4.6 Article

Priming of rhizobial nodulation signaling in the mycosphere accelerates nodulation of legume hosts

期刊

NEW PHYTOLOGIST
卷 235, 期 3, 页码 1212-1230

出版社

WILEY
DOI: 10.1111/nph.18192

关键词

bacterial-fungal interactions; Bradyrhizobium; flavonoid; nodulation; peanut (Arachis hypogaea); Phomopsis liquidambaris; symbiotic signaling pathway

资金

  1. National Natural Science Foundation of China [31870478, 32101277]
  2. Post-doctoral Science Foundation of China [2020M681657]
  3. Priority Academic Program Development (PAPD) of the Jiangsu Higher Education Institutions of China

向作者/读者索取更多资源

This study reveals the interactions between Bradyrhizobium, a rhizobial mutualist, and the facultatively biotrophic fungus Phomopsis liquidambaris before nodulation of peanut plants. The study demonstrates that fungal flavonoid production stimulates Bradyrhizobial nodulation signaling, enhancing the plant's early nodulation response. Additionally, flavonoids act as a strategy to alleviate oxidative stress during fungal-bacterial interactions. The study emphasizes the importance of flavonoids in tripartite interactions between legumes, beneficial fungi, and rhizobia.
The simultaneous symbiosis of leguminous plants with two root mutualists, endophytic fungi and rhizobia is common in nature, yet how two mutualists interact and co-exist before infecting plants and the concomitant effects on nodulation are less understood. Using a combination of metabolic analysis, fungal deletion mutants and comparative transcriptomics, we demonstrated that Bradyrhizobium and a facultatively biotrophic fungus, Phomopsis liquidambaris, interacted to stimulate fungal flavonoid production, and thereby primed Bradyrhizobial nodulation signaling, enhancing Bradyrhizobial responses to root exudates and leading to early nodulation of peanut (Arachis hypogaea), and such effects were compromised when disturbing fungal flavonoid biosynthesis. Stress sensitivity assays and reactive oxygen species (ROS) determination revealed that flavonoid production acted as a strategy to alleviate hyphal oxidative stress during P. liquidambaris-Bradyrhizobial interactions. By investigating the interactions between P. liquidambaris and a collection of 38 rhizobacteria, from distinct bacterial genera, we additionally showed that the flavonoid-ROS module contributed to the maintenance of fungal and bacterial co-existence, and fungal niche colonization under soil conditions. Our results demonstrate for the first time that rhizobial nodulation signaling can be primed by fungi before symbiosis with host plants and highlight the importance of flavonoid in tripartite interactions between legumes, beneficial fungi and rhizobia.

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