Moderate altitude exposure impacts extensive host-microbiota multi-kingdom connectivity with serum metabolome and fasting blood glucose.

IF 5.4 1区 农林科学 Q1 IMMUNOLOGY
Virulence Pub Date : 2025-12-01 Epub Date: 2025-07-13 DOI:10.1080/21505594.2025.2530660
Xiaoran Huang, Xiaoyan Gao, Yanqun Fan, Dingchen Wang, Xuanfu Chen, Xin Qi, Zhibo Yang, Yu-E Wang, Jinxiu Meng, Guoxiang Zou, Zhipeng Liu, Xin Li
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引用次数: 0

Abstract

The contributions and interactions of multi-kingdom microbiota (i.e. bacteriome, mycobiome, archaeome, and phageome) with serum metabolome and host phenome in healthy individuals under moderate altitude exposure remain unclear. We applied shotgun metagenomic sequencing in feces and targeted metabolomics technology in serum to explore how human gut multi-kingdom microorganisms influence the serum metabolome and phenome in healthy Chinese individuals following moderate altitude exposure. The results indicated that individuals with moderate altitude exposure exhibited more substantial alterations in gut bacteriome and phageome compared to those in mycobiome and archaeome. Both intra-kingdom and inter-kingdom correlations at baseline were denser than those following moderate altitude exposure. Bacteriophages-host interaction analysis revealed symbiosis between bacteriophages and Bacteroidetes, Proteobacteria, and short-chain fatty acids (SCFAs) producers. Furthermore, bacteriophage Shirahamavirus PTm1 (odds ratio (OR) = 3.82; 95% confidence interval (CI): 1.20-12.16), archaeon Crenarchaeota (OR = 3.70; 95% CI: 1.35-10.14) and bacterium Bacteroidetes (OR = 3.69; 95% CI: 1.34-10.15) showed a positive association with lowered fasting blood glucose (FBG) benefits, while bacteriophage Candidatus Nitrosopelagicus brevis (OR = 0.30; 95% CI: 0.10-0.89) and butyric acid (OR = 0.07; 95% CI: 0.01-0.37) exhibited a negative association with lowered FBG benefits. These findings suggest that targeting gut multi-kingdom microorganisms could serve as an alternative therapeutic approach to mitigate dysglycemia and its associated metabolic disorders.

中等海拔暴露会影响宿主-微生物群与血清代谢组和空腹血糖的广泛联系。
在中等海拔暴露条件下,健康人群血清代谢组和宿主表型与多界微生物群(即细菌组、真菌组、古菌组和噬菌体组)的作用和相互作用尚不清楚。我们利用鸟枪宏基因组测序技术对粪便进行测序,并利用靶向代谢组学技术对血清进行代谢组学检测,探讨人类肠道多领域微生物对中国健康人群中中等海拔暴露后血清代谢组和表型组的影响。结果表明,与真菌组和古菌组相比,中等海拔暴露个体肠道细菌组和噬菌体组发生了更大的变化。基线时王国内和王国间的相关性都比中等海拔暴露后要高。噬菌体-宿主相互作用分析揭示了噬菌体与拟杆菌门、变形杆菌门和短链脂肪酸(SCFAs)生产者之间的共生关系。此外,噬菌体Shirahamavirus PTm1(优势比(OR) = 3.82;95%可信区间(CI): 1.20-12.16),古菌绿古菌(OR = 3.70;95% CI: 1.35-10.14)和拟杆菌(OR = 3.69;95% CI: 1.34-10.15)与降低空腹血糖(FBG)的益处呈正相关,而短亚硝化候选噬菌体(OR = 0.30;95% CI: 0.10-0.89)和丁酸(OR = 0.07;95% CI: 0.01-0.37)与降低FBG的益处呈负相关。这些发现表明,靶向肠道多领域微生物可以作为缓解血糖异常及其相关代谢紊乱的替代治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virulence
Virulence IMMUNOLOGY-MICROBIOLOGY
CiteScore
9.20
自引率
1.90%
发文量
123
审稿时长
6-12 weeks
期刊介绍: Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication. Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.
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