Literature DB >> 11679926

Inhibition of purified recombinant reverse transcriptase from wild-type and zidovudine-resistant clinical isolates of human immunodeficiency virus type 1 by zidovudine, stavudine, and lamivudine triphosphates.

C Duan1, D Poticha, T C Stoeckli, C J Petropoulos, J M Whitcomb, C S McHenry, D R Kuritzkes.   

Abstract

Cross-resistance between zidovudine, stavudine, and lamivudine was studied, using purified recombinant reverse transcriptase from a zidovudine-susceptible and -resistant pair of clinical isolates of human immunodeficiency virus type 1. The zidovudine-resistant isolate exhibited low-level cross-resistance to both stavudine and lamivudine in drug susceptibility assays. Enzyme from the resistant isolate demonstrated reduced inhibition by zidovudine triphosphate and stavudine triphosphate and, to a lesser extent, lamivudine triphosphate. These findings provide additional evidence at the viral and enzyme level for cross-resistance between zidovudine and stavudine, and they suggest a possible effect of zidovudine resistance on susceptibility to lamivudine.

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Year:  2001        PMID: 11679926     DOI: 10.1086/323995

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  3 in total

1.  Pharmacokinetic Modeling of Lamivudine and Zidovudine Triphosphates Predicts Differential Pharmacokinetics in Seminal Mononuclear Cells and Peripheral Blood Mononuclear Cells.

Authors:  Julie B Dumond; Kuo H Yang; Racheal Kendrick; Y Sunila Reddy; Angela D M Kashuba; Luigi Troiani; Arlene S Bridges; Susan A Fiscus; Alan Forrest; Myron S Cohen
Journal:  Antimicrob Agents Chemother       Date:  2015-08-03       Impact factor: 5.191

Review 2.  Genotypic testing for human immunodeficiency virus type 1 drug resistance.

Authors:  Robert W Shafer
Journal:  Clin Microbiol Rev       Date:  2002-04       Impact factor: 26.132

3.  Genotoxic and Cytotoxic Effects of Antiretroviral Combinations in Mice Bone Marrow.

Authors:  Aroldo Vieira de Moraes Filho; Cláudia de Jesus Silva Carvalho; Cristiene Costa Carneiro; Camila Regina do Vale; Débora Cristina da Silva Lima; Wanessa Fernandes Carvalho; Thiago Bernardi Vieira; Daniela de Melo E Silva; Kênya Silva Cunha; Lee Chen-Chen
Journal:  PLoS One       Date:  2016-11-02       Impact factor: 3.240

  3 in total

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