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Use of amplification refractory mutation system PCR assay as a simple and effective tool to detect HIV-1 drug resistance mutations
- Publication Year :
- 2015
-
Abstract
- Access to genotyping assays to determine successful antiretroviral treatment (ART) is limited in resource-constrained settings by high cost, suggesting the need for a cost-effective and simplified method to identify HIV-1 drug resistance (HIVDR) mutations. In this study, an amplification refractory mutation system (ARMS)-PCR assay was developed and used to investigate the most frequent HIVDR mutations affecting first-line ART in settings where WHO ART guidelines are applied. Seventy-five HIV-positive (HIV+) samples from Cameroon were used to assess the performance of this assay. Sequencing of HIV-1 reverse transcriptase was simultaneously performed for comparison, and discordant samples were tested with a Trugene HIV-1 genotyping kit. The ARMS-PCR assay was able to detect M184V, T215Y/F, K103N, and Y181C mutations with sensitivities of 96.8%, 85.7%, 91.3%, and 70%, respectively, and specificities of 90.6%, 95%, 100%, 96.9%, respectively, compared with data on sequencing. The results indicated the highest positive predictive value for K103N (100%) and the highest negative predictive value for M184V (97.5%). ARMS-PCR's limits of detection for mutations M184V, T215Y/F, K103N, and Y181C were
- Subjects :
- Microbiology (medical)
Adult
Male
Genotyping Techniques
Cost-Benefit Analysis
Mutation, Missense
Drug Resistance
HIV Infections
Drug resistance
Microbial Sensitivity Tests
Biology
medicine.disease_cause
Polymerase Chain Reaction
Sensitivity and Specificity
law.invention
law
Predictive Value of Tests
Virology
Drug Resistance, Viral
medicine
Humans
Cameroon
Viral
Genotyping
Polymerase chain reaction
Settore MED/04 - Patologia Generale
Mutation
virus diseases
Middle Aged
Resistance mutation
Molecular biology
Reverse transcriptase
Predictive value of tests
HIV-1
Female
Missense
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....9ca326c0294e1785037eb8d5f7485a00