Transcriptomic analysis reveals vector attraction to potato virus Y is mediated through temporal regulation of TERPENE SYNTHASE 1 (TPS1)

IF 6.8 Q1 PLANT SCIENCES
Chad T. Nihranz , Prakriti Garg , Junha Shin , Madeleine Dumas , Sunnie Grace McCalla , Sushmita Roy , Clare L. Casteel
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Abstract

Viruses alter plant traits over time, which can further influence interactions between plants and insect vectors that transmit those viruses. However, the signaling pathways and regulators that control these temporal responses remain largely unknown. In this study, we used insect performance and preference bioassays, RNA-seq, and genetic tools to identify underlying mechanisms mediating temporal variation in plant-virus-vector interactions. We show that settlement and fecundity of the aphid vector, Myzus persicae, is increased on potato virus Y (PVY)-infected Nicotiana benthamiana plants two weeks post inoculation but not after six weeks. RNA-seq analysis revealed that transcripts related to plant defense and amino acid biosynthesis are upregulated in response to PVY infection and down regulated in response to aphid herbivory, and these patterns changed over time. Based on this analysis we identified a sesquiterpene synthase gene, terpene synthase 1 (NbTPS1), that is upregulated early in PVY infection, but not later in infection. Using virus-induced gene silencing and transient overexpression in N. benthamiana, we demonstrate that PVY induction of NbTPS1 is required for increased aphid attraction to PVY-infected plants in the early stages of infection. These findings reveal that PVY temporally modulates transcriptional pathways associated with plant defense responses and volatile organic compounds that influence the behavior of aphid vectors.
转录组学分析显示,载体对马铃薯Y病毒的吸引是通过TERPENE SYNTHASE 1 (TPS1)的时间调控介导的。
随着时间的推移,病毒会改变植物的性状,这可能进一步影响植物与传播这些病毒的昆虫媒介之间的相互作用。然而,控制这些时间反应的信号通路和调节因子在很大程度上仍然未知。在这项研究中,我们使用昆虫性能和偏好生物测定,RNA-seq和遗传工具来确定介导植物-病毒-载体相互作用时间变化的潜在机制。结果表明,蚜虫载体桃蚜(Myzus persicae)在马铃薯Y病毒(PVY)侵染的本烟(Nicotiana benthamiana)植株上的沉降和繁殖力在接种后2周增加,而在接种后6周没有增加。RNA-seq分析显示,植物防御和氨基酸生物合成相关转录本在PVY侵染下上调,在蚜虫侵染下下调,且这些模式随时间而改变。基于这一分析,我们发现了一个倍半萜合成酶基因,萜烯合成酶1 (NbTPS1),在PVY感染早期上调,但在感染后期没有上调。利用病毒诱导的基因沉默和在benthamiana中的短暂过表达,我们证明了PVY诱导NbTPS1是在感染PVY的早期阶段增加蚜虫对PVY感染植物的吸引力所必需的。这些发现表明,PVY暂时调节与植物防御反应和影响蚜虫媒介行为的挥发性有机化合物相关的转录途径。
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来源期刊
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
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