Analyze Diet
Journal of helminthology2003; 77(4); 335-339; doi: 10.1079/joh2003181

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

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.
Publication Date: 2003-11-25 PubMed ID: 14627451DOI: 10.1079/joh2003181Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article focuses on the role of digenetic trematodes, Acanthatrium sp. and Lecithodendrium sp., as potential vectors of Neorickettsia risticii, the agent causing Potomac horse fever. The study shows that bats and swallows may act as hosts for these trematodes and can be a potential natural storage site for N. risticii.

Research Methodology

  • The team pursued their investigation by collecting five bats (Myotis yumanensis) and three swallows (Hirundo rustica, Tachycineta bicolor) from a Potomac horse fever-endemic location in northern California.
  • The collected specimens were then dissected, and major organs were examined for presence of the trematodes and for Neorickettsia risticii DNA.
  • To detect the presence of N. risticii DNA, a ‘nested polymerase chain reaction’ (PCR) assay technique was employed. PCR is a common molecular biology method used to make multiple copies of a specific DNA segment, which allows the DNA to be visualized more easily.

Results and Findings

  • On scrutiny, the adult digenetic trematodes, Acanthatrium sp., and/or Lecithodendrium sp., were found within the gastrointestinal tract of all the examined bats and one swallow.
  • Three bats’ intestines, two bats’ spleens, one swallow’s liver, and spleen tested positive for N. risticii DNA.
  • Out of seven pools of identical digenetic trematodes derived from single hosts, two pools of Acanthatrium sp. and one pool of Lecithodendrium sp. also tested positive for N. risticii via PCR.

Implications of the Study

  • This research provides initial evidence that at least two trematodes from the Lecithodendriidae family could serve as vectors for N. risticii, the pathogen causing Potomac horse fever.
  • The findings also suggest that bats and swallows might not only act as definitive hosts for these trematodes but also as potential natural reservoirs for the N. risticii bacterium.

Cite This Article

APA
Pusterla N, Johnson EM, Chae JS, Madigan JE. (2003). Digenetic trematodes, Acanthatrium sp. and Lecithodendrium sp., as vectors of Neorickettsia risticii, the agent of Potomac horse fever. J Helminthol, 77(4), 335-339. https://doi.org/10.1079/joh2003181

Publication

ISSN: 0022-149X
NlmUniqueID: 2985115R
Country: England
Language: English
Volume: 77
Issue: 4
Pages: 335-339

Researcher Affiliations

Pusterla, N
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, One Shields Avenue, Davis, California 95616, USA. npusterla@ucdavis.edu
Johnson, E M
    Chae, J S
      Madigan, J E

        MeSH Terms

        • Anaplasmataceae Infections / parasitology
        • Anaplasmataceae Infections / transmission
        • Anaplasmataceae Infections / veterinary
        • Animals
        • Bird Diseases / parasitology
        • Chiroptera / parasitology
        • DNA, Helminth / analysis
        • Disease Vectors
        • Horse Diseases / parasitology
        • Horse Diseases / transmission
        • Horses
        • Intestines / parasitology
        • Neorickettsia risticii / isolation & purification
        • Songbirds / parasitology
        • Trematoda / isolation & purification
        • Trematoda / parasitology

        Citations

        This article has been cited 8 times.
        1. Alcantara DMC, Ikeda P, Souza CS, de Mello VVC, Torres JM, Lourenço EC, Bassini-Silva R, Herrera HM, Machado RZ, Barros-Battesti DM, Graciolli G, André MR. Multilayer Networks Assisting to Untangle Direct and Indirect Pathogen Transmission in Bats.. Microb Ecol 2023 Aug;86(2):1292-1306.
          doi: 10.1007/s00248-022-02108-3pubmed: 36166070google scholar: lookup
        2. Shaw SD, Stämpfli H. Diagnosis and Treatment of Undifferentiated and Infectious Acute Diarrhea in the Adult Horse.. Vet Clin North Am Equine Pract 2018 Apr;34(1):39-53.
          doi: 10.1016/j.cveq.2017.11.002pubmed: 29426709google scholar: lookup
        3. Xiong Q, Bekebrede H, Sharma P, Arroyo LG, Baird JD, Rikihisa Y. An Ecotype of Neorickettsia risticii Causing Potomac Horse Fever in Canada.. Appl Environ Microbiol 2016 Oct 1;82(19):6030-6.
          doi: 10.1128/AEM.01366-16pubmed: 27474720google scholar: lookup
        4. Greiman SE, Tkach M, Vaughan JA, Tkach VV. Laboratory maintenance of the bacterial endosymbiont, Neorickettsia sp., through the life cycle of a digenean, Plagiorchis elegans.. Exp Parasitol 2015 Oct;157:78-83.
          doi: 10.1016/j.exppara.2015.06.015pubmed: 26160679google scholar: lookup
        5. Greiman SE, Tkach VV, Pulis E, Fayton TJ, Curran SS. Large scale screening of digeneans for Neorickettsia endosymbionts using real-time PCR reveals new Neorickettsia genotypes, host associations and geographic records.. PLoS One 2014;9(6):e98453.
          doi: 10.1371/journal.pone.0098453pubmed: 24911315google scholar: lookup
        6. Greiman SE, Tkach VV, Vaughan JA. Transmission rates of the bacterial endosymbiont, Neorickettsia risticii, during the asexual reproduction phase of its digenean host, Plagiorchis elegans, within naturally infected lymnaeid snails.. Parasit Vectors 2013 Oct 22;6:303.
          doi: 10.1186/1756-3305-6-303pubmed: 24383453google scholar: lookup
        7. Gibson KE, Pastenkos G, Moesta S, Rikihisa Y. Neorickettsia risticii surface-exposed proteins: proteomics identification, recognition by naturally-infected horses, and strain variations.. Vet Res 2011 Jun 2;42(1):71.
          doi: 10.1186/1297-9716-42-71pubmed: 21635728google scholar: lookup
        8. Fried B, Graczyk TK, Tamang L. Food-borne intestinal trematodiases in humans.. Parasitol Res 2004 Jun;93(2):159-70.
          doi: 10.1007/s00436-004-1112-xpubmed: 15103556google scholar: lookup