HIV type 1 variants with nevirapine resistance mutations are rarely detected in antiretroviral drug-naive African women with subtypes A, C, and D

被引:9
作者
Church, Jessica D.
Hudelson, Sarah E.
Guay, Laura A.
Chen, Shu
Hoover, Donald R.
Parkin, Neil
Fiscus, Susan A.
Mmiro, Francis
Musoke, Philippa
Kumwenda, Newton
Jackson, J. Brooks
Taha, Taha E.
Eshleman, Susan H.
机构
[1] Johns Hopkins Univ, Dept Pathol, Sch Med, Johns Hopkins Med Inst, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[3] Rutgers State Univ, Dept Stat, Piscataway, NJ 08854 USA
[4] Rutgers State Univ, Inst Hlth Hlth Care Policy & Aging Res, Piscataway, NJ 08854 USA
[5] Monogram Biosci, San Francisco, CA 94080 USA
[6] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[7] Makerere Univ, Dept Obstet & Gynaecol, Kampala, Uganda
[8] Makerere Univ, Dept Paediat, Kampala, Uganda
关键词
D O I
10.1089/aid.2006.0272
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
K103N is frequently detected in HIV-infected women after single dose (SD) nevirapine (NVP). K103N-containing variants were detected more frequently by the ViroSeq HIV-1 Genotyping System in women with subtype C (69.2%) than subtypes A (19.4%, p < 0.0001) or D ( 36.1%, p < 0.0001). K103N-containing variants were also detected more frequently and at higher levels in women with subtype C by the LigAmp assay. In this report, we analyzed samples collected prior to or within hours after SD NVP administration from anti-retroviral drug-naive African women with subtypes A, C, and D. Only 1/254 samples had an NVP resistance mutation detected with the ViroSeq system, and only 4/236 samples had K103N detected at > 0.5% with the LigAmp assay [2/110 (1.8%) with subtype A, 1/46 (2.2%) with subtype C, and 1/80 (1.3%) with subtype D] ( p = 0.92). We did not detect significant differences in the pre-NVP frequency of NVP resistance mutations or the pre-NVP levels of K103N-containing variants in women with subtypes A, C, and D that explain the dramatic subtype-based differences in emergence of HIV-1 variants with these mutations after SD NVP exposure.
引用
收藏
页码:764 / 768
页数:5
相关论文
共 15 条
[1]   Reduced susceptibility of human immunodeficiency virus type 1 (HIV-1) from patients with primary HIV infection to nonnucleoside reverse transcriptase inhibitors is associated with variation at novel amino acid sites [J].
Brown, AJL ;
Precious, HM ;
Whitcomb, JM ;
Wong, JK ;
Quigg, M ;
Huang, W ;
Daar, ES ;
D'Aquila, RT ;
Keiser, PH ;
Connick, E ;
Hellmann, NS ;
Petropoulos, CJ ;
Richman, DD ;
Little, SJ .
JOURNAL OF VIROLOGY, 2000, 74 (22) :10269-10273
[2]   Sensitivity of the ViroSeq HIV-1 genotyping system for detection of the K103N resistance mutation in HIV-1 subtypes A, C, and D [J].
Church, Jessica D. ;
Jones, Dana ;
Flys, Tamara ;
Hoover, Donald ;
Marlowe, Natalia ;
Chen, Shu ;
Shi, Chanjuan ;
Eshleman, James R. ;
Guay, Laura A. ;
Jackson, J. Brooks ;
Kumwenda, Newton ;
Taha, E. Taha ;
Eshleman, Susan H. .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (04) :430-432
[3]   Phenotypic drug resistance patterns in subtype a HIV-1 clones with nonnucleoside reverse transcriptase resistance mutations [J].
Eshleman, SH ;
Jones, D ;
Galovich, J ;
Paxinos, EE ;
Petropoulos, CJ ;
Jackson, JB ;
Parkin, N .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2006, 22 (03) :289-293
[4]   Nevirapine (NVP) resistance in women with HIV-1 subtype C, compared with subtypes A and D, after the administration of single-dose NVP [J].
Eshleman, SH ;
Hoover, DR ;
Chen, S ;
Hudelson, SE ;
Guay, LA ;
Mwatha, A ;
Fiscus, SA ;
Mmiro, F ;
Musoke, P ;
Jackson, JB ;
Kumwenda, N ;
Taha, T .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (01) :30-36
[5]   Characterization of nevirapine resistance mutations in women with subtype A vs. D HIV-1 6-8 weeks after single-dose nevirapine (HIVNET 012) [J].
Eshleman, SH ;
Guay, LA ;
Mwatha, A ;
Brown, ER ;
Cunningham, SP ;
Musoke, P ;
Mmiro, F ;
Jackson, JB .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2004, 35 (02) :126-130
[6]   Sensitive drug-resistance assays reveal long-term persistence of HIV-1 variants with the K103N Nevirapine (NVP) resistance mutation in some women and infants after the administration of single-dose NVP: HIVNET 012 [J].
Flys, T ;
Nissley, DV ;
Claasen, CW ;
Jones, D ;
Shi, CJ ;
Guay, LA ;
Musoke, P ;
Mmiro, F ;
Strathern, JN ;
Jackson, JB ;
Eshleman, JR ;
Eshleman, SH .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (01) :24-29
[7]  
FLYS TS, 2006, J ACQ IMMUN DEF SYND, V42, P61
[8]   Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVMET 012 randomised trial [J].
Guay, LA ;
Musoke, P ;
Fleming, T ;
Bagenda, D ;
Allen, M ;
Nakabiito, C ;
Sherman, J ;
Bakaki, P ;
Ducar, C ;
Deseyve, M ;
Emel, L ;
Mirochnick, M ;
Fowler, MG ;
Mofenson, L ;
Miotti, P ;
Dransfield, K ;
Bray, D ;
Mmiro, F ;
Jackson, JB .
LANCET, 1999, 354 (9181) :795-802
[9]   Rare mutations at codon 103 of HIV-1 reverse transcriptase can confer resistance to non-nucleoside reverse transcriptase inhibitors [J].
Harrigan, PR ;
Mo, T ;
Wynhoven, B ;
Hirsch, J ;
Brumme, Z ;
McKenna, P ;
Pattery, T ;
Vingerhoets, J ;
Bacheler, LT .
AIDS, 2005, 19 (06) :549-554
[10]   Nevirapine-resistant human immunodeficiency virus: Kinetics of replication and estimated prevalence in untreated patients [J].
Havlir, DV ;
Eastman, S ;
Gamst, A ;
Richman, DD .
JOURNAL OF VIROLOGY, 1996, 70 (11) :7894-7899