| Literature DB >> 17604129 |
Tim Middleton1, Yupeng He, Tami Pilot-Matias, Rakesh Tripathi, Ben Hock Lim, Andrew Roth, Chih-Ming Chen, Gennadiy Koev, Teresa I Ng, Preethi Krishnan, Ron Pithawalla, Rubina Mondal, Tatyana Dekhtyar, Liangjun Lu, Hongmei Mo, Warren M Kati, Akhteruzzaman Molla.
Abstract
Hepatitis C virus (HCV) replicon-based shuttle vectors that permit phenotypes of NS5B polymerase genes from a large number of patient isolates to be rapidly assessed when transiently expressed in cultured cells were designed. When used to test responses to an inhibitor of HCV RNA-dependent RNA polymerase, IC(50) values for inhibition covered a several hundred-fold range among 47 patient samples tested. This observation highlights the variability that can be found by testing isolates derived from HCV-infected subjects. Partial suppression with a polymerase inhibitor of the most sensitive species permitted detection of minor quasispecies that were 7-200-fold more resistant than the bulk population in approximately half of the samples. Sequence analysis showed a wide range of amino acid changes not detected by conventional selection methods using laboratory-derived strains. This approach provides a means to assess variation in antiviral efficacy, and to predict possible responses in a clinical setting.Entities:
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Year: 2007 PMID: 17604129 DOI: 10.1016/j.jviromet.2007.05.016
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014