Red-light is an environmental effector for mutualism between begomovirus and its vector whitefly

文献类型： 外文期刊

第一作者： Zhao, Pingzhi

作者： Zhao, Pingzhi;Zhang, Xuan;Gong, Yuqing;Wang, Duan;Wang, Ning;Sun, Yanwei;Gao, Lianbo;Fang, Rong-Xiang;Ye, Jian;Zhao, Pingzhi;Gong, Yuqing;Wang, Duan;Fang, Rong-Xiang;Ye, Jian;Xu, Dongqing;Liu, Shu-Sheng;Deng, Xing Wang;Deng, Xing Wang;Kliebenstein, Daniel J.;Zhou, Xueping

作者机构：

期刊名称：PLOS PATHOGENS （ 影响因子：6.823； 五年影响因子：7.455 ）

ISSN： 1553-7366

年卷期： 2021 年 17 卷 1 期

页码：

收录情况： SCI

摘要： Author summary Climate change is driving disease rapidly spread, esp. for global distribution of insect-borne diseases. This paper reports red-light as an environmental factor to promote insect vector olfactory orientation behavior and increase viral disease transmission. Plant virus adapts the supplemental red lighting practice in modern agricultural greenhouse production under protection, therefore enhancing disease spreading globally. Environments such as light condition influence the spread of infectious diseases by affecting insect vector behavior. However, whether and how light affects the host defense which further affect insect preference and performance, remains unclear, nor has been demonstrated how pathogens co-adapt light condition to facilitate vector transmission. We previously showed that begomoviral beta C1 inhibits MYC2-mediated jasmonate signaling to establish plant-dependent mutualism with its insect vector. Here we show red-light as an environmental catalyzer to promote mutualism of whitefly-begomovirus by stabilizing beta C1, which interacts with PHYTOCHROME-INTERACTING FACTORS (PIFs) transcription factors. PIFs positively control plant defenses against whitefly by directly binding to the promoter of terpene synthase genes and promoting their transcription. Moreover, PIFs interact with MYC2 to integrate light and jasmonate signaling and regulate the transcription of terpene synthase genes. However, begomovirus encoded beta C1 inhibits PIFs' and MYC2' transcriptional activity via disturbing their dimerization, thereby impairing plant defenses against whitefly-transmitted begomoviruses. Our results thus describe how a viral pathogen hijacks host external and internal signaling to enhance the mutualistic relationship with its insect vector.

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