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Volume 22, Number 4—April 2016

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Definitive Hosts of Versteria Tapeworms (Cestoda: Taeniidae) Causing Fatal Infection in North America

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Laura M. Lee, Roberta S. Wallace, Victoria L. Clyde, Annette Gendron-Fitzpatrick, Samuel D. Sibley, Margot Stuchin, Michael Lauck, David H. O’Connor, Minoru Nakao, Antti Lavikainen, Eric P. Hoberg, and Tony L. GoldbergComments to Author 
Author affiliations: University of Wisconsin–Madison, Madison, Wisconsin, USA (L.M. Lee, A. Gendron-Fitzpatrick, S.D. Sibley, M. Lauck, D.H. O’Connor); Milwaukee County Zoo, Milwaukee, Wisconsin, USA (R.S. Wallace, V.L. Clyde, A. Gendron-Fitzpatrick); Colorado State University, Fort Collins, Colorado, USA (M. Stuchin); Wisconsin National Primate Research Center, Madison (M. Lauck, D.H. O’Connor, T.L. Goldberg); Asahikawa Medical University, Asahikawa, Hokkaido, Japan (M. Nakao); University of Helsinki, Helsinki, Finland (A. Lavikainen); United States National Parasite Collection, Beltsville, Maryland, USA (E.P. Hoberg)

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EID Lee LM, Wallace RS, Clyde VL, Gendron-Fitzpatrick A, Sibley SD, Stuchin M, et al. Definitive Hosts of Versteria Tapeworms (Cestoda: Taeniidae) Causing Fatal Infection in North America. Emerg Infect Dis. 2016;22(4):707-710. https://dx.doi.org/10.3201/eid2204.151446
AMA Lee LM, Wallace RS, Clyde VL, et al. Definitive Hosts of Versteria Tapeworms (Cestoda: Taeniidae) Causing Fatal Infection in North America. Emerging Infectious Diseases. 2016;22(4):707-710. doi:10.3201/eid2204.151446.
APA Lee, L. M., Wallace, R. S., Clyde, V. L., Gendron-Fitzpatrick, A., Sibley, S. D., Stuchin, M....Goldberg, T. L. (2016). Definitive Hosts of Versteria Tapeworms (Cestoda: Taeniidae) Causing Fatal Infection in North America. Emerging Infectious Diseases, 22(4), 707-710. https://dx.doi.org/10.3201/eid2204.151446.

Abstract

We previously reported fatal infection of a captive Bornean orangutan with metacestodes of a novel taeniid tapeworm, Versteria sp. New data implicate mustelids as definitive hosts of these tapeworms in North America. At least 2 parasite genetic lineages circulate in North America, representing separate introductions from Eurasia.

Taeniid tapeworms (Cestoda: Taeniidae) comprise 4 proposed genera: Taenia, Echinococcus, Hydatigera, and Versteria (1). Until recently, genetic data were absent for Versteria sp. in North America. However, in 2014, we reported an unusual case of fatal metacestode (larval stage of tapeworm) infection in a captive Bornean orangutan (Pongo pygmaeus); the causative agent was identified as a novel Versteria genotype (2).

As previously described (2), the orangutan was born at a zoo in Colorado, USA, and was rejected by his birth mother. Approximately 10 months later, he was transported to the Milwaukee County Zoo in Milwaukee, Wisconsin, USA, for adoption by a surrogate mother. At ≈5 years of age, he died unexpectedly from acute respiratory distress due to disseminated infection with an unknown agent. A combination of metagenomics and gene-specific DNA sequencing revealed the etiologic agent to be a previously unknown Versteria lineage in its larval form.

We obtained wild mustelids (carnivores of the family Mustelidae) from Colorado, near where the animal was born, and Wisconsin, near where the animal died. We targeted mustelids because they are definitive hosts of V. mustelae tapeworms in Europe (3) and V. brachyacantha tapeworms in Africa (4). Colorado samples were submissions to the Denver Museum of Nature and Science, and Wisconsin samples were obtained from a local fur trapper. We also examined mustelids from Oregon, USA, as part of an ongoing investigation of Versteria spp. tapeworms in the Nearctic region and Eurasia.

Figure 1

Thumbnail of Microscope image of a mature segment of an adult Versteria sp. tapeworm recovered from an ermine in Wisconsin, USA (original magnification ×10). Characteristic reproductive structures are visible, including genital pore (G), cirrus sac (C), vagina (V), ovary (O), testes (T), uterine stem (U), and vitelline gland (VG). Tapeworm specimens were preserved in 70% ethanol for concurrent morphologic and molecular analyses. A series of proglottids was subsampled from each worm as a basis fo

Figure 1. Microscope image of a mature segment of an adult Versteria sp. tapeworm recovered from an ermine in Wisconsin, USA (original magnification ×10). Characteristic reproductive structures are visible, including genital pore (G),...

From 4 mustelids from Colorado (1 otter [Lontra canadensis], 2 ermine [Mustela erminea], and 1 mink [Neovison vison]), we recovered 1 adult tapeworm from a female ermine collected 178 km from where the orangutan was born. From 17 mustelids from Wisconsin (1 mink, 5 long-tailed weasels [M. frenata], and 11 ermine), we recovered 1 adult tapeworm from a male ermine collected 56 km from where the orangutan died. From 17 mustelids from Oregon (1 mink, 1 ermine, and 15 long-tailed weasels), we recovered 1 adult tapeworm from an adult mink of unknown sex. All tapeworm specimens were fragmented, lacking intact scolices, or both, which prevented complete morphologic description; however, microscope examination of mature segments from the Wisconsin and Oregon specimens revealed structures consistent with those of parasites in the genus Versteria (Figure 1).

Figure 2

Thumbnail of Phylogenetic tree of members of the genus Versteria (Cestoda: Taeniidae). The tree was constructed from a DNA sequence alignment of cytochrome c oxidase subunit 1 genes. The maximum-likelihood method was used, with the likeliest model of molecular evolution (Hasegawa-Kishino-Yano model with invariable positions), which was chosen by using MEGA6 (6). Numbers next to branches indicate bootstrap values (%), estimated from 1,000 resamplings of the data, and the tree is rooted at the mid

Figure 2. Phylogenetic tree of members of the genus Versteria (Cestoda: Taeniidae). The tree was constructed from a DNA sequence alignment of cytochrome c oxidase subunit 1 genes. The maximum-likelihood method was used,...

We sequenced 396 bp of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene from the 3 new adult tapeworm specimens according to previously published methods (2). The sequences of the tapeworms from the Colorado ermine and the Oregon mink were 99.5% and 99.2% similar, respectively, to the sequence from the orangutan, placing these new specimens confidently within the same Versteria lineage (Figure 2). By contrast, the sequence from the tapeworm from the Wisconsin ermine was only 90.7% similar to the sequence from the orangutan, making it a heretofore unrecognized lineage that clusters more closely with parasites from Eurasia (Figure 2).

To investigate the hosts from which adult tapeworms were recovered, we amplified and sequenced 751 bp of the mustelid cytochrome b (cytb) gene, using DNA extracts from adult tapeworm material. To do this, we used previously published methods (7,8) with modified PCR primers MVZ45_must_F (5′-CAGTNATAGCAACAGCATTCATAGG-3′) and MVZ14_must_R (5′-GCTCTCCATTTTTGGTTTACAAGAC-3′). This effort was successful, demonstrating that adult tapeworm material contains sufficient host-associated DNA for such analyses. The resulting sequences indicated that the ermine from Colorado and Wisconsin (GenBank accession nos. KT223030 and KT223032, respectively) belonged to the continental clade, which is broadly distributed across the Nearctic region (9). The sequence for the Oregon mink (GenBank accession no. KT223031) closely matched published sequences for other mink from North America but was otherwise phylogeographically uninformative.

We next assessed whether parasites of the genus Versteria were present in wild carnivores on and near the grounds of the Milwaukee County Zoo. We conducted systematic searches of the zoo grounds (i.e., outside of enclosures) for carnivore feces. We also trapped carnivores, using live traps baited with fish, and then immediately released them, collecting any feces deposited in the trap, and we collected feces from mink from a local wildlife rehabilitation center. These efforts yielded 51 samples (3 from skunks [Mephitis mephitis], 3 from coyotes [Canis latrans], 6 from long-tailed weasels, 8 from mink, and 31 from raccoons [Procyon lotor]), which we examined by microscope, using standard flotation and sedimentation methods to identify parasite eggs (Table 1). We then used the ZR Fecal DNA MiniPrep kit (Zymo Research, Irvine, CA, USA) to extract DNA directly from feces samples and amplified and sequenced the cox1 gene (2). Resulting sequences were unambiguous and revealed a diversity of parasites (not only taeniids, and in some cases representing putative novel lineages), but none matched Versteria spp. (Table 2).

Our results demonstrate that the genus Versteria is a species complex in North America. The new lineage identified in Wisconsin clusters with parasites formerly known only from Eurasia (Figure 2). Preliminary assessments suggest that this same lineage infects ermine as far away as the Northwest Territories (NWT) of Canada (E.P. Hoberg et al., unpub. data) and that the lineage responsible for fatal infection of an orangutan (2) also infects muskrats (Ondatra zibethicus) in Idaho, USA, and the NWT (A. Lavikainen et al., unpub. data). To the extent that current sampling reflects the distribution of Versteria lineages in North America, there appears to be a western lineage (represented by Colorado, Oregon, and Idaho, and the NWT) and a northern continental lineage (represented by Wisconsin and the NWT), with sympatry in the NWT. We note that this pattern parallels the phylogeography of ermine in North America, perhaps reflecting postglacial expansion of host and parasite after the Pleistocene (9). More Versteria lineages will likely be found, as evidenced by a novel lineage in zokor (Eospalax baileyi, a fossorial rodent) recently described from Tibet (10) (Figure 2). Versteria lineages have clearly entered the Nearctic region from the Palearctic region at least twice, probably reflecting Beringian biogeographic processes of faunal expansion that are important drivers of the evolution of mammals and the organisms parasitizing them (11).

Our findings shed light on the origins of the infection that proved fatal to the orangutan. We found an adult Versteria sp. tapeworm with a nearly identical DNA sequence in Colorado, where the orangutan was born; however, a Versteria sp. tapeworm from Wisconsin, where the orangutan died, was genetically divergent. Moreover, we found no evidence of Versteria tapeworms on the grounds of the Milwaukee County Zoo or nearby. Taeniid metacestodes encyst and can remain dormant for years before asexual multiplication (12). We therefore suspect that the orangutan became infected where it was born (Colorado) and carried the latent infection to where it died ≈4 years later (Wisconsin). This animal’s sudden progression to disease remains a mystery, perhaps indicating immune deficiency or another precipitating factor, consistent with reports of disseminated taeniid infection in other hosts (13).

In general, our findings underscore that exotic animals in zoo settings are susceptible to infections harbored by local wildlife and that transport of such animals can complicate inferences about the origins of these locally acquired infections. We reiterate that taeniid tapeworms of the genus Versteria should be considered a threat to captive apes (2), and we recommend that wild mustelids, such as ermine and mink, be excluded or removed from the grounds of zoos where apes have access to outdoor environments. Given the close relationship between apes and humans, we also suggest increased vigilance for zoonotic infections.

Ms. Lee is a veterinary student who participated in this research as part of the University of Wisconsin-Madison School of Veterinary Medicine’s Summer Scholars Program. Her interests include wildlife medicine, small animal medicine, and infectious disease.

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Acknowledgments

We are grateful to the staff and administration of the Milwaukee County Zoo for their support, John Demboski and the Denver Museum of Nature and Science for access to mustelid specimens from Colorado, Katie Moriarty and Nicole Edmison for access to mustelid specimens from Oregon, Slade Noreen and Jorden Manasse for assistance with mustelid specimens from Wisconsin, and Daron Graves and Patricia Khan for assistance with obtaining samples from the grounds of the Milwaukee County Zoo.

This work was supported by the American Association of Zoological Veterinarians (award MSN173939). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Field collections in the Northwest Territories and broader explorations of diversity were conducted through the Collaborative Integrated Inventory of Biomes of the Arctic project, supported by the National Science Foundation (grants no. 0196095 and 0415668).

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References

  1. Nakao  M, Lavikainen  A, Iwaki  T, Haukisalmi  V, Konyaev  S, Oku  Y, Molecular phylogeny of the genus Taenia (Cestoda: Taeniidae): proposals for the resurrection of Hydatigera Lamarck, 1816 and the creation of a new genus Versteria. Int J Parasitol. 2013;43:42737. DOIPubMed
  2. Goldberg  TL, Gendron-Fitzpatrick  A, Deering  KM, Wallace  RS, Clyde  VL, Lauck  M, Fatal metacestode infection in Bornean orangutan caused by unknown Versteria species. Emerg Infect Dis. 2014;20:10913. DOIPubMed
  3. Loos-Frank  B. An up-date of Verster’s (1969) ‘Taxonomic revision of the genus Taenia Linnaeus’ (Cestoda) in table format. Syst Parasitol. 2000;45:15584. DOIPubMed
  4. Baer  JG, Fain  A. Newly discovered Cestoda in Belgian Congo [in French]. Acta Trop. 1951;8:5963 .PubMed
  5. Pritchard  MH, Kruse  GOW. The collection and preservation of animal parasites. Lincoln (Nebraska): University of Nebraska Press; 1982.
  6. Tamura  K, Stecher  G, Peterson  D, Filipski  A, Kumar  S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol. 2013;30:27259. DOIPubMed
  7. Smith  MF, Patton  JL. The diversification of South American murid rodents: evidence from mitochondrial DNA sequence data for the akodontine tribe. Biol J Linn Soc Lond. 1993;50:14977. DOI
  8. Fleming  MA, Cook  JA. Phylogeography of endemic ermine (Mustela erminea) in southeast Alaska. Mol Ecol. 2002;11:795807. DOIPubMed
  9. Dawson  NG, Hope  AG, Talbot  SL, Cook  JA. A multilocus evaluation of ermine (Mustela erminea) across the Holarctic, testing hypotheses of Pleistocene diversification in response to climate change. J Biogeogr. 2014;41:46475. DOI
  10. Zhao  F, Ma  JY, Cai  HX, Su  JP, Hou  ZB, Zhang  TZ, Molecular identification of Taenia mustelae cysts in subterranean rodent plateau zokors (Eospalax baileyi). Dongwuxue Yanjiu. 2014;35:313–8.
  11. Hoberg  EP, Galbreath  KE, Cook  JA, Kutz  SJ, Polley  L. Northern host–parasite assemblages: history and biogeography on the borderlands of episodic climate and environmental transition. Adv Parasitol. 2012;79:197. DOIPubMed
  12. Whitfield  PJ, Evans  NA. Parthenogenesis and asexual multiplication among parasitic platyhelminths. Parasitology. 1983;86:12160. DOIPubMed
  13. Hoberg  EP, Ebinger  W, Render  JA. Fatal cysticercosis by Taenia crassiceps (Cyclophyllidea: Taeniidae) in a presumed immunocompromised canine host. J Parasitol. 1999;85:11748. DOIPubMed

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DOI: 10.3201/eid2204.151446

Medline reports the last page should be "183" not "84" in reference 3 "Loos-Frank, 2000".

Medline indexes "Biol J Linn Soc Lond" but cannot find a listing for reference 7 "Smith, Patton, 1993". Please check the reference for accuracy.

Medline indexes "J Biogeogr" but cannot find a listing for reference 9 "Dawson, Hope, Talbot, Cook, 2014". Please check the reference for accuracy.

Table of Contents – Volume 22, Number 4—April 2016

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Tony L. Goldberg, University of Wisconsin-Madison, Department of Pathobiological Sciences, 1656 Linden Dr, Madison, WI 53706, USA


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