HpaP modulates type III effector secretion in Ralstonia solanacearum and harbours a substrate specificity switch domain essential for virulence. (19th February 2014)

• Record Type: Journal Article
• Authors: Lohou, David; Turner, Marie; Lonjon, Fabien; Cazalé, Anne‐Claire; Peeters, Nemo; Genin, Stéphane; Vailleau, Fabienne
• Is Part Of: Molecular plant pathology. Volume 15:Number 6(2014:Aug.)
• Page Start: 601
• Page End: 614
• Publication Date: 2014-02-19
• Subjects: Plant diseases -- Molecular aspects -- Periodicals; Plant-pathogen relationships -- Molecular aspects -- Periodicals; 571.936
• DOI: 10.1111/mpp.12119
• Languages: English
• ISSNs: 1464-6722

Abstract

<abstract abstract-type="main"> <title>Summary</title> <p>Many pathogenic bacteria have evolved a type III secretion system (T3SS) to successfully invade their host. This extracellular apparatus allows the translocation of proteins, called type III effectors (T3Es), directly into the host cells. T3Es are virulence factors that have been shown to interfere with the host's immunity or to provide nutrients from the host to the bacteria. The Gram‐negative bacterium <italic>Ralstonia solanacearum</italic> is a worldwide major crop pest whose virulence strongly relies on the T3SS. In <italic>R. solanacearum</italic>, transcriptional regulation has been extensively studied. However, very few data are available concerning the role played by type III‐associated regulators, such as type III chaperones and T3SS control proteins. Here, we characterized HpaP, a putative type III secretion substrate specificity switch (T3S4) protein of <italic>R. solanacearum</italic> which is not secreted by the bacterium or translocated in the plant cells. HpaP self‐interacts and interacts with the PopP1 T3E. HpaP modulates the secretion of early (HrpY pilin) and late (AvrA and PopP1 T3Es) type III substrates. HpaP is dispensable for the translocation of T3Es into the host cells. Finally, we identified two regions of five amino acids in the T3S4 domain that are essential for efficient PopP1 secretion and for HpaP's role in virulence on tomato and <italic>Arabidopsis thaliana</italic>, but not required for HpaP–HpaP and HpaP–PopP1 interactions. Taken together, our results indicate that HpaP is a putative <italic>R. solanacearum</italic> T3S4 protein important for full pathogenicity on several hosts, acting as a helper for PopP1 secretion, and repressing AvrA and HrpY secretion.</p> </abstract>