Potential for host-symbiont communication via neurotransmitters and neuromodulators in an aneural animal, the marine sponge Amphimedon queenslandica.

IF 3.4 3区 医学 Q2 NEUROSCIENCES Frontiers in Neural Circuits Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI:10.3389/fncir.2023.1250694
Xueyan Xiang, Arturo A Vilar Gomez, Simone P Blomberg, Huifang Yuan, Bernard M Degnan, Sandie M Degnan
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Abstract

Interkingdom signalling within a holobiont allows host and symbionts to communicate and to regulate each other's physiological and developmental states. Here we show that a suite of signalling molecules that function as neurotransmitters and neuromodulators in most animals with nervous systems, specifically dopamine and trace amines, are produced exclusively by the bacterial symbionts of the demosponge Amphimedon queenslandica. Although sponges do not possess a nervous system, A. queenslandica expresses rhodopsin class G-protein-coupled receptors that are structurally similar to dopamine and trace amine receptors. When sponge larvae, which express these receptors, are exposed to agonists and antagonists of bilaterian dopamine and trace amine receptors, we observe marked changes in larval phototactic swimming behaviour, consistent with the sponge being competent to recognise and respond to symbiont-derived trace amine signals. These results indicate that monoamines synthesised by bacterial symbionts may be able to influence the physiology of the host sponge.

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通过神经递质和神经调节剂与宿主共生体交流的潜力在非整倍体动物,海洋海绵昆士兰两栖动物中。
全生物体内的界间信号允许宿主和共生体交流并调节彼此的生理和发育状态。在这里,我们发现,在大多数有神经系统的动物中,一系列信号分子,特别是多巴胺和微量胺,作为神经递质和神经调节剂,完全由昆斯兰双足虫的细菌共生体产生。尽管海绵不具有神经系统,但昆士兰a.queenslandica表达与多巴胺和微量胺受体结构相似的视紫红质类G蛋白偶联受体。当表达这些受体的海绵幼虫暴露于双侧多巴胺和微量胺受体的激动剂和拮抗剂时,我们观察到幼虫的趋光游泳行为发生了显著变化,这与海绵能够识别和响应共生体衍生的微量胺信号相一致。这些结果表明,由细菌共生体合成的单胺可能能够影响宿主海绵的生理学。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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