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Viruses mobilize plant immunity to deter nonvector insect herbivores

机译:病毒动员植物免疫力来阻止非媒介昆虫食草动物

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摘要

A parasite-infected host may promote performance of associated insect vectors; but possible parasite effects on nonvector insects have been largely unexplored. Here, we show that Begomovirus, the largest genus of plant viruses and transmitted exclusively by whitefly, reprogram plant immunity to promote the fitness of the vector and suppress performance of nonvector insects (i.e., cotton bollworm and aphid). Infected plants accumulated begomoviral βC1 proteins in the phloem where they were bound to the plant transcription factor WRKY20. This viral hijacking of WRKY20 spatiotemporally redeployed plant chemical immunity within the leaf and had the asymmetrical benefiting effects on the begomoviruses and its whitefly vectors while negatively affecting two nonvector competitors. This type of interaction between a parasite and two types of herbivores, i.e., vectors and nonvectors, occurs widely in various natural and agricultural ecosystems; thus, our results have broad implications for the ecological significance of parasite-vector-host tripartite interactions.
机译:寄生虫感染的宿主可以促进相关昆虫载体的表现;但对非媒介昆虫可能产生的寄生虫影响尚未充分探讨。在这里,我们显示了植物病毒的最大属,且仅由粉虱传播的寄主虫重新编程植物免疫力,以促进载体的适应性并抑制非载体昆虫(即棉铃虫和蚜虫)的性能。受感染的植物在韧皮部中积累了begomoviralβC1蛋白,并与植物转录因子WRKY20结合。 WRKY20的这种病毒劫持在时空上重新部署了叶内的植物化学免疫性,并且对begomovirus及其粉虱载体具有不对称的有益作用,同时对两个非载体竞争者产生了负面影响。寄生虫与两种食草动物(媒介和非媒介)之间的这种相互作用广泛存在于各种自然和农业生态系统中。因此,我们的结果对寄生虫-载体-宿主三方相互作用的生态意义具有广泛的意义。

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