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Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis

Antibiotics are the most effective strategy to prevent and treat intramammary infections. However, their misuse has led to the dissemination of multidrug resistant bacteria (MDR) for both animals and humans. Efforts to develop new alternative strategies to control bacterial infections related to MDR...

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Autores principales: Bennett, Samantha, Ben Said, Laila, Lacasse, Pierre, Malouin, François, Fliss, Ismail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614789/
https://www.ncbi.nlm.nih.gov/pubmed/34827356
http://dx.doi.org/10.3390/antibiotics10111418
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author Bennett, Samantha
Ben Said, Laila
Lacasse, Pierre
Malouin, François
Fliss, Ismail
author_facet Bennett, Samantha
Ben Said, Laila
Lacasse, Pierre
Malouin, François
Fliss, Ismail
author_sort Bennett, Samantha
collection PubMed
description Antibiotics are the most effective strategy to prevent and treat intramammary infections. However, their misuse has led to the dissemination of multidrug resistant bacteria (MDR) for both animals and humans. Efforts to develop new alternative strategies to control bacterial infections related to MDR are continuously on the rise. The objective of this study was to evaluate the antimicrobial activity of different bacteriocins and reuterin against MDR Staphylococcus and Streptococcus clinical isolates involved in bovine mastitis. A bacterial collection including S. aureus (n = 19), S. dysgalactiae (n = 17) and S. uberis (n = 19) was assembled for this study. Antibiotic resistance profiles were determined by the disk diffusion method. In addition, sensitivity to bacteriocins and reuterin was evaluated by determining minimum inhibitory concentrations (MIC). A total of 21 strains (37.5%) were MDR. MICs ranged from ≤1.0 [Formula: see text] g/mL to ≥100 [Formula: see text] g/mL for nisin and 2.0 to ≥250 [Formula: see text] g/mL for bactofencin. Reuterin was active against all tested bacteria, and MICs vary between 70 and 560 [Formula: see text] g/mL. Interestingly, 20 MDR strains were inhibited by bactofencin at a concentration of ≤250 [Formula: see text] g/mL, while 14 were inhibited by nisin at an MIC of ≤100 [Formula: see text] g/mL. Pediocin did not show an inhibitory effect.
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spelling pubmed-86147892021-11-26 Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis Bennett, Samantha Ben Said, Laila Lacasse, Pierre Malouin, François Fliss, Ismail Antibiotics (Basel) Article Antibiotics are the most effective strategy to prevent and treat intramammary infections. However, their misuse has led to the dissemination of multidrug resistant bacteria (MDR) for both animals and humans. Efforts to develop new alternative strategies to control bacterial infections related to MDR are continuously on the rise. The objective of this study was to evaluate the antimicrobial activity of different bacteriocins and reuterin against MDR Staphylococcus and Streptococcus clinical isolates involved in bovine mastitis. A bacterial collection including S. aureus (n = 19), S. dysgalactiae (n = 17) and S. uberis (n = 19) was assembled for this study. Antibiotic resistance profiles were determined by the disk diffusion method. In addition, sensitivity to bacteriocins and reuterin was evaluated by determining minimum inhibitory concentrations (MIC). A total of 21 strains (37.5%) were MDR. MICs ranged from ≤1.0 [Formula: see text] g/mL to ≥100 [Formula: see text] g/mL for nisin and 2.0 to ≥250 [Formula: see text] g/mL for bactofencin. Reuterin was active against all tested bacteria, and MICs vary between 70 and 560 [Formula: see text] g/mL. Interestingly, 20 MDR strains were inhibited by bactofencin at a concentration of ≤250 [Formula: see text] g/mL, while 14 were inhibited by nisin at an MIC of ≤100 [Formula: see text] g/mL. Pediocin did not show an inhibitory effect. MDPI 2021-11-19 /pmc/articles/PMC8614789/ /pubmed/34827356 http://dx.doi.org/10.3390/antibiotics10111418 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bennett, Samantha
Ben Said, Laila
Lacasse, Pierre
Malouin, François
Fliss, Ismail
Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title_full Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title_fullStr Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title_full_unstemmed Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title_short Susceptibility to Nisin, Bactofencin, Pediocin and Reuterin of Multidrug Resistant Staphylococcus aureus, Streptococcus dysgalactiae and Streptococcus uberis Causing Bovine Mastitis
title_sort susceptibility to nisin, bactofencin, pediocin and reuterin of multidrug resistant staphylococcus aureus, streptococcus dysgalactiae and streptococcus uberis causing bovine mastitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614789/
https://www.ncbi.nlm.nih.gov/pubmed/34827356
http://dx.doi.org/10.3390/antibiotics10111418
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