Literature DB >> 12580281

A pseudomonas syringae pv. tomato DC3000 Hrp (Type III secretion) deletion mutant expressing the Hrp system of bean pathogen P. syringae pv. syringae 61 retains normal host specificity for tomato.

Derrick E Fouts1, Jorge L Badel, Adela R Ramos, Ryan A Rapp, Alan Collmer.   

Abstract

The plant pathogenic species Pseudomonas syringae is divided into numerous pathovars based on host specificity. For example, P. syringae pv. tomato DC3000 is pathogenic on tomato and Arabidopsis, whereas P. syringae pv. syringae 61 is pathogenic on bean. The ability of P. syringae strains to elicit the hypersensitive response (HR) in non-hosts or be pathogenic (or parasitic) in hosts is dependent on the Hrp (type III secretion) system and effector proteins this system is thought to inject into plant cells. To test the role of the Hrp system in determining host range, the hrp/hrc gene cluster (hrpK through hrpR) was deleted from DC3000 and complemented in trans with the orthologous cluster from strain 61. Mutant CUCPB5114 expressing the bean pathogen Hrp system on plasmid pCPP2071 retained the ability of wild-type DC3000 to elicit the HR in bean, to grow and cause bacterial speck in tomato, and to elicit a cultivar-specific (gene-for-gene) HR in tomato plants carrying the Pto resistance gene. However, the symptoms produced in compatible tomato plants involved markedly reduced chlorosis, and CUCPB5114(pCPP2071) did not grow or produce symptoms in Arabidopsis Col-0 although it was weakly virulent in NahG Arabidopsis. A hypersensitive-like collapse was produced by CUCPB5114(pCPP2071) in Arabidopsis Col-0 at 1 x 10(7) CFU/ml, but only if the bacteria also expressed AvrB, which is recognized by the RPM1 resistance gene in Col-0 and confers incompatibility. These observations support the concept that the P. syringae effector proteins, rather than secretion system components, are the primary determinants of host range at both the species and cultivar levels of host specificity.

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Year:  2003        PMID: 12580281     DOI: 10.1094/MPMI.2003.16.1.43

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


  11 in total

1.  Translocation of NopP by Sinorhizobium fredii USDA257 into Vigna unguiculata root nodules.

Authors:  Lisa M Schechter; Jeanette Guenther; Elizabeth A Olcay; Sungchan Jang; Hari B Krishnan
Journal:  Appl Environ Microbiol       Date:  2010-04-09       Impact factor: 4.792

2.  Pseudomonas syringae pv. tomato DC3000 CmaL (PSPTO4723), a DUF1330 family member, is needed to produce L-allo-isoleucine, a precursor for the phytotoxin coronatine.

Authors:  Jay N Worley; Alistair B Russell; Aaron G Wexler; Philip A Bronstein; Brian H Kvitko; Stuart B Krasnoff; Kathy R Munkvold; Bryan Swingle; Donna M Gibson; Alan Collmer
Journal:  J Bacteriol       Date:  2012-11-09       Impact factor: 3.490

3.  The membrane-anchored BOTRYTIS-INDUCED KINASE1 plays distinct roles in Arabidopsis resistance to necrotrophic and biotrophic pathogens.

Authors:  Paola Veronese; Hirofumi Nakagami; Burton Bluhm; Synan Abuqamar; Xi Chen; John Salmeron; Robert A Dietrich; Heribert Hirt; Tesfaye Mengiste
Journal:  Plant Cell       Date:  2005-12-09       Impact factor: 11.277

4.  Identification of harpins in Pseudomonas syringae pv. tomato DC3000, which are functionally similar to HrpK1 in promoting translocation of type III secretion system effectors.

Authors:  Brian H Kvitko; Adela R Ramos; Joanne E Morello; Hye-Sook Oh; Alan Collmer
Journal:  J Bacteriol       Date:  2007-09-14       Impact factor: 3.490

5.  Pseudomonas syringae HrpP Is a type III secretion substrate specificity switch domain protein that is translocated into plant cells but functions atypically for a substrate-switching protein.

Authors:  Joanne E Morello; Alan Collmer
Journal:  J Bacteriol       Date:  2009-03-06       Impact factor: 3.490

6.  Early detection of bean infection by Pseudomonas syringae in asymptomatic leaf areas using chlorophyll fluorescence imaging.

Authors:  Luis Rodríguez-Moreno; Mónica Pineda; Julia Soukupová; Alberto P Macho; Carmen R Beuzón; Matilde Barón; Cayo Ramos
Journal:  Photosynth Res       Date:  2007-11-14       Impact factor: 3.573

7.  Diverse evolutionary mechanisms shape the type III effector virulence factor repertoire in the plant pathogen Pseudomonas syringae.

Authors:  Laurence Rohmer; David S Guttman; Jeffery L Dangl
Journal:  Genetics       Date:  2004-07       Impact factor: 4.562

8.  Pseudomonas syringae type III secretion system targeting signals and novel effectors studied with a Cya translocation reporter.

Authors:  Lisa M Schechter; Kathy A Roberts; Yashitola Jamir; James R Alfano; Alan Collmer
Journal:  J Bacteriol       Date:  2004-01       Impact factor: 3.490

9.  Identification of Pseudomonas syringae pv. syringae 61 type III secretion system Hrp proteins that can travel the type III pathway and contribute to the translocation of effector proteins into plant cells.

Authors:  Adela R Ramos; Joanne E Morello; Sandeep Ravindran; Wen-Ling Deng; Hsiou-Chen Huang; Alan Collmer
Journal:  J Bacteriol       Date:  2007-05-25       Impact factor: 3.490

10.  Functional and computational analysis of amino acid patterns predictive of type III secretion system substrates in Pseudomonas syringae.

Authors:  Lisa M Schechter; Joy C Valenta; David J Schneider; Alan Collmer; Eric Sakk
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

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