A new natural product analog of blasticidin S reveals cellular uptake facilitated by the NorA multidrug transporter

Jack R. Davison, Katheryn M. Lohith, Xiaoning Wang, Kostyantyn Bobyk, Sivakoteswara R. Mandadapu, Su Lin Lee, Regina Cencic, Justin Nelson, Scott Simpkins, Karen M. Frank, Jerry Pelletier, Chad L. Myers, Jeff Piotrowski, Harold E. Smith, Carole A. Bewley

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The permeation of antibiotics through bacterial membranes to their target site is a crucial determinant of drug activity but in many cases remains poorly understood. During screening efforts to discover new broad-spectrum antibiotic compounds from marine sponge samples, we identified a new analog of the peptidyl nucleoside antibiotic blasticidin S that exhibited up to 16-fold-improved potency against a range of laboratory and clinical bacterial strains which we named P10. Whole-genome sequencing of laboratory-evolved strains of Staphylococcus aureus resistant to blasticidin S and P10, combined with genome-wide assessment of the fitness of barcoded Escherichia coli knockout strains in the presence of the antibiotics, revealed that restriction of cellular access was a key feature in the development of resistance to this class of drug. In particular, the gene encoding the well-characterized multidrug efflux pump NorA was found to be mutated in 69% of all S. aureus isolates resistant to blasticidin S or P10. Unexpectedly, resistance was associated with inactivation of norA, suggesting that the NorA transporter facilitates cellular entry of peptidyl nucleosides in addition to its known role in the efflux of diverse compounds, including fluoroquinolone antibiotics.

Original languageEnglish (US)
Article numbere02635-16
JournalAntimicrobial agents and chemotherapy
Volume61
Issue number6
DOIs
StatePublished - Jun 2017

Bibliographical note

Funding Information:
This work was supported by the Intramural Research Program, National Institutes of Health (NIDDK). C. L. Myers and J. Nelson are supported by National Institutes of Health grants 1R01HG005084, 1R01GM104975, and R01HG005853 and National Science Foundation grant DBI 0953881. J. S. Piotrowski is supported by National Institutes of Health grants 1R01HG005084 and 1R01GM104975.

Publisher Copyright:
© 2017 American Society for,Microbiology. All Rights Reserved.

Keywords

  • Antibiotic resistance
  • Chemical genomics
  • Natural products
  • Transporters

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