期刊论文详细信息
BMC Microbiology
The non-pathogenic Escherichia coli strain W secretes SslE via the virulence-associated type II secretion system beta
Rembrandt J F Haft1  Robert Landick3  Mark S DeCanio2 
[1] Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI, USA;Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA;Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA
关键词: Colonization factor;    Escherichia coli;    Surface display;    Type II secretion;   
Others  :  1143647
DOI  :  10.1186/1471-2180-13-130
 received in 2013-03-11, accepted in 2013-06-04,  发布年份 2013
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【 摘 要 】

Background

Many pathogenic E. coli strains secrete virulence factors using type II secretory systems, homologs of which are widespread in Gram-negative bacteria. Recently, the enteropathogenic Escherichia coli strain E2348/69 was shown to secrete and surface-anchor SslE, a biofilm-promoting virulence factor, via a type II secretion system. Genes encoding SslE and its associated secretion system are conserved in some non-pathogenic E. coli, including the commonly-used W (Waksman) strain.

Results

We report here that E. coli W uses its type II secretion system to export a cognate SslE protein. SslE secretion is temperature- and nutrient-dependent, being robust at 37°C in rich medium but strongly repressed by lower temperatures or nutrient limitation. Fusing either of two glycosyl hydrolases to the C-terminus of SslE prevented it from being secreted or surface-exposed. We screened mutations that inactivated the type II secretion system for stress-related phenotypes and found that inactivation of the secretion system conferred a modest increase in tolerance to high concentrations of urea. Additionally, we note that the genes encoding this secretion system are present at a hypervariable locus and have been independently lost or gained in different lineages of E. coli.

Conclusions

The non-pathogenic E. coli W strain shares the extracellular virulence factor SslE, and its associated secretory system, with pathogenic E. coli strains. The pattern of regulation of SslE secretion we observed suggests that SslE plays a role in colonization of mammalian hosts by non-pathogenic as well as pathogenic E. coli. Our work provides a non-pathogenic model system for the study of SslE secretion, and informs future research into the function of SslE during host colonization.

【 授权许可】

   
2013 DeCanio et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Korotkov KV, Sandkvist M, Hol WG: The type II secretion system: biogenesis, molecular architecture and mechanism. Nat Rev Microbiol 2012, 10:336-351.
  • [2]McLaughlin LS, Haft RJF, Forest KT: Structural insights into the type II secretion nanomachine. Curr Opin Struct Biol 2012, 22:208-216.
  • [3]Peabody CR, Chung YJ, Yen MR, Vidal-Ingigliardi D, Pugsley AP, Saier MH Jr: Type II protein secretion and its relationship to bacterial type IV pili and archaeal flagella. Microbiology 2003, 149:3051-3072.
  • [4]Hobbs M, Mattick JS: Common components in the assembly of type 4 fimbriae, DNA transfer systems, filamentous phage and protein-secretion apparatus: a general system for the formation of surface-associated protein complexes. Mol Microbiol 1993, 10:233-243.
  • [5]Cianciotto NP: Type II secretion: a protein secretion system for all seasons. Trends Microbiol 2005, 13:581-588.
  • [6]Sandkvist M: Type II secretion and pathogenesis. Infect Immun 2001, 69:3523-3535.
  • [7]Lathem WW, Grys TE, Witowski SE, Torres AG, Kaper JB, Tarr PI, Welch RA: StcE, a metalloprotease secreted by Escherichia coli O157:H7, specifically cleaves C1 esterase inhibitor. Mol Microbiol 2002, 45:277-288.
  • [8]Tauschek M, Gorrell RJ, Strugnell RA, Robins-Browne RM: Identification of a protein secretory pathway for the secretion of heat-labile enterotoxin by an enterotoxigenic strain of Escherichia coli. Proc Natl Acad Sci USA 2002, 99:7066-7071.
  • [9]Baldi DL, Higginson EE, Hocking DM, Praszkier J, Cavaliere R, James CE, Bennett-Wood V, Azzopardi KI, Turnbull L, Lithgow T, et al.: The type II secretion system and its ubiquitous lipoprotein substrate, SslE, are required for biofilm formation and virulence of enteropathogenic Escherichia coli. Infect Immun 2012, 80:2042-2052.
  • [10]Dunstan RA, Heinz E, Wijeyewickrema LC, Pike RN, Purcell AW, Evans TJ, Praszkier J, Robins-Browne RM, Strugnell RA, Korotkov KV, Lithgow T: Assembly of the type II secretion system such as found in Vibrio cholerae depends on the novel pilotin AspS. PLoS Pathog 2013, 9:e1003117.
  • [11]Yang J, Baldi DL, Tauschek M, Strugnell RA, Robins-Browne RM: Transcriptional regulation of the yghJ-pppA-yghG-gspCDEFGHIJKLM cluster, encoding the type II secretion pathway in enterotoxigenic Escherichia coli. J Bacteriol 2007, 189:142-150.
  • [12]Strozen TG, Li G, Howard SP: YghG (GspSβ) is a novel pilot protein required for localization of the GspSβ type II secretion system secretin of enterotoxigenic Escherichia coli. Infect Immun 2012, 80:2608-2622.
  • [13]Archer CT, Kim JF, Jeong H, Park JH, Vickers CE, Lee SY, Nielsen LK: The genome sequence of E. coli W (ATCC 9637): comparative genome analysis and an improved genome-scale reconstruction of E. coli. BMC Genomics 2011, 12:9. BioMed Central Full Text
  • [14]Blattner FR, Plunkett G, Bloch CA, Perna NT, Burland V, Riley M, Collado-Vides J, Glasner JD, Rode CK, Mayhew GF, et al.: The complete genome sequence of Escherichia coli K-12. Science 1997, 277:1453-1462.
  • [15]Lawley TD, Wilkins BM, Frost L: Bacterial conjugation in Gram-negative bacteria. In Plasmid biology. Edited by Phillips G, Funnell BE. Washington, D.C: ASM Press; 2004:203-226.
  • [16]Rumer L, Jores J, Kirsch P, Cavignac Y, Zehmke K, Wieler LH: Dissemination of pheU- and pheV-located genomic islands among enteropathogenic (EPEC) and enterohemorrhagic (EHEC) E. coli and their possible role in the horizontal transfer of the locus of enterocyte effacement (LEE). Int J Med Microbiol 2003, 292:463-475.
  • [17]Vimr ER, Steenbergen SM: Mobile contingency locus controlling Escherichia coli K1 polysialic acid capsule acetylation. Mol Microbiol 2006, 60:828-837.
  • [18]Schneider G, Dobrindt U, Bruggemann H, Nagy G, Janke B, Blum-Oehler G, Buchrieser C, Gottschalk G, Emody L, Hacker J: The pathogenicity island-associated K15 capsule determinant exhibits a novel genetic structure and correlates with virulence in uropathogenic Escherichia coli strain 536. Infect Immun 2004, 72:5993-6001.
  • [19]Francetic O, Pugsley AP: The cryptic general secretory pathway (gsp) operon of Escherichia coli K-12 encodes functional proteins. J Bacteriol 1996, 178:3544-3549.
  • [20]Filloux A: Secretion signal and protein targeting in bacteria: a biological puzzle. J Bacteriol 2010, 192:3847-3849.
  • [21]Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K: Short protocols in molecular biology. 5th edition. New York: Wiley; 2002.
  • [22]Neidhardt FC, Bloch PL, Smith DF: Culture medium for enterobacteria. J Bacteriol 1974, 119:736-747.
  • [23]Thomason L, Court DL, Bubunenko M, Costantino N, Wilson H, Datta S, Oppenheim A: Recombineering: genetic engineering in bacteria using homologous recombination. Curr Protoc Mol Biol 2007, Chapter 1(Unit 1):1.16.1-1.16.24.
  • [24]Baba T, Ara T, Hasegawa M, Takai Y, Okumura Y, Baba M, Datsenko KA, Tomita M, Wanner BL, Mori H: Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol Syst Biol 2006, 2:2006.0008.
  • [25]Haft RJ, Palacios G, Nguyen T, Mally M, Gachelet EG, Zechner EL, Traxler B: General mutagenesis of F plasmid TraI reveals its role in conjugative regulation. J Bacteriol 2006, 188:6346-6353.
  • [26]Amann E, Ochs B, Abel KJ: Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli. Gene 1988, 69:301-315.
  • [27]Haft RJF, Gardner JG, Keating DH: Quantitative colorimetric measurement of cellulose degradation under microbial culture conditions. Appl Microbiol Biotechnol 2012, 94:223-229.
  • [28]Collmer A, Ried JL, Mount MS: Assay methods for pectic enzymes. Methods Enzymol 1988, 161:329-335.
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