• 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
Characterization of the effects of salicylidene acylhydrazide compounds on type III secretion in Escherichia coli O157:H7.水杨醛酰肼化合物对大肠杆菌O157:H7Ⅲ型分泌作用的表征
Infect Immun. 2009 Oct;77(10):4209-20. doi: 10.1128/IAI.00562-09. Epub 2009 Jul 27.
2
Identification of bacterial target proteins for the salicylidene acylhydrazide class of virulence-blocking compounds.鉴定水杨酰腙类毒力阻断化合物的细菌靶蛋白。
J Biol Chem. 2011 Aug 26;286(34):29922-31. doi: 10.1074/jbc.M111.233858. Epub 2011 Jul 1.
3
Type III Secretion-Dependent Sensitivity of Escherichia coli O157 to Specific Ketolides.大肠杆菌O157对特定酮内酯的III型分泌依赖性敏感性
Antimicrob Agents Chemother. 2015 Nov 2;60(1):459-70. doi: 10.1128/AAC.02085-15. Print 2016 Jan.
4
Coumarins reduce biofilm formation and the virulence of Escherichia coli O157:H7.香豆素可减少大肠杆菌O157:H7的生物膜形成及毒力。
Phytomedicine. 2014 Jul-Aug;21(8-9):1037-42. doi: 10.1016/j.phymed.2014.04.008. Epub 2014 May 15.
5
Enterohaemorrhagic Escherichia coli O157:H7 target Peyer's patches in humans and cause attaching/effacing lesions in both human and bovine intestine.肠出血性大肠杆菌O157:H7侵袭人类的派尔集合淋巴结,并在人和牛的肠道中引发黏附-抹除性病变。
Gut. 2000 Sep;47(3):377-81. doi: 10.1136/gut.47.3.377.
6
Salicylidene acylhydrazides that affect type III protein secretion in Salmonella enterica serovar typhimurium.影响鼠伤寒沙门氏菌III型蛋白分泌的水杨醛酰肼类化合物。
Antimicrob Agents Chemother. 2007 Aug;51(8):2867-76. doi: 10.1128/AAC.00223-07. Epub 2007 Jun 4.
7
Inhibitory effects of broccoli extract on Escherichia coli O157:H7 quorum sensing and in vivo virulence.西兰花提取物对大肠杆菌 O157:H7 群体感应的抑制作用及其体内毒力。
FEMS Microbiol Lett. 2011 Aug;321(1):67-74. doi: 10.1111/j.1574-6968.2011.02311.x. Epub 2011 Jun 6.
8
Differences in adherence and virulence gene expression between two outbreak strains of enterohaemorrhagic Escherichia coli O157 : H7.两株肠出血性大肠杆菌 O157:H7 暴发菌株在黏附和毒力基因表达方面的差异。
Microbiology (Reading). 2010 Feb;156(Pt 2):408-419. doi: 10.1099/mic.0.033126-0. Epub 2009 Nov 5.
9
An investigation of the expression and adhesin function of H7 flagella in the interaction of Escherichia coli O157 : H7 with bovine intestinal epithelium.大肠杆菌O157:H7与牛肠上皮细胞相互作用中H7鞭毛的表达及黏附功能研究
Cell Microbiol. 2009 Jan;11(1):121-37. doi: 10.1111/j.1462-5822.2008.01244.x. Epub 2008 Oct 30.
10
Escherichia coli O157:H7 strains that persist in feedlot cattle are genetically related and demonstrate an enhanced ability to adhere to intestinal epithelial cells.存在于饲养场牛群中的大肠杆菌O157:H7菌株具有遗传相关性,并表现出更强的黏附于肠道上皮细胞的能力。
Appl Environ Microbiol. 2009 Sep;75(18):5927-37. doi: 10.1128/AEM.00972-09. Epub 2009 Jul 17.

引用本文的文献

1
Enterohaemorrhagic AdhE spirosome length correlates with enzymatic directionality and is perturbed by salicylidene acylhydrazides.肠出血性埃希氏菌黏附素螺旋体长度与酶促方向性相关,并受到水杨醛酰肼的干扰。
Open Biol. 2025 Jun;15(6):250041. doi: 10.1098/rsob.250041. Epub 2025 Jun 18.
2
Beyond Antibiotics: What the Future Holds.超越抗生素:未来会怎样。
Antibiotics (Basel). 2024 Sep 25;13(10):919. doi: 10.3390/antibiotics13100919.
3
Using next generation antimicrobials to target the mechanisms of infection.使用新一代抗菌药物来针对感染机制。
NPJ Antimicrob Resist. 2023;1(1):11. doi: 10.1038/s44259-023-00011-6. Epub 2023 Sep 22.
4
Targeting bacterial pathogenesis by inhibiting virulence-associated Type III and Type IV secretion systems.通过抑制与毒力相关的 III 型和 IV 型分泌系统来靶向细菌发病机制。
Front Cell Infect Microbiol. 2023 Jan 10;12:1065561. doi: 10.3389/fcimb.2022.1065561. eCollection 2022.
5
Five Plant Natural Products Are Potential Type III Secretion System Inhibitors to Effectively Control Soft-Rot Disease Caused by .五种植物天然产物是潜在的III型分泌系统抑制剂,可有效控制由……引起的软腐病。
Front Microbiol. 2022 Feb 22;13:839025. doi: 10.3389/fmicb.2022.839025. eCollection 2022.
6
Developing Cyclic Peptomers as Broad-Spectrum Type III Secretion System Inhibitors in Gram-Negative Bacteria.开发环状缩肽作为革兰氏阴性菌中广谱 III 型分泌系统抑制剂。
Antimicrob Agents Chemother. 2021 Jun 17;65(7):e0169020. doi: 10.1128/AAC.01690-20.
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
Innovation and Application of the Type III Secretion System Inhibitors in Plant Pathogenic Bacteria.III型分泌系统抑制剂在植物病原菌中的创新与应用
Microorganisms. 2020 Dec 9;8(12):1956. doi: 10.3390/microorganisms8121956.
9
On the road to structure-based development of anti-virulence therapeutics targeting the type III secretion system injectisome.在基于结构开发针对III型分泌系统注射体的抗毒力疗法的道路上。
Medchemcomm. 2019 Jun 20;10(8):1273-1289. doi: 10.1039/c9md00146h. eCollection 2019 Aug 1.
10
Transcriptional responses of Xanthomonas oryzae pv. oryzae to type III secretion system inhibitor ortho-coumaric acid.稻黄单胞菌对 III 型分泌系统抑制剂对香豆酸的转录反应。
BMC Microbiol. 2019 Jul 15;19(1):163. doi: 10.1186/s12866-019-1532-5.

本文引用的文献

1
Genomic instability in regions adjacent to a highly conserved pch prophage in Escherichia coli O157:H7 generates diversity in expression patterns of the LEE pathogenicity island.大肠杆菌O157:H7中高度保守的pch原噬菌体相邻区域的基因组不稳定性导致LEE致病岛表达模式的多样性。
J Bacteriol. 2009 Jun;191(11):3553-68. doi: 10.1128/JB.01738-08. Epub 2009 Mar 27.
2
An investigation of the expression and adhesin function of H7 flagella in the interaction of Escherichia coli O157 : H7 with bovine intestinal epithelium.大肠杆菌O157:H7与牛肠上皮细胞相互作用中H7鞭毛的表达及黏附功能研究
Cell Microbiol. 2009 Jan;11(1):121-37. doi: 10.1111/j.1462-5822.2008.01244.x. Epub 2008 Oct 30.
3
Super-shedding and the link between human infection and livestock carriage of Escherichia coli O157.超量排菌以及人类感染与大肠杆菌O157在牲畜中携带之间的联系。
Nat Rev Microbiol. 2008 Dec;6(12):904-12. doi: 10.1038/nrmicro2029.
4
Small-molecule type III secretion system inhibitors block assembly of the Shigella type III secreton.小分子III型分泌系统抑制剂可阻断志贺氏菌III型分泌装置的组装。
J Bacteriol. 2009 Jan;191(2):563-70. doi: 10.1128/JB.01004-08. Epub 2008 Nov 7.
5
Targeting QseC signaling and virulence for antibiotic development.靶向QseC信号传导和毒力用于抗生素研发。
Science. 2008 Aug 22;321(5892):1078-80. doi: 10.1126/science.1160354.
6
Virulence blockers as alternatives to antibiotics: type III secretion inhibitors against Gram-negative bacteria.作为抗生素替代品的毒力阻断剂:针对革兰氏阴性菌的III型分泌抑制剂
J Intern Med. 2008 Jul;264(1):17-29. doi: 10.1111/j.1365-2796.2008.01941.x. Epub 2008 Apr 3.
7
Global regulation by horizontally transferred regulators establishes the pathogenicity of Escherichia coli.通过水平转移的调节因子进行的全局调控确立了大肠杆菌的致病性。
DNA Res. 2008 Feb 29;15(1):25-38. doi: 10.1093/dnares/dsm033. Epub 2008 Jan 25.
8
RegulonDB (version 6.0): gene regulation model of Escherichia coli K-12 beyond transcription, active (experimental) annotated promoters and Textpresso navigation.RegulonDB(版本6.0):大肠杆菌K-12超越转录的基因调控模型、活跃(实验性)注释启动子及Textpresso导航
Nucleic Acids Res. 2008 Jan;36(Database issue):D120-4. doi: 10.1093/nar/gkm994. Epub 2007 Dec 23.
9
Efficacy of dose regimen and observation of herd immunity from a vaccine against Escherichia coli O157:H7 for feedlot cattle.针对育肥牛的大肠杆菌O157:H7疫苗剂量方案的疗效及群体免疫观察
J Food Prot. 2007 Nov;70(11):2561-7. doi: 10.4315/0362-028x-70.11.2561.
10
Enteropathogenic and enterohemorrhagic Escherichia coli virulence gene regulation.肠致病性和肠出血性大肠杆菌毒力基因调控
Infect Immun. 2007 Sep;75(9):4199-210. doi: 10.1128/IAI.01927-06. Epub 2007 Jun 18.

水杨醛酰肼化合物对大肠杆菌O157:H7Ⅲ型分泌作用的表征

Characterization of the effects of salicylidene acylhydrazide compounds on type III secretion in Escherichia coli O157:H7.

作者信息

Tree Jai J, Wang Dai, McInally Carol, Mahajan Arvind, Layton Abigail, Houghton Irene, Elofsson Mikael, Stevens Mark P, Gally David L, Roe Andrew J

机构信息

Zoonotic and Animal Pathogens Research Laboratory, Immunity and Infection Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, 49 Little France Crescent, Edinburgh EH16 4SB, United Kingdom.

出版信息

Infect Immun. 2009 Oct;77(10):4209-20. doi: 10.1128/IAI.00562-09. Epub 2009 Jul 27.

DOI:10.1128/IAI.00562-09
PMID:19635828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2747932/
Abstract

Recent work has highlighted a number of compounds that target bacterial virulence by affecting gene regulation. In this work, we show that small-molecule inhibitors affect the expression of the type III secretion system (T3SS) of Escherichia coli O157:H7 in liquid culture and when this bacterium is attached to bovine epithelial cells. Inhibition of T3SS expression resulted in a reduction in the capacity of the bacteria to form attaching and effacing lesions. Our results show that there is marked variation in the abilities of four structurally related compounds to inhibit the T3SS of a panel of isolates. Using transcriptomics, we performed a comprehensive analysis of the conserved and inhibitor-specific transcriptional responses to these four compounds. These analyses of gene expression show that numerous virulence genes, located on horizontally acquired DNA elements, are affected by the compounds, but the number of genes significantly affected varied markedly for the different compounds. Overall, we highlight the importance of assessing the effect of such "antivirulence" agents on a range of isolates and discuss the possible mechanisms which may lead to the coordinate downregulation of horizontally acquired virulence genes.

摘要

近期的研究工作突出了一些通过影响基因调控来靶向细菌毒力的化合物。在本研究中,我们表明小分子抑制剂在液体培养中以及当大肠杆菌O157:H7附着于牛上皮细胞时,会影响其三型分泌系统(T3SS)的表达。T3SS表达的抑制导致细菌形成紧密黏附并抹平损伤的能力降低。我们的结果表明,四种结构相关的化合物抑制一组分离株的T3SS的能力存在显著差异。利用转录组学,我们对这四种化合物的保守和抑制剂特异性转录反应进行了全面分析。这些基因表达分析表明,位于水平获得的DNA元件上的众多毒力基因受到这些化合物的影响,但不同化合物显著影响的基因数量差异明显。总体而言,我们强调评估此类“抗毒力”药物对一系列分离株的影响的重要性,并讨论可能导致水平获得的毒力基因协同下调的潜在机制。