Skip to main content

REVIEW article

Front. Vet. Sci., 21 February 2020
Sec. Zoological Medicine
Volume 7 - 2020 | https://doi.org/10.3389/fvets.2020.00003

Infectious Wildlife Diseases in Austria—A Literature Review From 1980 Until 2017

  • 1Department of Integrative Biology and Evolution, Research Institute of Wildlife Ecology, University of Veterinary Medicine Vienna, Vienna, Austria
  • 2Wildlife Conservation Society, Bronx, NY, United States

This literature review examines infectious wildlife disease research in Austria. We analyzed 226 research papers, published between 1980 and 2017. We determined that wildlife disease papers increased significantly from 0.8 ± 0.8 publications per year in the first decade (1980–1989) when compared to 2008–2017 with an average of 12.9 ± 4.1 publications per year. We illustrate information about the most investigated diseases and highlight the lack of research into certain wildlife pathogens. A special emphasis was given to diseases with zoonotic potential. The review showed that research focused on a few select species like the red fox (Vulpes vulpes), red deer (Cervus elaphus), and wild boar (Sus scrofa), all game species. Moreover, diseases affecting livestock and human health were seen more often. The review also found that only a low number of publications actually stated disease prevalence and confidence interval data. The reported diseases identified were classified according to their notifiable status and the distribution at the wildlife–human and wildlife–livestock interface. Furthermore, we try to argue why research into some diseases is prioritized, and why other diseases are underrepresented in current Austrian research. While spatiotemporal indicators could not be assessed due to the variability in methodologies and objectives of various studies, the information provided by this review offers the first comprehensive evaluation of the status of infectious wildlife disease research in Austria. Therefore, this study could assist investigators to identify further areas of priorities for research and conservation efforts and for wildlife management professionals to inform policy and funding strategies. With this review, we want to encourage research in the field of wildlife diseases in Austria to enhance current knowledge in the prevention of further loss in biodiversity and to find new measures to promote “One Health” on a global scale.

Introduction

We determined the status of infectious wildlife disease research in Austria based on a 37-year literature review between 1980 and 2017. The literature review was modeled on a similar study from the Republic of Korea in 2017 (1). One reason for conducting this review was to determine if an increase in so-called emerging infectious diseases (EIDs) had been noted in Austrian wildlife. It has previously been determined that that ~70% of EIDs have their origin in wildlife, and an estimated 60–80% of all EIDs also have zoonotic potential (2, 3). Increases in EIDs are related to the human impacts on landscapes (3, 4). In our constantly changing world, ecosystems continuously transform and offer pathogens novel opportunities to evolve, resulting in a greater diversity of adaptable and rapidly spreading infectious agents (5). Pathogens that can infect several species of hosts, so-called multihost pathogens, can also represent cause for concern with regard to wildlife conservation (6). Wildlife potentially contributes to the spread and maintenance of infectious diseases, and knowing the status supports addressing and mitigating impacts.

Austria has a population of ~8.8 million people (2017) with an average population density of 105 people/km2. The gross domestic product per capita is 37,100 euros (2016), which makes Austria one of the wealthiest countries in the European union (EU). A member of the European Union (EU) since 1995, the federal state of Austria is located in Central Europe and divided into nine provinces. Austria is a landlocked country with a land area of 83,879 km2 and a diversity of landscapes. About two-thirds of the land mass are mountainous, encompassing the Alps, the Carpathians, as well as the gneiss and granite highlands of the Bohemian Massif. The remaining third consists of the Vienna Basin and the Pannonian border regions of the Hungarian lowlands (79). The Austrian Fauna consists of roughly 45,870 different species, of which 626 are vertebrates. One hundred and ten vertebrates belong to the mammalian class, 418 to the avian class, 16 to the class of reptiles, 21 are amphibian species, and 60 species are fish (10).

Both active and passive surveillance programs for wildlife diseases exist in Austria (11, 12). Control programs were successful in eradicating rabies using widespread oral immunization of red fox (Vulpes vulpes). The last known rabies case occurred in 2003, and in 2008, Austria was declared rabies free. As of 2013, indicator animals (e.g., fox, badger, racoon dog, and raccoon) opportunistically were found dead, and all animals suspected of being rabid are examined at the National Reference Laboratory. Additional epizootic monitoring programs for Aujesky disease, bovine spongiform encephalopathy (BSE), scrapie, bluetongue virus, Brucella melitensis, bovine brucellosis, enzootic bovine leucosis, infectious bovine rhinotracheitis and infectious pustular vulvovaginitis, classical swine fever, and avian influenza are implemented. Only one zoonotic disease in wildlife is routinely monitored, namely, trichinosis in wild boars (Sus scrofa). In addition, in livestock animals, campylobacteriosis, echinococcosis, salmonellosis, trichinosis, and verotoxin-producing Escherichia coli are routinely monitored (13).

The wildlife-human interface in Austria consists of a number of critical points, such as game meat consumption, the hunting industry (e.g., direct contact between hunters, hunting dogs, and game animals) and tourism (e.g., hikers and recreational athletes). Occupations that involve a constant exposure to animals are related to a higher risk of infection, and this risk may be intensified through contact with livestock sharing pastures with wildlife. Risk groups include farmers, veterinarians, hunters, forestry workers, veterinary technicians, animal keepers, taxidermists, zookeepers, and people who prepare or consume game meat (1418).

Wildlife diseases are often not included in epidemiological reflections, as the main focus remains on diseases in livestock and transmission to humans. It is important to note that the wildlife-livestock interface is bidirectional and dynamic with frequent pathogen exchange through shared resources, such as habitats, water, and feed (19, 20). These factors increase the risk of transmitting infectious diseases from wildlife to domestic animals and subsequently to humans (19). Our review serves not only as an overview but also as a reminder that research on wildlife diseases is important and must be encouraged. This review is the first and only comprehensive review of infectious wildlife diseases in Austria.

Materials and Methods

A detailed literature search was conducted between October 2018 and December 2018 using the following literature data bases: “vetmedseeker” (vetmedseeker, University of Veterinary Medicine Vienna, Austria), “Scopus” (Scopus, Elsevier, Netherlands), “Ovid” (“Ovid Technologies,” Wolters Kluwer, Netherlands), “Web of Science” (Web of Science Core Collection, Clarivate Analytics, United States), and “PubMed” (NCBI Pubmed, National Center for Biotechnology Information, United States). Search terms used included “wildlife,” “diseases,” “infectious,” and “zoonosis” adjusted by setting the time frame to 1980–2017 and the affiliation to Austria. This resulted in 2,696 hits on “Scopus,” 1,284 hits on the “vetmedseeker,” 755 on “Ovid,” 473 on “PubMed,” and 180 on “Web of Science.” Only articles published in peer-reviewed journals were retained. Papers that addressed wildlife-human or wildlife-domestic disease transmission were also included. Additional articles found manually from the respective citations were included as well. A schematic step-by-step of the literature search can be found in Figure 1.

FIGURE 1
www.frontiersin.org

Figure 1. Overview of the work steps for drafting this review.

Following abstract review, 518 publications from “Scopus” appeared relevant. Papers were then compiled using a reference managing software (End Note Version X7.8, Thomson Reuters, United States). Duplicates, non-peer reviewed articles, book chapters, and conference proceedings were excluded in a first round. In a second round, we focused on infectious pathogens and diseases occurring in wild species. We excluded papers describing non-infectious, autoimmune, or idiopathic diseases. In addition, we restricted the search to vertebrates. Multicountry studies were only included in our review if “Austria” was mentioned in the materials and methods. In a third round, we excluded publications that addressed microbiological hygiene aspects in game meat. Subsequent to this process, it was clear that “Scopus” was the most efficient database for wildlife diseases, revealing 219 out of a total of 226 relevant publications. “PubMed,” in contrast, only showed 76 relevant articles. Finally, from all databases surveyed, 226 papers were retained and entered into a Microsoft Excel file for descriptive statistical analysis.

Publications were classified according to definitions by “Springer Nature” concerning article type (21) into original research articles, reviews, case reports, and short reports or letters. Original research articles were further subdivided into controlled studies and retrospective studies. Subsequently papers were categorized according to year of publication, type of pathogen, affected animal species, and group interface. The classification of group interfaces describes the primary group of interest (e.g., wildlife, humans, or livestock animals). Furthermore, we recorded whether the disease was notifiable according to the OIE List of notifiable diseases or the current Austrian legislation. If the paper covered various infectious agents, it was assigned to the categories “Notifiable in Austria” or “OIE-listed disease,” if at least one notifiable disease was included. In addition, it was noted if the prevalence and confidence intervals of the pathogen(s) were stated in the article.

Infectious agents were divided into parasitic, viral, bacterial, and fungal pathogens, and articles covering more than one pathogen or addressing more than one species were classified as “multiple infectious agents” or “multiple species affected.” Furthermore, agents were classified as zoonotic or having zoonotic potential. To determine the zoonotic potential of the diseases, the OIE list for infectious diseases, the “Merck Veterinary Manual” (22), as well as various textbooks (2326) were consulted. Diseases that are not yet known to have zoonotic potential or are currently being researched have been labeled as “unknown.”

Results

Publication Frequency

After review, we retained 226 publications, published between 1980 and 2017 (Figure 2). With the exception of the years 1981–1982, 1986, 1988, 1991, and 1993–1994, numerous wildlife disease papers were published. From 1995 onwards, there was a continuous increase in wildlife disease publications, with the most articles (n = 19) published in 2014. In 2007 and 2015, a drop in publications was noted, followed by an increase in the subsequent year. During the 37 years reviewed, 2000–2017 was most productive period with 89.4% of the retained articles published during this time period. Comparing the average yearly number of publications in the first decade (1980–1989 = 0.8 ± 0.8) to the last decade (2008–2017 = 12.9 ± 4.1) clearly shows a significant increase in interest in wildlife diseases (normality of data was tested by Shapiro-Wilk; two-tailed t-test: p = 0.01, t-statistics = −9.1178). Of the 226 papers, 146 publications were empirical studies, more specifically, 109 controlled studies, and 37 retrospective analyses. The rest was composed of 30 review articles, 34 case reports, and 16 letters or short reports (Figure 3).

FIGURE 2
www.frontiersin.org

Figure 2. Frequency of publications addressing wildlife diseases in Austria between 1980 and 2017.

FIGURE 3
www.frontiersin.org

Figure 3. Numerical amount of the different types of scientific publications according to the Springer classification.

Infectious Agents

The largest proportion of publications, namely 84 (37%), addressed infectious diseases caused by parasites (endoparasites: protozoa and helminths, or ectoparasites: arachnids and insects). A total of 67 (30%) of publications discussed viral diseases and 53 (23%) bacterial diseases, 9 (4%) dealt with diseases of fungal origin, and 13 (6%) papers mentioned multiple infectious agents (2741). We found no studies concerning diseases caused by prions (see Figure 4). In summary, we found 136 pathogens discussed in the 226 publications. For the complete list of all diseases and pathogens found in this study, see Table 1. Of these 136 infectious agents, 84 (62%) were only featured once, 23 (17%) were mentioned twice, and 12 (9%) were discussed three times. The remaining pathogens, namely 17 (12%), were featured more than three times. No clear trend was determined as to changes in which pathogenic agents were reported over the years (see Figure 5). Beyond the publications that discussed multiple pathogens (N > 10), Usutu virus was the most studied agent in Austria, with 14 published papers. It was followed by Echinococcus multilocularis (n = 11), West Nile Virus (n = 9), Trichinella sp. (n = 8), Toxoplasma gondii, Salmonella sp., Mycobacterium caprae, and Mycobacterium avium subsp. paratuberculosis with seven publications each. Also noteworthy are Fascioloides magna and Anaplasma phagocytophilum with six publications each, as well as Francisella tularensis, which was mentioned in five papers (see Figure 6).

FIGURE 4
www.frontiersin.org

Figure 4. Percentage of the infectious agents mentioned in all publications.

TABLE 1
www.frontiersin.org

Table 1. Infectious pathogens in alphabetical order, listing their zoonotic potential, notifiable status, animals affected, and authors, as found through our study.

FIGURE 5
www.frontiersin.org

Figure 5. Distribution of publications addressing either bacterial, viral, or parasitic diseases between 1980 and 2017.

FIGURE 6
www.frontiersin.org

Figure 6. Numerical depiction of diseases mentioned in all publications three times or more.

Zoonotic Potential

The review shows that 61% of papers discussed pathogens that have zoonotic potential, 21% of papers discussed diseases without zoonotic potential, and 5% discussed diseases with unclear zoonotic potential that would need further research (see Figures 7, 8).

FIGURE 7
www.frontiersin.org

Figure 7. Percentage of publications discussing the zoonotic potential of diseases.

FIGURE 8
www.frontiersin.org

Figure 8. Numbers of diseases with or without zoonotic potential, as well as diseases with currently unknown zoonotic potential.

Notifiable Status

A total of 77 publications addressed diseases notifiable in Austria according to Austrian legislation including the § 16. Federal law on epizootics, the Tuberculosis Act (1968), the Epidemic Act (1950), the Sexually Transmitted Diseases Act (1945), the BVD Regulation (2007), and the Paratuberculosis Ordinance (2006), while 67 publications mentioned OIE notifiable diseases (See Supplementary Tables 1, 2). Of the 77 publications addressing notifiable diseases in Austria, 48 also addressed notifiable diseases according to the OIE list. For 19 publications, our criteria were not applicable, as they did not mention an exact pathogen but multiple pathogens (N > 10) (see Figure 9). Of the 136 diseases detected, 24 diseases are notifiable according to current Austrian law. Six of these 24 diseases are notifiable as per the Austrian § 16. Federal law on epizootics, the remaining diseases are notifiable according to the above-mentioned laws (See Supplementary Tables 1, 2). Moreover, 20 diseases were found to be OIE-listed diseases (see Figure 10). Lastly, of the 24 diseases notifiable in Austria, 11 are also notifiable according to the OIE list.

FIGURE 9
www.frontiersin.org

Figure 9. Number of publications addressing diseases which are notifiable according to Austrian legislation and/or the OIE–World Organization for Animal Health compared to those addressing non-notifiable diseases.

FIGURE 10
www.frontiersin.org

Figure 10. Number of notifiable diseases described in retained papers according to Austrian legislation and the OIE compared to non-notifiable diseases.

Prevalence and Confidence Interval

Prevalence was indicated in a total of 99 (44%) publications. The confidence intervals, on the other hand, were only mentioned in 20 (9%) publications (see Figure 11).

FIGURE 11
www.frontiersin.org

Figure 11. Representation of the specification of prevalence and confidence interval (CI) in all the publications.

Animal Species

Both red deer (Cervus elaphus) and red foxes (V. vulpes) were each mentioned in 32 papers. These numbers were followed by wild boar (S. scrofa) (n = 25), chamois (Rupicapra rupicapra) (n = 21), roe deer (Capreolus capreolus) (n = 20), European brown hare (Lepus europeus) (n = 16), blackbird (Turdus merula) (n = 12), and fallow deer (Dama dama) (n = 10). Among the 10 most frequently described animal species, the domestic dog (Canis lupus familiaris) was the only domestic animal species. It occurred in a total of 12 papers. Furthermore, in 14 papers, multiple bird species were listed (see Figure 12).

FIGURE 12
www.frontiersin.org

Figure 12. Numerical occurrence of the individual wild animal species or group in the investigated literature.

In summary, we found 131 animal species or groups (e.g., genera, families, and orders) in the 226 publications. Of these, 58 were birds, followed by 55 mammal species, and 2 marsupial species. Reptiles and amphibians appear underrepresented by nine species or groups and seven species, respectively. Thirteen more categories were formed to describe those papers addressing more than 10 species or not stating an exact species. These included multiple bird, rodent, reptile psittacine bird, snake, amphibian and mammalian species, and domestic ruminants, wild ruminants, wild carnivores, wild ungulates, and game animals. Ninety six species or categories were mentioned once, whereas 12 were mentioned twice.

Risk Group Interfaces

A total of 163 publications addressed diseases that occurred exclusively in wild animals, conducted research solely with wild animals or took samples only from wildlife. In contrast, 12 papers dealt with diseases at the wildlife-human interface, and all of these diseases were zoonotic. In these 12 studies, humans and animals were sampled or results reported in humans and animals were discussed. Moreover, 25 publications addressed transmission and prevalence of diseases at the wildlife-livestock interface. Last but not least, 26 publications pertained to all interfaces, i.e., between wild animals, domesticated animals, and humans (see Figure 13).

FIGURE 13
www.frontiersin.org

Figure 13. Numerical allocation of the observed interfaces addressed in all publications.

Distinct Study Features

A total of 74 papers did not exhibit a specific trait according to our classification and were categorized under “No distinct feature.” In 53 publications, more than one specific pathogenic agent was mentioned. Furthermore, 46 papers referenced countries other than Austria. Diseases that emerged in captive wildlife were discussed in 44 publications. Thirteen studies addressed diseases emerging in wildlife but centered on human medicine (Figure 14). These included sampling of specific at-risk groups (e.g., hunters, veterinarians, animal keepers). Moreover, six papers dealt with game meat hygiene, and lastly, three publications were about environmental sampling for ubiquitous pathogens (e.g., Clostridium botulinum, avian botulism).

FIGURE 14
www.frontiersin.org

Figure 14. Distribution of different distinct features exhibited by all publications.

Discussion

According to the WHO, 75% of new EIDs or emerging diseases originate from animal reservoirs and thus have zoonotic potential. In the last 30 years, these EIDs have appeared as a consequence of the intensifying codependence in multiuse landscapes at the interface between animals and humans (249). This review provides a first insight into the state of knowledge on wildlife diseases in Austria between 1980 and 2017.

This literature review identified 226 publications between 1980 and 2017. More than half of the publications (65%) involved actively conducted research. The review also revealed that 15% of all papers were case reports. A majority of these case reports were based on pathology reports from the NRL of the AGES, the Institute of Pathology and the Research Institute of Wildlife Ecology at the University of Veterinary Medicine in Vienna. The existence of several facilities addressing wildlife pathogens and disease appears to have had a positive impact on the generation of knowledge in this field.

In comparison to a similar study from the Republic of Korea, which focused on the time span between 1982 and 2014 and found an average rate of 6.1 publications per year, our review yielded a higher total number of publications as well as a higher average amount of publications per year. (1). However, it has to be mentioned that our study covered a longer period of time. In the Korean review, viral diseases were reported on more often than in Austria. The most frequently researched diseases in Korea were avian influenza virus and rabies. In Austria, Usutu virus and E. multilocularis clearly dominated. As far as interfaces are concerned, research in Korea focused primarily on human and livestock diseases, whereas in Austria the main focus was on diseases in wildlife. In Korea, 24 zoonotic diseases were reported, whereas in Austria 78 have been investigated since 1980. Fifteen diseases that are notifiable according to the OIE list were mentioned in the Korean review; in contrast, 20 were reported in Austria. Birds dominated in the Korean review, while mammals, namely the red fox (V. vulpes) and the red deer (C. elaphus), were most reported on in Austria (1).

Infectious Agents

Parasitic diseases accounted for 37% of the papers, 30% were viral, and 23% were bacterial. Fungal diseases were only mentioned in 4% of all studies. Furthermore, we did not find a single study on transmissible spongiform encephalopathies or other diseases caused by prions. This may be due to the fact that only eight cases of BSE were detected in Austria between 2001 and 2010 (250). Austria was also declared as a country with negligible BSE risk by the OIE in 2012. However, it is prudent not to ignore TSEs in wildlife in view of the sudden emergence of chronic wasting disease in reindeer (Rangifer tarandus) and moose (Alces alces) in Finland and Norway in April 2016 (251).

Viral diseases were addressed in 30% of publications. The most studied viral pathogens were Usutu Virus and West Nile Virus. Since its first detection in 2001, Usutu Virus has been responsible for massive die-off of blackbirds (T. merula) in Europe. The first two human cases of Usutu Virus were detected in 2003 in Austria, generating a greater interest in this vector-borne disease (252). To a much lesser extent, avian Borna disease virus, avian pox virus, distemper virus, and Hantavirus/Puumala virus were also investigated.

Parasitic diseases accounted for 37% of papers. E. multilocularis, Trichinella sp., T. gondii, F. magna, A. phagocytophilum, and Neospora caninum were most often reported on. With the exception of F. magna and N. caninum, all of these are zoonotic.

When it comes to the bacterial pathogens, the most reported bacteria were Salmonella sp., M. caprae and M. avium subsp. paratuberculosis, F. tularensis, and methicillin-resistant Staphylococcus aureus. These are all zoonotic, potentially food borne and thus of high relevance to human health. The risk of a spillover or spillback of these bacterial diseases from wildlife to livestock is potentially quite high, as livestock and wildlife share mountain pastures in Austria.

Batrachochytrium dendrobatidis, a fungus that infects amphibians and is responsible for the global decline and even extinction of amphibians, was the most reported fungi and a classic EIDs (253).

Zoonotic Potential

The recovered papers are biased toward zoonotic diseases (61% n = 78). This is most likely due to funding being more readily available for diseases representing a human health risk. However, wildlife diseases without zoonotic potential should not be ignored, as they can also pose a risk to society, for example by causing major direct economic losses (e.g., ASF) and the loss of ecosystem services through species loss.

Notifiable Status

Of the 35 notifiable animal diseases in the Austrian federal law on epizootics, 7 were reported in the examined literature. In addition, the BVD Regulation 2007, BGBl. II No. 178/2007, and the Paratuberculosis Ordinance, BGBl. II No. 48/2006*, were of relevance, as both BVD and paratuberculosis were reported in wildlife (See Supplementary Tables 1, 2). The OIE list includes 117 diseases that can possibly infect or infest animals (254). In this review, we noted 20 diseases that are notifiable according to the OIE. Of the 29 diseases discussed more than two times, seven are notifiable according to the OIE list and the Austrian legislation, four are only notifiable in Austria, and three are only notifiable according to the OIE list.

Prevalence and Confidence Interval

Reporting prevalence is essential and provides insight into the epidemiological situation of a pathogen or disease entity in the sampled region. The disease prevalence was stated in 44% of publications. Of concern is that CI were only mentioned in 9% of the papers, thereby seriously limiting the significance of most studies and respective results. We found that 17 publications that provided a confidence interval for their results were research articles (e.g., controlled studies or retrospective studies). Providing confidence intervals did not increase over the 37 years reviewed. The authors of this study are of the opinion that appropriate descriptive statistics are not sufficiently employed in Austrian wildlife disease research at the present time.

Animal Species

Of roughly 626 different vertebrate species (including fish) native to Austria, only 21% have been addressed in this review. This demonstrates a huge untapped research potential in wildlife health research.

Mammals

The most studied mammalian species were the red fox (V. vulpes), the red deer (C. elaphus), the wild boar (S. scrofa), the chamois (R. rupicapra), the roe deer (C. capreolus), and the European brown hare (L. europeus). It is worth mentioning that these species represent the main game species in Austria. Again, it becomes clear that the primary focus of research has lain on species that serve as food source and offer recreational opportunities for humans. These animals pose a higher risk of transmitting zoonoses, generate funding, and therefore are more interesting to research. The wild boar is a species that has been of great interest to research, as populations are rapidly expanding both in absolute numbers and spatial distribution. Similar to many European countries, wild boar population management is increasingly difficult in Austria. One reason for the rapid reproduction of wild boar is climate change, resulting in increased food availability from beech nuts and acorns coupled with an increased number of litters and offspring survival. Since infection pressure potentially increases with population density, the wild boar population poses an important potential risk for domesticated pigs and humans from ASF or Trichinella spp. (214, 255).

Birds

The most studied bird species in Austria was the blackbird (T. merula) with references in 12 publications. Interestingly, all studies about blackbirds focused on Usutu virus related to the outbreak in Europe in 2000–2001. The mosquito-borne zoonotic Usutu virus has caused widespread deaths in blackbirds. Before the emergence of the disease in Austria, no previous research on this virus existed. Besides blackbirds, goshawks (Accipiter gentilis), feral pigeons (Columba livia domestica), and ducks were also of special interest to research. The Usutu virus highlights the fact that a large proportion of research related to wildlife diseases is opportunistic and initially reactive.

Reptiles and Amphibians

The captive bearded dragon (Pogona vitticeps) was the most studied reptile in Austria between 1980 and 2017 and appeared in four studies. However, no disease was mentioned more than once. Moreover, we were not able to identify any individual amphibian species that appeared more than once in the investigated publications. The reason for this low number of studies could be the scarcity of amphibian and reptile species in Austria. There are only 21 known native amphibian species and 16 reptile species in Austria (10).

Risk Group Interfaces

The majority (72%) of publications either prospectively sampled wild animal species or evaluated research results in retrospective studies. Numerous publications address the possibility of transmission of pathogens between the different interfaces (e.g., wildlife-livestock, wildlife-human). The remaining studies (28%) dealt with diseases affecting the interfaces between wildlife, livestock, and humans. These papers actively collected samples or performed retrospective studies on existing data across different interfaces. Our study shows that most of the publications addressed the fact that wildlife diseases can emerge in and cross various interfaces.

Distinct Study Features

We were able to identify seven categories within which we could further classify a subset of the papers. Publications could also exhibit more than one distinct feature. Fifty-three publications addressed more than one pathogen of which 42 were research papers. Six publications represented reviews. Furthermore, in 46 studies, countries other than Austria were mentioned. Only 44 studies dealt with captive wildlife or exotic pets. Research at the wildlife-human interface was documented in 13 studies, and these sampled both animals and humans. As the interface between wildlife and humans expands across Austria, it appears prudent to increase research and facilitate human and veterinary medical collaborations. Disease research on trichinosis, tularemia, tuberculosis, and echinococcosis would especially benefit from such collaborative one-health approaches.

Conclusion

Wildlife diseases will challenge research and medicine alike for years to come, as major changes due to the growing human population and environmental impacts increase. These impacts contribute to increased occurrence of diseases originating in wild animal species spilling over to humans. This review shows that increasing numbers of studies are being conducted in Austria. However, there is still room for further research. With the exception of prions, all infectious agents (viruses, bacteria, parasites, and fungi) have been investigated. Although there have been numerous studies on zoonoses, we have to stress the importance for future research to focus more strongly on disease dynamics and transmission at the wildlife-human interface. We acknowledge that wildlife disease studies frequently lack prevalence data, or data are of poor quality, to perform robust prevalence calculations. However, it appears that data essential to prevalence statement are not always available, especially in single case reports or due to the bias produced by passive surveillance sampling. Therefore, researchers may often decide not to include prevalence data, since it could be misinterpreted or even speculative. We would suggest that future wildlife disease-related studies should include prevalence data if possible, or state other appropriate measures and methods for statistical and epidemiological characterization of a disease event. Similarly, it appears important to expand the scope of the species investigated in the future. Funding is most often only available during impactful events, such as outbreaks, but is notably lacking for baseline research on wildlife, ecosystems, and diseases. Our assumption that there would be an increase in the number of publications on wildlife diseases in Austria over the period examined was confirmed. Considering our hypothesis, spatiotemporal indicators would have been beneficial to our review. However, due to the quality of the available data, its variability in consistency regarding study design, objectives, and methodologies of the investigated studies (e.g., multiple sampling sites, sampling across longer periods of time, multiple diseases in the same study), stating spatiotemporal indicators would have exceeded the clearly defined scope of this initial study. We believe this question would be best addressed in a separate and future analysis. We hope that this review provides information about the current research status for wildlife ecologists, veterinarians, and officials alike and incentivizes further research that employs “One Health” approaches.

Author Contributions

NT did the literature research and wrote the manuscript. CW planned the review concept and working steps, and edited the manuscript.

Funding

Funding was provided internally by the University of Veterinary Medicine of Vienna.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We would like to thank Dr. P. K. Walzer for improving and revising our manuscript in terms of grammar and style.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2020.00003/full#supplementary-material

Abbreviations

ADNS, Animal Disease Notification System; AGES, Austrian Agency for Health and Food Safety; ASF, African swine fever; AT, Austria; AVR, Annual Veterinary Report; BSE, Bovine spongiform encephalopathy; BVD, Bovine viral diarrhea; CI, Confidence interval; CWD, Chronic wasting disease; EFSA, European Food Safety Authority; EID, Emerging infectious disease; EU, European Union; KVG, Kommunikationsplattform VerbraucherInnengesundheit; MRSA, Methicillin-resistant Staphylococcus aureus; NA, Not applicable; NCBI, National Center for Biotechnology Information; NRL, National Reference Laboratory of the AGES; OIE, World Organization for Animal Health; RZZA, Report of Zoonoses and Zoonotic Agents; TSE, Transmissible spongiform encephalopathy; TSG, Tierseuchengesetz, Federal law on epizootics; WNV, West Nile Virus.

References

1. Hwang J, Lee K, Kim YJ, Sleeman JM, Lee H. Retrospective analysis of the epidemiologic literature, 1990–2015, on wildlife-associated diseases from the republic of Korea. J Wildlife Dis. (2017) 53:5–18. doi: 10.7589/2015-12-348

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Hassell JM, Begon M, Ward MJ, Fèvre EM. Urbanization and disease emergence: dynamics at the wildlife–livestock–human interface. Trends Ecol Evol. (2017) 32:55–67. doi: 10.1016/j.tree.2016.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, et al. Global trends in emerging infectious diseases. Nature. (2008) 451:990–3. doi: 10.1038/nature06536

PubMed Abstract | CrossRef Full Text | Google Scholar

4. McFarlane R, Sleigh A, McMichael T. Synanthropy of wild mammals as a determinant of emerging infectious diseases in the Asian-Australasian region. EcoHealth. (2012) 9:24–35. doi: 10.1007/s10393-012-0763-9

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Coker R, Rushton J, Mounier-Jack S, Karimuribo E, Lutumba P, Kambarage D, et al. Towards a conceptual framework to support one-health research for policy on emerging zoonoses. Lancet Infect Dis. (2011) 11:326–31. doi: 10.1016/S1473-3099(10)70312-1

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Gortázar C, Ferroglio E, Höfle U, Frölich K, Vicente J. Diseases shared between wildlife and livestock: a European perspective. Eur J Wildlife Res. (2007) 53:241–56. doi: 10.1007/s10344-007-0098-y

CrossRef Full Text | Google Scholar

7. StatistikAustria. Bevölkerung. (2019). Available online at: https://www.statistik.at/web_de/statistiken/menschen_und_gesellschaft/bevoelkerung/index.html (accessed February 8, 2019).

Google Scholar

8. Statisitk Austria. Austria. Data Figures Facts. (2018). Available online at: https://eu2018.statistik.at/fileadmin/euratspraesidentschaft/downloads/austria._data._figures._facts.pdf (accessed February 8, 2019).

9. Wikipedia. Austria. (2019). Available online at: https://en.wikipedia.org/wiki/Austria#Geography (accessed February 08, 2019).

Google Scholar

10. Geiser E. Wie viele tierarten leben in österreich? Erfassung, Hochrechnung und Abschätzung. Vcrii Zool Bot Ges Österreich. (1998) 135:81–93.

Google Scholar

11. Herzog U, Damoser J, Höflechner-Pöltl A. Annual Veterinary Report 2017. Federal Ministry of Labour, Social Affairs, Health and Consumer Protection and Austrian and Agency for Health and Food Safety (AGES), Vienna (2017). p. 1–84.

Google Scholar

12. Federal Ministry of Labour, Social Affairs, Health and Consumer Protection and Austrian Agency for Health and Food Safety. Zoonoses and Zoonotic agents in Austria. Report 2017. Vienna (2018). p. 1–84.

Google Scholar

13. Kommunikationsplattform VerbraucherInnengesundheit (KVG). Überwachung. (2019). Available online at: https://www.verbrauchergesundheit.gv.at/tiere/krankheiten/ueberwachung/ueberwachung.html (accessed May 8, 2019).

14. Deutz A, Fuchs K, Auer H, Schuller W, Nowotny N, Kerbl U, et al. Zoonoses, seroepidemiological examination of different persons for selected contact zoonoses: seroprevalences, risk factors and preventive measures. Fleischwirtschaft. (2002) 82:101–4.

15. Deutz A, Köfer J. Small game (fox, brown hare, pheasant and duck) as carriers of zoonoses. Berl Mun Tierarztl Wochenschr. (2000) 113:401–6. doi: 10.7748/paed.12.3.11.s15

CrossRef Full Text | Google Scholar

16. Fink M, Schleicher C, Gonano M, Prodinger WM, Pacciarini M, Glawischnig W, et al. Red deer as maintenance host for bovine tuberculosis, alpine region. Emerg Infect Dis. (2015) 21:464–7. doi: 10.3201/eid2103.141119

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Kainz R, Paulsen P. Changes in EU hygiene legislation for meat from hunted game. Wien Tierarztl Monatsschr. (2005) 92:150–6.

18. Posautz A, Gyuranecz M, Denes B, Knauer F, Dier H, Walzer C. Seroprevalence of Francisella tularensis in Austrian hunting dogs. Vector Borne Zoon Dis. (2017) 18:117–9. doi: 10.1089/vbz.2017.2193

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Wiethoelter AK, Beltrán-Alcrudo D, Kock R, Mor SM. Global trends in infectious diseases at the wildlife-livestock interface. Proc Natl Acad Sci USA. (2015) 112:9662–7. doi: 10.1073/pnas.1422741112

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Daszak P, Cunningham AA, Hyatt AD. Anthropogenic environmental change and the emergence of infectious diseases in wildlife. Acta Trop. (2001) 78:103–16. doi: 10.1016/S0001-706X(00)00179-0

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Springer. Types of Journal Articles. (2019). Avaialble online at: https://www.springer.com/gp/authors-editors/authorandreviewertutorials/writing-a-journal-manuscript/types-of-journal-articles/10285504 (accessed February 8, 2019).

Google Scholar

22. Aiello SE, Moses MA. The Merck Veterinary Manual. 11th ed. Kenilworth, NJ: Merck & Co., Inc. (2016).

Google Scholar

23. Boch J, Supperer R. Veterinärmedizinische Parasitologie. 3rd ed. Berlin: Parey (2006).

24. Deplazes P, Eckert J, Samson-Himmelstjerna GV, Zahner H. Lehrbuch der Parasitologie für die Tiermedizin. 3rd ed. Stuttgart: Enke (2013).

Google Scholar

25. Rolle M, Mayr A, Büttner M. Medizinische Mikrobiologie, Infektions- und Seuchenlehre. 8th ed. Stuttgart: Enke (2007).

Google Scholar

26. Selbit H-J, Truyen U, Valentin-Weigand P, Alber G. Tiermedizinische Mikrobiologie, Infektions- und Seuchenlehre. 9th ed. Stuttgart: Enke (2011).

Google Scholar

27. Rehbein S, Visser M. Die Endoparasiten des Sikawildes (Cervus nippon) in Österreich. Wien Klin Wochenschr. (2007) 119:96–101. doi: 10.1007/s00508-007-0865-5

CrossRef Full Text | Google Scholar

28. Winkelmayer R, Paulsen P. Parasites in free-living wild game: relevance for meat hygiene and possibilities of detection. Wien Tierarztl Monatsschr. (2011) 98:239–44.

29. Schwarz L, Frena M, Skalicky M, Prosl H. Endoparasite infestation of roe deer from a hunting ground in Lower Austria. Wien Tierarztl Monatsschr. (2011) 98:285–91.

Google Scholar

30. Hoby S, Walzer C, Slotta-Bachmayr L, Segner H, Robert N. Pathological investigations in free-ranging ungulates in the National Park Hohe Tauern, Austria. Wien Tierarztl Monatsschr. (2006) 93:104–12.

31. Juncker-Voss M, Prosl H, Lussy H, Enzenberg U, Auer H, Lassnig H, et al. Screening for antibodies against zoonoses among employees of the Zoological Garden of Vienna, Schönbrunn, Austria. Berl Munch Tierarztl Wochenschr. (2004) 117:404–9.

Google Scholar

32. Duscher G, Leschnik M, Führer HP, Joachim A. Wildlife reservoirs for vector-borne canine, feline and zoonotic infections in Austria. Int J Parasitol. (2015) 4:88–96. doi: 10.1016/j.ijppaw.2014.12.001

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Deutz A, Fuchs K, Schuller W, Nowotny N, Auer H, Aspock H, et al. Seroepidemiological studies of zoonotic infections in hunters in southeastern Austria - prevalences, risk factors, and preventive methods. Berl Munch Tierarztl Wochenschr. (2003) 116:306–11.

PubMed Abstract | Google Scholar

34. Duscher T, HodŽić A, Glawischnig W, Duscher G. The raccoon dog (Nyctereutes procyonoides) and the raccoon (Procyon lotor) - their role and impact of maintaining and transmitting zoonotic diseases in Austria, Central Europe. Parasitol Res. (2017) 116:1411–6. doi: 10.1007/s00436-017-5405-2

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Deutz A, Hinterdorfer F. Diseases in brown hare: Post-mortem findings, range of pathogens and zoonotic aspects. Tierarztl Umschau. (2000) 55:628–35.

Google Scholar

36. Khayal B, Hess M, Bagó Z. Pathomorphological investigations on wild birds during the winter season 2005/2006. Wien Tierarztl Monatsschr. (2010) 97:125–34.

Google Scholar

37. Wascher CAF, Bauer AC, Holtmann AR, Kotrschal K. Environmental and social factors affecting the excretion of intestinal parasite eggs in graylag geese. Behav Ecol. (2012) 23:1276–83. doi: 10.1093/beheco/ars113

CrossRef Full Text | Google Scholar

38. Rehbein S, Visser M, Jekel I, Silaghi C. Endoparasites of the fallow deer (Dama dama) of the Antheringer Au in Salzburg, Austria. Wien Klin Wochenschr. (2014) 126 (Suppl.1):37–41. doi: 10.1007/s00508-014-0506-8

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Schmidt-Ukaj S, Hochleithner M, Richter B, Hochleithner C, Brandstetter D, Knotek Z. A survey of diseases in captive bearded dragons: a retrospective study of 529 patients. Vet Med. (2017) 62:508–15. doi: 10.17221/162/2016-VETMED

CrossRef Full Text | Google Scholar

40. Hoby S, Schwarzenberger F, Doherr MG, Robert N, Walzer C. Steroid hormone related male biased parasitism in chamois, Rupicapra rupicapra. Vet Parasitol. (2006) 138:337–48. doi: 10.1016/j.vetpar.2006.01.028

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Deutz A, Köfer J. Pig and wild boar as carriers of zoonoses. Berl Munch Tierarztl Wochenschr. (1999) 112:305–10.

Google Scholar

42. Kübber-Heiss A, Benetka V, Filip T, Benyr G, Schilcher F, Pallan C, et al. First detection of an adenovirus infection in a bearded dragon (Pogona vitticeps) in Austria. Wien Tierarztl Monatsschr. (2006) 93:68–72.

43. Duscher G. Duncker's muscle fluke—Alaria alata in red foxes from Austria in relation to the occurrence of wild boars. Wien Tierarztl Monatsschr. (2011) 98:251–4.

44. Paulsen P, Ehebruster J, Irschik I, Lücker E, Riehn K, Winkelmayer R, et al. Findings of Alaria alata mesocercariae in wild boars (Sus scrofa) in eastern Austria. Eur J Wildlife Res. (2012) 58:991–5. doi: 10.1007/s10344-012-0642-2

CrossRef Full Text | Google Scholar

45. Sailer A, Glawischnig W, Irschik I, Lücker E, Riehn K, Paulsen P. Findings of Alaria alata mesocercariae in wild boar in Austria: current knowledge, identification of risk factors and discussion of risk management options. Wien Tierarztl Monatsschr. (2012) 99:346–52.

Google Scholar

46. Petrovec M, Sixl W, Schweiger R, Mikulašek S, Elke L, Wüst G, et al. Infections of wild animals with Anaplasma phagocytophila in Austria and the Czech republic. Ann NY Acad Sci. (2003) 990:103–6. doi: 10.1111/j.1749-6632.2003.tb07345.x

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Polin H, Hufnagl P, Haunschmid R, Gruber F, Ladurner G. Molecular evidence of Anaplasma phagocytophilum in Ixodes ricinus ticks and wild animals in Austria. J Clin Microbiol. (2004) 42:2285–6. doi: 10.1128/JCM.42.5.2285-2286.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Silaghi C, Hamel D, Pfister K, Rehbein S. Babesia species and co-infection with Anaplasma phagocytophilum in free-ranging ungulates from tyrol (Austria). Wien Tierarztl Monatsschr. (2011) 98:268–74.

Google Scholar

49. Silaghi C, Hamel D, Thiel C, Pfister K, Friche Passos LM, Rehbein S. Genetic variants of Anaplasma phagocytophilum in wild caprine and cervid ungulates from the alps in tyrol, Austria. Vector-Borne Zoonotic Dis. (2011) 11:355–62. doi: 10.1089/vbz.2010.0051

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Leschnik M, Kirtz G, Virányi Z, Wille-Piazzai W, Duscher G. Acute granulocytic anaplasmosis in a captive timber wolf (Canis lupus occidentalis). J Zoo Wildlife Med. (2012) 43:645–8. doi: 10.1638/2011-0224R.1

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Cezanne R, Mrowietz N, Eigner B, Duscher G, Glawischnig W, Führer HP. Molecular analysis of Anaplasma phagocytophilum and Babesia divergens in red deer (Cervus elaphus) in Western Austria. Mol Cell Probes. (2016) 31:55–8. doi: 10.1016/j.mcp.2016.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Kotsch V, Kübber-Heiss A, Url A, Walzer C, Schmidt P. Diseases of captive cheetahs (Acinonyx jubatus) within the European endangered species program (EEP)—A 22-year retrospective histopathological study. Wien Tierarztl Monatsschr. (2002) 89:341–50.

53. Pfeffer M, Dobler G. Emergence of zoonotic arboviruses by animal trade and migration. Parasit Vect. (2010) 3:35. doi: 10.1186/1756-3305-3-35

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Auer H. Parasites of huntable game dangerous for people in Austria. Wien Tierarztl Monatsschr. (2011) 98:245–50.

55. Frigerio D, Cibulski L, Ludwig SC, Campderrich I, Kotrschal K, Wascher CAF. Excretion patterns of coccidian oocysts and nematode eggs during the reproductive season in Northern Bald Ibis (Geronticus eremita). J Ornithol. (2016) 157:839–51. doi: 10.1007/s10336-015-1317-z

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Pardeike J, Weber S, Zarfl HP, Pagitz M, Zimmer A. Itraconazole-loaded nanostructured lipid carriers (NLC) for pulmonary treatment of aspergillosis in falcons. Eur J Pharm Biopharm. (2016) 108:269–76. doi: 10.1016/j.ejpb.2016.07.018

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Thaller D, Bilek A, Revilla-Fernández S, Bagó Z, Schildorfer H, Url A, et al. Diagnosis of aujeszky's disease in a dog in Austria. Wien Tierarztl Monatsschr. (2006) 93:62–7.

58. Leschnik M, Gruber A, Kübber-Heiss A, Bagó Z, Revilla-Fernández S, Wodak E, et al. Epidemiological aspects of aujeszky's disease in Austria by the means of six cases in dogs. Wien Tierarztl Monatsschr. (2012) 99:82–90.

59. Steinrigl A, Revilla-Fernández S, Kolodziejek J, Wodak E, Bagó Z, Nowotny N, et al. Detection and molecular characterization of Suid herpesvirus type 1 in Austrian wild boar and hunting dogs. Vet Microbiol. (2012) 157:276–84. doi: 10.1016/j.vetmic.2011.12.033

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Weissenböck H, Bakonyi T, Sekulin K, Ehrensperger F, Doneley RJT, Dürrwald R, et al. Avian bornaviruses in psittacine birds from Europe and Australia with proventricular dilatation disease. Emerg Infect Dis. (2009) 15:1453–9. doi: 10.3201/eid1509.090353

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Weissenböck H, Sekulin K, Bakonyi T, Högler S, Nowotny N. Novel Avian bornavirus in a nonpsittacine species (canary; Serinus canaria) with enteric ganglioneuritis and encephalitis. J Virol. (2009) 83:11367–71. doi: 10.1128/JVI.01343-09

PubMed Abstract | CrossRef Full Text

62. Weissenböck H, Fragner K, Nedorost N, Mostegl MM, Sekulin K, Maderner A, et al. Localization of avian bornavirus RNA by in situ hybridization in tissues of psittacine birds with proventricular dilatation disease. Vet Microbiol. (2010) 145:9–16. doi: 10.1016/j.vetmic.2010.02.030

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Nedorost N, Maderner A, Kolodziejek J, Lussy H, Nowotny N, Weissenböck H. Identification of mixed infections with different genotypes of avian bornaviruses in psittacine birds with proventricular dilatation disease. Avian Dis. (2012) 56:414–7. doi: 10.1637/10026-112911-ResNote.1

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Zhang X, Bilic I, Troxler S, Hess M. Evidence of genotypes 1 and 3 of Avian hepatitis E virus in wild birds. Virus Res. (2017) 228:75–8. doi: 10.1016/j.virusres.2016.11.028

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Globig A, Baumer A, Revilla-Fernández S, Beer M, Wodak E, Fink M, et al. Ducks as sentinels for avian influenza in wild birds. Emerg Infect Dis. (2009) 15:1633–6. doi: 10.3201/eid1510.090439

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Fink M, Fernández SR, Schobesberger H, Koefer J. Geographical spread of highly pathogenic avian influenza virus H5N1 during the 2006 outbreak in Austria. J Virol. (2010) 84:5815–23. doi: 10.1128/JVI.01642-09

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Loupal G, Schönbauer M, Jahn J. Pocken bei Zoo - und wildvögeln: licht - und elektronenmikroskopische untersuchungen. Z Vet Reihe B. (1985) 32:326–36. doi: 10.1111/j.1439-0450.1985.tb01969.x

CrossRef Full Text | Google Scholar

68. Reiter AS, Loupal G. A case of pox in the great bustard (Otis tarda) of the hanság population in Austria. J Ornithol. (1995) 136:221–3. doi: 10.1007/BF01651245

CrossRef Full Text

69. Gruber A, Grabensteiner E, Kolodziejek J, Nowotny N, Loupal G. Poxvirus infection in a great tit (Parus major). Avian Dis. (2007) 51:623–5. doi: 10.1637/0005-2086(2007)51[623:PIIAGT]2.0.CO;2

PubMed Abstract | CrossRef Full Text | Google Scholar

70. Pichler R, Posautz A, Beer T. Avian pox virus in a female bald eagle (Haliaeetus leucocephalus) - a case report. Wien Tierarztl Monatsschr. (2016) 103:321–5.

71. Mitková B, Hrazdilová K, D'Amico G, Duscher G, Suchentrunk F, Forejtek P, et al. Eurasian golden jackal as host of canine vector-borne protists. Parasit Vect. (2017) 10:183. doi: 10.1186/s13071-017-2110-z

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Duscher G, Führer HP, Kubber-Heiss A. Fox on the run - molecular surveillance of fox blood and tissue for the occurrence of tick-borne pathogens in Austria. Parasit Vect. (2014) 7:521. doi: 10.1186/PREACCEPT-1542240345144663

PubMed Abstract | CrossRef Full Text | Google Scholar

73. HodŽić A, Zörer J, Duscher G. Dermacentor reticulatus, a putative vector of Babesia cf. microti (syn. theileria annae) piroplasm. Parasitol Res. (2017) 116:1075–7. doi: 10.1007/s00436-017-5379-0

PubMed Abstract | CrossRef Full Text | Google Scholar

74. Corduneanu A, Hrazdilová K, Sándor AD, Matei IA, Ionicǎ AM, Barti L, et al. Babesia vesperuginis, a neglected piroplasmid: new host and geographical records, and phylogenetic relations. Parasit Vect. (2017) 10:598. doi: 10.1186/s13071-017-2536-3

PubMed Abstract | CrossRef Full Text | Google Scholar

75. Hinaidy HK. Blutparasiten der wildlebenden wiederkäuer österreichs. J Veterin Med Ser B. (1987) 34:81–97. doi: 10.1111/j.1439-0450.1987.tb00374.x

CrossRef Full Text | Google Scholar

76. Schmidt S, Essbauer SS, Mayer-Scholl A, Poppert S, Schmidt-Chanasit J, Klempa B, et al. Multiple infections of rodents with zoonotic pathogens in Austria. Vector Borne Zoo Dis. (2014) 14:467–75. doi: 10.1089/vbz.2013.1504

PubMed Abstract | CrossRef Full Text | Google Scholar

77. Richter B, Kübber-Heiss A. First detection of chytridiomycosis associated with fatalities in poison dart frogs (Dendrobates tinctorlus) in Austria. Wien Tierarztl Monatsschr. (2010) 97:157–60.

Google Scholar

78. Sztatecsny M, Glaser F. From the eastern lowlands to the western mountains: first records of the chytrid fungus Batrachochytrium dendrobatidis in wild amphibian populations from Austria. Herpetol J. (2011) 21:87–90.

Google Scholar

79. Lötters S, Kielgast J, Sztatecsny M, Wagner N, Schulte U, Werner P, et al. Absence of infection with the amphibian chytrid fungus in the terrestrial alpine salamander (Salamandra atra). Salamandra. (2012) 48:58–62. doi: 10.5167/uzh-62111

CrossRef Full Text | Google Scholar

80. d'Ovidio D, Pantchev N, Noviello E, Del Prete L, Maurelli MP, Cringoli G, et al. Survey of Baylisascaris spp. in captive striped skunks (mephitis mephitis) in some European areas. Parasitol Res. (2017) 116:483–6. doi: 10.1007/s00436-016-5307-8

PubMed Abstract | CrossRef Full Text | Google Scholar

81. Dürrwald R, Kolodziejek J, Muluneh A, Herzog S, Nowotny N. Epidemiological pattern of classical Borna disease and regional genetic clustering of Borna disease viruses point towards the existence of to-date unknown endemic reservoir host populations. Microb Infect. (2006) 8:917–29. doi: 10.1016/j.micinf.2005.08.013

PubMed Abstract | CrossRef Full Text | Google Scholar

82. Shibly S, Schmidt P, Robert N, Walzer C, Url A. Immunohistochemical screening for viral agents in cheetahs (Acinonyx jubatus) with myelopathy. Veterin Rec. (2006) 159:557–61. doi: 10.1136/vr.159.17.557

PubMed Abstract | CrossRef Full Text | Google Scholar

83. Weissenböck H, Bagó Z, Kolodziejek J, Hager B, Palmetzhofer G, Dürrwald R, et al. Infections of horses and shrews with Bornaviruses in upper Austria: a novel endemic area of borna disease. Emerg Microb Infect. (2017) 6:e52. doi: 10.1038/emi.2017.36

PubMed Abstract | CrossRef Full Text | Google Scholar

84. Leitner N, Schwarzmann L, Zittra C, Palmieri N, Eigner B, Otranto D, et al. Morphological and molecular identification of nasopharyngeal bot fly larvae infesting red deer (Cervus elaphus) in Austria. Parasitol Res. (2016) 115:4417–22. doi: 10.1007/s00436-016-5206-z

PubMed Abstract | CrossRef Full Text | Google Scholar

85. Krametter R, Nielsen SS, Loitsch A, Froetscher W, Benetka V, Moestl K, et al. Pestivirus exposure in free-living and captive deer in Austria. J Wildlife Dis. (2004) 40:791–5. doi: 10.7589/0090-3558-40.4.791

PubMed Abstract | CrossRef Full Text | Google Scholar

86. Glawischnig W, Schoepf K, Matt M. Monitoring for Bovine viral diarrhea virus in Austrian red deer (Cervus elaphus elaphus) by using ear-notch samples. J Wildlife Dis. (2010) 46:1269–73. doi: 10.7589/0090-3558-46.4.1269

PubMed Abstract | CrossRef Full Text | Google Scholar

87. Scholz HC, Hofer E, Vergnaud G, Fleche PL, Whatmore AM, Dahouk SA, et al. Isolation of Brucella microti from mandibular lymph nodes of red foxes, (Vulpes vulpes), in lower Austria. Vector Borne Zoo Dis. (2009) 9:153–5. doi: 10.1089/vbz.2008.0036

PubMed Abstract | CrossRef Full Text | Google Scholar

88. Al Dahouk S, Hofer E, Tomaso H, Vergnaud G, Le Flèche P, Cloeckaert A, et al. Intraspecies diodiversity of the genetically homologous species Brucella microti. Appl Environ Microbiol. (2012) 78:1534–43. doi: 10.1128/AEM.06351-11

PubMed Abstract | CrossRef Full Text | Google Scholar

89. Hofer E, Reisp K, Revilla-Fernández S, Plicka H, Romanek G, Bagó Z, et al. Isolation of Francisella tularensis and Brucella suis from red foxes (Vulpes vulpes). Tierarztli Umschau. (2010) 65:229–32.

Google Scholar

90. Scholz HC, Revilla-Fernández S, Dahouk SA, Hammerl JA, Zygmunt MS, Cloeckaert A, et al. Brucella vulpis sp. nov, isolated from mandibular lymph nodes of red foxes (Vulpes vulpes). Intl J Syst Evol Microbiol. (2016) 66:2090–8. doi: 10.1099/ijsem.0.000998

PubMed Abstract | CrossRef Full Text | Google Scholar

91. Winkelmayer R, Vodnansky M, Paulsen P, Gansterer A, Treml F. Explorative study on the seroprevalence of Brucella-, Francisella- and Leptospira antibodies in the European hare (Lepus europaeus) of the Austrian—Czech border region. Wien Tierarztl Monatsschr. (2005) 92:131–5.

Google Scholar

92. Hofer E, Revilla-Fernández S, Al Dahouk S, Riehm JM, Nöckler K, Zygmunt MS, et al. A potential novel Brucella species isolated from mandibular lymph nodes of red foxes in Austria. Vet Microbiol. (2012) 155:93–9. doi: 10.1016/j.vetmic.2011.08.009

PubMed Abstract | CrossRef Full Text | Google Scholar

93. Konicek C, VodráŽka P, Barták P, Knotek Z, Hess C, Račka K, et al. Detection of zoonotic pathogens in wild birds in the cross-border region Austria—Czech republic. J Wildlife Dis. (2016) 52:850–61. doi: 10.7589/2016-02-038

PubMed Abstract | CrossRef Full Text | Google Scholar

94. Troxler S, Hess C, Konicek C, Knotek Z, Barták P, Hess M. Microdilution testing reveals considerable and diverse antimicrobial resistance of Escherichia coli, thermophilic Campylobacter spp. and Salmonella spp. isolated from wild birds present in urban areas. Eur J Wildlife Res. (2017) 63:68. doi: 10.1007/s10344-017-1125-2

CrossRef Full Text | Google Scholar

95. HodŽić A, Cezanne R, Duscher G, Harl J, Glawischnig W, Führer HP. Candidatus Neoehrlichia sp. in an Austrian fox is distinct from candidatus neoehrlichia mikurensis, but closer related to candidatus neoehrlichia lotoris. Parasit Vectors. (2015) 8:1163. doi: 10.1186/s13071-015-1163-0

PubMed Abstract | CrossRef Full Text | Google Scholar

96. HodŽić A, Bruckschwaiger P, Duscher G, Glawischnig W, Führer HP. High prevalence of Eucoleus boehmi (syn. Capillaria boehmi) in foxes from western Austria. Parasitol Res. (2016) 115:3275–8. doi: 10.1007/s00436-016-5145-8

PubMed Abstract | CrossRef Full Text | Google Scholar

97. Führer HP. An overview of the host spectrum and distribution of Calodium hepaticum (syn. Capillaria hepatica): part 1 - Muroidea. Parasitol Res. (2014) 113:619–40. doi: 10.1007/s00436-013-3691-x

CrossRef Full Text | Google Scholar

98. Führer HP. An overview of the host spectrum and distribution of Calodium hepaticum (syn. Capillaria hepatica): part 2 - Mammalia (excluding Muroidea). Parasitol Res. (2014) 113:641–51. doi: 10.1007/s00436-013-3692-9

CrossRef Full Text | Google Scholar

99. Führer HP, Schneider R, Walochnik J, Auer H. Extraintestinal helminths of the common vole (Microtus arvalis) and the water vole (Arvicola terrestris) in Western Austria (Vorarlberg). Parasitol Res. (2010) 106:1001–4. doi: 10.1007/s00436-010-1753-x

PubMed Abstract | CrossRef Full Text | Google Scholar

100. Benetka V, Grabensteiner E, Gumpenberger M, Neubauer C, Hirschmüller B, Möstl K. First report of an iridovirus (Genus Ranavirus) infection in a leopard tortoise (Geochelone pardalis pardalis). Wien Tierarztl Monatsschr. (2007) 94:243–8.

Google Scholar

101. Stephan S, Guerra D, Pospischil A, Hilbe M, Weissenböck H, Novotný L, et al. Chlamydiaceae and chlamydia-like organisms in free-living small mammals in Europe and Afghanistan. J Wildlife Dis. (2014) 50:195–204. doi: 10.7589/2013-08-194

PubMed Abstract | CrossRef Full Text | Google Scholar

102. Schmidt-Ukaj S, Loncaric I, Klang A, Spergser J, Häbich AC, Knotek Z. Infection with Devriesea agamarum and Chrysosporium guarroi in an inland bearded dragon (Pogona vitticeps). Vet Dermatol. (2014) 25:555–97. doi: 10.1111/vde.12146

PubMed Abstract | CrossRef Full Text | Google Scholar

103. Kissling R, Krocza W. On the diagnosis of duck-sickness in an area near illmitz, Austria. Wien Tierarztl Monatsschr. (1984) 71:327–9.

104. Zechmeister TC, Kirschner AKT, Fuchsberger M, Gruber SG, Süß B, Rosengarten R, et al. Prevalence of botulinum neurotoxin C1 and its corresponding gene in environmental samples from low and high risk avian botulism areas. Altex. (2005) 22:185–95.

PubMed Abstract | Google Scholar

105. Sipos W, Fischer L, Schindler M, Schmoll F. Genotyping of Clostridium perfringens isolated from domestic and exotic ruminants and swine. J Veterin Med Ser B Infect Dis Veterin Pub Health. (2003) 50:360–2. doi: 10.1046/j.1439-0450.2003.00690.x

PubMed Abstract | CrossRef Full Text | Google Scholar

106. Burgstaller J, Burgstaller A, Mansfeld MD. Infection with Clostridium septicum in a chamois (Rupicapra rupicapra). Wien Tierarztl Monatsschr. (2014) 101:98–102.

Google Scholar

107. Burtscher H. Große coccidien-gewebszysten im gehirn von Gracula religiosa (Aves: Sturnidae). Zentralblatt Veterinärmedizin Reihe B. (1983) 30:590–9. doi: 10.1111/j.1439-0450.1983.tb01885.x

CrossRef Full Text | Google Scholar

108. Prosl H, Loupal G. Diagnosis of an infestation with Collyriclum faba (Bremser, 1831) in a starling (Sturnus vulgaris L.) in Vienna. Tierarztli Praxis. (1985) 13:177–179.

PubMed Abstract | Google Scholar

109. Foerster S, Chastel C, Kaleta EF. Crane hepatitis herpesviruses. J Veterin Med Ser B. (1989) 36:433–41. doi: 10.1111/j.1439-0450.1989.tb00625.x

PubMed Abstract | CrossRef Full Text | Google Scholar

110. Kielstein P, Hotzel H, Schmalreck A, Khaschabi D, Glawischnig W. Occurrence of Cryptococcus spp. in excreta of pigeons and pet birds Mycoses. (2000) 43:7–15. doi: 10.1046/j.1439-0507.2000.00534.x

PubMed Abstract | CrossRef Full Text | Google Scholar

111. Richter B, Nedorost N, Maderner A, Weissenböck H. Detection of Cryptosporidium species in feces or gastric contents from snakes and lizards as determined by polymerase chain reaction analysis and partial sequencing of the 18S ribosomal RNA gene. J Vet Diagn Invest. (2011) 23:430–5. doi: 10.1177/1040638711403415

PubMed Abstract | CrossRef Full Text | Google Scholar

112. Richter B, Kübber-Heiss A, Weissenböck H, Schmidt P. Detection of Cryptosporidium spp., Entamoeba spp. and Monocercomonas spp. in the gastrointestinal tract of snakes by in-situ hybridization. J Compar Pathol. (2008) 138:63–71. doi: 10.1016/j.jcpa.2007.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

113. Nemejc K, Sak B, Kvetonova D, Hanzal V, Janiszewski P, Forejtek P, et al. Cryptosporidium suis and Cryptosporidium scrofarum in Eurasian wild boars (Sus scrofa) in central Europe. Vet Parasitol. (2013) 197:504–8. doi: 10.1016/j.vetpar.2013.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

114. Brack M, Hochleithner C, Hochleithner M, Zenker W. Suspected dermatophilosis in an adult orangutan (Pongo pygmaeus pygmaeus). J Zoo Wildlife Med. (1997) 28:336–41.

PubMed Abstract | Google Scholar

115. Otcenásek M, Hubálek Z, Sixl W. Survey of dermatophytes in the hair of small mammals from Austria. Folia Parasitol. (1980) 27:83–7.

PubMed Abstract | Google Scholar

116. Führer HP, Auer H, Leschnik M, Silbermayr K, Duscher G, Joachim A. Dirofilaria in humans, dogs, and vectors in Austria (1978-2014)—from imported pathogens to the endemicity of Dirofilaria repens. PLoS Negl Trop Dis. (2016) 10:e0004547. doi: 10.1371/journal.pntd.0004547

CrossRef Full Text | Google Scholar

117. Kölbl S, Schnabel H, Mikula M. Distemper as the cause of death in badgers in Austria. Tierarztliche Praxis. (1990) 18:81–4.

PubMed Abstract | Google Scholar

118. Burtscher H, Url A. Evidence of canine distemper and suggestion of preceding parvovirus-myocarditis in a eurasian badger (Meles meles). J Zoo Wildlife Med. (2007) 38:139–42. doi: 10.1638/05-016.1

PubMed Abstract | CrossRef Full Text | Google Scholar

119. Benetka V, Leschnik M, Affenzeller N, Mösti K. Phylogenetic analysis of Austrian canine distemper virus strains from clinical samples from dogs and wild carnivores. Vet Rec. (2011) 168:377. doi: 10.1136/vr.c6404

PubMed Abstract | CrossRef Full Text | Google Scholar

120. Kreidl P, Allerberger F, Judmaier G, Auer H, Aspock H, Hall AJ. Domestic pets as risk factors for alveolar hydatid disease in Austria. Am J Epidemiol. (1998) 147:978–81. doi: 10.1093/oxfordjournals.aje.a009388

PubMed Abstract | CrossRef Full Text | Google Scholar

121. Eckert J, Conraths FJ, Tackmann K. Echinococcosis: an emerging or re-emerging zoonosis? Int J Parasitol. (2000) 30:1283–94. doi: 10.1016/S0020-7519(00)00130-2

CrossRef Full Text | Google Scholar

122. Vuitton DA, Zhou H, Bresson-Hadni S, Wang Q, Piarroux M, Raoul F, et al. Epidemiology of alveolar echinococcosis with particular reference to China and Europe. Parasitology. (2003) 127(Suppl.):87–107. doi: 10.1017/S0031182003004153

PubMed Abstract | CrossRef Full Text | Google Scholar

123. McCulloch CR, Prosl H, Schmidt P. A spontaneous and fatal jejunal intussusception in a European brown hare associated with Eimeria leporis. J Vet Med B Infect Dis Vet Public Health. (2004) 51:470–2. doi: 10.1111/j.1439-0450.2004.00806.x

PubMed Abstract | CrossRef Full Text | Google Scholar

124. Duscher G, Steineck T, Günter P, Prosl H, Joachim A. Echinococcus multilocularis in foxes in Vienna and surrounding territories. Wien Tierarztl Monatsschr. (2005) 92:16–20.

125. Duscher G, Pleydell D, Prosl H, Joachim A. Echinococcus multilocularis in Austrian foxes from 1991 until 2004. J Vet Med Series B. (2006) 53:138–44. doi: 10.1111/j.1439-0450.2006.00930.x

PubMed Abstract | CrossRef Full Text | Google Scholar

126. Schneider R, Aspöck H, Auer H. Unexpected increase of alveolar echincoccosis, Austria, 2011. Emerg Infect Dis. (2013) 19:475–7. doi: 10.3201/eid1903.120595

PubMed Abstract | CrossRef Full Text | Google Scholar

127. Gottstein B, Frey CF, Campbell-Palmer R, Pizzi R, Barlow A, Hentrich B, et al. Immunoblotting for the serodiagnosis of alveolar echinococcosis in alive and dead Eurasian beavers (Castor fiber). Vet Parasitol. (2014) 205:113–8. doi: 10.1016/j.vetpar.2014.06.017

PubMed Abstract | CrossRef Full Text | Google Scholar

128. Posautz A, Parz-Gollner R, Hölzler G, Gottstein B, Schwaiger L, Beiglböck C, et al. First record of Echinococcus multilocularis in Austrian beavers (Castor fiber). Wien Tierarztl Monatsschr. (2015) 102:74–9.

129. Führer HP, Blöschl I, Siehs C, Hassl A. Detection of Toxoplasma gondii, Neospora caninum, and Encephalitozoon cuniculi in the brains of common voles (Microtus arvalis) and water voles (Arvicola terrestris) by gene amplification techniques in western Austria (Vorarlberg). Parasitol Res. (2010) 107:469–73. doi: 10.1007/s00436-010-1905-z

CrossRef Full Text | Google Scholar

130. Richter B, Csokai J, Graner I, Eisenberg T, Pantchev N, Eskens HU, et al. Encephalitozoonosis in two inland bearded dragons (Pogona vitticeps). J Comp Pathol. (2013) 148:278–82. doi: 10.1016/j.jcpa.2012.05.009

PubMed Abstract | CrossRef Full Text | Google Scholar

131. Bartova E, Markova J, Sedlak K. Prevalence of antibodies to Encephalitozoon cuniculi in European hares (Lepus europaeus). Ann Agric Environ Med. (2015) 22:674–6. doi: 10.5604/12321966.1185773

PubMed Abstract | CrossRef Full Text | Google Scholar

132. Hinney B, Sak B, Joachim A, Kváč M. More than a rabbit's tale – Encephalitozoon spp. in wild mammals and birds. Int J Parasitol. (2016) 5:76–87. doi: 10.1016/j.ijppaw.2016.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

133. Nowotny N. Serological examinations in domestic cats for virus infections of wild rodents with potential human pathogenicity. Zentralbl Hyg Umweltmed. (1996) 198:452–61.

Google Scholar

134. Richter B, Kübber-Heiss A, Weissenböck H. Diphtheroid colitis in a Boa constrictor infected with amphibian Entamoeba sp. Vet Parasitol. (2008) 153:164–7. doi: 10.1016/j.vetpar.2008.01.013

PubMed Abstract | CrossRef Full Text | Google Scholar

135. Loncaric I, Stalder GL, Mehinagic K, Rosengarten R, Hoelzl F, Knauer F, et al. Comparison of ESBL - and AmpC producing enterobacteriaceae and Methicillin-Resistant Staphylococcus aureus (MRSA) isolated from migratory and resident population of rooks (Corvus frugilegus) in Austria. PLoS ONE. (2013) 8:e84048. doi: 10.1371/journal.pone.0084048

PubMed Abstract | CrossRef Full Text | Google Scholar

136. Loncaric I, Beiglböck C, Feßler AT, Posautz A, Rosengarten R, Walzer C, et al. Characterization of ESBL- and AmpC-producing and fluoroquinolone-resistant Enterobacteriaceae isolated from mouflons (Ovis orientalis musimon) in Austria and Germany. PLoS ONE. (2016) 11:e0155786. doi: 10.1371/journal.pone.0155786

PubMed Abstract | CrossRef Full Text | Google Scholar

137. Fuchs A, Weissenböck H. Comparative histopathological study of Rabbit haemorrhagic disease (RHD) and European brown hare syndrome (EBHS). J Comp Pathol. (1992) 107:103–13. doi: 10.1016/0021-9975(92)90100-9

PubMed Abstract | CrossRef Full Text | Google Scholar

138. Nowotny N, Ros Bascuñana C, Ballagi-Pordány A, Gavier-Widén D, Uhlén M, Belák S. Phylogenetic analysis of rabbit haemorrhagic disease and European brown hare syndrome viruses by comparison of sequences from the capsid protein gene. Arch Virol. (1997) 142:657–73. doi: 10.1007/s007050050109

PubMed Abstract | CrossRef Full Text | Google Scholar

139. Ursprung J, Joachim A, Prosl H. Epidemiology and control of the giant liver fluke, Fascioloides magna, in a population of wild ungulates in the Danubian wetlands east of Vienna. Berl Munch Tierarztl Wochenschr. (2006) 119:316–23.

Google Scholar

140. Haider M, Hörweg C, Liesinger K, Sattmann H, Walochnik J. Recovery of Fascioloides magna (Digenea) population in spite of treatment programme? Screening of Galba truncatula (Gastropoda, Lymnaeidae) from Lower Austria. Vet Parasitol. (2012) 187:445–51. doi: 10.1016/j.vetpar.2012.01.032

PubMed Abstract | CrossRef Full Text | Google Scholar

141. Hörweg C, Prosl H, Wille-Piazzai W, Joachim A, Sattmann H. Prevalence of Fascioloides magna in Galba truncatula in the Danube backwater area east of Vienna, Austria. Wien Tierarztl Monatsschr. (2011) 98:261–7.

Google Scholar

142. Ursprung J, Prosl H. The American Giant Liver Fluke (Fascioloides magna) in the Danube floodplain forests east of Vienna, Austria. Occurrence and control 2000 - 2010. Wien Tierarztl Monatsschr. (2011) 98:275–84.

143. Sattmann H, Hörweg C, Gaub L, Feix AS, Haider M, Walochnik J, et al. Wherefrom and whereabouts of an alien: the American liver fluke Fascioloides magna in Austria: an overview. Wiener klinische Wochenschrift. (2014) 126 (Suppl.1):23–31. doi: 10.1007/s00508-014-0499-3

PubMed Abstract | CrossRef Full Text | Google Scholar

144. Husch C, Sattmann H, Hoerweg C, Ursprung J, Walochnik J. Genetic homogeneity of Fascioloides magna in Austria. Vet Parasitol. (2017) 243:75–8. doi: 10.1016/j.vetpar.2017.06.007

PubMed Abstract | CrossRef Full Text | Google Scholar

145. Walzer C, Url A, Robert N, Kübber-Heiss A, Nowotny N, Schmidt P. Idiopathic acute onset myelopathy in cheetah (Acinonyx jubatus) cubs. J Zoo Wildlife Med. (2003) 34:36–46. doi: 10.1638/1042-7260(2003)34[0036:IAOMIC]2.0.CO;2

PubMed Abstract | CrossRef Full Text | Google Scholar

146. Weissenböck H, Hubálek Z, Bakonyi T, Nowotny N. Zoonotic mosquito-borne flaviviruses: Worldwide presence of agents with proven pathogenicity and potential candidates of future emerging diseases. Vet Microbiol. (2010) 140:271–80. doi: 10.1016/j.vetmic.2009.08.025

PubMed Abstract | CrossRef Full Text | Google Scholar

147. Hubálek Z, Sixl W, Halouzka J. Francisella tularensis in Dermacentor reticulatus ticks from the Czech Republic and Austria. Wiener klinische Wochenschrift. (1998) 110:909–10.

PubMed Abstract | Google Scholar

148. Deutz A, Guggenberger T, Gasteiner J, Steineck T, Bagó Z, Hofer E, et al. Investigation of the prevalence of tularaemia under the aspect of climate change. Wien Tierarztl Monatsschr. (2009) 96:107–13.

Google Scholar

149. Visser M, Messner C, Rehbein S. Massive infestation with fur mites (Lynxacarus mustelae) of a stone marten (Martes foina) from Tyrol. Wiener klinische Wochenschrift. (2011) 123 (Suppl. 1):36–42. doi: 10.1007/s00508-011-0005-0

PubMed Abstract | CrossRef Full Text | Google Scholar

150. Juncker-Voss M, Kübber-Heiss A, Kutzer E, Kanzler P, Schratter D, Prosl H. Geopetitia aspiculata: Endemic in zoobirds in Austria. Wien Tierarztl Monatsschr. (2001) 88:106–13.

151. Aberle SW, Lehner P, Ecker M, Aberle JH, Arneitz K, Khanakah G, et al. Nephropathia epidemica and Puumala virus in Austria. Eur J Clin Microbiol Infect Dis. (1999) 18:467–72. doi: 10.1007/s100960050325

PubMed Abstract | CrossRef Full Text | Google Scholar

152. Plyusnina A, Aberle S, Aberle J, Plyusnin A. Genetic analysis of Puumala hantavirus strains from Austria. Scand J Infect Dis. (2006) 38:512–9. doi: 10.1080/00365540600585040

PubMed Abstract | CrossRef Full Text | Google Scholar

153. Duscher G, Kubber-Heiss A, Richter B, Suchentrunk F. A golden jackal (Canis aureus) from Austria bearing Hepatozoon canis - import due to immigration into a non-endemic area? Ticks Tick Borne Dis. (2013) 4:133–7. doi: 10.1016/j.ttbdis.2012.10.040

PubMed Abstract | CrossRef Full Text | Google Scholar

154. Kübber-Heiss A, Schilcher F, Möstl K. Herpesvirus-infections in tortoises in Austria. Wien Tierarztl Monatsschr. (1999) 86:78–82.

155. Bauder B, Kübber-Heiss A, Steineck T, Kuttin ES, Kaufman L. Granulomatous skin lesions due to histoplasmosis in a badger (Meles meles) in Austria. Medical Mycology. (2000) 38:249–53. doi: 10.1080/mmy.38.3.249.253

PubMed Abstract | CrossRef Full Text | Google Scholar

156. Tsangaras K, Siracusa MC, Nikolaidis N, Ishida Y, Cui P, Vielgrader H, et al. Hybridization capture reveals evolution and conservation across the entire koala retrovirus genome. PLoS ONE. (2014) 9:e95633. doi: 10.1371/journal.pone.0095633

PubMed Abstract | CrossRef Full Text | Google Scholar

157. Deutz A, Fuchs K, Schuller W, Müller M, Kerbl U, Klement C. Studies on the seroprevalence of antibodies against Leptospira interrogans in hunters and wild boar from south-eastern Austria. Eur J Wildlife Res. (2002) 48:60–5. doi: 10.1007/BF02285358

CrossRef Full Text

158. Paulsen P, Winkelmayer R. Seasonal variation in the microbial contamination of game carcasses in an Austrian hunting area. Eur J Wildlife Res. (2004) 50:157–9. doi: 10.1007/s10344-004-0054-z

CrossRef Full Text | Google Scholar

159. Linke K, Rückerl I, Brugger K, Karpiskova R, Walland J, Muri-Klinger S, et al. Reservoirs of Listeria species in three environmental ecosystems. Appl Environ Microbiol. (2014) 80:5583–92. doi: 10.1128/AEM.01018-14

PubMed Abstract | CrossRef Full Text | Google Scholar

160. Benetka V, Krametter-Froetscher R, Baumgartner W, Moestl K. Investigation of the role of Austrian ruminant wildlife in the epidemiology of malignant catarrhal fever viruses. J Wildl Dis. (2009) 45:508–11. doi: 10.7589/0090-3558-45.2.508

PubMed Abstract | CrossRef Full Text | Google Scholar

161. Loncaric I, Kübber-Heiss A, Posautz A, Stalder GL, Hoffmann D, Rosengarten R, et al. Characterization of methicillin-resistant Staphylococcus spp. carrying the mecC gene, isolated from wildlife. J Antimicrob Chemother. (2013) 68:2222–5. doi: 10.1093/jac/dkt186

PubMed Abstract | CrossRef Full Text | Google Scholar

162. Loncaric I, Kübber-Heiss A, Posautz A, Stalder GL, Hoffmann D, Rosengarten R, et al. mecC- and mecA-positive meticillin-resistant Staphylococcus aureus (MRSA) isolated from livestock sharing habitat with wildlife previously tested positive for mecC-positive MRSA. Vet Dermatol. (2014) 25:147–8. doi: 10.1111/vde.12116

PubMed Abstract | CrossRef Full Text | Google Scholar

163. Deutz A, Spergser J, Rosengarten R, Köfer J. First detection of intrauterine transmission of paratuberculosis in red deer and chamois. Z Jagdwiss. (2003) 49:314–9. doi: 10.1007/BF02189639

CrossRef Full Text

164. Deutz A, Spergser J, Wagner P, Steineck T, Köfer J, Rosengarten R. Paratuberculosis in wild animals - An observed increase in the clinical incidence. Tierarztl Umsch. (2003) 58:482–9.

165. Deutz A, Spergser J, Wagner P, Rosengarten R, Köfer J. Mycobacterium avium subsp. paratuberculosis in wild animal species and cattle in Styria/Austria. Berl Munch Tierarztl Wochenschr. (2005) 118:314–20.

PubMed Abstract | Google Scholar

166. Glawischnig W, Steineck T, Spergser J. Infections caused by Mycobacterium avium subspecies avium, hominissuis, and paratuberculosis in free-ranging red deer (Cervus elaphus hippelaphus) in Austria, 2001-2004. J Wildlife Dis. (2006) 42:724–31. doi: 10.7589/0090-3558-42.4.724

PubMed Abstract | CrossRef Full Text | Google Scholar

167. Spergser J, Fuchs K, Deutz A. Molecular characterisation of M. avium subsp paratuberculosis isolated from cattle and wild animal species from Styria. Wien Tierarztl Monatsschr. (2006) 93:47–52.

168. Gerritsmann H, Stalder GL, Spergser J, Hoelzl F, Deutz A, Kuebber-Heiss A, et al. Multiple strain infections and high genotypic diversity among Mycobacterium avium subsp. paratuberculosis field isolates from diseased wild and domestic ruminant species in the eastern Alpine region of Austria. Infect Genet Evol. (2014) 21:244–51. doi: 10.1016/j.meegid.2013.11.009

PubMed Abstract | CrossRef Full Text | Google Scholar

169. Glawischnig W, Khaschabi D. Paratuberculosis in a free living red deer (Cervus elaphus hippelaphus) from Vorarlberg. Wien Tierarztl Monatsschr. (2001) 88:66–9.

170. Scope A, Spergser J, Vobornik A, Gumpenberger M, Hooijberg EH, Reifinger M. Atypical mycobacteriosis in a ural owl (Strix uralensis, PALLAS 1771) from the Austrian reintroduction project. Wien Tierarztl Monatsschr. (2013) 100:85–92.

Google Scholar

171. Rivière J, Carabin K, Le Strat Y, Hendrikx P, Dufour B. Bovine tuberculosis surveillance in cattle and free-ranging wildlife in EU Member States in 2013: A survey-based review. Vet Microbiol. (2014) 173:323–31. doi: 10.1016/j.vetmic.2014.08.013

PubMed Abstract | CrossRef Full Text | Google Scholar

172. Prodinger WM, Eigentler A, Allerberger F, Schönbauer M, Glawischnig W. Infection of red deer, cattle, and humans with Mycobacterium bovis subsp. caprae in western Austria. J Clin Microbiol. (2002) 40:2270–2. doi: 10.1128/JCM.40.6.2270-2272.2002

PubMed Abstract | CrossRef Full Text | Google Scholar

173. Glawischnig W, Allerberger F, Messner C, Schönbauer M, Prodinger WM. Tuberculosis in free-living red deer (Cervus elaphus hippelaphus) in the northern Alps. Wien Tierarztl Monatsschr. (2003) 90:38–44.

174. Prodinger WM, Brandstatter A, Naumann L, Pacciarini M, Kubica T, Boschiroli ML, et al. Characterization of Mycobacterium caprae isolates from Europe by mycobacterial interspersed repetitive unit genotyping. J Clin Microbiol. (2005) 43:4984–92. doi: 10.1128/JCM.43.10.4984-4992.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

175. Weikel J, Glawischnig W, Hofer E, Schoepf K. Tuberculosis in a deer (Capreolus capreolus) detected in Tyrol (Austria). Wien Tierarztl Monatsschr. (2010) 97:287–9.

Google Scholar

176. Schoepf K, Prodinger WM, Glawischnig W, Hofer E, Revilla-Fernandez S, Hofrichter J, et al. A two-years' survey on the prevalence of tuberculosis caused by Mycobacterium caprae in red deer (Cervus elaphus) in the Tyrol, Austria. Vet Sci. (2012) 2012:245138. doi: 10.5402/2012/245138

PubMed Abstract | CrossRef Full Text | Google Scholar

177. Rettinger A, Broeckl S, Fink M, Prodinger WM, Blum H, Krebs S, et al. The region of difference four is a robust genetic marker for subtyping mycobacterium caprae isolates and is linked to spatial distribution of three subtypes. Transbound Emerg Dis. (2017) 64:782–92. doi: 10.1111/tbed.12438

PubMed Abstract | CrossRef Full Text | Google Scholar

178. Belloy L, Janovsky M, Vilei EM, Pilo P, Giacometti M, Frey J. Molecular epidemiology of Mycoplasma conjunctivae in Caprinae: Transmission across species in natural outbreaks. Appl Environ Microbiol. (2003) 69:1913–9. doi: 10.1128/AEM.69.4.1913-1919.2003

PubMed Abstract | CrossRef Full Text | Google Scholar

179. Zimmermann L, Jambresic S, Giacometti M, Frey J. Specificity of Mycoplasma conjunctivae strains for alpine chamois Rupicapra r. rupicapra. Wildlife Biol. (2008) 14:118–24. doi: 10.2981/0909-6396(2008)14[118:SOMCSF]2.0.CO;2

CrossRef Full Text | Google Scholar

180. Friedrich C, Ingolic E, Freitag B, Kastberger G, Hohmann V, Skofitsch G, et al. A myxozoan-like parasite causing xenomas in the brain of the mole, Talpa europaea L., 1758 (Vertebrata, Mammalia). Parasitology. (2000) 121:483–92. doi: 10.1017/S0031182099006769

PubMed Abstract | CrossRef Full Text | Google Scholar

181. Wanha K, Edelhofer R, Gabler-Eduardo C, Prosl H. Prevalence of antibodies against Neospora caninum and Toxoplasma gondii in dogs and foxes in Austria. Vet Parasitol. (2005) 128:189–93. doi: 10.1016/j.vetpar.2004.11.027

PubMed Abstract | CrossRef Full Text | Google Scholar

182. Bartova E, Sedlak K, Treml F, Holko I, Literak I. Neospora caninum and Toxoplasma gondii antibodies in European brown hares in the Czech Republic, Slovakia and Austria. Vet Parasitol. (2010) 171:155–8. doi: 10.1016/j.vetpar.2010.03.002

PubMed Abstract | CrossRef Full Text | Google Scholar

183. Cronstedt-Fell A, Richter B, Voracek T, Kübber-Heiss A. Neosporosis in a Captive Parma Wallaby (Macropus parma). J Comp Pathol. (2012) 146:274–7. doi: 10.1016/j.jcpa.2011.05.002

PubMed Abstract | CrossRef Full Text | Google Scholar

184. Posautz A, Loncaric I, Kübber-Heiss A, Knoll A, Walzer C. Acute die-off of chamois (Rupicapra rupicapra) in the eastern Austrian alps due to bacterial bronchopneumonia with Pasteurellaceae. J Wildlife Dis. (2014) 50:616–20. doi: 10.7589/2013-04-090

PubMed Abstract | CrossRef Full Text | Google Scholar

185. Loupal G, Kutzer E. Infections with Plasmodium spec, in puffins (Fractercula arctica). Kleintierpraxis. (1996) 41:901–6.

186. Dinhopl N, Mostegl MM, Richter B, Nedorost N, Maderner A, Fragner K, et al. Application of in-situ hybridization for the detection and identification of avian malaria parasites in paraffin wax-embedded tissues from captive penguins. Avian Pathol. (2011) 40:315–20. doi: 10.1080/03079457.2011.569533

PubMed Abstract | CrossRef Full Text | Google Scholar

187. Dinhopl N, Nedorost N, Mostegl MM, Weissenbacher-Lang C, Weissenbock H. In situ hybridization and sequence analysis reveal an association of Plasmodium spp. with mortalities in wild passerine birds in Austria. Parasitol Res. (2015) 114:1455–62. doi: 10.1007/s00436-015-4328-z

PubMed Abstract | CrossRef Full Text | Google Scholar

188. Hess M, Scope A, Heincz U. Comparitive sensitivity of polymerase chain reaction diagnosis of psittacine beak and feather disease on feather samples, cloacal swabs and blood from budgerigars (Melopsittacus undulates, Shaw 18005). Avian Pathol. (2004) 33:477–81. doi: 10.1080/03079450400003619

PubMed Abstract | CrossRef Full Text | Google Scholar

189. Jahn J, Timischl W. Mathematical-analysis of the spread of wildlife rabies in Austria. Empirical and theoretical background. Wien Tierarztl Monatsschr. (1984) 71:149–55.

190. Kollaritsch H, Maurer W. Tollwut: Epidemiologie, prä- und postexpositionelle Immunisierung. Wien Klinis Wochenschr. (2006) 118:312–20. doi: 10.1007/s00508-006-0606-1

CrossRef Full Text | Google Scholar

191. Müller T, Bätza HJ, Beckert A, Bunzenthal C, Cox JH, Freuling CM, et al. Analysis of vaccine-virus-associated rabies cases in red foxes (Vulpes vulpes) after oral rabies vaccination campaigns in Germany and Austria. Arch Virol. (2009) 154:1081–91. doi: 10.1007/s00705-009-0408-7

PubMed Abstract | CrossRef Full Text | Google Scholar

192. Kölbl S, Settele J, Schönbauer M. The first appearance of infectious hemorrhagic disease of rabbits in Austria. Berl Munch Tierarztl Wochenschr. (1990) 103:261–6.

PubMed Abstract | Google Scholar

193. Ryll R, Bernstein S, Heuser E, Schlegel M, Dremsek P, Zumpe M, et al. Detection of Rat hepatitis E virus in wild Norway rats (Rattus norvegicus) and Black rats (Rattus rattus) from 11 European countries. Vet Microbiol. (2017) 208:58–68. doi: 10.1016/j.vetmic.2017.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

194. Erdélyi K, Gál J, Sugár L, Ursu K, Forgách P, Szeredi L, et al. Papillomavirus-associated fibropapillomas of red deer (Cervus elaphus). Acta Vet Hungar. (2009) 57:337–44. doi: 10.1556/AVet.57.2009.2.14

PubMed Abstract | CrossRef Full Text | Google Scholar

195. Geue L, Löschner U. Salmonella enterica in reptiles of German and Austrian origin. Vet Microbiol. (2002) 84:79–91. doi: 10.1016/S0378-1135(01)00437-0

PubMed Abstract | CrossRef Full Text | Google Scholar

196. Glawischnig W, Lazar J, Wallner A, Kornschober C. Cattle-derived Salmonella enterica serovar dublin infections in red foxes (Vulpes vulpes) in Tyrol, Austria. J Wildlife Dis. (2017) 53:361–3. doi: 10.7589/2016-04-087

PubMed Abstract | CrossRef Full Text | Google Scholar

197. Pfleger S, Benyr G, Sommer R, Hassl A. Pattern of Salmonella excretion in amphibians and reptiles in a vivarium. Int J Hyg Environ Health. (2003) 206:53–9. doi: 10.1078/1438-4639-00184

PubMed Abstract | CrossRef Full Text | Google Scholar

198. Awad-Masalmeh M, Romanik G, Herkal C. The occurrence of Salmonellae in reptiles kept privateley or in zoos in Austria. Tierarztliche Umschau. (2005) 60:70–4.

199. Paulsen P, Smulders FJM, Hilbert F. Salmonella in meat from hunted game: a Central European perspective. Food Res Int. (2012) 45:609–16. doi: 10.1016/j.foodres.2011.06.055

CrossRef Full Text | Google Scholar

200. Hilbert F, Smulders FJM, Chopra-Dewasthaly R, Paulsen P. Salmonella in the wildlife-human interface. Food Res Int. (2012) 45:603–8. doi: 10.1016/j.foodres.2011.08.015

CrossRef Full Text | Google Scholar

201. Fuchs K, Deutz A, Gressmann G. Detection of space-time clusters and epidemiological examinations of scabies in chamois. Vet Parasitol. (2000) 92:63–73. doi: 10.1016/S0304-4017(00)00269-7

PubMed Abstract | CrossRef Full Text | Google Scholar

202. Gressmann G, Deutz A. Considerations on reducing the risk of scabies infestation in chamois by targeted hunting of individual age classes. Z Jagdwiss. (2001) 47:34–42. doi: 10.1007/BF02242412

CrossRef Full Text

203. Monecke S, Gavier-Widén D, Hotzel H, Peters M, Guenther S, Lazaris A, et al. Diversity of Staphylococcus aureus isolates in european wildlife. PLoS ONE. (2016) 11:e0168433. doi: 10.1371/journal.pone.0168433

PubMed Abstract | CrossRef Full Text | Google Scholar

204. Führer HP, Siehs C, Schneider R, Auer H. Morphometrical analysis of Taenia taeniaeformis and Taenia crassiceps in the common vole (Microtus arvalis) and the water vole (Arvicola terrestris) in Vorarlberg, Austria. Helminthologia. (2012) 49:169–73. doi: 10.2478/s11687-012-0034-x

CrossRef Full Text | Google Scholar

205. Führer HP, Biro N, Harl J, Worliczek HL, Beiglbock C, Farkas R, et al. Molecular detection of Theileria sp. ZS TO4 in red deer (Cervus elaphus) and questing Haemaphysalis concinna ticks in Eastern Austria. Vet Parasitol. (2013) 197:653–7. doi: 10.1016/j.vetpar.2013.07.005

CrossRef Full Text | Google Scholar

206. Bagó Z, Bauder B, Kolodziejek J, Nowotny N, Weissenböck H. Tickborne encephalitis in a mouflon (Ovis ammon musimon). Vet Rec. (2002) 150:218–20. doi: 10.1136/vr.150.7.218

PubMed Abstract | CrossRef Full Text | Google Scholar

207. Duscher G, Wetscher M, Baumgartner R, Walder G. Roe deer sera used for TBE surveillance in Austria. Ticks Tick Borne Dis. (2015) 6:489–93. doi: 10.1016/j.ttbdis.2015.03.018

PubMed Abstract | CrossRef Full Text | Google Scholar

208. Deutz A, Fuchs K, Auer H, Kerbl U, Aspöck H, Köfer J. Toxocara-infestations in Austria: a study on the risk of infection of farmers, slaughterhouse staff, hunters and veterinarians. Parasitol Res. (2005) 97:390–4. doi: 10.1007/s00436-005-1469-5

PubMed Abstract | CrossRef Full Text | Google Scholar

209. Auer H, Aspöck H. The diagnosis of Toxocara infestations and of human toxocarosis. Lab Med. (2006) 30:1–12. doi: 10.1515/JLM.2006.001

CrossRef Full Text | Google Scholar

210. Basso W, Edelhofer R, Zenker W, Möstl K, Kübber-Heiss A, Prosl H. Toxoplasmosis in Pallas' cats (Otocolobus manul) raised in captivity. Parasitology. (2005) 130:293–9. doi: 10.1017/S0031182004006584

PubMed Abstract | CrossRef Full Text | Google Scholar

211. Edelhofer R, Prossinger H. Infection with Toxoplasma gondii during pregnancy: seroepidemiological studies in Austria. Zoonoses Public Health. (2010) 57:18–26. doi: 10.1111/j.1863-2378.2009.01279.x

PubMed Abstract | CrossRef Full Text | Google Scholar

212. Posautz A, Leidinger E, Knauer F, Hoffmann D, Suchentrunk F, Walzer C, et al. Seroprevalence of Treponema sp. in European brown hares (Lepus europaeus) in Austria and Germany. Wien Tierarztl Monatsschr. (2014) 101:281–5.

Google Scholar

213. Krois E, Nöckler K, Duscher G, Joachim A, Kapel CMO, Prosl H. Trichinella britovi in Austrian red foxes (Vulpes vulpes). Wien Tierarztl Monatsschr. (2005) 92:308–14.

214. Glawischnig W, Wunsch A, Fötschl H, Bagó Z, Vanek E. First report of Trichinella pseudospiralis in wild boar in Austria. Wien Tierarztl Monatsschr. (2016) 103:183–187.

215. Edelhofer R, Prosl H, Kutzer E. Trichinellosis and toxoplasmosis in wild pigs of Eastern Austria. Wien Tierarztl Monatsschr. (1996) 83:225–9.

216. Pozio E. Trichinellosis in the European union: epidemiology, ecology and economic impact. Parasitol Today. (1998) 14:35–8. doi: 10.1016/S0169-4758(97)01165-4

PubMed Abstract | CrossRef Full Text | Google Scholar

217. Paulsen P, Winkelmayer R, Gneist M, Riedl C, Gansterer A, Gabler C, et al. Establishing a Trichinella proficiency testing scheme in Austria. First communication: a preliminary study on Trichinella inspection of wild boar meat in Lower Austria by authorized trained hunters employing the compression method. Wien Tierarztl Monatsschr. (2003) 90:91–7.

218. Auer H. Human trichinellosis in Austria. Wien Tierarztl Monatsschr. (2005) 92:288–94.

219. Sattmann H, Prosl H. History of early research on trichinellae and trichinelloses. Wien Tierarztl Monatsschr. (2005) 92:283–7.

220. Winkelmayer R, Paulsen P. Trichinella examination of free range wild boar in Lower Austria. Wien Tierarztl Monatsschr. (2005) 92:322–4.

221. Duscher G, Winkelmayer R, Prosl H. Wild boar distribution in Austrian areas with Trichinella spp. findings in red foxes. Wien Tierarztl Monatsschr. (2005) 92:315–21.

222. Grabensteiner E, Bilic I, Kolbe T, Hess M. Molecular analysis of clonal trichomonad isolates indicate the existence of heterogenic species present in different birds and within the same host. Vet Parasitol. (2010) 172:53–64. doi: 10.1016/j.vetpar.2010.04.015

PubMed Abstract | CrossRef Full Text | Google Scholar

223. Ganas P, Jaskulska B, Lawson B, Zadravec M, Hess M, Bilic I. Multi-locus sequence typing confirms the clonality of Trichomonas gallinae isolates circulating in European finches. Parasitology. (2014) 141:652–61. doi: 10.1017/S0031182013002023

PubMed Abstract | CrossRef Full Text | Google Scholar

224. Schilcher F, Kübber-Heiss A, Breuer-Strosberg R, Barth S. Dermatomycosis due to Trichphyton terrestre in Madagascar Day Geckos (Phelsuma m. madagascariensis). Wien Tierarztl Monatsschr. (1998) 85:131–5.

Google Scholar

225. Mostegl MM, Richter B, Nedorost N, Maderner A, Dinhopl N, Kübber-Heiss A, et al. Identification of a putatively novel trichomonad species in the intestine of a common quail (Coturnix coturnix). Vet Parasitol. (2012) 183:369–72. doi: 10.1016/j.vetpar.2011.07.036

PubMed Abstract | CrossRef Full Text | Google Scholar

226. Weissenböck H, Kolodziejek J, Url A, Lussy H, Rebel-Bauder B, Nowotny N. Emergence of Usutu virus, an African mosquito-borne Flavivirus of the Japanese encephalitis virus group, central Europe. Emerg Infect Dis. (2002) 8:652–6. doi: 10.3201/eid0807.020094

PubMed Abstract | CrossRef Full Text | Google Scholar

227. Weissenböck H, Kolodziejek J, Fragner K, Kuhn R, Pfeffer M, Nowotny N. Usutu virus activity in Austria, 2001-2002. Microb Infect. (2003) 5:1132–6. doi: 10.1016/S1286-4579(03)00204-1

PubMed Abstract | CrossRef Full Text | Google Scholar

228. Chvala S, Kolodziejek J, Nowotny N, Weissenböck H. Pathology and viral distribution in fatal Usutu virus infections of birds from the 2001 and 2002 outbreaks in Austria. J Comp Pathol. (2004) 131:176–85. doi: 10.1016/j.jcpa.2004.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

229. Bakonyi T, Gould EA, Kolodziejek J, Weissenböck H, Nowotny N. Complete genome analysis and molecular characterization of Usutu virus that emerged in Austria in 2001: comparison with the South African Strain SAAR-1776 and other flaviviruses. Virology. (2004) 328:301–10. doi: 10.1016/S0042-6822(04)00525-2

PubMed Abstract | CrossRef Full Text | Google Scholar

230. Hassler D, Pfeffer M, Weissenbock H, Nowotny N. Usutu virus in Austria reminds one of the West Nile virus in the USA. Dtsch Med Wochenschr. (2004) 129:2339–40.

PubMed Abstract | Google Scholar

231. Weissenböck H, Bakonyi T, Chvala S, Nowotny N. Experimental Usutu virus infection of suckling mice causes neuronal and glial cell apoptosis and demyelination. Acta Neuropathol. (2004) 108:453–60. doi: 10.1007/s00401-004-0916-1

PubMed Abstract | CrossRef Full Text | Google Scholar

232. Chvala S, Bakonyi T, Bukovsky C, Meister T, Brugger K, Rubel F, et al. Monitoring of Usutu virus activity and spread by using dead bird surveillance in Austria, 2003-2005. Vet Microbiol. (2007) 122:237–45. doi: 10.1016/j.vetmic.2007.01.029

PubMed Abstract | CrossRef Full Text | Google Scholar

233. Meister T, Lussy H, Bakonyi T, Sikutova S, Rudolf I, Vogl W, et al. Serological evidence of continuing high Usutu virus (Flaviviridae) activity and establishment of herd immunity in wild birds in Austria. Vet Microbiol. (2008) 127:237–48. doi: 10.1016/j.vetmic.2007.08.023

PubMed Abstract | CrossRef Full Text | Google Scholar

234. Rubel F, Brugger K, Hantel M, Chvala-Mannsberger S, Bakonyi T, Weissenböck H, et al. Explaining Usutu virus dynamics in Austria: Model development and calibration. Prev Vet Med. (2008) 85:166–86. doi: 10.1016/j.prevetmed.2008.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

235. Brugger K, Rubel F. Simulation of climate-change scenarios to explain Usutu-virus dynamics in Austria. Prev Vet Med. (2009) 88:24–31. doi: 10.1016/j.prevetmed.2008.06.023

PubMed Abstract | CrossRef Full Text | Google Scholar

236. Buchebner N, Zenker W, Wenker C, Steinmetz HW, Sós E, Lussy H, et al. Low Usutu virus seroprevalence in four zoological gardens in central Europe. BMC Vet Res. (2013) 9:153. doi: 10.1186/1746-6148-9-153

PubMed Abstract | CrossRef Full Text | Google Scholar

237. Stiasny K, Aberle SW, Heinzl FX. Retrospective identification of human cases of West nile virus infection in Austria (2009 to 2010) by serological differentiation from Usutu and other flavivirus infections. Eurosurveillance. (2013) 18:20614. doi: 10.2807/1560-7917.ES2013.18.43.20614

PubMed Abstract | CrossRef Full Text | Google Scholar

238. Bakonyi T, Busquets N, Nowotny N. Comparison of complete genome sequences of Usutu virus strains detected in Spain, Central Europe, and Africa. Vector Borne Zoon Dis. (2014) 14:324–9. doi: 10.1089/vbz.2013.1510

PubMed Abstract | CrossRef Full Text | Google Scholar

239. Bakonyi T, Erdélyi K, Brunthaler R, Dán Á, Weissenböck H, Nowotny N. Usutu virus, Austria and Hungary, 2010-2016. Emerg Microb Infect. (2017) 6:85. doi: 10.1038/emi.2017.72

PubMed Abstract | CrossRef Full Text

240. Freidl G, Stalder G, Kostić T, Sessitsch A, Beiglböck C, Walzer C. Verocytotoxin-producing Escherichia coli in chamois (Rupicapra rupicapra) and cattle in Austria. J Wildlife Dis. (2011) 47:704–8. doi: 10.7589/0090-3558-47.3.704

PubMed Abstract | CrossRef Full Text | Google Scholar

241. Weissenböck H, Hubálek Z, Halouzka J, Pichlmair A, Maderner A, Fragner K, et al. Screening for West Nile virus infections of susceptible animal species in Austria. Epidemiol Infect. (2003) 131:1023–7. doi: 10.1017/S0950268803001031

PubMed Abstract | CrossRef Full Text | Google Scholar

242. Linke S, Muehlen M, Niedrig M, Ellerbrok H, Kaiser A, Fiedler W, et al. Assessing the exposure of German and Austrian bird ringers to West Nile virus (Flavivirus) and evaluating their potential risk of infection. J Ornithol. (2008) 149:271–5. doi: 10.1007/s10336-007-0270-x

CrossRef Full Text | Google Scholar

243. Wodak E, Richter S, Bagó Z, Revilla-Fernández S, Weissenböck H, Nowotny N, et al. Detection and molecular analysis of West Nile virus infections in birds of prey in the eastern part of Austria in 2008 and 2009. Vet Microbiol. (2011) 149:358–66. doi: 10.1016/j.vetmic.2010.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

244. Bakonyi T, Ferenczi E, Erdelyi K, Kutasi O, Csorgo T, Seidel B, et al. Explosive spread of a neuroinvasive lineage 2 West Nile virus in Central Europe, 2008/2009. Vet Microbiol. (2013) 165:61–70. doi: 10.1016/j.vetmic.2013.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

245. Beck C, Jimenez-Clavero MA, Leblond A, Durand B, Nowotny N, Leparc-Goffart I, et al. Flaviviruses in europe: complex circulation patterns and their consequences for the diagnosis and control of west nile disease. Int J Environ Res Public Health. (2013) 10:6049–83. doi: 10.3390/ijerph10116049

PubMed Abstract | CrossRef Full Text | Google Scholar

246. Hernández-Triana LM, Jeffries CL, Mansfield KL, Carnell G, Fooks AR, Johnson N. Emergence of West Nile virus lineage 2 in Europe: a review on the introduction and spread of a mosquito-borne disease. Front Public Health. (2014) 2:271. doi: 10.3389/fpubh.2014.00271

PubMed Abstract | CrossRef Full Text | Google Scholar

247. Rizzoli A, Jiménez-Clavero MA, Barzon L, Cordioli P, Figuerola J, Koraka P, et al. The challenge of West nile virus in Europe: knowledge gaps and research priorities. Eurosurveillance. (2015) 20:21135. doi: 10.2807/1560-7917.ES2015.20.20.21135

PubMed Abstract | CrossRef Full Text | Google Scholar

248. Bakonyi T, Gajdon GK, Schwing R, Vogl W, Häbich AC, Thaller D, et al. Chronic West Nile virus infection in kea (Nestor notabilis). Vet Microbiol. (2016) 183:135–9. doi: 10.1016/j.vetmic.2015.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

249. Bidaisee S, Macpherson CNL. Zoonoses and one health: a review of the literature. J Parasitol Res. (2014) 2014:874345. doi: 10.1155/2014/874345

PubMed Abstract | CrossRef Full Text | Google Scholar

250. Austrian Agency for Health and Food Safety (AGES). Transmissible Spongiforme Enzephalopathie (TSE). (2019). Available online at: https://www.ages.at/themen/krankheitserreger/tse-bsescrapiecwd/tab/3/ (accessed May 10, 2019).

Google Scholar

251. European Food Safety Authority (EFSA). Chronic Wasting Disease: Addressing Risks for the EU (CWD). (2017). Available online at: https://www.efsa.europa.eu/en/press/news/170118 (accessed May 6, 2019).

252. Austrian Agency for Health and Food Safety (AGES). Usutu Virus. (2019). Available online at: https://www.ages.at/themen/krankheitserreger/usutu-virus/tab/1/ (accessed May 9, 2019).

253. Dobson A, Foufopoulos J. Emerging infectious pathogens of wildlife. Philo Trans R Soc B Biol Sci. (2001) 356:1001–12. doi: 10.1098/rstb.2001.0900

PubMed Abstract | CrossRef Full Text | Google Scholar

254. World Organisation for Animal Health (OIE). OIE Listed Diseases. (2019). Available online at: http://www.oie.int/en/animal-health-in-the-world/oie-listed-diseases-2019/ (accessed May 7, 2019).

255. Vetter SG, Ruf T, Bieber C, Arnold W. What is a mild winter? Regional differences in within-species responses to climate change. PLoS ONE. (2015) 10:e0132178. doi: 10.1371/journal.pone.0132178

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: wildlife, infectious, diseases, zoonosis, Austria, game, one health, EID

Citation: Trimmel NE and Walzer C (2020) Infectious Wildlife Diseases in Austria—A Literature Review From 1980 Until 2017. Front. Vet. Sci. 7:3. doi: 10.3389/fvets.2020.00003

Received: 26 August 2019; Accepted: 02 January 2020;
Published: 21 February 2020.

Edited by:

Nicole Indra Stacy, University of Florida, United States

Reviewed by:

Martha Weber, Riverbanks Zoo and Garden, United States
Karoly Erdelyi, National Food Chain Safety Office, Hungary

Copyright © 2020 Trimmel and Walzer. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Nina Eva Trimmel, nina.trimmel@gmail.com

Download