• 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

相似文献

1
vttRA and vttRB Encode ToxR family proteins that mediate bile-induced expression of type three secretion system genes in a non-O1/non-O139 Vibrio cholerae strain.vttRA 和 vttRB 编码 ToxR 家族蛋白,这些蛋白介导非 O1/O139 霍乱弧菌株中胆汁诱导的 III 型分泌系统基因的表达。
Infect Immun. 2010 Jun;78(6):2554-70. doi: 10.1128/IAI.01073-09. Epub 2010 Apr 12.
2
Regulation by ToxR-Like Proteins Converges on vttRB Expression To Control Type 3 Secretion System-Dependent Caco2-BBE Cytotoxicity in Vibrio cholerae.类ToxR蛋白的调控作用集中于vttRB表达,以控制霍乱弧菌中依赖Ⅲ型分泌系统的Caco2-BBE细胞毒性。
J Bacteriol. 2016 May 13;198(11):1675-1682. doi: 10.1128/JB.00130-16. Print 2016 Jun 1.
3
The Vibrio cholerae trh gene is coordinately regulated in vitro with type III secretion system genes by VttR(A)/VttR(B) but does not contribute to Caco2-BBE cell cytotoxicity.霍乱弧菌 trh 基因在体外与 III 型分泌系统基因由 VttR(A)/VttR(B)共同调控,但不影响 Caco2-BBE 细胞的细胞毒性。
Infect Immun. 2012 Dec;80(12):4444-55. doi: 10.1128/IAI.00832-12. Epub 2012 Oct 8.
4
Vibrio cholerae VttR(A) and VttR(B) regulatory influences extend beyond the type 3 secretion system genomic island.霍乱弧菌 VttR(A) 和 VttR(B) 的调控影响超出了 III 型分泌系统基因组岛。
J Bacteriol. 2013 May;195(10):2424-36. doi: 10.1128/JB.02151-12. Epub 2013 Mar 22.
5
Identification of Vibrio cholerae type III secretion system effector proteins.霍乱弧菌 III 型分泌系统效应蛋白的鉴定。
Infect Immun. 2011 Apr;79(4):1728-40. doi: 10.1128/IAI.01194-10. Epub 2011 Jan 31.
6
ToxR regulates virulence gene expression in non-O1 strains of Vibrio cholerae that cause epidemic cholera.ToxR调节引起霍乱流行的霍乱弧菌非O1菌株中的毒力基因表达。
Infect Immun. 1994 Jan;62(1):72-8. doi: 10.1128/iai.62.1.72-78.1994.
7
[Chilean strains of clinical origin of non-O1, non-O139 Vibrio cholerae carry the genes vcsN2, vcsC2, vcsV2, vspD, toxR2 y vopF from secretion system T3SS2 present in an island of pathogenicity].[来自非O1、非O139霍乱弧菌临床分离株的智利菌株携带存在于一个致病岛中的III型分泌系统(T3SS2)的vcsN2、vcsC2、vcsV2、vspD、toxR2和vopF基因]
Rev Chilena Infectol. 2019 Jun;36(3):312-317. doi: 10.4067/S0716-10182019000300312.
8
Vibrio pathogenicity island and cholera toxin genetic element-associated virulence genes and their expression in non-O1 non-O139 strains of Vibrio cholerae.霍乱弧菌致病性岛和霍乱毒素遗传元件相关的毒力基因及其在霍乱弧菌非O1非O139菌株中的表达
Infect Immun. 2002 Aug;70(8):4735-42. doi: 10.1128/IAI.70.8.4735-4742.2002.
9
DksA coordinates bile-mediated regulation of virulence-associated phenotypes in type three secretion system-positive .DksA 协调胆盐介导的 III 型分泌系统阳性菌毒力相关表型的调控。
Microbiology (Reading). 2021 Feb;167(2). doi: 10.1099/mic.0.001006.
10
Molecular analysis of Vibrio cholerae O1, O139, non-O1, and non-O139 strains: clonal relationships between clinical and environmental isolates.霍乱弧菌O1、O139、非O1和非O139菌株的分子分析:临床分离株与环境分离株之间的克隆关系
Appl Environ Microbiol. 2001 Feb;67(2):910-21. doi: 10.1128/AEM.67.2.910-921.2001.

引用本文的文献

1
Antagonistic Effects of Actin-Specific Toxins on Typhimurium Invasion into Mammalian Cells.肌动蛋白特异性毒素对鼠伤寒沙门氏菌侵袭哺乳动物细胞的拮抗作用。
Biomolecules. 2024 Nov 9;14(11):1428. doi: 10.3390/biom14111428.
2
Antagonistic effects of actin-specific toxins on Typhimurium invasion into mammalian cells.肌动蛋白特异性毒素对鼠伤寒沙门氏菌侵入哺乳动物细胞的拮抗作用。
bioRxiv. 2024 Jul 2:2024.07.01.601609. doi: 10.1101/2024.07.01.601609.
3
An essential host dietary fatty acid promotes TcpH inhibition of TcpP proteolysis promoting virulence gene expression in .必需宿主膳食脂肪酸促进 TcpH 抑制 TcpP 蛋白水解,从而促进 中的毒力基因表达。
mBio. 2024 Aug 14;15(8):e0072124. doi: 10.1128/mbio.00721-24. Epub 2024 Jul 3.
4
Transmembrane Transcription Regulators Are Widespread in Bacteria and Archaea.跨膜转录调控因子在细菌和古菌中广泛存在。
Microbiol Spectr. 2023 Jun 15;11(3):e0026623. doi: 10.1128/spectrum.00266-23. Epub 2023 May 8.
5
Structural Insights into Regulation of Vibrio Virulence Gene Networks.结构洞察弧菌毒力基因网络的调控。
Adv Exp Med Biol. 2023;1404:269-294. doi: 10.1007/978-3-031-22997-8_14.
6
PsaF Is a Membrane-Localized pH Sensor That Regulates Expression in .PsaF 是一种膜定位的 pH 传感器,调节 在 中的表达。
J Bacteriol. 2021 Jul 22;203(16):e0016521. doi: 10.1128/JB.00165-21.
7
Molecular Targets and Strategies for Inhibition of the Bacterial Type III Secretion System (T3SS); Inhibitors Directly Binding to T3SS Components.抑制细菌 III 型分泌系统(T3SS)的分子靶点和策略;直接结合 T3SS 成分的抑制剂。
Biomolecules. 2021 Feb 19;11(2):316. doi: 10.3390/biom11020316.
8
DksA coordinates bile-mediated regulation of virulence-associated phenotypes in type three secretion system-positive .DksA 协调胆盐介导的 III 型分泌系统阳性菌毒力相关表型的调控。
Microbiology (Reading). 2021 Feb;167(2). doi: 10.1099/mic.0.001006.
9
Virulence Regulation and Innate Host Response in the Pathogenicity of .毒力调控与固有宿主反应在致病性中的作用
Front Cell Infect Microbiol. 2020 Sep 30;10:572096. doi: 10.3389/fcimb.2020.572096. eCollection 2020.
10
Animal Models of Type III Secretion System-Mediated Pathogenesis.III型分泌系统介导的发病机制的动物模型
Pathogens. 2019 Nov 22;8(4):257. doi: 10.3390/pathogens8040257.

本文引用的文献

1
Hfq negatively regulates type III secretion in EHEC and several other pathogens.Hfq对肠出血性大肠杆菌及其他几种病原体中的III型分泌起负调控作用。
Mol Microbiol. 2009 Oct;74(2):347-63. doi: 10.1111/j.1365-2958.2009.06856.x. Epub 2009 Aug 24.
2
Identification and characterization of a novel type III secretion system in trh-positive Vibrio parahaemolyticus strain TH3996 reveal genetic lineage and diversity of pathogenic machinery beyond the species level.对trh阳性副溶血性弧菌菌株TH3996中一种新型III型分泌系统的鉴定和表征揭示了物种水平之外致病机制的遗传谱系和多样性。
Infect Immun. 2009 Feb;77(2):904-13. doi: 10.1128/IAI.01184-08. Epub 2008 Dec 15.
3
The bile response repressor BreR regulates expression of the Vibrio cholerae breAB efflux system operon.胆汁反应阻遏物BreR调节霍乱弧菌breAB外排系统操纵子的表达。
J Bacteriol. 2008 Nov;190(22):7441-52. doi: 10.1128/JB.00584-08. Epub 2008 Sep 5.
4
Putative virulence traits and pathogenicity of Vibrio cholerae Non-O1, Non-O139 isolates from surface waters in Kolkata, India.来自印度加尔各答地表水体的霍乱弧菌非O1、非O139分离株的假定毒力特征及致病性
Appl Environ Microbiol. 2008 Sep;74(18):5635-44. doi: 10.1128/AEM.00029-08. Epub 2008 Jul 18.
5
Vibrio cholerae RND family efflux systems are required for antimicrobial resistance, optimal virulence factor production, and colonization of the infant mouse small intestine.霍乱弧菌RND家族外排系统是抗菌耐药性、最佳毒力因子产生以及在幼鼠小肠中定殖所必需的。
Infect Immun. 2008 Aug;76(8):3595-605. doi: 10.1128/IAI.01620-07. Epub 2008 May 19.
6
Distribution of genes for virulence and ecological fitness among diverse Vibrio cholerae population in a cholera endemic area: tracking the evolution of pathogenic strains.霍乱流行地区不同霍乱弧菌群体中毒力基因和生态适应性基因的分布:追踪致病菌株的进化
DNA Cell Biol. 2008 Jul;27(7):347-55. doi: 10.1089/dna.2008.0737.
7
Deoxycholate interacts with IpaD of Shigella flexneri in inducing the recruitment of IpaB to the type III secretion apparatus needle tip.脱氧胆酸盐在诱导IpaB募集至Ⅲ型分泌装置针尖的过程中与福氏志贺菌的IpaD相互作用。
J Biol Chem. 2008 Jul 4;283(27):18646-54. doi: 10.1074/jbc.M802799200. Epub 2008 May 1.
8
A type III secretion system in Vibrio cholerae translocates a formin/spire hybrid-like actin nucleator to promote intestinal colonization.霍乱弧菌中的III型分泌系统转运一种formin/spire杂合样肌动蛋白成核因子以促进肠道定殖。
Cell Host Microbe. 2007 Apr 19;1(2):95-107. doi: 10.1016/j.chom.2007.03.005.
9
Vibrio cholerae cytolysin is essential for high enterotoxicity and apoptosis induction produced by a cholera toxin gene-negative V. cholerae non-O1, non-O139 strain.霍乱弧菌细胞毒素对于霍乱毒素基因阴性的霍乱弧菌非O1、非O139菌株产生的高肠毒性和诱导细胞凋亡至关重要。
Microb Pathog. 2008 Feb;44(2):118-28. doi: 10.1016/j.micpath.2007.08.013. Epub 2007 Aug 31.
10
Regulatory networks controlling Vibrio cholerae virulence gene expression.控制霍乱弧菌毒力基因表达的调控网络。
Infect Immun. 2007 Dec;75(12):5542-9. doi: 10.1128/IAI.01094-07. Epub 2007 Sep 17.

vttRA 和 vttRB 编码 ToxR 家族蛋白,这些蛋白介导非 O1/O139 霍乱弧菌株中胆汁诱导的 III 型分泌系统基因的表达。

vttRA and vttRB Encode ToxR family proteins that mediate bile-induced expression of type three secretion system genes in a non-O1/non-O139 Vibrio cholerae strain.

机构信息

Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.

出版信息

Infect Immun. 2010 Jun;78(6):2554-70. doi: 10.1128/IAI.01073-09. Epub 2010 Apr 12.

DOI:10.1128/IAI.01073-09
PMID:20385759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2876560/
Abstract

Strain AM-19226 is a pathogenic non-O1/non-O139 serogroup Vibrio cholerae strain that does not encode the toxin-coregulated pilus or cholera toxin but instead causes disease using a type three secretion system (T3SS). Two genes within the T3SS pathogenicity island, herein named vttR(A) (locus tag A33_1664) and vttR(B) (locus tag A33_1675), are predicted to encode proteins that show similarity to the transcriptional regulator ToxR, which is found in all strains of V. cholerae. Strains with a deletion of vttR(A) or vttR(B) showed attenuated colonization in vivo, indicating that the T3SS-encoded regulatory proteins play a role in virulence. lacZ transcriptional reporter fusions to intergenic regions upstream of genes encoding the T3SS structural components identified growth in the presence of bile as a condition that modulates gene expression. Under this condition, VttR(A) and VttR(B) were necessary for maximal gene expression. In contrast, growth in bile did not substantially alter the expression of a reporter fusion to the vopF gene, which encodes an effector protein. Increased vttR(B) reporter fusion activity was observed in a DeltavttR(B) strain background, suggesting that VttR(B) may regulate its own expression. The collective results are consistent with the hypothesis that T3SS-encoded regulatory proteins are essential for pathogenesis and control the expression of selected T3SS genes.

摘要

菌株 AM-19226 是一种致病性非 O1/非 O139 血清群霍乱弧菌菌株,它不编码毒素调节菌毛或霍乱毒素,而是使用 III 型分泌系统(T3SS)引起疾病。T3SS 致病岛中的两个基因,在此命名为 vttR(A)(基因座标签 A33_1664)和 vttR(B)(基因座标签 A33_1675),预测编码与 ToxR 转录调节剂具有相似性的蛋白质,ToxR 存在于所有霍乱弧菌菌株中。vttR(A)或 vttR(B)缺失的菌株在体内定植能力减弱,表明 T3SS 编码的调节蛋白在毒力中发挥作用。与编码 T3SS 结构成分的基因间区上游的 lacZ 转录报告基因融合,鉴定出在胆汁存在的情况下生长是调节基因表达的条件。在这种条件下,VttR(A)和 VttR(B)是最大基因表达所必需的。相比之下,胆汁生长并没有实质性地改变编码效应蛋白的 vopF 基因的报告融合物的表达。在 DeltavttR(B) 菌株背景下观察到 vttR(B)报告融合物活性增加,表明 VttR(B)可能调节其自身表达。总的来说,结果与假设一致,即 T3SS 编码的调节蛋白对发病机制至关重要,并控制选定的 T3SS 基因的表达。