Virus population homogenization following acute human immunodeficiency virus type 1 infection

被引:77
作者
Learn, GH
Muthui, D
Brodie, SJ
Zhu, TF
Diem, K
Mullins, JI [1 ]
Corey, L
机构
[1] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[3] Univ Washington, Dept Med, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Program Infect Dis, Seattle, WA 98109 USA
关键词
D O I
10.1128/JVI.76.23.11953-11959.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Understanding the properties of human immunodeficiency virus type 1 (HIV-1) variants capable of establishing infection is critical to the development of a vaccine against AIDS. Previous studies of men have shown that the HIV-1 env gene is homogeneous early in infection, leading to the suggestion that infection is established by a single transmitted variant. However, we report here that all of eight homosexual men evaluated beginning 3.7 to 9 weeks following onset of symptoms of acute infection harbored diverse virus populations in their blood, with median genetic distances averaging 1.08% in the env C2V5 region and 0.81% in the gag p17 gene. Within another 4.7 to 11 weeks, the variant lineage in env became more homogeneous, while gag sequences continued to diversify. Thus, the homogenization that has been reported to characterize acute infection is actually preceded by the replication of multiple virus variants. This early selective process focuses on viral properties within Env but not Gag p17. Hence, the viral homogeneity observed early in HIV-1 infection results from a selective process that occurs during the establishment of infection.
引用
收藏
页码:11953 / 11959
页数:7
相关论文
共 33 条
[11]  
Long EM, 2000, NAT MED, V6, P71
[12]   GENOMIC HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RNA VARIATION IN MOTHER AND CHILD FOLLOWING INTRAUTERINE VIRUS TRANSMISSION [J].
MULDERKAMPINGA, GA ;
KUIKEN, C ;
DEKKER, J ;
SCHERPBIER, HJ ;
BOER, K ;
GOUDSMIT, J .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :1747-1756
[13]   Cytotoxic-T-cell responses, viral load, and disease progression in early human immunodeficiency virus type 1 infection [J].
Musey, L ;
Hughes, J ;
Schacker, T ;
Shea, T ;
Corey, L ;
McElrath, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (18) :1267-1274
[14]  
NEI M, 1986, MOL BIOL EVOL, V3, P418
[15]   Acute phase cytotoxic T lymphocyte escape is a hallmark of simian immunodeficiency virus infection [J].
O'Connor, DH ;
Allen, TM ;
Vogel, TU ;
Jing, PC ;
DeSouza, IP ;
Dodds, E ;
Dunphy, EJ ;
Melsaether, C ;
Mothé, B ;
Yamamoto, H ;
Horton, H ;
Wilson, N ;
Hughes, AL ;
Watkins, DI .
NATURE MEDICINE, 2002, 8 (05) :493-499
[16]   RAPID GENERATION OF SEQUENCE VARIATION DURING PRIMARY HIV-1 INFECTION [J].
PANG, S ;
SHLESINGER, Y ;
DAAR, ES ;
MOUDGIL, T ;
HO, DD ;
CHEN, ISY .
AIDS, 1992, 6 (05) :453-460
[17]   MODELTEST: testing the model of DNA substitution [J].
Posada, D ;
Crandall, KA .
BIOINFORMATICS, 1998, 14 (09) :817-818
[18]   Variants from the diverse virus population identified at seroconversion of a clade A human immunodeficiency virus type 1-infected woman have distinct biological properties [J].
Poss, M ;
Overbaugh, J .
JOURNAL OF VIROLOGY, 1999, 73 (07) :5255-5264
[19]   Evolution of envelope sequences from the genital tract and peripheral blood of women infected with clade A human immunodeficiency virus type 1 [J].
Poss, M ;
Rodrigo, AG ;
Gosink, JJ ;
Learn, GH ;
Panteleeff, DD ;
Martin, HL ;
Bwayo, J ;
Kreiss, JK ;
Overbaugh, J .
JOURNAL OF VIROLOGY, 1998, 72 (10) :8240-8251
[20]   COMPARISON OF VARIABLE REGION-3 SEQUENCES OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 FROM INFECTED CHILDREN WITH THE RNA AND DNA-SEQUENCES OF THE VIRUS POPULATIONS OF THEIR MOTHERS [J].
SCARLATTI, G ;
LEITNER, T ;
HALAPI, E ;
WAHLBERG, J ;
MARCHISIO, P ;
CLERICISCHOELLER, MA ;
WIGZELL, H ;
FENYO, EM ;
ALBERT, J ;
UHLEN, M ;
ROSSI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1721-1725