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Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay

[Image: see text] Antimicrobial resistance has emerged as a global public health threat, and development of novel therapeutics for treating infections caused by multi-drug resistant bacteria is urgent. Staphylococcus aureus is a major human and animal pathogen, responsible for high levels of morbidi...

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Autores principales: Pham, Nhan T., Alves, Joana, Sargison, Fiona A., Cullum, Reiko, Wildenhain, Jan, Fenical, William, Butler, Mark S., Mead, David A., Duggan, Brendan M., Fitzgerald, J. Ross, La Clair, James J., Auer, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425972/
https://www.ncbi.nlm.nih.gov/pubmed/37433130
http://dx.doi.org/10.1021/acsinfecdis.3c00049
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author Pham, Nhan T.
Alves, Joana
Sargison, Fiona A.
Cullum, Reiko
Wildenhain, Jan
Fenical, William
Butler, Mark S.
Mead, David A.
Duggan, Brendan M.
Fitzgerald, J. Ross
La Clair, James J.
Auer, Manfred
author_facet Pham, Nhan T.
Alves, Joana
Sargison, Fiona A.
Cullum, Reiko
Wildenhain, Jan
Fenical, William
Butler, Mark S.
Mead, David A.
Duggan, Brendan M.
Fitzgerald, J. Ross
La Clair, James J.
Auer, Manfred
author_sort Pham, Nhan T.
collection PubMed
description [Image: see text] Antimicrobial resistance has emerged as a global public health threat, and development of novel therapeutics for treating infections caused by multi-drug resistant bacteria is urgent. Staphylococcus aureus is a major human and animal pathogen, responsible for high levels of morbidity and mortality worldwide. The intracellular survival of S. aureus in macrophages contributes to immune evasion, dissemination, and resilience to antibiotic treatment. Here, we present a confocal fluorescence imaging assay for monitoring macrophage infection by green fluorescent protein (GFP)-tagged S. aureus as a front-line tool to identify antibiotic leads. The assay was employed in combination with nanoscaled chemical analyses to facilitate the discovery of a new, active rifamycin analogue. Our findings indicate a promising new approach for the identification of antimicrobial compounds with macrophage intracellular activity. The antibiotic identified here may represent a useful addition to our armory in tackling the silent pandemic of antimicrobial resistance.
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spelling pubmed-104259722023-08-16 Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay Pham, Nhan T. Alves, Joana Sargison, Fiona A. Cullum, Reiko Wildenhain, Jan Fenical, William Butler, Mark S. Mead, David A. Duggan, Brendan M. Fitzgerald, J. Ross La Clair, James J. Auer, Manfred ACS Infect Dis [Image: see text] Antimicrobial resistance has emerged as a global public health threat, and development of novel therapeutics for treating infections caused by multi-drug resistant bacteria is urgent. Staphylococcus aureus is a major human and animal pathogen, responsible for high levels of morbidity and mortality worldwide. The intracellular survival of S. aureus in macrophages contributes to immune evasion, dissemination, and resilience to antibiotic treatment. Here, we present a confocal fluorescence imaging assay for monitoring macrophage infection by green fluorescent protein (GFP)-tagged S. aureus as a front-line tool to identify antibiotic leads. The assay was employed in combination with nanoscaled chemical analyses to facilitate the discovery of a new, active rifamycin analogue. Our findings indicate a promising new approach for the identification of antimicrobial compounds with macrophage intracellular activity. The antibiotic identified here may represent a useful addition to our armory in tackling the silent pandemic of antimicrobial resistance. American Chemical Society 2023-07-11 /pmc/articles/PMC10425972/ /pubmed/37433130 http://dx.doi.org/10.1021/acsinfecdis.3c00049 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Pham, Nhan T.
Alves, Joana
Sargison, Fiona A.
Cullum, Reiko
Wildenhain, Jan
Fenical, William
Butler, Mark S.
Mead, David A.
Duggan, Brendan M.
Fitzgerald, J. Ross
La Clair, James J.
Auer, Manfred
Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title_full Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title_fullStr Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title_full_unstemmed Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title_short Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay
title_sort nanoscaled discovery of a shunt rifamycin from salinispora arenicola using a three-color gfp-tagged staphylococcus aureus macrophage infection assay
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425972/
https://www.ncbi.nlm.nih.gov/pubmed/37433130
http://dx.doi.org/10.1021/acsinfecdis.3c00049
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