Quantitative analysis of the endogenous reverse transcriptase reactions of HIV type 1 variants with decreased susceptibility to azidothymidine and nevirapine

被引:4
作者
Krogstad, P
Chen, ISY
Canon, J
Rey, O
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT MED,LOS ANGELES,CA 90095
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT MICROBIOL & IMMUNOL,LOS ANGELES,CA 90095
关键词
D O I
10.1089/aid.1996.12.977
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A large number of nucleoside analog and nonnucleoside inhibitors of HIV-1 reverse transcriptase (RT) have been developed for clinical use, Data confirm that;resistant variants of HIV-1 rapidly emerge in response to the selective pressure of treatment with these agents, Detection of drug resistance generally involves detection of specific mutations in the viral genome or demonstrating a failure of the drug to suppress virus replication in culture, We have developed a PCR-based method to quantitatively examine HIV-1 DNA synthesis in vitro in endogenous reverse transcription reactions and tested it as a method to detect resistance to RT inhibitors, Under certain conditions, we were able to distinguish HIV strains with high-level resistance to azidothymidine triphosphate inhibition from sensitive strains, This method was quite useful as an assay to detect resistance to nevirapine, a nonnucleoside RT inhibitor; in reconstruction experiments, nevirapine-resistant virus was detectable when it represented 10 to 25% of the total amount of virus present in reaction mixtures, These data are examined in the light of current models of the mechanisms of action of nucleoside and nonnucleoside RT inhibitors, This assay may be useful for detecting the emergence of drug-resistant HIV-1 variants during therapy.
引用
收藏
页码:977 / 983
页数:7
相关论文
共 25 条
[1]   ENZYMATIC GENE AMPLIFICATION - QUALITATIVE AND QUANTITATIVE METHODS FOR DETECTING PROVIRAL DNA AMPLIFIED INVITRO [J].
ABBOTT, MA ;
POIESZ, BJ ;
BYRNE, BC ;
KWOK, S ;
SNINSKY, JJ ;
EHRLICH, GD .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (06) :1158-1169
[2]   PRODUCTION OF ACQUIRED IMMUNODEFICIENCY SYNDROME-ASSOCIATED RETROVIRUS IN HUMAN AND NONHUMAN CELLS TRANSFECTED WITH AN INFECTIOUS MOLECULAR CLONE [J].
ADACHI, A ;
GENDELMAN, HE ;
KOENIG, S ;
FOLKS, T ;
WILLEY, R ;
RABSON, A ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1986, 59 (02) :284-291
[3]  
BACOLLA A, 1993, J BIOL CHEM, V268, P16871
[4]   2 SPECIES OF FULL-LENGTH CDNA ARE SYNTHESIZED IN HIGH-YIELD BY MELITTIN-TREATED AVIAN RETROVIRUS PARTICLES [J].
BOONE, LR ;
SKALKA, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (02) :847-851
[5]   DEVELOPMENT OF A HUMAN IMMUNODEFICIENCY VIRUS-1 IN-VITRO DNA-SYNTHESIS SYSTEM TO STUDY REVERSE-TRANSCRIPTASE INHIBITORS [J].
BORROTOESODA, K ;
BOONE, LR .
ANTIVIRAL RESEARCH, 1994, 23 (3-4) :235-249
[6]   EQUINE INFECTIOUS-ANEMIA VIRUS AND HUMAN-IMMUNODEFICIENCY-VIRUS DNA-SYNTHESIS INVITRO - CHARACTERIZATION OF THE ENDOGENOUS REVERSE-TRANSCRIPTASE REACTION [J].
BORROTOESODA, K ;
BOONE, LR .
JOURNAL OF VIROLOGY, 1991, 65 (04) :1952-1959
[7]   DEVELOPMENT OF AN ASSAY THAT DETECTS TRANSCRIPTIONALLY COMPETENT HUMAN-IMMUNODEFICIENCY-VIRUS TYPE ONE PARTICLES [J].
BUSSO, M ;
RESNICK, L .
JOURNAL OF VIROLOGICAL METHODS, 1994, 47 (1-2) :129-139
[8]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 POL GENE-MUTATIONS IN AN AIDS PATIENT TREATED WITH MULTIPLE ANTIRETROVIRAL DRUGS [J].
FITZGIBBON, JE ;
FARNHAM, AE ;
SPERBER, SJ ;
KIM, H ;
DUBIN, DT .
JOURNAL OF VIROLOGY, 1993, 67 (12) :7271-7275
[9]   DETAILED MODEL OF REVERSE TRANSCRIPTION AND TESTS OF CRUCIAL ASPECTS [J].
GILBOA, E ;
MITRA, SW ;
GOFF, S ;
BALTIMORE, D .
CELL, 1979, 18 (01) :93-100
[10]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VIRIONS COMPOSED OF UNPROCESSED GAG AND GAG-POL PRECURSORS ARE CAPABLE OF REVERSE TRANSCRIBING VIRAL GENOMIC RNA [J].
KAPLAN, AH ;
KROGSTAD, P ;
KEMPF, DJ ;
NORBECK, DW ;
SWANSTROM, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (12) :2929-2933