Fahnøe Ulrik, Bukh Jens
Copenhagen Hepatitis C Program (CO-HEP), Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre, Denmark.
Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Methods Mol Biol. 2019;1911:85-91. doi: 10.1007/978-1-4939-8976-8_5.
The purpose of this method is to amplify the full coding sequence of hepatitis C virus (HCV) by a single round reverse transcriptase-polymerase chain reaction (RT-PCR) approach. Our method relies on a highly robust and sensitive RNA extraction procedure and cutting-edge RT-PCR enzymes, all of which have been rigorously tested and optimized. This will not only allow for robust amplification of the entire open reading frame (ORF) of HCV for sequencing by Sanger or next-generation sequencing (NGS), but can also be used for cloning of the ORF of uncharacterized samples and for linkage analysis of mutations on individual genomes spanning the entire ORF. The method has been validated on a variety of samples, including sera from HCV patients and cell-culture supernatants.
该方法的目的是通过单轮逆转录-聚合酶链反应(RT-PCR)方法扩增丙型肝炎病毒(HCV)的完整编码序列。我们的方法依赖于高度稳健且灵敏的RNA提取程序以及前沿的RT-PCR酶,所有这些都经过了严格测试和优化。这不仅能够稳健地扩增HCV的整个开放阅读框(ORF)以便通过桑格测序法或新一代测序(NGS)进行测序,还可用于未表征样品ORF的克隆以及对跨越整个ORF的单个基因组上的突变进行连锁分析。该方法已在多种样品上得到验证,包括HCV患者的血清和细胞培养上清液。