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Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials
Lower respiratory tract infections and tuberculosis are responsible for the death of about 4.5 million people each year and are the main causes of mortality in children under 5 years of age. Streptococcus pneumoniae is the most common bacterial pathogen associated with severe pneumonia, although oth...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232686/ https://www.ncbi.nlm.nih.gov/pubmed/30459750 http://dx.doi.org/10.3389/fimmu.2018.02252 |
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author | Vázquez, Roberto García, Ernesto García, Pedro |
author_facet | Vázquez, Roberto García, Ernesto García, Pedro |
author_sort | Vázquez, Roberto |
collection | PubMed |
description | Lower respiratory tract infections and tuberculosis are responsible for the death of about 4.5 million people each year and are the main causes of mortality in children under 5 years of age. Streptococcus pneumoniae is the most common bacterial pathogen associated with severe pneumonia, although other Gram-positive and Gram-negative bacteria are involved in respiratory infections as well. The ability of these pathogens to persist and produce infection under the appropriate conditions is also associated with their capacity to form biofilms in the respiratory mucous membranes. Adding to the difficulty of treating biofilm-forming bacteria with antibiotics, many of these strains are becoming multidrug resistant, and thus the alternative therapeutics available for combating this kind of infections are rapidly depleting. Given these concerns, it is urgent to consider other unconventional strategies and, in this regard, phage lysins represent an attractive resource to circumvent some of the current issues in infection treatment. When added exogenously, lysins break specific bonds of the peptidoglycan and have potent bactericidal effects against susceptible bacteria. These enzymes possess interesting features, including that they do not trigger an adverse immune response and raise of resistance is very unlikely. Although Gram-negative bacteria had been considered refractory to these compounds, strategies to overcome this drawback have been developed recently. In this review we describe the most relevant in vitro and in vivo results obtained to date with lysins against bacterial respiratory pathogens. |
format | Online Article Text |
id | pubmed-6232686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62326862018-11-20 Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials Vázquez, Roberto García, Ernesto García, Pedro Front Immunol Immunology Lower respiratory tract infections and tuberculosis are responsible for the death of about 4.5 million people each year and are the main causes of mortality in children under 5 years of age. Streptococcus pneumoniae is the most common bacterial pathogen associated with severe pneumonia, although other Gram-positive and Gram-negative bacteria are involved in respiratory infections as well. The ability of these pathogens to persist and produce infection under the appropriate conditions is also associated with their capacity to form biofilms in the respiratory mucous membranes. Adding to the difficulty of treating biofilm-forming bacteria with antibiotics, many of these strains are becoming multidrug resistant, and thus the alternative therapeutics available for combating this kind of infections are rapidly depleting. Given these concerns, it is urgent to consider other unconventional strategies and, in this regard, phage lysins represent an attractive resource to circumvent some of the current issues in infection treatment. When added exogenously, lysins break specific bonds of the peptidoglycan and have potent bactericidal effects against susceptible bacteria. These enzymes possess interesting features, including that they do not trigger an adverse immune response and raise of resistance is very unlikely. Although Gram-negative bacteria had been considered refractory to these compounds, strategies to overcome this drawback have been developed recently. In this review we describe the most relevant in vitro and in vivo results obtained to date with lysins against bacterial respiratory pathogens. Frontiers Media S.A. 2018-10-16 /pmc/articles/PMC6232686/ /pubmed/30459750 http://dx.doi.org/10.3389/fimmu.2018.02252 Text en Copyright © 2018 Vázquez, García and García. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Vázquez, Roberto García, Ernesto García, Pedro Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title | Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title_full | Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title_fullStr | Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title_full_unstemmed | Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title_short | Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials |
title_sort | phage lysins for fighting bacterial respiratory infections: a new generation of antimicrobials |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232686/ https://www.ncbi.nlm.nih.gov/pubmed/30459750 http://dx.doi.org/10.3389/fimmu.2018.02252 |
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