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bacteria:t3e:xopah [2020/06/22 08:48] christianvbacteria:t3e:xopah [2025/02/21 11:35] (current) – [Conservation] rkoebnik
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-====== XopAH ======+====== The Type III Effector XopAH from //Xanthomonas// ======
  
-Author: Steven J. Roberts\\ +Author: [[https://www.researchgate.net/profile/Steven_Roberts8|Steven J. Roberts]]\\ 
-Internal reviewer: FIXME \\ +Internal reviewer: [[https://www.researchgate.net/profile/Christian_Verniere|Christian Vernière ]]
-Expert reviewerFIXME+
  
 Class: XopAH\\ Class: XopAH\\
 Family: XopAH\\ Family: XopAH\\
-Prototype: XopAH (AvrXccC(//Xanthomonas campestris// pv. //campestris// strain 8004 - //Qian et al//., 2005)\\ +Prototype: AvrXccC (//Xanthomonas campestris// pv. //campestris//strain 8004)\\ 
-RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/ABQ10636.1|ABQ10636.1]] (440 aa) (gene [[https://www.ncbi.nlm.nih.gov/nuccore/EF529437.1|EF529437.1]] 1323 bp)\\+GenBank ID: [[https://www.ncbi.nlm.nih.gov/protein/ABQ10636.1|ABQ10636.1]] (440 aa)\\ 
 +RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/WP_011037263.1|WP_011037263.1]] (331 aa, perhaps 109 aa too short since the 440-aa version would include a typical N-terminal palmitoylation signal, MGLC)\\ 
 +Synonym: AvrXccC (//Xanthomonas campestris// pv. //campestris//), AvrXccFM (//Xanthomonas campestris// pv. //campestris//) (Castañeda //et al.//, 2005)\\
 3D structure: Unknown 3D structure: Unknown
  
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 === How discovered? === === How discovered? ===
  
- AvrXccC was described during a genome comparison analysis between  CKGE_TMP_i Xanthomonas  CKGE_TMP_i citri pv. citri and  CKGE_TMP_i X. campestris CKGE_TMP_i  pv. campestris Xcc strain ATCC33913=NCPPB528 (Da Silva et al., 2002) and in   a search of annotated genome (Castenada //et al//., 2005).+AvrXccC was described during a genome comparison analysis between //Xanthomonas citri// pv. citri and //X. campestris// pv. campestris Xcc strain ATCC 33913 NCPPB 528 (Da Silva et al., 2002) and in a search of annotated genome (Castenada //et al//., 2005).
 === (Experimental) evidence for being a T3E === === (Experimental) evidence for being a T3E ===
  
-Secreted XopAH (AvrXccC) proteins were detected in culture fluid from //Xcc// 8004 and //hrcV// mutant complemented strains but not from the //hrcV// mutant (Wang //et al//., 2007). Insertion and deletion mutants affecting the locus (Xcc2109) in the type strain (Xcc 528) resulted in loss of virulence on the host Florida Broad Leaf Mustard (Castenada //et al//., 2005).+Secreted XopAH (AvrXccC) proteins were detected in culture fluid from //Xcc// 8004 and //hrcV// mutant complemented strains but not from the //hrcV// mutant (Wang //et al//., 2007). Insertion and deletion mutants affecting the locus (Xcc2109) in the type strain (Xcc 528) resulted in loss of virulence on the host Florida Broad Leaf Mustard (Castañeda //et al//., 2005).
 === Regulation === === Regulation ===
  
-Promoter activity assays showed that the expression of XopAH (//avrXccC)// is //hrpG/hrpX//-dependent (Wang //et al//., 2007).+Promoter activity assays showed that the expression of XopAH (//avrXccC//is //hrpG/hrpX//-dependent (Wang //et al//., 2007).
 === Phenotypes === === Phenotypes ===
  
-This effector is required for full virulence in the susceptible host cabbage (//Brassica oleracea//) (Wang //et al//., 2007) and results in avirulence in the resistant host mustard (//Brassica napiformis//) (Castenada //et al//., 2005; <font 10.5pt/inherit;;#333333;;inherit>He et al., 2007; Wang //et al</font>//., 2007). The intact AvrB-AvrC domain of //AvrXccC<sub>8004</sub> // is essential and sufficient to elicit defense responses in an //Arabidopsis// resistant ecotype (Col-0) (Ho et al., 2013). +This effector is required for full virulence in the susceptible host cabbage (//Brassica oleracea//) (Wang //et al//., 2007) and results in avirulence in the resistant host mustard (//Brassica napiformis//) (Castaneda //et al//., 2005; He //et al//., 2007; Wang //et al//., 2007). The intact AvrB-AvrC domain of //AvrXccC<sub>8004</sub> // is essential and sufficient to elicit defense responses in an //Arabidopsis// resistant ecotype (Col-0) (Ho //et al//., 2013).
- +
-<font 10.5pt/inherit;;#333333;;white>In the interaction  CKGE_TMP_i Arabidopsis CKGE_TMP_i CKGE_TMP_i Xcc CKGE_TMP_i  strain 8004,  CKGE_TMP_i AvrXccC<sub>8004</sub> CKGE_TMP_i  not only presented its avirulence activity to trigger plant defense response but also possessed its virulence activity to manipulate the component involved in the ABA signalling pathway leading to an increase of ABA concentrations (Ho et al., 2013).</font>+
  
 +In the interaction //Arabidopsis// / //Xcc// strain 8004, AvrXccC<sub>8004</sub> not only presented its avirulence activity to trigger plant defense response but also possessed its virulence activity to manipulate the component involved in the ABA signalling pathway leading to an increase of ABA concentrations (Ho //et al.//, 2013).
 === Localization === === Localization ===
  
-XopAH (AvrXccC) is anchored to the plant plasma membrane, and the N‐terminal myristoylation site (amino acids 2–7: GLcaSK) is essential for its localization (Wang //et al//., 2007).+XopAH (AvrXccC) is anchored to the plant plasma membrane, and the N‐terminal myristoylation site (amino acids 2–7: GLcaSK) is essential for its localization (Wang //et al.//, 2007).
 === Enzymatic function === === Enzymatic function ===
  
- XopAH has a Fido/AvrB domain derived from the fic (cyclic adenosine monophosphate (cAMP)-induced filamentation and doc (death on curing) domains (Kinch et al., 2009). Structural comparisons resulted in the inclusion of similar segments of the T3 effector AvrB from  CKGE_TMP_i Pseudomonas syringae CKGE_TMP_i  species (Kinch et al., 2009; White et al., 2009). T3 effectors in the XopAH group could trans-AMPylate plant host proteins. AMPylation represents a posttranslational modification used to stably modify proteins with AMP (Kinch et al., 2009). +XopAH has a Fido/AvrB domain derived from the fic (cyclic adenosine monophosphate (cAMP)-induced filamentation and doc (death on curing) domains (Kinch //et al//., 2009). Structural comparisons resulted in the inclusion of similar segments of the T3 effector AvrB from //Pseudomonas syringae// species (Kinch //et al//., 2009; White //et al//., 2009). T3 effectors in the XopAH group could trans-AMPylate plant host proteins. AMPylation represents a posttranslational modification used to stably modify proteins with AMP (Kinch //et al.//, 2009).
 === Interaction partners === === Interaction partners ===
  
- not known ?+Not known.
  
 ===== Conservation ===== ===== Conservation =====
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 === In xanthomonads === === In xanthomonads ===
  
-In //Xanthomonas campestris// pv. campestris.  XopAH is also present in  CKGE_TMP_i X. arboricola CKGE_TMP_i  pv. juglandis within strains causing Walnut Blight but is absent from the strains causing vertical oozing canker (Cesbron et al., 2015). +In //Xanthomonas campestris// pv. campestris. XopAH is also present in //X. arboricola// pv. juglandis within strains causing Walnut Blight but is absent from the strains causing vertical oozing canker (Cesbron //et al.//, 2015).
 === In other plant pathogens/symbionts === === In other plant pathogens/symbionts ===
  
-Yes (AvrB //Pseudomonas savastanoi//, //Pseudomonas syringae//)+Yes (AvrB //Pseudomonas savastanoi//, //Pseudomonas syringae//(Lee //et al.//, 2004; Desveaux //et al.//, 2007) 
 ===== References ===== ===== References =====
  
-Castenada A, Reddy JD, El-Yacoubi B, Gabriel DW (2005). Mutagenesis of all eight avr genes in //Xanthomonas campestris// pv. //campestris// had no detected effect on pathogenicity, but one avr gene affected race specificity. Mol. Plant-Microbe Interact. 18: 1306-1317. DOI: [[https://doi.org/10.1094/MPMI-18-1306|10.1094/MPMI-18-1306]].+Castañeda A, Reddy JD, El-Yacoubi B, Gabriel DW (2005). Mutagenesis of all eight avr genes in //Xanthomonas campestris// pv. //campestris// had no detected effect on pathogenicity, but one //avr// gene affected race specificity. Mol. Plant Microbe Interact. 18: 1306-1317. DOI: [[https://doi.org/10.1094/MPMI-18-1306|10.1094/MPMI-18-1306]] 
 + 
 +Cesbron S, Briand M, Essakhi S, Gironde S, Boureau T, Manceau C, Fischer-Le Saux M, Jacques MA (2015)Comparative genomics of pathogenic and nonpathogenic strains of //Xanthomonas arboricola// unveil molecular and evolutionary events linked to pathoadaptation. Front. Plant Sci. 6: 1126. DOI: [[https://doi.org/10.3389/fpls.2015.01126|10.3389/fpls.2015.01126]] 
 + 
 +da Silva AC, Ferro JA, Reinach FC, Farah CS, Furlan LR, Quaggio RB, Monteiro-Vitorello CB, Van Sluys MA, Almeida NF, Alves LM, do Amaral AM, Bertolini MC, Camargo LE, Camarotte G, Cannavan F, Cardozo J, Chambergo F, Ciapina LP, Cicarelli RM, Coutinho LL, Cursino-Santos JR, El-Dorry H, Faria JB, Ferreira AJ, Ferreira RC, Ferro MI, Formighieri EF, Franco MC, Greggio CC, Gruber A, Katsuyama AM, Kishi LT, Leite RP, Lemos EG, Lemos MV, Locali EC, Machado MA, Madeira AM, Martinez-Rossi NM, Martins EC, Meidanis J, Menck CF, Miyaki CY, Moon DH, Moreira LM, Novo MT, Okura VK, Oliveira MC, Oliveira VR, Pereira HA, Rossi A, Sena JA, Silva C, de Souza RF, Spinola LA, Takita MA, Tamura RE, Teixeira EC, Tezza RI, Trindade dos Santos M, Truffi D, Tsai SM, White FF, Setubal JC, Kitajima JP (2002). Comparison of the genomes of two //Xanthomonas// pathogens with differing host specificities. Nature 417: 459-463. DOI: [[https://doi.org/10.1038/417459a|10.1038/417459a]] 
 + 
 +Desveaux D, Singer AU, Wu AJ, McNulty BC, Musselwhite L, Nimchuk Z, Sondek J, Dangl JL (2007). Type III effector activation via nucleotide binding, phosphorylation, and host target interaction. PLoS Pathog. 3: e48. DOI: [[https://doi.org/10.1371/journal.ppat.0030048|10.1371/journal.ppat.0030048]]. Erratum in: PLoS Pathog. (2007) 3: e90. 
 + 
 +He YQ, Zhang L, Jiang BL, Zhang ZC, Xu RQ, Tang DJ, Qin J, Jiang W, Zhang X, Liao J, Cao JR, Zhang SS, Wei ML, Liang XX, Lu GT, Feng JX, Chen B, Cheng J, Tang JL (2007). Comparative and functional genomics reveals genetic diversity and determinants of host specificity among reference strains and a large collection of Chinese isolates of the phytopathogen //Xanthomonas campestris// pv. //campestris//. Genome Biol. 8: R218. DOI: [[https://doi.org/10.1186/gb-2007-8-10-r218|10.1186/gb-2007-8-10-r218]]
  
-<font 10.5pt/inherit;;inherit;;white>CesbronS.BriandM.EssakhiS., Gironde, S., Boureau, T., Manceau, C., Fischer-Le Saux, M., and Jacques, MA. 2015.</font><font 10.5pt/inherit;;inherit;;inherit>Comparative genomics of pathogenic and nonpathogenic strains of  CKGE_TMP_i Xanthomonas arboricola CKGE_TMP_i  unveil molecular and evolutionary events linked to pathoadaptationFrontiers in plant science 6:1126.</font>+Ho YPTan CMLi MYLin HDeng WLYang JY (2013)The AvrB_AvrC Domain of AvrXccC of //Xanthomonas campestris// pvcampestris is required to elicit plant defense responses and manipulate ABA homeostasisMolPlant Microbe Interact. 26: 419-430DOI: [[https://doi.org/10.1094/mpmi-06-12-0164-r|10.1094/mpmi-06-12-0164-r]]
  
-<font 10.5pt/inherit;;inherit;;white>Da SilvaA. C.Ferro, J. A., Reinach, F. C., Farah, C. S., Furlan, L. R., Quaggio, R. B., Monteiro-Vitorello, C. B., Van Sluys, M. A., Almeida, N. F., Alves, L. M., Do Amaral, A. M., Bertolini, M. C., Camargo, L. E., Camarotte, G., Cannavan, F., Cardozo, J., Chambergo, F., Ciapina, L. P., Cicarelli, R. M., Coutinho, L. L., Cursino-Santos, J. R., El-Dorry, H., Faria, J. B., Ferreira, A. J., Ferreira, R. C., Ferro, M. I., Formighieri, E. F., Franco, M. C., Greggio, C. C., Gruber, A., Katsuyama, A. M., Kishi, L. T., Leite, R. P., Lemos, E. G., Lemos, M. V., Locali, E. C., Machado, M. A., Madeira, A. M., Martinez-Rossi, N. M., Martins, E. C., Meidanis, J., Menck, C. F., Miyaki, C. Y., Moon, D. H., Moreira, L. M., Novo, M. T., Okura, V. K.Oliveira, M. C., OliveiraV. R.Pereira, HA., Rossi, A., Sena, JA., Silva, C., De Souza, RF., Spinola, LA., Takita, M. A., Tamura, R. E., Teixeira, E. C., Tezza, R. I., Trindade dos Santos, M., Truffi, D., Tsai, S. M., White, F. F., Setubal, J. C., and Kitajima, J. P. 2002. Comparison of the genomes of two  CKGE_TMP_i Xanthomonas CKGE_TMP_i  pathogens with differing host specificities. Nature 417:459-463.</font>+Kinch LNYarbrough MLOrth K, Grishin NV (2009)Fidoa novel AMPylation domain common to FicDocand AvrBPLoS One 4: e5818DOI: [[https://doi.org/10.1371/journal.pone.0005818|10.1371/journal.pone.0005818]]
  
-<font 10.5pt/inherit;;inherit;;white>HeY. Q.ZhangL.JiangB. L.ZhangZC., Xu, RQ., Tang, DJ., Qin, J., Jiang, W., Zhang, X., Liao, J., Cao, JR., Zhang, SS., Wei, M. L., Liang, X. X., Lu, G. T., Feng, J. X., Chen, B., Cheng, J., and Tang, J. L. 2007. Comparative and functional genomics reveals genetic diversity and determinants of host specificity among reference strains and a large collection of Chinese isolates of the phytopathogen  CKGE_TMP_i Xanthomonas campestris CKGE_TMP_i  pv. campestris. Genome Biology 8:R218.</font>+Lee CCWood MDNg KAndersen CBLiu YLuginbühl PSpraggon GKatagiri F (2004)Crystal structure of the type III effector AvrB from //Pseudomonas syringae//Structure 12: 487-494DOI: [[https://doi.org/10.1016/j.str.2004.02.013|10.1016/j.str.2004.02.013]]
  
-<font 10.5pt/inherit;;inherit;;white>Ho, Y. P.TanC. M.LiM. Y.Lin, H., Deng, WL.and YangJ. Y. 2013. The AvrB_AvrC Domain of AvrXccC of  CKGE_TMP_i Xanthomonas campestris CKGE_TMP_i  pv. campestris Is Required to Elicit Plant Defense Responses and Manipulate ABA HomeostasisMolPlant-Microbe Interact26:419-430.</font>+Qian WJia Y, Ren SXHe Y QFeng JXLu LFSun QYing G, Tang DJ, Tang H, Wu W, Hao P, Wang L, Jiang BLZeng S, Gu WY, Lu G, Rong L, Tian Y, Yao Z, Fu G, Chen B, Fang R, Qiang B, Chen Z, Zhao GP, Tang JL, He C (2005)Comparative and functional genomic analyses of the pathogenicity of phytopathogen //Xanthomonas campestris// pv. //campestris.// Genome Res15: 757-767DOI[[https://doi.org/10.1101/gr.3378705|10.1101/gr.3378705]]
  
-<font 10.5pt/inherit;;inherit;;inherit>Kinch, LN., Yarbrough, ML., Orth, K., and Grishin, NV2009Fido, a Novel AMPylation Domain Common to Fic, Doc, and AvrBPlos One 4: e5818.</font>+Wang L, Tang X, He C (2007)The bifunctional effector AvrXccC of //Xanthomonas campestris// pv//campestris// requires plasma membrane-anchoring for host recognitionMolPlant Pathol8: 491-501DOI: [[https://doi.org/10.1111/j.1364-3703.2007.00409.x|10.1111/j.1364-3703.2007.00409.x]]
  
-Qian WJia YRen SXHe Y Q, Feng JX, Lu LF, Sun Q, Ying G, Tang DJ, Tang H, Wu W, Hao P, Wang L, Jiang BL, Zeng S, Gu WY, Lu G, Rong L, Tian Y, Yao Z, Fu G, Chen B, Fang R, Qiang B, Chen Z, Zhao GP, Tang JL and He C (2005). Comparative and functional genomic analyses of the pathogenicity of phytopathogen //Xanthomonas campestris// pv//campestris.// Genome Research 15757-767. DOI: [[https://doi.org/10.1101/gr.3378705|10.1101/gr.3378705]].+White FFPotnis NJones JBKoebnik R (2009). The type III effectors of //Xanthomonas//MolPlant Pathol. 10749-766. DOI: [[https://doi.org/10.1111/j.1364-3703.2009.00590.x|10.1111/j.1364-3703.2009.00590.x]]
  
-Wang L, Tang X, He C (2007). The bifunctional effector AvrXccC of //Xanthomonas campestris// pv. //campestris// requires plasma membrane-anchoring for host recognition. Mol. Plant Pathol. 8: 491-501. DOI: [[https://doi.org/10.1111/j.1364-3703.2007.00409.x|10.1111/j.1364-3703.2007.00409.x]].+===== Acknowledgements =====
  
-<font 10.5pt/inherit;;inherit;;inherit>White, F. F., Potnis, N., Jones, J. B., and Koebnik, R. 2009. The type III effectors of  CKGE_TMP_i Xanthomonas CKGE_TMP_i .</font><font 10.5pt/inherit;;inherit;;inherit>Mol. Plant Pathol. 10:749-766.</font>+This fact sheet is based upon work from COST Action CA16107 EuroXanthsupported by COST (European Cooperation in Science and Technology).
  
bacteria/t3e/xopah.1592812137.txt.gz · Last modified: 2023/01/09 10:20 (external edit)