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Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter

The rise of antimicrobial resistant (AMR) bacteria is a global public health threat. AMR Achromobacter bacteria pose a challenging clinical problem, particularly for those with cystic fibrosis (CF) who are predisposed to chronic bacterial lung infections. Lytic bacteriophages (phages) offer a potent...

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Autores principales: Winzig, Franziska, Gandhi, Shiv, Lee, Alina, Würstle, Silvia, Stanley, Gail L., Capuano, Isabella, Neuringer, Isabel, Koff, Jonathan L., Turner, Paul E., Chan, Benjamin K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9765334/
https://www.ncbi.nlm.nih.gov/pubmed/36568830
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author Winzig, Franziska
Gandhi, Shiv
Lee, Alina
Würstle, Silvia
Stanley, Gail L.
Capuano, Isabella
Neuringer, Isabel
Koff, Jonathan L.
Turner, Paul E.
Chan, Benjamin K.
author_facet Winzig, Franziska
Gandhi, Shiv
Lee, Alina
Würstle, Silvia
Stanley, Gail L.
Capuano, Isabella
Neuringer, Isabel
Koff, Jonathan L.
Turner, Paul E.
Chan, Benjamin K.
author_sort Winzig, Franziska
collection PubMed
description The rise of antimicrobial resistant (AMR) bacteria is a global public health threat. AMR Achromobacter bacteria pose a challenging clinical problem, particularly for those with cystic fibrosis (CF) who are predisposed to chronic bacterial lung infections. Lytic bacteriophages (phages) offer a potential alternative to treat AMR infections, with the possible benefit that phage selection for resistance in target bacteria might coincide with reduced pathogenicity. The result is a genetic “trade-off,” such as increased sensitivity to chemical antibiotics, and/or decreased virulence of surviving bacteria that are phage resistant. Here, we show that two newly discovered lytic phages against Achromobacter were associated with stabilization of respiratory status when deployed to treat a chronic pulmonary infection in a CF patient using inhaled (nebulized) phage therapy. The two phages demonstrate traits that could be generally useful in their development as therapeutics, especially the possibility that the phages can select for clinically useful trade-offs if bacteria evolve phage resistance following therapy. We discuss the limitations of the current study and suggest further work that should explore whether the phages could be generally useful in targeting pulmonary or other Achromobacter infections in CF patients.
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spelling pubmed-97653342022-12-22 Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter Winzig, Franziska Gandhi, Shiv Lee, Alina Würstle, Silvia Stanley, Gail L. Capuano, Isabella Neuringer, Isabel Koff, Jonathan L. Turner, Paul E. Chan, Benjamin K. Yale J Biol Med Case Report The rise of antimicrobial resistant (AMR) bacteria is a global public health threat. AMR Achromobacter bacteria pose a challenging clinical problem, particularly for those with cystic fibrosis (CF) who are predisposed to chronic bacterial lung infections. Lytic bacteriophages (phages) offer a potential alternative to treat AMR infections, with the possible benefit that phage selection for resistance in target bacteria might coincide with reduced pathogenicity. The result is a genetic “trade-off,” such as increased sensitivity to chemical antibiotics, and/or decreased virulence of surviving bacteria that are phage resistant. Here, we show that two newly discovered lytic phages against Achromobacter were associated with stabilization of respiratory status when deployed to treat a chronic pulmonary infection in a CF patient using inhaled (nebulized) phage therapy. The two phages demonstrate traits that could be generally useful in their development as therapeutics, especially the possibility that the phages can select for clinically useful trade-offs if bacteria evolve phage resistance following therapy. We discuss the limitations of the current study and suggest further work that should explore whether the phages could be generally useful in targeting pulmonary or other Achromobacter infections in CF patients. YJBM 2022-12-22 /pmc/articles/PMC9765334/ /pubmed/36568830 Text en Copyright ©2022, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Case Report
Winzig, Franziska
Gandhi, Shiv
Lee, Alina
Würstle, Silvia
Stanley, Gail L.
Capuano, Isabella
Neuringer, Isabel
Koff, Jonathan L.
Turner, Paul E.
Chan, Benjamin K.
Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title_full Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title_fullStr Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title_full_unstemmed Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title_short Inhaled Bacteriophage Therapy for Multi-Drug Resistant Achromobacter
title_sort inhaled bacteriophage therapy for multi-drug resistant achromobacter
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9765334/
https://www.ncbi.nlm.nih.gov/pubmed/36568830
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