Key result
Fusidic acid reduces bacterial growth primarily via translocation inhibition, while recycling inhibition alters regulatory ORFs.
Why the study?
Fusidic acid inhibition of ribosome recycling by EF-G and RRF has remained obscure despite recent clarification of its inhibition of translocation.
Fusidic acid primarily inhibits bacterial growth through translocation inhibition, while its effect on ribosome recycling may drive resistance mechanisms.
Does not yet alter fusidic acid use; extends mechanistic understanding of translocation inhibition and resistance via ribosome recycling.
The antibiotic drug fusidic acid (FA) is commonly used in the clinic against gram-positive bacterial infections. FA targets ribosome-bound elongation factor G (EF-G), a translational GTPase that accelerates both messenger RNA (mRNA) translocation and ribosome recycling. How FA inhibits translocation was recently clarified, but FA inhibition of ribosome recycling by EF-G and ribosome recycling factor (RRF) has remained obscure. Here we use fast kinetics techniques to estimate mean times of ribosome splitting and the stoichiometry of GTP hydrolysis by EF-G at varying concentrations of FA, EF-G and RRF. These mean times together with previous data on uninhibited ribosome recycling were used to clarify the mechanism of FA inhibition of ribosome splitting. The biochemical data on FA inhibition of translocation and recycling were used to model the growth inhibitory effect of FA on bacterial populations. We conclude that FA inhibition of translocation provides the dominant cause of bacterial growth reduction, but that FA inhibition of ribosome recycling may contribute significantly to FA-induced expression of short regulatory open reading frames, like those involved in FA resistance.
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Borg et al. (2016) studied Gram-positive bacterial infections. Fusidic acid (FA) was evaluated on Mean times of ribosome splitting and the stoichiometry of GTP hydrolysis. Fusidic acid inhibition of translocation provides the dominant cause of bacterial growth reduction, but its inhibition of ribosome recycling may contribute to expression of short regulatory ORFs.