Biology subjects

Lecuyer, S.

Publications and source records attributed to Lecuyer, S..

4 recordsLinked to original sources

bioRxiv2026

Understanding the role of membrane lipids in mechanism of antimicrobial photodynamic therapy in Escherichia coli

Antimicrobial photodynamic therapy (aPDT) is a promising alternative to antibiotics, yet the molecular factors determining bacterial susceptibility remain unclear. This study investigates the critical role of bacterial lipids, particularly cardiolipin (CL) in the aPDT response of Escherichia coli using methylene blue as a photosensitizer. Through genetic deletion ({Delta}clsABC) and chemical modification via mannitol supplementation, we demonstrate that reduced CL levels significantly enhance bacterial sensitivity, leading to an additional reduction in viability exceeding 3 log10. Quantitative lipidomics (MS,GC) confirmed substantial CL depletion and altered fatty acid saturation. Interestingly, while live CL-deficient cells were more vulnerable, biomimetic giant unilamellar vesicles (GUVs) with higher CL content showed greater susceptibility to photo-oxidation. These findings suggest that CL-rich microdomains in living bacteria act as functional scaffolds for stress-defense systems rather than mere targets for oxidative damage. Modulating membrane lipid composition thus represents a novel strategy to potentiate aPDT efficacy.

microbiology↗

bioRxiv2025

Bacterial exploration of solid/liquid interfaces: developing platforms to control the physico-chemical microenvironment

Bacterial long-term contamination of surfaces is a promiscuous phenomenon often linked to harmful processes. Early bacterial exploration of interfaces, governed by adhesion and individual motility, is a known determinant of the subsequent development and persistence of bacterial colonies. However, the mechanisms by which bacteria integrate various environmental signals at these interfaces and modulate their behavior in response remain poorly understood. Here we present methods for designing precisely controlled microenvironments that enable the manipulation of both physical and chemical properties of solid-liquid interfaces, and also permit in situ monitoring of bacteria at these interfaces within microfluidic flow cells. Our aim is to provide an innovative toolbox for the interdisciplinary research community focused on elucidating the complex processes underlying bacterial surface exploration. We illustrate its use here by examining the surface motility of the pathogen Pseudomonas aeruginosa.

biophysics↗

bioRxiv2022

Substrate stiffness impacts early biofilm formation via a modulation of twitching motility

Surface-associated lifestyles dominate in the bacterial world. Large multicellular assemblies, called biofilms, are essential to the survival of bacteria in harsh environments, and are closely linked to antibiotic resistance in pathogenic strains. Biofilms stem from the surface colonization of a wide variety of substrates encountered by bacteria, from living tissues to inert materials. Here, we demonstrate experimentally that the promiscuous opportunistic pathogen Pseudomonas aeruginosa explores substrates differently based on their rigidity, leading to striking variations in biofilm structure, exopolysaccharides (EPS) distribution, strain mixing during co-colonization and phenotypic expression. Using simple kinetic models, we show that these phenotypes arise through a mechanical interaction between the elasticity of the substrate and the type IV pilus (T4P) machinery, that mediates the surface-based motility called twitching. Together, our findings reveal a new role for substrate softness in the spatial organization of bacteria in complex microenvironments, with far-reaching consequences on efficient biofilm formation.

biophysics↗

bioRxiv2017

Asymmetric adhesion of rod-shaped bacteria controls microcolony morphogenesis

Bacterial biofilms are spatially structured communities, within which bacteria can differentiate depending on environmental conditions. During biofilm formation, bacteria attach to a surface and use cell-cell contacts to convey the signals required for the coordination of biofilm morphogenesis. How bacteria can maintain both substrate adhesions and cell-cell contacts during the expansion of a microcolony is still a critical yet poorly understood phenomenon. Here, we describe the development of time-resolved methods to measure substrate adhesion at the single cell level during the formation of E. coli and P. aeruginosa microcolonies. We show that bacterial adhesion is asymmetrically distributed along the cell body. Higher adhesion forces at old poles put the daughter cells under tension and force them to slide along each other. These rearrangements increase cell-cell contacts and the circularity of the colony. We propose a mechanical model based on the microscopic details of adhesive links, which recapitulates microcolony morphogenesis and quantitatively predicts bacterial adhesion from simple time lapse movies. These results explain how the distribution of adhesion forces at the subcellular level directs the shape of bacterial colonies, which ultimately dictates the circulation of secreted signals.

biophysics↗