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Metabolic Screening of Gut Microbiota by Fourier-Transform Infrared Spectroscopy

dc.contributor.authorSayol Altarriba, Anna
dc.contributor.authorAira Gómez, Andrea
dc.contributor.authorMartín-López, Eva
dc.contributor.authorVillasante, Anna
dc.contributor.authorAlbarracín, Rosa
dc.contributor.authorFaneca, Joana
dc.contributor.authorPitart, Cristina
dc.contributor.authorRoca Subirà, Ignasi
dc.contributor.authorCasals Mercadal, Gregori
dc.contributor.authorMarco Colás, Santiago
dc.contributor.authorVillanueva Cañas, José Luis
dc.contributor.authorCasals Pascual, Climent
dc.date.accessioned2026-08-27T07:58:20Z
dc.date.embargoEndDateinfo:eu-repo/date/embargoEnd/2027-05-31
dc.date.issued2026-06-12
dc.date.updated2026-08-27T07:58:21Z
dc.description.abstractShort-chain fatty acids (SCFAs) are bacterial metabolites with crucial roles in host homeostasis and immune system modulation. Given their benefits, they have been proposed as markers of healthy microbiota. However, accurate SCFA quantification typically requires gas chromatography coupled with mass spectrometry (GC-MS), which is time-consuming, expensive, and requires specialized personnel and equipment, limiting its routine use for stool quality assessment in clinical contexts. In this initial feasibility study, we explored the use of Fourier transform infrared (FT-IR) spectroscopy as a rapid metabolic screening approach for stool samples. Analysis of SCFA-associated spectral windows enhanced discrimination between healthy and dysbiotic stool samples with <em>Clostridioides difficile</em> infection using principal component analysis. FT-IR is not intended to replace GC-MS for precise SCFA quantification but rather to provide a rapid screening of metabolically relevant differences. Although additional validation is still needed, the present study provides a robust proof-of-concept demonstrating the feasibility of applying FT-IR spectroscopy to clinical stool samples. Combined with the widespread availability of this technology in most hospitals, these advantages highlight its potential for future development as a tool for routine screening in clinical laboratories.
dc.embargo.lift2027-05-31
dc.format.extent22 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec771614
dc.identifier.issn2373-8227
dc.identifier.pmid42220213
dc.identifier.urihttps://hdl.handle.net/2445/231200
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/acsinfecdis.6c00128
dc.relation.ispartofACS Infectious Diseases, 2026, vol. 12, num.6, p. 2025-2032
dc.relation.urihttps://doi.org/10.1021/acsinfecdis.6c00128
dc.rights(c) American Chemical Society, 2026
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccess
dc.subject.classificationMicrobiota
dc.subject.classificationEspectroscòpia
dc.subject.classificationÀcids grassos
dc.subject.otherMicrobiota
dc.subject.otherSpectrum analysis
dc.subject.otherFatty acids
dc.titleMetabolic Screening of Gut Microbiota by Fourier-Transform Infrared Spectroscopy
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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