欧亚云杉树皮甲虫利用存在于几种功能感受器类型中的高表达特异性气味受体来检测羊毛脂酮。

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2024-11-20 DOI:10.1186/s12915-024-02066-x
Jothi Kumar Yuvaraj, Dineshkumar Kandasamy, Rebecca E Roberts, Bill S Hansson, Jonathan Gershenzon, Martin N Andersson
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引用次数: 0

摘要

背景:昆虫利用在触角嗅觉神经元(OSN)中表达的气味受体(ORs)来探测气味。具有重要生态意义的气味通常是由选择性的大量嗅觉神经元检测到的;因此,嗅觉神经元在触角上的表达量很高。然而,人们对甲虫中高表达 ORs 的功能知之甚少,因为很少有 ORs 具有功能特征。在这里,我们对云杉的主要害虫树皮甲虫 Ips typographus L.(鞘翅目,卷须科,鞘翅目)中表达量最高的 OR(ItypOR36)进行了功能表征。我们假设这种 OR 能检测到对甲虫的适应性很重要的化合物,如信息素成分。接下来,我们利用单感受器记录(SSR)和原位杂交技术研究了这种OR的触角分布情况,并通过野外和实验室实验评估了所发现配体的行为效应:结果:我们在 HEK293 细胞中表达了 ItypOR36,并用 64 种生态相关气味对其进行了挑战。OR只对源自单萜的酮类物质羊毛脂产生高灵敏度的反应。羊毛脂酮用于北美 Ips 物种的化学交流,但从未证明 I. typographus 产生过这种物质,也未对该物种的感官生理进行过研究。单感受器记录发现了一种新颖而丰富的羊毛脂酮反应性 OSN 类,其特异性反应与 ItypOR36 相同。令人吃惊的是,这些 OSN 与之前描述的七种不同的 OSN 类共同定位在感觉器中。现场实验表明,低释放率的羊毛脂酮可抑制甲虫对以聚集信息素为诱饵的诱捕器的吸引,对雄性甲虫的影响最大。在实验室步行生物测定中,雌性甲虫也会被羊毛甾酮吸引:我们的研究凸显了所谓的 "反向化学生态学 "方法在识别具有重要生态意义的昆虫物种的新型半化学物质方面的重要性。我们发现的涉及兰尼酮 OSN 类的共定位模式表明,不同昆虫纲之间的外周嗅觉存在组织差异。我们的行为实验表明,羊毛脂烯酮会引起雌雄甲虫不同的反应,这也取决于甲虫是在实验室中行走还是在野外飞行。要理解这些依赖于环境的行为,就需要揭示 typographus 自然环境中羊毛脂酮的来源。
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Eurasian spruce bark beetle detects lanierone using a highly expressed specialist odorant receptor, present in several functional sensillum types.

Background: Insects detect odours using odorant receptors (ORs) expressed in olfactory sensory neurons (OSNs) in the antennae. Ecologically important odours are often detected by selective and abundant OSNs; hence, ORs with high antennal expression. However, little is known about the function of highly expressed ORs in beetles, since few ORs have been functionally characterized. Here, we functionally characterized the most highly expressed OR (ItypOR36) in the bark beetle Ips typographus L. (Coleoptera, Curculionidae, Scolytinae), a major pest of spruce. We hypothesized that this OR would detect a compound important to beetle fitness, such as a pheromone component. We next investigated the antennal distribution of this OR using single sensillum recordings (SSR) and in situ hybridization, followed by field- and laboratory experiments to evaluate the behavioural effects of the discovered ligand.

Results: We expressed ItypOR36 in HEK293 cells and challenged it with 64 ecologically relevant odours. The OR responded exclusively to the monoterpene-derived ketone lanierone with high sensitivity. Lanierone is used in chemical communication in North American Ips species, but it has never been shown to be produced by I. typographus, nor has it been studied in relation to this species' sensory physiology. Single sensillum recordings revealed a novel and abundant lanierone-responsive OSN class with the same specific response as ItypOR36. Strikingly, these OSNs were co-localized in sensilla together with seven different previously described OSN classes. Field experiments revealed that low release rates of lanierone inhibited beetle attraction to traps baited with aggregation pheromone, with strongest effects on males. Female beetles were attracted to lanierone in laboratory walking bioassays.

Conclusions: Our study highlights the importance of the so-called 'reverse chemical ecology' approach to identify novel semiochemicals for ecologically important insect species. Our discovery of the co-localization pattern involving the lanierone OSN class suggests organizational differences in the peripheral olfactory sense between insect orders. Our behavioural experiments show that lanierone elicits different responses in the two sexes, which also depend on whether beetles are walking in the laboratory or flying in the field. Unravelling the source of lanierone in the natural environment of I. typographus is required to understand these context-dependent behaviours.

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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
期刊最新文献
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