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Infect Immun. 2013 Nov;81(11):4160-70. doi: 10.1128/IAI.00714-13. Epub 2013 Aug 26.
2
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The LspB protein is involved in the secretion of the LspA1 and LspA2 proteins by Haemophilus ducreyi.LspB蛋白参与了杜克雷嗜血杆菌对LspA1和LspA2蛋白的分泌过程。
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Activation of CpxRA in Haemophilus ducreyi primarily inhibits the expression of its targets, including major virulence determinants.在杜克嗜血杆菌中,CpxRA 的激活主要抑制其靶标的表达,包括主要毒力决定因子。
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8
Mutations in the lspA1 and lspA2 genes of Haemophilus ducreyi affect the virulence of this pathogen in an animal model system.杜氏嗜血杆菌lspA1和lspA2基因的突变影响该病原体在动物模型系统中的毒力。
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CpxA Phosphatase Inhibitor Activates CpxRA and Is a Potential Treatment for Uropathogenic Escherichia coli in a Murine Model of Infection.CpxA 磷酸酶抑制剂激活 CpxRA,有望成为尿路感染大肠杆菌感染小鼠模型的潜在治疗方法。
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1
Activation of CpxRA in Haemophilus ducreyi primarily inhibits the expression of its targets, including major virulence determinants.在杜克嗜血杆菌中,CpxRA 的激活主要抑制其靶标的表达,包括主要毒力决定因子。
J Bacteriol. 2013 Aug;195(15):3486-502. doi: 10.1128/JB.00372-13. Epub 2013 May 31.
2
Co-operative roles for DNA supercoiling and nucleoid-associated proteins in the regulation of bacterial transcription.DNA 超螺旋和类核相关蛋白在细菌转录调控中的合作作用。
Biochem Soc Trans. 2013 Apr;41(2):542-7. doi: 10.1042/BST20120222.
3
Carbon storage regulator A contributes to the virulence of Haemophilus ducreyi in humans by multiple mechanisms.碳储存调节剂 A 通过多种机制促进人类杜克雷嗜血杆菌的毒力。
Infect Immun. 2013 Feb;81(2):608-17. doi: 10.1128/IAI.01239-12. Epub 2012 Dec 10.
4
Development of a LacZ-based transcriptional reporter system for use with Moraxella catarrhalis.基于 LacZ 的转录报告系统的开发,用于卡他莫拉菌。
Plasmid. 2013 Mar;69(2):180-5. doi: 10.1016/j.plasmid.2012.11.003. Epub 2012 Dec 4.
5
Permeases of the sap transporter are required for cathelicidin resistance and virulence of Haemophilus ducreyi in humans.猪链球菌通透酶对于人类杜克雷嗜血菌的抗菌肽抗性和毒力是必需的。
J Infect Dis. 2012 Nov;206(9):1407-14. doi: 10.1093/infdis/jis525. Epub 2012 Aug 28.
6
Inhibition of acetyl phosphate-dependent transcription by an acetylatable lysine on RNA polymerase.乙酰磷酸盐依赖型转录的抑制作用由 RNA 聚合酶上的一个可乙酰化赖氨酸介导。
J Biol Chem. 2012 Sep 14;287(38):32147-60. doi: 10.1074/jbc.M112.365502. Epub 2012 Jul 24.
7
Sialylation of lipooligosaccharides is dispensable for the virulence of Haemophilus ducreyi in humans.唾液酸化脂寡糖对于杜克雷嗜血菌在人体中的毒力并非必需。
Infect Immun. 2012 Feb;80(2):679-87. doi: 10.1128/IAI.05826-11. Epub 2011 Dec 5.
8
Expression of the Flp proteins by Haemophilus ducreyi is necessary for virulence in human volunteers.杜克嗜血杆菌 Flp 蛋白的表达对人类志愿者的毒力是必需的。
BMC Microbiol. 2011 Sep 22;11:208. doi: 10.1186/1471-2180-11-208.
9
A Haemophilus ducreyi CpxR deletion mutant is virulent in human volunteers.杜克嗜血杆菌 CpxR 缺失突变体能在人类志愿者中引起毒力。
J Infect Dis. 2011 Jun 15;203(12):1859-65. doi: 10.1093/infdis/jir190.
10
Transcription of the plasmid-encoded toxin gene from enteroaggregative Escherichia coli is regulated by a novel co-activation mechanism involving CRP and Fis.肠聚集性大肠杆菌质粒编码毒素基因的转录受 CRP 和 Fis 共同激活机制调控。
Mol Microbiol. 2011 Jul;81(1):179-91. doi: 10.1111/j.1365-2958.2011.07685.x. Epub 2011 May 18.

杜克雷嗜血杆菌 Fis 蛋白参与控制 lspB-lspA2 操纵子和其他毒力因子的表达。

The Haemophilus ducreyi Fis protein is involved in controlling expression of the lspB-lspA2 operon and other virulence factors.

机构信息

Departments of Microbiology.

出版信息

Infect Immun. 2013 Nov;81(11):4160-70. doi: 10.1128/IAI.00714-13. Epub 2013 Aug 26.

DOI:10.1128/IAI.00714-13
PMID:23980107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3811840/
Abstract

Expression of the lspB-lspA2 operon encoding a virulence-related two-partner secretion system in Haemophilus ducreyi 35000HP is directly regulated by the CpxRA regulatory system (M. Labandeira-Rey, J. R. Mock, and E. J. Hansen, Infect. Immun. 77:3402-3411, 2009). In the present study, we show that this secretion system is also regulated by the small nucleoid-associated protein Fis. Inactivation of the H. ducreyi fis gene resulted in a reduction in expression of both the H. ducreyi LspB and LspA2 proteins. DNA microarray experiments showed that a H. ducreyi fis deletion mutant exhibited altered expression levels of genes encoding other important H. ducreyi virulence factors, including DsrA and Flp1, suggesting a possible global role for Fis in the control of virulence in this obligate human pathogen. While the H. ducreyi Fis protein has a high degree of sequence and structural similarity to the Fis proteins of other bacteria, its temporal pattern of expression was very different from that of enterobacterial Fis proteins. The use of a lacZ-based transcriptional reporter provided evidence which indicated that the H. ducreyi Fis homolog is a positive regulator of gyrB, a gene that is negatively regulated by Fis in enteric bacteria. Taken together, the Fis protein expression data and the observed regulatory effects of Fis in H. ducreyi suggest that this small DNA binding protein has a regulatory role in H. ducreyi which may differ in substantial ways from that of other Fis proteins.

摘要

lspB-lspA2 操纵子在杜克雷嗜血菌 35000HP 中的表达受 CpxRA 调控系统(M. Labandeira-Rey、J. R. Mock 和 E. J. Hansen,Infect. Immun. 77:3402-3411, 2009)直接调控。在本研究中,我们表明该分泌系统也受小核蛋白相关蛋白 Fis 的调控。杜克雷嗜血菌 fis 基因的失活导致 H. ducreyi LspB 和 LspA2 蛋白的表达减少。DNA 微阵列实验表明,H. ducreyi fis 缺失突变体显示出编码其他重要 H. ducreyi 毒力因子(包括 DsrA 和 Flp1)的基因表达水平的改变,表明 Fis 可能在控制这种专性人类病原体的毒力方面具有全局作用。虽然 H. ducreyi Fis 蛋白与其他细菌的 Fis 蛋白具有高度的序列和结构相似性,但它的表达模式与肠杆菌 Fis 蛋白非常不同。使用基于 lacZ 的转录报告提供了证据,表明 H. ducreyi Fis 同源物是 gyrB 的正调节剂,gyrB 基因在肠杆菌中受 Fis 负调控。总之,Fis 蛋白表达数据和 Fis 在 H. ducreyi 中的观察到的调节作用表明,这种小的 DNA 结合蛋白在 H. ducreyi 中具有调节作用,其方式可能与其他 Fis 蛋白有很大的不同。