AmelOBP4: an antenna-specific odor-binding protein gene required for olfactory behavior in the honey bee (Apis mellifera)

IF 2.6 2区 生物学 Q1 ZOOLOGY Frontiers in Zoology Pub Date : 2025-01-14 DOI:10.1186/s12983-024-00554-y
Fang Liu, Yu Lai, Lixian Wu, Qiang Li, Linyue Lei, Wei Yin, Yuan Zhang, Zachary Y. Huang, Hongxia Zhao
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Abstract

Odorant binding proteins (OBPs) initiate the process of odorant perception. Numerous investigations have demonstrated that OBPs bind a broad variety of chemicals and are more likely to carry pheromones or odor molecules with high binding affinities. However, few studies have investigated its effects on insect behavior. Previously, we found that AmelOBP4 has a significantly higher expression in the heads of foragers than that of nurses regardless of their ages, revealing its importance in foraging behaviour of the honey bee. RNA interference (RNAi) is the induction of sequence specific gene silencing by double-stranded RNA (dsRNA), it is a powerful tool that makes gene inactivation possible in organisms that were not amenable to genetic analysis before. In this study, we found that AmelOBP4 had high expression levels in the antennae of both nurses and foragers, and could be successfully inhibited by feeding double stranded RNA of AmelOBP4 (dsAmelOBP4). Foragers with inhibited AmelOBP4 showed significantly lower sugar responsiveness than control bees, and also significantly reduced EAG response to plant volatiles of nonanal, linalool and 1-Octen-3ol. On the other hand, nurses with inhibited AmelOBP4 showed significantly reduced EAG response to brood pheromone of ethyl oleate, methyl linoleate, methyl palmitate and β-ocimene. Finally, the Y-tube choice assay showed nurses only exhibited a significantly reduced preference to ethyl oleate, but foragers exhibited significantly reduced preference to all these three plant volatiles. The findings of our study suggested that AmelOBP4 plays an important role in the odorant binding process, especially in modulating olfactory behaviour in workers. Our results provide a foundation for exploring the olfactory mechanism of Apis mellifera.
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AmelOBP4:蜜蜂(Apis mellifera)嗅觉行为所需的触角特异性气味结合蛋白基因
气味结合蛋白(OBPs)启动气味感知过程。许多研究表明,obp结合多种化学物质,更有可能携带具有高结合亲和力的信息素或气味分子。然而,很少有研究调查其对昆虫行为的影响。在此之前,我们发现,在觅食蜂的头部中,AmelOBP4的表达明显高于看护蜂的头部,无论其年龄如何,这揭示了它在蜜蜂觅食行为中的重要性。RNA干扰(RNAi)是通过双链RNA (dsRNA)诱导序列特异性基因沉默,它是一种强大的工具,可以使以前无法进行遗传分析的生物体中的基因失活成为可能。在本研究中,我们发现AmelOBP4在护士和觅食者的触角中都有高表达水平,并且可以通过喂食AmelOBP4的双链RNA (dsAmelOBP4)成功地抑制。受AmelOBP4抑制的觅食蜂对糖的反应显著低于对照组,对植物挥发物壬醛、芳樟醇和1-辛烷醇的EAG反应也显著降低。另一方面,抑制AmelOBP4的护士对油酸乙酯、亚油酸甲酯、棕榈酸甲酯和β-辛烯等育苗信息素的EAG反应显著降低。最后,y管选择实验显示,护士对油酸乙酯的偏好显著降低,但觅食者对这三种植物挥发物的偏好显著降低。我们的研究结果表明,AmelOBP4在气味结合过程中起着重要作用,特别是在调节工人的嗅觉行为方面。本研究结果为探索蜜蜂的嗅觉机制提供了基础。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life. As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem. Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost. The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.
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