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--- bacteria:t3e:avrbs2 [2020/07/13 14:01]
rkoebnik [References]
+++ bacteria:t3e:avrbs2 [2020/07/17 10:29]
rkoebnik [References]
@@ Line 9: / Line 9: @@
 Prototype: AvrBs2 (//Xanthomonas euvesicatoria// pv. //euvesicatoria//, ex //Xanthomonas campestris// pv. //vesicatoria//; strain 85-10)\\
 RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/WP_011345810.1|WP_011345810.1]] (714 aa)\\
-Synonym: //avrRxc1/3// (Ignatov //et al.//, 2002)\\
+Synonym: AvrRxc1/3 (Ignatov //et al.//, 2002)\\
 D structure: Unknown
@@ Line 38: / Line 38: @@
   * AvrBs2 transiently expressed in //Arabidopsis//  protoplasts suppressed flg22-induced NHO1 expression (Li //et al//., 2015).
   * Induced expression of AvrBs2 in transgenic cell cultures was shown to dramatically suppress flg22-induced and chitin-induced immune responses, such as ROS burst and PR gene expression (Li //et al//., 2015).
-  * A ∆//xopK//  mutant strain of //Xanthomonas phaseoli//  pv. //manihotis//  (aka //Xanthomonas axonopodis//  pv. //manihotis//) showed reduced growth in planta and delayed spread through the vasculature system of cassava. Moreover, the ∆avrBs2 mutant strain exhibited reduced water-soaking symptoms at the site of inoculation (Mutka //et al.//, 2016).
+  * A ∆//xopK//  mutant strain of //Xanthomonas phaseoli//  pv. //manihotis//  showed reduced growth in planta and delayed spread through the vasculature system of cassava. Moreover, the ∆//avrBs2//  mutant strain exhibited reduced water-soaking symptoms at the site of inoculation (Mutka //et al.//, 2016).
 === Localization ===
@@ Line 106: / Line 106: @@
 Yes (//e.g.//, //X//. //arboricola//, //X//. //campestris//, //X//. //citri//, //X. euvesicatoria//, //X//. //fuscans//, //X. oryzae//, //X//. //phaseoli//).
-Field strains of //X. euvesicatoria//  pv. //euvesicatoria//  and //X//. //campestris//  pv. //campestris//  were found to accumulate mutations in the //avrBs2/////avrRxc1/3//  gene in order to overcome //Bs2/////Rxc1/////Rxc3//-mediated resistance (Swords //et al.//, 1996; Gassmann //et al.//, 2000; Ignatov //et al.//, 2002).
+Field strains of //X. euvesicatoria// pv. //euvesicatoria// and //X//. //campestris// pv. //campestris// were found to accumulate mutations in the //avrBs2/////avrRxc1/3// gene in order to overcome //Bs2/////Rxc1/////Rxc3//-mediated resistance (Swords //et al.//, 1996; Gassmann //et al.//, 2000; Ignatov //et al.//, 2002). Yet, the global //Xcv// population was found to be extremely clonal, with very little genetic variation throughout the chromosome, including //avrBs2// and the plasmid-borne //avrBs1//, a finding that is consistent with recent evolution or population expansion of the species (Wichmann //et al.//, 2005).
 === In other plant pathogens/symbionts ===
@@ Line 119: / Line 118: @@
 Coplin DL (1989). Plasmids and their role in the evolution of plant pathogenic bacteria. Ann. Rev. Phytopathol. 27: 187-212. DOI: [[https://doi.org/10.1146/annurev.py.27.090189.001155|10.1146/annurev.py.27.090189.001155]]
+Deb S, Ghosh P, Patel HK, Sonti RV (2020). Interaction of the //Xanthomonas// effectors XopQ and XopX results in induction of rice immune responses. Plant J., in press. DOI: [[https://doi.org/10.1111/tpj.14924|10.1111/tpj.14924]]
 Gassmann W, Dahlbeck D, Chesnokova O, Minsavage GV, Jones JB, Staskawicz BJ (2000). Molecular evolution of virulence in natural field strains of //Xanthomonas campestris// pv. //vesicatoria//. J. Bacteriol. 182: 7053-7059. DOI: [[https://doi.org/10.1128/jb.182.24.7053-7059.2000|10.1128/jb.182.24.7053-7059.2000]]

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