z-logo
Premium
Alteration of protein homeostasis mediates the interaction of Pseudomonas aeruginosa with Staphylococcus aureus
Author(s) -
Yang Nana,
Cao Qiao,
Hu Shuyang,
Xu Chenchen,
Fan Ke,
Chen Feifei,
Yang CaiGuang,
Liang Haihua,
Wu Min,
Bae Taeok,
Lan Lefu
Publication year - 2020
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.14519
Subject(s) - pseudomonas aeruginosa , biology , staphylococcus aureus , microbiology and biotechnology , quorum sensing , protease , bacteria , intracellular , bacteriocin , antimicrobial , pathogen , biofilm , biochemistry , genetics , enzyme
Intracellular protein degradation is essential for the survival of all organisms, but its role in interspecies interaction is unknown. Here, we show that the ClpXP protease of Pseudomonas aeruginosa suppresses its antimicrobial activity against Staphylococcus aureus , a common pathogen co‐isolated with P. aeruginosa from polymicrobial human infections. Using proteomic, biochemical, and molecular genetic approaches, we found that this effect is due to the inhibitory effects of ClpXP on the quorum sensing (QS) of P. aeruginosa , mainly by degrading proteins (e.g., PhnA, PhnB, PqsR, and RhlI) which are critical for the production of QS signal molecules PQS and C4‐HSL . We provide evidence that co‐culturing with S. aureus induces a decrease in the activity of ClpXP in P. aeruginosa , an effect which was also achieved by the treatment of P. aeruginosa with N‐acetylglucosamine (GlcNAc), a widespread chemical present on the surface of diverse cell types from bacteria to humans. These findings extend the range of biological events governed by proteolytic machinery to microbial community structure, thus also suggesting that a chemical‐induced alteration of protein homeostasis is a mechanism for interspecies interactions.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here