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Identification of bacterial factors involved in type 1 fimbria expression using an Escherichia coli K12 proteome chip.
Chen, Yi-Wen; Teng, Ching-Hao; Ho, Yu-Hsuan; Jessica Ho, Tien Yu; Huang, Wen-Chun; Hashimoto, Masayuki; Chiang, I-Yuan; Chen, Chien-Sheng.
Afiliación
  • Chen YW; From the ‡Graduate Institute of Systems Biology and Bioinformatics, National Central University, Jhongli City, Taiwan;
  • Teng CH; §Institute of Molecular Medicine, National Cheng Kung University Medical College, Tainan City, Taiwan; ¶Institute of Basic Medical Sciences, National Cheng Kung University Medical College, Tainan City, Taiwan; ‖Center of Infectious Disease and Signaling Research, National Cheng Kung University, Ta
  • Ho YH; From the ‡Graduate Institute of Systems Biology and Bioinformatics, National Central University, Jhongli City, Taiwan;
  • Jessica Ho TY; From the ‡Graduate Institute of Systems Biology and Bioinformatics, National Central University, Jhongli City, Taiwan;
  • Huang WC; ¶Institute of Basic Medical Sciences, National Cheng Kung University Medical College, Tainan City, Taiwan;
  • Hashimoto M; §Institute of Molecular Medicine, National Cheng Kung University Medical College, Tainan City, Taiwan; ‖Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan City, Taiwan;
  • Chiang IY; **Department of Nutrition and Health Sciences, Kainan University. No. 1, Kainan Road, Luzhu Township, Taoyuan Country, Taiwan.
  • Chen CS; From the ‡Graduate Institute of Systems Biology and Bioinformatics, National Central University, Jhongli City, Taiwan; cchen103@gmail.com.
Mol Cell Proteomics ; 13(6): 1485-94, 2014 Jun.
Article en En | MEDLINE | ID: mdl-24692643
ABSTRACT
Type 1 fimbriae are filamentous structures on Escherichia coli. These structures are important adherence factors. Because binding to the host cells is the first step of infection, type 1 fimbria is an important virulence factor of pathogenic E. coli. Expression of type 1 fimbria is regulated by a phase variation in which each individual bacterium can alternate between fimbriated (phase-ON) and nonfimbriated (phase-OFF) states. The phase variation is regulated by the flipping of the 314-bp fimS fragment, which contains the promoter driving the expression of the genes required for the synthesis of type 1 fimbria. Thus, the bacterial proteins able to interact with fimS are likely to be involved in regulating the expression of type 1 fimbria. To identify novel type 1 fimbria-regulating factors, we used an E. coli K12 proteome chip to screen for the bacterial factors able to interact with a 602-bp DNA fragment containing fimS and its adjacent regions. The Spr protein was identified by the proteome chip-based screening and further confirmed to be able to interact with fimS by electrophoretic mobility shift assay. Deletion of spr in the neonatal meningitis E. coli strain RS218 significantly increased the ratio of the bacterial colonies that contained the type 1 fimbria phase-ON cells on agar plates. In addition, Spr interfered with the interactions of fimS with the site-specific recombinases, FimB and FimE, which are responsible for mediating the flipping of fimS. These results suggest that Spr is involved in the regulation of type 1 fimbria expression through direct interaction with the invertible element fimS. These findings facilitate our understanding of the regulation of type 1 fimbria.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Fimbrias Bacterianas / Proteoma / Factores de Virulencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Fimbrias Bacterianas / Proteoma / Factores de Virulencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2014 Tipo del documento: Article