4.8 Article

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

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-019-10659-2

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资金

  1. NIH [AI114235, AI117841, AI120008, AI130005, AI122377, AI124776, AI135940, DA047034, HL134539, AI116228]
  2. Bill and Melinda Gates Foundation [OPP1066973, OPP1146433]
  3. Gilead Sciences, Inc. [00406]
  4. International AIDS Vaccine Initiative (IAVI) [UKZNRSA1001]
  5. NIAID [R37AI067073]
  6. Witten Family Foundation
  7. Dan and Marjorie Sullivan Foundation
  8. Mark and Lisa Schwartz Foundation
  9. AIDS Healthcare Foundation
  10. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NIAID) [P30 AI060354]
  11. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NCI) [P30 AI060354]
  12. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NICHD) [P30 AI060354]
  13. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NHLBI) [P30 AI060354]
  14. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NIDA) [P30 AI060354]
  15. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NIMH) [P30 AI060354]
  16. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: NIA) [P30 AI060354]
  17. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: FIC) [P30 AI060354]
  18. Harvard University Center for AIDS Research (CFAR - US National Institutes of Health: OAR) [P30 AI060354]
  19. Sub-Saharan African Network for TB/HIV Research Excellence (SANTHE), a DELTAS Africa Initiative [DEL-15-006]
  20. New Partnership for Africa's Development Planning and Coordinating Agency (NEPAD Agency)
  21. Wellcome Trust [107752/Z/15/Z]
  22. United Kingdom (UK) government
  23. Bill and Melinda Gates Foundation [OPP1146433, OPP1066973] Funding Source: Bill and Melinda Gates Foundation

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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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