4.7 Article

Previously Transmitted HIV-1 Strains Are Preferentially Selected During Subsequent Sexual Transmissions

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 206, 期 9, 页码 1433-1442

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OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jis503

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资金

  1. Division of Intramural Research, National Institutes of Allergy and Infectious Diseases (NIAID), National Institutes of Health
  2. NIAID [R01 A134826, R01 A134265, R01 AI077473]
  3. Eunice Kennedy Shriver National Institute of Child Health & Human Development [5P30HD06826]
  4. World Bank STI Project, Uganda
  5. Henry M. Jackson Foundation
  6. Fogarty Foundation [5D43TW00010]
  7. Bill and Melinda Gates Institute for Population and Reproductive Health at the Bloomberg School of Public Health, Johns Hopkins University

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Background. A genetic bottleneck is known to exist for human immunodeficiency virus (HIV) at the point of sexual transmission. However, the nature of this bottleneck and its effect on viral diversity over time is unclear. Methods. Interhost and intrahost HIV diversity was analyzed in a stable population in Rakai, Uganda, from 1994 to 2002. HIV-1 envelope sequences from both individuals in initially HIV-discordant relationships in which transmission occurred later were examined using Sanger sequencing of bulk polymerase chain reaction (PCR) products (for 22 couples), clonal analysis (for 3), and next-generation deep sequencing (for 9). Results. Intrahost viral diversity was significantly higher than changes in interhost diversity (P < .01). The majority of HIV-1-discordant couples examined via bulk PCR (16 of 22 couples), clonal analysis (3 of 3), and next-generation deep sequencing (6 of 9) demonstrated that the viral populations present in the newly infected recipient were more closely related to the donor partner's HIV-1 variants found earlier during infection as compared to those circulating near the estimated time of transmission (P = .03). Conclusions. These findings suggest that sexual transmission constrains viral diversity at the population level, partially because of the preferential transmission of ancestral as opposed to contemporary strains circulating in the transmitting partner. Future successful vaccine strategies may need to target these transmitted ancestral strains.

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