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Long-Range HIV Genotyping Using Viral RNA and Proviral DNA for Analysis of HIV Drug Resistance and HIV Clustering.
Novitsky, Vlad; Zahralban-Steele, Melissa; McLane, Mary Fran; Moyo, Sikhulile; van Widenfelt, Erik; Gaseitsiwe, Simani; Makhema, Joseph; Essex, M.
Afiliação
  • Novitsky V; Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
  • Zahralban-Steele M; Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
  • McLane MF; Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
  • Moyo S; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • van Widenfelt E; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Gaseitsiwe S; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Makhema J; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Essex M; Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana messex@hsph.harvard.edu.
J Clin Microbiol ; 53(8): 2581-92, 2015 Aug.
Article em En | MEDLINE | ID: mdl-26041893
ABSTRACT
The goal of the study was to improve the methodology of HIV genotyping for analysis of HIV drug resistance and HIV clustering. Using the protocol of Gall et al. (A. Gall, B. Ferns, C. Morris, S. Watson, M. Cotten, M. Robinson, N. Berry, D. Pillay, and P. Kellam, J Clin Microbiol 503838-3844, 2012, doi10.1128/JCM.01516-12), we developed a robust methodology for amplification of two large fragments of viral genome covering about 80% of the unique HIV-1 genome sequence. Importantly, this method can be applied to both viral RNA and proviral DNA amplification templates, allowing genotyping in HIV-infected subjects with suppressed viral loads (e.g., subjects on antiretroviral therapy [ART]). The two amplicons cover critical regions across the HIV-1 genome (including pol and env), allowing analysis of mutations associated with resistance to protease inhibitors, reverse transcriptase inhibitors (nucleoside reverse transcriptase inhibitors [NRTIs] and nonnucleoside reverse transcriptase inhibitors [NNRTIs]), integrase strand transfer inhibitors, and virus entry inhibitors. The two amplicons generated span 7,124 bp, providing substantial sequence length and numbers of informative sites for comprehensive phylogenic analysis and greater refinement of viral linkage analyses in HIV prevention studies. The long-range HIV genotyping from proviral DNA was successful in about 90% of 212 targeted blood specimens collected in a cohort where the majority of patients had suppressed viral loads, including 65% of patients with undetectable levels of HIV-1 RNA loads. The generated amplicons could be sequenced by different methods, such as population Sanger sequencing, single-genome sequencing, or next-generation ultradeep sequencing. The developed method is cost-effective-the cost of the long-range HIV genotyping is under $140 per subject (by Sanger sequencing)-and has the potential to enable the scale up of public health HIV prevention interventions.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Viral / RNA Viral / Infecções por HIV / HIV-1 / Farmacorresistência Viral / Técnicas de Genotipagem / Genótipo Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Viral / RNA Viral / Infecções por HIV / HIV-1 / Farmacorresistência Viral / Técnicas de Genotipagem / Genótipo Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article