Portal de Periódicos da CAPES

Sugar-based bactericides targeting phosphatidylethanolamine-enriched membranes

2018; Nature Portfolio; Volume: 9; Issue: 1 Linguagem: Inglês

10.1038/s41467-018-06488-4

2041-1723

Catarina Dias, João P. Pais, Rafael Nunes, M. Teresa Blázquez‐Sánchez, Joaquim T. Marquês, A. Filipa Almeida, Patrícia Serra, Nuno M. Xavier, Diogo Vila‐Viçosa, Miguel Machuqueiro, Ana S. Viana, Alice Martins, M. Soledade C.S. Santos, Ana Pelerito, Ricardo Dias, Rogério Tenreiro, M. Conceição Oliveira, Marialessandra Contino, Nicola Antonio Colabufo, Rodrigo F.M. de Almeida, Amélia P. Rauter,

Protein Structure and Dynamics

Anthrax is an infectious disease caused by Bacillus anthracis, a bioterrorism agent that develops resistance to clinically used antibiotics. Therefore, alternative mechanisms of action remain a challenge. Herein, we disclose deoxy glycosides responsible for specific carbohydrate-phospholipid interactions, causing phosphatidylethanolamine lamellar-to-inverted hexagonal phase transition and acting over B. anthracis and Bacillus cereus as potent and selective bactericides. Biological studies of the synthesized compound series differing in the anomeric atom, glycone configuration and deoxygenation pattern show that the latter is indeed a key modulator of efficacy and selectivity. Biomolecular simulations show no tendency to pore formation, whereas differential metabolomics and genomics rule out proteins as targets. Complete bacteria cell death in 10 min and cellular envelope disruption corroborate an effect over lipid polymorphism. Biophysical approaches show monolayer and bilayer reorganization with fast and high permeabilizing activity toward phosphatidylethanolamine membranes. Absence of bacterial resistance further supports this mechanism, triggering innovation on membrane-targeting antimicrobials.