Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA
1
Department of Microbiology and Immunology, University of Rochester School of Medicine, Rochester, NY 14642, USA
2
Department of Medicinal Chemistry and Molecular Pharmacology, College of Pharmacy, Purdue University, West Lafayette, IN 47906, USA
3
Purdue Institute of Inflammation, Immunology and Infectious Disease, Purdue University, West Lafayette, IN 47906, USA
4
Purdue Institute for Drug Discovery, Purdue University, West Lafayette, IN 47906, USA
*
Author to whom correspondence should be addressed.
Antibiotics 2019, 8(2), 48; https://doi.org/10.3390/antibiotics8020048
Received: 1 April 2019 / Revised: 23 April 2019 / Accepted: 25 April 2019 / Published: 28 April 2019
(This article belongs to the Special Issue Staphylococci Antimicrobial Resistance)
Staphylococcus aureus RnpA is thought to be a unique dual functional antimicrobial target that is required for two essential cellular processes, precursor tRNA processing and messenger RNA degradation. Herein, we used a previously described whole cell-based mupirocin synergy assay to screen members of a 53,000 compound small molecule diversity library and simultaneously enrich for agents with cellular RnpA inhibitory activity. A medicinal chemistry-based campaign was launched to generate a preliminary structure activity relationship and guide early optimization of two novel chemical classes of RnpA inhibitors identified, phenylcarbamoyl cyclic thiophene and piperidinecarboxamide. Representatives of each chemical class displayed potent anti-staphylococcal activity, limited the protein’s in vitro ptRNA processing and mRNA degradation activities, and exhibited favorable therapeutic indexes. The most potent piperidinecarboxamide RnpA inhibitor, JC2, displayed inhibition of cellular RnpA mRNA turnover, RnpA-depletion strain hypersusceptibility, and exhibited antimicrobial efficacy in a wax worm model of S. aureus infection. Taken together, these results establish that the whole cell screening assay used is amenable to identifying small molecule RnpA inhibitors within large chemical libraries and that the chemical classes identified here may represent progenitors of new classes of antimicrobials that target RnpA.
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Keywords:
Staphylococcus aureus; RnpA; mRNA degradation; tRNA processing; mupirocin
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MDPI and ACS Style
Colquhoun, J.M.; Ha, L.; Beckley, A.; Meyers, B.; Flaherty, D.P.; Dunman, P.M. Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA. Antibiotics 2019, 8, 48. https://doi.org/10.3390/antibiotics8020048
AMA Style
Colquhoun JM, Ha L, Beckley A, Meyers B, Flaherty DP, Dunman PM. Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA. Antibiotics. 2019; 8(2):48. https://doi.org/10.3390/antibiotics8020048
Chicago/Turabian StyleColquhoun, Jennifer M.; Ha, Lisha; Beckley, Andrew; Meyers, Brinkley; Flaherty, Daniel P.; Dunman, Paul M. 2019. "Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA" Antibiotics 8, no. 2: 48. https://doi.org/10.3390/antibiotics8020048
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