4.6 Article

Human immunodeficiency virus type 1 and influenza virus exit via different membrane Microdomains

Journal

JOURNAL OF VIROLOGY
Volume 81, Issue 22, Pages 12630-12640

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.01255-07

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Funding

  1. NCRR NIH HHS [P20 RR021905] Funding Source: Medline
  2. NIAID NIH HHS [R03 AI060679, T32 AI055402, R56 AI047727, R01 AI47727, R01 AI047727] Funding Source: Medline

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Directed release of human immunodeficiency virus type 1 (HIV-1) into the cleft of the virological synapse that can form between infected and uninfected T cells, for example, in lymph nodes, is thought to contribute to the systemic spread of this virus. In contrast, influenza virus, which causes local infections, is shed into the airways of the respiratory tract from free surfaces of epithelial cells. We now demonstrate that such differential release of HIV-1 and influenza virus is paralleled, at the subcellular level, by viral assembly at different microsegments of the plasma membrane of HeLa cells. HIV-1, but not influenza virus, buds through microdomains containing the tetraspanins CD9 and CD63. Consequently, the anti-CD9 antibody K41, which redistributes its antigen and also other tetraspanins to cell-cell adhesion sites, interferes with HIV-1 but not with influenza virus release. Altogether, these data strongly suggest that the bimodal egress of these two pathogenic viruses, like their entry into target cells, is guided by specific sets of host cell proteins.

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