Literature DB >> 8861207

The bundle-forming pili of enteropathogenic Escherichia coli: transcriptional regulation by environmental signals.

J L Puente1, D Bieber, S W Ramer, W Murray, G K Schoolnik.   

Abstract

The bundle-forming pili (BFP) of enteropathogenic Escherichia coil (EPEC) are required for the development of circumscribed colonies of bacteria attached to the surfaces of cultured epithelial cells, a process termed the localized adherence (LA) phenotype. Similar lesions are evident in jejunal biopsies from EPEC-infected children. BFP production is not constitutive, but instead occurs upon transfer of bacteria from nutrient broth to tissue culture media, indicating that the expression of BFP may be environmentally regulated. To learn more about how BFP protein expression is induced during epithelial-cell adherence, bfpA-cat transcriptional fusions and northern blot analyses were employed to monitor bfpA expression as a function of environmental signals and growth kinetics. bfpA expression was found to be regulated at the transcriptional level, and to require a separate locus on the EPEC adherence factor (EAF) plasmid. Expression occurred selectively during exponential-growth phase and was greatest between 35 and 37 degrees C, and in the presence of calcium. Ammonium (20 mM) significantly reduced bfpA mRNA and protein expression and the development of the LA phenotype. Analysis of the bfpA upstream sequence and identification of the transcription initiation site revealed a conventional sigma (70)-dependent promoter and an AT-rich tract that might affect promoter activity. Taken together, these findings further support the pathogenic role of BFP by explaining how BFP production would commence in the small intestine and terminate in the colon and in external habitats.

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Year:  1996        PMID: 8861207     DOI: 10.1111/j.1365-2958.1996.tb02491.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  81 in total

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2.  Transcriptional regulation of the orf19 gene and the tir-cesT-eae operon of enteropathogenic Escherichia coli.

Authors:  C Sánchez-SanMartín; V H Bustamante; E Calva; J L Puente
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3.  Novel group of virulence activators within the AraC family that are not restricted to upstream binding sites.

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4.  Structure-function analysis of BfpB, a secretin-like protein encoded by the bundle-forming-pilus operon of enteropathogenic Escherichia coli.

Authors:  S A Schmidt; D Bieber; S W Ramer; J Hwang; C Y Wu; G Schoolnik
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

5.  Expression of the bundle-forming pilus by enteropathogenic Escherichia coli strains of heterologous serotypes.

Authors:  Juana Gismero-Ordoñez; Monique Dall'Agnol; Luiz R Trabulsi; Jorge A Girón
Journal:  J Clin Microbiol       Date:  2002-06       Impact factor: 5.948

6.  Transcriptional regulation of the esp genes of enterohemorrhagic Escherichia coli.

Authors:  F Beltrametti; A U Kresse; C A Guzmán
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7.  Integration of a complex regulatory cascade involving the SirA/BarA and Csr global regulatory systems that controls expression of the Salmonella SPI-1 and SPI-2 virulence regulons through HilD.

Authors:  Luary C Martínez; Helen Yakhnin; Martha I Camacho; Dimitris Georgellis; Paul Babitzke; José L Puente; Víctor H Bustamante
Journal:  Mol Microbiol       Date:  2011-05-12       Impact factor: 3.501

8.  The type IV pilus assembly complex: biogenic interactions among the bundle-forming pilus proteins of enteropathogenic Escherichia coli.

Authors:  Sandra W Ramer; Gary K Schoolnik; Cheng-Yen Wu; Jaiweon Hwang; Sarah A Schmidt; David Bieber
Journal:  J Bacteriol       Date:  2002-07       Impact factor: 3.490

Review 9.  Virulence of enteropathogenic Escherichia coli, a global pathogen.

Authors:  S C Clarke; R D Haigh; P P E Freestone; P H Williams
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10.  The N-acetyltransferase RimJ responds to environmental stimuli to repress pap fimbrial transcription in Escherichia coli.

Authors:  Christine A White-Ziegler; Alia M Black; Stacie H Eliades; Sarah Young; Kimberly Porter
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

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