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Dismantling the bacterial virulence program

In the face of rising antimicrobial resistance, there is an urgent need for the development of efficient and effective anti‐infective compounds. Adaptive resistance, a reversible bacterial phenotype characterized by the ability to surmount antibiotic challenge without mutation, is triggered to cope...

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Detalles Bibliográficos
Autores principales: Alford, Morgan A., Pletzer, Daniel, Hancock, Robert E.W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465231/
https://www.ncbi.nlm.nih.gov/pubmed/30864265
http://dx.doi.org/10.1111/1751-7915.13388
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author Alford, Morgan A.
Pletzer, Daniel
Hancock, Robert E.W.
author_facet Alford, Morgan A.
Pletzer, Daniel
Hancock, Robert E.W.
author_sort Alford, Morgan A.
collection PubMed
description In the face of rising antimicrobial resistance, there is an urgent need for the development of efficient and effective anti‐infective compounds. Adaptive resistance, a reversible bacterial phenotype characterized by the ability to surmount antibiotic challenge without mutation, is triggered to cope in situ with several stressors and is very common clinically. Thus, it is important to target stress‐response effectors that contribute to in vivo adaptations and associated lifestyles such as biofilm formation. Interfering with these proteins should provide a means of dismantling bacterial virulence for treating infectious diseases, in combination with conventional antibiotics.
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spelling pubmed-64652312019-04-23 Dismantling the bacterial virulence program Alford, Morgan A. Pletzer, Daniel Hancock, Robert E.W. Microb Biotechnol Opinion In the face of rising antimicrobial resistance, there is an urgent need for the development of efficient and effective anti‐infective compounds. Adaptive resistance, a reversible bacterial phenotype characterized by the ability to surmount antibiotic challenge without mutation, is triggered to cope in situ with several stressors and is very common clinically. Thus, it is important to target stress‐response effectors that contribute to in vivo adaptations and associated lifestyles such as biofilm formation. Interfering with these proteins should provide a means of dismantling bacterial virulence for treating infectious diseases, in combination with conventional antibiotics. John Wiley and Sons Inc. 2019-03-12 /pmc/articles/PMC6465231/ /pubmed/30864265 http://dx.doi.org/10.1111/1751-7915.13388 Text en © 2019 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Opinion
Alford, Morgan A.
Pletzer, Daniel
Hancock, Robert E.W.
Dismantling the bacterial virulence program
title Dismantling the bacterial virulence program
title_full Dismantling the bacterial virulence program
title_fullStr Dismantling the bacterial virulence program
title_full_unstemmed Dismantling the bacterial virulence program
title_short Dismantling the bacterial virulence program
title_sort dismantling the bacterial virulence program
topic Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465231/
https://www.ncbi.nlm.nih.gov/pubmed/30864265
http://dx.doi.org/10.1111/1751-7915.13388
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