Four bottlenecks restrict colonization and invasion by the pathogen Ralstonia solanacearum in resistant tomato. (24th December 2019)

• Record Type: Journal Article
• Authors: Planas-Marquès, Marc; Kressin, Jonathan P; Kashyap, Anurag; Panthee, Dilip R; Louws, Frank J; Coll, Nuria S; Valls, Marc
• Editors: Bozhkov, Peter
• Is Part Of: Journal of experimental botany. Volume 71:Number 6(2020)
• Page Start: 2157
• Page End: 2171
• Publication Date: 2019-12-24
• Subjects: Bacterial wilt -- disease resistance -- Ralstonia solanacearum -- tomato -- vascular pathogen -- xylem; Botany -- Periodicals; Botany, Experimental -- Periodicals; Plant physiology -- Periodicals; 580
• DOI: 10.1093/jxb/erz562
• Languages: English
• ISSNs: 0022-0957

Abstract

Abstract : The spatio-temporal dynamics of the tomato– Ralstonia solanacearum interaction reveal spread of the pathogen out of the xylem and four different limitations to bacterial colonization in resistant tomato. Abstract: Ralstonia solanacearum is a bacterial vascular pathogen causing devastating bacterial wilt. In the field, resistance against this pathogen is quantitative and is available for breeders only in tomato and eggplant. To understand the basis of resistance to R. solanacearum in tomato, we investigated the spatio-temporal dynamics of bacterial colonization using non-invasive live monitoring techniques coupled to grafting of susceptible and resistant varieties. We found four 'bottlenecks' that limit the bacterium in resistant tomato: root colonization, vertical movement from roots to shoots, circular vascular bundle invasion, and radial apoplastic spread in the cortex. Radial invasion of cortical extracellular spaces occurred mostly at late disease stages but was observed throughout plant infection. This study shows that resistance is expressed in both root and shoot tissues, and highlights the importance of structural constraints to bacterial spread as a resistance mechanism. It also shows that R. solanacearum is not only a vascular pathogen but spreads out of the xylem, occupying the plant apoplast niche. Our work will help elucidate the complex genetic determinants of resistance, setting the foundations to decipher the molecular mechanisms that limit pathogen colonization, which may provide new precision tools to fight bacterial wilt in the field.