ORIGINAL RESEARCH article

Front. Vet. Sci., 06 December 2021
Sec.Veterinary Infectious Diseases
https://doi.org/10.3389/fvets.2021.784331

Serological Survey of Canine Vector-Borne Infections in North-Center Spain

Patricia Pérez Pérez1,2, Iván Rodríguez-Escolar1, Elena Carretón3*, José Ángel Sánchez Agudo4, Jacob Lorenzo-Morales2,5, José Alberto Montoya-Alonso3 and Rodrigo Morchón1*
  • 1Zoonotic Infections and One Health GIR, Laboratory of Parasitology, Faculty of Pharmacy, University of Salamanca, Salamanca, Spain
  • 2Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias (IUETSPC), Departamento de Obstetricia y Ginecología, Pediatría, Medicina Preventiva y Salud Pública, Toxicología, Medicina Legal y Forense y Parasitología, Universidad de La Laguna, La Laguna, Tenerife, Spain
  • 3Internal Medicine, Faculty of Veterinary Medicine, Research Institute of Biomedical and Health Sciences, University of Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain
  • 4Grupo de Investigación en Biodiversidad, Diversidad humana y Biología de la Conservación, Universidad de Salamanca, Salamanca, Spain
  • 5CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain

Various factors are currently causing an increase in vector-borne parasitic diseases at a global scale; among them, some stand out, such as climatic disturbances derived from global change, the increase in movements of reservoir animals, or changes in land made by human activity. In the European continent, there have been an increasing number of epidemiological studies focused on the detection of these diseases, especially in dogs. In Spain, there are few epidemiological studies focused on the evaluation of the biotic and abiotic factors that may influence the distribution, such as climatic zones, orography, or presence of water reservoirs. The aim of this study was to analyze the prevalence and distribution of several canine vector-borne diseases caused by Dirofilaria immitis, Leishmania infantum, Anaplasma platys, and Ehrlichia canis in the autonomous community of Castilla y León, the largest region of the Iberian Peninsula, providing a geospatial approach based on a geographic information system (GIS) analysis. Blood from a total of 1,475 domestic dogs from the nine provinces of Castilla y León were analyzed. Also, a GIS analysis of the sample locations was carried out, taking into account the most important predictor variables. The prevalence in dogs infected by D. immitis was 7.19%, and the seroprevalence by L. infantum was 4.61 and 1.56% for A. platys and E. canis. Most of the infected animals were located in areas with stagnant water, irrigated agriculture, or riverbanks, always close to forest and woodland vegetation. These results indicate that dogs living in Castilla y León should take prophylactic measures to avoid infections.

Introduction

Canine vector-borne diseases (CVBDs) are caused by several infectious agents, which are transmitted by a wide variety of arthropods, mainly fleas, ticks, mosquitoes, and sandflies. Many of them are zoonotic diseases and are among the most important health problems affecting both domestic dogs and humans worldwide (1). Temperature and humidity are two determining factors that act directly in the establishment and distribution of the vectors and the diseases, as well as other factors derived from human activity such as the increase in the mobility of people and infected animals, or modifications in the landscape, mainly caused by increased irrigated crops or intensive urbanization of new areas. These processes favor the development of some vectors and the infection of the hosts (24).

Many of the CVBDs are clinically important, even be fatal, and frequently show unspecific symptoms, which make them difficult to diagnose. These include several zoonotic diseases such as heartworm disease, canine leishmaniasis, and canine anaplasmosis (35). In addition, canine ehrlichiosis, although not classified as zoonotic, has been sporadically described in several clinical cases in humans (6, 7).

Nematode Dirofilaria immitis, transmitted by culicid mosquitoes, is the causative agent of canine heartworm disease, a chronic disease which can lead to the death of the animal, although many of these animals are asymptomatic and become uncontrolled reservoirs (8). It is a zoonotic parasite which can cause pulmonary dirofilariasis, an asymptomatic infection, but that can be mistaken for lung cancer (2, 911). Protozooan Leishmania infantum, transmitted by Phlebotomus spp., causes canine leishmaniosis and induces a severe disease with serious clinical signs which, if not treated, can lead to the death of the animal. In addition, L. infantum can cause cutaneous lesions in humans or visceral leishmaniasis, the latter being a serious condition especially in immunocompromised patients (12). Anaplasma platys is the causative agent of canine cyclic thrombocytopenia, while Ehrlichia canis is the causative agent of canine monocytic ehrlichiosis. These gram-negative bacteria are mainly transmitted by ticks, and the diseases are characterized by non-specific signs, making diagnosis difficult (1316). In humans, E. canis and A. platys have been reported in clinically ill human patients causing from mild, self-limiting febrile illness to fatal infections (6, 7, 17).

In Europe, many epidemiological studies have been published showing a wide variability in the prevalence of the mentioned CVBDs. These differences may be due to the influence exerted by the biotic and abiotic variables of each region as well as the different diagnostic tools used (5, 18). In Spain, few studies have been published on the epidemiological status of these diseases mostly reporting data at a global level without evaluating the influence of environmental factors (i.e., orography, vegetation, climate) of each of the areas studied, especially those focused on Anaplasma spp. and E. canis (3, 5, 19).

These are CVBDs that are spreading throughout Europe and are considered emerging diseases. Therefore, it is important to evaluate the influence of the possible factors that contribute to this expansion; in this way, more accurate prediction models and measures aimed at stopping this expansion can be studied. The present study is focused on Castilla y León, representing a significant extension of territory, with different orographic and climatic zones depending on the province analyzed, to study the prevalence of the mentioned CVBDs as well as the influence of several biotic and abiotic factors. Also, the implementation of global positioning systems for geolocation of data together with the analysis of the environmental variables of a territory through GIS and spatial correlation models has shown to have a great capacity to understand spatial patterns of distribution of biological events in a territory (20). This ecoinformatic methodology allows the elaboration of predictive models focused on the determination of potential risks of parasitic diseases on a global scope [i.e., (21)] or in specific areas (22, 23).

Therefore, the aim of this study was to deepen the prevalence as well as the geographic distribution patterns of selected causative agents of CVBDs in the autonomous community of Castilla y León (Spain) by using GIS, to understand the causal relationship between the environmental variables and the prevalence of the infections.

Methods

Study Area

The Autonomous Community of Castilla y León is located in the northwestern quadrant of the Iberian Peninsula (Figure 1). With an area of 94,224 km2, it is the largest region in Spain and one of the largest of Europe, being greater than seven state members of the European Union (Austria, Belgium, Denmark, Holland, Ireland, Luxembourg, and Portugal). The orography of Castilla y León is mainly formed by a plateau with an average altitude of around 800 m above sea level, surrounded by a belt of mountainous reliefs to the north, east, and south, and bordering the west with Portugal. Administratively, it is divided into nine provinces (León, Zamora, Salamanca, Valladolid, Palencia, Burgos, Soria, Segovia, and Ávila) (Figure 2), with León being the largest (15,851 km2) and Segovia the smallest (6,921 km2) (24, 25).

FIGURE 1
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Figure 1. Location of Autonomous Community of Castilla y León, Spain.

FIGURE 2
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Figure 2. Prevalence for D. immitis (A), and seroprevalences for L. infantum (B), A. platys (C), and E. canis (D) in the nine provinces of Castilla y León, Spain. 0% (•); 0.1–0.9% (yes); 1–4.9% (yes); 5–10% (yes); >10 (yes).1, León; 2, Zamora; 3, Salamanca; 4, Valladolid; 5, Palencia; 6, Burgos; 7, Soria; 8, Segovia; 9, Ávila.

According to Köppen's climate classification, Castilla y León falls within the continental's Mediterranean climate, presenting long and cold winters, with average temperatures between 3 and 6°C in January, as well as short, hot summers (average temperatures from 19 to 22°C). The average annual rainfall is about 450–500 mm, accentuated in mountain ranges, but with hardly any rainfall during the summer months. Furthermore, due to the great extension and the orographic diversity of this territory, different sub-climates can be distinguished. A large part falls within the temperate with dry or temperate summer (Csb) or temperate with a dry season and temperate summer (Cfb) sub-climates, the average of the warmest month being below 22°C but above 10°C for ≥5 months. In several areas of the central plateau, the sub-climate is classified as temperate with dry or hot summer (Csa) as it exceeds 22°C during the summer, or cold steppe (BSk), with average annual temperatures below 18°C. At high altitudes in the mountain areas, the climate present is cold temperate with average temperatures below 3°C in the coldest months and dry summers (Dsb or Dsc) (26).

According to the map of phytoclimatic series by Rivas Martínez (27), the vegetation of Castilla y León is mainly included in the Mediterranean region, supra-Mediterranean floor, Carpetano-Iberico-Leonesa biogeographic province. The potential forest formations of quercines are predominant in it: holm oaks (Quercus ilex subsp. ballota), pyrenean oaks (Q. pyrenaica), cork oaks (Q. suber), and quejigo oaks (Q. faginea), which are planted, managed, and regularly pruned, configuring a manmade ecosystem characterized by a savannah-like physiognomy, locally known as “dehesa systems.” These forests cover most of the plains and middle slopes, but some beech (Fagus sylvatica) and chestnut forests (Castanea sativa) are also present in the mountainous foothills. Sabinas and juniper trees (Juniperus sp.) practically complete most of this forest landscape, together with the riverside communities associated with the main rivers and streams that cross the territory.

Sample Collection

The study included a total of 1,475 blood samples from domestic dogs, collected between September 2019 and December 2020 (Table 1). Samples were collected from dogs undergoing medical examination in 44 veterinary clinics and hospitals, with at least four veterinary clinics for each province of Castilla y León. The participation of clinics and hospitals was voluntary, and samples were collected throughout the duration of the study. Samples came from both owned and shelter dogs. The criteria for inclusion were (a) no previous history of infection, (b) not receiving regular chemoprophylaxis for the studied vector-borne diseases, and (c) owner consent to participate in the survey. Epidemiological data, such as sex, age at presentation to the clinics, and habitat (indoor, outdoor, or indoor/outdoor: at least 1–50% of the time spent outdoors), were recorded.

TABLE 1
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Table 1. Prevalence and seroprevalences of the studied vector-borne infections by sex, age, and habitat in Castilla y León, Spain.

Blood samples were collected from the cephalic or jugular vein, placed in 3-ml serum tubes, and centrifuged. Serum samples were kept at −20°C until tests were performed. All samples were tested for the detection of D. immitis antigens and for the detection of antibodies against L. infantum, E. canis, and A. platys by using Uranotest Quattro (Uranovet, Barcelona Spain) following the manufacturer's instructions.

Statistical Analysis

Data were analyzed by using SPSS Base 20.0 software (SPSS Inc./IBM, Chicago, IL, USA). A descriptive analysis of the variables considered was carried out considering the proportions of the qualitative variables. Chi-square and Fisher exact tests to compare proportions were performed. Sex, age, and habitat were considered as variables in the analysis for the autonomous community of Castilla y León and for each province. For the statistical analysis, dogs were grouped into five age groups (<1 year, from 1 to 5 years, from 5 to 10 years, from 10 to 15 years, and >15 years). In all cases, the significance level was established at p < 0.05.

GIS Mapping

A map of the sampling area was constructed using ArcMap v.10.8 (ESRI, 2020 Redlands, CA, USA), including the following layers of relevant environmental information that have been considered to be relevant for the dynamics of the analyzed organisms and their transmission vectors: climate, potential vegetation, and surface waters and surface and edaphic humidity (rivers, lakes, lagoons, irrigated croplands, and parks) (28, 29). Thematic symbols were added for easier interpretation of the map. The canine samples were georeferenced by the location of health centers where the veterinary consultations occurred. Therefore, the points shown on the maps correspond to the centroids of the polygons of the postal codes where the analyses of the dogs were carried out. Inferences were drawn from a proximity analysis between the presence points and the environmental characteristics of the layers used. The coordinate system used was gcs_ETRS_1989.

Results

Of the studied dogs, 7.72% were positive for one or several causative agents of CVBDs. The overall prevalence of D. immitis was 7.19%, and the seroprevalences of L. infantum, A. platys, and E. canis were 4.61, 1.56, and 1.56%, respectively. Results by sex, age groups, and habitat are shown in Table 1. Results for each of the nine provinces of Castilla y León are shown in Figure 2 and Tables 25.

TABLE 2
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Table 2. Numbers of dogs sampled and prevalence of D. immitis by sex, age, and habitat in the nine provinces of Castilla y León, Spain.

TABLE 3
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Table 3. Numbers of dogs sampled and seroprevalence of L. infantum by sex, age, and habitat in the nine provinces of Castilla y León, Spain.

TABLE 4
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Table 4. Numbers of dogs sampled and seroprevalence of A. platys by sex, age, and habitat in the nine provinces of Castilla y León, Spain.

TABLE 5
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Table 5. Numbers of dogs sampled and seroprevalence of E. canis by sex, age, and habitat in the nine provinces of Castilla y León, Spain.

No significant differences were found by sex or age in any of the studied causative agents of CVBDs (Table 1). However, when habitat was assessed, significant differences were observed in the prevalence of D. immitis and seroprevalence of E. canis between indoor and outdoor dogs (p < 0.05) and between indoor and indoor/outdoor dogs (p < 0.05). Significant differences between outdoor and indoor/outdoor were observed in results for L. infantum (p < 0.05). By provinces, only significant differences were observed in the prevalence of D. immitis between indoor and outdoor dogs in Valladolid and between indoor and indoor/outdoor dogs in Segovia (p < 0.05) (Table 2).

Coinfections were observed in 0.95% of the infected dogs. Of them, 0.34% were infected by D. immitis + L. infantum, 0.14% by D. immitis + A. platys, 0.14% by D. immitis + E. canis, 0.14% by L. infantum + A. platys, 0.14% by L. infantum + E. canis, and 0.07% by A. platys + E. canis. By provinces, coinfections were found in 2.25% of the dogs from León, with 0.9% for D. immitis + L. infantum, 0.45% for L. infantum + A. platys, and 0.9% for L. infantum + E. canis. In Zamora, coinfections were found in 0.73% of the samples, corresponding to D. immitis + A. platys coinfections. In Valladolid, 0.6% tested positive for D. immitis + E. canis and 0.6% for L. infantum + A. platys. In Salamanca, only one dog was infected by D. immitis + A. platys (0.73%). In Palencia, there were two dogs infected by D. immitis + L. infantum (1.79%) and in Burgos 0.35% that tested positive for D. immitis + A. platys, D. immitis + E. canis, and A. platys + E. canis. In Soria, Segovia, and Avila, there were no coinfections in any of the samples analyzed.

Regarding D. immitis, the highest prevalences were located in the center and west of Castilla y León, where Csb and Cfb climates were present, while no infected dogs were found in Soria (east). Regarding L. infantum, the provinces with the highest seroprevalences were located in the south. On the other hand, seroprevalences for A. platys and E. canis were low but present in the whole region, except for the absence of A. platys in Palencia and Soria. According to climate, positive animals for L. infantum, A. platys, and E. canis were found in BSk, Cfb, Csa, and Csf sub-climates.

From a geospatial point of view (Figures 3, 4), 94.55% of infected animals were located in areas with high edaphic availability of water, as either stagnant water, irrigated agriculture, or river banks, as well as close to forest and groves vegetation, near holm oak, pyrenean oak groves, quejigo oak forest, or riparian forest, all of them mainly found in wet locations with a great abundance of irrigated arable land in the surrounding area. The remaining 5.45% of the infected animals (12/220) did not usually live in these locations but had been in the same or nearby areas with high soil availability of water and similar vegetation. In fact, 6.6% (7/106) were infected by D. immitis, 5.88% (4/68) by L. infantum, 0% (0/23) by A. platys, and 4.34% (1/23) by E. canis.

FIGURE 3
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Figure 3. Location of wetlands and rivers and geolocation of dogs infected by D. immitis (yes), and seroprevalences for L. infantum (yes), A. platys (yes), and E. canis (yes) in the nine provinces of Castilla y León, Spain.

FIGURE 4
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Figure 4. Location of phytoclimatic series and geolocation of dogs infected by D. immitis (yes), and seroprevalences for L. infantum (yes), A. platys (yes), and E. canis (yes) in the nine provinces of Castilla y León, Spain.

Discussion

This manuscript shows the prevalence and seroprevalence of four causative agents of CVBDs in Castilla y León, the largest region of the Iberian Peninsula and one of the largest territories of the European Union. The highest positivity detected was that of D. immitis (7.19%), followed by L. infantum (4.61%), A. platys, and E. canis (1.56%), although these seroprevalences varied according to the geographical location of the provinces and the distribution of the samples tested.

A slight increase in the global prevalence of D. immitis was found when compared to a previous study, which reported a prevalence of 6.23% for Castilla y León (3). Although the data should be considered carefully due to the short time between one study and another, it is necessary to keep a constant record of variations in epidemiology to determine if there is an increasing trend in prevalence, which could confirm the expansion of this parasitosis in Spain (8). In Castilla y León, data at the provincial level only had been previously published for Salamanca, where prevalence decreased from 12.3 to 5.8% within 30 years (3032); furthermore, a hyperendemic zone was previously reported in Salamanca, characterized by irrigated lands near the riverbank and presence of stagnant water, which showed a decreasing prevalence from 33.3 to 16.7% (8, 3032). The results of the present study showed a slight increase in Salamanca, which may be due to the spread of the disease as well. The occurrence of canine cardiopulmonary dirofilariasis depends mostly on climatic factors such as temperature and humidity, although changes in land use derived from the human activity (e.g., the increase of irrigated crops), and the management of domestic animals also influences on the presence of the parasite and vectors (33). Although initially relegated to south and east of Spain, studies have confirmed the expansion toward northern and colder areas (3, 8). In addition, the presence of Cx. pipiens, widely present in Salamanca, has also been demonstrated to transmit the disease in this province (34). The results of this study confirm the risk of transmission specially associated with the presence of stagnant water, irrigated agriculture, crops, riverbanks, forests, and wet vegetation, as was predicted by a geo-environmental model (35), since infected dogs were located in areas with high or very high risk of infection in all provinces of Castilla y León.

Canine leishmaniosis has traditionally been considered as a disease limited to the Mediterranean basin (36), but several studies have reported an incipient increase in the number of cases in some areas of the north and central regions of Spain (3, 5, 37, 38), although the number of published studies is still low (39). Previous studies carried out in Castilla y León are sporadic and with a low number of samples analyzed. One of them showed an overall seroprevalence of 5.74% (3), and at the provincial level, another study carried out in Valladolid showed a seroprevalence of 5.3% (40). Both showed slightly higher prevalences than those reported in the present study, which could be due to the difference in the sampling process (with lower number of samples) rather than a real decrease in the prevalence, since an increase of this disease is being reported in Spain (3, 5, 39). Although from a geographical and climatic point of view, conditions of Castilla y León are very different and less favorable for the development of sandfly vectors from those in Mediterranean regions considered as endemic for Leishmania, the disease is well-established since seropositive dogs were found in irrigated areas, with a range of vegetation prone to vector establishment, and, moreover, cases of human leishmaniosis have been reported in Castilla y León (39), so control measures are necessary. It is possible that this expansion found in heartworm and in leishmaniosis is due to the fact that both diseases are considered not present in Castilla y León and, therefore, are not subject to strict prophylactic measures between veterinarians and owners.

Regarding A. platys and E. canis, few epidemiological data are available in Spain, but those published report the presence of both infectious agents mainly distributed in the provinces along the Mediterranean, although prevalences between 1 and 4.9% have also been reported in inland and isolated areas of the Iberian Peninsula (3, 4). It seems that the presence in the studied territory has decreased, since previous studies reported global prevalences of 19.2% in 1996 and 2% in 2020 for E. canis (3, 40, 41). Similar findings have been seen for Anaplasma spp., which previous surveys have reported a global prevalence of 2.74% and prevalence of 19% in Valladolid (3, 40). This decrease is confirmed by the present results. Ixodes spp. and Rhipicephalus sanguineus, vectors of these diseases, are widely distributed throughout Castilla y León, the Iberian Peninsula, and Europe (42), being mainly located in areas with presence of grass, bushes, or trees. Furthermore, wild animals can act as reservoirs (43, 44), and in those provinces with higher seroprevalences there is a large population of wild animals (wolves, foxes) which in some cases live near houses and villages. In areas bordering the north of the region, where climatic and geographical conditions are much more favorable to vector development, previously reported seroprevalences were notably higher (5.01 and 3.13% to A. platys and E. canis, respectively) (45). It seems contradictory since climate changes favor the proliferation of ticks, but it could be due to the use of doxycycline for the treatment of several canine infections, as it is known that the dogs in this study did not receive adequate prophylaxis.

No significant differences were found by sex in this study, similar to other previous studies focused on these diseases such as other studies (3, 11, 19, 46). When age was assessed, no significant differences were observed between age groups, although differences have been observed in other epidemiological studies (4, 5, 11, 4750). Regarding habitat of the animals, significantly higher prevalences were found in outdoor and indoor/outdoor dogs, as described by other authors (3, 5, 11, 51), since outdoor animals are more exposed to vectors. However, the study showed infected dogs living indoors as well. This is because some arthropods, such as mosquitoes, have access to indoors, and because animals living indoors are not fully enclosed and have a certain amount of access to the outdoors. Therefore, prophylactic measures should be applied to all dogs equally.

The preliminary GIS analysis suggests the existence of patterns of appearance of the infections with certain bioclimatic and environmental variables. The presence of areas with stagnant water, irrigation systems, irrigated agriculture, river banks, and different types of climatologies and vegetation favorable for the development of the vectors detected in the same places where positive dogs have been recorded suggests the existence of patterns of occurrence of the reported diseases with certain bioclimatic and environmental variables (35, 52, 53). The establishment of causal circumstances that can serve to predict risk areas requires a more in-depth study both in the resolution of these variables and in the incorporation of others that can explain in a more precise way the interactions between the parasite, its hosts, and the dispersal vectors. Expanding the methodology through the incorporation of spatial correlation analysis is one of the needs in this epidemiological field.

In conclusion, the results of this epidemiological study show a wide distribution of the evaluated causative agents of CVBDs in Castilla y León, which is very significant given the great geographical extension of the territory. The data obtained reveal the influence of the climate, orography, and presence of water, which will allow to comprehend their evolution in Castilla y León. Given the risk of infection or exposure to pathogens, as their presence in humans in Spain has been described, a close relationship between veterinarians, physicians, and public health administrations under the concept of One Health is needed. This would allow effective control measures to be carried out on infected animals and vectors, mainly focused on prophylactic measures to be applied routinely on dogs.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The animal study was reviewed and approved by University of Las Palmas de Gran Canaria. Written informed consent was obtained from the owners for the participation of their animals in this study.

Author Contributions

EC, RM, and IR-E wrote the manuscript. EC, RM, and JM-A designed the study and obtained funding. PP, IR-E, and JS performed the fieldwork and collected the data. EC, RM, JM-A, and JL-M participated in the revision of the manuscript. All authors participated in the design and production of the figures and have read and agreed to the published version of the manuscript.

Funding

The study was carried out under the frame of CEVA Salud Animal (Spain), Fundación General de la Universidad de Salamanca, and Agencia de Desarrollo Económico de Castilla y León (cofinanced with FEDER funds-Art. 83).

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.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

The authors would like to thank Marta Ruiz-Somacarrera, degree student in Pharmacy (University of Salamanca), and Xiomara Murcia, masters student in Tropical Diseases (University of Salamanca), for their contribution to the study, and all veterinarians who kindly collaborated and provided samples for this research. Without their collaboration and dedication, this study could not have been carried out. Also, the authors would like to thank CEVA for their help and support throughout all the study.

References

1. Springer A, Montenegro VM, Schicht S, Pantchev N, Strube C. Seroprevalence and current infections of canine vector-borne diseases in Nicaragua. Parasit Vectors. (2018) 11:585. doi: 10.1186/s13071-018-3173-1

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Esteban-Mendoza MV, Arcila-Quiceno V, Albarracín-Navas J, Hernández I, Flechas-Alarcón MC, Morchón R. Current situation of the presence of Dirofilaria immitis in dogs and humans in Bucaramanga, Colombia. Front Vet Sci. (2020) 7:488. doi: 10.3389/fvets.2020.00488

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Montoya-Alonso JA, Morchón R, Costa-Rodríguez N, Matos JI, Falcón-Cordón Y, Carretón E. Current distribution of selected vector-borne diseases in dogs in Spain. Front Vet Sci. (2020) 7:564429. doi: 10.3389/fvets.2020.564429

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Sainz Á, Roura X, Miró G, Estrada-Peña A, Kohn B, Harrus S, et al. Guideline for veterinary practitioners on canine ehrlichiosis and anaplasmosis in Europe. Parasit Vectors. (2015) 8:75. doi: 10.1186/s13071-015-0649-0

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Montoya A, Checa R, Marino V, Gálvez R, Portero M, De Mari K, et al. Antibodies elicited by the CaniLeish® vaccine: long-term clinical follow-up study of dogs in Spain. Parasitol Res. (2021) 120:1471–9. doi: 10.1007/s00436-021-07091-1

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Perez M, Bodor M, Zhang C, Xiong Q, Rikihisa Y. Human infection with Ehrlichia canis accompanied by clinical signs in Venezuela. Ann N Y Acad Sci. (2010) 1212:130. doi: 10.1196/annals.1374.016

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Franco-Zetina M, Adame-Gallegos J, Dzul-Rosado K. Effectivity of diagnostic methods for the detection of human and canine monocytic ehrlichiosis. Rev Chilena Infectol. (2019) 36:650–5. doi: 10.4067/S0716-10182019000500650

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Morchón R, Carretón E, González-Miguel J, Mellado-Hernández I. Heartworm disease (Dirofilaria immitis) and their vectors in Europe - new distribution trends. Front Physiol. (2012) 3:196. doi: 10.3389/fphys.2012.00196

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Simón F, Muro A, Cordero M, Martin J. A seroepidemiologic survey of human dirofilariosis in Western Spain. Trop Med Parasitol. (1991) 42:106–8.

PubMed Abstract | Google Scholar

10. Savić S, Stosic MZ, Marcic D, Hernández I, Potkonjak A, Otasevic S, et al. Seroepidemiological study of canine and human dirofilariasis in the endemic region of Northern Serbia. Front Vet Sci. (2020) 7:571. doi: 10.3389/fvets.2020.00571

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Zumaquero L, Simón F, Carretón E, Hernández I, Sandoval C, Morchón R. Prevalence of canine and human dirofilariosis in Puebla, Mexico. Vet Parasitol. (2020) 282:109098. doi: 10.1016/j.vetpar.2020.109098

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Alvar J, Vélez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis Worldwide and global estimates of its incidence. PLoS ONE. (2012) 7:e35671. doi: 10.1371/journal.pone.0035671

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Harrus S. Perspectives on the pathogenesis and treatment of canine monocytic ehrlichiosis (Ehrlichia canis). Vet J. (2015) 204:239–40. doi: 10.1016/j.tvjl.2015.04.027

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Cazan CD, Ionică AM, Matei IA, D'Amico G, Muñoz C, Berriatua E, et al. Detection of Leishmania infantum DNA and antibodies against Anaplasma spp. Borrelia burgdorferi sl and Ehrlichia canis in a dog kennel in South-Central Romania. Acta Vet Scand. (2020) 62:42. doi: 10.1186/s13028-020-00540-4

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Dyachenko V, Pantchev N, Balzer HJ, Meyersen A, Straubinger RK. First case of Anaplasma platys infection in a dog from Croatia. Parasit Vect. (2012) 5:49. doi: 10.1186/1756-3305-5-49

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Bouzouraa T, René-Martellet M, Chêne J, Attipa C, Lebert I, Chalvet-Monfray K, et al. Clinical and laboratory features of canine Anaplasma platys infection in 32 naturally infected dogs in the Mediterranean basin. Ticks Tick Borne Dis. (2016) 7:1256–64. doi: 10.1016/j.ttbdis.2016.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Zobba R, Schianchi E, Ben Said M, Belkahia H, Messadi L, Piredda R, et al. gltA typing of Anaplasma strains related to A. platys: taxonomical and one health implications. Ticks Tick Borne Dis. (2021) 13:101850. doi: 10.1016/j.ttbdis.2021.101850

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Panarese R, Iatta R, Mendoza-Roldan JA, Szlosek D, Braff J, Liu J, et al. Comparison of diagnostic tools for the detection of Dirofilaria immitis infection in dogs. Pathogens. (2020) 9:499. doi: 10.3390/pathogens9060499

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Díaz-Regañón D, Roura X, Suárez ML, León M, Sainz Á. Serological evaluation of selected vector-borne pathogens in owned dogs from northern Spain based on a multicenter study using a commercial test. Parasit Vect. (2020) 13:301. doi: 10.1186/s13071-020-04172-5

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Pullan RL, Sturrock HJW, Soares Magalhaes RJ, Clements ACA, Brooker SK. Spatial parasite ecology and epidemiology: a review of methods and applications. Parasitology. (2012) 139:1870–87. doi: 10.1017/S0031182012000698

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Weiss DJ, Lucas TCD, Nguyen M, Nandi AK, Bisanzio D, Battle KE, et al. Mapping the global prevalence, incidence, and mortality of Plasmodium falciparum, 2000–17: a spatial and temporal modelling study. Lancet. (2019) 394:322–31. doi: 10.1016/S0140-6736(19)31097-9

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Sifaki-Pistola D, Ntais P, Christodoulou V, Mazeris A, Antoniou M. The use of spatial analysis to estimate the prevalence of canine leishmaniasis in Greece and Cyprus to predict its future variation and relate it to human disease. Am J Trop Med Hyg. (2014) 91:336–41. doi: 10.4269/ajtmh.13-0459

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Rinaldi L, Biggeri A, Carbone S, Musella V, Catelan D, Veneziano V, et al. Canine faecal contamination and parasitic risk in the city of Naples (southern Italy). BMC Vet Res. (2006) 2:29. doi: 10.1186/1746-6148-2-29

PubMed Abstract | CrossRef Full Text | Google Scholar

24. European Commission (2021). Available online at: https://ec.europa.eu/growth/tools-databases/regional-innovation-monitor/base-profile/castilla-y-leon (accessed July 6, 2021).

25. Research Innovation Strategy for Smart Specialisation (RIS3) of Castilla y León 2014-2020. (2021). Available online at: https://fuescyl.com/images/03innovacion_conocimiento/Comisionado/RIS3_Castilla_y_Leon_2014-2020_(eng).pdf (accessed September 29, 2021).

26. Agencia Estatal de Meteorología Ministerio de Agricultura Alimentación y Medio Ambiente. Iberian Climate Atlas. Air Temperature and Precipitation (1971-2000) (2021).

27. Rivas Martínez S,. Memoria del Mapa de Series de Vegetación de España 1: 400000 ICONA Ministerio de Agricultura. (1987). Available online at: https://www.mitecogobes/es/biodiversidad/servicios/banco-datos-naturaleza/informacion-disponible/memoria_mapa_series_veg_descargasaspx (accessed July 20, 2021).

28. Climate shifts. In: Worldmaps of Köppen-Geiger Climate Classification. (2019). Available online at: https://koeppen-geiger.vu-wien.ac.at/shifts.html (accessed July 20, 2021).

Google Scholar

29. Ministerio para la Transición Ecológica y el Reto Demográfico (2021. Available online at: https://www.miteco.gob.es/es/biodiversidad/ (accessed July 20, 2021).

Google Scholar

30. Diosdado A, Gómez PJ, González-Miguel J, Simón F, Morchón R. Current status of canine dirofilariosis in an endemic area of western Spain. J Helminthol. (2018) 92:520–3. doi: 10.1017/S0022149X17000591

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Morchón R, Mellado I, González-Miguel J, Hernández MV, Hernández L, Simón F. Prevalencia de la dirofilariosis cardiopulmonar canina. Argos. (2011) 126:30.

Google Scholar

32. Pérez-Sánchez R, Gómez-Bautista M, Grandes AE. Canine filariasis in Salamanca (northwest Spain). Ann Trop Med Parasitol. (1989) 83:143–50. doi: 10.1080/00034983.1989.11812322

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Simón F, Siles-Lucas M, Morchón R, González-Miguel J, Mellado I, Carretón E, et al. Human and animal dirofilariasis: the emergence of a zoonotic mosaic. Clin Microbiol Rev. (2012) 25:507–44. doi: 10.1128/CMR.00012-12

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Morchón R, Bargues MD, Latorre JM, Melero-Alcíbar R, Pou-Barreto C, Mas-Coma S, et al. Haplotype H1 of Culex pipiens implicated as natural vector of Dirofilaria immitis in an endemic area of Western Spain. Vector Borne Zoonot Dis. (2007) 7:653–8. doi: 10.1089/vbz.2007.0124

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Simón L, Afonin A, López-Díez LI, González-Miguel J, Morchón R, Carretón E, et al. Geo-environmental model for the prediction of potential transmission risk of Dirofilaria in an area with dry climate and extensive irrigated crops. The case of Spain. Vet Parasitol. (2014) 200:257–64. doi: 10.1016/j.vetpar.2013.12.027

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Fahrion A, Gasimov E, Joseph S, Grout L, Allan M, Postigo JR. Surveillance of leishmaniasis in the WHO European Region. Rev Épidémiol Santé Publique. (2018) 66:S394. doi: 10.1016/j.respe.2018.05.429

CrossRef Full Text | Google Scholar

37. González E, Jiménez M, Hernández S, Martín-Martín I, Molina R. Phlebotomine sand fly survey in the focus of leishmaniasis in Madrid, Spain (2012-2014): seasonal dynamics, Leishmania infantum infection rates and blood meal preferences. Parasit Vectors. (2017) 10:368. doi: 10.1186/s13071-017-2309-z

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Alcover MM, Ribas A, Guillén MC, Berenguer D, Tomás-Pérez M, Riera C, et al. Wild mammals as potential silent reservoirs of Leishmania infantum in a Mediterranean area. Prev Vet Med. (2020) 175:104874. doi: 10.1016/j.prevetmed.2019.104874

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Garrote JI, Gutiérrez MP, Izquierdo RL, Dueñas MA, Zarzosa P, Cañavate C, et al. Seroepidemiologic study of Leishmania infantum infection in Castilla-Leon, Spain. Am J Trop Med Hyg. (2004) 71:403–6. doi: 10.4269/ajtmh.2004.71.403

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Couto CG, Lorentzen L, Beall MJ, Shields J, Bertolone N, Couto JI, et al. Serological study of selected vector-borne diseases in shelter dogs in central Spain using point-of-care assays. Vector Borne Zoonotic Dis. (2010) 10:885–8. doi: 10.1089/vbz.2009.0063

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Sainz A, Delgado S, Amusátegui I, Tesouro MA. Seroprevalence of canine ehrlichiosis in Castilla-León (northwest of Spain). Prev Med Vet. (1996) 29:1–7. doi: 10.1016/S0167-5877(96)01060-4

CrossRef Full Text | Google Scholar

42. Nicholson WL, Allen KE, McQuiston JH, Breitschwerdt EB, Little SE. The increasing recognition of rickettsial pathogens in dogs and people. Trends Parasitol. (2010) 26:205–12. doi: 10.1016/j.pt.2010.01.007

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Fishman Z, Gonen L, Harrus S, Strauss-Ayali D, King R, Baneth G. A serosurvey of Hepatozoon canis and Ehrlichia canis antibodies in wild red foxes (Vulpes vulpes) from Israel. Vet Parasitol. (2004) 119:21–6. doi: 10.1016/j.vetpar.2003.08.012

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Alkishe A, Raghavan RK, Peterson AT. Likely geographic distributional shifts among medically important tick species and tick-associated diseases under climate change in North America: a review. Insects. (2021) 12:225. doi: 10.3390/insects12030225

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Amusategui I, Tesouro MA, Kakoma I, Sainz A. Serological reactivity to Ehrlichia canis, Anaplasma phagocytophilum, Neorickettsia risticii, Borrelia burgdorferi and Rickettsia conorii in dogs from northwestern Spain. Vector Borne Zoonot Dis. (2008) 8:797–803. doi: 10.1089/vbz.2007.0277

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Solano-Gallego L, Llull J, Osso M, Hegarty B, Breitschwerdt E. A serological study of exposure to arthropod-borne pathogens in dogs from northeastern Spain. Vet Res. (2006) 37:231–44. doi: 10.1051/vetres:2005054

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Encinas Grandes A, Gómez Bautista M, Martin Novo M, Simón F. Leishmaniasis in the province of Salamanca, Spain. Prevalence in dogs, and seasonal dynamics of vectors. Ann Parasitol Hum Comp. (1988) 63:387–97. doi: 10.1051/parasite/1988636387

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Fisa R, Gállego M, Castillejo S, Aisa MJ, Serra T, Riera C, et al. Epidemiology of canine leishmaniosis in Catalonia (Spain) the example of the Priorat focus. Vet Parasitol. (1999) 83:87–97. doi: 10.1016/S0304-4017(99)00074-6

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Portillo A, Pérez-Martínez L, Santibáñez S, Santibáñez P, Palomar AM, Oteo JA. Anaplasma spp. in wild mammals and Ixodes ricinus from the north of Spain. Vector Borne Zoonot Dis. (2011) 11:3–8. doi: 10.1089/vbz.2009.0214

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Vélez R, Ballart C, Domenech E, Abras A, Fernández-Arévalo A, Gómez SA, et al. Seroprevalence of canine Leishmania infantum infection in the Mediterranean region and identification of risk factors: the example of North-Eastern and Pyrenean areas of Spain. Prev Vet Med. (2019) 162:67–75. doi: 10.1016/j.prevetmed.2018.10.015

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Morillas F, Sanchez Rabasco F, Ocaña J, Martin-Sanchez J, Ocaña-Wihelmi J, Acedo C. Leishmaniasis in the focus of the Axarquía region, province of Málaga, southern Spain: a survey of humans, dogs, and vector. Parasitol Res. (1996) 82:569–70. doi: 10.1007/s004360050164

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Gálvez R, Montoya A, Cruz I, Fernández C, Martín O, Checa R, et al. Latest trends in Leishmania infantum infection in dogs in Spain, Part I: mapped seroprevalence and sand fly distributions. Parasit Vectors. (2020) 13:204. doi: 10.1186/s13071-020-04081-7

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Saleh MN, Allen KE, Lineberry MW, Little SE, Reichard MV. Ticks infesting dogs and cats in North America: biology, geographic distribution, and pathogen transmission. Vet Parasitol. (2021) 294:109392. doi: 10.1016/j.vetpar.2021.109392

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: canine vector borne disease, D. immitis, L. infantum, GIS, Spain, epidemiology, E. canis, A. platys.

Citation: Pérez Pérez P, Rodríguez-Escolar I, Carretón E, Sánchez Agudo JÁ, Lorenzo-Morales J, Montoya-Alonso JA and Morchón R (2021) Serological Survey of Canine Vector-Borne Infections in North-Center Spain. Front. Vet. Sci. 8:784331. doi: 10.3389/fvets.2021.784331

Received: 27 September 2021; Accepted: 05 November 2021;
Published: 06 December 2021.

Edited by:

Dirk Werling, Royal Veterinary College (RVC), United Kingdom

Reviewed by:

Dietmar Hamel, Boehringer Ingelheim Vetmedica GmbH, Germany
Roberta Iatta, University of Bari Aldo Moro, Italy

Copyright © 2021 Pérez Pérez, Rodríguez-Escolar, Carretón, Sánchez Agudo, Lorenzo-Morales, Montoya-Alonso and Morchón. 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: Elena Carretón, elena.carreton@ulpgc.es; Rodrigo Morchón, rmorgar@usal.es

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