Rational prioritization strategy allows the design of macrolide derivatives that overcome antibiotic resistance

Author:

König Gerhard,Sokkar PandianORCID,Pryk Niclas,Heinrich SaschaORCID,Möller David,Cimicata Giuseppe,Matzov Donna,Dietze Pascal,Thiel Walter,Bashan Anat,Bandow Julia ElisabethORCID,Zuegg Johannes,Yonath Ada,Schulz FrankORCID,Sanchez-Garcia ElsaORCID

Abstract

Antibiotic resistance is a major threat to global health; this problem can be addressed by the development of new antibacterial agents to keep pace with the evolutionary adaptation of pathogens. Computational approaches are essential tools to this end since their application enables fast and early strategical decisions in the drug development process. We present a rational design approach, in which acylide antibiotics were screened based on computational predictions of solubility, membrane permeability, and binding affinity toward the ribosome. To assess our design strategy, we tested all candidates for in vitro inhibitory activity and then evaluated them in vivo with several antibiotic-resistant strains to determine minimal inhibitory concentrations. The predicted best candidate is synthetically more accessible, exhibits higher solubility and binding affinity to the ribosome, and is up to 56 times more active against resistant pathogens than telithromycin. Notably, the best compounds designed by us show activity, especially when combined with the membrane-weakening drug colistin, against Acinetobacter baumanii, Pseudomonas aeruginosa, and Escherichia coli, which are the three most critical targets from the priority list of pathogens of the World Health Organization.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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