Mukhopadhya Indrani, Murdoch Heather, Berry Susan, Hunt Alison, Iturriza-Gomara Miren, Smith-Palmer Alison, Cameron J Claire, Hold Georgina L
Gastrointestinal Research Group, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK.
Vaccine Preventable Diseases, NHS National Services Scotland, Health Protection Scotland, Glasgow G2 6QE, UK.
Vaccine. 2017 Jan 3;35(1):156-163. doi: 10.1016/j.vaccine.2016.11.028. Epub 2016 Nov 18.
Rotaviruses (RV) are the leading cause of gastroenteritis in children less than five years of age worldwide. Rotarix®, a live attenuated monovalent vaccine containing a RV strain of G1P[8] specificity has been included in the childhood immunisation schedule from June 2013 in Scotland. This study aimed to characterise the prevalent RV strains in Scotland before and after the introduction of the RV vaccine.
RV positive faecal samples from Scottish virology laboratories covering the years 2012-2015 were genotyped. Viral RNA was extracted from faecal suspensions. VP7 and VP4 gene specific primers were used for multiplex hemi-nested PCRs and sequencing. Mann-Whitney U test and Chi-square test were used for statistical comparison.
There was a decrease in RV positive samples from the Scottish virology laboratories from 7409 samples in the pre-vaccination years (2009-2013) to 760 in 2014-2015, with an annual reduction of RV infections by 74.4% (RR-3.95; 95%-CI, 3.53-4.42, p<0.001). 362 samples from the pre-vaccination period and 278 samples from the post-vaccination were genotyped. There was a drop in prevalence of G1P[8] strains (72.1%, 95%-CI, 67.42-76.33 to 15%, 95%-CI, 11.38-19.79) after introduction of the vaccine. In the post-vaccination period G2P[4] was the dominant strain in Scotland (21.9%, 95%-CI, 17.48-27.17) with increase in G9P[8] (12.9%, 95%-CI, 9.50-7.41), G12P[8] (12.2%, 95%-CI, 8.89-16.60) and G3P[8] (11.9%, 95%-CI, 8.58-16.20) infections. Phylogenetic analysis of the VP7 and VP4 genes showed no major differences between the pre and post-vaccination G1P[8] strains.
This laboratory based surveillance study shows significant reduction in reported RV cases and a shift in proportion from G1P[8] to G2P[4] strains after introduction of RV vaccination in Scotland. The genotyping data from a subset of the total reported RV cases will be used to ascertain cross protection against strains and identify vaccine induced RV strain shifts in the years to come.
轮状病毒(RV)是全球五岁以下儿童肠胃炎的主要病因。Rotarix®是一种含有G1P[8]特异性RV毒株的减毒活单价疫苗,自2013年6月起被纳入苏格兰儿童免疫计划。本研究旨在描述RV疫苗引入前后苏格兰流行的RV毒株特征。
对2012 - 2015年苏格兰病毒学实验室的RV阳性粪便样本进行基因分型。从粪便悬液中提取病毒RNA。使用VP7和VP4基因特异性引物进行多重半巢式PCR和测序。采用Mann-Whitney U检验和卡方检验进行统计学比较。
苏格兰病毒学实验室的RV阳性样本数量从疫苗接种前几年(2009 - 2013年)的7409份降至2014 - 2015年的760份,RV感染年减少率为74.4%(RR = 3.95;95%置信区间,3.53 - 4.42,p < 0.001)。对疫苗接种前的362份样本和接种后的278份样本进行了基因分型。疫苗引入后,G1P[8]毒株的流行率下降(72.1%,95%置信区间,67.42 - 76.33降至15%,95%置信区间,11.38 - 19.79)。在疫苗接种后时期,G2P[4]是苏格兰的主要毒株(21.9%,95%置信区间,17.48 - 27.17),G9P[8](12.9%,95%置信区间,9.50 - 7.41)、G12P[8](12.2%,95%置信区间,8.89 - 16.60)和G3P[8](11.9%,95%置信区间,8.58 - 16.20)感染有所增加。VP7和VP4基因的系统发育分析显示,疫苗接种前后的G1P[8]毒株之间没有重大差异。
这项基于实验室的监测研究表明,在苏格兰引入RV疫苗后,报告的RV病例显著减少,且毒株比例从G1P[8]向G2P[4]发生了转变。来自全部报告的RV病例子集的基因分型数据将用于确定对各毒株的交叉保护作用,并在未来几年识别疫苗诱导的RV毒株转变情况。