Penedos Ana Raquel, Myers Richard, Hadef Besma, Aladin Farah, Brown Kevin E
Virus Reference Department, Public Health England, London, NW9 5EQ, United Kingdom.
PLoS One. 2015 Nov 16;10(11):e0143081. doi: 10.1371/journal.pone.0143081. eCollection 2015.
Measles is a highly infectious disease caused by measles virus (MeV). Despite the availability of a safe and cost-effective vaccine, measles is one of the world-leading causes of death in young children. Within Europe, there is a target for eliminating endemic measles in 2015, with molecular epidemiology required on 80% of cases for inclusion/exclusion of outbreak transmission chains. Currently, MeV is genotyped on the basis of a 450 nucleotide region of the nucleoprotein gene (N-450) and the hemagglutinin gene (H). However, this is not sufficiently informative for distinguishing endemic from imported MeV. We have developed an amplicon-based method for obtaining whole genome sequences (WGS) using NGS or Sanger methodologies from cell culture isolates or oral fluid specimens, and have sequenced over 60 samples, including 42 from the 2012 outbreak in the UK.
Overall, NGS coverage was over 90% for approximately 71% of the samples tested. Analysis of 32 WGS excluding 3' and 5' termini (WGS-t) obtained from the outbreak indicates that the single nucleotide difference found between the two major groups of N-450 sequences detected during the outbreak is most likely a result of stochastic viral mutation during endemic transmission rather than of multiple importation events: earlier strains appear to have evolved into two distinct strain clusters in 2013, one containing strains with both outbreak-associated N-450 sequences. Additionally, phylogenetic analysis of each genomic region of MeV for the strains in this study suggests that the most information is acquired from the non-coding region located between the matrix and fusion protein genes (M/F NCR) and the N-450 genotyping sequence, an observation supported by entropy analysis across genotypes.
We suggest that both M/F NCR and WGS-t could be used to complement the information from classical epidemiology and N-450 sequencing to address specific questions in the context of measles elimination.
麻疹是由麻疹病毒(MeV)引起的一种高度传染性疾病。尽管有安全且具成本效益的疫苗,但麻疹仍是全球幼儿死亡的主要原因之一。在欧洲,目标是到2015年消除地方性麻疹,要求对80%的病例进行分子流行病学分析,以确定是否属于疫情传播链。目前,MeV是根据核蛋白基因(N-450)的450个核苷酸区域和血凝素基因(H)进行基因分型的。然而,这对于区分地方性MeV和输入性MeV的信息还不够充分。我们开发了一种基于扩增子的方法,可使用下一代测序(NGS)或桑格测序方法从细胞培养分离株或口腔液体样本中获取全基因组序列(WGS),并且已经对60多个样本进行了测序,其中包括2012年英国疫情中的42个样本。
总体而言,约71%的测试样本的NGS覆盖率超过90%。对从疫情中获得的32个排除3'和5'末端的全基因组序列(WGS-t)进行分析表明,在疫情期间检测到的两组主要N-450序列之间发现的单核苷酸差异很可能是地方性传播过程中病毒随机突变的结果,而非多次输入事件导致的:早期毒株似乎在2013年演变成了两个不同的毒株簇,其中一个包含与疫情相关的两种N-450序列的毒株。此外,对本研究中各毒株的MeV每个基因组区域进行系统发育分析表明,从基质蛋白和融合蛋白基因之间的非编码区域(M/F NCR)和N-450基因分型序列中获得的信息最多,这一观察结果得到了各基因型熵分析的支持。
我们建议,M/F NCR和WGS-t均可用于补充经典流行病学和N-450测序的信息,以解决麻疹消除背景下的特定问题。