Inositol acylation of phosphatidylinositol mannosides: a rapid mass response to membrane fluidization in mycobacteria.
cell envelope
enzyme regulation
glycolipids
heat stress
lipids
membrane fluidity
metabolism
pathogens
plasma membrane integrity
stress response
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
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
100262Subventions
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.