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金黄色葡萄球菌 Ess 途径的分泌因子 EsaD。

EsaD, a secretion factor for the Ess pathway in Staphylococcus aureus.

机构信息

Department of Microbiology, University of Chicago, 920 East 58th St., CLSC 609, Chicago, IL 60637, USA.

出版信息

J Bacteriol. 2011 Apr;193(7):1583-9. doi: 10.1128/JB.01096-10. Epub 2011 Jan 28.

DOI:10.1128/JB.01096-10
PMID:21278286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3067666/
Abstract

Staphylococcus aureus encodes the Sec-independent Ess secretion pathway, an ortholog of mycobacterial T7 secretion systems which is required for the virulence of this Gram-positive microbe. The Ess (ESX secretion) pathway was previously defined as a genomic cluster of eight genes, esxA, esaA, essA, essB, esaB, essC, esaC, and esxB. essABC encode membrane proteins involved in the stable expression of esxA, esxB, and esaC, genes specifying three secreted polypeptide substrates. esaB, which encodes a small cytoplasmic protein, represses the synthesis of EsaC but not that of EsxA and EsxB. Here we investigated a hitherto uncharacterized gene, esaD, located downstream of esxB. Expression of esaD is activated by mutations in esaB and essB. EsaD, the 617-amino-acid product of esaD, is positioned in the membrane and is also accessible to EsaD-specific antibodies on the bacterial surface. S. aureus mutants lacking esaD are defective in the secretion of EsxA. Following intravenous inoculation of mice, S. aureus esaD mutants generate fewer abscesses with a reduced bacterial load compared to wild-type parent strain Newman. The chromosomes of Listeria and Bacillus species with Ess pathways also harbor esaD homologues downstream of esxB, suggesting that the contributory role of EsaD in Ess secretion may be shared among Gram-positive pathogens.

摘要

金黄色葡萄球菌编码 Sec 独立的 Ess 分泌途径,这是分枝杆菌 T7 分泌系统的同源物,是这种革兰氏阳性微生物毒力所必需的。Ess(ESX 分泌)途径以前被定义为八个基因的基因组簇,esxA、esaA、essA、essB、esaB、essC、esaC 和 esxB。essABC 编码参与 esxA、esxB 和 esaC 稳定表达的膜蛋白,这些基因指定三个分泌的多肽底物。esaB 编码一种小细胞质蛋白,抑制 EsaC 的合成,但不抑制 EsxA 和 EsxB 的合成。在这里,我们研究了一个迄今尚未表征的基因 esaD,它位于 esxB 的下游。esaB 和 essB 的突变激活 esaD 的表达。esaD 的产物是 617 个氨基酸的 EsaD,位于膜中,细菌表面的 EsaD 特异性抗体也可以接触到它。缺乏 esaD 的金黄色葡萄球菌突变体在 EsxA 的分泌中存在缺陷。与野生型亲本株 Newman 相比,经静脉接种小鼠后,金黄色葡萄球菌 esaD 突变体在形成脓肿方面的能力降低,细菌负荷减少。具有 Ess 途径的李斯特菌和芽孢杆菌的染色体也在 esxB 下游携带有 esaD 同源物,这表明 EsaD 在 Ess 分泌中的贡献作用可能在革兰氏阳性病原体中共享。

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