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Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective

[Image: see text] Virulence gene expression in Staphylococcus aureus is tightly regulated by intricate networks of transcriptional regulators and two-component signal transduction systems. There is now an emerging body of evidence to suggest that the blockade of S. aureus virulence gene expression s...

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Autores principales: Gordon, Christopher P., Williams, Paul, Chan, Weng C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585718/
https://www.ncbi.nlm.nih.gov/pubmed/23294220
http://dx.doi.org/10.1021/jm3014635
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author Gordon, Christopher P.
Williams, Paul
Chan, Weng C.
author_facet Gordon, Christopher P.
Williams, Paul
Chan, Weng C.
author_sort Gordon, Christopher P.
collection PubMed
description [Image: see text] Virulence gene expression in Staphylococcus aureus is tightly regulated by intricate networks of transcriptional regulators and two-component signal transduction systems. There is now an emerging body of evidence to suggest that the blockade of S. aureus virulence gene expression significantly attenuates infection in experimental models. In this Perspective, we will provide insights into medicinal chemistry strategies for the development of chemical reagents that have the capacity to inhibit staphylococcal virulence expression. These reagents can be broadly grouped into four categories: (1) competitive inhibitors of the accessory gene regulator (agr) quorum sensing system, (2) inhibitors of AgrA–DNA interactions, (3) RNAIII transcription inhibitors, and (4) inhibitors of the SarA family of transcriptional regulators. We discuss the potential of specific examples of antivirulence agents for the management and treatment of staphylococcal infections.
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spelling pubmed-35857182013-03-04 Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective Gordon, Christopher P. Williams, Paul Chan, Weng C. J Med Chem [Image: see text] Virulence gene expression in Staphylococcus aureus is tightly regulated by intricate networks of transcriptional regulators and two-component signal transduction systems. There is now an emerging body of evidence to suggest that the blockade of S. aureus virulence gene expression significantly attenuates infection in experimental models. In this Perspective, we will provide insights into medicinal chemistry strategies for the development of chemical reagents that have the capacity to inhibit staphylococcal virulence expression. These reagents can be broadly grouped into four categories: (1) competitive inhibitors of the accessory gene regulator (agr) quorum sensing system, (2) inhibitors of AgrA–DNA interactions, (3) RNAIII transcription inhibitors, and (4) inhibitors of the SarA family of transcriptional regulators. We discuss the potential of specific examples of antivirulence agents for the management and treatment of staphylococcal infections. American Chemical Society 2013-01-07 2013-02-28 /pmc/articles/PMC3585718/ /pubmed/23294220 http://dx.doi.org/10.1021/jm3014635 Text en Copyright © 2013 American Chemical Society
spellingShingle Gordon, Christopher P.
Williams, Paul
Chan, Weng C.
Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title_full Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title_fullStr Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title_full_unstemmed Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title_short Attenuating Staphylococcus aureus Virulence Gene Regulation: A Medicinal Chemistry Perspective
title_sort attenuating staphylococcus aureus virulence gene regulation: a medicinal chemistry perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585718/
https://www.ncbi.nlm.nih.gov/pubmed/23294220
http://dx.doi.org/10.1021/jm3014635
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