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Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V

Nisin A is the most thoroughly investigated member of the lantibiotic family of antimicrobial peptides. In addition to a long history of safe use as a food antimicrobial, its activity against multi‐drug resistant pathogens has resulted in a renewed interest in applying nisin as a chemotherapeutic to...

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Detalles Bibliográficos
Autores principales: Field, Des, Quigley, Lisa, O'Connor, Paula M., Rea, Mary C., Daly, Karen, Cotter, Paul D., Hill, Colin, Ross, R. Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815813/
https://www.ncbi.nlm.nih.gov/pubmed/21255345
http://dx.doi.org/10.1111/j.1751-7915.2010.00184.x
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author Field, Des
Quigley, Lisa
O'Connor, Paula M.
Rea, Mary C.
Daly, Karen
Cotter, Paul D.
Hill, Colin
Ross, R. Paul
author_facet Field, Des
Quigley, Lisa
O'Connor, Paula M.
Rea, Mary C.
Daly, Karen
Cotter, Paul D.
Hill, Colin
Ross, R. Paul
author_sort Field, Des
collection PubMed
description Nisin A is the most thoroughly investigated member of the lantibiotic family of antimicrobial peptides. In addition to a long history of safe use as a food antimicrobial, its activity against multi‐drug resistant pathogens has resulted in a renewed interest in applying nisin as a chemotherapeutic to treat bacterial infections. The wealth of Nisin‐related information that has been generated has also led to the development of the biotechnological capacity to engineer novel Nisin variants with a view to improving the function and physicochemical properties of this already potent peptide. However, the identification of bioengineered Nisin derivatives with enhanced antimicrobial activity against Gram‐positive targets is a recent event. In this study, we created stable producers of the most promising derivatives of Nisin A generated to date [M21V (hereafter Nisin V) and K22T (hereafter Nisin T)] and assessed their potency against a range of drug‐resistant clinical, veterinary and food pathogens. Nisin T exhibited increased activity against all veterinary isolates, including streptococci and staphylococci, and against a number of multi‐drug resistant clinical isolates including MRSA, but not vancomycin‐resistant enterococci. In contrast, Nisin V displayed increased potency against all targets tested including hVISA strains and the hyper‐virulent Clostridium difficile ribotype 027 and against important food pathogens such as Listeria monocytogenes and Bacillus cereus. Significantly, this enhanced activity was validated in a model food system against L. monocytogenes. We conclude that Nisin V possesses significant potential as a novel preservative or chemotherapeutic compound.
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spelling pubmed-38158132014-02-12 Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V Field, Des Quigley, Lisa O'Connor, Paula M. Rea, Mary C. Daly, Karen Cotter, Paul D. Hill, Colin Ross, R. Paul Microb Biotechnol Research Articles Nisin A is the most thoroughly investigated member of the lantibiotic family of antimicrobial peptides. In addition to a long history of safe use as a food antimicrobial, its activity against multi‐drug resistant pathogens has resulted in a renewed interest in applying nisin as a chemotherapeutic to treat bacterial infections. The wealth of Nisin‐related information that has been generated has also led to the development of the biotechnological capacity to engineer novel Nisin variants with a view to improving the function and physicochemical properties of this already potent peptide. However, the identification of bioengineered Nisin derivatives with enhanced antimicrobial activity against Gram‐positive targets is a recent event. In this study, we created stable producers of the most promising derivatives of Nisin A generated to date [M21V (hereafter Nisin V) and K22T (hereafter Nisin T)] and assessed their potency against a range of drug‐resistant clinical, veterinary and food pathogens. Nisin T exhibited increased activity against all veterinary isolates, including streptococci and staphylococci, and against a number of multi‐drug resistant clinical isolates including MRSA, but not vancomycin‐resistant enterococci. In contrast, Nisin V displayed increased potency against all targets tested including hVISA strains and the hyper‐virulent Clostridium difficile ribotype 027 and against important food pathogens such as Listeria monocytogenes and Bacillus cereus. Significantly, this enhanced activity was validated in a model food system against L. monocytogenes. We conclude that Nisin V possesses significant potential as a novel preservative or chemotherapeutic compound. Blackwell Publishing Ltd 2010-07 2010-06-24 /pmc/articles/PMC3815813/ /pubmed/21255345 http://dx.doi.org/10.1111/j.1751-7915.2010.00184.x Text en Copyright © 2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
Field, Des
Quigley, Lisa
O'Connor, Paula M.
Rea, Mary C.
Daly, Karen
Cotter, Paul D.
Hill, Colin
Ross, R. Paul
Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title_full Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title_fullStr Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title_full_unstemmed Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title_short Studies with bioengineered Nisin peptides highlight the broad‐spectrum potency of Nisin V
title_sort studies with bioengineered nisin peptides highlight the broad‐spectrum potency of nisin v
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815813/
https://www.ncbi.nlm.nih.gov/pubmed/21255345
http://dx.doi.org/10.1111/j.1751-7915.2010.00184.x
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