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JVI Accepts, published online ahead of print on 16 May 2007
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J. Virol. doi:10.1128/JVI.00281-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Virus-subtype specific features of natural SIVsmm infection in sooty mangabeys

Cristian Apetrei*, Rajeev Gautam, Beth Sumpter, Anders C. Carter, Thaidra Gaufin, Silvija I. Staprans, James Else, Mary Barnes, Robert Cao Jr., Seema Garg, Jeffrey M. Milush, Donald L. Sodora, Ivona Pandrea, and Guido Silvestri

Divisions of Microbiology and Comparative Pathology, Tulane National Primate Research Center, Covington, LA 70433; Department of Tropical Medicine of the School of Public Health and Department of Pathology, School of Medicine, Tulane University, New Orleans, LA 70112; Emory Vaccine Center and Yerkes National Research Primate Center, Emory University, Atlanta, GA; University of Texas Southwestern Medical Center, Dallas, TX; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19107

* To whom correspondence should be addressed. Email: capetrei{at}tulane.edu.


   Abstract

SIVsmm naturally infects sooty mangabeys (SMs) and is the source virus of pathogenic infections with HIV-2 and SIVmac of humans and macaques, respectively. In previous studies we characterized SIVsmm diversity in naturally SIV-infected SMs and identified 9 different phylogenetic subtypes whose genetic distances are similar to those reported for the different HIV-1 group M subtypes.

Here we report that, within the colony of SMs housed at the Yerkes National Primate Research Center, at least four SIVsmm subtypes co-circulate, with the vast majority of animals infected with SIVsmm subtype 1, 2, or 3, resulting in the emergence of occasional recombinant forms. While SIVsmm-infected SMs show a typically non-pathogenic course of infection, we have observed that different SIVsmm subtypes are in fact associated with specific immunologic features. Notably, while subtypes 1, 2, and 3 are associated with a very benign course of infection and preservation of normal CD4+ T-cell counts, three out of four SMs infected with subtype 5 show a significant depletion of CD4+ T-cells. The fact that virus replication in SMs infected with subtype 5 is similar to that of SMs infected with other SIVsmm subtypes suggest that the subtype 5-associated CD4+ T-cell depletion is unlikely to simply reflect higher levels of virus-mediated direct killing of CD4+ T-cells. Taken together, this systematic analysis of the subtype-specific features of SIVsmm infection in natural SM hosts identifies subtype-specific differences in the pathogenicity of SIVsmm infection.




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