A modular toolbox for Golden‐Gate‐based plasmid assembly streamlines the generation of Ralstonia solanacearum species complex knockout strains and multi‐cassette complementation constructs. (1st February 2018)

• Record Type: Journal Article
• Authors: Wu, Dousheng; Schandry, Niklas; Lahaye, Thomas
• Is Part Of: Molecular plant pathology. Volume 19:Number 6(2018)
• Page Start: 1511
• Page End: 1522
• Publication Date: 2018-02-01
• Subjects: effector -- Golden‐Gate cloning -- modular cloning -- Ralstonia solanacearum species complex (Rssc) -- type III secretion system (T3SS); Plant diseases -- Molecular aspects -- Periodicals; Plant-pathogen relationships -- Molecular aspects -- Periodicals; 571.936
• DOI: 10.1111/mpp.12632
• Languages: English
• ISSNs: 1464-6722

Abstract

Summary: Members of the Ralstonia solanacearum species complex ( Rssc ) cause bacterial wilt, a devastating plant disease that affects numerous economically important crops. Like other bacterial pests, Rssc injects a cocktail of effector proteins via the bacterial type III secretion system into host cells that collectively promote disease. Given their functional relevance in disease, the identification of Rssc effectors and the investigation of their in planta function are likely to provide clues on how to generate pest‐resistant crop plants. Accordingly, molecular analysis of effector function is a focus of Rssc research. The elucidation of effector function requires corresponding gene knockout strains or strains that express the desired effector variants. The cloning of DNA constructs that facilitate the generation of such strains has hindered the investigation of Rssc effectors. To overcome these limitations, we have designed, generated and functionally validated a toolkit consisting of DNA modules that can be assembled via Golden‐Gate (GG) cloning into either desired gene knockout constructs or multi‐cassette expression constructs. The Ralstonia ‐GG‐kit is compatible with a previously established toolkit that facilitates the generation of DNA constructs for in planta expression. Accordingly, cloned modules, encoding effectors of interest, can be transferred to vectors for expression in Rssc strains and plant cells. As many effector genes have been cloned in the past as GATEWAY entry vectors, we have also established a conversion vector that allows the implementation of GATEWAY entry vectors into the Ralstonia ‐GG‐kit. In summary, the Ralstonia ‐GG‐kit provides a valuable tool for the genetic investigation of genes encoding effectors and other Rssc genes.