TY - JOUR
T1 - Phosphatidylinositol-phospholipase C2 regulates pattern-triggered immunity in Nicotiana benthamiana
AU - Kiba, Akinori
AU - Nakano, Masahito
AU - Hosokawa, Miki
AU - Galis, Ivan
AU - Nakatani, Hiroko
AU - Shinya, Tomonori
AU - Ohnishi, Kouhei
AU - Hikichi, Yasufumi
N1 - Funding Information:
The authors thank Dr David C. Baulcombe of the Sainsbury Laboratory, John Innes Centre, UK, and G. Martin of Cornell University, USA, for providing the PVX vector and Pseudomonas fluorescens 55, respectively. The authors also thank Dr Y. Ichinose for kindly providing Pseudomonas syringae pv. tabaci 6605. This work was supported by a Cabinet Office Grants-in-Aid, the Advanced Next-Generation Greenhouse Horticulture by the Internet of Plants (IoP), Japan.This research was also supported by the Ministry of Education, Culture, Sports, Science and Technology as part of the Joint Research Program implemented at the Institute of Plant Science and Resources, Okayama University, Japan. LC-MS/MS instrumentation was supported by the Japan Advanced Plant Science Network. AK is also grateful for financial support from a Grants-in-Aid for Scientific Research (24580066) from the Ministry of Education, Science, Sports, and Culture, Japan, the Asahi Glass Foundation, the Agricultural Chemical Research Foundation, and the Sapporo Bioscience Foundation. We thank Dr Lesley Benyon from the Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript.
Funding Information:
The authors thank Dr David C. Baulcombe of the Sainsbury Laboratory, John Innes Centre, UK, and G. Martin of Cornell University, USA, for providing the PVX vector and Pseudomonas fluorescens 55, respectively. The authors also thank Dr Y. Ichinose for kindly providing Pseudomonas syringae pv. tabaci 6605. This work was supported by a Cabinet Office Grants-in-Aid,the Advanced Next-Generation Greenhouse Horticulture by the Internet of Plants (IoP), Japan.This research was also supported by the Ministry of Education, Culture, Sports, Science and Technology as part of the Joint Research Program implemented at the Institute of Plant Science and Resources, Okayama University, Japan. LC-MS/MS instrumentation was supported by the Japan Advanced Plant Science Network. AK is also grateful for financial support from a Grants-in-Aid for Scientific Research (24580066) from the Ministry of Education, Science, Sports, and Culture, Japan, the Asahi Glass Foundation, the Agricultural Chemical Research Foundation, and the Sapporo Bioscience Foundation. We thank Dr Lesley Benyon from the Edanz Group (www.edanzediting. com/ac) for editing a draft of this manuscript.
Publisher Copyright:
© 2020 Oxford University Press. All rights reserved.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Phospholipid signaling plays an important role in plant immune responses against phytopathogenic bacteria in Nicotiana benthamiana. Here, we isolated two phospholipase C2 (PLC2) orthologs in the N. benthamiana genome, designated as PLC2-1 and 2-2. Both NbPLC2-1 and NbPLC2-2 were expressed in most tissues and were induced by infiltration with bacteria and flg22. NbPLC2-1 and NbPLC2-2 (NbPLC2s) double-silenced plants showed a moderately reduced growth phenotype. The induction of the hypersensitive response was not affected, but bacterial growth and the appearance of bacterial wilt were accelerated in NbPLC2s-silenced plants when they were challenged with a virulent strain of Ralstonia solanacearum that was compatible with N. benthamiana. NbPLC2s-silenced plants showed reduced expression levels of NbPR-4, a marker gene for jasmonic acid signaling, and decreased jasmonic acid and jasmonoyl-L-isoleucine contents after inoculation with R. solanacearum. The induction of pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) marker genes was reduced in NbPLC2s-silenced plants after infiltration with R. solanacearum or Pseudomonas fluorescens. Accordingly, the resistance induced by flg22 was compromised in NbPLC2s-silenced plants. In addition, the expression of flg22-induced PTI marker genes, the oxidative burst, stomatal closure, and callose deposition were all reduced in the silenced plants. Thus, NbPLC2s might have important roles in pre- and post-invasive defenses, namely in the induction of PTI.
AB - Phospholipid signaling plays an important role in plant immune responses against phytopathogenic bacteria in Nicotiana benthamiana. Here, we isolated two phospholipase C2 (PLC2) orthologs in the N. benthamiana genome, designated as PLC2-1 and 2-2. Both NbPLC2-1 and NbPLC2-2 were expressed in most tissues and were induced by infiltration with bacteria and flg22. NbPLC2-1 and NbPLC2-2 (NbPLC2s) double-silenced plants showed a moderately reduced growth phenotype. The induction of the hypersensitive response was not affected, but bacterial growth and the appearance of bacterial wilt were accelerated in NbPLC2s-silenced plants when they were challenged with a virulent strain of Ralstonia solanacearum that was compatible with N. benthamiana. NbPLC2s-silenced plants showed reduced expression levels of NbPR-4, a marker gene for jasmonic acid signaling, and decreased jasmonic acid and jasmonoyl-L-isoleucine contents after inoculation with R. solanacearum. The induction of pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) marker genes was reduced in NbPLC2s-silenced plants after infiltration with R. solanacearum or Pseudomonas fluorescens. Accordingly, the resistance induced by flg22 was compromised in NbPLC2s-silenced plants. In addition, the expression of flg22-induced PTI marker genes, the oxidative burst, stomatal closure, and callose deposition were all reduced in the silenced plants. Thus, NbPLC2s might have important roles in pre- and post-invasive defenses, namely in the induction of PTI.
KW - Jasmonic acid
KW - Nicotiana benthamiana
KW - Pathogen-associated molecular pattern-triggered immunity
KW - Phosphatidylinositol-phospholipase C2
KW - Ralstonia solanacearum
KW - Virus-induced gene silencing
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U2 - 10.1093/jxb/eraa233
DO - 10.1093/jxb/eraa233
M3 - Article
AN - SCOPUS:85091407587
SN - 0022-0957
VL - 71
SP - 5027
EP - 5038
JO - Journal of Experimental Botany
JF - Journal of Experimental Botany
IS - 16
ER -