性别特异性小鼠死后微生物组动力学:对死亡定义的影响。

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Yangkui Xue, Mengliang Huang, Jianing Zhang, Shrestha Navin, Yahao Tao, Gang Zeng
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引用次数: 0

摘要

肠道微生物与其宿主形成复杂而动态的共生关系。然而,在宿主死亡后的早期阶段,微生物的反应在很大程度上仍然是未知的。在本研究中,我们采用小鼠模型系统表征了肠道微生物群的死后反应,并分析了雄性和雌性小鼠死亡后早期(死后0、0.5、2、6、12和24小时)微生物组成的动态变化。我们的研究结果表明,微生物组组成的性别二态变化早在死后2小时就发生了。雄性小鼠表现出更多的功能冗余和延迟的社区重组,而雌性小鼠表现出更早的社区转移。这些性别特异性模式伴随着代谢途径活性和生物标志物分类群的差异。值得注意的是,肠道微生物在宿主死亡后所观察到的调节能力的保留,为死亡本身的概念化提供了一个新的视角。我们提出“生态死亡”一词来描述死亡后宿主相关微生物生态系统的不可逆转的崩溃,这标志着肠道微生物群功能和结构完整性的关键转变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-specific postmortem microbiome dynamics in mice: implications for death definitions.

Gut microbes form a complex and dynamic symbiotic relationship with their host. However, the microbial response during the early stages following host death remains largely uncharacterized. In this study, we employed a mouse model to systematically characterize the postmortem response of the intestinal microbiota, and analyzed the dynamic changes in microbial composition during the early stages after death in both male and female mice (at 0, 0.5, 2, 6, 12, and 24 h postmortem). Our findings reveal that sex-dimorphic shifts in microbiome composition occur as early as 2 h postmortem. Male mice exhibited increased functional redundancy and delayed community restructuring, whereas female mice displayed earlier community shifts. These sex-specific patterns were accompanied by differences in metabolic pathway activity and biomarker taxa. Notably, the observed retention of regulatory capacity by intestinal microbes after host death offers a novel perspective on the conceptualization of death itself. We propose the term "ecological death" to describe the irreversible collapse of the host-associated microbial ecosystem following death, marking a critical transition in the functional and structural integrity of the intestinal microbiota.

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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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