کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6133681 | 1593471 | 2014 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Targeted deep sequencing of HIV-1 using the IonTorrentPGM platform
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کلمات کلیدی
transmitted/founderSingle genome amplificationvRNAEPCRDEPCSGANATT/FCATTDSCTLViral RNA - RNA ویروسیPlasma viral load - بار ویروسی پلاسماReverse transcriptase - ترانس کریپتاز معکوس یا وارونویسnucleic acid testing - تست اسید نوکلئیکNext-generation sequencing - تعیین توالی نسل بعدیMolecular evolution - تکامل مولکولیdiethylpyrocarbonate - دیاتیلپیر کربناتPASS - عبورcytotoxic T lymphocyte - لنفوسیت T سیتوتوکسیکPVL - مقاله از استخراج اجباریHIV-1 - ویروس اچ آی وی نوع یکSingle nucleotide polymorphism - پلیمورفیسم تک نوکلئوتیدیSNP - چندریختی تک-نوکلئوتیدchloramphenicol acetyltransferase - کلرامفنیکول استیل ترانسفراز
موضوعات مرتبط
علوم زیستی و بیوفناوری
ایمنی شناسی و میکروب شناسی
ویروس شناسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
The characterization of mixed HIV-1 populations is a key question in clinical and basic research settings. This can be achieved through targeted deep sequencing (TDS), where next-generation sequencing is used to examine in depth a sub-genomic region of interest. This study explores the suitability of IonTorrent PGM(LifeTechnologies) for the TDS-based analysis of HIV-1 evolution. Using laboratory reagents and primary specimens sampled at pre-peak viremia the error rates from misincorporation and in vitro recombination were <0.5%. The sequencing error rate was 2- to 3-fold higher in/around homopolymeric tracts, and could be discerned from true polymorphism using bidirectional sequencing. The limit of detection of complex variants was further lowered by using haplotyping. The application of this system was illustrated on primary samples from an individual infected with HIV-1 followed from pre-peak viremia through six months post-acquisition. TDS provided an augmented view of the extent of genetic diversity, the covariation among polymorphisms, the evolutionary pathways, and the boundaries of the mutational space explored by the viral swarm. Based on its performance, the system can be applied for the characterization of minor viral variants in support of studies of viral evolution, which can inform the rational design of the next generation of vaccines and therapeutics.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Virological Methods - Volume 205, 1 September 2014, Pages 7-16
Journal: Journal of Virological Methods - Volume 205, 1 September 2014, Pages 7-16
نویسندگان
Gustavo H. Kijak, Eric Sanders-Buell, Elizabeth A. Harbolick, Phuc Pham, Agnes L. Chenine, Leigh Anne Eller, Kathleen Rono, Merlin L. Robb, Nelson L. Michael, Jerome H. Kim, Sodsai Tovanabutra,