Demonstration of equine infectious anemia virus in primary leukocyte cultures by electron microscopy.
Abstract: Electron microscopy was used to demonstrate the presence of viral particles in primary cultures of leukocytes taken from a horse after SC inoculation with the Wyoming strain of equine infectious anemia virus. Unlike previous studies, the exposure virus was not passaged through cell culture prior to horse inoculation. Cultures were begun approximately 1 week before and 1 week after the 1st pyrexic period after inoculation. In both samples, viral particles and cytoplasmic alterations were observed resembling those previously reported in equine infectious anemia virus and other retravirus-infected cells.
Publication Date: 1977-12-01 PubMed ID: 202180
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- Journal Article
- Research Support
- U.S. Gov't
- Non-P.H.S.
Summary
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The study examines the presence of equine infectious anemia virus in the leukocytes of a horse, using electron microscopy.
Objective of the Research
- The main aim of the research was to investigate traces of equine infectious anemia virus in primary leukocyte cultures of a horse. Electron microscopy was the principal method utilized to detect the presence of the viral particles.
Methodology and Approach
- The researchers used the Wyoming strain of equine infectious anemia virus for the inoculation process. This particular strain was directly injected subcutaneously (SC) into the horse without being passaged through cell culture first, as is typically done in similar studies.
- The scientists set up cultures approximately one week before and one week after the horse’s first feverish period following the inoculation. These timeframes were strategically chosen to give the virus adequate time to manifest and to observe and capture any significant variations at two critical stages of the infection.
Observations and Findings
- Both the pre-fever and post-fever cultures exhibited signs of equine infectious anemia virus when analyzed under the electron microscope. Visible evidence of viral particles, as well as changes in the cellular structures, akin to those previously reported with equine infectious anemia virus and other retrovirus-infected cells, were noted.
- The research, therefore, successfully demonstrates the presence of equine infectious anemia virus in leukocytes using electron microscopy. Furthermore, it suggests that this methodology could be a reliable way to detect viral particles directly in the primary leukocytes of a horse without the need for intermediary cell culture passages.
Cite This Article
APA
McConnel MB, Katada M, McConnell S, Moore R.
(1977).
Demonstration of equine infectious anemia virus in primary leukocyte cultures by electron microscopy.
Am J Vet Res, 38(12), 2067-2069.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cells, Cultured
- Equine Infectious Anemia / microbiology
- Female
- Horses
- Infectious Anemia Virus, Equine / ultrastructure
- Leukocytes / microbiology
- Leukocytes / ultrastructure
Citations
This article has been cited 6 times.- Sellon DC, Fuller FJ, McGuire TC. The immunopathogenesis of equine infectious anemia virus.. Virus Res 1994 May;32(2):111-38.
- Montelaro RC, Lohrey N, Parekh B, Blakeney EW, Issel CJ. Isolation and comparative biochemical properties of the major internal polypeptides of equine infectious anemia virus.. J Virol 1982 Jun;42(3):1029-38.
- 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.
- Rice NR, Henderson LE, Sowder RC, Copeland TD, Oroszlan S, Edwards JF. Synthesis and processing of the transmembrane envelope protein of equine infectious anemia virus.. J Virol 1990 Aug;64(8):3770-8.
- 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.
- Kim CH, Casey JW. Genomic variation and segregation of equine infectious anemia virus during acute infection.. J Virol 1992 Jun;66(6):3879-82.
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