Abstract

To understand the pathogenicity of acquired immune deficiency syndrome (AIDS), it is important to clarify where, when and how the virus replicates in the body of infected individuals. To identify the major virus replication site at the end stage of SHIV infection, we investigated the systemic tissues of SHIV-infected monkeys that developed AIDS-like disease. We quantified proviral DNA, and compared the mutation patterns of the viruses in various systemic tissues and in peripheral blood through phylogenetic analysis of the full genome sequence. We found that the amounts of proviral DNA detected in internal tissues were higher than those in peripheral blood mononuclear cells. In the sequence and phylogenetic tree analyses, the mutation patterns of the viruses in each tissue were generally different. However, the mutation pattern of the viruses in the jejunum and mesenteric lymph node were most similar to that of plasma viral RNA among the tissues examined in all three monkeys. In two of the three monkeys, which were euthanized earlier, viruses in the jejunum and mesenteric lymph node occupied the root position of the phylogenetic tree. Furthermore, in these tissues, more than 50% of SHIV-expressing cells were identified as macrophages based on co-expression of CD68. These results suggest that macrophages of the small intestine and/or mesenteric lymph node are the major virus production site at the end stage of SHIV infection of macaques.

Highlights

  • To understand the pathogenicity of acquired immune deficiency syndrome (AIDS), it is important to clarify where, when and how HIV replicates in the body of infected individuals

  • To understand the pathogenicity of AIDS, it is important to clarify where, when and how HIV replicates in the body of infected individuals

  • simian immunodeficiency virus (SIV) is closely related to HIV-2, but not HIV-1; in particular, the immune response of SIV env is thought to be different from the immune response of HIV-1 (Overbaugh et al, 1991)

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Summary

Introduction

To understand the pathogenicity of AIDS, it is important to clarify where, when and how HIV replicates in the body of infected individuals. SIV is closely related to HIV-2, but not HIV-1; in particular, the immune response of SIV env is thought to be different from the immune response of HIV-1 (Overbaugh et al, 1991) Another animal model is that comprising simian-human immunodeficiency virus (SHIV) and the macaque. SHIVs are chimeric viruses that contain HIV-1 env, rev, tat, and vpu genes on a background of SIVmac, and some strains of SHIV cause AIDS-like disease (Reimann et al, 1996, 1999; Joag et al, 1997; Harouse et al, 1998) One such virus is SHIV-KS661, which is characterized by the profound depletion of CD4+ T cells and maintenance of high viral loads (Fukazawa et al, 2008). SHIV-infected macaques develop CD4+ T cell depletion within several weeks, and acute AIDS-like disease from several weeks to months (Joag et al, 1996; Reimann et al, 1996)

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