Journal Article

Depleting Cationic Lipids Involved in Antimicrobial Resistance Drives Adaptive Lipid Remodeling in Enterococcus faecalis

Allen, Doug K., Rashid, Rafi, Chen, Swaine L., Wenk, Markus R., Kline, Kimberly A., Nair, Zeus Jaren, Morley, Stewart A., Chia, Dominic Ming Hao, Chong, Kelvin Kian Long, Chng, Shu Sin, Cazenave Gassiot, Amaury

2023

Overview

The cell membrane plays a pivotal role in protecting bacteria against external threats, such as antibiotics. Cationic phospholipids such as lysyl-phosphatidyglycerol (L-PG) resist the action of cationic antimicrobial peptides through electrostatic repulsion. The bacterial cell membrane is an interface for cell envelope synthesis, protein secretion, virulence factor assembly, and a target for host cationic antimicrobial peptides (CAMPs). To resist CAMP killing, several Gram-positive pathogens encode the multiple peptide resistance factor (MprF) enzyme that covalently attaches cationic amino acids to anionic phospholipids in the cell membrane. While E. faecalis encodes two mprF paralogs, MprF2 plays a dominant role in conferring resistance to killing by the CAMP human β-defensin 2 (hBD-2) in E. faecalis strain OG1RF. The goal of the current study is to understand the broader lipidomic and functional roles of E. faecalis mprF. We analyzed the lipid profiles of parental wild-type and mprF mutant strains and show that while Δ mprF2 and Δ mprF1 Δ mprF2 mutants completely lacked cationic lysyl-phosphatidylglycerol (L-PG), the Δ mprF1 mutant synthesized ~70% of L-PG compared to the parent. Unexpectedly, we also observed a significant reduction of PG in Δ mprF2 and Δ mprF1 Δ mprF2 . In the mprF mutants, particularly Δ mprF1 Δ mprF2 , the decrease in L-PG and phosphatidylglycerol (PG) is compensated by an increase in a phosphorus-containing lipid, glycerophospho-diglucosyl-diacylglycerol (GPDGDAG), and D-ala-GPDGDAG. These changes were accompanied by a downregulation of de novo fatty acid biosynthesis and an accumulation of long-chain acyl-acyl carrier proteins (long-chain acyl-ACPs), suggesting that the suppression of fatty acid biosynthesis was mediated by the transcriptional repressor FabT. Growth in chemically defined media lacking fatty acids revealed severe growth defects in the Δ mprF1 Δ mprF2 mutant strain, but not the single mutants, which was partially rescued through supplementation with palmitic and stearic acids. Changes in lipid homeostasis correlated with lower membrane fluidity, impaired protein secretion, and increased biofilm formation in both Δ mprF2 and Δ mprF1 Δ mprF2 , compared to the wild type and Δ mprF1 . Collectively, our findings reveal a previously unappreciated role for mprF in global lipid regulation and cellular physiology, which could facilitate the development of novel therapeutics targeting MprF. IMPORTANCE The cell membrane plays a pivotal role in protecting bacteria against external threats, such as antibiotics. Cationic phospholipids such as lysyl-phosphatidyglycerol (L-PG) resist the action of cationic antimicrobial peptides through electrostatic repulsion. Here we demonstrate that L-PG depletion has several unexpected consequences in Enterococcus faecalis , including a reduction of phosphatidylglycerol (PG), enrichment of a phosphorus-containing lipid, reduced fatty acid synthesis accompanied by an accumulation of long-chain acyl-acyl carrier proteins (long chain acyl-ACPs), lower membrane fluidity, and impaired secretion. These changes are not deleterious to the organism as long as exogenous fatty acids are available for uptake from the culture medium. Our findings suggest an adaptive mechanism involving compensatory changes across the entire lipidome upon removal of a single phospholipid modification. Such adaptations must be considered when devising antimicrobial strategies that target membrane lipids.

• Publisher: American Society for Microbiology
• Subject: adaptive remodeling / Anti-Bacterial Agents - metabolism / Anti-Bacterial Agents - pharmacology / Anti-Infective Agents - metabolism / Antibiotics / Antimicrobial agents / Antimicrobial Cationic Peptides - metabolism / Antimicrobial Cationic Peptides - pharmacology / Antimicrobial peptides / Antimicrobial resistance / Bacteria / Bacterial Proteins - metabolism / Bacteriology / Biofilms / Camps / Carrier Proteins - metabolism / Cationic antimicrobial peptides / cationic antimicrobial peptides (CAMPs) / Cations - metabolism / Cell culture / Cell membranes / Chromatography / Defensins / Diglycerides / Drug development / Drug resistance / Drug Resistance, Bacterial / Enterococcus faecalis / Enterococcus faecalis - metabolism / Fatty acids / Fatty Acids - metabolism / Fluidity / Genes / Gram-positive bacteria / Homeostasis / Humans / Infections / lipid homeostasis / lipid metabolism / Lipids / lysyl-phosphatidylglycerol (L-PG) / Membrane fluidity / multiple peptide resistance factor (MprF) / Mutants / Mutation / Peptides / Phosphatidylglycerol / Phosphatidylglycerols - metabolism / Phospholipids / Phospholipids - metabolism / Phosphorus / Protein biosynthesis / Research Article / Secretion / Virulence factors