Cell tropism of simian immunodeficiency virus in culture is not predictive of in vivo tropism or pathogenesis

Juan T. Borda, Xavier Alvarez, Ivanela Kondova, Pyone Aye, Meredith A. Simon, Ronald Charles Desrosiers, Andrew A. Lackner

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

SIVmac239/316 is a molecular clone derived from SIVmac239 that differs from the parental virus by nine amino acids in env. This virus, unlike the parental SIVmac239, is able to replicate well in alveolar macrophages in culture. We have not however, observed macrophage-associated inflammatory disease in any animal infected with SIVmac239/316. Therefore, we sought to examine the cell tropism of this virus in vivo in multiple tissues using in situ hybridization combined with immunohistochemistry and multilabel confocal microscopy for viral nucleic acid and multiple cell-type-specific markers for macrophages and T lymphocytes. Tissues examined included brain, heart, lung, lymph nodes, spleen, thymus, and small and large intestine. Matched tissues from macaques infected with the parental SIVmac239 and uninfected macaques were also examined. Many infected cells were detected in the tissues of animals infected with SIVmac239 and SIVmac239/316 although there appeared to be fewer positive cells in animals infected with SIVmac239/316. Surprisingly, in light of the cell culture observations, nearly every simian immunodeficiency virus-infected cell in animals inoculated with SIVmac239/316 was a T lymphocyte rather than a macrophage. This was true both during early infection (first 2 months) and in terminal disease. In contrast, as previously described, SIVmac239 was found in both T cells and macrophages in tissues as early as 21 days after infection. These studies indicate that during both acute and chronic SIVmac239/316 infection T lymphocytes rather than macrophages are the principal targets in vivo. These data combined with the absence of macrophage-associated lesions in SIVmac239/316-infected animals indicate that in vitro cell tropism is not predictive of in vivo tropism or disease pathogenesis.

Original languageEnglish (US)
Pages (from-to)2111-2122
Number of pages12
JournalAmerican Journal of Pathology
Volume165
Issue number6
StatePublished - Dec 2004
Externally publishedYes

Fingerprint

Simian Immunodeficiency Virus
Tropism
Macrophages
T-Lymphocytes
Macaca
Viruses
Infection
Large Intestine
Alveolar Macrophages
Confocal Microscopy
Thymus Gland
Nucleic Acids
Small Intestine
In Situ Hybridization
Spleen
Clone Cells
Cell Culture Techniques
Lymph Nodes
Immunohistochemistry
Amino Acids

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Borda, J. T., Alvarez, X., Kondova, I., Aye, P., Simon, M. A., Desrosiers, R. C., & Lackner, A. A. (2004). Cell tropism of simian immunodeficiency virus in culture is not predictive of in vivo tropism or pathogenesis. American Journal of Pathology, 165(6), 2111-2122.

Cell tropism of simian immunodeficiency virus in culture is not predictive of in vivo tropism or pathogenesis. / Borda, Juan T.; Alvarez, Xavier; Kondova, Ivanela; Aye, Pyone; Simon, Meredith A.; Desrosiers, Ronald Charles; Lackner, Andrew A.

In: American Journal of Pathology, Vol. 165, No. 6, 12.2004, p. 2111-2122.

Research output: Contribution to journalArticle

Borda, JT, Alvarez, X, Kondova, I, Aye, P, Simon, MA, Desrosiers, RC & Lackner, AA 2004, 'Cell tropism of simian immunodeficiency virus in culture is not predictive of in vivo tropism or pathogenesis', American Journal of Pathology, vol. 165, no. 6, pp. 2111-2122.
Borda, Juan T. ; Alvarez, Xavier ; Kondova, Ivanela ; Aye, Pyone ; Simon, Meredith A. ; Desrosiers, Ronald Charles ; Lackner, Andrew A. / Cell tropism of simian immunodeficiency virus in culture is not predictive of in vivo tropism or pathogenesis. In: American Journal of Pathology. 2004 ; Vol. 165, No. 6. pp. 2111-2122.
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