Mattick K L, Green J, Punia P, Belda F J, Gallimore C I, Brown D W
Regional Virology Laboratory, Leeds Public Health Laboratory, UK.
J Virol Methods. 2000 Jun;87(1-2):161-9. doi: 10.1016/s0166-0934(00)00170-1.
Molecular epidemiological studies of Norwalk-like viruses (NLVs), previously known as small round structured viruses (SRSVs), are dependant currently on DNA sequencing of PCR amplicons, which is expensive and time consuming. The Heteroduplex Mobility assay (HMA) was evaluated as a method for identification of PCR amplicons from the commonly circulating NLV strains without DNA sequencing. The procedure was developed for use with two reference strains, a Mexico virus-like strain (MXV-like; Hu¿NLV¿RBH¿1993¿UK) and the Grimsby virus strain (Hu¿NLV¿Gimsby¿1995¿UK), and was optimised with regards to the annealing and electrophoresis conditions and the electrophoresis gel matrix. Using the optimised conditions, amplicons of less than 90% sequence identity formed visible heteroduplexes, allowing the strains to be placed into three categories; Mexico-like, Grimsby-like and non-Mexico virus/non-Grimsby virus strains. Outbreak strains 'genotyped' previously by DNA sequencing as Mexico virus or Grimsby virus were identified correctly by the heteroduplex mobility assay. The procedure was applied prospectively to strains from 130 outbreaks occurring in the UK between 1997 and 1998. Heteroduplex mobility assay was successful on 120 (92%) strains of which 68 (57%) were GRV-like strains, three (2.5%) were Mexico virus-like strains and 49 (41%) were categorised as non- Mexico/non-Grimsby virus strains. Amplicons from 50 of the 120 strains were sequenced and there was perfect correlation between the heteroduplex mobility assay categorisation and phylogenetic analysis. HMA offers a rapid, robust and far cheaper alternative to sequencing for the identification of prevalent Norwalk-like virus genotypes for molecular epidemiological studies.
诺如病毒(Norwalk-like viruses,NLVs),以前被称为小圆结构病毒(small round structured viruses,SRSVs),目前的分子流行病学研究依赖于PCR扩增子的DNA测序,这既昂贵又耗时。异源双链迁移率分析(Heteroduplex Mobility assay,HMA)被评估为一种无需DNA测序即可鉴定常见流行NLV毒株PCR扩增子的方法。该程序是针对两种参考毒株开发的,一种是墨西哥病毒样毒株(MXV-like;Hu¿NLV¿RBH¿1993¿UK)和格里姆斯比病毒毒株(Hu¿NLV¿Gimsby¿1995¿UK),并在退火、电泳条件和电泳凝胶基质方面进行了优化。使用优化后的条件,序列同一性低于90%的扩增子形成可见的异源双链,从而可将毒株分为三类:墨西哥样、格里姆斯比样和非墨西哥病毒/非格里姆斯比病毒毒株。先前通过DNA测序“基因分型”为墨西哥病毒或格里姆斯比病毒的暴发毒株,通过异源双链迁移率分析被正确鉴定。该程序被前瞻性地应用于1997年至1998年间在英国发生的130起疫情的毒株。异源双链迁移率分析在120株(92%)毒株上取得成功,其中68株(57%)为GRV样毒株,3株(2.5%)为墨西哥病毒样毒株,49株(41%)被归类为非墨西哥/非格里姆斯比病毒毒株。对120株中的50株扩增子进行了测序,异源双链迁移率分析分类与系统发育分析之间存在完美的相关性。对于分子流行病学研究中常见诺如病毒基因型的鉴定,HMA提供了一种快速、可靠且成本低得多的测序替代方法。