Comparative proteomic analysis of Salmonella enterica serovar Typhimurium ppGpp-deficient mutant to identify a novel virulence protein required for intracellular survival in macrophages

被引:13
|
作者
Haneda, Takeshi [1 ]
Sugimoto, Mariko [1 ]
Yoshida-Ohta, Yukie [1 ]
Kodera, Yoshio [2 ]
Oh-Ishi, Masamichi [2 ]
Maeda, Tadakazu [2 ]
Shimizu-Izumi, Satomi [1 ]
Miki, Tsuyoshi [1 ]
Kumagai, Yoshinori [1 ]
Danbara, Hirofumi [1 ]
Okada, Nobuhiko [1 ]
机构
[1] Kitasato Univ, Sch Pharm, Dept Microbiol, Minato Ku, Tokyo 1088641, Japan
[2] Kitasato Univ, Sch Sci, Dept Phys, Lab Biomol Dynam,Minami Ku, Sagamihara, Kanagawa 2520373, Japan
来源
BMC MICROBIOLOGY | 2010年 / 10卷
关键词
III SECRETION SYSTEM; 2-DIMENSIONAL GEL-ELECTROPHORESIS; BACTERIAL SIGNAL MOLECULE; ESCHERICHIA-COLI; SHIGELLA-FLEXNERI; EPITHELIAL-CELLS; MASS PROTEINS; AGAROSE GELS; GENES; IDENTIFICATION;
D O I
10.1186/1471-2180-10-324
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: The global ppGpp-mediated stringent response in pathogenic bacteria plays an important role in the pathogenesis of bacterial infections. In Salmonella enterica serovar Typhimurium ( S. Typhimurium), several genes, including virulence genes, are regulated by ppGpp when bacteria are under the stringent response. To understand the control of virulence genes by ppGpp in S. Typhimurium, agarose 2-dimensional electrophoresis (2-DE) combined with mass spectrometry was used and a comprehensive 2-DE reference map of amino acid-starved S. Typhimurium strain SH100, a derivative of ATCC 14028, was established. Results: Of the 366 examined spots, 269 proteins were successfully identified. The comparative analysis of the wild-type and ppGpp(0) mutant strains revealed 55 proteins, the expression patterns of which were affected by ppGpp. Using a mouse infection model, we further identified a novel virulence-associated factor, STM3169, from the ppGpp-regulated and Salmonella-specific proteins. In addition, Salmonella strains carrying mutations in the gene encoding STM3169 showed growth defects and impaired growth within macrophage-like RAW264.7 cells. Furthermore, we found that expression of stm3169 was controlled by ppGpp and SsrB, a response regulator of the two-component system located on Salmonella pathogenicity island 2. Conclusions: A proteomic approach using a 2-DE reference map can prove a powerful tool for analyzing virulence factors and the regulatory network involved in Salmonella pathogenesis. Our results also provide evidence of a global response mediated by ppGpp in S. enterica.
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页数:13
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