寄主蚂蚁的大脑和触角转录组揭示了社会寄生群体行为和功能之间的潜在联系

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2023-08-04 DOI:10.1111/mec.17092
Marah Stoldt, Erwann Collin, Maide Nesibe Macit, Susanne Foitzik
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引用次数: 0

摘要

昆虫群居寄生虫的特点是利用寄主的社会行为。为什么宿主会对这些寄生虫和它们的后代直接采取照顾行为,这在很大程度上仍未得到研究。一种假设是,寄主没有意识到它们的社会环境被改变了,而是接受了寄生群体。我们使用了双性专性社会性寄生虫Harpagoxenus sublaevis的宿主尖钩胸蚁(Leptothorax acervorum),通过对比年轻寄主工蜂的组织特异性转录组,揭示了行为剥削的分子机制。寄主蛹被实验性地(重新)引入到它们原来的、另一个同种的、异种的或寄生的群体的片段中。对羽化后在实验蚁群中生活至少50天的成年蚂蚁提取脑和触角mRNA并进行测序。由此得到的尖孢乳杆菌转录组揭示了蚂蚁确实受到其社会环境的影响。群居寄生虫的存在改变了宿主的脑转录组,这表明寄生环境影响大脑活动,这可能与行为变化有关。触角的转录活性随着不相关个体的存在而变化最大,无论它们是同种个体还是寄生虫。这表明气味感知的早期启动,这进一步支持了气味的感官知觉作为差异表达基因的丰富功能。此外,在取样前,触角中的基因表达与工蚁的行为相对应,而不是大脑中的基因表达。我们的研究表明,寄生蜂对社会行为的利用与中枢和周围神经系统的转录组改变有关。
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Brain and antennal transcriptomes of host ants reveal potential links between behaviour and the functioning of socially parasitic colonies

Insect social parasites are characterized by exploiting the hosts' social behaviour. Why exactly hosts direct their caring behaviour towards these parasites and their offspring remains largely unstudied. One hypothesis is that hosts do not perceive their social environment as altered and accept the parasitic colony as their own. We used the ant Leptothorax acervorum, host of the dulotic, obligate social parasite Harpagoxenus sublaevis, to shed light on molecular mechanisms underlying behavioural exploitation by contrasting tissue-specific transcriptomes in young host workers. Host pupae were experimentally (re-)introduced into fragments of their original, another conspecific, heterospecific or parasitic colony. Brain and antennal mRNA was extracted and sequenced from adult ants after they had lived in the experimental colony for at least 50 days after eclosion. The resulting transcriptomes of L. acervorum revealed that ants were indeed affected by their social environment. Host brain transcriptomes were altered by the presence of social parasites, suggesting that the parasitic environment influences brain activity, which may be linked to behavioural changes. Transcriptional activity in the antennae changed most with the presence of unrelated individuals, regardless of whether they were conspecifics or parasites. This suggests early priming of odour perception, which was further supported by sensory perception of odour as an enriched function of differentially expressed genes. Furthermore, gene expression in the antennae, but not in the brain corresponded to ant worker behaviour before sampling. Our study demonstrated that the exploitation of social behaviours by brood parasites correlates with transcriptomic alterations in the central and peripheral nervous systems.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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