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Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes

Staphylococcus aureus is a widely acknowledged Gram-positive pathogen for forming biofilm and virulence gene expressions by quorum sensing (QS), a cell to cell communication process. The quorum regulator SarA of S. aureus up-regulates the expression of many virulence factors including biofilm format...

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Autores principales: Balamurugan, P., Praveen Krishna, V., Bharath, D., Lavanya, Raajaraam, Vairaprakash, Pothiappan, Adline Princy, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504099/
https://www.ncbi.nlm.nih.gov/pubmed/28744275
http://dx.doi.org/10.3389/fmicb.2017.01290
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author Balamurugan, P.
Praveen Krishna, V.
Bharath, D.
Lavanya, Raajaraam
Vairaprakash, Pothiappan
Adline Princy, S.
author_facet Balamurugan, P.
Praveen Krishna, V.
Bharath, D.
Lavanya, Raajaraam
Vairaprakash, Pothiappan
Adline Princy, S.
author_sort Balamurugan, P.
collection PubMed
description Staphylococcus aureus is a widely acknowledged Gram-positive pathogen for forming biofilm and virulence gene expressions by quorum sensing (QS), a cell to cell communication process. The quorum regulator SarA of S. aureus up-regulates the expression of many virulence factors including biofilm formation to mediate pathogenesis and evasion of the host immune system in the late phases of growth. Thus, inhibiting the production or blocking SarA protein might influence the down-regulation of biofilm and virulence factors. In this context, here we have synthesized 2-[(Methylamino)methyl]phenol, which was specifically targeted toward the quorum regulator SarA through in silico approach in our previous study. The molecule has been evaluated in vitro to validate its antibiofilm activity against clinical S. aureus strains. In addition, antivirulence properties of the inhibitor were confirmed with the observation of a significant reduction in the expression of representative virulence genes like fnbA, hla and hld that are governed under S. aureus QS. Interestingly, the SarA targeted inhibitor showed negligible antimicrobial activity and markedly reduced the minimum inhibitory concentration of conventional antibiotics when used in combination making it a more attractive lead for further clinical tests.
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spelling pubmed-55040992017-07-25 Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes Balamurugan, P. Praveen Krishna, V. Bharath, D. Lavanya, Raajaraam Vairaprakash, Pothiappan Adline Princy, S. Front Microbiol Microbiology Staphylococcus aureus is a widely acknowledged Gram-positive pathogen for forming biofilm and virulence gene expressions by quorum sensing (QS), a cell to cell communication process. The quorum regulator SarA of S. aureus up-regulates the expression of many virulence factors including biofilm formation to mediate pathogenesis and evasion of the host immune system in the late phases of growth. Thus, inhibiting the production or blocking SarA protein might influence the down-regulation of biofilm and virulence factors. In this context, here we have synthesized 2-[(Methylamino)methyl]phenol, which was specifically targeted toward the quorum regulator SarA through in silico approach in our previous study. The molecule has been evaluated in vitro to validate its antibiofilm activity against clinical S. aureus strains. In addition, antivirulence properties of the inhibitor were confirmed with the observation of a significant reduction in the expression of representative virulence genes like fnbA, hla and hld that are governed under S. aureus QS. Interestingly, the SarA targeted inhibitor showed negligible antimicrobial activity and markedly reduced the minimum inhibitory concentration of conventional antibiotics when used in combination making it a more attractive lead for further clinical tests. Frontiers Media S.A. 2017-07-11 /pmc/articles/PMC5504099/ /pubmed/28744275 http://dx.doi.org/10.3389/fmicb.2017.01290 Text en Copyright © 2017 Balamurugan, Praveen Krishna, Bharath, Lavanya, Vairaprakash and Adline Princy. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Balamurugan, P.
Praveen Krishna, V.
Bharath, D.
Lavanya, Raajaraam
Vairaprakash, Pothiappan
Adline Princy, S.
Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title_full Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title_fullStr Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title_full_unstemmed Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title_short Staphylococcus aureus Quorum Regulator SarA Targeted Compound, 2-[(Methylamino)methyl]phenol Inhibits Biofilm and Down-Regulates Virulence Genes
title_sort staphylococcus aureus quorum regulator sara targeted compound, 2-[(methylamino)methyl]phenol inhibits biofilm and down-regulates virulence genes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504099/
https://www.ncbi.nlm.nih.gov/pubmed/28744275
http://dx.doi.org/10.3389/fmicb.2017.01290
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