Marcel Haas1*
Lisa Segeritz1Ole Anders2Tomma Lilli Middelhoff2Akary Myat Tun3
Seyed Sajjad Hasheminasab1Berardino Cocchiararo4
Alena Dusch1
Anja Taubert1
Carlos Hermosilla1- 1Institute of Parasitology, Biomedical Research Center Seltersberg, Justus Liebig University Giessen, Giessen, Germany
- 2Harz National Park, Wernigerode, Germany
- 3Lplan – Planning Office for Landscape and Aquatic Ecology, Erlensee, Germany
- 4Centre for Wildlife Genetics, Senckenberg Research Institute and Natural History Museum Frankfurt, Gelnhausen, Germany
The formerly widely spread Eurasian lynx (Lynx lynx) nowadays represents an endangered large wild felid species in Germany. Recent and ongoing conservation efforts have succeeded in establishing small but stable lynx populations in distinct parts of Germany. However, very little is known on the occurrence of neglected and re-emerging gastropod-borne cardiopulmonary nematodes in wild L. lynx populations in Europe. Therefore, the aim of current study was to estimate metastrongyloid infections in, a group of seven free-ranging, (sub-) adult Eurasian lynxes from the Harz Mountains (Germany) which were equipped with GPS/GSMS collars and in resident gastropod intermediate host populations. Both, lynx scat samples (n = 24) and terrestrial gastropods (n = 153) were collected in close proximity to prey remains left behind by Eurasian lynxes respectively in natural habitats in a non-invasive and un-molested manner. Fresh fecal samples were analyzed for the presence of metastrongyloid first-stage larvae (L1) by standard Baermann funnel technique and morphologically identified to genus level. Morphological metastrongyloid L1 were additionally investigated by PCR for final species identification. Terrestrial gastropods (i.e., slugs, semi-slugs, snails) were morphologically identified to genus level, thereafter artificially digested and analyzed for the presence of lungworm larvae. This work delivers a first report on the occurrence of patent Troglostrongylus brevior-, and Crenosoma sp.-infections in wild Eurasian lynxes in Germany and re-confirms recent findings on Aelurostrongylus abstrusus- and Angiostrongylus sp. infections in these lynxes. Overall, a total lungworm occurrence of 37,5% (9/24) was detected in assessed Eurasian lynx samples and 51.1% (4/7) of lynxes showed patent metastrongyloid infections. In digested terrestrial gastropods, 1.3% (2/153) contained A. vasorum larvae, underlining a successful propagation of A. vasorum life cycle in the Harz Mountains. Hence, we recommend regular monitoring for metastrongyloid infections not only in wild Eurasian lynxes but also in obligate intermediate hosts to better understand their impact on animal and population health to support current conservation efforts on this endangered large felid species in Europe.
1 Introduction
The Eurasian lynx (Lynx lynx) represents the largest felid apex predator in Europe and, in consequence, plays a fundamental role in the maintenance of ecosystem health by not only influencing food web composition but also increasing biodiversity in natural biomes (1–7). Consistently, as a natural apex predator, L. lynx might affect prey behavior, number and composition and thereby indirectly influencing flora and fauna biodiversity (5–7). Additionally, the surrounding of the remains of Eurasian lynx prey, also referred to as killing sites, can be recognized as such for several weeks, since lynx feed on their prey multiple times, depending on the prey size and eventual disturbances. Killing sites are nowadays considered as important micro-ecosystems influencing environmental biomes (5–8). Consistently, killing sites can provide valuable data on predator-prey relationships, on complex host-parasite interactions, and additionally serve as nutritional sources for numerous vertebrates, invertebrates and microbes (8–16). Despite a positive impact of wild Eurasian lynxes on ecosystem preservation, their crucial role in biodiversity improvement is generally underestimated in Germany and elsewhere (2–7).
Two hundred years ago, the geographic distribution of Eurasian lynxes ranged from the European mainland to Central Asia and from the Tibetan plateau of China to Eastern parts of Russia (17–22). The Eurasian lynx has the IUCN (International Union for the Conservation of Nature) status least concern and is strictly protected by the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), the Council Regulation (EC) 338/97 and Federal Species Protection Regulations (FSPR) in face of its population vulnerability (19, 21). However, according to the IUCN, the total Eurasian lynx population is listed as “least concern” since it shows a wide distribution in sparsely populated geographic areas of Eastern Europe and Asia (19, 21, 23). In contrast, in Germany, Eurasian lynxes are still facing extinction and are therefore listed as “critically endangered” according to the IUCN and the German Red List Centre (GRLC), based on their low individual numbers and critical population fragmentation (18–25). Main threats for L. lynx survival in Central Europe are poaching, traffic accidents, habitat fragmentation, habitat loss and insufficient presence of prey. Moreover, infectious diseases like viral infections (e.g., canine distemper, FeLV, FIV) and parasite infestations (e.g., Sarcoptes) negatively impact small Eurasian lynx populations as it is the case for the re-introduced Harz Mountain population (23, 26). Given that ecto- and endoparasitoses are well-known as causes of suffering and decline (27, 28), regular monitoring seems relevant for conservation issues. Accordingly, feline gastropod-borne metastrongyloid nematodes, such as Aelurostrogylus abstrusus, Angiostrongylus chabaudi, Crenosoma vismani, and Troglostrongylus brevior, can cause bronchopneumonia and cardiopulmonary disorders in various definite hosts, including wild felids and lynxes (29–32). Alongside, some of these lungworm species parasitize domestic/feral cats (Felis catus) and wild cats (Felis silvestris) (33–42). Nonetheless, very little is currently known on these infections in free-ranging Eurasian lynxes. The crenosomatid lungworm species T. brevior and C. vismani parasitize the bronchi and bronchioles of feline definite hosts whilst A. abstrusus resides in subpleural parenchyma and alveoli (32, 37, 43, 44). Conversely, the angiotropic nematode A. chabaudi parasitizes the pulmonary arteries and the right heart of mainly wild cats (30, 33, 45). Embryonated metastrongyloid eggs are deposited, first-stage larvae (L1) hatch and migrate via lung tissues to larynx/pharynx, are swallowed and shed via defecation into the environment during patency. Thereafter, exogenous L1 infect terrestrial gastropods (i.e., slugs, semi-slugs, snails) acting as obligate intermediate hosts. In gastropods, L1 develop into second-(L2) and infective third-(L3) larval stages within approximately 2–4 weeks, depending on the parasite species. Eurasian lynxes become infected either after ingesting L3-infected gastropods or via consumption of paratenic hosts (amphibians, reptiles, birds, rodents) carrying infective L3. Alternatively, but more unlikely, wild Eurasian lynxes might become infected from standing waters containing dead intermediate hosts and/or released infective L3 (46). In case of T. brevior, also lactogenic transmission was recently demonstrated for domestic cats in Italy (42).
Feline troglostrongylosis has gained scientific interest in Europe where it is considered as a spill-over event from wild cats (F. silvestris) to feral cats (30, 32, 37, 42, 47–52). Pathological alterations of troglostrongylosis in lynx include multifocal, consolidated, firm tan to gray areas in various lung lobes with thickened alveoli walls, filled with necrotic debris, leukocyte infiltration and degenerated inflammatory cells, as well as parasite larvae and eggs and a lung oedema (32), thereby corroborating histopathological findings of T. brevior-infected wild cats (F. silvestris) (35, 36, 53). In line, proteinaceous lung oedema was described in wild bobcats (Lynx rufus) infected with closely related Troglostrongylus wilsoni (54). Of note, a recent study identified T. brevior in terrestrial gastropods in South America thereby expanding its geographic distribution (55). Obviously, spill-over of metastrongyloid infections from feral cats to free-ranging Eurasian lynxes or wild cats may occur when sharing the same biome (31). As already stated, only few studies exist on patent metastrongyloid infections in wild Eurasian lynxes and on their impact on population health (29, 31, 32, 37, 38). Therefore, the current study aims to add epizootiological data by evaluating not only patent metastrongyloid infections in free-living Eurasian lynxes but also in gastropod intermediate hosts in the Harz Mountains, being habitat of the largest L. lynx population in Germany.
2 Material and methods
2.1 Study area
Collection sites were allocated along the western part of the Harz Mountains nearby the Harz National Park (HNP; 51.6946953, 10.5674415) in Germany. This mountainous area outside the HNP is characterized by opened landscapes, vast forested and meadow areas, provincial towns and some large country roads. An illustration of the study area is given in Figure 1, the respective geographic map was generated by QGIS V.3.28.1 (QGIS Geographic Information System. QGIS Association. http://www.qgis.org).
Figure 1. Study area with fecal sampling sites (dots) and gastropod collection sites (triangles) according to the associated lynxes (for clarification which lynx is associated see Table 1). The Harz National Park (black outline drawing), and country roads (orange) in the area of study.
2.2 Collection of scat samples and gastropods at Eurasian lynx killing sites
Wild Eurasian lynxes sampled in this study included 6 young/sub-adult animals and an adult male. Four of these lynxes (F10, M18, M19, and M20) were rehabilitated animals, which were originally found as orphans and raised in enclosures before being released again into the wild. The other three animals (F11, F12, and M22) were captured weak, and were rehabilitated before release, none of them showed any clinical respiratory signs. All animals were equipped with GPS/GSM-transmitting collars (VECTRONIC AEROSPACE, Berlin) by the staff of the HNP before release (see Figure 2). Moreover, parasitological examinations of collared juvenile Eurasian lynxes were performed, which excludes M22 which was captured as an adult animal. All juvenile animals were tested with copromicroscopy and were all found positive for Toxocara cati and thus received anthelmintic treatments (Ivomec®, ivermectin, 0.5 mg/kg, Boehringer Ingelheim), before being released again. Lynx killing sites were identified using two handheld GPS devices (GPSMAP® 64s and GPSMAP® 65s, Garmin, Olathe, USA) and by profiting from received repeated collar-transmitted signals from distinct geographic spots, thereby proving the presence of lynxes at this locations (see above). In the current study, hidden prey animals included roe deer (Capreolus capreolus), hares (Lepus europaeus) and red foxes (Vulpes vulpes). A variety of arthropods (e.g., flies, maggots, carrion beetles, ants and isopods) as well as different terrestrial gastropods (i.e., slugs, semi-slugs and snails) were found in close proximity to killing sites (please refer to Figures 3, 5). In total, 41 killing sites or Eurasian lynx habitats were identified via GPS tracking and on 25 sites, scat- and/or gastropod samples were successfully collected.
Figure 2. A wild Eurasian lynx (Lynx lynx) wearing a GPS collar.
Figure 3. A typical Eurasian lynx (Lynx lynx) killing site at the Harz Mountains. (A) Leftovers of a killed roe deer (Capreolus capreolus). Initially the carcass was found entirely covered with grass, leaves, branches and soil particles; (B) a red-breasted carrion beetle (Oiceoptoma thoracicum) feeding on meat leftovers of a roe deer pelvis. (C) An excavated Eurasian lynx faecal sample which was also found entirely hidden under grass, leaves and branches. (D) Terrestrial slug (Arion sp.; indicated by red circle) found on a bone.
Figure 4. Coproscopic findings of metastrongyloid first-stage larvae (L1) in Eurasian lynx fecal samples. (A) Aelurostrongylus abstrusus, 366 μm length, 15 μm width; (B) Troglostrongylus brevior, 340 μm length, 19 μm width; (C) Angiostrongylus sp.-larvae 370 μm length, 15 μm width; (D) Crenosoma sp. 314 μm length, 14 μm width.
Figure 5. Example of collected terrestrial gastropods. (A) Juvenile Arion sp. (breathing hole in cranial part of the mantle); (B) adult Arion cf. rufus (breathing hole in cranial part of the mantle, rocking behavior, orange coloration); (C) Daudebardia cf. brevipes (grey-blueish body, specific shell formation); (D) Cepaea hortensis (yellow mouthlip of the shell).
Overall, 24 individual fecal samples originating from the seven individuals mentioned above, were collected during six visits of killing sites between March 2022 and February 2023. As mentioned before these samples could be associated with the different individual lynx by the sampling methods here used. Following this 3/24 samples originated from M18 (12,5%), 6/24 from M19 (25%), 1/24 from M20 (4,2%), 3/24 from M22 (12,5%), 3/24 from F10 (12,5%), 4/24 from F11 (16,6%), 1/24 from F12 (4,2%) and 3/24 from a meeting point of F12 + M22 (12,5%). Scat samples were identified based on characteristic morphology, size, composition (mainly containing roe deer hair), emission of lynx-specific odor, as well as the feline specific covering behavior of the feces with surrounding material. All the before mentioned characteristics in combination lead to the diagnosis of lynx feces. Collected scat samples were labeled, kept at 4°C and immediately transferred to the Institute of Parasitology of the Justus Liebig University Giessen for further parasitological analysis. In cases of uncertainty of the scat origin, fecal samples were additionally analyzed by molecular approaches at the Centre for Wildlife Genetics, Senckenberg Research Institute and Natural History Museum, Gelnhausen, Germany (for detailed description of this methodology refer to Section 2.3).
Besides scat samples, a total of 153 terrestrial gastropods were collected during 2021 and 2023 at 14 previously selected GPS-tracked killing sites or in Eurasian lynx habitats during scat sampling (please refer to Table 1, Figures 1, 5), and surrounding areas (up to 1 km radius). All gastropods were collected manually by wearing gloves in search for humid mollusc hiding places (i.e., beneath leaves, rocks or rotten wood) or in close proximity to killing sites. Some slugs were directly collected from carcasses, bones or beneath carcasses, as illustrated in Figure 3. All GPS-identified lynx killing sites were visited during daytime to avoid disturbance of nocturnal Eurasian lynxes and prey animals and with a time delay of at least 3 days to not disturb lynxes in their feeding behavior.
Table 1. Sample collection sides with associated lynxes.
2.3 Molecular analysis of lynx feces
At the Centre for Wildlife Genetics (Senckenberg Research Institute and Natural History Museum, Gelnhausen, Germany) DNA from fecal samples were extracted, this and the following steps were performed by using the QIAamp Fast DNA Stool Mini Kit (Qiagen, Germany) and using the Qiacube-Robotic-System (Qiagen, Germany). Two mitochondrial markers were employed for species identification. The first marker consisted of the two primers L15995 (5′-CTCCACTATCAGCACCCAAAG-3′) and H16498 (5′-CCTGAAGTAAGAACCAGATG-3′) (56) and was used for general confirmation of a mammal species. The second marker consisted of the two primers LF4 (5′-GACATAATAGTGCTTAATCGTGC-3′) (57) and H16498 (5′-CCTGAAGTAAGAACCAGATG-3′) (58) detecting particularly members of the family Felidae. For PCR, 5 μl SensiFAST SYBR No-ROX Kit (Biocat, Germany), 0.4 μl of the respective primer pair, 1.2 μl of nucleic acid-free Water (Carl Roth, Germany) and 3 μl of DNA extract were mixed. The cycling protocol included 1 × 3 min at 95°C, 40 × 95°C for 5 s and 60°C for 30 s, 10°C for storage. Before Sanger sequencing, PCR products were purified by ExoSAP-IT (Thermofisher Scientific, USA) following the manufacturer's instructions. The BLAST tool (59) was used for species determination of the obtained sequences.
2.4 Detection of metastrongyloid first-stage larvae in fecal samples
Fecal samples were processed at the day of collection by using the standard Baermann funnel technique (60, 61). After 24 h of incubation, samples were microscopically analyzed using an Olympus BH-2®light microscope (Olympus, Tokyo, Japan) equipped with a digital camera (SC30®, Olympus, Tokyo, Japan). Metastrongyloid L1 were morphologically characterized, and in cases of high larval motility, treated with Lugol's iodine solution [iodine-potassium iodide solution according to Lugol (1% iodine), Carl Roth, Germany] to immobilize larvae (62). Lungworm larvae were identified to genus level according to their typical morphological and morphometric characteristics using several larvae per sample [i.e., body length, detail of anterior extremity, oesophagal shape (non-rhabditiform) and length (1/3–1/2 the length of larvae), and typical tail morphology] (31, 32, 34, 35, 47, 48, 63, 64) (see Figure 4).
2.5 Gastropod digestion for metastrongyloid larvae detection
Gastropods were first identified to genus level via morphological characteristics, then cryo-euthanized and stored at −20°C until further processing (55), artificially digested and sieved according to Penagos-Tabares et al. (55). In brief, frozen gastropods were cut into small pieces and immersed in a digestion solution [10 g pepsin powder 2000 FIP-U/g (Carl Roth, Germany), 8.5 g NaCl, 30 mL HCl 37% (Carl Roth, Germany) adjusted to 1 L by distilled water] for 3 h at 37°C in 50 ml sterile plastic tubes (Greiner) under permanent shaking. After digestion, samples were sieved through a 300 μm pore-sized metal sieve (Retsch) to remove undigested material/debris and then passed through a 25 μm pore-sized metal sieve (Retsch). Remnants of the latter sieving process, were then transferred to 10 ml tubes and sedimented at 800 g for 5 min at room temperature (RT). The sediments were examined microscopically for the presence of metastrongyloid larvae (Olympus BH-2®, Olympus, Tokyo, Japan).
2.6 Molecular identification of metastrongyloid species
All larvae-positive samples (n = 11, 9 fecal- and 2 gastropod samples) were additionally analyzed by molecular techniques. Therefore, all larvae from each Baermann sediment were collected via careful pipetting and each sediment were analyzed individually by metastrongyloid-specific PCRs, and finally sequenced to species level. Therefore, DNA was isolated from larvae using a commercial kit (DNeasy Blood and Tissue Kit®, Qiagen, Hilden, Germany). PCRs were performed using the universal nematode primers NC1 (5′-ACGTCTGGTTCAGGGTTGTT-3′) and NC2 (5′-TTAGTTTCTTTTCCTCCGCT-3′) (65). Using a total reaction volume of 50 μl, HOT FIREPol® Blend Master Mix (Solis BioDyne, Tartu, Estonia) and 5 μl of DNA template, cycling was performed at the following conditions: denaturation at 95°C for 15 min, 35 cycles of denaturation at 95°C for 20 s, annealing at 52°C for 30 s and extension at 72°C for 30 s, followed by a final elongation step at 72°C for 5 min as reported elsewhere (65). In cases when metastrongyloid PCRs yielded negative or inconclusive results, and the quantity of amplicon-DNA from initial PCR was low, a second nested conventional PCR was conducted using the primers NC1 (5′-ACGTCTGGTTCAGGGTTGTT-3′) and MetR (5′-CCGCTAAATGATATGCTTA-3′) (66). Obtained amplicons were purified via gel electrophoresis, sent to a commercial sequencing service (LGC Genomics, Berlin, Germany) and analyzed by BLAST search (http://www.ncbi.nlm.nih.gov/BLAST/; accessed on 15 December 2022).
3 Results
3.1 Locations of GPS-tracked killing sites
GPS-tracked lynx killing sites included areas of wastewater treatment plants, abandoned quarries, private shooting grounds and former ammunition depots, all in vicinity to wooded areas (see Figure 1).
3.2 Occurrence of metastrongyloid infections in wild Eurasian lynxes
Out of 24 lynx fecal samples, 37.5% (9/24) revealed positive for metastrongyloid L1 and 57.1% (4/7) Eurasian lynxes showed metastrongyloid-positive fecal samples for at least one lungworm species (for details see Table 1). All L1 were identified as parasitic nematode larvae belonging to the family Metastrongylidae. In total, four different cardiopulmonary parasites were identified to genus level: Aelurostrongylus, Angiostrongylus, Crenosoma, and Troglostrongylus (see Figure 4).
Three PCR products obtained from Eurasian lynx fecal samples proved positive for feline metastrongyloid-specific DNA and were thereafter analyzed by sequencing. Based on molecular analyses, two parasitic larvae were additionally identified to species level as T. brevior and A. abstrusus. However, the molecular identification of Angiostrongylus and Crenosoma L1 remained un-conclusive. The gene sequencing results were deposited at GenBank® under the accession numbers: OQ225253 (for A. abstrusus) and OQ222066 + OQ222065 (for T. brevior), respectively. In one Eurasian lynx (M20), a patent co-infection with A. abstrusus and Angiostrongylus sp. was detected. One lynx (M19) showed in one sample Angiostrongylus sp. L1 whereas in a later scat sample this finding could not be reconfirmed. Another lynx (M22) showed Crenosoma sp. L1 and T. brevior L1 in two different samples from the same location, in a later sample T. brevior L1 could be reconfirmed.
3.3 Gastropod species diversity and metastrongyloid infections in gastropods
The most common gastropod species found at lynx killing sites or in the surroundings were slugs of the genus Arion (59.5%; 91/153), followed by snails of the genus Cepaea (11.1%; 17/153) and the Leopard slug (Limax maximus, 10.5%; 16/153). Rare semi-slug species of the genus Daudebarida (2.6%; 4/153) with small translucent shells were also collected (see Figure 5). For more details on terrestrial gastropod species diversity please refer to Table 1.
Of digested terrestrial gastropods (n = 153), 1.3% of them (2/153) contained metastrongyloid larvae and were identified as A. vasorum (see Figure 6). All two positive slugs belonged to the genus Arion. Referring to slug larval burden, one Arion slug carried two A. vasorum larvae whilst the other one proved highly infected with a total larval burden of 34 larvae. Overall, all three larval development stages of A. vasorum, i.e., L1, L2, and L3, were found in the latter slug.
Figure 6. Lungworm larvae found in Arion cf. vulgaris (A) A. vasorum L1, (B) A. vasorum L3.
4 Discussion
The killing site-based, non-invasive sample collection included several advantages like an efficient, un-molested scat and gastropod collection leading to less harm and stress for both humans and animals and being in accordance to current animal welfare and wildlife conservation strategies in contrast to other sampling methods, which might require stressful animal capture. Thus, GPS-based identification of killing sites (see above) seems feasible for non-invasive scat sample- and terrestrial gastropod collections.
Based on the biological behavior of lynxes, actual killing sites were sometimes hard to discover in the field, since lynxes typically deeply hide their prey under thorny bushes, foliage and branches or deposit them in very remote areas. In most cases, feces were found entirely covered by leaves and branch piles reflecting typical feline behavior. Most of the places with killing sides share the characteristic of beeing human-dominated areas, with a low level of human interaction.
The current study is based on a lynx population consisting of sub-adult and adult individuals, which were re-introduced into nature after their capture and rearing (below 1 year). Proceedings of re-introduction included obligatory anthelminthic treatments of sub-adult lynxes (M18, M19, M20, F10, F11, and F12) with ivermectin to eliminate T. cati and potential other nematode infections before release. It is to mention that currently there is no explicit study which shows the specific effectiveness of ivermectin against all the metastrongyloid lungworms, which were found in this survey. However there are different reports which show the effectiveness of ivermectin against lungworms of the genus Crenosoma (67, 68). Against Aelurostrongylus abstrusus ivermectin seems to have an incomplete effectiveness (69, 70). For the use of ivermectin against Angiostrongylus sp. and Troglostrongylus sp. in felids there is currently insufficient scientific knowledge. We therefore recommend to review reintroduction protocols for wild felids using ivermectin and maybe switch to better working compounds if the aim is to eradicate metastrongyloid lungworm infections. If ivermectin is to be used, the animals should be tested again with the Baermann funnel after treatment to detect possibly surviving metastrongyloid lungworms and if the result is positive, the animals should be treated with another more specific compound. A complete absence of metastrongyloid lungworm infections in the reintroduced lynxes, mentioned in this manuscript, prior their release into the wild, can therefore not to be ruled out and given that the results of the copromicroscopic analysis yielded negative for metastrongyloid lungworm infections, it seems still highly feasible to assume that patent metastrongyloid infections detected in the current study were acquired within the study area either by ingesting metastrongyloid-infected gastropod intermediate hosts and/or after consumption of infected paratenic hosts including amphibians, reptiles, birds and rodents.
The metastrongyloid genera Aelurostrongylus, Angiostrongylus, and Troglostrongylus have previously been described not only in wild Eurasian lynxes but also in wild cats (F. silvestris) and domestic cats (30, 37, 50). In contrast, Crenosoma infections in wild felids were reported exclusively for L. lynx and identified as C. vismani (29). Of note, current parasitological results include the broadest metastrongyloid species diversity for wild Eurasian lynxes compared to former reports (31, 37, 38, 71). This species diversity might be explained by the current method, i.e., examination of fresh feces by the Baermann funnel, which allows the detection of living larvae. Of note, this technique is still considered as gold standard for lungworm larvae diagnostics (72–80). In contrast, other studies on Eurasian lynx lungworms either analyzed preserved (i.e., fixed or frozen) fecal samples or examined carcasses and/or did not apply the Baermann funnel technique, thereby potentially reducing the sensitivity of lungworm detection (31, 38, 71, 81). Another explanation for current parasite diversity may be related to the age structure of analyzed Eurasian lynxes, consisting mainly of sub-adult animals. Correspondingly, juvenile domestic cats and young wild cats also showed a broader range of metastrongyloid species, thereby being predisposed for these cardiopulmonary infections by age, we would assume that this will be the case for Eurasian lynx as well (30, 48, 51, 82–84).
A recent study on endoparasites of free-ranging Eurasian lynxes (n = 24) of the Harz Mountains reported a prevalence of 12.5% (3/24) for metastrongyloid L1, among them Angiostrongylus spp.-like larvae and A. abstrusus, nonetheless neither T. brevior- nor Crenosoma spp.-larvae were detected in this study (31). Interestingly, the present study revealed a lungworm species that has never been reported before in free-ranging German Eurasian lynxes, the metastrongyloid lungworm Troglostrongylus brevior. Moreover, current findings on troglostrongylosis represents the third-ever report in literature for this feline host species in Europe. Hence, the first and second report on T. brevior infections in Eurasian lynxes came from Bosnia and Herzegovina in 2015 (32) and from Romania in 2022 (37), respectively. Conversely, in North America the closely related species T. wilsoni was reported to occur in Canadian lynxes (Lynx canadensis) (85) and in wild bobcats (Lynx rufus) (54, 86–88). In line with rare reports on lynx troglostrongylosis, the occurrence of aelurostrongylosis in Eurasian lynxes has only been described for three countries so far, i.e., Switzerland, Poland and Germany (31, 38, 89). Troglostrongylus seems to be of more clinical concern, than A. abstrusus as they seem to show in general a more severe clinical picture (90–92). In Switzerland, analyses of 58 fecal samples from dead L. lynx were in five cases (9%) positive for A. abstrusus. Interestingly, in one of the examined Swiss Eurasian lynx, histopathological findings unveiled a multifocal mild granulomatous pneumonia (89). In Poland, a much higher A. abstrusus prevalence of 21% was reported (38). Current findings re-confirm A. abstrusus as circulating in free-ranging Eurasian lynxes in Germany and highlight the importance of regular monitoring on gastropod-borne aelurostrongylosis (31). Recently, feline crenosomosis was reported in wild Eurasian lynxes in Latvia. Based on morphological and morphometric characteristics, C. vismani was identified as the related infective pathogen (29). In the current study, we failed to identify the Crenosoma species for the detected larvae by molecular tools. It has to be noted that, it cannot be ruled out, that the here identified Crenosoma-L1 might also have originated from an infected prey animal [i.e., red fox (Crenosoma vulpis) or European hedgehog (Crenosoma striatum)] (41, 93–99). Accordingly, three carcasses of killed red foxes were found at one killing site. Equally, current findings on Angiostrongylus-L1 might have originated from other infected prey, predator/mesopredator living within the same biome. Hence, interactions of wild Eurasian lynxes with badgers (Meles meles), racoons (Procyon lotor) and wild cats sharing the same habitats of the Harz Mountains might result in spill-overs and spill-backs of Angiostrongylus spp.-infections as previously postulated (27, 30, 31, 100, 101). Particularly feral cats and domestic dogs may pose a risk in reverse of spill-overs for endangered Eurasian lynxes (31). Wildlife studies have already demonstrated that especially feral cats play a significant role in transmitting parasites to wild lynx populations as reported for re-introduced Iberian lynxes in Spain and Portugal (27, 100, 101).
In the present study, we failed to molecularly confirm the endemic A. chabaudi parasite to species level for the current German lynx samples. Nevertheless, this species has already been reported for wild cats in Germany (30), and from other European countries (35, 36, 102). However, patent A. chabaudi-infections have not yet been detected in wild Eurasian lynxes. Given that wild cats and Eurasian lynxes cohabit the same biome in the Harz Mountains, transmission of A. chabaudi seems plausible through consumption of either infected intermediate hosts or paratenic hosts (31, 64, 103), but further investigations are needed for conclusive data on lynx angiostrongylosis in Germany.
In this study lungworm larvae only of the species A. vasourm were found in gastropods of the genus Arion sp. The origin of infection of the sampled lynxes, with the lungworms, which were found during the analysis of the Baermann funnel, has to be investigated in further studies. Until this time their way of infection is speculative. Felids tend to get infected with metastrongyloid lungworms by ingesting paratenic hosts (e.g., rodents and birds) rather than by ingesting gastropods, this case seems also feasible for Eurasian lynxes and is therefore a highly reasonable cause of infection (39, 104). Wild cats (F. silvestris) seem to be a reservoir for T. brevior (49), and as they are occurring syntop with the Eurasian lynx in the Harz Mountains they could be a source of infection. The majority of the collected slugs belonged to the species Arion cf. vulgaris, which is in accordance to other studies the most common slug species in Germany and mainly found in urbanized areas due to its synanthropic behavior (105). Nonetheless, also Arion cf. rufus slugs were here found in the lynx biomes of the Harz Mountains. Unfortunately, the species determination of collected Cepaea snails was impossible since pivotal morphological characteristics for proper identification (e.g., color of the mouthlip of the shell, internal morphology of reproductive organs) were missing due to beginning autolysis or fragmentation of the shell (106). The susceptibility of gastropod species to lungworm infections is explained by different factors e.g., intermediate host behavior and size of the gastropod (52, 107, 108). The exact parameters which influence the susceptibility of gastropod species have to be investigated in further studies, for example with a broader sample size or experimental infections. The prevalence of metastrongyloid lungworms in gastropod intermediate hosts has already been done in several studies (52, 55, 109).
Considering present metastrongyloid findings in digested gastropod intermediate hosts, exclusively A. vasorum larvae in two Arion cf. vulgaris slugs were found. Most probably these infections result from marked coprophagic behavior of this slug species (16, 110) when compared to other investigated gastropod genera (e.g., Cepaea and Daudebardia), what makes them good intermediate hosts. When referring to definite hosts of A. vasorum, the most predominant species in the Harz Mountains are red foxes followed by gray wolves (Canis lupus), besides domestic dogs, while felines are usually considered as rare and inadequate hosts (111, 112). Especially red foxes are well-known to show high A. vasorum prevalences in Germany (93, 113). Moreover, it cannot be ruled out that the presence of A. vasorum larvae in Arion slugs was due to intermediesis, where nematode stages are transferred from one infected gastropod to another by carnivorous behavior or by contact with L3 released from dead intermediate hosts (114, 115).
5 Conclusion
To the best of current knowledge, this work represents the first report on patent T. brevior-infections in wild Eurasian lynxes in Germany. Additionally, current data re-confirmed patent A. abstrusus infections to be circulating in the L. lynx population inhabiting the Harz Mountains, which is the largest one in Germany. Our findings emphasize the necessity for additional research on neglected cardiopulmonary diseases, such as feline angiostrongylosis and crenosomosis, in wild Eurasian lynxes to increase the current understanding on their epizootiology, pathogenesis, immunity, and clinical relevance. Moreover, the presence of A. vasorum larvae in gastropods was here reported for the first time for the Harz Mountains within the Federal State of Lower Saxony. Even though our study is limited in terms of low animals numbers, its significance lies in the importance of exploring wildlife-associated parasitoses in a non-disturbing manner to uncover potential threats to endangered large felid apex predators. Considering the limited knowledge on the pathological and clinical findings induced by lungworm infections in wild felids, regular veterinary monitoring is crucial to evaluate the population health status, which could additionally be done by the examination of samples from other regions as wells as clinical assessments of animals in rescue centers or necropsies of dead animals to get broader insights in metastrongyloid lungworm infections in Eurasian lynxes. These regular veterinary monitoring programs will play a crucial role for future re-introduction programs and should encompass not only the target but also sympatric species.
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/supplementary material.
Ethics statement
Ethical approval was not required for the study involving animals in accordance with the local legislation and institutional requirements because the study was done on fecal samples, which were gained from the field, with no disturbances of the animals.
Author contributions
MH: Investigation, Visualization, Writing – original draft, Writing – review & editing, Methodology. LS: Investigation, Writing – review & editing. OA: Methodology, Resources, Writing – review & editing. TM: Methodology, Resources, Writing – review & editing. AM: Investigation, Visualization, Writing – review & editing. SH: Writing – review & editing. BC: Methodology, Writing – review & editing. AD: Investigation, Methodology, Writing – review & editing. AT: Funding acquisition, Resources, Supervision, Validation, Writing – review & editing. CH: Conceptualization, Funding acquisition, Resources, Supervision, Validation, Writing – review & editing.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. The study was partially funded by the Institute of Parasitology, Faculty of Veterinary Medicine of the Justus Liebig University Giessen (JLU) and the Harz National Park (HNP), Germany.
Acknowledgments
We express our deepest gratitude to Dr. Manuel Uribe for assisting with mapping in QGIS and by providing valuable support in the field. Special thanks to all the land owners and hunting tenants for allowance to observe their areas for signs of Eurasian lynxes activities, as well as the authorities of the State Forests of Lower Saxony, for the allowance to pass through and search in their territories for killing sites. Our special appreciation extends to the authorities of the Harz National Park (HNP) for their constant and kind cooperation, logistical support, and the necessary driving permits. For extraordinary help in the determination of gastropod species we thank the malacologists Dr. Frank Walther and Dr. Vollrath Wiese. Further, we acknowledge Christine Henrich for her valuable assistance in conducting molecular analysis of collected metastrongyloid larvae. Finally, we thank Dr. Daniela Grob for her assistance in gastropod sampling.
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.
Generative AI statement
The author(s) declare that no Gen AI was used in the creation of this manuscript.
Publisher's note
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Keywords: Aelurostrongylus abstrusus, Angiostrongylus, Crenosoma, Eurasian lynx, Lynx lynx, Troglostrongylus brevior, wildlife
Citation: Haas M, Segeritz L, Anders O, Middelhoff TL, Myat Tun A, Hasheminasab SS, Cocchiararo B, Dusch A, Taubert A and Hermosilla C (2025) Patent Troglostrongylus brevior-, Aelurostrongylus abstrusus-, Angiostrongylus sp.-, and Crenosoma sp. infections in wild Eurasian lynxes (Lynx lynx) and their habitat-sharing gastropod intermediate hosts. Front. Vet. Sci. 12:1515507. doi: 10.3389/fvets.2025.1515507
Received: 23 October 2024; Accepted: 23 May 2025;
Published: 03 July 2025.
Edited by:
Consuelo Rubio-Guerri, Universidad CEU Cardenal Herrera, SpainReviewed by:
Erica Marchiori, University of Padua, ItalySergey Naidenko, Severtsov Institute of Ecology and Evolution (RAS) Moscow, Russia
Hugo Vilhena, University of Porto, Portugal
Copyright © 2025 Haas, Segeritz, Anders, Middelhoff, Myat Tun, Hasheminasab, Cocchiararo, Dusch, Taubert and Hermosilla. 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: Marcel Haas, TWFyY2VsLkhhYXNAdmV0bWVkLnVuaS1naWVzc2VuLmRl