Spatially resolved analysis of Pseudomonas aeruginosa biofilm proteomes measured by laser ablation sample transfer

Heterogeneity in the distribution of nutrients and oxygen gradients during biofilm growth gives rise to changes in phenotype. There has been long term interest in identifying spatial differences during biofilm development including clues that identify chemical heterogeneity. Laser ablation sample transfer (LAST) allows site-specific sampling combined with label free proteomics to distinguish radially and axially resolved proteomes for Pseudomonas aeruginosa biofilms. Specifically, differential protein abundances on oxic vs. anoxic regions of a biofilm were observed by combining LAST with bottom up proteomics. This study reveals a more active metabolism in the anoxic region of the biofilm with respect to the oxic region for this clinical strain of P. aeruginosa, despite this organism being considered an aerobe by nature. Protein abundance data related to cellular acclimations to chemical gradients include identification of glucose catabolizing proteins, high abundance of proteins from arginine and polyamine metabolism, and proteins that could also support virulence and environmental stress mediation in the anoxic region. Finally, the LAST methodology requires only a few mm(2) of biofilm area to identify hundreds of proteins.

Automated summary

The study using LAST technology combined with proteomics revealed differential protein abundances between oxic and anoxic regions in Pseudomonas aeruginosa biofilms, showing a more active metabolism in the anoxic zone. Cellular adaptations to chemical gradients in the biofilm include glucose catabolizing proteins, high abundance of proteins from arginine and polyamine metabolism, and proteins that may support virulence and stress mediation in the anoxic region. The LAST methodology can identify hundreds of proteins using just a small area of biofilm.