Literature DB >> 9618447

Type III protein secretion systems in bacterial pathogens of animals and plants.

C J Hueck1.   

Abstract

Various gram-negative animal and plant pathogens use a novel, sec-independent protein secretion system as a basic virulence mechanism. It is becoming increasingly clear that these so-called type III secretion systems inject (translocate) proteins into the cytosol of eukaryotic cells, where the translocated proteins facilitate bacterial pathogenesis by specifically interfering with host cell signal transduction and other cellular processes. Accordingly, some type III secretion systems are activated by bacterial contact with host cell surfaces. Individual type III secretion systems direct the secretion and translocation of a variety of unrelated proteins, which account for species-specific pathogenesis phenotypes. In contrast to the secreted virulence factors, most of the 15 to 20 membrane-associated proteins which constitute the type III secretion apparatus are conserved among different pathogens. Most of the inner membrane components of the type III secretion apparatus show additional homologies to flagellar biosynthetic proteins, while a conserved outer membrane factor is similar to secretins from type II and other secretion pathways. Structurally conserved chaperones which specifically bind to individual secreted proteins play an important role in type III protein secretion, apparently by preventing premature interactions of the secreted factors with other proteins. The genes encoding type III secretion systems are clustered, and various pieces of evidence suggest that these systems have been acquired by horizontal genetic transfer during evolution. Expression of type III secretion systems is coordinately regulated in response to host environmental stimuli by networks of transcription factors. This review comprises a comparison of the structure, function, regulation, and impact on host cells of the type III secretion systems in the animal pathogens Yersinia spp., Pseudomonas aeruginosa, Shigella flexneri, Salmonella typhimurium, enteropathogenic Escherichia coli, and Chlamydia spp. and the plant pathogens Pseudomonas syringae, Erwinia spp., Ralstonia solanacearum, Xanthomonas campestris, and Rhizobium spp.

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Year:  1998        PMID: 9618447      PMCID: PMC98920          DOI: 10.1128/MMBR.62.2.379-433.1998

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  490 in total

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2.  Transcriptional organization and expression of the large hrp gene cluster of Pseudomonas solanacearum.

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Journal:  Mol Plant Microbe Interact       Date:  1992 Mar-Apr       Impact factor: 4.171

3.  Genetic and transcriptional organization of the hrp cluster of Pseudomonas syringae pv. phaseolicola.

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Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

4.  Nucleotide sequences of Bacillus subtilis flagellar biosynthetic genes fliP and fliQ and identification of a novel flagellar gene, fliZ.

Authors:  D S Bischoff; M D Weinreich; G W Ordal
Journal:  J Bacteriol       Date:  1992-06       Impact factor: 3.490

5.  Protein tyrosine phosphatase activity of an essential virulence determinant in Yersinia.

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Journal:  Science       Date:  1990-08-03       Impact factor: 47.728

Review 6.  Biogenesis of lipoproteins in bacteria.

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Journal:  Curr Top Microbiol Immunol       Date:  1986       Impact factor: 4.291

7.  Genetic analysis of an invasion region by use of a Tn3-lac transposon and identification of a second positive regulator gene, invE, for cell invasion of Shigella sonnei: significant homology of invE with ParB of plasmid P1.

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Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

8.  Cytoplasmic and membrane proteins of yersiniae cultivated under conditions simulating mammalian intracellular environment.

Authors:  S C Straley; R R Brubaker
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

9.  Plasmid and chromosomal elements involved in the pathogenesis of attaching and effacing Escherichia coli.

Authors:  A E Jerse; K G Gicquelais; J B Kaper
Journal:  Infect Immun       Date:  1991-11       Impact factor: 3.441

10.  Nucleotide sequence of the ipaBCD structural genes of Shigella dysenteriae.

Authors:  R Yao; S Palchaudhuri
Journal:  Mol Microbiol       Date:  1991-09       Impact factor: 3.501

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  763 in total

Review 1.  Bacteriophages in the evolution of pathogen-host interactions.

Authors:  E A Miao; S I Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

2.  Role of the Hrp type III protein secretion system in growth of Pseudomonas syringae pv. syringae B728a on host plants in the field.

Authors:  S S Hirano; A O Charkowski; A Collmer; D K Willis; C D Upper
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

3.  IpaC induces actin polymerization and filopodia formation during Shigella entry into epithelial cells.

Authors:  G Tran Van Nhieu; E Caron; A Hall; P J Sansonetti
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

4.  Genetic analysis of assembly of the Salmonella enterica serovar Typhimurium type III secretion-associated needle complex.

Authors:  A Sukhan; T Kubori; J Wilson; J E Galán
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

5.  SigE is a chaperone for the Salmonella enterica serovar Typhimurium invasion protein SigD.

Authors:  K H Darwin; L S Robinson; V L Miller
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

6.  Type III secretion chaperone-dependent regulation: activation of virulence genes by SicA and InvF in Salmonella typhimurium.

Authors:  K H Darwin; V L Miller
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

7.  Spa33, a cell surface-associated subunit of the Mxi-Spa type III secretory pathway of Shigella flexneri, regulates Ipa protein traffic.

Authors:  R Schuch; A T Maurelli
Journal:  Infect Immun       Date:  2001-04       Impact factor: 3.441

8.  Enteropathogenic Escherichia coli mediates antiphagocytosis through the inhibition of PI 3-kinase-dependent pathways.

Authors:  J Celli; M Olivier; B B Finlay
Journal:  EMBO J       Date:  2001-03-15       Impact factor: 11.598

Review 9.  Chunnel vision. Export and efflux through bacterial channel-tunnels.

Authors:  C Andersen; C Hughes; V Koronakis
Journal:  EMBO Rep       Date:  2000-10       Impact factor: 8.807

Review 10.  Molecular basis of the interaction of Salmonella with the intestinal mucosa.

Authors:  K H Darwin; V L Miller
Journal:  Clin Microbiol Rev       Date:  1999-07       Impact factor: 26.132

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