Meloidogyne enterolobiiMeMSP1 effector targets the glutathione‐S‐transferase phi GSTF family in Arabidopsis to manipulate host metabolism and promote nematode parasitism

Author:

Chen Yongpan1ORCID,Liu Qian12ORCID,Sun Xuqian1ORCID,Liu Lei1,Zhao Jianlong3ORCID,Yang Shanshan4ORCID,Wang Xiangfeng5,Quentin Michaël6ORCID,Abad Pierre6ORCID,Favery Bruno6ORCID,Jian Heng1ORCID

Affiliation:

1. Department of Plant Pathology and MOA Key Laboratory of Pest Monitoring and Green Management China Agricultural University Beijing 100193 China

2. Sanya Institute of China Agricultural University Sanya 572024 China

3. Institute of Vegetables and Flowers Chinese Academy of Agricultural Science Beijing 100081 China

4. College of Agriculture Guangxi University Nanning Guangxi 530004 China

5. National Maize Improvement Center, College of Agronomy and Biotechnology China Agricultural University Beijing 100193 China

6. INRAE Université Côte d'Azur, CNRS, ISA Sophia Antipolis F‐06903 France

Abstract

Summary Meloidogyne enterolobii is an emerging root‐knot nematode species that overcomes most of the nematode resistance genes in crops. Nematode effector proteins secreted in planta are key elements in the molecular dialogue of parasitism. Here, we show the MeMSP1 effector is secreted into giant cells and promotes M. enterolobii parasitism. Using co‐immunoprecipitation and bimolecular fluorescent complementation assays, we identified glutathione‐S‐transferase phi GSTFs as host targets of the MeMSP1 effector. This protein family plays important roles in plant responses to abiotic and biotic stresses. We demonstrate that MeMSP1 interacts with all Arabidopsis GSTF. Moreover, we confirmed that the N‐terminal region of AtGSTF9 is critical for its interaction, and atgstf9 mutant lines are more susceptible to root‐knot nematode infection. Combined transcriptome and metabolome analyses showed that MeMSP1 affects the metabolic pathways of Arabidopsis thaliana, resulting in the accumulation of amino acids, nucleic acids, and their metabolites, and organic acids and the downregulation of flavonoids. Our study has shed light on a novel effector mechanism that targets plant metabolism, reducing the production of plant defence‐related compounds while favouring the accumulation of metabolites beneficial to the nematode, and thereby promoting parasitism.

Funder

Agence Nationale de la Recherche

China Scholarship Council

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Plant Science,Physiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3