Littorina snails and Microphallus trematodes: Diverse consequences of the trematode-induced metabolic shifts.

IF 1.8 3区 医学 Q2 PARASITOLOGY Parasitology Research Pub Date : 2024-05-31 DOI:10.1007/s00436-024-08244-8
Egor A Repkin, Elizaveta R Gafarova, Marina A Varfolomeeva, Dmitrii S Kurjachii, Dmitrii E Polev, Alexei L Shavarda, Georgiy P Maslakov, Roman I Mullakhmetov, Ekaterina V Zubova, Timur B Bariev, Andrei I Granovitch, Arina L Maltseva
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Abstract

The intricate relationships between parasites and hosts encompass a wide range of levels, from molecular interactions to population dynamics. Parasites influence not only the physiological processes in the host organism, but also the entire ecosystem, affecting mortality of individuals, the number of offspring through parasitic castration, and matter and energy cycles. Understanding the molecular mechanisms that govern host-parasite relationships and their impact on host physiology and environment remains challenging. In this study, we analyzed how infection with Microphallus trematodes affects the metabolome of two Littorina snail species inhabiting different intertidal zone shore levels. We applied non-targeted GC-MS-based metabolomics to analyze biochemical shifts induced by trematode infection in a host organism. We have identified changes in energy, amino acid, sugar, and lipid metabolism. In particular, we observed intensified amino acid catabolism and nitrogenous catabolites (glutamine, urea) production. These changes primarily correlated with infection and interspecies differences of the hosts rather than shore level. The changes detected in the host metabolism indicate that other aspects of life may have been affected, both within the host organism and at a supra-organismal level. Therefore, we explored changes in microbiota composition, deviations in the host molluscs behavior, and acetylcholinesterase activity (ACE, an enzyme involved in neuromuscular transmission) in relation to infection. Infected snails displayed changes in their microbiome composition. Decreased ACE activity in snails was associated with reduced mobility, but whether it is associated with trematode infection remains unclear. The authors suggest a connection between the identified biochemical changes and the deformation of the shell of molluscs, changes in their behavior, and the associated microbiome. The role of parasitic systems formed by microphallid trematodes and Littorina snails in the nitrogen cycle at the ecosystem level is also assumed.

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Littorina 蜗牛与小球藻吸虫:震颤虫引起的新陈代谢变化的不同后果
寄生虫与宿主之间错综复杂的关系涵盖了从分子相互作用到种群动态等多个层面。寄生虫不仅影响宿主生物的生理过程,还影响整个生态系统,通过寄生阉割影响个体死亡率、后代数量以及物质和能量循环。了解宿主与寄生虫关系的分子机制及其对宿主生理和环境的影响仍然具有挑战性。在这项研究中,我们分析了感染小球吸虫如何影响栖息在不同潮间带海岸水平的两种 Littorina 蜗牛的代谢组。我们采用基于 GC-MS 的非靶向代谢组学分析了宿主生物感染吸虫后引起的生化变化。我们发现了能量、氨基酸、糖和脂质代谢的变化。特别是,我们观察到氨基酸分解代谢和含氮分解物(谷氨酰胺、尿素)的产生都有所加强。这些变化主要与宿主的感染和种间差异有关,而不是与海岸水平有关。在宿主新陈代谢中检测到的变化表明,生命的其他方面可能也受到了影响,包括宿主生物内部和超生物层面。因此,我们探讨了微生物群组成的变化、宿主软体动物行为的偏差以及乙酰胆碱酯酶活性(ACE,一种参与神经肌肉传递的酶)与感染的关系。受感染蜗牛的微生物组组成发生了变化。蜗牛体内乙酰胆碱酯酶活性的降低与活动能力下降有关,但是否与吸虫感染有关仍不清楚。作者认为,已发现的生化变化与软体动物外壳的变形、行为的改变以及相关的微生物组之间存在联系。此外,作者还假设了由小球吸虫和Littorina蜗牛形成的寄生系统在生态系统氮循环中的作用。
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来源期刊
Parasitology Research
Parasitology Research 医学-寄生虫学
CiteScore
4.10
自引率
5.00%
发文量
346
审稿时长
6 months
期刊介绍: The journal Parasitology Research covers the latest developments in parasitology across a variety of disciplines, including biology, medicine and veterinary medicine. Among many topics discussed are chemotherapy and control of parasitic disease, and the relationship of host and parasite. Other coverage includes: Protozoology, Helminthology, Entomology; Morphology (incl. Pathomorphology, Ultrastructure); Biochemistry, Physiology including Pathophysiology; Parasite-Host-Relationships including Immunology and Host Specificity; life history, ecology and epidemiology; and Diagnosis, Chemotherapy and Control of Parasitic Diseases.
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