Warkad Shrikant Dashrath, Nimse Satish Balasaheb, Song Keum-Soo, Kim Taisun
Institute of Applied Chemistry and Department of Chemistry, Hallym University, Chuncheon 24252, South Korea.
ACS Omega. 2020 May 8;5(19):10794-10799. doi: 10.1021/acsomega.0c00386. eCollection 2020 May 19.
The World Health Organization and the World Health Assembly recommended eradicating hepatitis as a public threat by 2030. The accurate genotyping of hepatitis C virus (HCV) is crucial to achieving this goal because it is vital for the selection of anti-HCV therapy required for complete cure of HCV infection. We report the development of a method for accurate genotyping of HCV 1a, 1b, 2, 3, 4, and 6 genotypes. The merits of the developed method for HCV genotyping include (i) requirement of a single polymerase chain reaction (PCR) primer set, (ii) room-temperature detection in 30 min after the PCR, (iii) no need of highly trained professionals, (iv) highly accurate HCV genotyping results afforded by highly specific DNA-DNA hybridization, and (v) probe sequences that can be used on other platforms.
世界卫生组织和世界卫生大会建议到2030年消除作为公共威胁的肝炎。丙型肝炎病毒(HCV)的准确基因分型对于实现这一目标至关重要,因为它对于选择彻底治愈HCV感染所需的抗HCV治疗至关重要。我们报告了一种对HCV 1a、1b、2、3、4和6基因型进行准确基因分型的方法的开发。所开发的HCV基因分型方法的优点包括:(i)只需一组聚合酶链反应(PCR)引物;(ii)PCR后30分钟可在室温下检测;(iii)无需高技能专业人员;(iv)通过高度特异性的DNA-DNA杂交获得高度准确的HCV基因分型结果;(v)可在其他平台上使用的探针序列。