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Pre-infestation of Tomato Plants by Aphids Modulates Transmission-Acquisition Relationship among Whiteflies Tomato Yellow Leaf Curl Virus (TYLCV) and Plants

机译:蚜虫对番茄植物的预侵染调节粉虱番茄黄叶卷毛病毒(TYLCV)和植物之间的传播-获取关系

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摘要

Herbivory defense systems in plants are largely regulated by jasmonate-(JA) and salicylate-(SA) signaling pathways. Such defense mechanisms may impact insect feeding dynamic, may also affect the transmission-acquisition relationship among virus, plants and vectoring insects. In the context of the tomato – whitefly – Tomato Yellow Leaf Curl Virus (TYLCV) biological model, we tested the impact of pre-infesting plants with a non-vector insect (aphid Myzus persicae) on feeding dynamics of a vector insect (whitefly Bemisia tabaci) as well as virus transmission-acquisition. We showed that an aphid herbivory period of 0–48 h led to a transient systemic increase of virus concentration in the host plant (root, stem, and leaf), with the same pattern observed in whiteflies feeding on aphid-infested plants. We used real-time quantitative PCR to study the expression of key genes of the SA- and JA-signaling pathways, as well as electrical penetration graph (EPG) to characterize the impact of aphid pre-infestation on whitefly feeding during TYLCV transmission (whitefly to tomato) and acquisition (tomato to whitefly). The impact of the duration of aphid pre-infestation (0, 24, or 48 h) on phloem feeding by whitefly (E2) during the transmission phase was similar to that of global whitefly feeding behavior (E1, E2 and probing duration) during the acquisition phase. In addition, we observed that a longer phase of aphid pre-infestation prior to virus transmission by whitefly led to the up-regulation and down-regulation of SA- and JA-signaling pathway genes, respectively. These results demonstrated a significant impact of aphid pre-infestation on the tomato – whitefly – TYLCV system. Transmission and acquisition of TYLCV was positively correlated with feeding activity of B. tabaci, and both were mediated by the SA- and JA-pathways. TYLCV concentration during the transmission phases was modulated by up- and down-regulation of SA- and JA-pathways, respectively. The two pathways were inconsistent during the acquisition phase; SA- related genes were up-regulated, whereas those up- and down-stream of the JA pathway showed a more complex relationship. These findings enhance our understanding of plant – herbivore – virus interactions, which are potentially important for development of ecologically sound pest and pathogen management programs.
机译:植物中的草食防御系统在很大程度上受茉莉酸(JA)和水杨酸(SA)信号通路的调节。这种防御机制可能会影响昆虫的摄食动态,也可能会影响病毒,植物和媒介昆虫之间的传播与获取关系。在番茄–粉虱–番茄黄叶卷毛病毒(TYLCV)生物学模型的背景下,我们测试了非矢量昆虫(蚜虫Myzus persicae)的侵染前植物对矢量昆虫(粉虱Bemisia)进食动力学的影响烟粉虱)以及病毒传播获取。我们发现,蚜虫的草食期为0–48 h,导致宿主植物(根,茎和叶)中病毒浓度的短暂系统性增加,在以蚜虫侵染的植物为食的粉虱中观察到了相同的模式。我们使用实时定量PCR来研究SA和JA信号通路关键基因的表达以及电渗透图(EPG),以表征在TYLCV传播过程中蚜虫预先侵染对粉虱取食的影响(粉虱)番茄)和采集(番茄到粉虱)。在传播阶段,蚜虫预侵染的持续时间(0、24或48小时)对粉虱(E2)进食韧皮部的影响与该期间全球粉虱的进食行为(E1,E2和探测持续时间)相似。获取阶段。此外,我们观察到,粉虱在病毒传播之前,蚜虫预侵染的时间较长,分别导致SA和JA信号通路基因的上调和下调。这些结果证明了蚜虫预侵染对番茄–烟粉虱– TYLCV系统的重大影响。 TYLCV的传播和获得与烟粉虱的摄食活性呈正相关,二者均通过SA途径和JA途径介导。传播阶段的TYLCV浓度分别通过SA和JA途径的上调和下调来调节。在获取阶段这两个途径是不一致的。 SA相关基因被上调,而JA途径的上游和下游则显示出更复杂的关系。这些发现增强了我们对植物-草食动物-病毒相互作用的理解,这对于开发生态上合理的病虫害和病原体管理计划可能具有重要意义。

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