Lipidomic Analysis Reveals Differences in Bacteroides Species Driven Largely by Plasmalogens, Glycerophosphoinositols and Certain Sphingolipids

Author:

Ryan Eileen12ORCID,Gonzalez Pastor Belén13,Gethings Lee A.456,Clarke David J.13,Joyce Susan A.12ORCID

Affiliation:

1. APC Microbiome Ireland, University College Cork, T12 K8AF Cork, Ireland

2. School of Biochemistry & Cell Biology, University College Cork, T12 K8AF Cork, Ireland

3. School of Microbiology, University College Cork, T12 K8AF Cork, Ireland

4. Waters, Stamford Avenue, Altrincham Road, Wilmslow SK9 4AX, UK

5. Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Institute of Biotechnology, University of Manchester, Manchester M1 7DN, UK

6. Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey GU2 7XH, UK

Abstract

There has been increasing interest in bacterial lipids in recent years due, in part, to their emerging role as molecular signalling molecules. Bacteroides thetaiotaomicron is an important member of the mammalian gut microbiota that has been shown to produce sphingolipids (SP) that pass through the gut epithelial barrier to impact host SP metabolism and signal into host inflammation pathways. B. thetaiotaomicron also produces a novel family of N-acyl amines (called glycine lipids) that are potent ligands of host Toll-like receptor 2 (TLR2). Here, we specifically examine the lipid signatures of four species of gut-associated Bacteroides. In total we identify 170 different lipids, and we report that the range and diversity of Bacteroides lipids is species specific. Multivariate analysis reveals that the differences in the lipid signatures are largely driven by the presence and absence of plasmalogens, glycerophosphoinositols and certain SP. Moreover, we show that, in B. thetaiotaomicron, mutations altering either SP or glycine lipid biosynthesis result in significant changes in the levels of other lipids, suggesting the existence of a compensatory mechanisms required to maintain the functionality of the bacterial membrane.

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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