Authors
Jesus F Salazar-Gonzalez, Maria G Salazar, Brandon F Keele, Gerald H Learn, Elena E Giorgi, Hui Li, Julie M Decker, Shuyi Wang, Joshua Baalwa, Matthias H Kraus, Nicholas F Parrish, Katharina S Shaw, M Brad Guffey, Katharine J Bar, Katie L Davis, Christina Ochsenbauer-Jambor, John C Kappes, Michael S Saag, Myron S Cohen, Joseph Mulenga, Cynthia A Derdeyn, Susan Allen, Eric Hunter, Martin Markowitz, Peter Hraber, Alan S Perelson, Tanmoy Bhattacharya, Barton F Haynes, Bette T Korber, Beatrice H Hahn, George M Shaw
Publication date
2009/6/8
Journal
Journal of Experimental Medicine
Volume
206
Issue
6
Pages
1273-1289
Publisher
The Rockefeller University Press
Description
Identification of full-length transmitted HIV-1 genomes could be instrumental in HIV-1 pathogenesis, microbicide, and vaccine research by enabling the direct analysis of those viruses actually responsible for productive clinical infection. We show in 12 acutely infected subjects (9 clade B and 3 clade C) that complete HIV-1 genomes of transmitted/founder viruses can be inferred by single genome amplification and sequencing of plasma virion RNA. This allowed for the molecular cloning and biological analysis of transmitted/founder viruses and a comprehensive genome-wide assessment of the genetic imprint left on the evolving virus quasispecies by a composite of host selection pressures. Transmitted viruses encoded intact canonical genes (gag-pol-vif-vpr-tat-rev-vpu-env-nef) and replicated efficiently in primary human CD4+ T lymphocytes but much less so in monocyte-derived macrophages. Transmitted viruses …
Total citations
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