Abstract
Pyrithione (2-mercaptopyridine-N-oxide) is a metal binding modified pyridine, the anti-bacterial activity of which was described over 60 years ago. The formulation of zinc-pyrithione is commonly used in the topical treatment of certain dermatological conditions. However, the charac-terisation of the cellular uptake of pyrithione has not been elucidated, although an unsubstantiated assumption has persisted that pyrithione and/or its metal complexes undergo a passive diffusion through cell membranes. Here, we have profiled specific membrane transporters from an unbiased interrogation of 532 E. coli strains of knockouts of genes encoding membrane proteins from the Keio collection. Two membrane transporters, FepC and MetQ, seemed involved in the uptake of pyrithi-one and its cognate metal complexes with copper, iron, and zinc. Additionally, the phenotypes displayed by CopA and ZntA knockouts suggested that these two metal effluxers drive the extrusion from the bacterial cell of potentially toxic levels of copper, and perhaps zinc, which hyperaccumu-late as a function of pyrithione. The involvement of these distinct membrane transporters contrib-utes to the understanding of the mechanisms of action of pyrithione specifically and highlights, more generally, the important role that membrane transporters play in facilitating the uptake of drugs, including metal–drug compounds.
Original language | English |
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Article number | 5826 |
Journal | Molecules |
Volume | 26 |
Issue number | 19 |
Number of pages | 19 |
ISSN | 1420-3049 |
DOIs | |
Publication status | Published - 1 Oct 2021 |
Bibliographical note
Funding Information:Acknowledgments: We thank the Keuhn lab at Duke University for generously providing individual Keio deletions strains, and Hannah D’Ambrosio and the Derbyshire lab for their assistance with PCR. We thank Martina Ralle for collecting ICP-MS data at the Oregon Health Sciences University Elemental Analysis Core, with partial support from NIH instrumentation grant S10RR025512.
Funding Information:
Funding: This research was funded in part by the National Institutes of Health (R01GM084176 to K.J.F.); J.M.Z.-B. acknowledges fellowship support from the Duke Pharmacological Sciences Training Program (T32 GM007105). D.B.K. thanks the Novo Nordisk Foundation for financial support (grant NNF20CC0035580).
Publisher Copyright:
© 2021 by the author. Licensee MDPI, Basel, Switzerland.
Keywords
- Copper
- E. coli
- Gram-negative
- Iron
- Keio collection
- Membrane transporters
- Metal ions
- Pyrithione
- Zinc