High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men

نویسندگان

  • Hui Li
  • Katharine J. Bar
  • Shuyi Wang
  • Julie M. Decker
  • Yalu Chen
  • Chuanxi Sun
  • Jesus F. Salazar-Gonzalez
  • Maria G. Salazar
  • Gerald H. Learn
  • Charity J. Morgan
  • Joseph E. Schumacher
  • Peter Hraber
  • Elena E. Giorgi
  • Tanmoy Bhattacharya
  • Bette T. Korber
  • Alan S. Perelson
  • Joseph J. Eron
  • Myron S. Cohen
  • Charles B. Hicks
  • Barton F. Haynes
  • Martin Markowitz
  • Brandon F. Keele
  • Beatrice H. Hahn
  • George M. Shaw
چکیده

Elucidating virus-host interactions responsible for HIV-1 transmission is important for advancing HIV-1 prevention strategies. To this end, single genome amplification (SGA) and sequencing of HIV-1 within the context of a model of random virus evolution has made possible for the first time an unambiguous identification of transmitted/founder viruses and a precise estimation of their numbers. Here, we applied this approach to HIV-1 env analyses in a cohort of acutely infected men who have sex with men (MSM) and found that a high proportion (10 of 28; 36%) had been productively infected by more than one virus. In subjects with multivariant transmission, the minimum number of transmitted viruses ranged from 2 to 10 with viral recombination leading to rapid and extensive genetic shuffling among virus lineages. A combined analysis of these results, together with recently published findings based on identical SGA methods in largely heterosexual (HSX) cohorts, revealed a significantly higher frequency of multivariant transmission in MSM than in HSX [19 of 50 subjects (38%) versus 34 of 175 subjects (19%); Fisher's exact p = 0.008]. To further evaluate the SGA strategy for identifying transmitted/founder viruses, we analyzed 239 overlapping 5' and 3' half genome or env-only sequences from plasma viral RNA (vRNA) and blood mononuclear cell DNA in an MSM subject who had a particularly well-documented virus exposure history 3-6 days before symptom onset and 14-17 days before peak plasma viremia (47,600,000 vRNA molecules/ml). All 239 sequences coalesced to a single transmitted/founder virus genome in a time frame consistent with the clinical history, and a molecular clone of this genome encoded replication competent virus in accord with model predictions. Higher multiplicity of HIV-1 infection in MSM compared with HSX is consistent with the demonstrably higher epidemiological risk of virus acquisition in MSM and could indicate a greater challenge for HIV-1 vaccines than previously recognized.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2010