Recombineering and stable integration of the Pseudomonas syringae pv. syringae 61 hrp/hrc cluster into the genome of the soil bacterium Pseudomonas fluorescens Pf0-1

被引:104
作者
Thomas, William J. [1 ,2 ]
Thireault, Caitlin A. [1 ]
Kimbrel, Jeffrey A. [1 ,2 ]
Chang, Jeff H. [1 ,2 ,3 ]
机构
[1] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Mol & Cellular Biol Program, Corvallis, OR 97331 USA
[3] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
关键词
type-III secretion system; hrp; hrc; type-III effectors; plant defense; Pseudomonas syringae; virulence; AVIRULENCE GENE AVRRPT2; PROGRAMMED CELL-DEATH; III EFFECTOR PROTEINS; RANGE CLONING VECTOR; TOMATO DC3000; DISEASE RESISTANCE; HOMOLOGOUS RECOMBINATION; INNATE IMMUNITY; PLANT IMMUNITY; PHYTOPATHOGENIC BACTERIA;
D O I
10.1111/j.1365-313X.2009.03998.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
P>Many Gram-negative bacteria use a type III secretion system (T3SS) to establish associations with their hosts. The T3SS is a conduit for direct injection of type-III effector proteins into host cells, where they manipulate the host for the benefit of the infecting bacterium. For plant-associated pathogens, the variations in number and amino acid sequences of type-III effectors, as well as their functional redundancy, make studying type-III effectors challenging. To mitigate this challenge, we developed a stable delivery system for individual or defined sets of type-III effectors into plant cells. We used recombineering and Tn5-mediated transposition to clone and stably integrate, respectively, the complete hrp/hrc region from Pseudomonas syringae pv. syringae 61 into the genome of the soil bacterium Pseudomonas fluorescens Pf0-1. We describe our development of Effector-to-Host Analyzer (EtHAn), and demonstrate its utility for studying effectors for their in planta functions.
引用
收藏
页码:919 / 928
页数:10
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