HIV-1 Drug Resistance Genotyping in Resource Limited Settings: Current and Future Perspectives in Sequencing Technologies

被引:10
|
作者
Manyana, Sontaga [1 ]
Gounder, Lilishia [1 ]
Pillay, Melendhran [1 ]
Manasa, Justen [2 ]
Naidoo, Kogieleum [3 ,4 ]
Chimukangara, Benjamin [1 ,3 ]
机构
[1] Univ KwaZulu Natal, Sch Lab Med & Med Sci, Dept Virol, Natl Hlth Lab Serv, ZA-4058 Durban, South Africa
[2] Univ Zimbabwe, Fac Med & Hlth Sci, Dept Lab Med & Investigat Sci, Harare, Zimbabwe
[3] Ctr AIDS Programme Res South Africa CAPRISA, ZA-4013 Durban, South Africa
[4] South African Med Res Council SAMRC, CAPRISA HIV TB Pathogenesis & Treatment Res Unit, ZA-4013 Durban, South Africa
来源
VIRUSES-BASEL | 2021年 / 13卷 / 06期
关键词
HIV-1 drug resistance; Sanger sequencing; next generation sequencing; resource limited settings; BLOOD SPOT SPECIMENS; ANTIRETROVIRAL THERAPY; ASSAY; PERFORMANCE; INTEGRASE; MUTATIONS; PLASMA; SYSTEM;
D O I
10.3390/v13061125
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Affordable, sensitive, and scalable technologies are needed for monitoring antiretroviral treatment (ART) success with the goal of eradicating HIV-1 infection. This review discusses use of Sanger sequencing and next generation sequencing (NGS) methods for HIV-1 drug resistance (HIVDR) genotyping, focusing on their use in resource limited settings (RLS). Sanger sequencing remains the gold-standard method for detecting HIVDR mutations of clinical relevance but is mainly limited by high sequencing costs and low-throughput. NGS is becoming a more common sequencing method, with the ability to detect low-abundance drug-resistant variants and reduce per sample costs through sample pooling and massive parallel sequencing. However, use of NGS in RLS is mainly limited by infrastructure costs. Given these shortcomings, our review discusses sequencing technologies for HIVDR genotyping, focusing on common in-house and commercial assays, challenges with Sanger sequencing in keeping up with changes in HIV-1 treatment programs, as well as challenges with NGS that limit its implementation in RLS and in clinical diagnostics. We further discuss knowledge gaps and offer recommendations on how to overcome existing barriers for implementing HIVDR genotyping in RLS, to make informed clinical decisions that improve quality of life for people living with HIV.
引用
收藏
页数:9
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