An optimised monophasic faecal extraction method for LC-MS analysis and its application in gastrointestinal disease

Kelly, P. E., Ng, H. J., Farrell, G., McKirdy, S., Russell, R. K., Hansen, R., Rattray, Z., Gerasimidis, K. and Rattray, N. J. W. (2022) An optimised monophasic faecal extraction method for LC-MS analysis and its application in gastrointestinal disease. Metabolites, 12(11), 1110. (doi: 10.3390/metabo12111110) (PMID:36422250) (PMCID:PMC9698041)

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Abstract

Liquid chromatography coupled with mass spectrometry (LC-MS) metabolomic approaches are widely used to investigate underlying pathogenesis of gastrointestinal disease and mechanism of action of treatments. However, there is an unmet requirement to assess faecal metabolite extraction methods for large-scale metabolomics studies. Current methods often rely on biphasic extractions using harmful halogenated solvents, making automation and large-scale studies challenging. The present study reports an optimised monophasic faecal extraction protocol that is suitable for untargeted and targeted LC-MS analyses. The impact of several experimental parameters, including sample weight, extraction solvent, cellular disruption method, and sample-to-solvent ratio, were investigated. It is suggested that a 50 mg freeze-dried faecal sample should be used in a methanol extraction (1:20) using bead beating as the means of cell disruption. This is revealed by a significant increase in number of metabolites detected, improved signal intensity, and wide metabolic coverage given by each of the above extraction parameters. Finally, we addressed the applicability of the method on faecal samples from patients with Crohn’s disease (CD) and coeliac disease (CoD), two distinct chronic gastrointestinal diseases involving metabolic perturbations. Untargeted and targeted metabolomic analysis demonstrated the ability of the developed method to detect and stratify metabolites extracted from patient groups and healthy controls (HC), highlighting characteristic changes in the faecal metabolome according to disease. The method developed is, therefore, suitable for the analysis of patients with gastrointestinal disease and can be used to detect and distinguish differences in the metabolomes of CD, CoD, and HC.

Item Type:Articles
Additional Information:This study was supported by Shimadzu UK and the University of Strathclyde through joint contribution to P.E.K.’s studentship. The clinical studies were funded by the Glasgow Children Hospital Charity and the Nutricia Research Foundation. Z.R. want to acknowledge the EPSRC Multiscale Metrology Suite (EP/V028960/1).
Keywords:Mass spectrometry, metabolite extraction, inflammatory bowel disease, Crohn’s disease, coeliac disease.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Hansen, Dr Richard and Russell, Dr Richard and Kelly, Miss Patricia and Ng, Ms Hwei and Mckirdy, Miss Shona and Gerasimidis, Professor Konstantinos
Authors: Kelly, P. E., Ng, H. J., Farrell, G., McKirdy, S., Russell, R. K., Hansen, R., Rattray, Z., Gerasimidis, K., and Rattray, N. J. W.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
Journal Name:Metabolites
Publisher:MDPI
ISSN:2218-1989
ISSN (Online):2218-1989
Published Online:14 November 2022
Copyright Holders:Copyright © 2022 The Authors
First Published:First published in Metabolites 12(11): 1110
Publisher Policy:Reproduced under a Creative Commons License

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