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本文引用的文献

1
Vibrio cholerae leuO Transcription Is Positively Regulated by ToxR and Contributes to Bile Resistance.霍乱弧菌leuO转录受ToxR正调控并有助于胆汁抵抗。
J Bacteriol. 2015 Nov;197(22):3499-510. doi: 10.1128/JB.00419-15. Epub 2015 Aug 24.
2
Stationary-phase induction of vvpS expression by three transcription factors: repression by LeuO and activation by SmcR and CRP.三种转录因子对vvpS表达的稳定期诱导:LeuO的抑制作用以及SmcR和CRP的激活作用。
Mol Microbiol. 2015 Jul;97(2):330-46. doi: 10.1111/mmi.13028. Epub 2015 May 9.
3
Vibrio cholerae ToxR downregulates virulence factor production in response to cyclo(Phe-Pro).霍乱弧菌 ToxR 通过响应环(苯丙氨酸-脯氨酸)下调毒力因子的产生。
mBio. 2013 Aug 27;4(5):e00366-13. doi: 10.1128/mBio.00366-13.
4
Effects of polyamines on Vibrio cholerae virulence properties.多胺对霍乱弧菌毒力特性的影响。
PLoS One. 2013 Apr 10;8(4):e60765. doi: 10.1371/journal.pone.0060765. Print 2013.
5
The Vibrio parahaemolyticus ToxRS regulator is required for stress tolerance and colonization in a novel orogastric streptomycin-induced adult murine model.副溶血性弧菌 ToxRS 调节子是一种新型经口给予链霉素诱导的成年鼠模型中应激耐受和定植所必需的。
Infect Immun. 2012 May;80(5):1834-45. doi: 10.1128/IAI.06284-11. Epub 2012 Mar 5.
6
Comparative genomics of Vibrio cholerae from Haiti, Asia, and Africa.海地、亚洲和非洲霍乱弧菌的比较基因组学研究。
Emerg Infect Dis. 2011 Nov;17(11):2113-21. doi: 10.3201/eid1711.110794.
7
Novel roles of LeuO in transcription regulation of E. coli genome: antagonistic interplay with the universal silencer H-NS.LeuO 在大肠杆菌基因组转录调控中的新作用:与通用沉默子 H-NS 的拮抗相互作用。
Mol Microbiol. 2011 Oct;82(2):378-97. doi: 10.1111/j.1365-2958.2011.07818.x. Epub 2011 Sep 14.
8
The LysR-type virulence activator AphB regulates the expression of genes in Vibrio cholerae in response to low pH and anaerobiosis.LysR 型毒力激活因子 AphB 响应低 pH 值和无氧环境调节霍乱弧菌基因的表达。
J Bacteriol. 2010 Aug;192(16):4181-91. doi: 10.1128/JB.00193-10. Epub 2010 Jun 18.
9
Growth in a biofilm induces a hyperinfectious phenotype in Vibrio cholerae.生物膜中的生长会诱导霍乱弧菌产生超感染表型。
Infect Immun. 2010 Aug;78(8):3560-9. doi: 10.1128/IAI.00048-10. Epub 2010 Jun 1.
10
The cyclic dipeptide cyclo(Phe-Pro) inhibits cholera toxin and toxin-coregulated pilus production in O1 El Tor Vibrio cholerae.环二肽环(苯丙氨酸-脯氨酸)抑制 O1 型埃尔托霍乱弧菌的霍乱毒素和毒素调节菌毛的产生。
J Bacteriol. 2010 Jul;192(14):3829-32. doi: 10.1128/JB.00191-10. Epub 2010 May 7.

LysR 型调节因子 LeuO 调控霍乱弧菌的耐酸反应。

The LysR-type regulator LeuO regulates the acid tolerance response in Vibrio cholerae.

作者信息

Ante Vanessa M, Bina X Renee, Bina James E

机构信息

Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

出版信息

Microbiology (Reading). 2015 Dec;161(12):2434-43. doi: 10.1099/mic.0.000194. Epub 2015 Sep 29.

DOI:10.1099/mic.0.000194
PMID:26424466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4811655/
Abstract

Vibrio cholerae is a neutrophilic enteric pathogen that is extremely sensitive to acid. As V. cholerae passages through the host gastrointestinal tract it is exposed to a variety of environmental stresses including low pH and volatile fatty acids. Exposure to acidic environments induces expression of the V. cholerae acid tolerance response. A key component of the acid tolerance response is the cad system, which is encoded by cadC and the cadBA operon. CadB is a lysine/cadaverine antiporter and CadA is a lysine decarboxylase and these function together to counter low intracellular and extracellular pH. CadC is a membrane-associated transcription factor that activates cadBA expression in response to acidic conditions. Herein we investigated the role of the LysR-type transcriptional regulator LeuO in the V. cholerae acid tolerance response. Transcriptional reporter assays revealed that leuO expression repressed cadC transcription, indicating that LeuO was a cadC repressor. Consistent with this, leuO expression was inversely linked to lysine decarboxylase production and leuO overexpression resulted in increased sensitivity to organic acids. Overexpression of leuO in a cadA mutant potentiated killing by organic acids, suggesting that the function of leuO in the acid tolerance response extended beyond its regulation of the cad system. Collectively, these studies have identified a new physiological role for LeuO in V. cholerae acid tolerance.

摘要

霍乱弧菌是一种嗜中性肠道病原体,对酸极为敏感。当霍乱弧菌通过宿主胃肠道时,它会受到包括低pH值和挥发性脂肪酸在内的各种环境压力。暴露于酸性环境会诱导霍乱弧菌酸耐受反应的表达。酸耐受反应的一个关键组成部分是cad系统,它由cadC和cadBA操纵子编码。CadB是一种赖氨酸/尸胺反向转运蛋白,CadA是一种赖氨酸脱羧酶,它们共同作用以应对细胞内和细胞外的低pH值。CadC是一种膜相关转录因子,可响应酸性条件激活cadBA的表达。在此,我们研究了LysR型转录调节因子LeuO在霍乱弧菌酸耐受反应中的作用。转录报告分析表明,leuO的表达抑制了cadC的转录,表明LeuO是cadC的阻遏物。与此一致的是,leuO的表达与赖氨酸脱羧酶的产生呈负相关,并且leuO的过表达导致对有机酸的敏感性增加。在cadA突变体中过表达leuO增强了有机酸的杀伤作用,这表明leuO在酸耐受反应中的功能超出了其对cad系统的调节。总的来说,这些研究确定了LeuO在霍乱弧菌酸耐受中的新生理作用。