Citrobacter rodentium espB Is Necessary for Signal Transduction and for Infection of Laboratory Mice

ABSTRACT Citrobacter rodentium is the causative agent of transmissible murine colonic hyperplasia and contains a locus of enterocyte effacement (LEE) similar to that found in enteropathogenicEscherichia coli (EPEC). EPEC espB is necessary for intimate attachment and signal transduction between EPEC and cultured cell monolayers. Mice challenged with wild-type C. rodentium develop a mucosal immunoglobulin A response to EspB. In this study, C. rodentium espB has been cloned and its nucleotide sequence has been determined. C. rodentium espBwas found to have 90% identity to EPEC espB. A nonpolar insertion mutation in C. rodentium espB was constructed and used to replace the chromosomal wild-type allele. The C. rodentium espB mutant exhibited reduced cell association and had no detectable fluorescent actin staining activity on cultured cell monolayers. The C. rodentium espB mutant also failed to colonize laboratory mice following experimental inoculation. TheespB mutation could be complemented with a plasmid-encoded copy of the gene, which restored both cell association and fluorescent actin staining activity, as well as the ability to colonize laboratory mice. These studies indicate that espB is necessary for signal transduction and for colonization of laboratory mice by C. rodentium.

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  M. Schmidt,et al.  Insertion of EspD into epithelial target cell membranes by infecting enteropathogenic Escherichia coli , 1999, Molecular microbiology.

[3]  G. Schoolnik,et al.  Type IV pili, transient bacterial aggregates, and virulence of enteropathogenic Escherichia coli. , 1998, Science.

[4]  M. Pallen,et al.  A novel EspA‐associated surface organelle of enteropathogenic Escherichia coli involved in protein translocation into epithelial cells , 1998, The EMBO journal.

[5]  T. McDaniel,et al.  The complete sequence of the locus of enterocyte effacement (LEE) from enteropathogenic Escherichia coli E2348/69 , 1998 .

[6]  E. Hanski,et al.  Protein translocation into host epithelial cells by infecting enteropathogenic Escherichia coli , 1998, Molecular microbiology.

[7]  J. Kaper,et al.  EspB and EspD require a specific chaperone for proper secretion from enteropathogenic Escherichia coli , 1998, Molecular microbiology.

[8]  B. Finlay,et al.  Enteropathogenic E. coli (EPEC) Transfers Its Receptor for Intimate Adherence into Mammalian Cells , 1997, Cell.

[9]  S. Savkovic,et al.  Activation of NF-κB in intestinal epithelial cells by enteropathogenic Escherichia coli. , 1997, American journal of physiology. Cell physiology.

[10]  B. Finlay,et al.  Characterization of two virulence proteins secreted by rabbit enteropathogenic Escherichia coli, EspA and EspB, whose maximal expression is sensitive to host body temperature , 1997, Infection and immunity.

[11]  J. Oh,et al.  Activation of host cell protein kinase C by enteropathogenic Escherichia coli , 1997, Infection and immunity.

[12]  B. Finlay,et al.  Enteropathogenic Escherichia coli protein secretion is induced in response to conditions similar to those in the gastrointestinal tract , 1997, Infection and immunity.

[13]  B. Finlay,et al.  Intimin-dependent binding of enteropathogenic Escherichia coli to host cells triggers novel signaling events, including tyrosine phosphorylation of phospholipase C-gamma1 , 1997, Infection and immunity.

[14]  K. Stone,et al.  A third secreted protein that is encoded by the enteropathogenic Escherichia coli pathogenicity island is required for transduction of signals and for attaching and effacing activities in host cells , 1997, Infection and immunity.

[15]  B. Finlay,et al.  Characterization of EspC, a 110-kilodalton protein secreted by enteropathogenic Escherichia coli which is homologous to members of the immunoglobulin A protease-like family of secreted proteins , 1996, Journal of bacteriology.

[16]  B. Finlay,et al.  Enteropathogenic Escherichia coli markedly decreases the resting membrane potential of Caco-2 and HeLa human epithelial cells , 1996, Infection and immunity.

[17]  T. Savidge,et al.  Epithelial cell proliferation in childhood enteropathies. , 1996, Gut.

[18]  B. Finlay,et al.  EspA, a protein secreted by enteropathogenic Escherichia coli, is required to induce signals in epithelial cells , 1996, Molecular microbiology.

[19]  B. Finlay,et al.  Protein secretion by enteropathogenic Escherichia coli is essential for transducing signals to epithelial cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[20]  A. Steigerwalt,et al.  Genetic and biochemical characterization of Citrobacter rodentium sp. nov , 1995, Journal of clinical microbiology.

[21]  S. Miller,et al.  PhoP/PhoQ transcriptional repression of Salmonella typhimurium invasion genes: evidence for a role in protein secretion , 1995, Molecular microbiology.

[22]  T. McDaniel,et al.  A genetic locus of enterocyte effacement conserved among diverse enterobacterial pathogens. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[23]  B. Finlay,et al.  The eaeB gene of enteropathogenic Escherichia coli is necessary for signal transduction in epithelial cells , 1994, Infection and immunity.

[24]  B. Finlay,et al.  A diarrheal pathogen, enteropathogenic Escherichia coli (EPEC), triggers a flux of inositol phosphates in infected epithelial cells , 1994, The Journal of experimental medicine.

[25]  S. Falkow,et al.  The eae gene of Citrobacter freundii biotype 4280 is necessary for colonization in transmissible murine colonic hyperplasia , 1993, Infection and immunity.

[26]  R. Ménard,et al.  Nonpolar mutagenesis of the ipa genes defines IpaB, IpaC, and IpaD as effectors of Shigella flexneri entry into epithelial cells , 1993, Journal of bacteriology.

[27]  M. McKee,et al.  The role of the eae gene of enterohemorrhagic Escherichia coli in intimate attachment in vitro and in a porcine model. , 1993, The Journal of clinical investigation.

[28]  M. Levine,et al.  Role of the eaeA gene in experimental enteropathogenic Escherichia coli infection. , 1993, The Journal of clinical investigation.

[29]  J. Yu,et al.  A second chromosomal gene necessary for intimate attachment of enteropathogenic Escherichia coli to epithelial cells , 1993, Journal of bacteriology.

[30]  S. Falkow,et al.  Attaching and effacing locus of a Citrobacter freundii biotype that causes transmissible murine colonic hyperplasia , 1993, Infection and immunity.

[31]  B. Finlay,et al.  Signal transduction between enteropathogenic Escherichia coli (EPEC) and epithelial cells: EPEC induces tyrosine phosphorylation of host cell proteins to initiate cytoskeletal rearrangement and bacterial uptake. , 1992, The EMBO journal.

[32]  G. Schoolnik,et al.  An inducible bundle-forming pilus of enteropathogenic Escherichia coli. , 1991, Science.

[33]  J. Dixon,et al.  Tyrosine phosphate hydrolysis of host proteins by an essential Yersinia virulence determinant. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[34]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[35]  J. Cantey,et al.  Production of diarrhea in the rabbit by a mutant of Escherichia coli (RDEC-1) that does not express adherence (AF/R1) pili. , 1989, The Journal of infectious diseases.

[36]  P. Williams,et al.  Actin accumulation at sites of bacterial adhesion to tissue culture cells: basis of a new diagnostic test for enteropathogenic and enterohemorrhagic Escherichia coli , 1989, Infection and immunity.

[37]  M. Wolf,et al.  Characterization of the plasmid from Escherichia coli RDEC-1 that mediates expression of adhesin AF/R1 and evidence that AF/R1 pili promote but are not essential for enteropathogenic disease , 1988, Infection and immunity.

[38]  J. Mekalanos,et al.  A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR , 1988, Journal of bacteriology.

[39]  M. Levine,et al.  The diarrheal response of humans to some classic serotypes of enteropathogenic Escherichia coli is dependent on a plasmid encoding an enteroadhesiveness factor. , 1985, The Journal of infectious diseases.

[40]  M. Levine,et al.  Attaching and effacing activities of rabbit and human enteropathogenic Escherichia coli in pig and rabbit intestines , 1983, Infection and immunity.

[41]  S. Barthold,et al.  The ultrastructure of transmissible murine colonic hyperplasia. , 1979, The American journal of pathology.

[42]  G. L. Coleman,et al.  Transmissible Murine Colonic Hyperplasia , 1978, Veterinary pathology.

[43]  M. Lipkin Biology of large bowel cancer. Present status and research frontiers , 1975, Cancer.

[44]  P. W. Luther,et al.  The EspB protein of enteropathogenic Escherichia coli is targeted to the cytoplasm of infected HeLa cells. , 1998, Infection and immunity.

[45]  S. Barthold,et al.  Autoradiographic cytokinetics of colonic mucosal hyperplasia in mice. , 1979, Cancer research.

[46]  B. Finlay,et al.  Copyright © 1997, American Society for Microbiology Common Themes in Microbial Pathogenicity Revisited , 2022 .