Skip to main content

Is the red fox (Vulpes vulpes) a competent definitive host for Taenia multiceps?



Shepherd and stray dogs are thought to represent the primary definitive hosts of Coenurosis by Taenia multiceps, due to their feeding habits which translate into high chances of coming into contact with infected intermediate hosts. Nonetheless, little attention has been paid to the role of the red fox (Vulpes vulpes) in the epidemiology of coenurosis. In fact a knowledge gap exists on the role played by red foxes in the epidemiology of Taenia multiceps and the capability of this parasite to produce fertile and viable eggs in this wild canid, i.e. on the occurrence of a sylvatic cycle.

This study investigates the role of the red fox (Vulpes vulpes) in the epidemiology of T. multiceps and related metacestodoses.


The small intestine of 63 red foxes was macroscopically examined for the presence of cestodes. Adult parasites were identified morphologically as being T. multiceps. Tapeworm eggs were counted and stored at 4 °C in physiological saline solution prior to experimental infection of four sheep and one goat. Sheep were inoculated orally on Day 0 with 3000 (sheep 1), 5000 (sheep 2 and 3) or 7000 eggs (sheep 4), while the goat was infected with 5000 eggs of T. multiceps. The animals were followed-up regularly by MRI and underwent surgical treatment between days 180 to day 240 post infection. Collected coenuri were identified using morphological and molecular methods.


A total of 6.3 % of red foxes were found infected with T. multiceps and the eggs obtained from the worms were determined to have a viability of 45.4 %. Two of the challenged sheep and the goat developed disease compatible with T. multiceps. Morphometrical features of the cysts were consistent with those of T. multiceps; nucleotide amplification and sequencing of mitochondrial genes (i.e., cox1 and Nd1) from the metacestode material confirmed the identification.


The present study is the first to provide evidence of the role of the red fox as a competent definitive host for T. multiceps, thus changing the epidemiological scenarios of infections by this cestode.


Coenurosis or “Gid”, known previously as Coenurus cerebralis, is a parasitic disease caused by the metacestode stage of Taenia multiceps (Cestoda, Teniidae). The adult tapeworm inhabits the small intestine of a number of domestic and wild carnivores, including dogs, jackals, foxes and coyotes [1]. Eggs of T. multiceps are excreted in the environment with the faeces of the definitive hosts and ingested by intermediate herbivore hosts including sheep, goats, horses, cattle, camels, deer and pigs [2, 3]. Following the ingestion of the eggs, the oncosphere hatches, burrows its way through the intestinal wall and reaches the central nervous system (CNS) and other organs via the bloodstream [4]. The infection is often lethal in intermediate hosts and the parasite is a significant cause of economic losses in many areas of the world [5].

Coenurosis has been documented in scattered foci in the Americas and parts of Europe, Asia and Africa, although its distribution is most likely global, with the exception of Australia [6]. The infection is more common in temperate regions, such as the Mediterranean basin and Sardinia Island, where different intraspecific genetic variants have been identified [79]. In particular, a genetic variant of this parasite (i.e. Tm4) is also responsible for non-cerebral coenurosis in goats, where the parasite invades the subcutaneous fascia, peritoneal areas, and intramuscular tissues [1014].

Coenurosis is a zoonotic disease in which humans act as accidental hosts and may develop different forms of neurological diseases. Over 100 human cases have been described from different countries including Italy, Egypt and the United States [6].

Shepherd and stray dogs are thought to represent the primary definitive hosts of this metacestodosis, due to their feeding habits, which translate into high chances of coming into contact with infected intermediate hosts [5]. Nonetheless, little attention has been paid to the role of the red fox (Vulpes vulpes) in the epidemiology of coenurosis. Several authors have reported T. multiceps from fox species, but with prevalences usually under 1 % [1518]. A survey in the Tartar Republic of Russia identified 28.2 % positivity for T. multiceps in necropsied foxes (n = 350) [19]. Other descriptions of T. multiceps in red foxes originated from Germany (3.3 %) [20], Perù (2 %) [21], Jordan (3.8 %) [22], Iran (4.8 and 8.2 %) [23, 24] and China (6 % in Tibetan sand foxes) [25]. To date, T. multiceps has never been described from red foxes of Sardinia, Italy [26, 27], where sheep coenurosis is endemic.

A knowledge gap exists on the role played by red foxes in the epidemiology of T. multiceps and the capability of this parasite to produce fertile and viable eggs in the intestine of red foxes, i.e. on the occurrence of an alternative lifecycle.

Therefore, in this study, the role of the red fox as a competent definitive host for T. multiceps was investigated to better understand the epidemiology of this important taeniid and of the metacestodosis it causes.


This study was approved by the National Research Centre (NRC) – Medical Research Ethics Committee (MREC) on animal ethics, Registration number 14099 of 14/09/2014 and executed following the recommendations of European Council Directive (86/609/EEC) on the protection of animals used for experimental purposes.


Between 2012 and 2014, 63 carcasses of red foxes (Vulpes vulpes), road-killed or legally hunted in Sardinia Island (Western Mediterranean, Italy - 40° 00′ 00″ N; 9° 00′ 00″ E), were referred to the Laboratory of Parasitology of the Veterinary Teaching Hospital in Sassari, for necropsy. At necropsy, the small intestine was macroscopically examined and dissected under a stereomicroscope for detection of cestodes. Parasites collected were washed in saline solution and the gravid segments were collected and stored at 4 °C in TCM 199 (Minitüb GmbH, Tiefenbach, Germany). Cestode specimens were individually mounted on glass slides and morphologically identified using morphometrical keys [28, 29]. A section of each parasite was stored for molecular identification using protocols described elsewhere [7, 30].

Eggs were separated from gravid proglottids using a surgical blade, counted in a McMaster slide and stored at 4 °C in physiological saline solution prior to experimental infections. Egg vitality tests were performed according to the methodology described by Deplazes et al. [31]. Briefly, 0.3 ml of Sodium Hypochlorite (SH) solution (2 % active chlorine, pH 12) was added to 0.4 ml egg suspension (2500 eggs/ml). Within 1 min (i.e. before destruction of embryophores occurred), the total number of eggs was determined in a McMaster-chamber. Four to 5 min later, oncospheres with intact membranes were counted again. SH resistance was calculated from triplicate counts as percentage of intact oncospheres. Eggs were subsequently diluted in PBS, and a batch of eggs (5000/ml) was prepared for the challenge in the intermediate hosts.

Four 16-week old male sheep and one goat, kept indoors since birth, were dewormed prior to the trial (4 ml /40 kg b.w. of Albendazole 1.9 %; Valbazen, Zoetis). The egg suspension was enclosed into capsules resistant to gastric digestion (Sansyoiyaku, Shizuoka, Japan) and animals were orally inoculated using a rumen bolus applicator at Day 0 (D0) with 3000 (Sheep 1), 5000 (Sheep 2 and Sheep 3) and 7000 eggs (Sheep 4), while the goat was infected with 5000 eggs of T. multiceps.

Following experimental infection, animals were housed under usual conditions with free access to food and water. Animals were checked daily to detect clinical signs and behavioural changes (i.e., temperature, physiologic functions, symptoms related to coenurosis or other diseases). A neurological examination and magnetic resonance imaging (MRI) scan according to Manunta et al. [32] was performed for each animal every 30 days, and the size, localization and number of coenuri detected were documented. Surgical treatment of positive animals was performed at the end of the challenge.

The coenuri collected at surgery were examined under a light microscope without staining, in order to assess viability, number and size of clusters of protoscoleces, hook size and numbers. Microscopical images and measurements were acquired using a digital image processing system (LC micro Image Acquisition Software V.5.2, Olympus). Aliquots of protoscoleces were used for molecular identification [7].


Four (6.3 %) out of the 63 examined red foxes were infected by T. multiceps (Figs. 1 and 2). The percentage of intact oncospheres at the viability test was 45.4 % (567.7/1172 in 0.4 ml of egg suspension).

Fig. 1
figure 1

Gravid proglottids of Taenia multiceps recovered in the rectum of a necropsied fox

Fig. 2
figure 2

Eggs of Taenia multiceps obtained from gravid proglottids (200× magnification)

Three of the animals challenged with T. multiceps eggs developed coenurosis as assessed by MRI (Fig. 3) (Table 1) at 30 days. Two sheep developed one coenurus each while sheep 4 and the goat developed 4 and 3 coenuri, respectively.

Fig. 3
figure 3

Screenshot of magnetic resonance imaging (MRI) scan of a sheep challenged with 5000 Taenia multiceps eggs

Table 1 Animals, challenge doses of Taenia multiceps eggs and number and location of coenuri found

Following surgical procedure for the removal of the coenuri (day 180–240), all animals fully recovered. All recovered metacestodes were viable, with visible protoscoleces. The size of the cysts as well the number of clusters of protoscoleces, their size and the morphometric data of the hooks (Fig. 4) were consistent with T. multiceps cysts (Table 2). Molecular analyses of both adult tapeworms and metacestodes displayed 100 % nucleotide identity to T. multiceps Tm1 strain [Genbank accession numbers: AY669089.2; DQ309767.1] [7].

Fig. 4
figure 4

Light microscopy, hooks of a protoscolex (50× magnification)

Table 2 Features and size of recovered coenuri in animals challenged with Taenia multiceps eggs


The present study provides experimental evidence of the role of the red fox as a competent definitive host for T. multiceps, clearly indicating that coenurosis by T. multiceps can be maintained and spread by wild canids.

In spite of previous speculations hypothesising a possible role for the red fox in transmitting T. multiceps, this is the first study providing unequivocal data showing that foxes excrete proglottids with viable and infective eggs that could therefore maintain the parasite lifecycle.

A similar issue has surrounded another important cestode, Echinococcus granulosus, with some authors claiming that parasites infecting red foxes were unable to produce fertile eggs [26, 33] and others reporting an active role for this canid as a valid definitive host for this cestode [34].

In the past, several authors have also questioned the role of the red fox as a definitive host for T. multiceps, because of the presumptive inability of this carnivore to access the sheep CNS through the skull [35]. However, it has been reported that the presence of cysts is associated with thinner skull bones, thus facilitating access, even to foxes [6]; the first author of the present paper has personally witnessed foxes accessing the full content of a sheep skull (CNS and eventually coenuri) via the foramen magnum without breaking the skull itself [Varcasia A., personal observations].

The red fox is the most widespread wild member of the Carnivora, distributed from the Arctic Circle to subtropical regions in North America and Eurasia as well as in in North Africa. Its distribution range has increased alongside human expansion, and it now includes Australia. Red fox populations are increasing in numbers and their expansion towards urban areas has been reported over the last two decades. This is considered to have contributed to the enlarging distribution of Echinococcus multilocularis (EM) and alveolar echinococcosis cases in urban areas of Europe and North America [36].

Home ranges of red foxes in the United States span from 2. to 19.9 km2, ~50 km2 in Iran, from 4 to 12 km2 in Sweden, and from 0.21 (urban) to 10.0 (rural) km2 in England, with males occupying larger home ranges than females [37].

For this reason the role of foxes in the epidemiology of coenurosis must not be underestimated. During the mating period in spring, males are able to travel several kilometres, both for mating and hunting. This time span also coincides with the period in which replacement sheep (3–4 months animals) are usually taken out at pasture for the first time in many Mediterranean locations. This period is considered to be crucial for infection of replacement sheep [8, 9].

Control of T. multiceps transmission by foxes is bound to be challenging, given the large home ranges and the scary and suspicious attitude of this species. The sanitary education of the farmers and the prophylactic measures (e.g., concerning the proper disposal of dead/ butchered animals) are of primary importance in the prevention of the disease and to reduce the risk of infection of foxes in areas where coenurosis is endemic. One of the first steps that should be implemented in these areas is represented by mandatory slaughtering of T. multiceps infected animals at diagnosis, to avoid contact between infected carcasses and dogs and foxes in the field, as well as appropriate disposal of skull and offal of slaughtered animals [5].

In endemic areas for E. multilocularis, the use of praziquantel baits every 1–6 km has been effective in reducing the cestode parasite pressure in foxes. This approach is also cost effective if implemented for several decades in restricted, most relevant areas for the transmission of the parasites [36]. For T. multiceps, the use of Praziquantel baits could be useful particularly in inaccessible and wild areas where the disease is endemic, as well as in proximity of urbanized areas. Vaccination of intermediate hosts (with combinations of parasite antigens expressed in recombinant form), and in particular of replacement animals, has been shown to be effective and could represent an alternative control method for coenurosis, together with other metacestodoses such as cystic echinococcosis [8, 9].

According to Verster and Tustin [38], the number of eggs necessary to develop Coenurosis in sheep is in excess of 5000 eggs; the results of our experiments, even conducted on a limited number of animals, are consistent with this finding.

Two of the challenged animals did not develop Coenurosis; this could be related to some animals being refractory to the infection, for instance due to genetic factors or immune responses to the parasite [8].

The Coenuri detected in the challenged animals displayed morphological features and size typical of T. multiceps. Molecular identification confirmed the diagnosis and revealed that all the cysts removed belonged to the genetic variant Tm1, which represents the most common genotype detected in intermediate hosts in Sardinia as well as in other geographical areas [7, 13].

Considering the genetic variant involved in this report and the number of cysts recovered in all challenged animals, it seems that the number of coenuri in infected animals should be more related to the quantity and viability of eggs ingested rather than to a particular strain (ie. Tm1/Tm3), as had been speculated in the past [7].


Based on the findings of the present study, we argue that the red fox should be recognised as an alternative definitive host of T. multiceps and, considering that this species is becoming increasingly widespread in several European countries, the role of this carnivore must be taken into account when planning control strategies for the prevention of this metacestodosis in livestock, as well as public health-related risks.


  1. Rostami S, Beech RN, Salavati R, Baneshi MR, Kamyabi H, Harandi MF. Morphometric analysis of larval rostellar hooks in Taenia multiceps of sheep in Iran and its association with mitochondrial gene variability. Iran J Parasitol. 2013;8:579–85.

    PubMed  PubMed Central  Google Scholar 

  2. Scala A, Cancedda GM, Varcasia A, Ligios C, Garippa G, Genchi C. A survey of Taenia multiceps coenurosis in Sardinian sheep. Vet Parasitol. 2007;143:294–8.

    Article  CAS  PubMed  Google Scholar 

  3. Varcasia A, Pipia AP, Arru D, Pes AM, Tamponi C, Dore F, et al. Morphological and molecular characterization of bovine coenurosis in Sardinia, Italy. Parasitol Res. 2013;112:2079–82.

    Article  CAS  PubMed  Google Scholar 

  4. Paltrinieri S, Varcasia A, Cazzaniga S, Giordano A, Pipia AP, Marrosu R, et al. Brain creatine kinase isoenzyme (CK-BB) as a possible biomarker for the diagnosis in vivo of ovine coenurosis in a naturally infected flock. Small Ruminant Res. 2010;94:180–4.

    Article  Google Scholar 

  5. Varcasia A, Tanda B, Giobbe M, Solinas C, Pipia AP, Malgor R, et al. Cystic echinococcosis in Sardinia: farmers’ knowledge and dog infection in sheep farms. Vet Parasitol. 2011;181:335–40.

    Article  CAS  PubMed  Google Scholar 

  6. Scala A, Varcasia A. Updates on morphobiology, epidemiology and molecular characterization of coenurosis in sheep. Parassitologia. 2006;48:61–3.

    CAS  PubMed  Google Scholar 

  7. Varcasia A, Lightowlers MW, Cattoli G, Cancedda GM, Canu S, Garippa G, et al. Genetic variation within Taenia multiceps in Sardinia, Western Mediterranean (Italy). Parasitol Res. 2006;99:622–6.

    Article  CAS  PubMed  Google Scholar 

  8. Gauci C, Vural G, Oncel T, Varcasia A, Damian V, Kyngdon CT, et al. Vaccination with recombinant oncosphere antigens reduces the susceptibility of sheep to infection with Taenia multiceps. Int J Parasitol. 2008;38:1041–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Varcasia A, Tosciri G, Coccone GN, Pipia AP, Garippa G, Scala A, et al. Preliminary field trial of a vaccine against coenurosis caused by Taenia multiceps. Vet Parasitol. 2009;162:285–9.

    Article  CAS  PubMed  Google Scholar 

  10. Oryan A, Nazifi S, Sharifiyazdi H, Ahmadnia S. Pathological, molecular, and biochemical characterization of Coenurus gaigeri in Iranian native goats. J Parasitol. 2010;96:961–7.

    Article  CAS  PubMed  Google Scholar 

  11. Schuster RK, Sivakumar S, Wieckowsky T. Non-cerebral coenurosis in goats. Parasitol Res. 2010;107:721–6.

    Article  PubMed  Google Scholar 

  12. Varcasia A, Jia WZ, Yan HB, Manunta ML, Pipia AP, Garippa G, et al. Molecular characterization of subcutaneous and muscular coenurosis of goats in United Arab Emirates. Vet Parasitol. 2012;190:604–7.

    Article  CAS  PubMed  Google Scholar 

  13. Oryan A, Akbari M, Moazeni M, Amrabadi OR. Cerebral and non-cerebral coenurosis in small ruminants. Trop Biomed. 2014;31:1–16.

    CAS  PubMed  Google Scholar 

  14. Akbari M, Moazeni M, Oryan A, Sharifiyazdi H, Amrabadi O. Experimental cerebral and non-cerebral coenurosis in goats: A comparative study on the morphological and molecular characteristics of the parasite. Vet Parasitol. 2015; (In press).

  15. Shaldybin LS. Helminth fauna of hunting animals in the Mordova state reserve (In Russian), Thesis. Moscow: All Union Helminthological Institute; 1950.

    Google Scholar 

  16. Kadenacii AN. Helminth fauna of mammals of Crimea and trial to control major helminthoses in farm animals (In Russian) (source not given), Omsk: 1957;124. cited in Bondareva V.I. Coenurus invasion in domestic and wild animals. Academy of Sciences of the Kazakh 1963, SSR publishing house, Almaty, 355 pp.

  17. Igrashev. On the helminth fauna of domestic and wild animals in Samarkand region (In Russian). Uzbekistan Biol J. 1958;5:62–8.

    Google Scholar 

  18. Muminov P Ch. On the helminth fauna of of foxes in Uzbekistan (In Russian). Theses of papers of the scientific conference of Allunion Helminthological Society 1962 (part 2). Moscow: Academy of Sciences. cited in Bondareva VI: Coenurus invasion in domestic and wild animals. Academy of Sciences of the Kazakh 1963, SSR publishing house, Almaty, 355 pp.

  19. Troickaja AA. Materials on the helminth fauna of foxes in the Tartar Autonomous Sovjet Republic (In Russian). Papers of the Allunion Scientific Institute of Hunting Industry 1955; 14. Cited in Bondareva VI: Coenurus invasion in domestic and wild animals. Academy of Sciences of the Kazakh 1963, SSR publishing house, Almaty, 355 pp.

  20. Ballek D, Takla M, Ising-Volmer S, Stoye M. The helminth fauna of red foxes (Vulpes vulpes Linnaeus 1758) in north Hesse and east Westphalia. 1. Cestodes. Dtsch Tierarztl Wochenschr. 1992;99:362–5.

    CAS  PubMed  Google Scholar 

  21. Moro PL, Ballarta J, Gilman RH, Leguia G, Rojas M, Montes G. Intestinal parasites of the grey fox (Pseudalopex culpaeus) in the central Peruvian Andes. J Helminthol. 1998;72:87–9.

    Article  CAS  PubMed  Google Scholar 

  22. El-Shehabi FS, Abdel-Hafez SK, Kamhawi SA. Prevalence of intestinal helminths of dogs and foxes from Jordan. Parasitol Res. 1999;85:928–34.

    Article  CAS  PubMed  Google Scholar 

  23. Dalimi A, Sattari A, Motamedi G. A study on intestinal helminthes of dogs, foxes and jackals in the western part of Iran. Vet Parasitol. 2006;142:129–33.

    Article  CAS  PubMed  Google Scholar 

  24. Nabavi R, Manouchehri Naeini K, Zebardast N, Hashemi H. Epidemiological study of gastrointestinal helminthes of canids in Chaharmahal and Bakhtiari province of Iran. Iran J Parasitol. 2014;9:276–81.

    PubMed  PubMed Central  Google Scholar 

  25. Li W, Guo Z, Duo H, Fu Y, Peng M, Shen X, et al. Survey on helminths in the small intestine of wild foxes in Qinghai, China. J Vet Med. 2013;75:1329–33.

    Google Scholar 

  26. Deaina S, Arru E. Echinococcus granulosus in Vulpes vulpes della Sardegna. Parassitologia. 1962;23(4):267–75.

    Google Scholar 

  27. Leoni A, Garippa G, Masala S. Osservazioni sull’elmintofauna della volpe (Vulpes vulpes) in Sardegna. Parassitologia. 1986;28:268–9.

    Google Scholar 

  28. Verster A. A taxonomic revision of the genus Taenia Linnaeus, 1758 s.str. Onderstepoort J Vet Res. 1969;36:3–58.

    CAS  PubMed  Google Scholar 

  29. Loos-Frank B. An update of Versters (1969): ‘Taxonomic revision of the genus Taenia Linnaeus’ (Cestoda) in table format. Syst Parasitol. 2000;45:155–83.

    Article  CAS  PubMed  Google Scholar 

  30. Otranto D, Varcasia A, Solinas C, Scala A, Brianti E, Dantas-Torres F, et al. Redescription of Cercopithifilaria bainae Almeida & Vicente, 1984 (Spirurida, Onchocercidae) from a dog in Sardinia, Italy. Parasit Vectors. 2013;6:132.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Deplazes P, Grimm F, Sydler T, Tanner I, Kapel CMO. Experimental alveolar echinococcosis in pigs, lesion development and serological follow up. Vet Parasitol. 2005;130:213–22.

    Article  CAS  PubMed  Google Scholar 

  32. Manunta ML, Evangelisti MA, Burrai GP, Columbano N, Ligios C, Varcasia A, et al. Magnetic resonance imaging of the brain and skull of sheep with cerebral coenurosis. Am J Vet Res. 2012;73:1913–8.

    Article  PubMed  Google Scholar 

  33. Gemmell MA. Hydatid disease in Australia.VI. Observations on the carnivora of New South Wales as definitive hosts of Echinococcus granulosus (Batsch, 17E6) (Rudolphi, 1801), and their role in the spread of hydatidiasis in domestic animals. Aust Vet J. 1959;35:450–55.

  34. Thompson RCA. The susceptibility of the European red fox (Vulpes vulpes) to infection with Echinococcus granulosus of Australian sheep origin. Ann Trop Med Parasitol. 1983;77:75–82.

    CAS  PubMed  Google Scholar 

  35. Deiana S. Stato attuale della diffusione della Cenurosi cerebrale negli ovini e nell’uomo in Sardegna. Parassitologia. 1971;13:173–5.

    CAS  PubMed  Google Scholar 

  36. Hegglin D, Deplazes P. Control of Echinococcus multilocularis: strategies, feasibility and cost-benefit analyses. Int J Parasitol. 2013;43:327–37.

    Article  PubMed  Google Scholar 

  37. Rountree GH. Comparative study of the home range and habitat usage of red foxes and gray foxes in an urban setting: a preliminary report. In: Shaw WW, Harris LK & Van Druff L (Eds.) 2004;238–244. Proceedings of the 4th International Symposium on Urban Wildlife Conservation, May 1–5, 1999. Tucson, Arizona, 368 pp.

  38. Verster A, Tustin RC. Treatment of the larval stage of Taenia multiceps with praziquantel. J S Afr Vet Assoc. 1982;53:107–8.

    CAS  PubMed  Google Scholar 

Download references


Authors thank Bayer HealthCare AG (Leverkusen, Germany) for covering publication fees of the article and Cinzia Cantacessi (Senior Lecturer, Department of Veterinary Medicine, University of Cambridge, United Kingdom) for the critical review of the manuscript.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Antonio Varcasia.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

AV, CT and AS conceived the study and drafted the manuscript. CT, GT, AV and FD collected parasites, performed the morphological identification and the challenge in sheep and the goat. AV and APP carried out the molecular genetic studies, sequence alignment and phylogenetic analyses, and drafted the manuscript. AS and RKS revised the drafts of manuscript. OMK participated in molecular genetic and phylogenetic studies and revised and implemented the drafts of the manuscript. All authors read and approved the final version of manuscript.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Varcasia, A., Tamponi, C., Tosciri, G. et al. Is the red fox (Vulpes vulpes) a competent definitive host for Taenia multiceps?. Parasites Vectors 8, 491 (2015).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: