A genotypic assay for the amplification and sequencing of gag and protease from diverse human immunodeficiency virus type 1 group M subtypes

被引:16
作者
Van Laethem, K
Schrooten, Y
Dedecker, S
Van Heeswijck, L
Deforche, K
Van Wijngaerden, E
Van Ranst, M
Vandamme, AM
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
[2] Univ Hosp Leuven, Aids Reference Lab, Louvain, Belgium
关键词
RNA extraction; cDNA synthesis; PCR; HIV-1; subtypes; sensitivity;
D O I
10.1016/j.jviromet.2005.10.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In human immunodeficiency virus type 1 (HIV-1), an interaction exists between the in vivo evolution of Gag protein and protease to escape from antiretroviral drug selective pressure. Therefore, it was decided to develop a genotypic assay for the amplification and sequencing of HIV-1 gag and protease. As the HIV-1 pandemic is characterised by a large genetic diversity, the assay developed was evaluated on a panel of 28 genetically divergent samples belonging to the following subtypes A1, B, C, D, F1, F2, G, H, J, CRF01-AE, CRF02-AG and CRF13-cpx. The assay displayed a detection limit ranging between 500 RNA copies/ml and 5000 RNA copies/ml plasma. Full-length sequences could be obtained for 25 samples. The population sequences of the three other samples lacked a part of the sequence because of heterogeneous signal, probably due to the presence of quasispecies with insertions/deletions of a different length. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 186
页数:6
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