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Volume 21, Number 10—October 2015
Letter

Alaria alata Mesocercariae among Feral Cats and Badgers, Denmark

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To the Editor: The digenean trematode Alaria alata is considered an emerging zoonotic parasite in Europe because of increased findings in wild boars during Trichinella inspection. No human illness caused by A. alata mesocercariae (infective larvae) has been reported, but concern remains because the closely related North American species A. americana has caused illnesses among humans, including 1 death (1).

In Denmark, high prevalence of A. alata trematodes in final hosts has been shown (2), but limited data on potential paratenic hosts are available. Therefore, samples from 406 domestic pigs, 130 wild boars, 9 badgers, and 99 cats were collected by convenience sampling during October 2013–September 2014. We used pig and wild boar samples from multiple geographic areas of Denmark were leftover tissue samples from ongoing Trichinella spp. surveillance. Badgers had died naturally or were hit by vehicles (8 from Jutland, 1 from Zealand) and collected as part of a wildlife monitoring program. Cats (all from Zealand) were either feral (n = 92) or domesticated (n = 7) and had been euthanized as part of a national control program. Carcasses were necropsied in our laboratory; we collected 30 g of tissue samples according to Riehn et al. (3). All samples were analyzed by the modified A. alata mesocercariae migration technique (3). In brief, the sample was cut into ≈0.5-cm edge pieces, wrapped in gauze, and suspended for 90 min by 2 wooden sticks in a conical glass with ≈300 mL of water (46°C–48°C). Approximately 15 mL of sediment was collected from the bottom of the glass by suction by using a glass pipette and examined by microscopy (magnification ×20).

A. alata mesocercariae were isolated from 3 cats and 6 badgers (Technical Appendix Table 1). All 3 cats were female (2 pregnant, 1 lactating); prevalence was significantly higher in pregnant or lactating females (3/12) than other intact females (0/24) (p = 0.031 by Fisher exact test). This finding might be related to increased exposure because an increase in predation by the cats during pregnancy and lactation to meet higher protein and energy demand. However, because A. marcianae mesocercariae can be transmitted through milk in cats (4), lactating females may also be predisposed to an increased chance for A. alata mesocercariae reaching their offspring. Examination of the intestines of all cats by sedimentation and counting technique (5) revealed no A. alata adults. Although A. alata adults have been found in cats in Uruguay (6), reports from Europe are lacking, and thus it is still uncertain whether cats can act as amphiparatenic or final hosts. Natural infection of cats with other Alaria spp. has been reported in the United States (7), indicating biologic differences among Alaria spp.

Zoonotic risk for A. alata infection through ingestion of cat meat is probably minimal in Europe but may be important in Asia and South America, where cats are occasionally consumed. Badgers are, however, sometimes consumed as game meat or road kill meat in Europe. In Russia, 10.6% of trichinellosis outbreaks during 1998–2002 were caused by consumption of badger meat (8). Thus, the zoonotic potential of infections in this animal, although a protected species, should not be ignored.

Negative findings in domestic pigs and wild boars in this study may reflect underestimation because those samples were below the recommended 30 g and often taken from sites that are not typically infected with mesocercariae (3). A follow-up study with better sampling strategy would be of value to determine the risk for A. alata transmission from domestic pigs and wild boars.

Figure

Thumbnail of Neighbor-joining phylogenetic tree of Alaria alata isolates based on the analysis of partial mitochondrial cytochrome c oxidase subunit 1 gene sequences (332 bp). Bootstrap values are indicated to the left of the nodes and are based on 10,000 replicates. GenBank accession numbers are listed to the right. Scale bar indicates base substitutions per site.

Figure. Neighbor-joining phylogenetic tree of Alaria alata isolates based on the analysis of partial mitochondrial cytochrome c oxidase subunit 1 gene sequences (332 bp). Bootstrap values are indicated to the left of...

Identification of isolated mesocercariae was confirmed by PCR and sequencing of a fragment (332 bp) of the mitochondrial cytochrome c oxidase subunit 1 gene (cox1) (9). By neighbor-joining analysis (10), the consensus cox1 sequences were compared with the trematode Neodiplostomum seoulense (outgroup), 1 A. alata isolate from a Danish red fox, and all 7 cox1 sequences of Alaria spp. available in GenBank as of October 2014. (Sequences from this study have been deposited into GenBank under accession nos. KP123417–KP123422 [badgers] KP123423–KP123425 [feral cats].) The inferred phylogenetic tree (Figure) showed marked genetic variation among A. alata isolates from Denmark and other parts of Europe but no apparent separation of most A. alata isolates from Europe based on host species or country, except for that from badger 1 (Technical Appendix Table 2). This animal originated from Northern Jutland, where host and parasite populations are geographically isolated by a large fjord separating the region from the rest of the country. The marked genetic variation within cox1 sequences suggests the usefulness of this marker, but additional genetic markers should be included in future studies to explore the genetic flow of A. alata within natural hosts.

In conclusion, A. alata mesocercariae seem to favorably infect pregnant or lactating cats, thereby increasing the chance of vertical transmission. Further, detection of A. alata infection in numerous badgers suggests potential high zoonotic risk associated with ingestion of such exotic meat. These results should, however, be interpreted with caution because of the small sample size and unknown efficacy of the modified A. alata mesocercariae migration technique.

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Acknowledgment

We thank the staff of the Danish Veterinary and Food Administration and Mariann Chriél, Helena Mejer, Caroline S. Olsen, Mia Jensen, and Tina V. Hansen for providing animals for the project. We thank Boi-Tien Thi Pham for conducting molecular analysis.

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Nao Takeuchi-Storm, Mohammed N.S. Al-Sabi, Stig M. Thamsborg, and Heidi L. EnemarkComments to Author 
Author affiliations: Technical University of Denmark, Copenhagen, Denmark (N. Takeuchi-Storm, M.N. Solaiman Al-Sabi, H.L. Enemark); University of Copenhagen (S.M. Thamsborg)

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References

  1. Möhl  K, Große  K, Hamedy  A, Wüste  T, Kabelitz  P, Lücker  E. Biology of Alaria spp. and human exposition risk to Alaria mesocercariae–a review. Parasitol Res. 2009;105:115 . DOIPubMedGoogle Scholar
  2. Al-Sabi  MNS, 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.
  3. Riehn  K, Hamedy  A, Große  K, Zeitler  L, Lücker  E. A novel detection method for Alaria alata mesocercariae in meat. Parasitol Res. 2010;107:21320. DOIPubMedGoogle Scholar
  4. Shoop  WL, Corkum  KC. Maternal transmission by Alaria marcianae and the concept of amphiparatenesis. J Parasitol. 1987;73:1105. DOIPubMedGoogle Scholar
  5. Eckert  J, Deplazes  P, Craig  P, Gemmell  M, Gottstein  B, Heath  D, Echinococcosis in animals: clinical aspects, diagnosis and treatment. WHO/OIE manual on echinococcosis in humans and animals: a public health problem of global concern. 2001:73–99.http://apps.who.int/iris/bitstream/10665/42427/1/929044522X.pdf
  6. Castro  O, Venzal  JM, Felix  ML. Two new records of helminth parasites of domestic cat from Uruguay: Alaria alata (Goeze, 1782) (Digenea, Diplostomidae) and Lagochilascaris major Leiper, 1910 (Nematoda, Ascarididae). Vet Parasitol. 2009;160:3447. DOIPubMedGoogle Scholar
  7. Lucio-Forster  A, Bowman  DD. Prevalence of fecal-borne parasites detected by centrifugal flotation in feline samples from two shelters in upstate New York. J Feline Med Surg. 2011;13:3003. DOIPubMedGoogle Scholar
  8. Ozeretskovskaya  NN, Mikhailova  LG, Sabgaida  TP, Dovgalev  AS. New trends and clinical patterns of human trichinellosis in Russia at the beginning of the XXI century. Vet Parasitol. 2005;132:16771. DOIPubMedGoogle Scholar
  9. Bowles  J, Blair  D, McManus  DP. Genetic variants within the genus Echinococcus identified by mitochondrial DNA sequencing. Mol Biochem Parasitol. 1992;54:16573. DOIPubMedGoogle Scholar
  10. Tamura  K, Stecher  G, Peterson  D, Filipski  A, Kumar  S. MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol. 2013;30:27259. DOIPubMedGoogle Scholar

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Cite This Article

DOI: 10.3201/eid2110.141817

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Heidi L Enemark, Norwegian Veterinary Institute, PO Box 750 Sentrum, NO-0106 Oslo, Norway

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Page created: September 22, 2015
Page updated: September 22, 2015
Page reviewed: September 22, 2015
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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