Literature DB >> 7579617

The complete hrp gene cluster of Pseudomonas syringae pv. syringae 61 includes two blocks of genes required for harpinPss secretion that are arranged colinearly with Yersinia ysc homologs.

H C Huang1, R H Lin, C J Chang, A Collmer, W L Deng.   

Abstract

Pseudomonas syringae pv. syringae 61 contains a 25-kb hrp cluster that is sufficient to elicit the hypersensitive response (HR) in nonhost plants. Previous studies have shown that mutations in complementation groups VIII, IX, and XI in the hrp cluster abolished the ability of the bacterium to cause the HR. The sequence of a 3.7-kb SmaI-SstI fragment covering groups VIII and IX now reveals five open reading frames (ORFs) in the same transcript, designated as hrpU, hrpW, hrpO, hrpX, and hrpY, and predicted to encode proteins of 14,795, 23,211, 9,381, 28,489, and 39,957 Da, respectively. The hrpU, hrpW, hrpO, hrpX, and hrpY genes are homologous and arranged colinearly with the yscQ/spa33/spaO, yscR/spa24/spaP, yscS/spa9/spaQ, yscT/spa29/spaR, and yscU/spa40/spaS genes of Yersinia spp., Shigella flexneri, and Salmonella typhimurium, respectively. These proteins also show similarity to Fli/Flh proteins of Bacillus and enteric bacteria. The Ysc and Spa proteins are involved in the secretion of virulence factors, like the Yop and Ipa proteins. Fli/Flh proteins are involved in flagellar biogenesis. The sequence of a 2.9-kb EcoRV-EcoRI DNA fragment containing mainly group XI revealed five ORFs, designated hrpC, hrpD, hrpE, hrpF, and hrpG, predicted to encode proteins of 29,096, 15,184, 21,525, 7,959, and 13,919 Da, respectively. The first three genes belong to an operon containing hrpZ, which encodes an extracellular protein that elicits the HR. hrpF and hrpG are two potential ORFs upstream of hrpH in the hrpH operon. HrpC is homologous to Yersinia YscJ, Pseudomonas solanacearum HrpI, Xanthomonas compestris pv. vesicatoria HrpB3, and Rhizobium fredii NolT. HrpE is similar to YscL of Yersinia spp. P. s. pv. syringae 61 Hrp proteins are most similar to Ysc proteins among those homologs. TnphoA insertions in hrpC, hrpE, hrpW, hrpX, and hrpY abolished the ability of P. s.pv. syringae 61 to secrete HrpZ (harpinPss), as determined by immunoblot analysis of cell-bound and culture supernatant fractions. Thus, many of the proteins required for flagellar biogenesis and virulence protein secretion in plant and animal pathogens may have a common ancestry.

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Year:  1995        PMID: 7579617     DOI: 10.1094/mpmi-8-0733

Source DB:  PubMed          Journal:  Mol Plant Microbe Interact        ISSN: 0894-0282            Impact factor:   4.171


  34 in total

1.  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

2.  Bacterial Pathogens in Plants: Life up against the Wall.

Authors:  J. R. Alfano; A. Collmer
Journal:  Plant Cell       Date:  1996-10       Impact factor: 11.277

3.  Elicitation of Plant Hypersensitive Response by Bacteria.

Authors:  S. Y. He
Journal:  Plant Physiol       Date:  1996-11       Impact factor: 8.340

4.  The hrpA and hrpC operons of Erwinia amylovora encode components of a type III pathway that secretes harpin.

Authors:  J F Kim; Z M Wei; S V Beer
Journal:  J Bacteriol       Date:  1997-03       Impact factor: 3.490

Review 5.  Type III protein secretion systems in bacterial pathogens of animals and plants.

Authors:  C J Hueck
Journal:  Microbiol Mol Biol Rev       Date:  1998-06       Impact factor: 11.056

6.  Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp.

Authors:  A J Bogdanove; Z M Wei; L Zhao; S V Beer
Journal:  J Bacteriol       Date:  1996-03       Impact factor: 3.490

7.  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.

Authors:  A O Charkowski; H C Huang; A Collmer
Journal:  J Bacteriol       Date:  1997-06       Impact factor: 3.490

Review 8.  The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death.

Authors:  J R Alfano; A Collmer
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

9.  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

10.  The Active Oxygen Response of Cell Suspensions to Incompatible Bacteria Is Not Sufficient to Cause Hypersensitive Cell Death.

Authors:  J. A. Glazener; E. W. Orlandi; C. J. Baker
Journal:  Plant Physiol       Date:  1996-03       Impact factor: 8.340

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