Turnover of env variable region 1 and 2 genotypes in subjects with late-stage human immunodeficiency virus type 1 infection

被引:48
作者
Kitrinos, KM
Hoffman, NG
Nelson, JAE
Swanstrom, R
机构
[1] Univ N Carolina, Lineberger Canc Ctr 22 062, UNC Ctr AIDS Res, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
关键词
D O I
10.1128/JVI.77.12.6811-6822.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The env gene of human immunodeficiency virus type 1 (HIV-1) includes some of the most genetically diverse regions of the viral genome, which are called variable regions 1 through 5 (V1 through V5). We have developed a heteroduplex tracking assay to detect changes in variable regions 1 and 2 of env (V1/V2-HTA). Using sequences from two molecular clones as probes, we have studied the nature of longitudinal virus population changes in a cohort of HIV-1-infected subjects. Viral sequences present in 21 subjects with late-stage HIV-1 infection were initially screened for stability of the virus population by V1/V2-HTA. The virus populations at entry comprised an average of five coexisting V1/V2 genotypic variants (as identified by HTA). Eight of the 21 subjects were examined in detail because of the dynamic behavior of their env variants over an approximately 9-month period. In each of these cases we detected a single discrete transition of V1/V2 genotypes based on monthly sampling. The major V1/V2 genotypes (those present at >10% abundance) from the eight subjects were cloned and sequenced to define the nature of V1/V2 variability associated with a discrete transition. Based on a comparison of V1/V2 genotypic variants present at entry with the newly emerged variants we categorized the newly emerged variants into two groups: variants without length differences and variants with length differences. Variants without length differences had fewer nucleotide substitutions, with the changes biased to either V1 or V2, suggestive of recent evolutionary events. Variants with length differences included ones with larger numbers of changes that were distributed, suggestive of recall of older genotypes. Most length differences were located in domains where the codon motif AVT (V = A, G, C) had become enriched and fixed. Finally, recombination events were detected in two subjects, one of which resulted in the reassortment of V1 and V2 regions. We suggest that turnover in V1/V2 populations was largely driven by selection on either V1 or V2 and that escape was accomplished either through changes focused in the region under selection or by the appearance of a highly divergent variant.
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页码:6811 / 6822
页数:12
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共 83 条
  • [1] PRODUCTION OF ACQUIRED IMMUNODEFICIENCY SYNDROME-ASSOCIATED RETROVIRUS IN HUMAN AND NONHUMAN CELLS TRANSFECTED WITH AN INFECTIOUS MOLECULAR CLONE
    ADACHI, A
    GENDELMAN, HE
    KOENIG, S
    FOLKS, T
    WILLEY, R
    RABSON, A
    MARTIN, MA
    [J]. JOURNAL OF VIROLOGY, 1986, 59 (02) : 284 - 291
  • [2] Natural variation in HIV-1 protease, gag p7 and p6, and protease cleavage sites within Gag/Pol polyproteins: Amino acid substitutions in the absence of protease inhibitors in mothers and children infected by human immunodeficiency virus type 1
    Barrie, KA
    Perez, E
    Lamers, SL
    Farmerie, WG
    Dunn, BM
    Sleasman, JW
    Goodenow, MM
    [J]. VIROLOGY, 1996, 219 (02) : 407 - 416
  • [3] THE CONTRASTING STRUCTURES OF MISMATCHED DNA-SEQUENCES CONTAINING LOOPED-OUT BASES (BULGES) AND MULTIPLE MISMATCHES (BUBBLES)
    BHATTACHARYYA, A
    LILLEY, DMJ
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (17) : 6821 - 6840
  • [4] INSERTION OF N-LINKED GLYCOSYLATION SITES IN THE VARIABLE REGIONS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 SURFACE GLYCOPROTEIN THROUGH AAT TRIPLET REITERATION
    BOSCH, ML
    ANDEWEG, AC
    SCHIPPER, R
    KENTER, M
    [J]. JOURNAL OF VIROLOGY, 1994, 68 (11) : 7566 - 7569
  • [5] Randomised placebo-controlled trial of ritonavir in advanced HIV-1 disease
    Cameron, DW
    Heath-Chiozzi, M
    Danner, S
    Cohen, C
    Kravcik, S
    Maurath, C
    Sun, E
    Henry, D
    Rode, R
    Potthoff, A
    Leonard, J
    [J]. LANCET, 1998, 351 (9102) : 543 - 549
  • [6] Replication and neutralization of human immunodeficiency virus type 1 lacking the V1 and V2 variable loops of the gp120 envelope glycoprotein
    Cao, J
    Sullivan, N
    Desjardin, E
    Parolin, C
    Robinson, J
    Wyatt, R
    Sodroski, J
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (12) : 9808 - 9812
  • [7] Specific N-linked and O-linked glycosylation modifications in the envelope V1 domain of simian immunodeficiency virus variants that evolve in the host alter recognition by neutralizing antibodies
    Chackerian, B
    Rudensey, LM
    Overbaugh, J
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (10) : 7719 - 7727
  • [8] Selection for neutralization resistance of the simian human immunodeficiency virus SHIVSF33A variant in vivo by virtue of sequence changes in the extracellular envelope glycoprotein that modify N-linked glycosylation
    Cheng-Mayer, C
    Brown, A
    Harouse, J
    Luciw, PA
    Mayer, AJ
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (07) : 5294 - 5300
  • [9] Insertion/deletion frequencies match those of point mutations in the hypervariable regions of the simian immunodeficiency virus surface envelope gene
    Cheynier, R
    Kils-Hütten, L
    Meyerhans, A
    Wain-Hobson, S
    [J]. JOURNAL OF GENERAL VIROLOGY, 2001, 82 : 1613 - 1619
  • [10] Identification of determinants on a dualtropic human immunodeficiency virus type 1 envelope glycoprotein that confer usage of CXCR4
    Cho, MW
    Lee, MK
    Carney, MC
    Berson, JF
    Doms, RW
    Martin, MA
    [J]. JOURNAL OF VIROLOGY, 1998, 72 (03) : 2509 - 2515