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The prevalence of intestinal nematodes among red foxes (Vulpes vulpes) in north-western Poland



The red fox (Vulpes vulpes) is widely distributed in the Northern Hemisphere and Australia. The presence of nematode-infected foxes in urbanized areas increases the risk of transmission of nematodes to domestic dogs and thus, to humans. The aim of this study was to determine the prevalence and species composition of intestinal nematodiasis in red foxes in Western Pomerania, a province in north-western Poland. The intestinal contents of 620 red foxes killed during a government reduction shooting programme were examined for adult nematodes using the sedimentation and counting technique (SCT).


Intestinal nematodes, including Toxocara canis, Toxascaris leonina, Uncinaria stenocephala and Trichuris vulpis, were found in 77.3% (95% CI 73.8–80.4%) of the examined foxes with a mean infection burden of 20.1 nematode per animal. Male and female foxes had similar infection burdens.


The nematodes are present in high prevalence and intensity among foxes in north-western Poland. Furthermore, this high prevalence of nematodes in foxes may likely constitute a health risk to humans and domestic animals due to increasing fox densities in urban and periurban areas.


The red fox (Vulpes vulpes) is widely distributed in the Northern Hemisphere and Australia [1]. A rapid increase in its number has been observed in many European countries since the late twentieth century [2,3,4]. This growth may be explained by a reduction in mortality rate due to intensive rabies vaccination campaigns and the opportunistic behaviour of the fox itself [2].

The growth in the fox population has resulted in its expansion to new habitats. Unfortunately, as foxes may be infected by zoonotic intestinal nematodes, their presence in urbanized areas increases the risk of transmission of these nematodes to humans, either directly, or indirectly through infection of domestic dogs [5,6,7]. Infected foxes can contaminate sandpits, parks and squares with their faeces, thus exposing humans to the eggs of zoonotic nematode species such as Toxocara canis, Toxascaris leonina and Trichuris vulpis, and nematodes from the Ancylostomatidae family [8,9,10,11,12].

The most widespread helminth zoonosis in developed countries is toxocariasis, known to cause visceral and ocular larva migrans syndrome [3, 13, 14]. In humans, as paratenic hosts, the larvae of T. canis, responsible for toxocariasis, do not develop into an adult stage but migrate throughout the tissues and remain as L3 arrested larvae for an extended period of time [15].

The prevalence of T. canis seropositive cases in humans has been estimated at 2.4% in Denmark [16], 7% in Sweden [17] and 6.3% in Austria [18]. A significant proportion of the human population in Poland have also been found to harbour T. canis antibodies, with a seroprevalence ranging from 18.6 to 43% depending on the region [19, 20]. Similar symptoms can be observed following infection with T. leonina and T. vulpis larvae [21].

An additional threat is also posed to humans by hookworms, i.e. nematodes of the Ancylostomatidae family, such as Ancylostoma caninum and Uncinaria stenocephala, with approximately 1.3 billion people being estimated to be infected by a nematode from this family [22]. Hookworm infection rarely results in mortality but leads to anaemia and malnutrition [23], which lead to chronic health problems such as lethargy and impaired physical and cognitive development [24].

A number of studies, including one carried out from 1996 to 1998 in north-western Poland by Bieńko [25], indicate that the occurrence of nematodes in foxes varies considerably [26,27,28,29,30]. Therefore, the aim of the present study was to determine the prevalence of intestinal nematoidiasis in red foxes (Vulpes vulpes) in north-western Poland and investigate other parameters associated with its presence, e.g. examine its distribution between sexes and predilection.


The study was conducted in Western Pomerania, a province of north-western Poland. The material comprised a total of 620 red foxes (236 females and 384 males) culled during a government reduction shooting programme in 18 counties in the region. The remains of the foxes were acquired from the Departments of Veterinary Hygiene in Szczecin and Koszalin during the hunting seasons of 2008/2009, 2009/2010 and 2010/2011. The minimum sample size was calculated according to the Cochran formula.

Parasitological analyses were carried out at the Department of Veterinary Hygiene in Szczecin and Koszalin. Fox carcasses delivered to the department by hunters were initially frozen at − 70 °C for four days to prevent transmission of infective Echinococcus multilocularis eggs. The carcasses were then thawed and examined.

The alimentary tracts of the foxes were subjected to parasitological analysis using sectional methods described by Eckert et al. [31, 32] and by Stefański and Żarnowski [33]. Briefly, the alimentary tract samples were isolated from the animals and divided into oral cavity, oesophagus, stomach, small intestine, caecum and large intestine samples. In addition, the small intestine was further divided into three sections: duodenum, jejunum and ileum. The organs were opened along their entire length. Visible parasites were removed immediately from the mucosa and placed in Petri dishes with water. Other parasites were collected using the sedimentation and counting technique (SCT). The sex of the animals was identified based on the gonads. The recovered nematodes were identified according to Stefański and Żarnowski [33] and preserved in 70% alcohol.

The Jaccard coexistence index (J) [34] was used to compare the coexistence of particular species of nematodes, where the feature is the presence of a species in the sample (environment). A value ​​of 100% indicates that two analysed nematode species always co-occur, regardless of their numbers, and 0% indicates that the two species are never observed together.

$$ Jp1p2 = \;\frac{c}{a + b - c}\; \times \;100$$

where: Jp1p2—coexistence index between species p1 and p2; a—the number of occurrences of species p1; b—the number of occurrences of species p2; c—the number of common occurrences of species p1 and p2 in the habitat.

The obtained results were analysed using Statistica 10.0. The occurrence of individual nematode species was compared between the sex of the host was determined using the Mann–Whitney U-test. The occurrence of nematodes was compared between individual sections of the gastrointestinal tract using the Kruskal–Wallis test. The confidence interval of a proportion was calculated by the modified Wald method, as recommended by Agresti and Coull [35].


Nematodes were found in 77.3% (95% CI 73.8–80.4%) of analysed foxes, while the mean infection intensity was 20.1 nematodes per animal. T. canis, T. leonina, U. stenocephala and T. vulpis were isolated from the tested foxes. Of these, U. stenocephala was the most prevalent (34.0%, 95% CI 30.4–37.9%), with an intermediate intensity of infection (20.7) (Table 1).

Table 1 Parameters of occurrence of nematodes in red fox

T. canis was more commonly observed in male foxes (32.0%, 95% CI 27.6–36.9%) than females (27.1%, 95% CI 21.8–33.1%), while U. stenocephala was more common in female foxes (37.7%, 95% CI 31.8–44.0%) than males (31.8%, 95% CI 27.3–36.6%). These differences in incidence were not statistically significant (p > 0.05). In both males and females, the highest mean intensity of infection was found for U. stenocephala, which displayed similar intensities in female (21.7) and male foxes (19.9) (Table 2).

Table 2 Incidence of nematodes in red foxes with regard to sex of host

Nematodes were observed in the duodenum, jejunum, ileum and caecum; however, none were noted in the oral cavity, the oesophagus, the stomach or the large intestine. The parts of the alimentary tract where nematodes were found were then subjected to further analysis; among these, significantly higher numbers of nematodes were found in the jejunum than in the duodenum or ileum (Kruskal–Wallis; H = 96.7; p = 0.000) (Table 3).

Table 3 The occurrence of nematodes in red foxes according to location in the intestine

Regarding T. canis, its numbers differed significantly between the duodenum and the ileum and between the jejunum and the ileum (Kruskal–Wallis; H = 50.6; p < 0.001). In addition, the occurrence of T. leonina significantly differed between the duodenum and the ileum, and between the jejunum and the ileum (Kruskal–Wallis; H = 52.0; p < 0.001), and U. stenocephala differed significantly between the duodenum and the jejunum, and between the jejunum and the ileum (Kruskal–Wallis; H = 55.8; p < 0.001) (Table 3).

In the duodenum, the most common nematodes were U. stenocephala (20.7%, 95% CI 17.6–24.0%) and T. canis (20.7%, 95% CI 17.6–24.0%); however, the highest mean intensity of infection was found for U. stenocephala (4.3) (Table 3). Of the identified nematodes, the prevalence and the highest mean intensity of infection were noted for U. stenocephala in the jejunum (31.6% [95% CI 28.1–35.4%], 16.3, respectively) and the ileum [14.2% (95% CI 11.7–17.2%), 7.0, respectively] (Table 3). T. vulpis (11.9%, 95% CI 9.6–14.7%) was found only in the caecum (Table 3).

Our findings indicate variations in both the chance of encountering certain pairs of nematode species and the strength of the relationship between them, as measured by the Jaccard index (J). The most common pairs comprised U. stenocephala and T. canis (66 joint occurrences, J = 14.2%) and U. stenocephala and T. leonina (40 joint occurrences, J = 9.7%) (Table 4).

Table 4 Frequency of coexistence of individual nematode species in a single host organism


The most frequently-observed gastro-intestinal nematode in the red foxes examined in the present study was U. stenocephala. This finding is in line with previous studies on red foxes in Europe in general [3, 36,37,38,39] and in studies in northern and southern Poland [40, 41]. However, other studies conducted in western and southern Poland showed a significantly lower prevalence, ranging from 11 to 35% [42,43,44]. A higher prevalence of U. stenocephala has been found in Estonia (84.3%) [45], Lithuania (76.9%) [46] and Italy (75.4%) [37]; however, U. stenocephala are less common in Ukraine (27.1%) [47], Romania (15.0%) [48], the Czech Republic (10.0%) [2], Switzerland (5.3%) [6] and Norway (1.6%) [49].

The prevalence of U. stenocephala in foxes has been found to increase in recent years, from 39.0% in 2008 to 65.0% in 2010 in Sweden [50], and from 68.6% in 2006 to 84.1% in 2013 in Denmark [36, 51].

In the present study, T. canis was more common than T. leonina. A similar trend was observed in earlier studies in the same region, with the frequency of T. leonina infection increasing more than 12-fold over the test period [25]; however, the prevalence of T. canis was found to be higher than in the present study (42.3%). This situation could be caused by the availability of food, mostly rodents, in the environment occupied by the foxes. Okulewicz et al. [52] highlight the role of small rodents as paratenic hosts of nematodes and note that rodents may contribute significantly to the spread of T. canis and T. leonina in the environment. Pucek et al. [53] report that most species of rodents display cycles characterised by periodic and rapid changes in population density. In the case of forest mice and voles, their numbers are directly influenced by mast years of deciduous tree species (oak, beech, hornbeam) and weather conditions in the winter season [54].

The abundance of T. canis and T. leonina in foxes is also influenced by the growing number of animals infected with the parasites, the large numbers of eggs excreted into the environment, and the considerable resistance of the eggs to adverse environmental conditions. Given appropriate temperature and humidity conditions, eggs are known to remain infective for at least a year [54]. Otranto and Deplazes [55] note that T. canis infections are generally higher in young foxes, i.e. under six months of age, although adult foxes with weak immunity also demonstrate a relatively high infection rate by intestinal parasites in endemic areas.

A higher prevalence of T. canis than T. leonina has also been found in other countries, including Denmark (59.4 and 0.6%) [51], Italy (52.6 and 0%) [37], Slovakia (25.8 and 17.5%) [56], and Kyrgyzstan (30.4 and 5.9%, respectively) [57]. However, T. leonina has been found to predominate over T. canis in other countries, such as Sweden (65.0 and 30.0%) [50], Turkey (65.0 and 20.0%) [58], and Norway (12.9 and 1.6%, respectively) [49]. An exception was the Czech Republic, where both species were present in foxes in equal numbers [2].

The most rarely-found parasite in this study was T. vulpis. This finding confirms the results of Karamon et al. [40] from Poland, who estimate its prevalence among foxes to be 1.3% in south-eastern Poland and 4.4% in northern Poland. A high prevalence (64.4%) has only been reported in southern Poland [59]. Interestingly, this parasite has not been found in central Poland [60].

In other European countries, the occurrence of T. vulpis among foxes varies considerably. In Italy, 12.3% of tested foxes were found to be infected [37], while the prevalence was found to 7.7% in Sweden, 5.5% in Switzerland, 4.8% in Ukraine, and 1.6% in Norway [6, 37, 47, 49]. However, as surveillance in foxes is often limited to the small intestine, T. vulpis, which is localized in the large intestine, is not typically considered during post-mortem parasitological investigations [40].

In the present study, similar nematode prevalence levels were observed between male and female foxes. Similarly, previous studies have also reported no sex-related differences in prevalence [2, 41]. Vervaeke et al. [61] suggest that these observed lack of sex-driven differences in the prevalence of nematodes may result from the fact that both male and female foxes feed on the same type of food. Their main diet is rodents, which are intermediate hosts of many parasite species. However, the higher prevalence of T. canis observed in males in the present study might be a result of behavioural differences between the sexes. Male foxes are more active than females, and their hunting grounds are larger than those of females. Moreover, males are larger than females, and have higher food requirements [62].

Unfortunately, it is difficult to find suitable comparisons for our results regarding the distribution of parasites in the digestive tract of the studied foxes, as literature in this area is scarce. Based on the present findings, the nematodes T. canis and T. leonina prefer to colonize the duodenum and jejunum and are significantly less commonly observed in the ileum. U. stenocephala colonizes the jejunum far more readily than the duodenum or ileum. One exception is T. vulpis, which was observed only in the caecum, suggesting that this may be the predilection site of the parasite. A similar prevalence was found by Fiocchi et al. [37] in the caeca of seven foxes (12.3%).

U. stenocephala was found to co-occur most often with T. canis (J = 14.2%) and less often with T. leonina (J = 9.7%). T. canis and T. leonina were found to co-occur in only 14 foxes (J = 3.8%). Therefore, the high prevalence of T. canis in foxes and pets may lead to a low prevalence of T. leonina and vice versa [50]; however, Jankovska et al. [2] report the co-occurrence of these two nematode species in 70.6% of tested foxes in the Czech Republic.

The differences observed in the prevalence of nematodes between specific European countries might be an effect of the variable diet of the foxes, which depends on the geographical location and species variability of prey in a given region [62]. Foxes prefer to hunt for small rodents in their hunting range. This is particularly noted in areas with large populations of some rodent species, such as voles; for example, in western and northern Poland, markedly greater consumption of voles and other field rodents may be observed in the summer and autumn seasons. In central and eastern Poland, however, the winter diet of foxes is dominated by rodents, hares and carrion; hares and birds dominate in spring, and large amounts of fruit appear in the diet in summer and autumn [63]. In places where voles are absent, e.g., in Ireland, foxes readily eat other rodent species, such as rats [64]. Carrion is a regular component of the diet of foxes, irrespective of their place of occurrence; in fact, under specific circumstances, carrion may constitute almost half of their diet [62]. A substantial share of carrion in the diet is observed in mountain areas and forests in the Northern Hemisphere because thick and long-lasting snow cover makes catching small rodents difficult [65].

The foxes inhabiting north-western Poland demonstrate are frequently hosts to nematodes. A number of studies suggest that the prevalence of geohelminths is associated with climate conditions, inter alia temperature, air and soil humidity, and mean annual rainfall, which extend the lifespan of their free-living developmental stages [2, 40, 66,67,68]. The region of north-western Poland is particularly suitable for the development of parasites, being situated close to the sea, with substantial forest cover and a temperate climate, a total annual rainfall of 500–800 mm, a mean annual temperature of 7–9 °C and high humidity. Such conditions certainly increase the threat to the health of humans and pets by increasing the risk of parasite transmission. This risk is further increased by the growing number of foxes searching for new places to live in areas inhabited by humans.


Our findings demonstrate that nematodes are present in high prevalence and intensity among foxes in north-western Poland. Furthermore, this high prevalence of nematodes in foxes may likely constitute a health risk to humans and domestic animals due to increasing fox densities in urban and periurban areas.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on request.


J: :

The Jaccard coexistence index


  1. 1.

    Hoffmann M, Sillero-Zubiri C. Vulpes vulpes. The IUCN Red List of Threatened Species. 2016.

  2. 2.

    Jankovská I, Brožová A, Matějů Z, Langrová I, Lukešová D, Sloup V. Parasites with possible zoonotic potential in the small intestines of red foxes (Vulpes vulpes) from Northwest Bohemia (CzR). Helminthol. 2016;53:290–3.

    Article  Google Scholar 

  3. 3.

    Magi M, Guardone L, Mignone W, Prati MC, Macchioni F. Intestinal helminths of red foxes (Vulpes vulpes) in north-west Italy. Helminthol. 2016;53:31–8.

    Article  Google Scholar 

  4. 4.

    Veronesi F, Morganti G, Di Cesare A, Lepri E, Cassini R, Zanet S, et al. Eucoleus boehmi infection in red fox (Vulpes vulpes) from Italy. Vet Parasitol. 2014;206:232–9.

    PubMed  Article  PubMed Central  Google Scholar 

  5. 5.

    Gloor S, Bontadina F, Hegglin D, Deplazes P, Breitenmoser U. The rise of urban fox population in Switzerland. Mamm Biol. 2001;66:155–64.

    Google Scholar 

  6. 6.

    Koller B, Hegglin D, Schnyder M. A grid-cell based fecal sampling scheme reveals: land-use and altitude affect prevalence rates of Angiostrongulus vasorum and other parasites of red foxes (Vulpes vulpes). Parasitol Res. 2019;118:2235–45.

    PubMed  Article  PubMed Central  Google Scholar 

  7. 7.

    Reperant LA, Hegglin D, Fischer C, Kohler L, Weber JM, Deplazes P. Influence of urbanization on the epidemiology of intestinal helminths of the red fox (Vulpes vulpes) in Geneva, Switzerland. Parasitol Res. 2007;101:605–11.

    PubMed  Article  PubMed Central  Google Scholar 

  8. 8.

    Lotsch F, Vingerling R, Spijker R, Grobusch MP. Toxocariasis in humans in Africa—a systematic review. Travel Med Infect Dis. 2017;20:15–25.

    PubMed  Article  PubMed Central  Google Scholar 

  9. 9.

    Maleki B, Khorshidi A, Gorgipour M, Mirzapour A, Majidiani H, Foroutan M. Prevalence of Toxocara spp. Eggs in soil of public areas in Iran: a systematic review and meta-analysis. Alexandria J Med. 2018;54:97–101.

    Article  Google Scholar 

  10. 10.

    Nijsse R, Mughini-Gras L, Wagenaar JA, Franssen F, Ploeger HW. Environmental contamination with Toxocara eggs: a quantative approach to estimate the relative contributions of dogs, cats and foxes, and to assess the efficacy of advised interventions in dogs. Parasit Vectors. 2015;8:397.

    PubMed  PubMed Central  Article  Google Scholar 

  11. 11.

    Ondriska F, Macuhova K, Melicherova J, Reiterova K, Valentova D, Beladicova V, et al. Toxocariasis in urban environment of western Slovakia. Helminthol. 2013;50:261–8.

    Article  Google Scholar 

  12. 12.

    Papajova I, Pipkova J, Papaj J, Cizmar A. Parasitic contamination of urban and rural environments in the Slovak Republic: dog’s excrements as a source. Helminthol. 2014;51:273–80.

    Article  Google Scholar 

  13. 13.

    Aghamolaie S, Seyyedtabaei SJ, Behniafar H, Foroutan M, Saber V, Hanifehpur H, et al. Seroepidemiology, modifiable risk factors and clinical symptoms of Toxocara spp. infection in northern Iran. Trans R Soc Trop Med Hyg. 2019;113:116–22.

    PubMed  Article  PubMed Central  Google Scholar 

  14. 14.

    Zibaei M. Helminth infections and cardiovascular diseases: Toxocara species in contributing to the disease. Curr Cardiol Rev. 2017;13:56–62.

    PubMed  PubMed Central  Article  Google Scholar 

  15. 15.

    Strube C, Heuer L, Janecek E. Toxocara spp. infection in paratenic hosts. Vet Parasitol. 2013;193:375–89.

    PubMed  Article  PubMed Central  Google Scholar 

  16. 16.

    Stensvold CR, Skov J, Moller LN, Jensen PM, Kapel CMO, Petersen E, et al. Seroprevalence of human toxocariasis in Denmark. Clin Lab Immunol. 2009;16:1372–3.

    CAS  Google Scholar 

  17. 17.

    Ma G, Holland CV, Wang T, Hofmann A, Fan CK, Maizels RM, et al. Human toxocariasis. Lancet Infect Dis. 2018;18:14–24.

    Article  Google Scholar 

  18. 18.

    Poeppl W, Herkner H, Tobudic S. Exposure to Echinococcus multilocularis, Toxocara canis, and Toxocara cati in Austria: a nationwide cross-sectional seroprevalence study. Vector Borne Zoonotic Dis. 2013;13:798–803.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  19. 19.

    Hermanowska-Szpakowicz T, Kondrusik M, Świerzbińska R, Zajkowska J, Pancewicz S. Incidence of antibody detection against Toxocara canis and clinical symptoms in inhabitants of North-Eastern Poland. Pol Merkur Lekarski. 2001;10:168–70.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Balicka-Ramisz A, Horodnicka-Jóźwa A, Ramisz A, Laurans Ł, Wnuk W, Pilarczyk B. Toxocariasis in dogs and the presence of antibodies against Toxocara canis in children. Med Wet. 2005;61:786–8.

    Google Scholar 

  21. 21.

    Despommier D. Toxocariasis: clinical aspects, epidemiology, medical ecology and molecular aspects. Clin Microbiol Rev. 2003;16:265–72.

    PubMed  PubMed Central  Article  Google Scholar 

  22. 22.

    Chan MS. The global burden of intestinal nematode infections—fifty years on. Parasitol Today. 1997;13:438–43.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  23. 23.

    Hotez PJ, Bethony JM, Diemert DJ, Pearson M, Loukas A. Developing vaccines to combat hookworm infection and intestinal schistosomiasis. Nat Rev Microbiol. 2010;8:814–26.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  24. 24.

    Hotez PJ, Brooker S, Bethony JM, Bottazzi ME, Loukas A, Xiao S. Hookworm infection. N Engl J Med. 2004;351:799–807.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  25. 25.

    Bieńko R. Research on parasitofauna and the role of a free living foxes as a reservoir of parasite zoonoses in north-western Poland. Szczecin: Agricultural University (dissertation); 2000.

  26. 26.

    Andras T. Data on the parasitological status of the red fox in Hungary. Mag Allat Lapja. 2001;123:100–7.

    Google Scholar 

  27. 27.

    Cisek A, Ramisz A, Balicka-Ramisz A, Pilarczyk B, Laurans Ł. The extensity of Toxocara canis (Werner, 1782) in dogs and foxes in north-western Poland. Wiad Parazytol. 2004;50:641–6.

    PubMed  PubMed Central  Google Scholar 

  28. 28.

    Criado-Fornelio A, Gutierrez-Garcia L, Rodriguez-Caabeiro F, Reus-Garcia E, Roldan-Soriano MA, Diaz-Sanchez MA. A parasitological survey of wild red foxes (Vulpes vulpes) from the province of Guadalajara. Spain Vet Parasitol. 2000;92:245–51.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  29. 29.

    Di Cerbo AR, Manfredi MT, Bregoli M, Ferro N, Cova M. Wild carnivores as source of zoonotic helminths in north-eastern Italy. Helminthol. 2008;45:13–9.

    Article  Google Scholar 

  30. 30.

    Zoltan S, Tamas S, Istvan V. Prevalence, veterinary and public health aspects of gastrointestinal parasites in red foxes (Vulpes vulpes) in Hungary. Magy Allatorvosok. 2004;126:293–9.

    Google Scholar 

  31. 31.

    Eckert J, Deplazes P, Ewald D, Gottstein B. Parasitological and immunological methods of detecting Echinococcus multilocularis in foxes. Mitt Österr Ges Tropenmed Parasitol. 1991;13:25–30.

    Google Scholar 

  32. 32.

    Eckert J, Kutzer E, Rommel M, Bürger HJ, Körting W. Veterinary parasitology. Berlin and Hamburg: Verlag Paul Parey; 1992.

    Google Scholar 

  33. 33.

    Stefański W, Żarnowski E. Recognition of parasitic invasions in animals. Warsaw: PWRiL; 1971.

    Google Scholar 

  34. 34.

    Magurran AE. Measuring biological diversity. Oxford: Blackwell Publishing; 2004.

    Google Scholar 

  35. 35.

    Agresti A, Coull BA. Approximate is better than “exact” for interval estimation of binomial proportions. Am Stat. 1998;52:119–26.

    Google Scholar 

  36. 36.

    Al-Sabi MN, Chriél M, Jensen TH, Enemark HL. Endoparasites of the raccoon dog (Nyctereutes procyonoides) and the red fox (Vulpes vulpes) in Denmark 2009–2012—a comparative study. Int J Parasitol Parasites Wildl. 2013;2:144–51.

    PubMed  PubMed Central  Article  Google Scholar 

  37. 37.

    Fiocchi A, Gustinelli A, Gelmini L, Rugna G, Renzi M, Fontana MC, et al. Helminth parasites of the red fox Vulpes vulpes (L., 1758) and the wolf Canis lupus italicus Altobello, 1921 in Emilia-Romagna, Italy. Ital J Zool. 2016;83:503–13.

    CAS  Article  Google Scholar 

  38. 38.

    Rataj AV, Posedi J, Zele D, Vengust G. Intestinal parasites of the red fox (Vulpes vulpes) in Slovenia. Acta Vet Hung. 2013;61:454–62.

    Article  Google Scholar 

  39. 39.

    Schuster RK, Shimalov VV. A comparative study of helminths of raccoon dogs (Nyctereutes procynoides) and red foxes (Vulpes vulpes) sharing the same territory. Asian Pac J Trop Dis. 2017;7:708–14.

    Article  Google Scholar 

  40. 40.

    Karamon J, Dąbrowska J, Kochanowski M, Samorek-Pieróg M, Sroka J, Różycki M, et al. Prevalence of intestinal helminths of red foxes (Vulpes vulpes) in central Europe (Poland): a significant zoonotic threat. Parasit Vectors. 2018;11:1–10.

    Article  Google Scholar 

  41. 41.

    Karamon J, Samorek-Pieróg M, Moskwa B, Różycki M, Bilska-Zając E, Zdybel J, et al. Intestinal helminths of racoon dogs (Nyctereutes procyonoides) and red foxes (Vulpes vulpes) from the Augustów Primeval Forest (north-eastern Poland). J Vet Res. 2016;60:273–7.

    Article  Google Scholar 

  42. 42.

    Balicka-Ramisz A, Ramisz A, Pilarczyk B, Bieńko R. Fauna of gastro-intestinal parasites in red foxes in western Poland. Med Wet. 2003;59:922–5.

    Google Scholar 

  43. 43.

    Borecka A, Gawor J, Malczewska M, Malczewski A. Prevalence of zoonotic helminth parasites of the small intestine in red foxes from central Poland. Med Wet. 2009;65:33–5.

    Google Scholar 

  44. 44.

    Pacoń J, Sołtysiak Z, Nicpoń J, Janczak M. Prevalence of internal helminths in red foxes (Vulpes vulpes) in selected regions of Lower Silesia. Med Wet. 2006;62:67–9.

    Google Scholar 

  45. 45.

    Laurimaa L, Moks E, Soe E, Valdmann H, Saarma U. Echinococcus multilocularis and other zoonotic parasites in red foxes in Estonia. Parasitol. 2016;143:1450–8.

    Article  Google Scholar 

  46. 46.

    Bruzinskaite-Schmidhalter R, Sarkunas M, Malakauskas A, Mathis A, Torgerson PR, Deplazes P. Helminths of red foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonides) in Lithuania. Parasitol. 2012;139:120–7.

    Article  Google Scholar 

  47. 47.

    Varodi EI, Malega AM, Kuzmin YI, Kornyushin VV. Helminths of wild predatory mammals of Ukraine. Nematodes Vestnik Zoologii. 2017;51:187–202.

    Article  Google Scholar 

  48. 48.

    Siko SB, Deplazes P, Ceika C, Tivadar CS, Gogolin I, Popescu S, et al. Echinococcus multilocularis in south-eastern Europe (Romania). Parasitol Res. 2011;108:1093–7.

    PubMed  Article  PubMed Central  Google Scholar 

  49. 49.

    Myskova E, Broz M, Fuglei E, Kvicerova J, Macova A, Sak B, et al. Gastrointestinal parasites of arctic foxes (Vulpes lagopus) and sibling voles (Microtus levis) in Spitsbergen. Svalbard Parasitol Res. 2019;118:3409–18.

    PubMed  Article  PubMed Central  Google Scholar 

  50. 50.

    Meijer T, Mattsson R, Angerbjörn A, Osterman-Lind E, Fernandez-Aguilar X, Gavier-Widen D. Endoparasites in the endangered Fennoscandian population of arctic foxes (Vulpes lagopus). Eur J Wildlife Res. 2011;57:923–7.

    Article  Google Scholar 

  51. 51.

    Saeed I, Maddox-Hyttel C, Monrad J, Kapel CMO. Helminths of red foxes (Vulpes vulpes) in Denmark. Vet Parasitol. 2006;139:168–79.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  52. 52.

    Okulewicz A, Perec-Matysiak A, Buńkowska K, Hildebrand J. Toxocara canis, Toxocara cati and Toxascaris leonina in wild and domestic carnivores. Helminthol. 2012;49:3–10.

    Article  Google Scholar 

  53. 53.

    Pucek Z, Jędrzejewski W, Jędrzejewska B, Pucek M. Rodent population dynamics in a primeval deciduous forest (Białowieża National Park) in relation to weather, seed crop and predation. Acta Theriol. 1993;38:199–232.

    Article  Google Scholar 

  54. 54.

    Overgaauw PAM, van Knapen F. Toxocarosis, an important zoonosis. EJCAP. 2008;18:259–66.

    Google Scholar 

  55. 55.

    Otranto D, Deplazes P. Zoonotic nematodes of wild carnivores. Int J Parasitol Parasites Wildl. 2019;9:370–83.

    PubMed  PubMed Central  Article  Google Scholar 

  56. 56.

    Letkova V, Lazar P, Curlik J, Goldova M, Kocisova A, Kosuthova L, et al. The red fox (Vulpes vulpes L.) as a source of zoonoses. Vet Athiv. 2006;76:73–81.

    Google Scholar 

  57. 57.

    Ziadinov I, Deplazes P, Mathis A, Mutunova B, Abdykerimov K, Nurgaziev R, et al. Frequency distribution of Echinococcus multilocularis and other helminths of foxes in Kyrgyzstan. Vet Parasitol. 2010;171:286–92.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  58. 58.

    Gicik Y, Kara M, Sari BI, Kilic K, Arslan O. Intestinal parasites of red foxes (Vulpes vulpes) and their zoonotic importance for humans in Kars province. KAÜ Veteriner Fakültesi. 2009;15:135–40.

    Google Scholar 

  59. 59.

    Borecka A, Gawor J, Zięba F. A survey of intestinal helminths in wild carnivores from the Tatra National Park, southern Poland. Ann Parasitol. 2013;59:169–72.

    PubMed  PubMed Central  Google Scholar 

  60. 60.

    Borecka A, Gawor J. Helminth intestine fauna in foxes from central Poland. Mag Wet. 2009;18:1061–6.

    Google Scholar 

  61. 61.

    Vervaeke M, Dorny P, de Bruyn L, Vercammen F, Jordaens K, van den Berge K, et al. A survey of intestinal helminths of red foxes (Vulpes vulpes) in northern Belgium. Acta Parasitol. 2005;50:221–7.

    Google Scholar 

  62. 62.

    Goszczyński J. Fox. Natural and hunting monograph. Warsaw: Oikos; 1995

  63. 63.

    Goszczyński J. Connection between predatory birds and mammals and their prey. Acta Theriol. 1977;22:399–430.

    Article  Google Scholar 

  64. 64.

    Robertson RA, Whelan J. The food of the red fox (Vulpes vulpes) in Co. Kildare, Ireland. J Zool. 1987;313:740–3.

    Article  Google Scholar 

  65. 65.

    Voigt DR. Red fox. Ontario: Ministry of Natural Resources and Forestry; 1987.

    Google Scholar 

  66. 66.

    Dybing NA, Fleming PA, Adams PJ. Environmental conditions predict helminth prevalence in red foxes in Western Australia. Int J Parasitol Parasites Wildl. 2013;2:165–72.

    PubMed  PubMed Central  Article  Google Scholar 

  67. 67.

    Eslahi AV, Badri M, Khorshidi A, Majidiani H, Hooshmand E, Hosseini H, et al. Prevalence of Toxocara and Toxascaris infection among human and animals in Iran with meta-analysis approach. BMC Infect Dis. 2020;20:1–17.

    Article  Google Scholar 

  68. 68.

    Mork T, Ims RA, Killengreen ST. Rodent population cycle as a determinant of gastrointestinal nematode abundance in a low-arctic population of the red fox. Int J Parasitol Parasites Wildl. 2019;9:36–41.

    PubMed  PubMed Central  Article  Google Scholar 

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Study conception and design was carried out by AT and BP. Manuscript preparation was carried out by AT, BP, ATM and RP. Laboratory work was performed by AT. All authors read and approved the final manuscript.

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Correspondence to Agnieszka Tylkowska.

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Tylkowska, A., Pilarczyk, B., Tomza-Marciniak, A. et al. The prevalence of intestinal nematodes among red foxes (Vulpes vulpes) in north-western Poland. Acta Vet Scand 63, 19 (2021).

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  • Ecological indicators
  • Helminths
  • Nematodes
  • Prevalence
  • Red fox