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Discordance between genotypic resistance and pseudovirus phenotypic resistance in AIDS patients after long-term antiretroviral therapy and virological failure
被引:4
|作者:
Yang, Jing
[1
,2
]
Geng, Wenqing
[1
]
Zhang, Min
[1
]
Han, Xiaoxu
[1
]
Shang, Hong
[1
]
机构:
[1] China Med Univ, Affiliated Hosp 1, Minist Hlth, Key Lab AIDS Immunol,Dept Lab Med, Shenyang 110001, Peoples R China
[2] Gen Hosp Shenyang Mil Area Command, Infect Control Dept, Shenyang, Peoples R China
关键词:
HIV-1;
Drug resistance;
Genotype-phenotype resistance;
Highly Active Antiretroviral Therapy (HAART);
IMMUNODEFICIENCY-VIRUS TYPE-1;
DRUG-RESISTANCE;
HIV-1;
SUSCEPTIBILITY;
D O I:
10.1002/jobm.201300415
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Sixteen original recombinant pseudoviruses were generated by cloning the reverse transcriptase and protease genes of human immunodeficiency virus (HIV)-1 from patients into a plasmid vector (pNL4-3-E-EGFP). By site-directed mutagenesis two restriction endonuclease sites, ApaI and AgeI, were inserted into pNL4-3-E-EGFP. Phenotypic susceptibility of recombinant pseudoviruses to five different classes of antiretroviral drugs was determined using a luciferase reporter assay system. The results were subjected to comparative analyses to detect genotype-phenotype associations. Among 16 strains tested, 12 strains had a discordant genotype-phenotype resistance pattern to at least one drug. In five strains resistance to two, in two strains to three, and in one strain resistance to four drugs was detected. HIV resistance genotyping could predict the phenotype for nevirapine and azidothymidine. For lamivudine, 2-3-didehydro-2-3dideoxythymidine and didanosine, phenotypic resistance testing was necessary. The study showed that in patients who experienced long-term highly active antiretroviral therapy and virological failure, there is some discordance between genotypic and phenotypic HIV drug resistance. To address the issue of limited resources in China, genotypic and phenotypic resistance testing should be done for different drugs in order to guide clinical therapy more effectively.
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页码:1120 / 1125
页数:6
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