{"title":"色氨酸代谢的季节性可塑性为蛇冬眠的生理适应提供了新的见解","authors":"Yuting Wei, Zexiu Zhang, Xiaohong Lin, Gangning Wei, Pengyue Zhang, Huirong Mao, Biao Chen, Jianhao Ji, Yunlin Zheng, Zhiyi Luo, Xiaolong Hu","doi":"10.1002/ece3.72202","DOIUrl":null,"url":null,"abstract":"<p>Hibernation is a common behavioral strategy for snakes to cope with extreme environments. This phenomenon has raised important scientific questions regarding its physiological adaptation mechanisms. Although tryptophan and its metabolites have been widel y studied for their roles in various physiological processes in animals—including immune regulation, metabolic homeostasis, and circadian rhythms—the impact of snake hibernation on tryptophan metabolism remains unexplored. In the present study, an integrated multi-omics approach that combines targeted metabolomics, transcriptomics, and microbiome was used to reveal the tryptophan metabolism mechanisms in active and hibernating snakes. Our results revealed that the higher gut indole concentrations observed in active snakes indicate a greater reliance on microbial pathways in their tryptophan metabolism. Correlation analyses between gut microbiota and indole levels further identified specific bacterial genera—<i>Paeniclostridium, Romboutsia</i>, and <i>Clostridium sensu stricto 1</i>—as potential key contributors to tryptophan conversion into indole. Additionally, the higher serum concentrations of metabolites such as kynurenic acid and 5-hydroxytryptophol, along with the upregulated expression of key genes, indicate that hibernating snakes exhibit an increased reliance on the kynurenine and 5-hydroxytryptamine pathways for tryptophan metabolism. These findings collectively suggested that the seasonal plasticity of tryptophan metabolism may mediate physiological adaptations during snake hibernation, thereby providing deeper cognition into the mechanisms underlying reptilian hibernation strategies.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"15 9","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece3.72202","citationCount":"0","resultStr":"{\"title\":\"Seasonal Plasticity in Tryptophan Metabolism Provides New Insights Into Physiological Adaptation in Snake Hibernation\",\"authors\":\"Yuting Wei, Zexiu Zhang, Xiaohong Lin, Gangning Wei, Pengyue Zhang, Huirong Mao, Biao Chen, Jianhao Ji, Yunlin Zheng, Zhiyi Luo, Xiaolong Hu\",\"doi\":\"10.1002/ece3.72202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Hibernation is a common behavioral strategy for snakes to cope with extreme environments. This phenomenon has raised important scientific questions regarding its physiological adaptation mechanisms. Although tryptophan and its metabolites have been widel y studied for their roles in various physiological processes in animals—including immune regulation, metabolic homeostasis, and circadian rhythms—the impact of snake hibernation on tryptophan metabolism remains unexplored. In the present study, an integrated multi-omics approach that combines targeted metabolomics, transcriptomics, and microbiome was used to reveal the tryptophan metabolism mechanisms in active and hibernating snakes. Our results revealed that the higher gut indole concentrations observed in active snakes indicate a greater reliance on microbial pathways in their tryptophan metabolism. Correlation analyses between gut microbiota and indole levels further identified specific bacterial genera—<i>Paeniclostridium, Romboutsia</i>, and <i>Clostridium sensu stricto 1</i>—as potential key contributors to tryptophan conversion into indole. Additionally, the higher serum concentrations of metabolites such as kynurenic acid and 5-hydroxytryptophol, along with the upregulated expression of key genes, indicate that hibernating snakes exhibit an increased reliance on the kynurenine and 5-hydroxytryptamine pathways for tryptophan metabolism. 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引用次数: 0
摘要
冬眠是蛇应对极端环境的一种常见行为策略。这一现象对其生理适应机制提出了重要的科学问题。尽管色氨酸及其代谢物在动物各种生理过程中的作用已被广泛研究,包括免疫调节、代谢稳态和昼夜节律,但蛇的冬眠对色氨酸代谢的影响仍未被探索。本研究采用综合多组学方法,结合靶向代谢组学、转录组学和微生物组学,揭示了活动和冬眠蛇的色氨酸代谢机制。我们的研究结果显示,在活性蛇中观察到的较高肠道吲哚浓度表明它们在色氨酸代谢中更依赖于微生物途径。肠道微生物群与吲哚水平之间的相关性分析进一步确定了特定的细菌属- paeniclostridium, Romboutsia和Clostridium sensu stricto 1 -作为色氨酸转化为吲哚的潜在关键因素。此外,较高的血清代谢物浓度,如犬尿氨酸和5-羟色胺,以及关键基因的上调表达,表明冬眠蛇对犬尿氨酸和5-羟色胺途径的色氨酸代谢依赖性增加。这些发现共同表明,色氨酸代谢的季节性可塑性可能介导了蛇冬眠期间的生理适应,从而为爬行动物冬眠策略的机制提供了更深入的认识。
Seasonal Plasticity in Tryptophan Metabolism Provides New Insights Into Physiological Adaptation in Snake Hibernation
Hibernation is a common behavioral strategy for snakes to cope with extreme environments. This phenomenon has raised important scientific questions regarding its physiological adaptation mechanisms. Although tryptophan and its metabolites have been widel y studied for their roles in various physiological processes in animals—including immune regulation, metabolic homeostasis, and circadian rhythms—the impact of snake hibernation on tryptophan metabolism remains unexplored. In the present study, an integrated multi-omics approach that combines targeted metabolomics, transcriptomics, and microbiome was used to reveal the tryptophan metabolism mechanisms in active and hibernating snakes. Our results revealed that the higher gut indole concentrations observed in active snakes indicate a greater reliance on microbial pathways in their tryptophan metabolism. Correlation analyses between gut microbiota and indole levels further identified specific bacterial genera—Paeniclostridium, Romboutsia, and Clostridium sensu stricto 1—as potential key contributors to tryptophan conversion into indole. Additionally, the higher serum concentrations of metabolites such as kynurenic acid and 5-hydroxytryptophol, along with the upregulated expression of key genes, indicate that hibernating snakes exhibit an increased reliance on the kynurenine and 5-hydroxytryptamine pathways for tryptophan metabolism. These findings collectively suggested that the seasonal plasticity of tryptophan metabolism may mediate physiological adaptations during snake hibernation, thereby providing deeper cognition into the mechanisms underlying reptilian hibernation strategies.
期刊介绍:
Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment.
Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.