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2000 - 2007年山东省风疹病毒分子流行病学分析

[Analysis on molecular epidemiology of rubella virus in Shandong province during 2000-2007].

作者信息

Wang Chang-Yin, Zhu Zhen, Xu Ai-Qiang, Xiong Ping, Song Li-Zhi, Xu Qing, Feng Lei, Xu Wen-Bo

机构信息

Shandong Provincial Key Laboratory for Infectious Disease Control and Prevention, Shandong Province Center for Disease Control and Prevention, Jinan 250014, China.

出版信息

Bing Du Xue Bao. 2010 Nov;26(6):471-6.

Abstract

Analyze the genetic characteristics of sixteen strains of wild-type rubella viruses derived from Vero cells, Rk13 cells or Vero/slam cells, and isolated from throat samples in Shandong province during 2000-2007. The 1107 nucleotide sequence of nucleoprotein (E1) gene of these isolates were amplified by RT-PCR, and the PCR products were directly sequenced. Comparing with the gene tree that was constructed based on the 739 gene sequences of the WHO reference strains, twelve isolated strains belonged to 1E genotype, one strain belonged to 1F genotype, three strains belonged to 2A genotype. The first strain belonged to 1E genotype was isolated in Shandong province in 2001, then genotype 1E became dominant genotype of wild rubella viruses circulated. The 1E genotype circulated from 2006-2007 was different compared with that circulated from 2001 to 2002, but no significant deviation in temporal and geographic distribution was found. The strain belonged to Genotype 1F was only isolated during 2000 to 2001. The three strains of 2A genotype of rubella viruses were similar to rubella viruses vaccine strain (BRDII). The most nucleotide mutation of rubella viruses among the sixteen strains were nonsense mutation, and the amino acid sequences were highly conservative with no change in important antigen sites. Alike the previous reports, there was the same amino acid mutation in protein E1 at the site of 338 in all of the 1E genotype rubella viruses isolated during 2001- 2007 in Shandong (Leu338 --> Phe338).

摘要

分析2000年至2007年期间从山东省咽喉样本中分离出的、源自Vero细胞、Rk13细胞或Vero/slam细胞的16株野生型风疹病毒的基因特征。通过RT-PCR扩增这些分离株核蛋白(E1)基因的1107个核苷酸序列,并对PCR产物进行直接测序。与基于世界卫生组织参考株的739个基因序列构建的基因树进行比较,12株分离株属于1E基因型,1株属于1F基因型,3株属于2A基因型。第一株属于1E基因型的毒株于2001年在山东省分离得到,随后1E基因型成为流行的野生风疹病毒的主导基因型。2006 - 2007年流行的1E基因型与2001年至2002年流行的不同,但在时间和地理分布上未发现明显偏差。属于1F基因型的毒株仅在2000年至2001年期间分离得到。3株2A基因型风疹病毒与风疹病毒疫苗株(BRDII)相似。16株风疹病毒中大多数核苷酸突变是无义突变,氨基酸序列高度保守,重要抗原位点无变化。与之前的报道一样,2001 - 2007年在山东分离的所有1E基因型风疹病毒在E1蛋白338位点存在相同的氨基酸突变(Leu338 --> Phe338)。

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