Elsevier

Virology

Volume 260, Issue 1, 20 July 1999, Pages 116-124
Virology

Regular Article
Isolation and Partial Characterization of a Lentivirus from Talapoin Monkeys (Myopithecus talapoin)

https://doi.org/10.1006/viro.1999.9794Get rights and content
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Abstract

We have identified a novel lentivirus prevalent in talapoin monkeys (Myopithecus talapoin), extending previous observations of human immunodeficiency virus-1 cross-reactive antibodies in the serum of these monkeys. We obtained a virus isolate from one of three seropositive monkeys initially available to us. The virus was tentatively named simian immunodeficiency virus from talapoin monkeys (SIVtal). Despite the difficulty of isolating this virus, it was readily passed between monkeys in captivity through unknown routes of transmission. The virus could be propagated for short terms in peripheral blood mononuclear cells of talapoin monkeys but not in human peripheral blood mononuclear cells or human T cell lines. The propagated virus was used to infect a naive talapoin monkey, four rhesus macaques (M. mulatta), and two cynomolgus macaques (M. fascicularis). All animals seroconverted and virus could be reisolated during a short period after experimental infection. A survey of SIVtal-infected captive talapoin monkeys revealed a relative decrease in CD4+ cell numbers in chronically (>2 years) infected animals. No other signs of immunodeficiency were observed in any of the infected animals. PCR amplification followed by DNA sequencing of two fragments of the polymerase gene revealed that SIVtal is different from the presently known lentiviruses and perhaps most related to the SIV from Sykes monkeys.

Cited by (0)

1

Present address: Laboratory of Virology, Erasmus University, Rotterdam, The Netherlands.

2

Present address: Department of Pathobiology, University of Washington, Seattle, WA 98195.

3

Present address: Primate Research Center and School of Veterinary Medicine, Institut Pertanian Bogor, Bogor, Indonesia.

4

To whom reprint requests should be addressed. Fax: (206) 543-3873. E-mail: [email protected].