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Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins

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Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins. / Schechter, Lisa M; Vencato, Monica; Jordan, Katy L et al.
In: Molecular plant-microbe interactions : MPMI, Vol. 19, No. 11, 14.02.2007, p. 1180-92.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Schechter, LM, Vencato, M, Jordan, KL, Schneider, SE, Schneider, DJ & Collmer, A 2007, 'Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins', Molecular plant-microbe interactions : MPMI, vol. 19, no. 11, pp. 1180-92. https://doi.org/10.1094/MPMI-19-1180

APA

Schechter, L. M., Vencato, M., Jordan, K. L., Schneider, S. E., Schneider, D. J., & Collmer, A. (2007). Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins. Molecular plant-microbe interactions : MPMI, 19(11), 1180-92. https://doi.org/10.1094/MPMI-19-1180

Vancouver

Schechter LM, Vencato M, Jordan KL, Schneider SE, Schneider DJ, Collmer A. Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins. Molecular plant-microbe interactions : MPMI. 2007 Feb 14;19(11):1180-92. doi: 10.1094/MPMI-19-1180

Author

Schechter, Lisa M ; Vencato, Monica ; Jordan, Katy L et al. / Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins. In: Molecular plant-microbe interactions : MPMI. 2007 ; Vol. 19, No. 11. pp. 1180-92.

Bibtex

@article{90f38889c8f445e1b63a3b58521c294d,
title = "Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins",
abstract = "Pseudomonas syringae pv. tomato DC3000 is a pathogen of tomato and Arabidopsis that translocates virulence effector proteins into host cells via a type III secretion system (T3SS). Many effector-encoding hypersensitive response and pathogenicity (Hrp) outer protein (hop) genes have been identified previously in DC3000 using bioinformatic methods based on Hrp promoter sequences and characteristic N-terminal amino acid patterns that are associated with T3SS substrates. To approach completion of the Hop/effector inventory in DC3000, 44 additional candidates were tested by the Bordetella pertussis calmodulin-dependent adenylate cyclase (Cya) translocation reporter assay; 10 of the high-probability candidates were confirmed as T3SS substrates. Several previously predicted hop genes were tested for their ability to be expressed in an HrpL-dependent manner in culture or to be expressed in planta. The data indicate that DC3000 harbors 53 hop/avr genes and pseudogenes (encoding both injected effectors and T3SS substrates that probably are released to the apoplast); 33 of these genes are likely functional in DC3000, 12 are nonfunctional members of valid Hop families, and 8 are less certain regarding their production at functional levels. Growth of DC3000 in tomato and Arabidopsis Col-0 was not impaired by constitutive expression of repaired versions of two hops that were disrupted naturally by transposable elements or of hop genes that are naturally cryptic. In summary, DC3000 carries a complex mixture of active and inactive hop genes, and the hop genes in P. syringae can be identified efficiently by bioinformatic methods; however, a precise inventory of the subset of Hops that are important in pathogenesis awaits more knowledge based on mutant phenotypes and functions within plants.",
keywords = "Adenylate Cyclase Toxin/genetics, Arabidopsis/microbiology, Bacterial Outer Membrane Proteins/genetics, Bacterial Proteins/genetics, Bordetella pertussis/genetics, DNA-Binding Proteins/genetics, Genes, Plant, Solanum lycopersicum/microbiology, Protein Transport, Pseudomonas syringae/genetics, Sigma Factor/genetics, Tobacco, Virulence",
author = "Schechter, {Lisa M} and Monica Vencato and Jordan, {Katy L} and Schneider, {Sarah E} and Schneider, {David J} and Alan Collmer",
year = "2007",
month = feb,
day = "14",
doi = "10.1094/MPMI-19-1180",
language = "English",
volume = "19",
pages = "1180--92",
journal = "Molecular plant-microbe interactions : MPMI",
issn = "0894-0282",
publisher = "American Phytopathological Society",
number = "11",

}

RIS

TY - JOUR

T1 - Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins

AU - Schechter, Lisa M

AU - Vencato, Monica

AU - Jordan, Katy L

AU - Schneider, Sarah E

AU - Schneider, David J

AU - Collmer, Alan

PY - 2007/2/14

Y1 - 2007/2/14

N2 - Pseudomonas syringae pv. tomato DC3000 is a pathogen of tomato and Arabidopsis that translocates virulence effector proteins into host cells via a type III secretion system (T3SS). Many effector-encoding hypersensitive response and pathogenicity (Hrp) outer protein (hop) genes have been identified previously in DC3000 using bioinformatic methods based on Hrp promoter sequences and characteristic N-terminal amino acid patterns that are associated with T3SS substrates. To approach completion of the Hop/effector inventory in DC3000, 44 additional candidates were tested by the Bordetella pertussis calmodulin-dependent adenylate cyclase (Cya) translocation reporter assay; 10 of the high-probability candidates were confirmed as T3SS substrates. Several previously predicted hop genes were tested for their ability to be expressed in an HrpL-dependent manner in culture or to be expressed in planta. The data indicate that DC3000 harbors 53 hop/avr genes and pseudogenes (encoding both injected effectors and T3SS substrates that probably are released to the apoplast); 33 of these genes are likely functional in DC3000, 12 are nonfunctional members of valid Hop families, and 8 are less certain regarding their production at functional levels. Growth of DC3000 in tomato and Arabidopsis Col-0 was not impaired by constitutive expression of repaired versions of two hops that were disrupted naturally by transposable elements or of hop genes that are naturally cryptic. In summary, DC3000 carries a complex mixture of active and inactive hop genes, and the hop genes in P. syringae can be identified efficiently by bioinformatic methods; however, a precise inventory of the subset of Hops that are important in pathogenesis awaits more knowledge based on mutant phenotypes and functions within plants.

AB - Pseudomonas syringae pv. tomato DC3000 is a pathogen of tomato and Arabidopsis that translocates virulence effector proteins into host cells via a type III secretion system (T3SS). Many effector-encoding hypersensitive response and pathogenicity (Hrp) outer protein (hop) genes have been identified previously in DC3000 using bioinformatic methods based on Hrp promoter sequences and characteristic N-terminal amino acid patterns that are associated with T3SS substrates. To approach completion of the Hop/effector inventory in DC3000, 44 additional candidates were tested by the Bordetella pertussis calmodulin-dependent adenylate cyclase (Cya) translocation reporter assay; 10 of the high-probability candidates were confirmed as T3SS substrates. Several previously predicted hop genes were tested for their ability to be expressed in an HrpL-dependent manner in culture or to be expressed in planta. The data indicate that DC3000 harbors 53 hop/avr genes and pseudogenes (encoding both injected effectors and T3SS substrates that probably are released to the apoplast); 33 of these genes are likely functional in DC3000, 12 are nonfunctional members of valid Hop families, and 8 are less certain regarding their production at functional levels. Growth of DC3000 in tomato and Arabidopsis Col-0 was not impaired by constitutive expression of repaired versions of two hops that were disrupted naturally by transposable elements or of hop genes that are naturally cryptic. In summary, DC3000 carries a complex mixture of active and inactive hop genes, and the hop genes in P. syringae can be identified efficiently by bioinformatic methods; however, a precise inventory of the subset of Hops that are important in pathogenesis awaits more knowledge based on mutant phenotypes and functions within plants.

KW - Adenylate Cyclase Toxin/genetics

KW - Arabidopsis/microbiology

KW - Bacterial Outer Membrane Proteins/genetics

KW - Bacterial Proteins/genetics

KW - Bordetella pertussis/genetics

KW - DNA-Binding Proteins/genetics

KW - Genes, Plant

KW - Solanum lycopersicum/microbiology

KW - Protein Transport

KW - Pseudomonas syringae/genetics

KW - Sigma Factor/genetics

KW - Tobacco

KW - Virulence

U2 - 10.1094/MPMI-19-1180

DO - 10.1094/MPMI-19-1180

M3 - Journal article

C2 - 17073301

VL - 19

SP - 1180

EP - 1192

JO - Molecular plant-microbe interactions : MPMI

JF - Molecular plant-microbe interactions : MPMI

SN - 0894-0282

IS - 11

ER -