Human immunodeficiency virus type 1 genetic evolution in children with different rates of development of disease

被引:138
作者
Ganeshan, S
Dickover, RE
Korber, BTM
Bryson, YJ
Wolinsky, SM
机构
[1] NORTHWESTERN UNIV,SCH MED,DEPT MED,CHICAGO,IL 60611
[2] UNIV CALIF LOS ANGELES,DEPT PEDIAT,LOS ANGELES,CA 90095
[3] LOS ALAMOS NATL LAB,DIV THEORET,LOS ALAMOS,NM 87545
关键词
D O I
10.1128/JVI.71.1.663-677.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The rate of development of disease varies considerably among human immunodeficiency virus type I (HIV-1)-infected children. The reasons for these observed differences are not clearly understood but most probably depend on the dynamic interplay between the HIV-1 quasispecies virus population and the immune constraints imposed by the host. To study the relationship between disease progression and genetic diversity, we analyzed the evolution of viral sequences within six perinatally infected children by examining proviral sequences spanning the C2 through V5 regions of the viral envelope gene by PCR of blood samples obtained at sequential visits. PCR product DNAs from four sample time points per child were cloned, and 10 to 13 clones from each sample were sequenced. Greater genetic distances relative to the time of infection were found for children with low virion-associated RNA burdens and slow progression to disease relative to those found for children with high virion-associated RNA burdens and rapid progression to disease. The greater branch lengths observed in the phylogenetic reconstructions correlated with a higher accumulation rate of nonsynonymous base substitutions per potential nonsynonymous site, consistent with positive selection for change rather than a difference in replication kinetics. Viral sequences from children with slow progression to disease also showed a tendency to form clusters that associated with different sampling times. These progressive shifts in the viral population were not found in viral sequences from children with rapid progression to disease. Therefore, despite the HIV-1 quasispecies being a diverse, rapidly evolving, and competing population of genetic variants, different rates of genetic evolution could be found under different selective constraints. These data suggest that the evolutionary dynamics exhibited by the HIV-1 quasispecies virus populations are compatible with a Darwinian system evolving under the constraints of natural selection.
引用
收藏
页码:663 / 677
页数:15
相关论文
共 94 条
  • [21] DECLINE IN CD4+ CELL NUMBERS REFLECTS INCREASE IN HIV-1 REPLICATION
    DEWOLF, F
    ROOS, M
    LANGE, JMA
    HOUWELING, JTM
    COUTINHO, RA
    VANDERNOORDAA, J
    SCHELLEKENS, PT
    GOUDSMIT, J
    [J]. AIDS RESEARCH AND HUMAN RETROVIRUSES, 1988, 4 (06) : 433 - 440
  • [22] RAPID INCREASES IN LOAD OF HUMAN-IMMUNODEFICIENCY-VIRUS CORRELATE WITH EARLY DISEASE PROGRESSION AND LOSS OF CD4 CELLS IN VERTICALLY INFECTED INFANTS
    DICKOVER, RE
    DILLON, M
    GILLETTE, SG
    DEVEIKIS, A
    KELLER, M
    PLAEGERMARSHALL, S
    CHEN, I
    DIAGNE, A
    STIEHM, ER
    BRYSON, Y
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) : 1279 - 1284
  • [23] DICKOVER RE, 1996, JAMA-J AM MED ASSOC, V278, P566
  • [24] SUBCLONAL COMPONENTS OF CONSENSUS FITNESS IN AM RNA VIRUS CLONE
    DUARTE, EA
    NOVELLA, IS
    LEDESMA, S
    CLARKE, DK
    MOYA, A
    ELENA, SF
    DOMINGO, E
    HOLLAND, JJ
    [J]. JOURNAL OF VIROLOGY, 1994, 68 (07) : 4295 - 4301
  • [25] DULIEGE AM, 1992, PEDIATR INFECT DIS J, V11, P630
  • [26] Eigen M., 1988, RNA Genetics, Vol. III, VIII, P211
  • [27] MULTIPLE ALIGNED SEQUENCE EDITOR (MASE)
    FAULKNER, DV
    JURKA, J
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1988, 13 (08) : 321 - 322
  • [28] PHYLOGENIES FROM MOLECULAR SEQUENCES - INFERENCE AND RELIABILITY
    FELSENSTEIN, J
    [J]. ANNUAL REVIEW OF GENETICS, 1988, 22 : 521 - 565
  • [29] FELSENSTEIN J, 1974, GENETICS, V78, P737
  • [30] FELSENSTEIN J, 1993, PHYLIP VERSION 3