TY - JOUR
T1 - Previously transmitted HIV-1 strains are preferentially selected during subsequent sexual transmissions
AU - Redd, Andrew
AU - Collinson-Streng, Aleisha N.
AU - Chatziandreou, Nikolaos
AU - Mullis, Caroline E.
AU - Laeyendecker, Oliver B.
AU - Martens, Craig
AU - Ricklefs, Stacy
AU - Kiwanuka, Noah
AU - Nyein, Phyu Hninn
AU - Lutalo, Tom
AU - Grabowski, Mary K.
AU - Kong, Xiangrong
AU - Manucci, Jordyn
AU - Sewankambo, Nelson
AU - Wawer, Maria
AU - Gray, Ronald H
AU - Porcella, Stephen F.
AU - Fauci, Anthony S.
AU - Sagar, Manish
AU - Serwadda, David
AU - Quinn, Thomas C
N1 - Funding Information:
Financial support. This work was supported in part by funding from the Division of Intramural Research, National Institutes of Allergy and Infectious Diseases (NIAID), National Institutes of Health; the NIAID (grants R01 A134826, R01 A134265 and R01 AI077473 to M. S.); the Eunice Kennedy Shriver National Institute of Child Health & Human Development (grant 5P30HD06826); the World Bank STI Project, Uganda; the Henry M. Jackson Foundation; the Fogarty Foundation (grant 5D43TW00010); and the Bill and Melinda Gates Institute for Population and Reproductive Health at the Bloomberg School of Public Health, Johns Hopkins University. Potential conflicts of interest. All authors: No reported conflicts.
PY - 2012/11/1
Y1 - 2012/11/1
N2 - 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.
AB - 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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U2 - 10.1093/infdis/jis503
DO - 10.1093/infdis/jis503
M3 - Article
C2 - 22997233
AN - SCOPUS:84867562000
SN - 0022-1899
VL - 206
SP - 1433
EP - 1442
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 9
ER -