cwrA, a gene that specifically responds to cell wall damage in Staphylococcus aureus

被引:18
作者
Balibar, Carl J. [1 ]
Shen, Xiaoyu [1 ]
McGuire, Dorothy [1 ]
Yu, Donghui [1 ]
McKenney, David [1 ]
Tao, Jianshi [1 ]
机构
[1] Novartis Inst BioMed Res, Dept Infect Dis, Cambridge, MA 02139 USA
来源
MICROBIOLOGY-SGM | 2010年 / 156卷
关键词
LIPOTEICHOIC ACID; TEICHOIC-ACIDS; DLT OPERON; INSERTIONAL INACTIVATION; METHICILLIN-RESISTANT; MEVALONATE PATHWAY; STRESS STIMULON; BIOSYNTHESIS; VIRULENCE; MEMBRANE;
D O I
10.1099/mic.0.036129-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transcriptional profiling data accumulated in recent years for the clinically relevant pathogen Staphylococcus aureus have established a cell wall stress stimulon, which comprises a coordinately regulated set of genes that are upregulated in response to blockage of cell wall biogenesis. In particular, the expression of cwrA (SA2343, N315 notation), which encodes a putative 63 amino acid polypeptide of unknown biological function, increases over 100-fold in response to cell wall inhibition. Herein, we seek to understand the biological role that this gene plays in S. aureus. cwrA was found to be robustly induced by all cell wall-targeting antibiotics tested - vancomycin, oxacillin, penicillin G, phosphomycin, imipenem, hymeglusin and bacitracin - but not by antibiotics with other mechanisms of action, including ciprofloxacin, erythromycin, chloramphenicol, triclosan, rifampicin, novobiocin and carbonyl cyanide 3-chlorophenylhydrazone. Although a Delta cwrA S. aureus strain had no appreciable shift in MICs for cell wall-targeting antibiotics, the knockout was shown to have reduced cell wall integrity in a variety of other assays. Additionally, the gene was shown to be important for virulence in a mouse sepsis model of infection.
引用
收藏
页码:1372 / 1383
页数:12
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