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The Journal of veterinary medical science2012; 74(6); 813-815; doi: 10.1292/jvms.11-0552

Analysis of antibody responses by commercial western blot assay in horses with alveolar echinococcosis.

Abstract: Commercial western blot (WB) assay was used to detect serum antibodies specific to Echinococcus multilocularis in 23 horses in which infection was confirmed by postmortem inspection at a slaughterhouse. Livers contained from 1 to >20 nodular lesions; foci diameter ranged from 1 to 25 mm. Antibody tests of serum from all 23 animals were negative for antigen bands at 7, 16, 18, and 26-28 kDa, which show specificity in the serum of human patients. However, sera from two infected horses with the largest nodules (diameter, 25 mm) showed positive response to one of the 22-kDa and 30-kDa antigen bands. It may be possible to diagnose E. multilocularis infection in horses based on the detection of these bands on commercial WB assay.
Publication Date: 2012-01-20 PubMed ID: 22261148DOI: 10.1292/jvms.11-0552Google Scholar: Lookup
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  • Comparative Study
  • 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 explores the use of a commercial western blot assay to identify antibody reactions in horses infected with the Echinococcus multilocularis parasite as confirmed through postmortem examination. The researchers found that it may be possible to diagnose this infection by detecting specific antigen bands using this assay.

Background

  • The research focuses on Echinococcus multilocularis, a tiny tapeworm that can cause a parasitic infection called alveolar echinococcosis in animals and humans.
  • The aim of the study was to identify if the commercial western blot (WB) assay, a commonly used lab technique to detect specific proteins in a sample, could be used as a diagnostic tool in identifying these infections in horses.
  • By observing antibody responses specific to E. multilocularis in horses, the researchers hoped to enhance diagnostic capabilities and tackle this parasitic infection more effectively.

Methodology

  • The researchers collected samples from 23 horses which were confirmed to be infected with E. multilocularis through a postmortem inspection carried out in a slaughterhouse.
  • The infection in the horses had manifested as numerous nodular lesions in their livers, with diameters ranging from 1 to 25 mm.
  • These samples were then subjected to the WB assay to detect serum antibodies specific to E. multilocularis.

Findings

  • The antibody tests of serum conducted on all 23 animals turned out negative for antigen bands at 7, 16, 18, and 26-28 kDa. These bands typically indicate specificity in the serum of human patients with this infection.
  • However, the researchers observed a positive response to the 22-kDa and 30-kDa antigen bands in the sera of two horses that had the largest nodules (diameter, 25 mm).
  • This suggests that the detection of these bands on the WB assay could potentially be used to diagnose E. multilocularis infection in horses.

Conclusion

  • This study provides implications for the detection and diagnosis of E. multilocularis infection in horses using commercially available WB assays.
  • While additional research is needed, these preliminary findings suggest that looking for specific antigen bands can aid in diagnosing this parasitic infection.
  • This could lead to improved care and health outcomes for infected horses and aid in the prevention of potential zoonotic transmission of E. multilocularis.

Cite This Article

APA
Ueno M, Kuroda N, Yahagi K, Ohtaki T, Kawanaka M. (2012). Analysis of antibody responses by commercial western blot assay in horses with alveolar echinococcosis. J Vet Med Sci, 74(6), 813-815. https://doi.org/10.1292/jvms.11-0552

Publication

ISSN: 1347-7439
NlmUniqueID: 9105360
Country: Japan
Language: English
Volume: 74
Issue: 6
Pages: 813-815

Researcher Affiliations

Ueno, Masahiro
  • Yamagata Prefectural Nairiku Meat Inspection Center, Yamagata 990-0892, Japan.
Kuroda, Nobuhiko
    Yahagi, Kazue
      Ohtaki, Toshihiko
        Kawanaka, Masanori

          MeSH Terms

          • Animals
          • Antibodies, Helminth / blood
          • Blotting, Western / methods
          • Blotting, Western / veterinary
          • Echinococcosis
          • Echinococcosis, Hepatic / diagnosis
          • Echinococcosis, Hepatic / immunology
          • Echinococcosis, Hepatic / veterinary
          • Echinococcus multilocularis / immunology
          • Female
          • Horse Diseases / diagnosis
          • Horse Diseases / immunology
          • Horse Diseases / parasitology
          • Horses
          • Humans
          • Liver / parasitology
          • Liver / pathology
          • Male
          • Polymerase Chain Reaction / veterinary
          • Polymorphism, Restriction Fragment Length / genetics

          Citations

          This article has been cited 3 times.
          1. Hifumi T, Tanaka T, Suzu I, Sato M, Akioka K, Fujimata C, Shinkai R, Maeda T, Kusakisako K, Ikadai H, Miyoshi N. Molecular phylogenetic analysis of Echinococcus multilocularis from horses raised in Canada or Japan, using mitochondrial cytochrome b gene-targeted PCR. Food Waterborne Parasitol 2024 Mar;34:e00219.
            doi: 10.1016/j.fawpar.2024.e00219pubmed: 38298421google scholar: lookup
          2. Delling C, Helm C, Heinze P, Friedman M, Böttcher D. First report of infection with metacestode stages of Echinococcus multilocularis in a kulan (Equus hemionus kulan) from Slovakia. Int J Parasitol Parasites Wildl 2023 Dec;22:80-83.
            doi: 10.1016/j.ijppaw.2023.09.003pubmed: 37736617google scholar: lookup
          3. Hifumi T, Tanaka T, Sato M, Akioka K, Fujimata C, Miyoshi N. Rapid detection of alveolar echinococcosis in hepatic nodules of horses by recombinase polymerase amplification assay. Vet Anim Sci 2023 Jun;20:100291.
            doi: 10.1016/j.vas.2023.100291pubmed: 36936549google scholar: lookup