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Direct analysis by ultra-high-resolution mass spectrometry of lipid A and phospholipids from Acinetobacter baumannii cells.

Authors :
Vergoz D
Schaumann A
Schmitz I
van Agthoven M
Martí S
Vila J
Afonso C
Dé E
Loutelier-Bourhis C
Alexandre S
Source :
Biochimie [Biochimie] 2024 Dec; Vol. 227 (Pt B), pp. 3-11. Date of Electronic Publication: 2024 Sep 24.
Publication Year :
2024

Abstract

Acinetobacter baumannii, classified as priority number one by the World Health Organization (WHO), is an opportunistic pathogen responsible for infection and is able to develop antibiotic resistance easily. Membranes are bacteria's first line of defense against external aggression, such as antibiotics. A chemical modification of a lipid family or a change in lipid composition can lead to resistance to antibiotics. In this work, we analyzed different A. baumannii strains from various environments with different antibiotic resistance profiles, using matrix-assisted laser desorption ionization-Fourier transform ion cyclotron resonance mass spectrometry (MALDI-FT-ICR MS). This study shows that it is possible to describe the main lipidome (phospholipids and lipid A) from the simple preparation of lysed cells, and that despite the complexity of the mixture. This ultra-high resolution mass spectrometry technique enables the separation of isobaric ion, to report a new class of lipids. Given its performance, this technique can be used to quickly and reliably characterize the lipidome of clinical strains from different environments.<br />Competing Interests: Declaration of competing interest The authors declare no competing interest concerning the research authorship and or publication of this article.<br /> (Copyright © 2024 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM). All rights reserved.)

Details

Language :
English
ISSN :
1638-6183
Volume :
227
Issue :
Pt B
Database :
MEDLINE
Journal :
Biochimie
Publication Type :
Academic Journal
Accession number :
39326489
Full Text :
https://doi.org/10.1016/j.biochi.2024.09.012