HIV-1 DNA sequence diversity and evolution during acute subtype C infection

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作者
Guinevere Q. Lee
Kavidha Reddy
Kevin B. Einkauf
Kamini Gounder
Joshua M. Chevalier
Krista L. Dong
Bruce D. Walker
Xu G. Yu
Thumbi Ndung’u
Mathias Lichterfeld
机构
[1] Ragon Institute of MGH,HIV Pathogenesis Programme, Nelson R. Mandela School of Medicine
[2] MIT and Harvard,undefined
[3] Brigham and Women’s Hospital,undefined
[4] Harvard Medical School,undefined
[5] University of KwaZulu-Natal,undefined
[6] Africa Health Research Institute,undefined
[7] Broad Institute of MIT and Harvard,undefined
[8] Howard Hughes Medical Institute,undefined
[9] Max Planck Institute for Infection Biology,undefined
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Little is known about the genotypic make-up of HIV-1 DNA genomes during the earliest stages of HIV-1 infection. Here, we use near-full-length, single genome next-generation sequencing to longitudinally genotype and quantify subtype C HIV-1 DNA in four women identified during acute HIV-1 infection in Durban, South Africa, through twice-weekly screening of high-risk participants. In contrast to chronically HIV-1-infected patients, we found that at the earliest phases of infection in these four participants, the majority of viral DNA genomes are intact, lack APOBEC-3G/F-associated hypermutations, have limited genome truncations, and over one year show little indication of cytotoxic T cell-driven immune selections. Viral sequence divergence during acute infection is predominantly fueled by single-base substitutions and is limited by treatment initiation during the earliest stages of disease. Our observations provide rare longitudinal insights of HIV-1 DNA sequence profiles during the first year of infection to inform future HIV cure research.
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