TY - JOUR
T1 - Priming for enhanced ARGONAUTE2 activation accompanies induced resistance to cucumber mosaic virus in Arabidopsis thaliana
AU - Ando, Sugihiro
AU - Jaskiewicz, Michal
AU - Mochizuki, Sei
AU - Koseki, Saeko
AU - Miyashita, Shuhei
AU - Takahashi, Hideki
AU - Conrath, Uwe
N1 - Funding Information:
This work was supported, in part, by the Japan Society for the Promotion of Science KAKENHI (grants 15K07307, 16H06185, 17K19257, 19H02953, 20K06045, and 26292022), Grant-in-Aid for Scientific Research on Innovative Areas of the Ministry of Education, Culture, Science, Sports and Technology (MEXT) of Japan (grants 16H06429, 16K21723, and 16H06435), and by the Japan Society for the Promotion of Science Core-to-Core Program of Advanced Research Networks entitled “Establishment of international agricultural immunology research-core for a quantum improvement in food safety”. We thank Syngenta Crop Protection AG for providing a WP formulation of BTH to the Conrath laboratory. This article does not contain any studies on humans or animals performed by any of the authors. The authors declare that they have no conflicts of interest. Open access funding enabled and organized by Projekt DEAL.
Funding Information:
This work was supported, in part, by the Japan Society for the Promotion of Science KAKENHI (grants 15K07307, 16H06185, 17K19257, 19H02953, 20K06045, and 26292022), Grant‐in‐Aid for Scientific Research on Innovative Areas of the Ministry of Education, Culture, Science, Sports and Technology (MEXT) of Japan (grants 16H06429, 16K21723, and 16H06435), and by the Japan Society for the Promotion of Science Core‐to‐Core Program of Advanced Research Networks entitled “Establishment of international agricultural immunology research‐core for a quantum improvement in food safety”. We thank Syngenta Crop Protection AG for providing a WP formulation of BTH to the Conrath laboratory. This article does not contain any studies on humans or animals performed by any of the authors. The authors declare that they have no conflicts of interest.
Publisher Copyright:
© 2020 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd
PY - 2021/1
Y1 - 2021/1
N2 - Systemic acquired resistance (SAR) is a broad-spectrum disease resistance response that can be induced upon infection from pathogens or by chemical treatment, such as with benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester (BTH). SAR involves priming for more robust activation of defence genes upon pathogen attack. Whether priming for SAR would involve components of RNA silencing remained unknown. Here, we show that upon leaf infiltration of water, BTH-primed Arabidopsis thaliana plants accumulate higher amounts of mRNA of ARGONAUTE (AGO)2 and AGO3, key components of RNA silencing. The enhanced AGO2 expression is associated with prior-to-activation trimethylation of lysine 4 in histone H3 and acetylation of histone H3 in the AGO2 promoter and with induced resistance to the yellow strain of cucumber mosaic virus (CMV[Y]). The results suggest that priming A. thaliana for enhanced defence involves modification of histones in the AGO2 promoter that condition AGO2 for enhanced activation, associated with resistance to CMV(Y). Consistently, the fold-reduction in CMV(Y) coat protein accumulation by BTH pretreatment was lower in ago2 than in wild type, pointing to reduced capacity of ago2 to activate BTH-induced CMV(Y) resistance. A role of AGO2 in pathogen-induced SAR is suggested by the enhanced activation of AGO2 after infiltrating systemic leaves of plants expressing a localized hypersensitive response upon CMV(Y) infection. In addition, local inoculation of SAR-inducing Pseudomonas syringae pv. maculicola causes systemic priming for enhanced AGO2 expression. Together our results indicate that defence priming targets the AGO2 component of RNA silencing whose enhanced expression is likely to contribute to SAR.
AB - Systemic acquired resistance (SAR) is a broad-spectrum disease resistance response that can be induced upon infection from pathogens or by chemical treatment, such as with benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester (BTH). SAR involves priming for more robust activation of defence genes upon pathogen attack. Whether priming for SAR would involve components of RNA silencing remained unknown. Here, we show that upon leaf infiltration of water, BTH-primed Arabidopsis thaliana plants accumulate higher amounts of mRNA of ARGONAUTE (AGO)2 and AGO3, key components of RNA silencing. The enhanced AGO2 expression is associated with prior-to-activation trimethylation of lysine 4 in histone H3 and acetylation of histone H3 in the AGO2 promoter and with induced resistance to the yellow strain of cucumber mosaic virus (CMV[Y]). The results suggest that priming A. thaliana for enhanced defence involves modification of histones in the AGO2 promoter that condition AGO2 for enhanced activation, associated with resistance to CMV(Y). Consistently, the fold-reduction in CMV(Y) coat protein accumulation by BTH pretreatment was lower in ago2 than in wild type, pointing to reduced capacity of ago2 to activate BTH-induced CMV(Y) resistance. A role of AGO2 in pathogen-induced SAR is suggested by the enhanced activation of AGO2 after infiltrating systemic leaves of plants expressing a localized hypersensitive response upon CMV(Y) infection. In addition, local inoculation of SAR-inducing Pseudomonas syringae pv. maculicola causes systemic priming for enhanced AGO2 expression. Together our results indicate that defence priming targets the AGO2 component of RNA silencing whose enhanced expression is likely to contribute to SAR.
KW - chromatin modification
KW - cucumber mosaic virus
KW - defence priming
KW - histone modification
KW - induced resistance
KW - RNA silencing
KW - systemic acquired resistance
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UR - http://www.scopus.com/inward/citedby.url?scp=85092623944&partnerID=8YFLogxK
U2 - 10.1111/mpp.13005
DO - 10.1111/mpp.13005
M3 - Article
C2 - 33073913
AN - SCOPUS:85092623944
SN - 1464-6722
VL - 22
SP - 19
EP - 30
JO - Molecular Plant Pathology
JF - Molecular Plant Pathology
IS - 1
ER -