• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伤寒沙门氏菌Vi抗原B区域的分子克隆

Molecular cloning of the ViaB region of Salmonella typhi.

作者信息

Hashimoto Y, Ezaki T, Li N, Yamamoto H

机构信息

Department of Microbiology, Gifu University School of Medicine, Japan.

出版信息

FEMS Microbiol Lett. 1991 Dec 15;69(1):53-6. doi: 10.1016/0378-1097(91)90645-q.

DOI:10.1016/0378-1097(91)90645-q
PMID:1664401
Abstract

The ViaB region required for Vi antigen production in Salmonella typhi was cloned. The plasmid pGBM124 containing a 14-kb S. typhi chromosomal DNA fragment conferred the ability to produce Vi antigen on Escherichia coli HB101 and ViaB-deleted S. typhi GIFU10007-3. Tn5 insertion analysis showed that the 14-kb DNA was split into three regions. Region 1 and region 2 are involved in the biosynthesis of Vi polysaccharide. Region 3 is involved in translocation of the Vi polysaccharide to the cell surface. Southern blot hybridization showed that regions 2 and 3 but not region 1, were considerably homologous to the DNA of Vi-positive Citrobacter freundii.

摘要

伤寒沙门氏菌中Vi抗原产生所需的ViaB区域被克隆。含有14kb伤寒沙门氏菌染色体DNA片段的质粒pGBM124赋予大肠杆菌HB101和缺失ViaB的伤寒沙门氏菌GIFU10007-3产生Vi抗原的能力。Tn5插入分析表明,14kb的DNA被分成三个区域。区域1和区域2参与Vi多糖的生物合成。区域3参与Vi多糖向细胞表面的转运。Southern印迹杂交表明,区域2和区域3而非区域1与Vi阳性弗氏柠檬酸杆菌的DNA有相当高的同源性。

相似文献

1
Molecular cloning of the ViaB region of Salmonella typhi.伤寒沙门氏菌Vi抗原B区域的分子克隆
FEMS Microbiol Lett. 1991 Dec 15;69(1):53-6. doi: 10.1016/0378-1097(91)90645-q.
2
The Vi antigen of Salmonella typhi: molecular analysis of the viaB locus.伤寒沙门氏菌的Vi抗原:viaB基因座的分子分析
J Gen Microbiol. 1992 Feb;138(2):297-304. doi: 10.1099/00221287-138-2-297.
3
Complete nucleotide sequence and molecular characterization of ViaB region encoding Vi antigen in Salmonella typhi.伤寒沙门氏菌中编码Vi抗原的ViaB区域的完整核苷酸序列及分子特征
J Bacteriol. 1993 Jul;175(14):4456-65. doi: 10.1128/jb.175.14.4456-4465.1993.
4
Comparison of ViaB regions of Vi-positive organisms.Vi阳性生物体的Vi抗原区域比较。
FEMS Microbiol Lett. 1997 Dec 1;157(1):55-7. doi: 10.1111/j.1574-6968.1997.tb12752.x.
5
Expression of Vi antigen in Escherichia coli K-12: characterization of ViaB from Citrobacter freundii and identity of ViaA with RcsB.大肠杆菌K-12中Vi抗原的表达:弗氏柠檬酸杆菌ViaB的特性及ViaA与RcsB的同一性
J Bacteriol. 1992 Sep;174(18):5910-5. doi: 10.1128/jb.174.18.5910-5915.1992.
6
Role of the viaB locus in synthesis, transport and expression of Salmonella typhi Vi antigen.ViA位点在伤寒沙门氏菌Vi抗原合成、转运及表达中的作用。
Microbiology (Reading). 1995 Dec;141 ( Pt 12):3039-47. doi: 10.1099/13500872-141-12-3039.
7
Specific insertion and deletion of insertion sequence 1-like DNA element causes the reversible expression of the virulence capsular antigen Vi of Citrobacter freundii in Escherichia coli.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4402-5. doi: 10.1073/pnas.85.12.4402.
8
Development of a DNA probe to detect Salmonella typhi.用于检测伤寒沙门氏菌的DNA探针的研制。
J Clin Microbiol. 1985 Oct;22(4):600-5. doi: 10.1128/jcm.22.4.600-605.1985.
9
Characterization of the rcsA and rcsB genes from Salmonella typhi: rcsB through tviA is involved in regulation of Vi antigen synthesis.伤寒沙门氏菌rcsA和rcsB基因的特性:rcsB通过tviA参与Vi抗原合成的调控。
J Bacteriol. 1996 Mar;178(6):1691-8. doi: 10.1128/jb.178.6.1691-1698.1996.
10
Characterization of defined ompR mutants of Salmonella typhi: ompR is involved in the regulation of Vi polysaccharide expression.伤寒沙门氏菌特定ompR突变体的特性:ompR参与Vi多糖表达的调控。
Infect Immun. 1994 Sep;62(9):3984-93. doi: 10.1128/iai.62.9.3984-3993.1994.

引用本文的文献

1
The invasome of Salmonella Dublin as revealed by whole genome sequencing.通过全基因组测序揭示的都柏林沙门氏菌侵袭体
BMC Infect Dis. 2017 Aug 4;17(1):544. doi: 10.1186/s12879-017-2628-x.
2
Molecular characterization of the viaB locus encoding the biosynthetic machinery for Vi capsule formation in Salmonella Typhi.志贺氏菌属生物合成 Vi 荚膜形成的 viaB 基因座的分子特征。
PLoS One. 2012;7(9):e45609. doi: 10.1371/journal.pone.0045609. Epub 2012 Sep 21.
3
Structure, diversity, and mobility of the Salmonella pathogenicity island 7 family of integrative and conjugative elements within Enterobacteriaceae.
肠杆菌科中沙门氏菌致病性岛 7 家族的整合和共轭元件的结构、多样性和迁移性。
J Bacteriol. 2012 Mar;194(6):1494-504. doi: 10.1128/JB.06403-11. Epub 2012 Jan 13.
4
A safe vaccine (DV-STM-07) against Salmonella infection prevents abortion and confers protective immunity to the pregnant and new born mice.一种安全的沙门氏菌感染疫苗(DV-STM-07)可预防流产,并为怀孕和新生小鼠提供保护免疫力。
PLoS One. 2010 Feb 10;5(2):e9139. doi: 10.1371/journal.pone.0009139.
5
Regulation of Vi capsular polysaccharide synthesis in Salmonella enterica serotype Typhi.伤寒沙门氏菌中Vi荚膜多糖合成的调控。
J Infect Dev Ctries. 2008 Dec 1;2(6):412-20. doi: 10.3855/jidc.154.
6
The capsule encoding the viaB locus reduces interleukin-17 expression and mucosal innate responses in the bovine intestinal mucosa during infection with Salmonella enterica serotype Typhi.在感染伤寒沙门氏菌血清型伤寒期间,编码viaB位点的荚膜会降低牛肠道黏膜中白细胞介素-17的表达和黏膜固有免疫反应。
Infect Immun. 2007 Sep;75(9):4342-50. doi: 10.1128/IAI.01571-06. Epub 2007 Jun 25.
7
Vi antigen expression in Salmonella enterica serovar Typhi clinical isolates from Pakistan.来自巴基斯坦的伤寒沙门氏菌临床分离株中Vi抗原的表达。
J Clin Microbiol. 2005 Mar;43(3):1158-65. doi: 10.1128/JCM.43.3.1158-1165.2005.
8
Positive autoregulation of vipR expression in ViaB region-encoded Vi antigen of Salmonella typhi.伤寒沙门氏菌Viab区域编码的Vi抗原中vipR表达的正自调控
J Bacteriol. 1996 Mar;178(5):1430-6. doi: 10.1128/jb.178.5.1430-1436.1996.
9
Regulation of expression of group IA capsular polysaccharides in Escherichia coli and related extracellular polysaccharides in other bacteria.大肠杆菌中IA族荚膜多糖及其他细菌中相关胞外多糖表达的调控。
J Ind Microbiol. 1995 Oct;15(4):361-71. doi: 10.1007/BF01569992.
10
Complete nucleotide sequence and molecular characterization of ViaB region encoding Vi antigen in Salmonella typhi.伤寒沙门氏菌中编码Vi抗原的ViaB区域的完整核苷酸序列及分子特征
J Bacteriol. 1993 Jul;175(14):4456-65. doi: 10.1128/jb.175.14.4456-4465.1993.