Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. Pseudintermedius
Author
O’Neill, A.M.Worthing, K.A.
Kulkarni, N.
Li, F.
Nakatsuji, T.
McGrosso, D.
Mills, R.H.
Kalla, G.
Cheng, J.Y.
Norris, J.M.
Pogliano, K.
Pogliano, J.
Gonzalez, D.J.
Gallo, R.L.
Affiliation
College of Veterinary Medicine, University of Arizona,Issue Date
2021
Metadata
Show full item recordPublisher
eLife Sciences Publications LtdCitation
O’Neill, A. M., Worthing, K. A., Kulkarni, N., Li, F., Nakatsuji, T., McGrosso, D., Mills, R. H., Kalla, G., Cheng, J. Y., Norris, J. M., Pogliano, K., Pogliano, J., Gonzalez, D. J., & Gallo, R. L. (2021). Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. Pseudintermedius. ELife.Journal
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Copyright © O'Neill et al. This article is distributed under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Methicillin-resistant Staphylococcus pseudintermedius (MRSP) is an important emerging zoonotic pathogen that causes severe skin infections. To combat infections from drug- resistant bacteria, the transplantation of commensal antimicrobial bacteria as a therapeutic has shown clinical promise. We screened a collection of diverse staphylococcus species from domestic dogs and cats for antimicrobial activity against MRSP. A unique strain (S. felis C4) was isolated from feline skin that inhibited MRSP and multiple gram-positive pathogens. Whole genome sequencing and mass spectrometry revealed several secreted antimicrobials including a thiopeptide bacteriocin micrococcin P1 and phenol-soluble modulin beta (PSMP) peptides that exhibited antimicrobial and anti-inflammatory activity. Fluorescence and electron microscopy revealed that S. felis antimicrobials inhibited translation and disrupted bacterial but not eukaryotic cell membranes. Competition experiments in mice showed that S. felis significantly reduced MRSP skin colonization and an antimicrobial extract from S. felis significantly reduced necrotic skin injury from MRSP infection. These findings indicate a feline commensal bacterium that could be utilized in bacteriotherapy against difficult-to-treat animal and human skin infections. © 2021, eLife Sciences Publications Ltd. All rights reserved.Note
Open access journalISSN
2050-084XVersion
Final published versionae974a485f413a2113503eed53cd6c53
10.7554/eLife.66793
Scopus Count
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Except where otherwise noted, this item's license is described as Copyright © O'Neill et al. This article is distributed under the terms of the Creative Commons Attribution License.

