Effect of naturally-occurring gp41 HR1 variations on susceptibility of HIV-1 to fusion inhibitors

被引:27
作者
Chinnadurai, R [1 ]
Münch, J [1 ]
Kirchhoff, F [1 ]
机构
[1] Univ Ulm Klinikum, Dept Virol, D-89081 Ulm, Germany
关键词
HIV-1; entry inhibitors; T-20; T-1249; resistance;
D O I
10.1097/01.aids.0000180785.25800.de
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Sequence variations in the gp41 heptad repeat 1 (HR1) region have been identified in some treatment-naive HIV-1-infected patients but it remained elusive whether they confer resistance to fusion inhibitors. Objective: To evaluate whether naturally occurring sequence variations in the HIV-1 group M gp41 HRI region affect the sensitivity to inhibition by T-20 and T-1249. Methods: Site-directed mutagenesis was used to generate HIV-1 NL4-3 mutants containing changes in the gp4l HR1 domain which have been previously identified in treatment-naive patients infected with various HIV-1 group M subtypes. HIV-1 variants were produced by transient transfection of 293T cells and used to determine viral infectivity and sensitivity to the fusion inhibitors T-20 and T-1249. Results: Most naturally occurring sequence variations in the HR1 domain did not reduce viral infectivity. Three of the 10 HIV-1 variants analysed containing a single substitution of L33V, which is frequently present in subtype D isolates, or combined changes of L54M/Q56K or L34M/L54M/Q56R showed about fivefold reduced sensitivity to inhibition by T-20. In comparison, none of these HRI sequence variations conferred resistance to T-1249. Conclusion: Some naturally occurring sequence variations in the gp41 HR1 region reduce sensitivity of HIV-1 to inhibition by T-20 but not T-1249. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1401 / 1405
页数:5
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