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OPTIMATRIX v2.0:用于人体远端结肠模型的微型基质生物反应器平台中减轻微生物大量繁殖的优化方案。

OPTIMATRIX v2.0: Optimised protocol to mitigate microbial blooms in the micro-Matrix bioreactor platform used as an human distal colon model.

作者信息

Mukherjee Arghya, Leali Nicola Ferremi, Salvetti Elisa, Torriani Sandra, Cotter Paul D, Mathur Harsh

机构信息

Teagasc Food Research Centre, Moorepark, Fermoy, Cork, Ireland.

APC Microbiome Ireland, Cork, Ireland.

出版信息

MethodsX. 2025 Mar 22;14:103275. doi: 10.1016/j.mex.2025.103275. eCollection 2025 Jun.

Abstract

We previously reported optimisation of the methodology to mitigate blooms and associated loss of microbial diversity when using the micro-Matrix bioreactor platform as an model of the human distal colon. Here, we provide further critical insights that we have gained in this regard through follow-up experiments. We tested four separate faecal fermentation media compositions for the purposes of such distal colon model experiments and found that the media composition described by MacFarlane is the most suitable for mitigating such microbial blooms, and concurrently, maintaining microbial diversity. We also tested if pooled or individual donor faecal samples were more suitable and found that pooled samples performed better in terms of maintaining gut microbiota diversity in such batch culture model experiments using the micro-Matrix system. Finally, we determined that prolonged experiments, i.e. for durations of up to 96 h, may be warranted with a view to affording particularly fastidious gut microbes an opportunity to grow and compete with their less fastidious counterparts. Essentially, we provide critical insights into:•Optimal faecal fermentation media to minimise blooms and preserve diversity in colon model experiments•Optimal faecal inoculum source and duration of experiments.

摘要

我们之前报道过,在使用微矩阵生物反应器平台作为人类远端结肠模型时,对减轻菌群大量繁殖及相关微生物多样性丧失的方法进行了优化。在此,我们提供通过后续实验在这方面获得的进一步关键见解。为了进行此类远端结肠模型实验,我们测试了四种不同的粪便发酵培养基成分,发现麦克法兰描述的培养基成分最适合减轻此类微生物大量繁殖,同时维持微生物多样性。我们还测试了混合或个体供体粪便样本是否更合适,发现在使用微矩阵系统的此类分批培养模型实验中,混合样本在维持肠道微生物群多样性方面表现更好。最后,我们确定可能有必要进行长时间实验,即长达96小时,以便为特别挑剔的肠道微生物提供生长机会,并与不那么挑剔的同类微生物竞争。本质上,我们提供了关于以下方面的关键见解:

• 在结肠模型实验中使菌群大量繁殖最小化并保持多样性的最佳粪便发酵培养基

• 最佳粪便接种物来源和实验持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad4/11986543/bc01fad25a8c/ga1.jpg

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