Detection of equine infectious anemia virus in horse leukocyte cultures derived from horses in various stages of equine infectious anemia viral infection.
Abstract: The enzyme-linked immunosorbent assay (ELISA) antigen-positive and agar-gel immunodiffusion test (AGID)-negative horses do not have infective equine infectious anemia (EIA) virus. The ELISA testing of horse leukocyte culture (HLC) supernatants did detect EIA virus in a HLC that was infected with the Wyoming strain of EIA virus and in HLC derived from horses in febrile, acute, or subacute stages of EIA infection. In supernatants of HLC derived from chronic and inapparent carrier horses, EIA virus was not detected with ELISA. Direct fluorescent antibody tests detected EIA virus in HLC infected with 10(6)TCID50 of the Wyoming strain of EIA virus and in 50% of the HLC from febrile acute or subacute horses. The direct fluorescent antibody testing of HLC derived from chronic and inapparent carrier horses did not detect cell-associated EIA virus. The pony inoculation test proved to be the most reliable and accurate method for detecting infective EIA virus in horses in various stages of EIA infection and accurately correlated with the AGID test.
Publication Date: 1984-01-01 PubMed ID: 6322623
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
- Antibodies
- Clinical Study
- Diagnosis
- Diagnostic Technique
- Disease
- Disease Diagnosis
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Epidemiology
- Equine Health
- Equine Infectious Anemia
- Horses
- Immunology
- In Vitro Research
- Infection
- Infectious Disease
- Laboratory Methods
- Leukocytes
- Veterinary Medicine
- Veterinary Research
- Virology
- Virus
Summary
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This research investigates the detection of equine infectious anemia (EIA) virus in horse leukocyte cultures obtained from horses at different stages of the EIA infection, and finds that the pony inoculation test is most reliable for detecting this virus.
Overview
Using different testing methodologies, the study analyzed the presence of the EIA virus in Horse leukocyte cultures (HLC), which are cell cultures derived from horses. These horses were at different stages of the EIA infection, including febrile (feverish), acute, subacute, chronic, and inapparent carrier stages.
Use of Different Methods for Virus Detection
- The research applied ELISA (enzyme-linked immunosorbent assay), a common lab test used for detecting antigens (substances that evoke immune responses), to detect the virus in HLC supernatants (liquid component of a culture). It found that those horses with ELISA-positive and AGID (agar-gel immunodiffusion test)-negative results did not carry the infective EIA virus.
- EIA virus was detected in a HLC infected with the Wyoming strain of EIA virus, and in HLC from horses in the febrile, acute, or subacute stages. However, the virus was not found in HLC from chronic and inapparent (symptomless) carrier horses.
Fluorescent Antibody Tests for Virus Detection
- Fluorescent antibody tests were used to detect the virus in HLC infected with other doses of the virus and in half of the HLC from febrile acute or subacute horses.
- However, using this method, the virus was not detected in HLC derived from chronic and inapparent carrier horses.
The Best Method for Detecting EIA Virus
- The pony inoculation test, where a test pony is injected with potentially contaminated material and then monitored for disease, was found to be the most reliable and accurate method for detecting the infective EIA virus. This test’s results accurately correlated with the AGID test, often used as a reference for EIA detection.
Cite This Article
APA
Evans KS, Carpenter SL, Sevoian M.
(1984).
Detection of equine infectious anemia virus in horse leukocyte cultures derived from horses in various stages of equine infectious anemia viral infection.
Am J Vet Res, 45(1), 20-25.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antigens, Viral / analysis
- Carrier State / microbiology
- Carrier State / veterinary
- Cells, Cultured
- Enzyme-Linked Immunosorbent Assay
- Equine Infectious Anemia / microbiology
- Fluorescent Antibody Technique
- Horses
- Immunodiffusion / veterinary
- Infectious Anemia Virus, Equine / immunology
- Infectious Anemia Virus, Equine / isolation & purification
- Leukocytes / microbiology
- Lymphocyte Culture Test, Mixed
Citations
This article has been cited 7 times.- Oaks JL, McGuire TC, Ulibarri C, Crawford TB. Equine infectious anemia virus is found in tissue macrophages during subclinical infection.. J Virol 1998 Sep;72(9):7263-9.
- Sellon DC, Fuller FJ, McGuire TC. The immunopathogenesis of equine infectious anemia virus.. Virus Res 1994 May;32(2):111-38.
- Rice NR, Lequarre AS, Casey JW, Lahn S, Stephens RM, Edwards J. Viral DNA in horses infected with equine infectious anemia virus.. J Virol 1989 Dec;63(12):5194-200.
- Carpenter S, Chesebro B. Change in host cell tropism associated with in vitro replication of equine infectious anemia virus.. J Virol 1989 Jun;63(6):2492-6.
- Carpenter S, Evans LH, Sevoian M, Chesebro B. Role of the host immune response in selection of equine infectious anemia virus variants.. J Virol 1987 Dec;61(12):3783-9.
- Alexandersen S, Carpenter S. Characterization of variable regions in the envelope and S3 open reading frame of equine infectious anemia virus.. J Virol 1991 Aug;65(8):4255-62.
- Sellon DC, Perry ST, Coggins L, Fuller FJ. Wild-type equine infectious anemia virus replicates in vivo predominantly in tissue macrophages, not in peripheral blood monocytes.. J Virol 1992 Oct;66(10):5906-13.
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