A conserved protein family in mirid bug <i>Riptortus pedestris</i> plays dual roles in regulating plant immunity

The mirid bug (Riptortus pedestris), a major soybean pest, migrates into soybean fields during the pod filling stage and causes staygreen syndrome, which leads to substantial yield losses. The mechanism by which R. pedestris elicits soybean (Glycine max) defenses and counter-defenses remains largely unexplored. In this study, we characterized a protein family from R. pedestris, designated R.pedestris HAMP 1 (RPH1), and its putative paralogs (RPH1L1, 2, 3, 4, and 5), whose members exhibit dual roles in triggering and inhibiting plant immunity. RPH1 and RPH1L1 function as herbivore-associated molecular patterns (HAMPs), activating pattern-triggered immunity (PTI) in tobacco (Nicotiana benthamiana) and G. max. Furthermore, RPH1 stimulates jasmonic acid and ethylene biosynthesis in G. max, thereby enhancing its resistance to R. pedestris feeding. Additionally, RPH1 homologs are universally conserved across various herbivorous species, with many homologs also acting as HAMPs that trigger plant immunity. Interestingly, the remaining RPH1 putative paralogs (RPH1L2-5) serve as effectors that counteract RPH1-induced PTI, likely by disrupting the extracellular perception of RPH1. This research uncovers a HAMP whose homologs are conserved in both chewing and piercing-sucking insects. Moreover, it unveils an extracellular evasion mechanism utilized by herbivores to circumvent plant immunity using functionally differentiated paralogs.

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Publication Details

Journal
PLANT PHYSIOLOGY
Published
2024-09-04
DOI
https://doi.org/10.1093/plphys/kiae468
Citations
9
Primary Topic
Insect-Plant Interactions and Control
Type
article
Field-Weighted Citation Impact
4.86

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article

A conserved protein family in mirid bug Riptortus pedestris plays dual roles in regulating plant immunity

Dong‐Lei Yang, Zhiyuan Yin, Yurong Ma, Yuanchao Wang et al.
9 citations
PLANT PHYSIOLOGY
Insect-Plant Interactions and Control
4.86
article

A conserved protein family in mirid bug Riptortus pedestris plays dual roles in regulating plant immunity

Dong‐Lei Yang, Zhiyuan Yin, Yurong Ma, Yuanchao Wang, Danyu Shen, Daolong Dou, Jiangxuan Zhou, Ai Xia, Gan Ai, Qingsong Zhang, Xiaoxi Li, Yumei Dong, Yong Pei, Yujie OYang, Lanping Ding
article en
9 citations

Abstract

The mirid bug (Riptortus pedestris), a major soybean pest, migrates into soybean fields during the pod filling stage and causes staygreen syndrome, which leads to substantial yield losses. The mechanism by which R. pedestris elicits soybean (Glycine max) defenses and counter-defenses remains largely unexplored. In this study, we characterized a protein family from R. pedestris, designated R.pedestris HAMP 1 (RPH1), and its putative paralogs (RPH1L1, 2, 3, 4, and 5), whose members exhibit dual roles in triggering and inhibiting plant immunity. RPH1 and RPH1L1 function as herbivore-associated molecular patterns (HAMPs), activating pattern-triggered immunity (PTI) in tobacco (Nicotiana benthamiana) and G. max. Furthermore, RPH1 stimulates jasmonic acid and ethylene biosynthesis in G. max, thereby enhancing its resistance to R. pedestris feeding. Additionally, RPH1 homologs are universally conserved across various herbivorous species, with many homologs also acting as HAMPs that trigger plant immunity. Interestingly, the remaining RPH1 putative paralogs (RPH1L2-5) serve as effectors that counteract RPH1-induced PTI, likely by disrupting the extracellular perception of RPH1. This research uncovers a HAMP whose homologs are conserved in both chewing and piercing-sucking insects. Moreover, it unveils an extracellular evasion mechanism utilized by herbivores to circumvent plant immunity using functionally differentiated paralogs.

PLANT PHYSIOLOGYVol. 196(4)
Nanjing Agricultural University (CN), Hangzhou Normal University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 5%
Insect-Plant Interactions and Control
4.86
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