[1]史沛举,等.2型猪链球菌中国强毒株05ZYH33 ofs N-片段基因敲除株的构建[J].南京师大学报(自然科学版),2009,32(02):87-92.
 Shi Peiju,Hao Xina,Ge Junchao,et al.Deletion of the N-terminal Fragment of ofs Gene in Streptococcus Suis Serotype 2 Chinese Highly Virulent Strain 05ZYH33[J].Journal of Nanjing Normal University(Natural Science Edition),2009,32(02):87-92.
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2型猪链球菌中国强毒株05ZYH33 ofs N-片段基因敲除株的构建()
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《南京师大学报(自然科学版)》[ISSN:1001-4616/CN:32-1239/N]

卷:
第32卷
期数:
2009年02期
页码:
87-92
栏目:
生命科学
出版日期:
2009-06-30

文章信息/Info

Title:
Deletion of the N-terminal Fragment of ofs Gene in Streptococcus Suis Serotype 2 Chinese Highly Virulent Strain 05ZYH33
作者:
史沛举1 2 郝喜娜1 2 葛俊超1 2 王长军2 王晶2 潘秀珍1 2 唐家琪2
1. 南京师范大学生命科学学院, 江苏南京210046
2. 南京军区军事医学研究所, 江苏南京210002
Author(s):
Shi Peiju12Hao Xina12Ge Junchao12Wang Changjun2Wang Jing2Pan Xiuzhen12Tang Jiaqi2
1.School of Life Sciences,Nanjing Normal University,Nanjing 210046,China
关键词:
2型猪链球菌 of s 基因敲除株
Keywords:
strep to coccus suis sero type 2 ofs gene knock -out mutant
分类号:
R378.12
摘要:
通过生物信息学分析2型猪链球菌(Streptococcus suisserotype 2,S.suis2)中国强毒株05ZYH33的基因组,预测并发现猪链球菌血清浑浊因子(Opacity factor ofS.suis,OFS)的编码基因ofs.为了构建ofsN-末端片段ofs 37-683的基因敲除株,首先构建中间为壮观霉素抗性基因,两侧为ofs 37-683上、下游同源序列的基因敲除质粒,并对该质粒进行PCR和酶切鉴定.根据同源重组的原理,通过电转化方法筛选得到ofs 37-683基因敲除株.PCR、测序和RT- PCR 分析结果均显示ofs 37- 683已完全被壮观霉素抗性基因替代, 证实of s 37- 683基因敲除株构建成功. 该敲除株的获得为进一步研究ofs 在猪链球菌2型致病机制中的作用奠定基础.
Abstract:
The gene o f Opac ity factor o fS. suis ( ofs) w as pred icted in the g enom e o fS trep tococcus suis sero type 2 (S. su- is 2) Chinese h ighly v iru lent stra in 05ZYH 33 and its prote in structure was charac terized w ith B io informa tics too ls. To de lete theN term ina l fragment of ofs in 05ZYH 33, recom b inant gene knock ou t p lasm id w ith a Sp cr casse tte flanked w ith hom o logy arm s was constructed. The p lasm id w as confirm ed by PCR and restriction enzym e d igestion. Accord ing to the pr inciple of hom ologous recom b ina tion, the isogenic of s 37- 683 de fic ient mutant was screened through e lectroporation transform ation. PCR am plication, sequenc ing o f its produc t and RT - PCR analysis con firm ed that the target gene was replaced by Sp crcassette. Th is m utated 05ZYH 33 provided a potent too l fo r assessing the role of ofs in the S. suis 2 infection.

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备注/Memo

备注/Memo:
基金项目: 国家自然科学基金( 30730081, 30600533, 30670105 )、江苏省自然科学基金( BK 2007013, BK2008066)、南京军区医学科技创新课题( 07Z045 )、南京军区卫生专业人才培养“ 122”工程项目.
通讯联系人: 潘秀珍, 博士, 研究员, 研究方向: 自然疫源性疾病病原等. E-m ail: panxiu zhen- 2004@ 163. com
更新日期/Last Update: 2013-04-23