EuroXanth DokuWiki

User Tools

Site Tools

Trace:
bacteria:t3e:xopx

Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revisionPrevious revision
Next revision		Previous revision
bacteria:t3e:xopx [2025/02/13 12:56] – jfpothierbacteria:t3e:xopx [2025/07/24 22:54] (current) – jfpothier
Line 2: Line 2:
  
 Author: [[https://www.researchgate.net/profile/Lucas_Moriniere|Lucas Morinière]] & [[https://www.researchgate.net/profile/Sohini_Deb|Sohini Deb]]\\ Author: [[https://www.researchgate.net/profile/Lucas_Moriniere|Lucas Morinière]] & [[https://www.researchgate.net/profile/Sohini_Deb|Sohini Deb]]\\
-Internal reviewer: Coline Sciallano\\ +Internal reviewer: [[https://www.researchgate.net/profile/Coline-Sciallano|Coline Sciallano]]\\ 
-Expert reviewer: Ramesh V. Sonti+Expert reviewer: [[https://www.researchgate.net/profile/Ramesh_Sonti|Ramesh V. Sonti]]\\
  
 Class: XopX\\ Class: XopX\\
Line 17: Line 17:
  
 XopX was discovered through the screening of a genomic cosmid library of //X. euvesicatoria// strain GM98-38 conjugated in //X. campestris// pv. //campestris// that allowed //Xcc// to elicit an //Xcv// cell death-like response when inoculated on //N. benthamiana// (Metz //et al//., 2005). XopX was discovered through the screening of a genomic cosmid library of //X. euvesicatoria// strain GM98-38 conjugated in //X. campestris// pv. //campestris// that allowed //Xcc// to elicit an //Xcv// cell death-like response when inoculated on //N. benthamiana// (Metz //et al//., 2005).
 +
 === (Experimental) evidence for being a T3E === === (Experimental) evidence for being a T3E ===
  
 Translational fusions of XopX with the calmodulin-dependent adenylate cyclase domain of //Bordetella pertussis// (Cya) were exchanged by simple homologous recombination into the genomic copy of //xopX// of //X. euvesicatoria// strains 85* (constitutive //hrp// expression mutant), 85* Δ//hrcV// (T3SS-defective mutant) and wild-type GM98-38. All Cya fusion strains except 85* Δ//hrcV// still induced cell death response activity in //N. benthamiana//. Moreover, leaf extracts of //N. benthamiana// inoculated with these fusion strains were assayed for cAMP, and only strains with a functional T3SS showed an increase in cAMP levels due to translocation of the Cya reporter protein into the plant (Metz //et al//., 2005). Translational fusions of XopX with the calmodulin-dependent adenylate cyclase domain of //Bordetella pertussis// (Cya) were exchanged by simple homologous recombination into the genomic copy of //xopX// of //X. euvesicatoria// strains 85* (constitutive //hrp// expression mutant), 85* Δ//hrcV// (T3SS-defective mutant) and wild-type GM98-38. All Cya fusion strains except 85* Δ//hrcV// still induced cell death response activity in //N. benthamiana//. Moreover, leaf extracts of //N. benthamiana// inoculated with these fusion strains were assayed for cAMP, and only strains with a functional T3SS showed an increase in cAMP levels due to translocation of the Cya reporter protein into the plant (Metz //et al//., 2005).
 +
 === Regulation === === Regulation ===
  
 qRT-PCR revealed that transcript levels of 15 out of 18 tested non-TAL effector genes (as well as the regulatory genes //hrpG// and //hrpX//), including //xopX//, were significantly reduced in the //Xanthomonas oryzae// pv. //oryzae// Δ//xrvC// mutant compared with those in the wild-type strain PXO99<sup>A</sup> (Liu //et al.//, 2016). qRT-PCR revealed that transcript levels of 15 out of 18 tested non-TAL effector genes (as well as the regulatory genes //hrpG// and //hrpX//), including //xopX//, were significantly reduced in the //Xanthomonas oryzae// pv. //oryzae// Δ//xrvC// mutant compared with those in the wild-type strain PXO99<sup>A</sup> (Liu //et al.//, 2016).
 +
 === Phenotypes === === Phenotypes ===
  
Line 28: Line 31:
   * During infection of rice (//Oryza sativa//) with //Xanthomonas oryzae// pv. //oryzae//, XopX was shown to be an inhibitor of rice innate immune response, as it suppresses LipA-induced callose deposition (Sinha //et al//., 2013).   * During infection of rice (//Oryza sativa//) with //Xanthomonas oryzae// pv. //oryzae//, XopX was shown to be an inhibitor of rice innate immune response, as it suppresses LipA-induced callose deposition (Sinha //et al//., 2013).
   * XopX is required for the development of //X. euvesicatoria//- induced symptoms in the bacterial spot disease of tomato (//Solanum lycopersicum//) and pepper (//Capsicum annuum//). Indeed, it promotes ethylene production, and therefore chlorosis and plant cell death during infection by //X. euvesicatoria// of susceptible tomato and in transient expression assays in tobacco. Interestingly, it also suppresses flagellin-induced production of reactive oxygen species (ROS) while promoting the accumulation of pattern-triggered immunity (PTI) gene transcripts (Stork //et al//., 2015). Eventually, the complex behavior of XopX //in planta//, which combines activation and suppression of immunity-related plant responses at the same time, allows to classify this effector with the T3Es that activates the plant ‘default to death and defense’ response (Lindeberg //et al//., 2012; Stork //et al//., 2015).   * XopX is required for the development of //X. euvesicatoria//- induced symptoms in the bacterial spot disease of tomato (//Solanum lycopersicum//) and pepper (//Capsicum annuum//). Indeed, it promotes ethylene production, and therefore chlorosis and plant cell death during infection by //X. euvesicatoria// of susceptible tomato and in transient expression assays in tobacco. Interestingly, it also suppresses flagellin-induced production of reactive oxygen species (ROS) while promoting the accumulation of pattern-triggered immunity (PTI) gene transcripts (Stork //et al//., 2015). Eventually, the complex behavior of XopX //in planta//, which combines activation and suppression of immunity-related plant responses at the same time, allows to classify this effector with the T3Es that activates the plant ‘default to death and defense’ response (Lindeberg //et al//., 2012; Stork //et al//., 2015).
-  *XopX is required for full virulence in //Xanthomonas axonopodis// pv. //manihotis//CIO151 strain. A //Xam// strain deleted for //xopX//  showed decreased ability to produce symptoms in leaves of cassava. Also, the// xopX //KO reached more than one log unit lower populations than those observed for the wild‐type strain. This underlies the importance of this effector for disease developement (Medina //et al//., 2018).+  *XopX is required for full virulence in //Xanthomonas axonopodis// pv. //manihotis//CIO151 strain. A //Xam// strain deleted for //xopX//  showed decreased ability to produce symptoms in leaves of cassava. Also, the //xopX// KO reached more than one log unit lower populations than those observed for the wild‐type strain. This underlies the importance of this effector for disease developement (Medina //et al//., 2018).
   * When expressed in //Pseudomonas fluorescens// 55 (//Pf//55), a non‐pathogenic bacterium capable of eliciting PTI (callose deposit) in //Arabidopsis// Col‐0 plants, XopX is not able to reduce callose deposit, suggesting in these conditions, the effector is not able to suppress PTI. Using the same heterologuous system, XopX is not able to suppress the HR triggered by Pf 55 HopA1 on tobacco, suggesting that is these conditions, XopX do not act as an ETI suppressor. (Medina //et al//., 2018).   * When expressed in //Pseudomonas fluorescens// 55 (//Pf//55), a non‐pathogenic bacterium capable of eliciting PTI (callose deposit) in //Arabidopsis// Col‐0 plants, XopX is not able to reduce callose deposit, suggesting in these conditions, the effector is not able to suppress PTI. Using the same heterologuous system, XopX is not able to suppress the HR triggered by Pf 55 HopA1 on tobacco, suggesting that is these conditions, XopX do not act as an ETI suppressor. (Medina //et al//., 2018).
   * When transiently expressed in //N. benthamiana// by //Agrobacterium tumefaciens//–mediated expression system, XopX from //X. oryzae// pv. //oryzicola// cause the nonhost HR at approximately 2 days (Li //et al., //2015).   * When transiently expressed in //N. benthamiana// by //Agrobacterium tumefaciens//–mediated expression system, XopX from //X. oryzae// pv. //oryzicola// cause the nonhost HR at approximately 2 days (Li //et al., //2015).
bacteria/t3e/xopx.1739451416.txt.gz · Last modified: 2025/02/13 12:56 by jfpothier

Page Tools

Except where otherwise noted, content on this wiki is licensed under the following license: CC Attribution-Share Alike 4.0 International
CC Attribution-Share Alike 4.0 International Donate Powered by PHP Valid HTML5 Valid CSS Driven by DokuWiki