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金黄色葡萄球菌CodY负向调控毒力基因表达。

Staphylococcus aureus CodY negatively regulates virulence gene expression.

作者信息

Majerczyk Charlotte D, Sadykov Marat R, Luong Thanh T, Lee Chia, Somerville Greg A, Sonenshein Abraham L

机构信息

Tufts University Sackler School of Graduate Biomedical Sciences, Boston, Massachusetts 02111, USA.

出版信息

J Bacteriol. 2008 Apr;190(7):2257-65. doi: 10.1128/JB.01545-07. Epub 2007 Dec 21.

Abstract

CodY is a global regulatory protein that was first discovered in Bacillus subtilis, where it couples gene expression to changes in the pools of critical metabolites through its activation by GTP and branched-chain amino acids. Homologs of CodY can be found encoded in the genomes of nearly all low-G+C gram-positive bacteria, including Staphylococcus aureus. The introduction of a codY-null mutation into two S. aureus clinical isolates, SA564 and UAMS-1, through allelic replacement, resulted in the overexpression of several virulence genes. The mutant strains had higher levels of hemolytic activity toward rabbit erythrocytes in their culture fluid, produced more polysaccharide intercellular adhesin (PIA), and formed more robust biofilms than did their isogenic parent strains. These phenotypes were associated with derepressed levels of RNA for the hemolytic alpha-toxin (hla), the accessory gene regulator (agr) (RNAII and RNAIII/hld), and the operon responsible for the production of PIA (icaADBC). These data suggest that CodY represses, either directly or indirectly, the synthesis of a number of virulence factors of S. aureus.

摘要

CodY是一种全局性调控蛋白,最初在枯草芽孢杆菌中被发现,在那里它通过被GTP和支链氨基酸激活,将基因表达与关键代谢物库的变化联系起来。几乎所有低G+C革兰氏阳性菌的基因组中都编码有CodY的同源物,包括金黄色葡萄球菌。通过等位基因替换,将codY缺失突变引入两株金黄色葡萄球菌临床分离株SA564和UAMS-1中,导致几个毒力基因的过表达。与同基因亲本菌株相比,突变菌株的培养液对兔红细胞具有更高水平的溶血活性,产生更多的多糖细胞间黏附素(PIA),并形成更坚固的生物膜。这些表型与溶血α毒素(hla)、辅助基因调节因子(agr)(RNAII和RNAIII/hld)以及负责PIA产生的操纵子(icaADBC)的RNA去阻遏水平相关。这些数据表明,CodY直接或间接抑制金黄色葡萄球菌多种毒力因子的合成。

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