Inositol acylation of phosphatidylinositol mannosides: a rapid mass response to membrane fluidization in mycobacteria.


Journal

Journal of lipid research
ISSN: 1539-7262
Titre abrégé: J Lipid Res
Pays: United States
ID NLM: 0376606

Informations de publication

Date de publication:
09 2022
Historique:
received: 28 05 2022
revised: 25 07 2022
accepted: 29 07 2022
pubmed: 12 8 2022
medline: 5 10 2022
entrez: 11 8 2022
Statut: ppublish

Résumé

Mycobacteria share an unusually complex, multilayered cell envelope, which contributes to adaptation to changing environments. The plasma membrane is the deepest layer of the cell envelope and acts as the final permeability barrier against outside molecules. There is an obvious need to maintain the plasma membrane integrity, but the adaptive responses of the plasma membrane to stress exposure remain poorly understood. Using chemical treatment and heat stress to fluidize the membrane, we show here that phosphatidylinositol (PI)-anchored plasma membrane glycolipids known as PI mannosides (PIMs) are rapidly remodeled upon membrane fluidization in Mycobacterium smegmatis. Without membrane stress, PIMs are predominantly in a triacylated form: two acyl chains of the PI moiety plus one acyl chain modified at one of the mannose residues. Upon membrane fluidization, we determined the fourth fatty acid is added to the inositol moiety of PIMs, making them tetra-acylated variants. Additionally, we show that PIM inositol acylation is a rapid response independent of de novo protein synthesis, representing one of the fastest mass conversions of lipid molecules found in nature. Strikingly, we found that M. smegmatis is more resistant to the bactericidal effect of a cationic detergent after benzyl alcohol pre-exposure. We further demonstrate that fluidization-induced PIM inositol acylation is conserved in pathogens such as Mycobacterium tuberculosis and Mycobacterium abscessus. Our results demonstrate that mycobacteria possess a mechanism to sense plasma membrane fluidity change. We suggest that inositol acylation of PIMs is a novel membrane stress response that enables mycobacterial cells to resist membrane fluidization.

Identifiants

pubmed: 35952902
pii: S0022-2275(22)00095-5
doi: 10.1016/j.jlr.2022.100262
pmc: PMC9490103
pii:
doi:

Substances chimiques

Benzyl Alcohols 0
Detergents 0
Fatty Acids 0
Glycolipids 0
Mannosides 0
Phosphatidylinositols 0
phosphatidylinositol mannoside 0
Inositol 4L6452S749
Mannose PHA4727WTP

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

100262

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI144748
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM139789
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that they have no conflicts of interest with the contents of this article.

Auteurs

Peter P Nguyen (PP)

Department of Microbiology, University of Massachusetts, Amherst, MA, USA.

Takehiro Kado (T)

Department of Microbiology, University of Massachusetts, Amherst, MA, USA.

Malavika Prithviraj (M)

Department of Microbiology, University of Massachusetts, Amherst, MA, USA.

M Sloan Siegrist (MS)

Department of Microbiology, University of Massachusetts, Amherst, MA, USA; Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA, USA.

Yasu S Morita (YS)

Department of Microbiology, University of Massachusetts, Amherst, MA, USA; Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA, USA. Electronic address: ymorita@umass.edu.

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Classifications MeSH