Selection promotes organ compartmentalization in HIV-1:: Evidence from gag and pol genes

被引:9
|
作者
Borderia, Antonio V.
Codoner, Francisco M.
Sanjuan, Rafael
机构
[1] Univ Politecn Valencia, CSIC, Inst Biol Mol & Celular Plantas, Valencia 46022, Spain
[2] Univ Dublin Trinity Coll, Smurfit Inst Genet, Dublin 2, Ireland
[3] Natl Univ Ireland Maynooth, Dept Biol, Inst Immunol, Maynooth, Kildare, Ireland
[4] Inst Salud Carlos III, Ctr Nacl Microbiol, Serv Virol Mol, Madrid 28220, Spain
[5] CUNY Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
关键词
adaptation; gene flow; molecular evolution; population genetics; viral evolution;
D O I
10.1111/j.1558-5646.2007.00025.x
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
The existence of organ-specific human immunodeficiency virus type 1 (HIV-1) populations within infected hosts has been long lasting studied. Previous work established that population subdivision by organs occurs at the envelope env gene, but less is known about other genomic regions. Here, we used a population genetics approach to detect organ compartmentalization in proviral sequences of HIV-1 gag and pol genes. Significant population structure was found in pol (100% of cases) and gag (33%) pair-wise organ comparisons. The degree of compartmentalization positively correlated with the ratio of nonsynonymous to synonymous substitutions, and codons showing organ compartmentalization were more likely to be under significantly positive selection. This suggests that HIV-1 populations dynamically adapt to locally variable intra-host environments. In the case of pol gene, differential penetration of antiretroviral drugs might account for the observed pattern, whereas for gag gene, local selective pressures remain unexplored.
引用
收藏
页码:272 / 279
页数:8
相关论文
共 50 条
  • [1] NATURAL-SELECTION ON THE GAG, POL, AND ENV GENES OF HUMAN-IMMUNODEFICIENCY-VIRUS-1 (HIV-1)
    SEIBERT, SA
    HOWELL, CY
    HUGHES, MK
    HUGHES, AL
    MOLECULAR BIOLOGY AND EVOLUTION, 1995, 12 (05) : 803 - 813
  • [2] Modulation of HIV-1 Gag/Gag-Pol frameshifting by tRNA abundance
    Korniy, Natalia
    Goyal, Akanksha
    Hoffmann, Markus
    Samatova, Ekaterina
    Peske, Frank
    Poehlmann, Stefan
    Rodnina, Marina V.
    NUCLEIC ACIDS RESEARCH, 2019, 47 (10) : 5210 - 5222
  • [3] Persistence of processed HIV-1 Gag and Gag-Pol proteins following treatment with HIV-1 protease inhibitors.
    Speck, RR
    Yu, XF
    Flexner, C
    FASEB JOURNAL, 2000, 14 (04): : A185 - A185
  • [4] Effects of reduced gag cleavage efficiency on HIV-1 Gag-Pol package
    Yi-Ru Lin
    Shih-Ming Chu
    Fu-Hsien Yu
    Kuo-Jung Huang
    Chin-Tien Wang
    BMC Microbiology, 22
  • [5] Effects of reduced gag cleavage efficiency on HIV-1 Gag-Pol package
    Lin, Yi-Ru
    Chu, Shih-Ming
    Yu, Fu-Hsien
    Huang, Kuo-Jung
    Wang, Chin-Tien
    BMC MICROBIOLOGY, 2022, 22 (01)
  • [6] Accumulation of HIV-1 Gag and Gag-Pol processing intermediates in the presence of non-peptidomimetic HIV-1 protease inhibitors
    Speck, RR
    Yu, XF
    Flexner, C
    ANTIVIRAL RESEARCH, 2000, 46 (01) : A71 - A71
  • [7] A COMPARISON OF GAG, POL AND REV ANTISENSE OLIGODEOXYNUCLEOTIDES AS INHIBITORS OF HIV-1
    KINCHINGTON, D
    GALPIN, S
    JAROSZEWSKI, JW
    GHOSH, K
    SUBASINGHE, C
    COHEN, JS
    ANTIVIRAL RESEARCH, 1992, 17 (01) : 53 - 62
  • [8] CHARACTERIZATION OF RIBOSOMAL FRAMESHIFTING IN HIV-1 GAG-POL EXPRESSION
    JACKS, T
    POWER, MD
    MASIARZ, FR
    LUCIW, PA
    BARR, PJ
    VARMUS, HE
    NATURE, 1988, 331 (6153) : 280 - 283
  • [9] Functional human immunodeficiency virus type 1 (HIV-1) gag-pol or HIV-1 Gag-Pol and Env expressed from a single rhabdovirus-based vaccine vector genome
    McGettigan, JP
    Naper, K
    Orenstein, J
    Koser, M
    McKenna, PM
    Schnell, MJ
    JOURNAL OF VIROLOGY, 2003, 77 (20) : 10889 - 10899
  • [10] PHYLOGENETIC ANALYSIS OF GAG AND ENV GENES FROM INTERNATIONAL HIV-1 ISOLATES AND EVIDENCE FOR MULTIPLE GENOTYPES
    LOUWAGIE, J
    MCCUTCHAN, F
    JANSSENS, W
    VANDERGROEN, G
    BURKE, D
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 1994, 10 : S39 - S39