Affordable in-house antiretroviral drug resistance assay with good performance in non-subtype B HIV-1

The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is...

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Published inJournal of virological methods Vol. 163; no. 2; pp. 505 - 508
Main Authors Wallis, Carole L., Papathanasopoulos, Maria A., Lakhi, Shabir, Karita, Etienne, Kamali, Anatoli, Kaleebu, Pontiano, Sanders, Eduard, Anzala, Omu, Bekker, Linda-Gail, Stevens, Gwynn, Wit, Tobias F. Rinke de, Stevens, Wendy
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.02.2010
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Abstract The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is common. This study developed and evaluated an affordable “in–house” genotyping assay to monitor HIV-1 drug resistance in Africa, particularly South Africa. An “in-house” assay using automated RNA extraction, and subtype C specific PCR and sequencing primers was developed and successfully evaluated 396 patient samples (viral load ranges 1000–1.6 million RNA copies/ml). The “in-house” assay was validated by comparing sequence data and drug resistance profiles from 90 patient and 10 external quality control samples to data from the ViroSeq™ HIV-1 Genotyping kit. The “in-house” assay was more efficient, amplifying all 100 samples, compared to 91 samples using Viroseq. The “in house” sequences were 99.2% homologous to the ViroSeq sequences, and identical drug resistance mutation profiles were observed in 96 samples. Furthermore, the “in-house” assay genotyped 260 of 295 samples from seven African sites, where 47% were non-subtype C. Overall, the newly validated “in-house” drug resistance assay is suited for use in Africa as it overcomes the obstacle of subtype diversity.
AbstractList The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is common. This study developed and evaluated an affordable "in-house" genotyping assay to monitor HIV-1 drug resistance in Africa, particularly South Africa. An "in-house" assay using automated RNA extraction, and subtype C specific PCR and sequencing primers was developed and successfully evaluated 396 patient samples (viral load ranges 1000-1.6 million RNA copies/ml). The "in-house" assay was validated by comparing sequence data and drug resistance profiles from 90 patient and 10 external quality control samples to data from the ViroSeq HIV-1 Genotyping kit. The "in-house" assay was more efficient, amplifying all 100 samples, compared to 91 samples using Viroseq. The "in house" sequences were 99.2% homologous to the ViroSeq sequences, and identical drug resistance mutation profiles were observed in 96 samples. Furthermore, the "in-house" assay genotyped 260 of 295 samples from seven African sites, where 47% were non-subtype C. Overall, the newly validated "in-house" drug resistance assay is suited for use in Africa as it overcomes the obstacle of subtype diversity.
The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is common. This study developed and evaluated an affordable “in–house” genotyping assay to monitor HIV-1 drug resistance in Africa, particularly South Africa. An “in-house” assay using automated RNA extraction, and subtype C specific PCR and sequencing primers was developed and successfully evaluated 396 patient samples (viral load ranges 1000–1.6 million RNA copies/ml). The “in-house” assay was validated by comparing sequence data and drug resistance profiles from 90 patient and 10 external quality control samples to data from the ViroSeq™ HIV-1 Genotyping kit. The “in-house” assay was more efficient, amplifying all 100 samples, compared to 91 samples using Viroseq. The “in house” sequences were 99.2% homologous to the ViroSeq sequences, and identical drug resistance mutation profiles were observed in 96 samples. Furthermore, the “in-house” assay genotyped 260 of 295 samples from seven African sites, where 47% were non-subtype C. Overall, the newly validated “in-house” drug resistance assay is suited for use in Africa as it overcomes the obstacle of subtype diversity.
The introduction of antiretroviral therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is common. This study developed and evaluated an affordable “in–house” genotyping assay to monitor HIV-1 drug resistance in Africa, particularly South Africa. An “in-house” assay using automated RNA extraction, and subtype C specific PCR and sequencing primers was developed and successfully evaluated 396 patient samples (viral load ranges 1,000->1.6million RNA copies/ml). The “in-house” assay was validated by comparing sequence data and drug resistance profiles from 90 patient and 10 external quality control samples to data from the ViroSeq TM HIV-1 Genotyping kit. The “in-house” assay was more efficient, amplifying all 100 samples, compared to 91 samples using Viroseq. The “in house” sequences were 99.2%) homologous to the ViroSeq sequences, and identical drug resistance mutation profiles were observed in 96 samples. Furthermore, the “in-house” assay genotyped 260 of 295 samples from seven African sites, where 47% were non-subtype C. Overall, the newly validated “in-house” drug resistance assay is suited for use in Africa as it overcomes the obstacle of subtype diversity.
Author Karita, Etienne
Kaleebu, Pontiano
Wallis, Carole L.
Papathanasopoulos, Maria A.
Lakhi, Shabir
Stevens, Gwynn
Kamali, Anatoli
Wit, Tobias F. Rinke de
Bekker, Linda-Gail
Anzala, Omu
Stevens, Wendy
Sanders, Eduard
AuthorAffiliation 8 Internation AIDS Vaccine Initiative Johannesburg, South Africa
11 National Health Laboratory Services (NHLS), Johannesburg., South Africa
2 Zambia Emory HIV Research Project (ZEHRP), Lusaka, Zambia
3 Project San Francisco (PSF) , Kigali, Rwanda
7 Desmond Tutu HIV Foundation, Cape Town, South Africa
1 Department of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa
6 Kenya AIDS Vaccine Initiative, Nairobi, Kenya
9 Linking African and Asian Societies for an Enhanced Response to HIV/AIDS (LAASER)
10 PharmAccess Foundation, Amsterdam, The Netherlands
5 Centre for Geographic Medicine Research-Coast (CGMRC), Kenya Medical Research Institute (KEMRI) - Kilifi, Kenya
4 MRC/UVRI Uganda Virus Research Unit on AIDS, , Uganda
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Issue 2
Keywords Antiretroviral drug resistance
HIV-1 subtype C
Affordable
Mutation profile
Antiretroviral agent
HIV-1 virus
Retroviridae
Method
Lentivirus
Virus
Resistance
Antiviral
Human immunodeficiency virus
Mutation
Subtype
Language English
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Snippet The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected...
The introduction of antiretroviral therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals....
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SubjectTerms Affordable
Anti-Retroviral Agents - pharmacology
Antiretroviral drug resistance
Antiviral agents
Automation
Biological and medical sciences
DNA Primers - genetics
Drug Resistance, Viral
Fundamental and applied biological sciences. Psychology
Genes, Viral
Genotype
HIV-1 - drug effects
HIV-1 - genetics
HIV-1 - isolation & purification
HIV-1 subtype C
Human immunodeficiency virus 1
Humans
Microbial Sensitivity Tests - economics
Microbial Sensitivity Tests - methods
Microbiology
Mutation profile
Reverse Transcriptase Polymerase Chain Reaction - methods
RNA, Viral - genetics
RNA, Viral - isolation & purification
Sensitivity and Specificity
South Africa
Techniques used in virology
Virology
Title Affordable in-house antiretroviral drug resistance assay with good performance in non-subtype B HIV-1
URI https://dx.doi.org/10.1016/j.jviromet.2009.11.011
https://www.ncbi.nlm.nih.gov/pubmed/19917318
https://search.proquest.com/docview/733618721
https://search.proquest.com/docview/744612993
https://pubmed.ncbi.nlm.nih.gov/PMC2932961
Volume 163
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