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Veterinary parasitology1985; 18(2); 139-153; doi: 10.1016/0304-4017(85)90063-9

Pathogenesis of helminths in equines.

Abstract: This review summarizes information on the clinical signs, gross and microscopic lesions associated with nematode and cestode infections and discusses the development of these conditions in the equine host.
Publication Date: 1985-08-01 PubMed ID: 2930935DOI: 10.1016/0304-4017(85)90063-9Google Scholar: Lookup
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  • Journal Article
  • Review

Summary

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The research is a detailed analysis of the effects and development of nematode and cestode infections, commonly known as helminths, in equines, mainly focusing on the clinical signs and related microscopic and gross lesions.

Overview of the Research

  • The research provides an in-depth review of the pathogenesis of helminths, specifically nematodes and cestodes, in horses, ponies, donkeys, and other equine species.
  • Being parasitic worms, nematodes and cestodes pose significant health concerns for equines. The research discusses the manifestations of these infections, including the clinical signs observed and the lesions that occur as a result of the pathogens.

Clinical Signs and Lesions

  • Discussion on clinical signs involves how infection of helminths presents itself in equines. These include symptoms such as weight loss, colic, anemia, and other related physical changes that indicate an infestation.
  • Gross lesions refer to observable tissue changes that occur as a result of the infection. The study also covers microscopic lesions, which are cellular alterations that are not visible to the naked eye but are detected under a microscope.

Development of Conditions

  • Beyond the symptoms and effects of the infections, the study also delves into the development of these conditions within the host. It explores how the equine’s body reacts to the presence of these parasites, what factors enable these parasites to thrive, and the progression of the disease within the host’s body.

Implications of the Review

  • This comprehensive review contributes significantly to the understanding of helminthic infections in equines. It provides a basis for the identification of infection signs and an understanding of the pathophysiology of the disease. Thus, it can guide equine health practitioners in devising effective diagnosis, treatment, and prevention strategies.

Cite This Article

APA
Slocombe JO. (1985). Pathogenesis of helminths in equines. Vet Parasitol, 18(2), 139-153. https://doi.org/10.1016/0304-4017(85)90063-9

Publication

ISSN: 0304-4017
NlmUniqueID: 7602745
Country: Netherlands
Language: English
Volume: 18
Issue: 2
Pages: 139-153

Researcher Affiliations

Slocombe, J O

    MeSH Terms

    • Animals
    • Ascaridoidea
    • Cestode Infections / etiology
    • Cestode Infections / veterinary
    • Colic / etiology
    • Colic / veterinary
    • Helminthiasis, Animal / etiology
    • Horse Diseases / etiology
    • Horses
    • Nematode Infections / etiology
    • Nematode Infections / veterinary
    • Onchocerciasis / etiology
    • Onchocerciasis / veterinary
    • Species Specificity
    • Spirurida Infections / etiology
    • Strongyle Infections, Equine / etiology
    • Strongyle Infections, Equine / pathology
    • Strongyle Infections, Equine / physiopathology
    • Strongyloidea / pathogenicity
    • Strongyloidiasis / etiology
    • Strongyloidiasis / veterinary

    Citations

    This article has been cited 7 times.
    1. Stummer M, Frisch V, Glitz F, Hinney B, Spergser J, Krücken J, Diekmann I, Dimmel K, Riedel C, Cavalleri JV, Rümenapf T, Joachim A, Lyrakis M, Auer A. Presence of Equine and Bovine Coronaviruses, Endoparasites, and Bacteria in Fecal Samples of Horses with Colic.. Pathogens 2023 Aug 15;12(8).
      doi: 10.3390/pathogens12081043pubmed: 37624003google scholar: lookup
    2. Özben M, von Samson-Himmelstjerna G, Freiin von Streit MKB, Wilkes EJA, Hughes KJ, Krücken J. Absence of Polymorphisms in Codons 167, 198 and 200 of All Seven β-Tubulin Isotypes of Benzimidazole Susceptible and Resistant Parascaris spp. Specimens from Australia.. Pathogens 2022 Apr 20;11(5).
      doi: 10.3390/pathogens11050490pubmed: 35631011google scholar: lookup
    3. Živković S, Pavlović I, Mijatović B, Trailović I, Trailović D. Prevalence, Intensity and Risks Involved in Helminth Infections in Domestic Mountain Pony and Balkan Donkey in Nature Park Stara Planina, Serbia.. Iran J Parasitol 2021 Apr-Jun;16(2):318-326.
      doi: 10.18502/ijpa.v16i2.6283pubmed: 34557248google scholar: lookup
    4. Ghorbanzadeh B, Naem S, Farshid AA. Microscopic Study of Mechanoreceptors and Chemoreceptors of Anterior and Posterior Ends of Toxocara Canis Using Scanning Electron Microscopy and Light Microscope.. Arch Razi Inst 2021 Jul;76(2):311-322.
      doi: 10.22092/ari.2020.342252.1457pubmed: 34223730google scholar: lookup
    5. Lindroth KM, Dicksved J, Pelve E, Båverud V, Müller CE. Faecal bacterial composition in horses with and without free faecal liquid: a case control study.. Sci Rep 2021 Feb 26;11(1):4745.
      doi: 10.1038/s41598-021-83897-4pubmed: 33637818google scholar: lookup
    6. Jenkins E, Backwell AL, Bellaw J, Colpitts J, Liboiron A, McRuer D, Medill S, Parker S, Shury T, Smith M, Tschritter C, Wagner B, Poissant J, McLoughlin P. Not playing by the rules: Unusual patterns in the epidemiology of parasites in a natural population of feral horses (Equus caballus) on Sable Island, Canada.. Int J Parasitol Parasites Wildl 2020 Apr;11:183-190.
      doi: 10.1016/j.ijppaw.2020.02.002pubmed: 32095427google scholar: lookup
    7. Hubert JD, Seahorn TL, Klei TR, Hosgood G, Horohov DW, Moore RM. Clinical signs and hematologic, cytokine, and plasma nitric oxide alterations in response to Strongylus vulgaris infection in helminth-naïve ponies.. Can J Vet Res 2004 Jul;68(3):193-200.
      pubmed: 15352544