Two-component system VraSR positively modulates the regulation of cell-wall biosynthesis pathway in Staphylococcus aureus

被引:414
|
作者
Kuroda, M
Kuroda, H
Oshima, T
Takeuchi, F
Mori, H
Hiramatsu, K
机构
[1] Juntendo Univ, Bunkyo Ku, Tokyo 1138421, Japan
[2] Nara Inst Sci & Technol, Res & Educ Ctr Genet Informat, Ikoma 6300101, Japan
[3] Int Med Ctr Japan, Res Inst, Shinjuku Ku, Tokyo 1628655, Japan
[4] Org Pharmaceut Safety & Res, Chiyoda Ku, Tokyo 1000013, Japan
关键词
D O I
10.1046/j.1365-2958.2003.03599.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA microarray covering the whole genome of Staphylococcus aureus strain N315 was prepared to investigate transcription profiles. The microarray analyses revealed that vancomycin induces transcription of 139 genes. Forty-six genes among them failed to be induced in the vraSR null mutant KVR. Part of the genes regulated by VraSR system is associated with cell-wall biosynthesis, such as PBP2, SgtB and MurZ. Other cell-wall synthesis inhibitors also induced VraSR, suggesting that the sensor kinase VraS responds to the damage of cell-wall structure or inhibition of cell-wall biosynthesis. Additionally, the vraSR null mutants derived from hetero- and homomethicillin-resistant S. aureus showed significant decrease of resistance against teicoplanin, beta-lactam, bacitracin and fosfomycin but not Of D-Cycloserine and levofloxacin. The observation strongly indicates that VraSR constitutes a positive regulator of cell-wall peptidoglycan synthesis, and that is deeply involved in the expression of beta-lactam and glycopeptide resistance in S. aureus.
引用
收藏
页码:807 / 821
页数:15
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