Identification of I50L as the signature atazanavir (ATV)-resistance mutation in treatment-naive HIV-1-infected patients receiving ATV-containing regimens

被引:109
作者
Colonno, R
Rose, R
McLaren, C
Thiry, A
Parkin, N
Friborg, J
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Wallingford, CT 06492 USA
[2] ViroLogic, San Francisco, CA USA
关键词
D O I
10.1086/386291
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Atazanavir (ATV) is a once-daily human immunodeficiency virus (HIV) protease inhibitor (PI) shown to be effective and well tolerated. ATV has a distinct resistance profile relative to other PIs, with susceptibility maintained against 86% of isolates resistant to 1 - 2 PIs. Clinical isolates obtained from PI-naive patients designated as experiencing virologic failure while receiving ATV-containing regimens contained a unique isoleucine-to-leucine substitution at amino acid residue 50 (I50L) of the HIV-1 protease. The I50L substitution, observed in all isolates exhibiting phenotypic resistance to ATV, emerged in a variety of different backgrounds and was most frequently accompanied by A71V, K45R, and/or G73S. Viruses containing an I50L substitution were growth impaired, displayed ATV-specific resistance, and had increased susceptibilities ( less than or equal to0.4 of reference strain) to other PIs. Comparison of viruses bearing I50L with those bearing I50V revealed specific resistance to ATV and amprenavir, respectively, with no evidence of cross-resistance. The unique I50L substitution is the signature mutation for resistance to ATV.
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页码:1802 / 1810
页数:9
相关论文
共 32 条
  • [1] Polymorphism of HIV type 1 Gag p7/p1 and p1/p6 cleavage sites: Clinical significance and implications for resistance to protease inhibitors
    Bally, F
    Martinez, R
    Peters, S
    Sudre, P
    Telenti, A
    [J]. AIDS RESEARCH AND HUMAN RETROVIRUSES, 2000, 16 (13) : 1209 - 1213
  • [2] Activities of atazanavir (BMS-232632) against a large panel of human immunodeficiency virus type 1 clinical isolates resistant to one or more approved protease inhibitors
    Colonno, RJ
    Thiry, A
    Limoli, K
    Parkin, N
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (04) : 1324 - 1333
  • [3] Human immunodeficiency virus type 1 protease cleavage site mutations associated with protease inhibitor cross-resistance selected by indinavir, ritonavir, and/or saquinavir
    Côté, HCF
    Brumme, ZL
    Harrigan, PR
    [J]. JOURNAL OF VIROLOGY, 2001, 75 (02) : 589 - 594
  • [4] Second locus involved in human immunodeficiency virus type 1 resistance to protease inhibitors
    Doyon, L
    Croteau, G
    Thibeault, D
    Poulin, F
    Pilote, L
    Lamarre, D
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (06) : 3763 - 3769
  • [5] In vitro resistance profile of the human immunodeficiency virus type 1 protease inhibitor BMS-232632
    Gong, YF
    Robinson, BS
    Rose, RE
    Deminie, C
    Spicer, TP
    Stock, D
    Colonno, RJ
    Lin, PF
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) : 2319 - 2326
  • [6] Phenotypic and genotypic analysis of clinical HIV-1 isolates reveals extensive protease inhibitor cross-resistance: a survey of over 6000 samples
    Hertogs, K
    Bloor, S
    Kemp, SD
    Van den Eynde, C
    Alcorn, TM
    Pauwels, R
    Van Houtte, M
    Staszewski, S
    Miller, V
    Larder, BA
    [J]. AIDS, 2000, 14 (09) : 1203 - 1210
  • [7] Antiretroviral drug resistance testing in adult HIV-1 infection -: Recommendations of an International AIDS Society-USA panel
    Hirsch, MS
    Brun-Vézinet, F
    D'Aquila, RT
    Hammer, SM
    Johnson, VA
    Kuritzkes, DR
    Loveday, C
    Mellors, JW
    Clotet, B
    Conway, B
    Demeter, LM
    Vella, S
    Jacobsen, DM
    Richman, DD
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (18): : 2417 - 2426
  • [8] Johnson V.A., 1990, Techniques in HIV-Research, P71
  • [9] Emergence of resistance to protease inhibitor amprenavir in human immunodeficiency virus type 1-infected patients: Selection of four alternative viral protease genotypes and influence of viral susceptibility to coadministered reverse transcriptase nucleoside inhibitors
    Maguire, M
    Shortino, D
    Klein, A
    Harris, W
    Manohitharajah, V
    Tisdale, M
    Elston, R
    Yeo, J
    Randall, S
    Xu, F
    Parker, H
    May, J
    Snowden, W
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) : 731 - 738
  • [10] Changes in human immunodeficiency virus type 1 Gag at positions L449 and P453 are linked to 150V protease mutants in vivo and cause reduction of sensitivity to amprenavir and improved viral fitness in vitro
    Maguire, MF
    Guinea, R
    Griffin, P
    Macmanus, S
    Elston, RC
    Wolfram, J
    Richards, N
    Hanlon, MH
    Porter, DJT
    Wrin, T
    Parkin, N
    Tisdale, M
    Furfine, E
    Petropoulos, C
    Snowden, BW
    Kleim, JP
    [J]. JOURNAL OF VIROLOGY, 2002, 76 (15) : 7398 - 7406