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Digenetic trematodes, Acanthatrium sp. and Lecithodendrium sp., as vectors of Neorickettsia risticii, the agent of Potomac horse fever

Published online by Cambridge University Press:  12 April 2024

N. Pusterla*
Affiliation:
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, One Shields Avenue, Davis, California 95616, USA
E.M. Johnson
Affiliation:
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, One Shields Avenue, Davis, California 95616, USA
J.S. Chae
Affiliation:
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, One Shields Avenue, Davis, California 95616, USA
J.E. Madigan
Affiliation:
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, One Shields Avenue, Davis, California 95616, USA
*
*Fax: (530) 752 9815 E-mail: npusterla@ucdavis.edu

Abstract

Neorickettsia (formerly Ehrlichia) risticii, the agent of Potomac horse fever (PHF), has been recently detected in trematode stages found in the secretions of freshwater snails and in aquatic insects. Insectivores, such as bats and birds, may serve as the definitive host of the trematode vector. To determine the definitive helminth vector, five bats (Myotis yumanensis) and three swallows (Hirundo rustica, Tachycineta bicolor) were collected from a PHF endemic location in northern California. Bats and swallows were dissected and their major organs examined for trematodes and for N. risticii DNA using a nested polymerase chain reaction (PCR) assay. Adult digenetic trematodes, Acanthatrium sp. and/or Lecithodendrium sp., were recovered from the gastrointestinal tract of all bats and from one swallow. The intestine of three bats, the spleen of two bats and one swallow as well as the liver of one swallow tested PCR positive for N. risticii. From a total of seven pools of identical digenetic trematodes collected from single hosts, two pools of Acanthatrium sp. and one pool of Lecithodendrium sp. tested PCR positive. The results of this investigation provide preliminary evidence that at least two trematodes in the family Lecithodendriidae are vectors of N. risticii. The data also suggest that bats and swallows not only act as a host for trematodes but also as a possible natural reservoir for N. risticii.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2003

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References

Azim, A.M. (1936) On the life-history of Lecithodendrium pyramidum Looss, 1896, and its development from a xiphidocercaria, C. pyramidum sp. nov., from Melania tuberculata . Annals of Tropical Medicine and Parasitology 30, 351356.CrossRefGoogle Scholar
Barlough, J.E., Rikihisa, Y. & Madigan, J.E. (1997) Nested polymerase chain reaction for detection of Ehrlichia risticii genomic DNA in infected horses. Veterinary Parasitology 68, 367373.CrossRefGoogle ScholarPubMed
Barlough, J.E., Reubel, G.H., Madigan, J.E., Vredevoe, L.K., Miller, P.E. & Rikihisa, Y. (1998) Detection of Ehrlichia risticii, the agent of Potomac horse fever, in freshwater stream snails (Pleuroceridae: Juga spp.) from northern California. Applied and Environmental Microbiology 64, 28882893.CrossRefGoogle ScholarPubMed
Burns, W.C. (1961) Penetration and development of Allassogonoporus vespertilionis and Acanthatrium oregonense (Trematoda: Lecithodendriidae) cercariae in caddis fly larvae. Journal of Parasitology 47, 927932.CrossRefGoogle ScholarPubMed
Chae, J.S., Pusterla, N., Johnson, E., Derock, E., Lawler, S.P. & Madigan, J.E. (2000) Infection of aquatic insects with trematode metacercariae carrying Ehrlichia risticii, the cause of Potomac horse fever. Journal of Medical Entomology 37, 619625.CrossRefGoogle ScholarPubMed
Chae, J., Kim, M. & Madigan, J. (2002) Detection of Neorickettsia (Ehrlichia) risticii in tissues of mice experimentally infected with cercariae of trematodes by in situ hybridization. Veterinary Microbiology 88, 233243.CrossRefGoogle ScholarPubMed
Hahn, N.E., Fletcher, M., Rice, R.M., Kocan, K.M., Hansen, J.W., Hair, J.A., Barker, R.W. & Perry, B.D. (1990) Attempted transmission of Ehrlichia risticii, causative agent of Potomac horse fever by the ticks, Dermacentor variabilis, Rhipicephalus sanguineus, Ixodes scapularis, and Amblyomma americanum . Experimental and Applied Acarology 8, 4150.CrossRefGoogle ScholarPubMed
Kanter, M., Mott, J., Ohashi, N., Fried, B., Reed, S., Lin, Y.C. & Rikihisa, Y. (2000) Analysis of 16S rRNA and 51-kilodalton antigen gene and transmission in mice of Ehrlichia risticii in virgulate trematodes from Elimia livescens snails in Ohio. Journal of Clinical Microbiology 38, 33493358.CrossRefGoogle ScholarPubMed
Knight, R.A. & Pratt, I. (1955) The life histories of Allassogonoporus vespertilionis Macy and Acanthatrium oregonense Macy (Trematoda: Lecithodendriidae). Journal of Parasitology 41, 248255.CrossRefGoogle ScholarPubMed
Kumar, V. (1999) Lecithodendriid infections. pp. 343344 . in Kumar, V. (Ed.) Trematode infections and diseases of man and animals. Boston, Kluwer Academic Publishers.CrossRefGoogle Scholar
Levine, J.F., Levy, M.G., Nicholson, W.L. & Gager, R.B. (1990) Attempted Ehrlichia risticii transmission with Dermacentor variabilis (Acari: Ixodidae). Journal of Medical Entomology 27, 931933.CrossRefGoogle ScholarPubMed
Madigan, J.E. & Pusterla, N. (2000) Ehrlichial diseases. Veterinary Clinics of North America Equine Practice 16, 487499.CrossRefGoogle ScholarPubMed
Madigan, J.E., Pusterla, N., Johnson, E., Chae, J.-S., Berger Pusterla, J., DeRock, E. & Lawler, S.P. (2000) Transmission of Ehrlichia risticii, the agent of Potomac horse fever, using naturally infected aquatic insects and helminth vectors: preliminary report. Equine Veterinary Journal 32, 275279.CrossRefGoogle ScholarPubMed
Pretzman, C., Ralph, D., Stothard, D.R., Fuerst, P.A. & Rikihisa, Y. (1995) 16S rRNA gene sequence of Neorickettsia helminthoeca and its phylogenetic alignment with members of the genus Ehrlichia . International Journal of Systematic Bacteriology 45, 207211.CrossRefGoogle ScholarPubMed
Pusterla, N., Madigan, J.E., Chae, J.-S., DeRock, E., Johnson, E. & Berger Pusterla, J. (2000) Helminthic transmission and isolation of Ehrlichia risticii, the causative agent of Potomac horse fever, by using trematode stages from freshwater stream snails. Journal of Clinical Microbiology 38, 12931297.CrossRefGoogle ScholarPubMed
Reubel, G.H., Barlough, J.E. & Madigan, J.E. (1998) Production and characterization of Ehrlichia risticii, the agent of Potomac horse fever, from snails (Pleuroceridae: Juga spp.) in aquarium culture and genetic comparison to equine strains. Journal of Clinical Microbiology 36, 15011511.CrossRefGoogle ScholarPubMed
Rikihisa, Y. (1991a) Cross-reacting antigens between Neorickettsia helminthoeca and Ehrlichia species, shown by immunofluoresence and Western immunoblotting. Journal of Clinical Microbiology 29, 20242029.CrossRefGoogle Scholar
Rikihisa, Y. (1991b) The tribe Ehrlichieae and ehrlichial diseases. Clinical Microbiology Reviews 4, 286308.CrossRefGoogle ScholarPubMed
Schell, S.C. (1970) Family Lecithodendriidae. pp. 274284 in Schell, S.C. (Ed.) How to know the trematodes. Dubuque, Brown Company Publishers.Google Scholar
Schmidtmann, E.T., Robl, M.G. & Carroll, J.F. (1986) Attempted transmission of Ehrlichia risticii by field-captured Dermacentor variabilis (Acari: Ixodidae). American Journal of Veterinary Research 47, 23932395.Google ScholarPubMed