Eshleman Susan H, Jones Dana, Galovich Justin, Paxinos Ellen E, Petropoulos Christos J, Jackson J Brooks, Parkin Neil
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
AIDS Res Hum Retroviruses. 2006 Mar;22(3):289-93. doi: 10.1089/aid.2006.22.289.
We analyzed the nonnucleoside reverse transcriptase (RT) inhibitor (NNRTI) susceptibility of 29 subtype A HIV-1 clones isolated from 10 Ugandan women after single-dose nevirapine (NVP) administration. Six clones had no NNRTI resistance-associated mutations ("wild type"), eight had K103N, nine had Y181C, five had G190A, and one had Y181S. Three clones displayed unexpected phenotypic drug susceptibility/resistance based on their RT genotypes. One wild-type clone had reduced susceptibility to NVP, delavirdine (DLV), and efavirenz (EFV), one clone with K103N was susceptible to all three NNRTIs, and one clone with G190A had extreme hypersusceptibility to DLV. Three unusual HIV-1 RT amino acid substitutions may have contributed to the unexpected phenotypes of the clones: I31T, N136S, and N265D. These polymorphisms were rarely detected among 47,900 HIV-1 genotypes from clinical samples of predominantly United States origin. Further studies are needed to define the genetic correlates of antiretroviral drug resistance in nonsubtype B HIV-1.
我们分析了从10名乌干达女性中分离出的29个A型HIV-1克隆在单剂量奈韦拉平(NVP)给药后的非核苷类逆转录酶(RT)抑制剂(NNRTI)敏感性。6个克隆没有与NNRTI耐药相关的突变(“野生型”),8个有K103N突变,9个有Y181C突变,5个有G190A突变,1个有Y181S突变。3个克隆根据其RT基因型表现出意外的表型药物敏感性/耐药性。1个野生型克隆对NVP、地拉韦啶(DLV)和依非韦伦(EFV)的敏感性降低,1个有K103N突变的克隆对所有三种NNRTIs敏感,1个有G190A突变的克隆对DLV极度敏感。三种不寻常的HIV-1 RT氨基酸取代可能导致了克隆的意外表型:I31T、N136S和N265D。在美国主要来源的临床样本的47900个HIV-1基因型中很少检测到这些多态性。需要进一步研究来确定非B型HIV-1中抗逆转录病毒药物耐药性的遗传相关性。