Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence
Author(s) -
Carlos MolinaSantiago,
David VelaCorcía,
Daniel Petras,
Luis DíazMartínez,
Alicia Isabel PérezLorente,
Sara SopeñaTorres,
J. R. A. Pearson,
Andrés Mauricio CaraballoRodríguez,
Pieter C. Dorrestein,
Antonio de Vicente,
Diego Romero
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109449
Subject(s) - pseudomonas chlororaphis , bacillus amyloliquefaciens , glycerol kinase , antagonism , biology , elongation factor , multidrug tolerance , bacillus (shape) , bacteria , genetics , microbiology and biotechnology , biochemistry , pseudomonas , gene , biofilm , receptor , rna , ribosome
Summary Bacterial communities are in a continuous adaptive and evolutionary race for survival. In this work we expand our knowledge on the chemical interplay and specific mutations that modulate the transition from antagonism to co-existence between two plant-beneficial bacteria, Pseudomonas chlororaphis PCL1606 and Bacillus amyloliquefaciens FZB42. We reveal that the bacteriostatic activity of bacillaene produced by Bacillus relies on an interaction with the protein elongation factor FusA of P. chlororaphis and how mutations in this protein lead to tolerance to bacillaene and other protein translation inhibitors. Additionally, we describe how the unspecific tolerance of B. amyloliquefaciens to antimicrobials associated with mutations in the glycerol kinase GlpK is provoked by a decrease of Bacillus cell membrane permeability, among other pleiotropic responses. We conclude that nutrient specialization and mutations in basic biological functions are bacterial adaptive dynamics that lead to the coexistence of two primary competitive bacterial species rather than their mutual eradication.
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