The Global Regulator CodY Regulates Toxin Gene Expression in Bacillus anthracis and Is Required for Full Virulence

被引:69
作者
van Schaik, Willem [1 ]
Chateau, Alice [1 ]
Dillies, Marie-Agnes
Coppee, Jean-Yves
Sonenshein, Abraham L. [2 ]
Fouet, Agnes [1 ]
机构
[1] Inst Pasteur, Unite Toxines & Pathogenie Bacterienne, CNRS, URA 2172, F-75724 Paris 15, France
[2] Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA
关键词
GRAM-POSITIVE BACTERIA; STATIONARY-PHASE; STREPTOCOCCUS-PYOGENES; STAPHYLOCOCCUS-AUREUS; DIFFERENTIAL ANALYSIS; LACTOCOCCUS-LACTIS; SUBTILIS CODY; PLASMID; CEREUS; IDENTIFICATION;
D O I
10.1128/IAI.00716-09
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In gram-positive bacteria, CodY is an important regulator of genes whose expression changes upon nutrient limitation and acts as a repressor of virulence gene expression in some pathogenic species. Here, we report the role of CodY in Bacillus anthracis, the etiologic agent of anthrax. Disruption of codY completely abolished virulence in a toxinogenic, noncapsulated strain, indicating that the activity of CodY is required for full virulence of B. anthracis. Global transcriptome analysis of a codY mutant and the parental strain revealed extensive differences. These differences could reflect direct control for some genes, as suggested by the presence of CodY binding sequences in their promoter regions, or indirect effects via the CodY-dependent control of other regulatory proteins or metabolic rearrangements in the codY mutant strain. The differences included reduced expression of the anthrax toxin genes in the mutant strain, which was confirmed by lacZ reporter fusions and immunoblotting. The accumulation of the global virulence regulator AtxA protein was strongly reduced in the mutant strain. However, in agreement with the microarray data, expression of atxA, as measured using an atxA-lacZ transcriptional fusion and by assaying atxA mRNA, was not significantly affected in the codY mutant. An atxA-lacZ translational fusion was also unaffected. Overexpression of atxA restored toxin component synthesis in the codY mutant strain. These results suggest that CodY controls toxin gene expression by regulating AtxA accumulation posttranslationally.
引用
收藏
页码:4437 / 4445
页数:9
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