{"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. 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":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.72202","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
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.