Protocol for preparing murine fecal microbiota transplant and fecal microbiota metabolites for in vivo and in vitro use

Accumulating evidence demonstrates that microbiota-derived metabolites can modulate host immune responses and influence complex pathologies. Despite their therapeutic potential, the isolation of fecal microbial metabolites and their scalable ex vivo production remain challenging. Here, we present a protocol for preparing murine fecal microbiota transplant (FMT) and fecal microbiota metabolites for in vivo and in vitro use. We describe steps for collecting and preparing donor feces, isolating fecal microbial metabolites, and producing fecal microbial metabolites ex vivo with a broth expansion culture. For complete details on the use and execution of this protocol, please refer to Phelps et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2025-11-28
DOI
https://doi.org/10.1016/j.xpro.2025.104240
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
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0.00
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article

Protocol for preparing murine fecal microbiota transplant and fecal microbiota metabolites for in vivo and in vitro use

Marlies Meisel, K.J. Dhanaraj, Catherine M. Phelps
STAR Protocols
Clostridium difficile and Clostridium perfringens research
article

Protocol for preparing murine fecal microbiota transplant and fecal microbiota metabolites for in vivo and in vitro use

Marlies Meisel, K.J. Dhanaraj, Catherine M. Phelps
article en

Abstract

Accumulating evidence demonstrates that microbiota-derived metabolites can modulate host immune responses and influence complex pathologies. Despite their therapeutic potential, the isolation of fecal microbial metabolites and their scalable ex vivo production remain challenging. Here, we present a protocol for preparing murine fecal microbiota transplant (FMT) and fecal microbiota metabolites for in vivo and in vitro use. We describe steps for collecting and preparing donor feces, isolating fecal microbial metabolites, and producing fecal microbial metabolites ex vivo with a broth expansion culture. For complete details on the use and execution of this protocol, please refer to Phelps et al.<sup>1</sup>.

STAR ProtocolsVol. 6(4)
University of Pittsburgh (US)
Openalex Percentile: Top 56%
Clostridium difficile and Clostridium perfringens research
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