کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5673081 | 1593434 | 2017 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: HIV drug resistance testing among patients failing second line antiretroviral therapy. Comparison of in-house and commercial sequencing HIV drug resistance testing among patients failing second line antiretroviral therapy. Comparison of in-house and commercial sequencing](/preview/png/5673081.png)
- In-house sequencing can provide reliable genotyping information.
- Low-cost sequencing achieved by adopting SATURN protocol.
- In-house and commercial sequencing make testing feasible, accessible and affordable.
- High quality resistance testing improves patient care.
IntroductionHIV genotyping is often unavailable in low and middle-income countries due to infrastructure requirements and cost. We compared genotype resistance testing in patients with virologic failure, by amplification of HIV pol gene, followed by “in-house” sequencing and commercial sequencing.MethodsRemnant plasma samples from adults and children failing second-line ART were amplified and sequenced using in-house and commercial di-deoxysequencing, and analyzed in Harare, Zimbabwe and at Stanford, U.S.A, respectively. HIV drug resistance mutations were determined using the Stanford HIV drug resistance database.ResultsTwenty-six of 28 samples were amplified and 25 were successfully genotyped. Comparison of average percent nucleotide and amino acid identities between 23 pairs sequenced in both laboratories were 99.51 (±0.56) and 99.11 (±0.95), respectively. All pairs clustered together in phylogenetic analysis. Sequencing analysis identified 6/23 pairs with mutation discordances resulting in differences in phenotype, but these did not impact future regimens.ConclusionsThe results demonstrate our ability to produce good quality drug resistance data in-house. Despite discordant mutations in some sequence pairs, the phenotypic predictions were not clinically significant.
Journal: Journal of Virological Methods - Volume 243, May 2017, Pages 151-157