Literature DB >> 9190801

Altered localization of HrpZ in Pseudomonas syringae pv. syringae hrp mutants suggests that different components of the type III secretion pathway control protein translocation across the inner and outer membranes of gram-negative bacteria.

A O Charkowski1, H C Huang, A Collmer.   

Abstract

Pseudomonas syringae pv. syringae 61 (Pss61) secretes the HrpZ harpin by a type III protein secretion pathway encoded by a cluster of hrp (hypersensitive response and pathogenicity) and hrc genes. The nine hrc genes represent a subset of hrp genes that are also conserved in the type III virulence protein secretion systems of animal pathogenic Yersinia, Shigella, and Salmonella spp. The hrpJ and hrpU operons contain seven hrc genes (counting hrcQ(A) and hrcQ(B) as one gene), all with additional homologs involved in flagellar biogenesis and secretion, and five of which encode predicted inner membrane proteins. The hrpC and hrpZ operons encode HrcC and HrcJ, respectively, which are associated with the outer membrane. Interposon mutants affected in all of the hrc genes in the hrpJ and hrpU operons and TnphoA-induced hrcC and hrcJ mutants were assayed for altered localization of HrpZ in mid-log-phase cultures by immunoblotting sodium dodecyl sulfate-polyacrylamide gels that were run with various cell fractions. The hrpJ and hrpU operon mutants revealed a novel phenotype of partially reduced accumulation of HrpZ in the total culture (despite wild-type levels of hrpZ operon transcription), all of which was cell bound and equivalent in level to that of cell-bound HrpZ in the wild type. The hrcC and hrcJ mutant cultures accumulated the same total amount of HrpZ as the wild type, but the HrpZ was cell bound. Among all the strains tested, only the hrcC mutant accumulated significant amounts of HrpZ in the periplasm, as indicated by selective release through spheroplasting. Analysis of nonpolar mutations in the hrpU and hrpC operons support the results obtained with polar mutations. These observations indicate that a constant pool of HrpZ is maintained in the cytoplasm of Pss61 despite secretion deficiencies, that the hrpJ and hrpU operons encode an alternative to the Sec (general protein export) pathway for translocation across the inner membrane, that genes in the hrpC operon are necessary for translocation across the outer membrane, and that the Pss61 Hrp system permits study of two genetically distinguishable stages in type III protein secretion.

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Year:  1997        PMID: 9190801      PMCID: PMC179194          DOI: 10.1128/jb.179.12.3866-3874.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  63 in total

1.  Unified nomenclature for broadly conserved hrp genes of phytopathogenic bacteria.

Authors:  A J Bogdanove; S V Beer; U Bonas; C A Boucher; A Collmer; D L Coplin; G R Cornelis; H C Huang; S W Hutcheson; N J Panopoulos; F Van Gijsegem
Journal:  Mol Microbiol       Date:  1996-05       Impact factor: 3.501

2.  Yersinia pestis LcrV forms a stable complex with LcrG and may have a secretion-related regulatory role in the low-Ca2+ response.

Authors:  M L Nilles; A W Williams; E Skrzypek; S C Straley
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

3.  Protease secretion by Erwinia chrysanthemi: the specific secretion functions are analogous to those of Escherichia coli alpha-haemolysin.

Authors:  S Létoffé; P Delepelaire; C Wandersman
Journal:  EMBO J       Date:  1990-05       Impact factor: 11.598

4.  Functional analysis of the Salmonella typhimurium invasion genes invl and invJ and identification of a target of the protein secretion apparatus encoded in the inv locus.

Authors:  C M Collazo; M K Zierler; J E Galán
Journal:  Mol Microbiol       Date:  1995-01       Impact factor: 3.501

5.  Pseudomonas syringae pv. syringae harpinPss: a protein that is secreted via the Hrp pathway and elicits the hypersensitive response in plants.

Authors:  S Y He; H C Huang; A Collmer
Journal:  Cell       Date:  1993-07-02       Impact factor: 41.582

6.  The Pseudomonas syringae pv. syringae 61 hrpH product, an envelope protein required for elicitation of the hypersensitive response in plants.

Authors:  H C Huang; S Y He; D W Bauer; A Collmer
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

7.  The HrpZ proteins of Pseudomonas syringae pvs. syringae, glycinea, and tomato are encoded by an operon containing Yersinia ysc homologs and elicit the hypersensitive response in tomato but not soybean.

Authors:  G Preston; H C Huang; S Y He; A Collmer
Journal:  Mol Plant Microbe Interact       Date:  1995 Sep-Oct       Impact factor: 4.171

8.  Regulated underexpression of the FliM protein of Escherichia coli and evidence for a location in the flagellar motor distinct from the MotA/MotB torque generators.

Authors:  H Tang; D F Blair
Journal:  J Bacteriol       Date:  1995-06       Impact factor: 3.490

9.  Phenotypic expression of Pseudomonas syringae avr genes in E. coli is linked to the activities of the hrp-encoded secretion system.

Authors:  M U Pirhonen; M C Lidell; D L Rowley; S W Lee; S Jin; Y Liang; S Silverstone; N T Keen; S W Hutcheson
Journal:  Mol Plant Microbe Interact       Date:  1996-05       Impact factor: 4.171

10.  Characterization of the hrpJ and hrpU operons of Pseudomonas syringae pv. syringae Pss61: similarity with components of enteric bacteria involved in flagellar biogenesis and demonstration of their role in HarpinPss secretion.

Authors:  M C Lidell; S W Hutcheson
Journal:  Mol Plant Microbe Interact       Date:  1994 Jul-Aug       Impact factor: 4.171

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  32 in total

1.  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

2.  Cellular locations of Pseudomonas syringae pv. syringae HrcC and HrcJ proteins, required for harpin secretion via the type III pathway.

Authors:  W L Deng; H C Huang
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

3.  Structure of HrcQB-C, a conserved component of the bacterial type III secretion systems.

Authors:  Vasiliki E Fadouloglou; Anastasia P Tampakaki; Nicholas M Glykos; Marina N Bastaki; Jonathan M Hadden; Simon E Phillips; Nicholas J Panopoulos; Michael Kokkinidis
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-23       Impact factor: 11.205

4.  Secretin of the enteropathogenic Escherichia coli type III secretion system requires components of the type III apparatus for assembly and localization.

Authors:  Annick Gauthier; Jose Luis Puente; B Brett Finlay
Journal:  Infect Immun       Date:  2003-06       Impact factor: 3.441

Review 5.  Type III secretion systems and bacterial flagella: insights into their function from structural similarities.

Authors:  Ariel Blocker; Kaoru Komoriya; Shin-Ichi Aizawa
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-11       Impact factor: 11.205

6.  Components of the Salmonella flagellar export apparatus and classification of export substrates.

Authors:  T Minamino; R M Macnab
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

7.  Characterization of the hrpC and hrpRS operons of Pseudomonas syringae pathovars syringae, tomato, and glycinea and analysis of the ability of hrpF, hrpG, hrcC, hrpT, and hrpV mutants to elicit the hypersensitive response and disease in plants.

Authors:  W L Deng; G Preston; A Collmer; C J Chang; H C Huang
Journal:  J Bacteriol       Date:  1998-09       Impact factor: 3.490

8.  Cloning, nucleotide sequence, and expression in Escherichia coli of levansucrase genes from the plant pathogens Pseudomonas syringae pv. glycinea and P. syringae pv. phaseolicola.

Authors:  U Hettwer; F R Jaeckel; J Boch; M Meyer; K Rudolph; M S Ullrich
Journal:  Appl Environ Microbiol       Date:  1998-09       Impact factor: 4.792

9.  Negative regulation of hrp genes in Pseudomonas syringae by HrpV.

Authors:  G Preston; W L Deng; H C Huang; A Collmer
Journal:  J Bacteriol       Date:  1998-09       Impact factor: 3.490

10.  Nonhost resistance of tomato to the bean pathogen Pseudomonas syringae pv. syringae B728a is due to a defective E3 ubiquitin ligase domain in avrptobb728a.

Authors:  Ching-Fang Chien; Johannes Mathieu; Chun-Hua Hsu; Patrick Boyle; Gregory B Martin; Nai-Chun Lin
Journal:  Mol Plant Microbe Interact       Date:  2013-04       Impact factor: 4.171

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