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Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius

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 scree...

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Autores principales: O'Neill, Alan M, Worthing, Kate A, Kulkarni, Nikhil, Li, Fengwu, Nakatsuji, Teruaki, McGrosso, Dominic, Mills, Robert H, Kalla, Gayathri, Cheng, Joyce Y, Norris, Jacqueline M, Pogliano, Kit, Pogliano, Joe, Gonzalez, David J, Gallo, Richard L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592530/
https://www.ncbi.nlm.nih.gov/pubmed/34664551
http://dx.doi.org/10.7554/eLife.66793
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author O'Neill, Alan M
Worthing, Kate A
Kulkarni, Nikhil
Li, Fengwu
Nakatsuji, Teruaki
McGrosso, Dominic
Mills, Robert H
Kalla, Gayathri
Cheng, Joyce Y
Norris, Jacqueline M
Pogliano, Kit
Pogliano, Joe
Gonzalez, David J
Gallo, Richard L
author_facet O'Neill, Alan M
Worthing, Kate A
Kulkarni, Nikhil
Li, Fengwu
Nakatsuji, Teruaki
McGrosso, Dominic
Mills, Robert H
Kalla, Gayathri
Cheng, Joyce Y
Norris, Jacqueline M
Pogliano, Kit
Pogliano, Joe
Gonzalez, David J
Gallo, Richard L
author_sort O'Neill, Alan M
collection PubMed
description 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 (PSMβ) 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.
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spelling pubmed-85925302021-11-16 Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius O'Neill, Alan M Worthing, Kate A Kulkarni, Nikhil Li, Fengwu Nakatsuji, Teruaki McGrosso, Dominic Mills, Robert H Kalla, Gayathri Cheng, Joyce Y Norris, Jacqueline M Pogliano, Kit Pogliano, Joe Gonzalez, David J Gallo, Richard L eLife Microbiology and Infectious Disease 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 (PSMβ) 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. eLife Sciences Publications, Ltd 2021-10-19 /pmc/articles/PMC8592530/ /pubmed/34664551 http://dx.doi.org/10.7554/eLife.66793 Text en © 2021, O'Neill et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
O'Neill, Alan M
Worthing, Kate A
Kulkarni, Nikhil
Li, Fengwu
Nakatsuji, Teruaki
McGrosso, Dominic
Mills, Robert H
Kalla, Gayathri
Cheng, Joyce Y
Norris, Jacqueline M
Pogliano, Kit
Pogliano, Joe
Gonzalez, David J
Gallo, Richard L
Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title_full Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title_fullStr Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title_full_unstemmed Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title_short Antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant S. pseudintermedius
title_sort antimicrobials from a feline commensal bacterium inhibit skin infection by drug-resistant s. pseudintermedius
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592530/
https://www.ncbi.nlm.nih.gov/pubmed/34664551
http://dx.doi.org/10.7554/eLife.66793
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