Ciprofloxacin binding to GyrA causes global changes in the proteome of Pseudomonas aeruginosa.
FEMS microbiology letters
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Jedrey, H., Lilley, K., & Welch, M. (2018). Ciprofloxacin binding to GyrA causes global changes in the proteome of Pseudomonas aeruginosa.. FEMS microbiology letters, 365 (13)https://doi.org/10.1093/femsle/fny134
Ciprofloxacin is one of the most widely-used antibiotics, and has proven especially effective at controlling infections associated with the opportunistic human pathogen, Pseudomonas aeruginosa. In this work, we show that sub-inhibitory concentrations of ciprofloxacin induce discrete changes in the intracellular proteome. Central metabolism and cell envelope-associated functions are particularly affected. In spite of the low magnitude of the intracellular proteomic changes, we found that sub-lethal concentrations of ciprofloxacin had substantial effects on motility and exoprotein secretion. Crucially, the proteomic and phenotypic modulations that we observed were absolutely dependent upon the presence of wild-type GyrA; an isogenic strain of P. aeruginosa carrying a ciprofloxacin-insensitive form of GyrA (a T83→I mutant) did not display ciprofloxacin-dependent changes unless complemented with wild-type gyrA in trans. These results show that the diverse effects of sub-inhibitory ciprofloxacin on the cell are routed through its primary target in the cell, DNA gyrase.
Pseudomonas aeruginosa, Ciprofloxacin, DNA Gyrase, Bacterial Proteins, Proteome, Anti-Bacterial Agents, Microbial Sensitivity Tests, Mutation
This work was supported by BBSRC grants BB/C500252/1 and BB/M019411/1.
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External DOI: https://doi.org/10.1093/femsle/fny134
This record's URL: https://www.repository.cam.ac.uk/handle/1810/278703
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Licence URL: http://creativecommons.org/licenses/by/4.0/
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