期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
乙型脑炎病毒减毒SA14-14-2-B3株基因组全序列分析
1
作者 张学涛 赵明秋 +4 位作者 琚春梅 赵启祖 康艳梅 沈海燕 陈金顶 《中国预防兽医学报》 CAS CSCD 北大核心 2010年第8期632-634,654,共4页
为进一步了解乙型脑炎病毒(JEV)减毒疫苗株基因组变异和分子遗传特性,本研究根据已发表的JEV基因组序列,设计合成了8对引物,应用RT-PCR对SA14-14-2-B3株基因组进行了克隆和序列测定,获得了该株病毒的全基因组序列(10977nt)并推导出其编... 为进一步了解乙型脑炎病毒(JEV)减毒疫苗株基因组变异和分子遗传特性,本研究根据已发表的JEV基因组序列,设计合成了8对引物,应用RT-PCR对SA14-14-2-B3株基因组进行了克隆和序列测定,获得了该株病毒的全基因组序列(10977nt)并推导出其编码的氨基酸序列(3432aa)。序列分析表明:SA14-14-2-B3株与疫苗株SA14-14-2和SA(A)及野毒株SA14的核苷酸和氨基酸相似性较高,分别为99.8%、99.9%、99.4%和99.7%、99.8%、99.1%,与猪源分离株HEN0701和KV1899的核苷酸与氨基酸相似性较低,分别为88.5%、88.5%和97.6%、96.6%,比较显示在SA14-14-2-B3株基因组第10700nt处有一碱基"G"的插入。以全基因组为基础,对SA14-14-2-B3株进行遗传进化关系分析,结果表明:SA14-14-2-B3株与SA14源病毒株SA14、SA14-14-2、SA(A)、SA(V)及分离株Beijing-1、p3、WHe和HW的遗传关系较近,与XJP613株和HEN0701株的遗传关系较远。以E基因为基础,对SA14-14-2-B3株进行遗传进化关系分析,结果表明SA14-14-2-B3株属于JEV基因Ⅲ型。 展开更多
关键词 乙型脑炎病毒 sa14-14-2-b3 基因组 序列分析
下载PDF
A retrospective investigation on the phenotype and stability of the E-protein gene in Japanese Encephalitis (JE) virus strain SA14-14-2 used live-attenuated JE vaccine
2
作者 LI LI JIA YONG XIN YU +2 位作者 YING HUANG ZHI WEI WANG GUAN MU DONG 《Journal of Microbiology and Immunology》 2005年第4期241-245,共5页
To detect retrospectively the phenotype and stability of the E-protein gene in Japanese Encephalitis (JE) virus strain SA14-14-2 used in the live-attenuated JE vaccine prepears, the viral titer was titrated by plaqu... To detect retrospectively the phenotype and stability of the E-protein gene in Japanese Encephalitis (JE) virus strain SA14-14-2 used in the live-attenuated JE vaccine prepears, the viral titer was titrated by plaque formation in BHK-21 cell cultures, and the neuro-virulence of viruses was assayed in mice with body weight of 12-14 g by intracerebral inoculation. Meanwhile, the total RNA of virus gene was extracted and amplified by RT-PCR with the designed primers, and then it was purified and cloned to the expression vector pGEM-T. The recombinant plasmid was purified and sequenced. It was found that the loss of viral titer of vaccines stored in -20℃ for longer than 10 years was less than 0.5 Lg PFU/ml. No mice inoculated intracerebrally showed signs of illness or even death. The size of plagues of the vaccine virus remained to be small, and the E genes of primary virus seed SA14-14-2 and the vaccines prepared at different years (1987-2001) were unchanged, in- cluding the 8 critical amino acid sites which were different from the parent wild virus strain SA14 and the related neuro-virulence. These results indicate that the genotypic and biological characteristics of the attenuated JE virus strain SA14-14-2 and its vaccines sion noted. prepared are quite stable without any reversion noted. 展开更多
关键词 Live attenuated Japanese Encephalitis virus strain sa14-14-2) Live attenuated vaccinePhenotype Genetic stability of E protein
下载PDF
乙型脑炎病毒SA14-14-2株NS3基因的克隆及原核表达 被引量:1
3
作者 叶琳 张鹏艳 +1 位作者 郑庆纹 姚亚夫 《中国生物制品学杂志》 CAS CSCD 2009年第8期758-761,共4页
目的克隆并表达乙型脑炎病毒SA14-14-2株NS3编码区的基因片段,为重组蛋白进一步的功能研究奠定基础。方法提取乙脑病毒SA14-14-2株总RNA,用RT-PCR法扩增NS3-1、NS3-2基因片段,克隆入原核表达载体pET15bTAT中,构建重组原核表达质粒,转化... 目的克隆并表达乙型脑炎病毒SA14-14-2株NS3编码区的基因片段,为重组蛋白进一步的功能研究奠定基础。方法提取乙脑病毒SA14-14-2株总RNA,用RT-PCR法扩增NS3-1、NS3-2基因片段,克隆入原核表达载体pET15bTAT中,构建重组原核表达质粒,转化大肠杆菌Rosetta2,IPTG诱导表达。表达产物经Ni2+亲和层析柱纯化后,进行Western blot鉴定。结果重组原核表达质粒pET15bTAT-NS3-1和pET15bTAT-NS3-2经酶切证明构建正确。表达的重组蛋白相对分子质量约为27000和20000,主要以包涵体的形式表达。重组蛋白纯化后纯度可达80%以上,并可被小鼠抗乙型脑炎病毒SA14-14-2株血清识别。结论已成功克隆了乙型脑炎病毒SA14-14-2株NS3-1和NS3-2基因,并在大肠杆菌Rosetta2中获得表达。 展开更多
关键词 乙型脑炎病毒 sa14-14—2株 NS3基因 克隆 原核表达
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部