白蛉与portiera共生合成的苯丙氨酸可提高真菌侵染下寄主的存活率

IF 4.3 1区 农林科学 Q1 ENTOMOLOGY
Chao Lv, Song-Xue Zhang, Ji-Sheng Hong, Tian-Yu Wang, Bing-Qi Liu, Chu-Qiao Li, Jin-Yang Yan, Jun-Bo Luan
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引用次数: 0

摘要

寄主及其专性共生体之间的苯丙氨酸合成代谢合作在半翅目昆虫中广泛存在。然而,苯丙氨酸合成的机制及其在半足类昆虫中的作用在很大程度上是未知的。我们之前的研究表明,白蝇烟粉虱谷氨酸-草酰乙酸转氨酶基因GOT2补偿了Portiera缺失的tyrB。本研究发现,粉虱的GOT2和Portiera主要通过沉默GOT2来协同合成苯丙氨酸。我们进一步发现白蛉与portiera共生合成的苯丙氨酸促进了成年白蛉角质层的形成。然后,我们证明了通过沉默白蝇GOT2抑制苯丙氨酸合成在高温低湿条件下不会显著提高白蝇的死亡率,但当白蝇感染球孢白僵菌时,它会提高白蝇的死亡率。我们的研究结果为共生如何促进成年白蝇角质层的形成提供了实验证据,揭示了寄主合成的苯丙氨酸和寄主的共生体促进共生细菌细胞的昆虫角质层形成的平行历史。本研究表明,虫菌共生合成的苯丙氨酸可能赋予昆虫对昆虫病原真菌的适应性。我们的发现也将有助于我们制定害虫控制的昆虫共生破坏策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The phenylalanine synthesized by whitefly–Portiera symbiosis enhances host survival under fungi infection

The metabolic cooperation for the phenylalanine synthesis between the host and its obligate symbiont is widespread in hemipteran insects. However, the mechanisms underlying phenylalanine synthesis and its role in hemipteran insects are largely unknown. Our previous study indicates that the whitefly Bemisia tabaci glutamate–oxaloacetate transaminase gene GOT2 compensates for tyrB missing from Portiera. Here, we found that the whitefly GOT2 and Portiera can cooperate for the synthesis of phenylalanine mainly by silencing GOT2. We further revealed that the phenylalanine synthesized by whitefly–Portiera symbiosis promotes cuticle formation on adult whiteflies. Then, we demonstrated that repression of phenylalanine synthesis by silencing whitefly GOT2 does not significantly increase the whitefly mortality under high temperature and low humidity conditions, but it enhances the whitefly mortality when whiteflies were infected with the entomopathogenic fungi Beauveria bassiana. Our results provide experimental evidence on how symbiosis contributes to adult whitefly cuticle formation, revealing parallel histories of the phenylalanine synthesized by the host and its obligate symbiont facilitated cuticle formation in insects housing the bacteriocyte symbionts. This study indicates that the phenylalanine synthesized by insect–bacteria symbiosis may confer the insect adaptation to entomopathogenic fungi. Our findings will also help us to develop an insect symbiosis disruption strategy for pest control.

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来源期刊
Journal of Pest Science
Journal of Pest Science 生物-昆虫学
CiteScore
10.40
自引率
8.30%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Journal of Pest Science publishes high-quality papers on all aspects of pest science in agriculture, horticulture (including viticulture), forestry, urban pests, and stored products research, including health and safety issues. Journal of Pest Science reports on advances in control of pests and animal vectors of diseases, the biology, ethology and ecology of pests and their antagonists, and the use of other beneficial organisms in pest control. The journal covers all noxious or damaging groups of animals, including arthropods, nematodes, molluscs, and vertebrates. Journal of Pest Science devotes special attention to emerging and innovative pest control strategies, including the side effects of such approaches on non-target organisms, for example natural enemies and pollinators, and the implementation of these strategies in integrated pest management. Journal of Pest Science also publishes papers on the management of agro- and forest ecosystems where this is relevant to pest control. Papers on important methodological developments relevant for pest control will be considered as well.
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