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作 者:周俊梅[1] 方丹云[1] 梁瑜[1] 尹悦[1] 江丽芳[1]
机构地区:[1]中山大学中山医学院微生物学教研室,广东广州510080
出 处:《生物技术》2009年第3期1-3,共3页Biotechnology
基 金:广东省自然科学基金团队项目(05200638;06201946);广东省自然科学基金项目(7001516)资助
摘 要:目的:对登革病毒2型海南分离株NS1全序列进行测定和生物信息学分析,了解其系统进化和分子流行病学特征。方法:采用RT-PCR法扩增D2-Hainan全长NS1基因,将其克隆入载体pPIcZαB,测序,采用相关软件进行生物信息学分析。结果:获得D2-Hainan株NS1全长基因1056bp,其序列与登革病毒2型NGC株的同源性为95%。系统进化树分析显示该毒株与登革病毒2型China04株的亲缘关系最近。初步分析了NS1蛋白的氨基酸序列特征和二级结构。结论:登革病毒流行株存在地域性和复杂性,对D2-Hainan株NS1基因及其编码蛋白信息特征的了解,有助于进一步研究其基因特征与病毒毒力的关系。Objective: Determine and analyze the entire sequence of the NS1 gene of dengue 2 virus strain isolated in Hainan which is to understand the characteristic of its molecular evolution. Method:The nucleotides of NS1 of D2 - Hainan was amplified by RT- PCR and the sequence was determined by Sanger method. Then the gene and the encoding protein were analyzed by BLAST, MEGA, Clustal X, nnPredict, HNN, and DAS software. Result: It showed that the whole nueleotide sequence of D2- Hainan NS1 was 1 056bp and had the 95% homology with that of NGC strain. It was most closely to China04 strain with the homology 99.3%. Bioinformatics analysis proved there were 352 deduced amino acids of NS1 protein and it shared the twelve highly conserved eysteine sequence among flavivimses. Conclusion: By carrying out sequencing and bioinformaties of NS1, our research established foundation of further explore for the relationship between the NS1 gene character and dengue virus vimlence.
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