Cargando…

Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus

The β-lactams imipenem and cefoxitin are used for the treatment of Mycobacterium abscessus lung infections. Here, we show that these cell wall synthesis inhibitors trigger a lethal bacterial ATP burst by increasing oxidative phosphorylation. Cotreatment of M. abscessus with the antimycobacterial ATP...

Descripción completa

Detalles Bibliográficos
Autores principales: Lindman, Marissa, Dick, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658768/
https://www.ncbi.nlm.nih.gov/pubmed/31182531
http://dx.doi.org/10.1128/AAC.00827-19
_version_ 1783439016005206016
author Lindman, Marissa
Dick, Thomas
author_facet Lindman, Marissa
Dick, Thomas
author_sort Lindman, Marissa
collection PubMed
description The β-lactams imipenem and cefoxitin are used for the treatment of Mycobacterium abscessus lung infections. Here, we show that these cell wall synthesis inhibitors trigger a lethal bacterial ATP burst by increasing oxidative phosphorylation. Cotreatment of M. abscessus with the antimycobacterial ATP synthase inhibitor bedaquiline suppresses this ATP burst and eliminates the bactericidal activity of β-lactams. Thus, the addition of bedaquiline to β-lactam-containing regimes may negatively affect treatment outcome.
format Online
Article
Text
id pubmed-6658768
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-66587682019-08-07 Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus Lindman, Marissa Dick, Thomas Antimicrob Agents Chemother Mechanisms of Action: Physiological Effects The β-lactams imipenem and cefoxitin are used for the treatment of Mycobacterium abscessus lung infections. Here, we show that these cell wall synthesis inhibitors trigger a lethal bacterial ATP burst by increasing oxidative phosphorylation. Cotreatment of M. abscessus with the antimycobacterial ATP synthase inhibitor bedaquiline suppresses this ATP burst and eliminates the bactericidal activity of β-lactams. Thus, the addition of bedaquiline to β-lactam-containing regimes may negatively affect treatment outcome. American Society for Microbiology 2019-07-25 /pmc/articles/PMC6658768/ /pubmed/31182531 http://dx.doi.org/10.1128/AAC.00827-19 Text en Copyright © 2019 Lindman and Dick. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mechanisms of Action: Physiological Effects
Lindman, Marissa
Dick, Thomas
Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title_full Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title_fullStr Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title_full_unstemmed Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title_short Bedaquiline Eliminates Bactericidal Activity of β-Lactams against Mycobacterium abscessus
title_sort bedaquiline eliminates bactericidal activity of β-lactams against mycobacterium abscessus
topic Mechanisms of Action: Physiological Effects
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658768/
https://www.ncbi.nlm.nih.gov/pubmed/31182531
http://dx.doi.org/10.1128/AAC.00827-19
work_keys_str_mv AT lindmanmarissa bedaquilineeliminatesbactericidalactivityofblactamsagainstmycobacteriumabscessus
AT dickthomas bedaquilineeliminatesbactericidalactivityofblactamsagainstmycobacteriumabscessus