Chen Ying-Fang Elaine, Lee Chung-Chan, Chiu Cheng-Hsun, Chang Yu-Chung, Tsai Chi-Neu, Chao Hsun-Ching, Kong Shu-Sing, Chen Shih-Yen
Division of Neonatology, Department of Pediatrics, Taipei Medical University Shuang Ho Hospital, New Taipei City.
Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital.
Medicine (Baltimore). 2020 Feb;99(9):e19253. doi: 10.1097/MD.0000000000019253.
Despite the development of vaccines in 2006, rotavirus is still a major cause of acute gastroenteritis worldwide. This study was performed to analyze the presence of circulating rotaviruses before and after the introduction of rotavirus vaccines to allow phylogenetic comparisons of vaccine strains in northern Taiwan.Rotavirus genotyping and sequencing of rotavirus VP7 and VP4 PCR products were performed by Reverse Transcriptase Polymerase Chain Reaction and DNA autosequencing. Phylogenies were constructed by the neighbor-joining and maximum-likelihood methods using CLUSTAL W software included in the MEGA software package (version 6.0).Between April 2004 and December 2012, a total of 101 rotavirus specimens from pediatric patients with acute gastroenteritis hospitalized in Chang Gung Children's Hospital were amplified, and their VP4 and VP7 sequences were determined. These 101 specimens consisted of 55 pre-vaccine strains (G1 [13, 23.6%], G2 [12, 21.8%], G3 [16, 29.1%], and G9 [14, 25.5%]) and 46 post-vaccine strains (G1 [25, 54.3%], G2 [12, 26.1%], G3 [5, 10.9%], and G9 [4, 8.7%]). The most common combination of the G and P types was G2P[4], accounting for 36% cases, followed by G9P[8] (25%), G1P[8] (20%), G3P[4] (15%), G3P[8] (10%), G1P[4] (5%), and G2P[8] (5%). Phylogenetic analysis showed that only the G1 and P[8] genotypes clustered in the same lineages with the rotavirus vaccine strains.Based on our results, the inclusion of G9, modified G2 and G3 with target lineages, and the combination G2P[4] and G9P[8] in the rotavirus vaccines in Taiwan is warranted as a vaccination strategy.
尽管2006年就研发出了轮状病毒疫苗,但轮状病毒仍是全球急性肠胃炎的主要病因。本研究旨在分析引入轮状病毒疫苗前后流行的轮状病毒情况,以便对台湾北部的疫苗毒株进行系统发育比较。通过逆转录聚合酶链反应和DNA自动测序对轮状病毒VP7和VP4 PCR产物进行轮状病毒基因分型和测序。使用MEGA软件包(版本6.0)中包含的CLUSTAL W软件,通过邻接法和最大似然法构建系统发育树。2004年4月至2012年12月期间,对长庚儿童医院收治的101例急性肠胃炎患儿的轮状病毒标本进行了扩增,并测定了其VP4和VP7序列。这101个标本包括55株疫苗接种前毒株(G1型[13株,23.6%]、G2型[12株,21.8%]、G3型[16株,29.1%]和G9型[14株,25.5%])和46株疫苗接种后毒株(G1型[25株,54.3%]、G2型[12株,26.1%]、G3型[5株,10.9%]和G9型[4株,8.7%])。G型和P型最常见的组合是G2P[4],占36%的病例,其次是G9P[8](25%)、G1P[8](20%)、G3P[4](15%)、G3P[8](10%)、G1P[4](5%)和G2P[8](5%)。系统发育分析表明,只有G1和P[8]基因型与轮状病毒疫苗毒株聚集在同一谱系中。根据我们的研究结果,台湾轮状病毒疫苗中纳入G9、经过改良的G2和G3以及目标谱系,以及G2P[4]和G9P[8]组合作为疫苗接种策略是有必要的。