HIV type 2 protease, reverse transcriptase, and envelope viral variation in the PBMC and genital tract of ARV-naive women in Senegal

被引:8
作者
Gottlieb, Geoffrey S. [1 ]
Hawes, Stephen E. [2 ]
Wong, Kim G. [3 ]
Raugi, Dana N. [3 ]
Agne, Habibatou D. [4 ]
Critchlow, Cathy W. [2 ]
Kiviat, Nancy B. [5 ]
Sow, Papa Salif [4 ]
机构
[1] Univ Washington, Dept Med, Div Allergy & Infect Dis, Sch Med, Seattle, WA 98195 USA
[2] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98195 USA
[4] Univ Dakar, Dakar, Senegal
[5] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
关键词
D O I
10.1089/aid.2008.0015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unique viral variants and resistance mutations may occur in the genital tract of HIV-2 ARV-naive infected women. We sequenced and phylogenetically analyzed protease (PR), reverse transcriptase (RT), and envelope (ENV) from PBMC and genital tract samples from four ARV-naive women in Senegal. HIV-2 protease polymorphisms that predict HIV-1 protease inhibitor (PI) resistance were common. Two subjects had protease mutations (T77I and I64V) in genital tract samples that were not found in PBMCs. One subject had the HIV-2 reverse transcriptase M184I mutation in CVL DNA (but not PBMCs) that is known to confer 3TC/FTC resistance in HIV-2. In another subject, the reverse transcriptase A62V mutation was also found in CVL-RNA but not PBMCs. We found no significant difference in ENV variants between PBMCs and the genital tract. HIV-2 RT and PR mutations in the genital tract of ARV-naive females may have implications for transmitted HIV-2 resistance and ARV therapy.
引用
收藏
页码:857 / 864
页数:8
相关论文
共 16 条
[1]   Polymorphism of the human immunodeficiency virus type 2 (HIV-2) protease gene and selection of drug resistance mutations in HIV-2-infected patients treated with protease inhibitors [J].
Damond, F ;
Brun-Vezinet, F ;
Matheron, S ;
Peytavin, G ;
Campa, P ;
Pueyo, S ;
Mammano, F ;
Lastere, S ;
Farfara, I ;
Simon, F ;
Chene, G ;
Descamps, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (01) :484-487
[2]   EPIDEMIOLOGY AND TRANSMISSION OF HIV-2 - WHY THERE IS NO HIV-2 PANDEMIC [J].
DECOCK, KM ;
ADJORLOLO, G ;
EKPINI, E ;
SIBAILLY, T ;
KOUADIO, J ;
MARAN, M ;
BRATTEGAARD, K ;
VETTER, KM ;
DOORLY, R ;
GAYLE, HD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (17) :2083-2086
[3]  
DECOCK KM, 1994, JAMA-J AM MED ASSOC, V271, P196
[4]   GENETIC DIVERSITY OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-2 - EVIDENCE FOR DISTINCT SEQUENCE SUBTYPES WITH DIFFERENCES IN VIRUS BIOLOGY [J].
GAO, F ;
YUE, L ;
ROBERTSON, DL ;
HILL, SC ;
HUI, HX ;
BIGGAR, RJ ;
NEEQUAYE, AE ;
WHELAN, TM ;
HO, DD ;
SHAW, GM ;
SHARP, PM ;
HAHN, BH .
JOURNAL OF VIROLOGY, 1994, 68 (11) :7433-7447
[5]   Molecular epidemiology of dual HIV-1/HIV-2 seropositive adults from Senegal, West Africa [J].
Gottlieb, GS ;
Sow, PS ;
Hawes, SE ;
Ndoye, I ;
Coll-Seck, AM ;
Curlin, ME ;
Critchlow, CW ;
Kiviat, NB ;
Mullins, JI .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2003, 19 (07) :575-584
[6]   Equal plasma viral loads predict a similar rate of CD4+ T cell decline in human immunodeficiency virus (HIV) type 1-and HIV-2-infected individuals from Senegal, West Africa [J].
Gottlieb, GS ;
Sow, PS ;
Hawes, SE ;
Ndoye, L ;
Redman, M ;
Coll-Seek, AM ;
Faye-Niang, MA ;
Diop, A ;
Kuypers, JM ;
Critchlow, CW ;
Respess, R ;
Mullins, JI ;
Kiviat, NB .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (07) :905-914
[7]   SLOWER HETEROSEXUAL SPREAD OF HIV-2 THAN HIV-1 [J].
KANKI, PJ ;
TRAVERS, KU ;
MBOUP, S ;
HSIEH, CC ;
MARLINK, RG ;
GUEYENDIAYE, A ;
SIBY, T ;
THIOR, I ;
HERNANDEZAVILA, M ;
SANKALE, JL ;
NDOYE, I ;
ESSEX, ME .
LANCET, 1994, 343 (8903) :943-946
[8]   REDUCED RATE OF DISEASE DEVELOPMENT AFTER HIV-2 INFECTION AS COMPARED TO HIV-1 [J].
MARLINK, R ;
KANKI, P ;
THIOR, I ;
TRAVERS, K ;
EISEN, G ;
SIBY, T ;
TRAORE, I ;
HSIEH, CC ;
DIA, MC ;
GUEYE, E ;
HELLINGER, J ;
GUEYENDIAYE, A ;
SANKALE, JL ;
NDOYE, I ;
MBOUP, S ;
ESSEX, M .
SCIENCE, 1994, 265 (5178) :1587-1590
[9]   HIV-2 protease sequences of subtypes A and B harbor multiple mutations associated with protease inhibitor resistance in HIV-1 [J].
Pieniazek, D ;
Rayfield, M ;
Hu, DJ ;
Nkengasong, JN ;
Soriano, V ;
Heneine, W ;
Zeh, C ;
Agwale, SM ;
Wambebe, C ;
Odama, L ;
Wiktor, SZ ;
Kalish, ML .
AIDS, 2004, 18 (03) :495-502
[10]  
Rodés B, 2000, J CLIN MICROBIOL, V38, P1370