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Integrative genomic analysis identifies isoleucine and CodY as regulators of Listeria monocytogenes virulence.整合基因组分析确定异亮氨酸和 CodY 是李斯特菌毒力的调节剂。
PLoS Genet. 2012 Sep;8(9):e1002887. doi: 10.1371/journal.pgen.1002887. Epub 2012 Sep 6.
2
Fatty acids regulate stress resistance and virulence factor production for Listeria monocytogenes.脂肪酸调节李斯特菌的应激抗性和毒力因子的产生。
J Bacteriol. 2012 Oct;194(19):5274-84. doi: 10.1128/JB.00045-12. Epub 2012 Jul 27.
3
Borrelia burgdorferi cp32 BpaB modulates expression of the prophage NucP nuclease and SsbP single-stranded DNA-binding protein.伯氏疏螺旋体 cp32 BpaB 调节噬菌体 NucP 核酸内切酶和 SsbP 单链 DNA 结合蛋白的表达。
J Bacteriol. 2012 Sep;194(17):4570-8. doi: 10.1128/JB.00661-12. Epub 2012 Jun 22.
4
Control of a Salmonella virulence locus by an ATP-sensing leader messenger RNA.ATP 感应前导信使 RNA 控制沙门氏菌毒力基因座。
Nature. 2012 Jun 13;486(7402):271-5. doi: 10.1038/nature11090.
5
Effect of levels of acetate on the mevalonate pathway of Borrelia burgdorferi.乙酰辅酶 A 水平对伯氏疏螺旋体甲羟戊酸途径的影响。
PLoS One. 2012;7(5):e38171. doi: 10.1371/journal.pone.0038171. Epub 2012 May 31.
6
EbfC (YbaB) is a new type of bacterial nucleoid-associated protein and a global regulator of gene expression in the Lyme disease spirochete.EbFC(YbaB)是一种新型的细菌核相关蛋白,也是莱姆病螺旋体基因表达的全局调控因子。
J Bacteriol. 2012 Jul;194(13):3395-406. doi: 10.1128/JB.00252-12. Epub 2012 Apr 27.
7
Borrelia burgdorferi requires the alternative sigma factor RpoS for dissemination within the vector during tick-to-mammal transmission.伯氏疏螺旋体(Borrelia burgdorferi)在蜱向哺乳动物传播过程中需要替代 sigma 因子 RpoS 进行传播。
PLoS Pathog. 2012 Feb;8(2):e1002532. doi: 10.1371/journal.ppat.1002532. Epub 2012 Feb 16.
8
Of ticks, mice and men: understanding the dual-host lifestyle of Lyme disease spirochaetes.论 ticks、mice 和 men:理解莱姆病螺旋体的双重宿主生活方式。
Nat Rev Microbiol. 2012 Jan 9;10(2):87-99. doi: 10.1038/nrmicro2714.
9
BpaB and EbfC DNA-binding proteins regulate production of the Lyme disease spirochete's infection-associated Erp surface proteins.BpaB 和 EbfC DNA 结合蛋白调节莱姆病螺旋体感染相关 Erp 表面蛋白的产生。
J Bacteriol. 2012 Feb;194(4):778-86. doi: 10.1128/JB.06394-11. Epub 2011 Dec 9.
10
BosR (BB0647) controls the RpoN-RpoS regulatory pathway and virulence expression in Borrelia burgdorferi by a novel DNA-binding mechanism.BosR(BB0647)通过一种新的 DNA 结合机制控制伯氏疏螺旋体中的 RpoN-RpoS 调控途径和毒力表达。
PLoS Pathog. 2011 Feb 10;7(2):e1001272. doi: 10.1371/journal.ppat.1001272.

细菌生长速率的变化控制着伯氏疏螺旋体 OspC 和 Erp 感染相关表面蛋白的表达。

Changes in bacterial growth rate govern expression of the Borrelia burgdorferi OspC and Erp infection-associated surface proteins.

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky College of Medicine, Lexington, KY, USA.

出版信息

J Bacteriol. 2013 Feb;195(4):757-64. doi: 10.1128/JB.01956-12. Epub 2012 Dec 7.

DOI:10.1128/JB.01956-12
PMID:23222718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3562092/
Abstract

The Lyme disease spirochete controls production of its OspC and Erp outer surface proteins, repressing protein synthesis during colonization of vector ticks but increasing expression when those ticks feed on vertebrate hosts. Early studies found that the synthesis of OspC and Erps can be stimulated in culture by shifting the temperature from 23°C to 34°C, leading to a hypothesis that Borrelia burgdorferi senses environmental temperature to determine its location in the tick-mammal infectious cycle. However, borreliae cultured at 34°C divide several times faster than do those cultured at 23°C. We developed methods that disassociate bacterial growth rate and temperature, allowing a separate evaluation of each factor's impacts on B. burgdorferi gene and protein expression. Altogether, the data support a new paradigm that B. burgdorferi actually responds to changes in its own replication rate, not temperature per se, as the impetus to increase the expression of the OspC and Erp infection-associated proteins.

摘要

莱姆病螺旋体控制其 OspC 和 Erp 外表面蛋白的产生,在载体蜱虫的定殖过程中抑制蛋白质合成,但在这些蜱虫以脊椎动物宿主为食时增加表达。早期研究发现,通过将温度从 23°C 升高到 34°C,可以刺激 OspC 和 Erps 在培养物中的合成,这导致了一种假设,即伯氏疏螺旋体可以感知环境温度来确定其在蜱-哺乳动物感染周期中的位置。然而,在 34°C 下培养的博氏疏螺旋体比在 23°C 下培养的博氏疏螺旋体分裂速度快几倍。我们开发了将细菌生长速度和温度分开的方法,允许分别评估每个因素对伯氏疏螺旋体基因和蛋白质表达的影响。总的来说,这些数据支持了一个新的范例,即伯氏疏螺旋体实际上是对其自身复制率的变化做出反应,而不是温度本身,这是增加 OspC 和 Erp 感染相关蛋白表达的动力。