Detection of humoral antigen and antibody by enzyme-linked immunosorbent assay in horses with experimentally induced Ehrlichia equi infection.
Abstract: An enzyme-linked immunosorbent assay (ELISA) was used to detect antigen in plasma and antibody in serum of 3 horses inoculated with Ehrlichia equi. Clinical signs, including rectal temperature, were correlated with the antigen and antibody detection. ELISA was very efficient in detection of serum antibody. Antigen detection using monoclonal antibodies to E. equi and ELISA should be considered as a diagnostic method.
Publication Date: 1993-01-01 PubMed ID: 8466978DOI: 10.1177/104063879300500109Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Antibodies
- Antigen
- Clinical Pathology
- Clinical Signs
- Diagnosis
- Diagnostic Technique
- Disease
- Disease Diagnosis
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Equine Health
- Experimental Methods
- Horses
- Immunology
- Infection
- Infectious Disease
- Monoclonal Antibodies
- Plasma
- Serum
- Theileria equi
- Veterinary Medicine
- Veterinary Research
Summary
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The study attempted to detect the presence of a specific infection, Ehrlichia equi, in horses by using an enzyme-linked immunosorbent assay (ELISA). Clinical observations were correlated with the assay results, and the scientists found ELISA to be an effective method for diagnosing E. equi in horses.
Objective of the Study
- The research aimed to test the ELISA’s efficiency in detecting the Ehrlichia equi bacteria in horses, an infection that can cause fever, loss of appetite, edema, and anemia.
Methods
- Three horses were intentionally inoculated with Ehrlichia equi.
- The enzyme-linked immunosorbent assay (ELISA) was employed to detect the presence of the antigen (the Ehrlichia equi bacteria) in the horse’s plasma, and the antibodies produced by the horse’s immune system to fight the infection in the serum.
- Clinical observations such as rectal temperature were associated with the presence of the antigen and the antibody to confirm the direct correlation between the presence of the infection and the symptoms.
Findings
- Evidence showed that ELISA was very efficient in identifying the antibodies in the serum, demonstrating the horse’s effort to fight the infection.
- The study suggests that antigen identification using monoclonal antibodies specific to Ehrlichia equi, together with the ELISA, could be a promising diagnostic method.
Implication of the Research
- The research plays a significant role in veterinary medicine as it identifies a potentially effective method for diagnosing Ehrlichia equi in horses.
- Since clinical signs were shown to correlate with antigen and antibody detection, this could refine the understanding of the disease’s progression and, subsequently, improve its management.
- The study could pave the way for further research in this area to confirm ELISA’s efficacy in detecting similar infections in different types of animals.
Cite This Article
APA
Corstvet RE, Gaunt SD, Karns PA, McBride JW, Battistini RA, Mauterer LA, Austin FW.
(1993).
Detection of humoral antigen and antibody by enzyme-linked immunosorbent assay in horses with experimentally induced Ehrlichia equi infection.
J Vet Diagn Invest, 5(1), 37-39.
https://doi.org/10.1177/104063879300500109 Publication
Researcher Affiliations
- Department of Veterinary Science, LSU Agricultural Center, Baton Rouge.
MeSH Terms
- Animals
- Antibodies, Monoclonal
- Antibodies, Viral / blood
- Antigens, Viral / blood
- Ehrlichia / immunology
- Ehrlichiosis / blood
- Ehrlichiosis / diagnosis
- Ehrlichiosis / veterinary
- Enzyme-Linked Immunosorbent Assay / methods
- Horse Diseases / blood
- Horse Diseases / diagnosis
- Horse Diseases / immunology
- Horses
- Immunoglobulin G / blood
- Immunoglobulin M / blood
Citations
This article has been cited 1 times.- Nicholson WL, Comer JA, Sumner JW, Gingrich-Baker C, Coughlin RT, Magnarelli LA, Olson JG, Childs JE. An indirect immunofluorescence assay using a cell culture-derived antigen for detection of antibodies to the agent of human granulocytic ehrlichiosis. J Clin Microbiol 1997 Jun;35(6):1510-6.
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