The prebiotic potential of dietary onion extracts: shaping gut microbial structures and promoting beneficial metabolites.

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-01-21 Epub Date: 2024-12-23 DOI:10.1128/msystems.01189-24
Yebeen Yoo, Seongok Kim, WonJune Lee, Jinwoo Kim, Bokyung Son, Kwang Jun Lee, Hakdong Shin
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引用次数: 0

Abstract

Onions are well-known vegetables that offer various health benefits. This study explores the impact of onion extracts on gut microbiome using an in vitro fecal incubation model and metabolome analysis. Fecal samples were collected from 19 healthy donors and incubated in the presence or absence of onion extracts for 24 h. To reduce inter-individual variability in the gut microbiome, we employed enterotyping based on baseline fecal microbiota: 14 subjects with a Bacteroides-dominant type (enterotype B) and 5 subjects with Prevotella-dominant type (enterotype P). Alpha diversity was significantly reduced in the onion-treated group compared to the non-treated control group in both Bacteroides- and Prevotella-dominant types. However, significant structural differences in bacterial communities were observed based on weighted UniFrac distance. Notably, short-chain fatty acid (SCFA)-producing bacteria, such as Bifidobacterium_388775, Feacalibacterium, and Fusicatenibacter, were overrepresented in response to onion extracts in enterotype B. Furthermore, genes related to butyrate production were significantly overrepresented in the onion-treated group within enterotype B. Consistent with the enriched taxa and the predicted metabolic pathways, SCFAs and their related metabolites were significantly enriched in the onion-treated group. Additionally, tryptophan metabolism-derived metabolites, including indolelactate (ILA) and indolepropionate (IPA), were elevated by 4- and 32-fold, respectively, in the onion-treated group compared to the control group. In vitro growth assays showed an increase in lactobacilli strains in the presence of onion extracts. These results provide evidence that onion extracts could serve as promising prebiotics by altering gut microbial structure and promoting the production of beneficiary metabolites, including SCFAs and indole derivatives, and enhancing the growth of probiotics.IMPORTANCEThis study is significant as it provides compelling evidence that onion extracts have the potential to serve as effective prebiotics. Utilizing an in vitro fecal incubation model and enterotyping to reduce inter-individual variability, the research demonstrates how onion extracts can alter gut microbial structure and promote the production of beneficial metabolites, including SCFAs and indole derivatives like ILA and IPA. Additionally, onion extract treatment enhances the growth of beneficial probiotics. The findings underscore the potential of onion extracts to improve gut health by enriching specific beneficial bacteria and metabolic pathways, thereby supporting the development of functional foods aimed at improving gut microbiota composition and metabolic health.

膳食洋葱提取物的益生元潜力:塑造肠道微生物结构和促进有益代谢产物。
洋葱是众所周知的有益健康的蔬菜。本研究通过体外粪便培养模型和代谢组分析探讨了洋葱提取物对肠道微生物组的影响。从19名健康供体中收集粪便样本,并在存在或不存在洋葱提取物的情况下孵育24小时。为了减少肠道微生物组的个体间差异,我们采用了基于基线粪便微生物群的肠道分型:14例为拟杆菌(Bacteroides)优势型(肠型B), 5例为普雷沃菌(prevotella)优势型(肠型P)。与未处理对照组相比,洋葱处理组在拟杆菌(Bacteroides)和普雷沃菌(prevotella)优势型中α多样性均显著降低。然而,根据加权UniFrac距离,观察到细菌群落的显著结构差异。值得注意的是,短链脂肪酸(SCFA)产生细菌,如双歧杆菌(Bifidobacterium_388775)、Feacalibacterium和Fusicatenibacter,在肠型b中对洋葱提取物的反应中被过度代表。此外,与丁酸盐产生相关的基因在肠型b中被显著过度代表。与富集的分类群和预测的代谢途径一致,洋葱处理组中SCFA及其相关代谢物显著富集。此外,色氨酸代谢衍生的代谢物,包括吲哚乳酸酯(ILA)和吲哚丙酸酯(IPA),在洋葱处理组中分别比对照组升高了4倍和32倍。体外生长试验表明,在洋葱提取物的存在下,乳酸杆菌菌株增加。这些结果表明,洋葱提取物可以通过改变肠道微生物结构,促进有益代谢物(包括短链脂肪酸和吲哚衍生物)的产生,促进益生菌的生长,从而成为有前景的益生元。这项研究具有重要意义,因为它提供了令人信服的证据,证明洋葱提取物具有作为有效益生元的潜力。该研究利用体外粪便培养模型和肠道分型来减少个体间的差异,展示了洋葱提取物如何改变肠道微生物结构并促进有益代谢物的产生,包括短链脂肪酸和吲哚衍生物如ILA和IPA。此外,洋葱提取物处理促进有益益生菌的生长。这些发现强调了洋葱提取物通过丰富特定的有益细菌和代谢途径来改善肠道健康的潜力,从而支持旨在改善肠道微生物群组成和代谢健康的功能性食品的开发。
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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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