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Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus

Within a sufficiently large bacterial population, some members will naturally adopt an alternate, metabolically-active state that favors small molecule synthesis over cell division. These isogenic “tolerant” subpopulations have variable responses during antibiotic exposure and can remain viable in t...

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Autores principales: Berti, Andrew D., Harven, Lauren T., Bingley, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695155/
https://www.ncbi.nlm.nih.gov/pubmed/33171631
http://dx.doi.org/10.3390/antibiotics9110789
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author Berti, Andrew D.
Harven, Lauren T.
Bingley, Victoria
author_facet Berti, Andrew D.
Harven, Lauren T.
Bingley, Victoria
author_sort Berti, Andrew D.
collection PubMed
description Within a sufficiently large bacterial population, some members will naturally adopt an alternate, metabolically-active state that favors small molecule synthesis over cell division. These isogenic “tolerant” subpopulations have variable responses during antibiotic exposure and can remain viable in the presence of typically bactericidal concentrations. In this study, we determine the ability of typical and atypical antistaphylococcal therapies to reduce the viability of mupirocin-induced tolerant Staphylococcus aureus bacteria. Overall, tolerance-induced staphylococci exhibited a markedly decreased rate and extent of killing following antibiotic exposure. However, oritavancin remained effective at maintaining a similar extent of killing. Further studies to investigate the role of oritavancin against recurrent or relapse staphylococcal infection are warranted.
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spelling pubmed-76951552020-11-28 Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus Berti, Andrew D. Harven, Lauren T. Bingley, Victoria Antibiotics (Basel) Communication Within a sufficiently large bacterial population, some members will naturally adopt an alternate, metabolically-active state that favors small molecule synthesis over cell division. These isogenic “tolerant” subpopulations have variable responses during antibiotic exposure and can remain viable in the presence of typically bactericidal concentrations. In this study, we determine the ability of typical and atypical antistaphylococcal therapies to reduce the viability of mupirocin-induced tolerant Staphylococcus aureus bacteria. Overall, tolerance-induced staphylococci exhibited a markedly decreased rate and extent of killing following antibiotic exposure. However, oritavancin remained effective at maintaining a similar extent of killing. Further studies to investigate the role of oritavancin against recurrent or relapse staphylococcal infection are warranted. MDPI 2020-11-08 /pmc/articles/PMC7695155/ /pubmed/33171631 http://dx.doi.org/10.3390/antibiotics9110789 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Berti, Andrew D.
Harven, Lauren T.
Bingley, Victoria
Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title_full Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title_fullStr Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title_full_unstemmed Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title_short Distinct Effectiveness of Oritavancin against Tolerance-Induced Staphylococcus aureus
title_sort distinct effectiveness of oritavancin against tolerance-induced staphylococcus aureus
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695155/
https://www.ncbi.nlm.nih.gov/pubmed/33171631
http://dx.doi.org/10.3390/antibiotics9110789
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