Synergistic gut microbiome-mediated degradation of Astragalus membranaceus polysaccharides and Codonopsis pilosula polysaccharides into butyric acid: a metatranscriptomic analysis.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
XinQian Rong, LingFeng Zhu, QingLong Shu
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引用次数: 0

Abstract

Astragalus membranaceus and Codonopsis pilosula are traditional Chinese medicines known for their tonifying effects, which are linked to the metabolism of their polysaccharide components in the gut. However, the role of gut microbiota in the degradation of these polysaccharides to butyric acid remains unclear. This study aims to investigate the in vitro degradation of polysaccharides from Astragalus membranaceus and Codonopsis pilosula by healthy mice fecal microbiota, focusing on butyric acid production and the associated microbial gene expression. We conducted an in vitro analysis of the degradation of homogeneous polysaccharides. from Astragalus membranaceus and Codonopsis pilosula using fecal microbiota cultures derived from healthy mice. The fecal microbiota was cultured with the polysaccharides for 48 hours, after which the degradation liquid was collected for butyric acid quantification and metatranscriptome analysis of the microbiota. The degradation of Astragalus membranaceus polysaccharide resulted in a significant increase in butyric acid levels compared to those produced from Codonopsis pilosula polysaccharide or fructooligosaccharide (control). Differential gene expression analysis indicated an upregulation of carbohydrate-active enzymes and genes associated with butyrate production during the degradation of Astragalus membranaceus polysaccharides. Additionally, the findings suggested that synergistic interactions between polysaccharide-degrading and butyrate-producing bacteria play a crucial role in the microbiota's response to specific polysaccharides. This study highlights the potential of Astragalus polysaccharides to enhance butyric acid production through specific gut microbiota interactions, suggesting their beneficial effects on gut health and metabolism. Further research may provide insights into the therapeutic applications of these traditional medicines in modulating gut microbiota and improving health outcomes.IMPORTANCEThis study significantly advances our understanding of the role of gut microbiota in the metabolism of traditional Chinese medicinal polysaccharides, specifically those from Astragalus membranaceus and Codonopsis pilosula. By demonstrating that Astragalus membranaceus polysaccharide enhances butyric acid production more effectively than Codonopsis pilosula polysaccharide or fructooligosaccharides, the research highlights the potential of these natural compounds in modulating gut health. The identification of upregulated carbohydrate-active enzymes and butyrate production genes provides valuable insights into the microbial mechanisms underlying polysaccharide degradation. This work not only contributes to the field of microbiome research but also supports the development of functional foods and therapeutics aimed at enhancing gut health through targeted polysaccharide consumption.

协同肠道微生物介导的黄芪多糖和党参多糖转化为丁酸的降解:一项亚转录组学分析。
黄芪和党参是传统的中药,以其补益作用而闻名,这与肠道中多糖成分的代谢有关。然而,肠道微生物群在这些多糖降解为丁酸中的作用尚不清楚。本研究旨在研究健康小鼠粪便微生物群对黄芪和党参多糖的体外降解,重点研究丁酸的产生和相关微生物基因的表达。我们对均相多糖的体外降解进行了分析。从黄芪和党参中提取,利用健康小鼠的粪便微生物培养物。将粪便微生物群与多糖一起培养48小时,收集降解液对微生物群进行丁酸定量和亚转录组分析。与党参多糖或低聚果糖(对照)相比,黄芪多糖的降解导致丁酸水平显著增加。差异基因表达分析表明,在黄芪多糖降解过程中,糖活性酶和与丁酸盐产生相关的基因表达上调。此外,研究结果表明,多糖降解细菌和丁酸盐产生细菌之间的协同作用在微生物群对特定多糖的反应中起着至关重要的作用。该研究强调了黄芪多糖通过特定肠道菌群相互作用促进丁酸产生的潜力,表明它们对肠道健康和代谢有有益作用。进一步的研究可能会为这些传统药物在调节肠道微生物群和改善健康结果方面的治疗应用提供见解。重要意义本研究显著提高了我们对肠道菌群在中药多糖代谢中的作用的认识,特别是黄芪和党参多糖的代谢。通过证明黄芪多糖比党参多糖或低聚果糖更有效地促进丁酸的产生,该研究强调了这些天然化合物在调节肠道健康方面的潜力。碳水化合物活性酶和丁酸盐生产基因的上调鉴定为多糖降解的微生物机制提供了有价值的见解。这项工作不仅为微生物组研究领域做出了贡献,而且还支持了旨在通过有针对性地摄入多糖来增强肠道健康的功能性食品和疗法的开发。
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
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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