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Infection of bone marrow macrophages by equine infectious anemia virus.

Abstract: To characterize infection of bone marrow-derived macrophages (BMDM) with equine infectious anemia virus (EIAV) by determining virus production, effects on viability, and induction of cytokines. Methods: BMDM obtained from bone marrow of 6 clinically normal adult horses. Methods: BMDM were infected with EIAV at a multiplicity of infection of 8. Cell viability, percentage of cells with detectable viral protein, reverse transcriptase activity, and concentrations of infective virus (focus-forming units/ml), interleukin 6, and tumor necrosis factor-alpha were measured in culture supernatant samples obtained at various days after infection. Results: Cell viability was decreased on day 4 and was maximally decreased on day 8. The number of cells with detectable viral protein and supernatant reverse transcriptase activity increased significantly on day 4 and increased until day 6. Virus concentration (focus-forming units per milliliter) peaked on day 4 after infection and was constant thereafter. Infection with EIAV caused significant induction of interleukin 6 production by BMDM. The maximal difference was seen on day 4 after infection. Control and infected BMDM produced only negligible amounts of tumor necrosis factor-alpha. Conclusions: BMDM are useful, as a cell population, to study the effects of infection with EIAV, including cell death and induction of interleukin 6 but not tumor necrosis factor-alpha production.
Publication Date: 1997-12-24 PubMed ID: 9401688
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the infection of bone marrow-derived macrophages (BMDM) by the equine infectious anemia virus (EIAV), its impact on cell viability, and the induction of cytokines.

Method of Research

  • BMDM were collected from the bone marrow of six healthy adult horses for this study.
  • The BMDM cells were then infected with the EIAV at a multiplicity of infection of 8.
  • Various metrics were then studied from culture supernatant samples taken at different times after infection. These statistics included:
    • Cell viability,
    • Percentage of cells with detectable viral protein,
    • Reverse transcriptase activity, and
    • Concentrations of infective virus (measured in focus-forming units per milliliter), interleukin 6, and tumor necrosis factor-alpha.

Results of Research

  • Cell viability declined noticeably on the 4th day and was at its last on the 8th day.
  • There was a significant increase in the number of cells revealing viral protein and amplified reverse transcriptase activity from the 4th day until the 6th day.
  • The virus concentration peaked on the 4th day after infection and remained steady after this period.
  • Infection with EIAV induced a significant rise in the production of interleukin 6 by BMDM, with the most noticeable difference observed on the 4th day.
  • Tumor necrosis factor-alpha production remained negligible in both control and infected BMDM.

Conclusions of Research

  • The BMDM cellular group is effective for studying the impact of EIAV infection, such as cell death and the induction of interleukin 6, while the work does not produce significant amounts of tumor necrosis factor-alpha.
  • The research gives profound insights on how to contain and understand the infection rates of EIAV. It also provides valuable information about the behavior of the disease in regards to cell life and the production of interleukin 6.

Cite This Article

APA
Swardson CJ, Lichtenstein DL, Wang S, Montelaro RC, Kociba GJ. (1997). Infection of bone marrow macrophages by equine infectious anemia virus. Am J Vet Res, 58(12), 1402-1407.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 58
Issue: 12
Pages: 1402-1407

Researcher Affiliations

Swardson, C J
  • Department of Veterinary Biosciences, College of Veterinary Medicine, Ohio State University, Columbus 43210, USA.
Lichtenstein, D L
    Wang, S
      Montelaro, R C
        Kociba, G J

          MeSH Terms

          • Analysis of Variance
          • Animals
          • Bone Marrow / pathology
          • Bone Marrow / virology
          • Cell Survival
          • Cells, Cultured
          • Cytopathogenic Effect, Viral
          • Equine Infectious Anemia / immunology
          • Equine Infectious Anemia / pathology
          • Horses
          • Infectious Anemia Virus, Equine / physiology
          • Interleukin-6 / biosynthesis
          • Macrophages / metabolism
          • Macrophages / pathology
          • Macrophages / virology
          • Microscopy, Electron / methods
          • Microscopy, Electron / veterinary
          • RNA-Directed DNA Polymerase / metabolism
          • Tumor Necrosis Factor-alpha / biosynthesis
          • Viral Proteins / metabolism
          • Virion / isolation & purification

          Citations

          This article has been cited 1 times.
          1. Harrold SM, Cook SJ, Cook RF, Rushlow KE, Issel CJ, Montelaro RC. Tissue sites of persistent infection and active replication of equine infectious anemia virus during acute disease and asymptomatic infection in experimentally infected equids.. J Virol 2000 Apr;74(7):3112-21.