Patterns of HIV-1 evolution in individuals with differing rates of CD4 T cell decline

被引:94
作者
Markham, RB [1 ]
Wang, WC
Weisstein, AE
Wang, Z
Munoz, A
Templeton, A
Margolick, J
Vlahov, D
Quinn, T
Farzadegan, H
Yu, XF
机构
[1] Johns Hopkins Sch Hyg & Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Johns Hopkins Sch Hyg & Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[3] Washington Univ, Dept Biol, St Louis, MO 63130 USA
[4] NIAID, NIH, Bethesda, MD 20892 USA
[5] Johns Hopkins Sch Med, Dept Med, Baltimore, MD 21205 USA
关键词
D O I
10.1073/pnas.95.21.12568
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Evolution of HIV-1 env sequences was studied in 15 seroconverting injection drug users selected for differences in the extent of CD4 T cell decline. The rates of increase of either sequence diversity at a given visit or divergence from the first seropositive visit were both higher in progressors than in nonprogressors. Viral evolution in individuals with rapid or moderate disease progression showed selection favoring nonsynonymous mutations, while nonprogressors with low viral loads selected against the nonsynonymous mutations that might have resulted in viruses with higher levels of replication. For 10 of the 15 subjects no single variant predominated over time. Evolution away from a dominant variant was followed frequently at a later time point by return to dominance of strains closely related to that variant. The observed evolutionary pattern is consistent with either selection against only the predominant virus or independent evolution occurring in different environments within the host. Differences in the level to which CD4 T cells fall in a given time period reflect not only quantitative differences in accumulation of mutations, but differences in the types of mutations that pro,ide the best adaptation to the host environment.
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页码:12568 / 12573
页数:6
相关论文
共 51 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]   Multiple extracellular elements of CCR5 and HIV-1 entry: Dissociation from response to chemokines [J].
Atchison, RE ;
Gosling, J ;
Monteclaro, FS ;
Franci, C ;
Digilio, L ;
Charo, IF ;
Goldsmith, MA .
SCIENCE, 1996, 274 (5294) :1924-1926
[3]   ELEPHANT SEALS - GENETIC-VARIATION AND NEAR EXTINCTION [J].
BONNELL, ML ;
SELANDER, RK .
SCIENCE, 1974, 184 (4139) :908-909
[4]   QUIESCENT LYMPHOCYTES-T AS AN INDUCIBLE VIRUS RESERVOIR IN HIV-1 INFECTION [J].
BUKRINSKY, MI ;
STANWICK, TL ;
DEMPSEY, MP ;
STEVENSON, M .
SCIENCE, 1991, 254 (5030) :423-427
[5]   THE REGION OF THE ENVELOPE GENE OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RESPONSIBLE FOR DETERMINATION OF CELL TROPISM [J].
CANN, AJ ;
CHURCHER, MJ ;
BOYD, M ;
OBRIEN, W ;
ZHAO, JQ ;
ZACK, J ;
CHEN, ISY .
JOURNAL OF VIROLOGY, 1992, 66 (01) :305-309
[6]   The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates [J].
Choe, H ;
Farzan, M ;
Sun, Y ;
Sullivan, N ;
Rollins, B ;
Ponath, PD ;
Wu, LJ ;
Mackay, CR ;
LaRosa, G ;
Newman, W ;
Gerard, N ;
Gerard, C ;
Sodroski, J .
CELL, 1996, 85 (07) :1135-1148
[7]   Quantification of latent tissue reservoirs and total body viral load in HIV-1 Infection [J].
Chun, TW ;
Carruth, L ;
Finzi, D ;
Shen, XF ;
DiGiuseppe, JA ;
Taylor, H ;
Hermankova, M ;
Chadwick, K ;
Margolick, J ;
Quinn, TC ;
Kuo, YH ;
Brookmeyer, R ;
Zeiger, MA ;
BarditchCrovo, P ;
Siliciano, RF .
NATURE, 1997, 387 (6629) :183-188
[8]  
DEAN AM, 1989, GENETICS, V123, P441
[9]   Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene [J].
Dean, M ;
Carrington, M ;
Winkler, C ;
Huttley, GA ;
Smith, MW ;
Allikmets, R ;
Goedert, JJ ;
Buchbinder, SP ;
Vittinghoff, E ;
Gomperts, E ;
Donfield, S ;
Vlahov, D ;
Kaslow, R ;
Saah, A ;
Rinaldo, C ;
Detels, R ;
OBrien, SJ .
SCIENCE, 1996, 273 (5283) :1856-1862
[10]   Slower evolution of human immunodeficiency virus type I quasispecies during progression to AIDS [J].
Delwart, EL ;
Pan, H ;
Sheppard, HW ;
Wolpert, D ;
Neumann, AU ;
Korber, B ;
Mullins, JI .
JOURNAL OF VIROLOGY, 1997, 71 (10) :7498-7508