Molecular mechanisms of bacterial virulence: type III secretion and pathogenicity islands.
暂无分享,去创建一个
[1] J. Bresee,et al. Synopses , 1988, Sarcoma.
[2] D. Berg,et al. Two pathogenicity islands in uropathogenic Escherichia coli J96: cosmid cloning and sample sequencing , 1996, Infection and immunity.
[3] T. Bergman,et al. Modulation of Virulence Factor Expression by Pathogen Target Cell Contact , 1996, Science.
[4] R. Harshey,et al. Spinning tails: homologies among bacterial flagellar systems. , 1996, Trends in microbiology.
[5] R. Ménard,et al. Bacterial entry into epithelial cells: the paradigm of Shigella. , 1996, Trends in microbiology.
[6] H. Wolf‐Watz,et al. The Yersinia YpkA Ser/Thr kinase is translocated and subsequently targeted to the inner surface of the HeLa cell plasma membrane , 1996, Molecular microbiology.
[7] G. Cornelis,et al. Customized secretion chaperones in pathogenic bacteria , 1996, Molecular microbiology.
[8] B. Finlay,et al. EspA, a protein secreted by enteropathogenic Escherichia coli, is required to induce signals in epithelial cells , 1996, Molecular microbiology.
[9] B. Finlay,et al. Identification of a Salmonella virulence gene required for formation of filamentous structures containing lysosomal membrane glycoproteins within epithelial cells , 1996, Molecular microbiology.
[10] J. Galán. Molecular genetic bases of Salmonella entry into host cells , 1996, Molecular microbiology.
[11] J. Shea,et al. Identification of a virulence locus encoding a second type III secretion system in Salmonella typhimurium. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[12] R. Ménard,et al. The secreted Ipa complex of Shigella flexneri promotes entry into mammalian cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[13] F. Taddei,et al. Genetic barriers among bacteria. , 1996, Trends in microbiology.
[14] J. Kaper,et al. Cloning and sequence of a region encoding a surface polysaccharide of Vibrio cholerae O139 and characterization of the insertion site in the chromosome of Vibrio cholerae O1 , 1996, Molecular microbiology.
[15] S. Aizawa. Flagellar assembly in Salmonella typhimurium , 1996, Molecular microbiology.
[16] R. Macnab,et al. Flagella and motility , 1996 .
[17] Leeds Ca. Pathogenicity islands and the evolution of bacterial pathogens. , 1996 .
[18] C. Lee. Pathogenicity islands and the evolution of bacterial pathogens. , 1996, Infectious agents and disease.
[19] G. Cornelis,et al. Mutational analysis of the Yersinia enterocolitica virC operon: characterization of yscE, F, G, I, J, K required for Yop secretion and yscH encoding YopR , 1995, Molecular microbiology.
[20] A. Holmström,et al. Cell‐surface‐bound Yersinia translocate the protein tyrosine phosphatase YopH by a polarized mechanism into the target cell , 1995, Molecular microbiology.
[21] H. Wolf‐Watz,et al. Functional conservation of the secretion and translocation machinery for virulence proteins of yersiniae, salmonellae and shigellae. , 1995, The EMBO journal.
[22] T. McDaniel,et al. Enteropathogenic Escherichia coli contains a putative type III secretion system necessary for the export of proteins involved in attaching and effacing lesion formation. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[23] R. Ménard,et al. Functional conservation of the Salmonella and Shigella effectors of entry into epithelial cells , 1995, Molecular microbiology.
[24] R. Perry,et al. Environmental modulation of gene expression and pathogenesis in Yersinia. , 1995, Trends in microbiology.
[25] S. Naitza,et al. H-NS regulation of virulence gene expression in enteroinvasive Escherichia coli harboring the virulence plasmid integrated into the host chromosome , 1995, Journal of bacteriology.
[26] S. Falkow,et al. Entry of microbes into the host: using M cells to break the mucosal barrier. , 1995, Current opinion in immunology.
[27] H. Ochman,et al. Relationship between evolutionary rate and cellular location among the Inv/Spa invasion proteins of Salmonella enterica. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[28] G. Cornelis,et al. VirG, a Yersinia enterocolitica lipoprotein involved in Ca2+ dependency, is related to exsB of Pseudomonas aeruginosa , 1995, Journal of bacteriology.
[29] J. Shea,et al. Simultaneous identification of bacterial virulence genes by negative selection. , 1995, Science.
[30] G. Plano,et al. Mutations in yscC, yscD, and yscG prevent high-level expression and secretion of V antigen and Yops in Yersinia pestis , 1995, Journal of bacteriology.
[31] W. Rabsch,et al. tRNA genes and pathogenicity islands: influence on virulence and metabolic properties of uropathogenic Escherichia coli , 1995, Molecular microbiology.
[32] M. Watarai,et al. Contact of Shigella with host cells triggers release of Ipa invasins and is an essential function of invasiveness. , 1995, The EMBO journal.
[33] R. Rosqvist,et al. The chaperone‐like protein YerA of Yersinia pseudotuberculosis stabilizes YopE in the cytoplasm but is dispensible for targeting to the secretion loci , 1995, Molecular microbiology.
[34] J. Heesemann,et al. Evidence for two evolutionary lineages of highly pathogenic Yersinia species , 1995, Journal of bacteriology.
[35] C. Boucher,et al. The hrp gene locus of Pseudomonas solanacearum, which controls the production of a type III secretion system, encodes eight proteins related to components of the bacterial flagellar biogenesis complex , 1995, Molecular microbiology.
[36] 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.
[37] Jeff F. Miller,et al. Ectopic expression of the flagellar regulon alters development of the bordetella-host interaction , 1995, Cell.
[38] A. Caprioli,et al. Gene clusters encoding the cytotoxic necrotizing factor type 1, Prs-fimbriae and alpha-hemolysin form the pathogenicity island II of the uropathogenic Escherichia coli strain J96. , 1995, FEMS microbiology letters.
[39] C. Ginocchio,et al. Functional conservation among members of the Salmonella typhimurium InvA family of proteins , 1995, Infection and immunity.
[40] Catherine A. Lee,et al. A 40 kb chromosomal fragment encoding Salmonella typhimurium invasion genes is absent from the corresponding region of the Escherichia coli K‐12 chromosome , 1995, Molecular microbiology.
[41] F. Mooi,et al. Genesis of the novel epidemic Vibrio cholerae O139 strain: evidence for horizontal transfer of genes involved in polysaccharide synthesis. , 1995, The EMBO journal.
[42] G. Nair,et al. Studies on the genesis of Vibrio cholerae O139: identification of probable progenitor strains. , 1995, Journal of medical microbiology.
[43] H. Ochman,et al. The evolution of invasion by enteric bacteria. , 1995, Canadian journal of microbiology.
[44] D. Dykhuizen,et al. Clonal divergence in Escherichia coli as a result of recombination, not mutation. , 1994, Science.
[45] R. Ménard,et al. Extracellular association and cytoplasmic partitioning of the IpaB and IpaC invasins of S. flexneri , 1994, Cell.
[46] G. Cornelis,et al. Translocation of a hybrid YopE‐adenylate cyclase from Yersinia enterocolitica into HeLa cells , 1994, Molecular microbiology.
[47] R. Ménard,et al. The secretion of the Shigella flexneri Ipa invasins is activated by epithelial cells and controlled by IpaB and IpaD. , 1994, The EMBO journal.
[48] R. Perry,et al. The pigmentation locus of Yersinia pestis KIM6+ is flanked by an insertion sequence and includes the structural genes for pesticin sensitivity and HMWP2 , 1994, Molecular microbiology.
[49] J. L. Montagne,et al. Emerging infectious diseases. , 1994, The Journal of infectious diseases.
[50] J. Galán,et al. The Salmonella typhimurium invasion genes invF and invG encode homologues of the AraC and PulD family of proteins , 1994, Molecular microbiology.
[51] G. Cornelis,et al. YscU, a Yersinia enterocolitica inner membrane protein involved in Yop secretion , 1994, Journal of bacteriology.
[52] P. Cossart,et al. The virulence gene cluster of Listeria monocytogenes is also present in Listeria ivanovii, an animal pathogen, and Listeria seeligeri, a nonpathogenic species , 1994, Infection and immunity.
[53] M. Waldor,et al. Vibrio cholerae 0139 specific gene sequences , 1994, The Lancet.
[54] T. Bergman,et al. The lcrB (yscN/U) gene cluster of Yersinia pseudotuberculosis is involved in Yop secretion and shows high homology to the spa gene clusters of Shigella flexneri and Salmonella typhimurium , 1994, Journal of bacteriology.
[55] G. Cornelis,et al. YscN, the putative energizer of the Yersinia Yop secretion machinery , 1994, Journal of bacteriology.
[56] C. Ginocchio,et al. Contact with epithelial cells induces the formation of surface appendages on Salmonella typhimurium , 1994, Cell.
[57] K. A. Fields,et al. A low-Ca2+ response (LCR) secretion (ysc) locus lies within the lcrB region of the LCR plasmid in Yersinia pestis , 1994, Journal of bacteriology.
[58] K. Magnusson,et al. Target cell contact triggers expression and polarized transfer of Yersinia YopE cytotoxin into mammalian cells. , 1994, The EMBO journal.
[59] J. Hacker,et al. Adhesin regulatory genes within large, unstable DNA regions of pathogenic Escherichia coli: cross‐talk between different adhesin gene clusters , 1994, Molecular microbiology.
[60] J. Hacker,et al. Excision of large DNA regions termed pathogenicity islands from tRNA-specific loci in the chromosome of an Escherichia coli wild-type pathogen , 1994, Infection and immunity.
[61] A. Salyers,et al. Bacterial Pathogenesis: A Molecular Approach , 1994 .
[62] G. Cornelis,et al. Yersinia pathogenicity factors. , 1994, Current topics in microbiology and immunology.
[63] J. G. Hastings. Molecular Biology of Bacterial Infection. Current Status and Future Perspectives: Edited by C. E. HORMAECHE, C. W. PENN and C. J. SMYTH.1992. ISBN 0 521 43298 7. Cambridge University Press. Pp.329. £55.00. , 1993 .
[64] R. Kolter,et al. ABC transporters: bacterial exporters , 1993, Microbiological reviews.
[65] K. Hughes,et al. Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator. , 1993, Science.
[66] H. Ochman,et al. Cognate gene clusters govern invasion of host epithelial cells by Salmonella typhimurium and Shigella flexneri. , 1993, The EMBO journal.
[67] S. Straley,et al. LcrG, a secreted protein involved in negative regulation of the low-calcium response in Yersinia pestis , 1993, Journal of bacteriology.
[68] G. Baranton,et al. Relationship between loss of pigmentation and deletion of the chromosomal iron-regulated irp2 gene in Yersinia pestis: evidence for separate but related events , 1993, Infection and immunity.
[69] D. Platt. Molecular Biology of Bacterial Infection. Current Status and Future Perspectives , 1993 .
[70] T. Whittam,et al. Clonal relationships among Escherichia coli strains that cause hemorrhagic colitis and infantile diarrhea , 1993, Infection and immunity.
[71] C. Sasakawa,et al. Eight genes in region 5 that form an operon are essential for invasion of epithelial cells by Shigella flexneri 2a , 1993, Journal of bacteriology.
[72] A. Pugsley. The complete general secretory pathway in gram-negative bacteria. , 1993, Microbiological reviews.
[73] T. Bergman,et al. YopB and YopD constitute a novel class of Yersinia Yop proteins , 1993, Infection and immunity.
[74] Philip J. Reeves,et al. Membrance traffic wardens and protein secretion in Gram-negative bacteria , 1993 .
[75] G. Salmond,et al. Membrane traffic wardens and protein secretion in gram-negative bacteria. , 1993, Trends in biochemical sciences.
[76] R. Perry,et al. Loss of the pigmentation phenotype in Yersinia pestis is due to the spontaneous deletion of 102 kb of chromosomal DNA which is flanked by a repetitive element , 1992, Molecular microbiology.
[77] U. Bonas,et al. Determinants of pathogenicity in Xanthomonas campestris pv. vesicatoria are related to proteins involved in secretion in bacterial pathogens of animals. , 1992, Molecular plant-microbe interactions : MPMI.
[78] A. Maurelli,et al. Temperature regulation of Shigella virulence: identification of the repressor gene virR, an analogue of hns, and partial complementation by tyrosyl transfer RNA (tRNA1Tyr) , 1992, Molecular microbiology.
[79] S. Straley,et al. Structure and regulation of the Yersinia pestis yscBCDEF operon , 1992, Journal of bacteriology.
[80] H. Wolf‐Watz,et al. A novel protein, LcrQ, involved in the low-calcium response of Yersinia pseudotuberculosis shows extensive homology to YopH , 1992, Journal of bacteriology.
[81] H. Wolf‐Watz,et al. Intracellular targeting of the Yersinia YopE cytotoxin in mammalian cells induces actin microfilament disruption , 1991, Infection and immunity.
[82] S. Barve,et al. LcrD, a membrane-bound regulator of the Yersinia pestis low-calcium response , 1991, Journal of bacteriology.
[83] G. Cornelis,et al. Analysis of virC, an operon involved in the secretion of Yop proteins by Yersinia enterocolitica , 1991, Journal of bacteriology.
[84] V. Kutyrev,et al. Integration of the plasmid encoding the synthesis of capsular antigen and murine toxin into Yersinia pestis chromosome. , 1991, Microbial pathogenesis.
[85] J. Sun,et al. Association of a retroelement with a P4-like cryptic prophage (retronphage phi R73) integrated into the selenocystyl tRNA gene of Escherichia coli , 1991, Journal of bacteriology.
[86] S. Inouye,et al. Retronphage phi R73: an E. coli phage that contains a retroelement and integrates into a tRNA gene. , 1991, Science.
[87] M. Skurnik,et al. The surface‐located YopN protein is involved in calcium signal transduction in Yersinia pseudotuberculosis , 1991, Molecular microbiology.
[88] B. Colonna,et al. Virulence plasmids of enteroinvasive Escherichia coli and Shigella flexneri integrate into a specific site on the host chromosome: integration greatly reduces expression of plasmid-carried virulence genes , 1991, Infection and immunity.
[89] 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.
[90] R. Brasseur,et al. Secretion of Yop proteins by Yersiniae , 1990, Infection and immunity.
[91] G. Cornelis,et al. Oral immunization of mice with a live recombinant Yersinia enterocolitica O:9 strain that produces the cholera toxin B subunit , 1990, Infection and immunity.
[92] S. Falkow,et al. The ability of Salmonella to enter mammalian cells is affected by bacterial growth state. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[93] T. Bergman,et al. The cytotoxic protein YopE of Yersinia obstructs the primary host defence , 1990, Molecular microbiology.
[94] J Hacker,et al. Deletions of chromosomal regions coding for fimbriae and hemolysins occur in vitro and in vivo in various extraintestinal Escherichia coli isolates. , 1990, Microbial pathogenesis.
[95] J. Galán,et al. Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[96] B. Finlay,et al. Common themes in microbial pathogenicity , 1989, Microbiological reviews.
[97] W. Reiter,et al. Transfer RNA genes frequently serve as integration sites for prokaryotic genetic elements. , 1989, Nucleic acids research.
[98] S. Falkow,et al. A molecular strategy for the study of bacterial invasion. , 1987, Reviews of infectious diseases.
[99] F. Neidhardt,et al. Escherichia Coli and Salmonella: Typhimurium Cellular and Molecular Biology , 1987 .
[100] J Hacker,et al. Large, unstable inserts in the chromosome affect virulence properties of uropathogenic Escherichia coli O6 strain 536 , 1986, Journal of bacteriology.
[101] K. Żukowski,et al. Integration of the Vwa plasmid into the chromosome of Yersinia pestis strains harboring F' plasmids of Escherichia coli , 1985, Infection and immunity.
[102] M. Surgalla,et al. Repression of the Virulence of Yersinia pestis by an F' Plasmid , 1983, Infection and immunity.
[103] W. Hayes. The genetics of bacteria and their viruses , 1964 .