Literature DB >> 19458001

Is the gut the major source of virus in early simian immunodeficiency virus infection?

Matthew D H Lay1, Janka Petravic, Shari N Gordon, Jessica Engram, Guido Silvestri, Miles P Davenport.   

Abstract

The acute phases of human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infection are characterized by rapid and profound depletion of CD4+ T cells from the guts of infected individuals. The large number of CD4+ T cells in the gut (a large fraction of which are activated and express the HIV/SIV coreceptor CCR5), the high level of infection of these cells, and the temporal coincidence of this CD4+ T-cell depletion with the peak of virus in plasma in acute infection suggest that the intestinal mucosa may be the major source of virus driving the peak viral load. Here, we used data on CD4+ T-cell proportions in the lamina propria of the rectums of SIV-infected rhesus macaques (which progress to AIDS) and sooty mangabeys (which do not progress) to show that in both species, the depletion of CD4+ T cells from this mucosal site and its maximum loss rate are often observed several days before the peak in viral load, with few CD4+ T cells remaining in the rectum by the time of peak viral load. In contrast, the maximum loss rate of CD4+ T cells from bronchoalveolar lavage specimens and lymph nodes coincides with the peak in virus. Analysis of the kinetics of depletion suggests that, in both rhesus macaques and sooty mangabeys, CD4+ T cells in the intestinal mucosa are a highly susceptible population for infection but not a major source of plasma virus in acute SIV infection.

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Year:  2009        PMID: 19458001      PMCID: PMC2708631          DOI: 10.1128/JVI.00552-09

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  24 in total

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Authors:  Qingsheng Li; Lijie Duan; Jacob D Estes; Zhong-Min Ma; Tracy Rourke; Yichuan Wang; Cavan Reilly; John Carlis; Christopher J Miller; Ashley T Haase
Journal:  Nature       Date:  2005-04-28       Impact factor: 49.962

Review 3.  Perils at mucosal front lines for HIV and SIV and their hosts.

Authors:  Ashley T Haase
Journal:  Nat Rev Immunol       Date:  2005-10       Impact factor: 53.106

4.  Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection.

Authors:  Joseph J Mattapallil; Daniel C Douek; Brenna Hill; Yoshiaki Nishimura; Malcolm Martin; Mario Roederer
Journal:  Nature       Date:  2005-04-28       Impact factor: 49.962

5.  Gastrointestinal tract as a major site of CD4+ T cell depletion and viral replication in SIV infection.

Authors:  R S Veazey; M DeMaria; L V Chalifoux; D E Shvetz; D R Pauley; H L Knight; M Rosenzweig; R P Johnson; R C Desrosiers; A A Lackner
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6.  Influence of peak viral load on the extent of CD4+ T-cell depletion in simian HIV infection.

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7.  Rapid turnover of plasma virions and CD4 lymphocytes in HIV-1 infection.

Authors:  D D Ho; A U Neumann; A S Perelson; W Chen; J M Leonard; M Markowitz
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8.  Estimating the infectivity of CCR5-tropic simian immunodeficiency virus SIV(mac251) in the gut.

Authors:  David P Wilson; Joseph J Mattapallil; Matthew D H Lay; Lei Zhang; Mario Roederer; Miles P Davenport
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9.  Microbial translocation is a cause of systemic immune activation in chronic HIV infection.

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2.  TCR triggering transcriptionally downregulates CCR5 expression on rhesus macaque CD4(+) T-cells with no measurable effect on susceptibility to SIV infection.

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3.  Early Antiretroviral Therapy Prevents Viral Infection of Monocytes and Inflammation in Simian Immunodeficiency Virus-Infected Rhesus Macaques.

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4.  Blocking of α4β7 gut-homing integrin during acute infection leads to decreased plasma and gastrointestinal tissue viral loads in simian immunodeficiency virus-infected rhesus macaques.

Authors:  Aftab A Ansari; Keith A Reimann; Ann E Mayne; Yoshiaki Takahashi; Susan T Stephenson; Rijian Wang; Xinyue Wang; Jichu Li; Andrew A Price; Dawn M Little; Mohammad Zaidi; Robert Lyles; Francois Villinger
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5.  Integrin alpha4beta7 is downregulated on the surfaces of simian immunodeficiency virus SIVmac239-infected cells.

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7.  Vaccination-induced noncytolytic effects in the acute phase of SHIV infection.

Authors:  Janka Petravic; Miles P Davenport
Journal:  PLoS One       Date:  2010-11-30       Impact factor: 3.240

8.  Similar impact of CD8+ T cell responses on early virus dynamics during SIV infections of rhesus macaques and sooty mangabeys.

Authors:  Roger D Kouyos; Shari N Gordon; Silvija I Staprans; Guido Silvestri; Roland R Regoes
Journal:  PLoS Comput Biol       Date:  2010-08-26       Impact factor: 4.475

9.  Viral CTL escape mutants are generated in lymph nodes and subsequently become fixed in plasma and rectal mucosa during acute SIV infection of macaques.

Authors:  Thomas H Vanderford; Chelsea Bleckwehl; Jessica C Engram; Richard M Dunham; Nichole R Klatt; Mark B Feinberg; David A Garber; Michael R Betts; Guido Silvestri
Journal:  PLoS Pathog       Date:  2011-05-19       Impact factor: 6.823

10.  Repressive effect of primary virus replication on superinfection correlated with gut-derived central memory CD4(+) T cells in SHIV-infected Chinese rhesus macaques.

Authors:  Jing Xue; Zhe Cong; Jing Xiong; Wei Wang; Hong Jiang; Ting Chen; Fangxin Wu; Kejian Liu; Aihua Su; Bin Ju; Zhiwei Chen; Marcelo A Couto; Qiang Wei; Chuan Qin
Journal:  PLoS One       Date:  2013-09-02       Impact factor: 3.240

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