A rapid and standardized workflow for functional assessment of bacterial biosensors in fecal samples.

diagnostics engineered bacteria gut microbiome metabolite detection synthetic biology whole-cell biosensor

Journal

Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513

Informations de publication

Date de publication:
2022
Historique:
received: 21 01 2022
accepted: 05 07 2022
entrez: 8 9 2022
pubmed: 9 9 2022
medline: 9 9 2022
Statut: epublish

Résumé

Gut metabolites are pivotal mediators of host-microbiome interactions and provide an important window on human physiology and disease. However, current methods to monitor gut metabolites rely on heavy and expensive technologies such as liquid chromatography-mass spectrometry (LC-MS). In that context, robust, fast, field-deployable, and cost-effective strategies for monitoring fecal metabolites would support large-scale functional studies and routine monitoring of metabolites biomarkers associated with pathological conditions. Living cells are an attractive option to engineer biosensors due to their ability to detect and process many environmental signals and their self-replicating nature. Here we optimized a workflow for feces processing that supports metabolite detection using bacterial biosensors. We show that simple centrifugation and filtration steps remove host microbes and support reproducible preparation of a physiological-derived media retaining important characteristics of human feces, such as matrix effects and endogenous metabolites. We measure the performance of bacterial biosensors for benzoate, lactate, anhydrotetracycline, and bile acids, and find that they are highly sensitive to fecal matrices. However, encapsulating the bacteria in hydrogel helps reduce this inhibitory effect. Sensitivity to matrix effects is biosensor-dependent but also varies between individuals, highlighting the need for case-by-case optimization for biosensors' operation in feces. Finally, by detecting endogenous bile acids, we demonstrate that bacterial biosensors could be used for future metabolite monitoring in feces. This work lays the foundation for the optimization and use of bacterial biosensors for fecal metabolites monitoring. In the future, our method could also allow rapid pre-prototyping of engineered bacteria designed to operate in the gut, with applications to

Identifiants

pubmed: 36072290
doi: 10.3389/fbioe.2022.859600
pii: 859600
pmc: PMC9444133
doi:

Types de publication

Journal Article

Langues

eng

Pagination

859600

Informations de copyright

Copyright © 2022 Zúñiga, Muñoz-Guamuro, Boivineau, Mayonove, Conejero, Pageaux, Altwegg and Bonnet.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Ana Zúñiga (A)

Centre de Biologie Structurale (CBS), INSERM U1054, CNRS UMR5048, University of Montpellier, Montpellier, France.

Geisler Muñoz-Guamuro (G)

Centre de Biologie Structurale (CBS), INSERM U1054, CNRS UMR5048, University of Montpellier, Montpellier, France.

Lucile Boivineau (L)

Hepatogastroenterology and Bacteriology Service at CHU Montpellier, University of Montpellier, Montpellier, France.

Pauline Mayonove (P)

Centre de Biologie Structurale (CBS), INSERM U1054, CNRS UMR5048, University of Montpellier, Montpellier, France.

Ismael Conejero (I)

Department of Psychiatry, CHU Nimes, University of Montpellier, Montpellier, France.

Georges-Philippe Pageaux (GP)

Hepatogastroenterology and Bacteriology Service at CHU Montpellier, University of Montpellier, Montpellier, France.

Romain Altwegg (R)

Hepatogastroenterology and Bacteriology Service at CHU Montpellier, University of Montpellier, Montpellier, France.

Jerome Bonnet (J)

Centre de Biologie Structurale (CBS), INSERM U1054, CNRS UMR5048, University of Montpellier, Montpellier, France.

Classifications MeSH