酵母衍生的挥发物与东方粘虫蛾协调了昆虫-酵母的共生关系

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Baiwei Ma, Hetan Chang, Mengbo Guo, Dong Ai, Jiayu Wang, Run Chen, Xiaolan Liu, Bingzhong Ren, Bill S. Hansson, Guirong Wang
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引用次数: 0

摘要

昆虫、植物和微生物之间的相互作用是生态系统动力学的基础,花蜜和花粉是各种生物的关键资源。酵母,如常见于花蜜中的reukaufii,通过挥发性化合物(VOCs)影响蜜的吸引力,但其潜在的生物学机制尚不清楚。在这里,我们发现异戊醇,一种突出的酵母挥发性有机化合物,吸引东方粘虫蛾(Mythimna separata)到富含花粉的酵母发酵花蜜。在一系列的电生理和行为分析中,我们发现异戊醇激活了一类表达嗅觉受体MsepOR8的高度特异性嗅觉感觉神经元。在飞蛾的触角叶中,这些神经元以AM2肾小球为目标,后者对异戊醇有反应。MsepOR8的遗传破坏导致对异戊醇的生理和行为反应完全取消,导致定位花蜜来源的能力受损。此外,我们发现异戊醇诱导的觅食行为在一定程度上促进了酵母和飞蛾之间的互惠关系,促进了酵母的扩散和飞蛾的繁殖成功率。我们的研究结果揭示了一种高度特异性的机制,通过酵母衍生的VOC促进昆虫-酵母共生,为授粉生态系统中昆虫-微生物的相互作用提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Yeast-derived volatiles orchestrate an insect-yeast mutualism with oriental armyworm moths

Yeast-derived volatiles orchestrate an insect-yeast mutualism with oriental armyworm moths

Interactions among insects, plants, and microorganisms are fundamental to ecosystem dynamics, with floral nectar and pollen serving as key resources for various organisms. Yeasts, such as Metschnikowia reukaufii, commonly found in nectar, influence nectarial attraction through volatile compounds (VOCs), yet the underlying biological mechanisms remain elusive. Here, we show that isoamyl alcohol, a prominent yeast VOC, attracts oriental armyworm moths (Mythimna separata) to pollen-rich, yeast-fermented nectar. In a series of electrophysiological and behavioral assays, we show that isoamyl alcohol activates a single class of highly specific olfactory sensory neurons expressing the olfactory receptor MsepOR8. In the moth antennal lobe, these neurons target the AM2 glomerulus, which responds to isoamyl alcohol. Genetic disruption of MsepOR8 leads to complete abolition of both physiological and behavioral responses to isoamyl alcohol, resulting in an impaired ability to locate nectar sources. Moreover, we show that isoamyl alcohol-induced foraging behavior fosters a mutualistic relationship between yeast and moths to some extent, enhancing yeast dispersal and increasing moth reproductive success. Our results unveil a highly specific mechanism by which a yeast-derived VOC facilitates insect-yeast mutualism, providing insights into insect-microbe interactions within pollination ecosystems.

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来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
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