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[2009年山东省甲型H1N1流感大流行4起疫情的病原学分析]

[Analysis of etiology of four pandemic influenza A (H1N1) virus outbreaks in Shandong province, in 2009].

作者信息

Li Zhong, Liu Ti, Lin Yi, Zhang Sheng-Yang, Liu Jun, Jiang Wen-Guo, Wang Xian-Jun, Xu Ai-Qiang, Bi Zhen-Qiang

机构信息

Shandong Center for Disease Control and Prevention, Key Lab of Infectious Diseases in Shandong Province, Shandong University Institute for Prevention Medicine, Jinan 250014, China.

出版信息

Zhonghua Yu Fang Yi Xue Za Zhi. 2010 Dec;44(12):1069-74.

Abstract

OBJECTIVE

To isolate and identify the influenza virus that caused four influenza-like-illness outbreaks in Jining city of Shandong Province in 2009 and analyze the genetic characteristics of hemagglutinin (HA) and neuraminidase (NA) gene, the variation of these genes were studied.

METHODS

34 nasopharyngeal swabs from fever patients of four influenza-like-illness outbreaks were collected and diagnosed by real time quantitative RT-PCR method. The positive samples were incubated and cultured for virus. HA and NA genes of isolated pandemic influenza A (H1N1) virus were sequenced, the homology analysis was done with DNAStar software and the genetic evolution and amino acid substitutions were performed with Mega 4.0 software. The sequences were compared with WHO recommended vaccine virus, native reference virus.

RESULTS

Seventeen of 34 nasopharyngeal swabs were positive, 11 pandemic influenza A (H1N1) viruses were isolated and HA and NA genes of 7 strains were sequenced. Phylogenetic analysis for hemagglutinin and neuraminidase gene of Shandong outbreak strains showed that there were 98.4% - 99.6% and 99.2% - 100.0% sequence identity. Compared with WHO-recommended vaccine strain, the reference virus in mainland China strain, eleven amino acids were changed for HA protein, including position 38, 40, 56, 90, 100, 145, 172, 173, 220, 303 and 338, and 38, 40, 303 of HA protein were located in the antigenic determination C cluster, 172, 173 in the D cluster, 56 in the E cluster, site 40 of HA protein were glycosylated. In NA protein, seven amino acids were changed, including position 80, 106, 241, 248, 351, 369 and 386, site 40 of NA protein were glycosylated. No mutations of 275 in NA protein were found.

CONCLUSION

The HA and NA genes of the epidemic strains showed high homology, some mutations in the HA and NA proteins were found, the antigenic site and glycosylation site of some strains were changed during the epidemic process.

摘要

目的

分离并鉴定引起2009年山东省济宁市4起流感样疾病暴发的流感病毒,分析血凝素(HA)和神经氨酸酶(NA)基因的遗传特征,研究这些基因的变异情况。

方法

采集4起流感样疾病暴发中发热患者的34份鼻咽拭子,采用实时定量RT-PCR方法进行诊断。对阳性样本进行病毒培养。对分离的甲型H1N1大流行性流感病毒的HA和NA基因进行测序,使用DNAStar软件进行同源性分析,使用Mega 4.0软件进行遗传进化和氨基酸替换分析。将序列与世界卫生组织推荐的疫苗病毒、本土参考病毒进行比较。

结果

34份鼻咽拭子中有17份呈阳性,分离出11株甲型H1N1大流行性流感病毒,对其中7株的HA和NA基因进行了测序。山东暴发株HA和NA基因的系统发育分析显示,序列同源性分别为98.4% - 99.6%和99.2% - 100.0%。与世界卫生组织推荐的疫苗株、中国大陆参考病毒株相比,HA蛋白有11个氨基酸发生改变,包括第38、40、56、90、100、145、172、173、220、303和338位,其中HA蛋白的第38、40、303位位于抗原决定簇C簇,172、173位位于D簇,56位位于E簇,HA蛋白的40位发生糖基化。NA蛋白有7个氨基酸发生改变,包括第80、106、241、248、351、369和386位,NA蛋白的40位发生糖基化。未发现NA蛋白第275位有突变。

结论

流行株的HA和NA基因显示出高度同源性,HA和NA蛋白存在一些突变,部分毒株的抗原位点和糖基化位点在流行过程中发生了改变。

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