Analyze Diet
Journal of medical entomology2000; 37(4); 619-625; doi: 10.1603/0022-2585-37.4.619

Infection of aquatic insects with trematode metacercariae carrying Ehrlichia risticii, the cause of Potomac horse fever.

Abstract: We provide evidence of Ehrlichia risticii Holland, the agent of Potomac horse fever, in trematode stages found in aquatic insects collected from a pasture stream in northern California, using nested polymerase chain reaction (PCR) amplification and sequence analyses of the 16S rRNA, 51 kDa major antigen and groEL heat shock protein genes. E. risticii was detected in metacercariae found in the immatures and adults of the following insects: caddisflies (Trichoptera), mayflies (Ephemeroptera), damselflies (Odonata, Zygoptera), dragonflies (Odonata, Anisoptera), and stoneflies (Plecoptera). The prevalence of E. risticii was 31.9% (n = 454 individuals) in aquatic insects (13 of 17 species were positive). Prevalence within orders was as follows: 43.5% (n = 207) in caddisflies, 15.2% (n = 92) in mayflies, 13.9% (n = 115) in damselflies, 10.0% (n = 10) in dragonflies, and 80.0% (n = 30) in stoneflies. This study demonstrates a broad intermediate host range for trematodes that act as vector for E. risticii. Insects are likely to play an important role in the epidemiology of this disease.
Publication Date: 2000-08-01 PubMed ID: 10916305DOI: 10.1603/0022-2585-37.4.619Google 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.

The research article provides an in-depth investigation into aquatic insects carrying E. risticii, the bacterium causing Potomac horse fever, through infection by trematode stages. The study was conducted in a pasture stream in northern California, and the presence of the bacterium was validated through different gene analyses.

Methodology for detection of E. risticii

  • The research utilized nested polymerase chain reaction (PCR), an amplification process used to make multiple copies of a specific DNA segment, to detect the presence of E. risticii in the trematode stages of the aquatic insects.
  • For further validation, sequence analyses of the 16S rRNA, 51 kDa major antigen, and groEL heat shock protein genes were conducted. These genes were chosen due to their distinctive structures in E. risticii bacterium, thus assisting in its accurate identification.

Detection of E. risticii in various aquatic insects

  • The bacterium was detected in metacercariae, a developmental stage of certain parasites including trematodes, found in both the immature and adult stages of various aquatic insects.
  • The aquatic insects that were found to be carriers included caddisflies, mayflies, damselflies, dragonflies, and stoneflies – making these an intermediate host range for the said trematodes acting as vectors for E. risticii.

Prevalence of E. risticii in aquatic insects

  • The overall prevalence of E. risticii in the examined aquatic insects was 31.9% (with 454 individuals tested), and 13 out of the 17 species were found to be positive.
  • Among different insect orders, the prevalence of E. risticii varied, with caddisflies at 43.5% (in 207 individuals), mayflies at 15.2% (92 individuals), damselflies at 13.9% (115 individuals), dragonflies at 10.0% (10 individuals), and stoneflies at the highest, 80.0% (30 individuals).
  • These numbers demonstrate the ability of E. risticii to survive and possibly propagate in a broad range of insect hosts, indicating their potential role in the lifecycle and spread of this bacterium.

Implications on Disease Epidemiology

  • The study suggests that the aquatic insect hosts might play a significant role in the epidemiology of Potomac horse fever.
  • This information is crucial for formulating disease control strategies, like vector management, thus minimizing the instances of Potomac horse fever, which can be devastating to equine populations.

Cite This Article

APA
Chae JS, Pusterla N, Johnson E, Derock E, Lawler SP, Madigan JE. (2000). Infection of aquatic insects with trematode metacercariae carrying Ehrlichia risticii, the cause of Potomac horse fever. J Med Entomol, 37(4), 619-625. https://doi.org/10.1603/0022-2585-37.4.619

Publication

ISSN: 0022-2585
NlmUniqueID: 0375400
Country: England
Language: English
Volume: 37
Issue: 4
Pages: 619-625

Researcher Affiliations

Chae, J S
  • College of Veterinary Medicine, Chonbuk National University, Chonju, Korea.
Pusterla, N
    Johnson, E
      Derock, E
        Lawler, S P
          Madigan, J E

            MeSH Terms

            • Animals
            • Antigens, Bacterial
            • Antigens, Surface / genetics
            • Base Sequence
            • Cells, Cultured
            • Chaperonin 60 / genetics
            • DNA, Bacterial
            • Ehrlichia / genetics
            • Ehrlichia / isolation & purification
            • Ehrlichiosis / microbiology
            • Ehrlichiosis / veterinary
            • Horse Diseases / microbiology
            • Horses
            • Insecta / microbiology
            • Mice
            • Molecular Sequence Data
            • RNA, Ribosomal, 16S / analysis

            Citations

            This article has been cited 9 times.
            1. Budachetri K, Lin M, Yan Q, Chien RC, Hostnik LD, Haanen G, Leclère M, Waybright W, Baird JD, Arroyo LG, Rikihisa Y. Real-Time PCR Differential Detection of Neorickettsia findlayensis and N. risticii in Cases of Potomac Horse Fever.. J Clin Microbiol 2022 Jul 20;60(7):e0025022.
              doi: 10.1128/jcm.00250-22pubmed: 35695520google scholar: lookup
            2. Abbasi M, Doosti S, Vatandoost H, Hosseini-Vasoukolaei N. Study on the Fauna of Aquatic Insects in Northwestern Iran.. J Arthropod Borne Dis 2020 Mar;14(1):1-7.
              doi: 10.18502/jad.v14i1.2698pubmed: 32766343google scholar: lookup
            3. Shaeghi M, Dehghan H, Pakdad K, Nikpour F, Absavaran A, Sofizadeh A, Akhavan AA, Vatandoost H, Aghai-Afshar A. Faunistic Study of the Aquatic Arthropods in a Tourism Area in Northern Iran.. J Arthropod Borne Dis 2017 Jun;11(2):286-301.
              pubmed: 29062853
            4. 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
            5. Shayeghi M, Vatandoost H, Gorouhi A, Sanei-Dehkordi AR, Salim-Abadi Y, Karami M, Jalil-Navaz MR, Akhavan AA, Shiekh Z, Vatandoost S, Arandian MH. Biodiversity of Aquatic Insects of Zayandeh Roud River and Its Branches, Isfahan Province, Iran.. J Arthropod Borne Dis 2014 Dec;8(2):197-203.
              pubmed: 26114133
            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. Baird JD, Arroyo LG. Historical aspects of Potomac horse fever in Ontario (1924-2010).. Can Vet J 2013 Jun;54(6):565-72.
              pubmed: 24155447
            8. 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
            9. Mott J, Muramatsu Y, Seaton E, Martin C, Reed S, Rikihisa Y. Molecular analysis of Neorickettsia risticii in adult aquatic insects in Pennsylvania, in horses infected by ingestion of insects, and isolated in cell culture.. J Clin Microbiol 2002 Feb;40(2):690-3.
              doi: 10.1128/JCM.40.2.690-693.2002pubmed: 11825999google scholar: lookup