Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>

<i>Staphylococcus aureus</i> is one of the major pathogens responsible for antimicrobial resistance-associated death. <i>S. aureus</i> can secrete various exotoxins, and staphylococcal biofilms play critical roles in antibiotic tolerance and the persistence of chronic infecti...

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Main Authors: Sanghun Kim, Jin-Hyung Lee, Yong-Guy Kim, Yulong Tan, Jintae Lee
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/18/10683
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author Sanghun Kim
Jin-Hyung Lee
Yong-Guy Kim
Yulong Tan
Jintae Lee
author_facet Sanghun Kim
Jin-Hyung Lee
Yong-Guy Kim
Yulong Tan
Jintae Lee
author_sort Sanghun Kim
collection DOAJ
description <i>Staphylococcus aureus</i> is one of the major pathogens responsible for antimicrobial resistance-associated death. <i>S. aureus</i> can secrete various exotoxins, and staphylococcal biofilms play critical roles in antibiotic tolerance and the persistence of chronic infections. Here, we investigated the inhibitory effects of 18 hydroquinones on biofilm formation and virulence factor production by <i>S. aureus</i>. It was found that 2,5-bis(1,1,3,3-tetramethylbutyl) hydroquinone (TBHQ) at 1 µg/mL efficiently inhibits biofilm formation by two methicillin-sensitive and two methicillin-resistant <i>S. aureus</i> strains with MICs of 5 µg/mL, whereas the backbone compound hydroquinone did not (MIC > 400 µg/mL). In addition, 2,3-dimethylhydroquinone and <i>tert</i>-butylhydroquinone at 50 µg/mL also exhibited antibiofilm activity. TBHQ at 1 µg/mL significantly decreased the hemolytic effect and lipase production by <i>S. aureus</i>, and at 5–50 µg/mL was non-toxic to the nematode <i>Caenorhabditis elegans</i> and did not adversely affect <i>Brassica rapa</i> seed germination or growth. Transcriptional analyses showed that TBHQ suppressed the expression of <i>RNAIII</i> (effector of quorum sensing). These results suggest that hydroquinones, particularly TBHQ, are potentially useful for inhibiting <i>S. aureus</i> biofilm formation and virulence.
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spelling doaj.art-cf3d914bd71942dfb31e500a37b7d68d2023-11-23T16:46:16ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-09-0123181068310.3390/ijms231810683Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>Sanghun Kim0Jin-Hyung Lee1Yong-Guy Kim2Yulong Tan3Jintae Lee4School of Chemical Engineering, Yeungnam University, Gyeongsan 38541, KoreaSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, KoreaSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, KoreaSpecial Food Research Institute, Qingdao Agricultural University, Qingdao 266109, ChinaSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Korea<i>Staphylococcus aureus</i> is one of the major pathogens responsible for antimicrobial resistance-associated death. <i>S. aureus</i> can secrete various exotoxins, and staphylococcal biofilms play critical roles in antibiotic tolerance and the persistence of chronic infections. Here, we investigated the inhibitory effects of 18 hydroquinones on biofilm formation and virulence factor production by <i>S. aureus</i>. It was found that 2,5-bis(1,1,3,3-tetramethylbutyl) hydroquinone (TBHQ) at 1 µg/mL efficiently inhibits biofilm formation by two methicillin-sensitive and two methicillin-resistant <i>S. aureus</i> strains with MICs of 5 µg/mL, whereas the backbone compound hydroquinone did not (MIC > 400 µg/mL). In addition, 2,3-dimethylhydroquinone and <i>tert</i>-butylhydroquinone at 50 µg/mL also exhibited antibiofilm activity. TBHQ at 1 µg/mL significantly decreased the hemolytic effect and lipase production by <i>S. aureus</i>, and at 5–50 µg/mL was non-toxic to the nematode <i>Caenorhabditis elegans</i> and did not adversely affect <i>Brassica rapa</i> seed germination or growth. Transcriptional analyses showed that TBHQ suppressed the expression of <i>RNAIII</i> (effector of quorum sensing). These results suggest that hydroquinones, particularly TBHQ, are potentially useful for inhibiting <i>S. aureus</i> biofilm formation and virulence.https://www.mdpi.com/1422-0067/23/18/10683biofilmshydroquinones<i>RNAIII</i><i>Staphylococcus</i> <i>aureus</i>virulence factors
spellingShingle Sanghun Kim
Jin-Hyung Lee
Yong-Guy Kim
Yulong Tan
Jintae Lee
Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
International Journal of Molecular Sciences
biofilms
hydroquinones
<i>RNAIII</i>
<i>Staphylococcus</i> <i>aureus</i>
virulence factors
title Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
title_full Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
title_fullStr Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
title_full_unstemmed Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
title_short Hydroquinones Inhibit Biofilm Formation and Virulence Factor Production in <i>Staphylococcus aureus</i>
title_sort hydroquinones inhibit biofilm formation and virulence factor production in i staphylococcus aureus i
topic biofilms
hydroquinones
<i>RNAIII</i>
<i>Staphylococcus</i> <i>aureus</i>
virulence factors
url https://www.mdpi.com/1422-0067/23/18/10683
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AT yongguykim hydroquinonesinhibitbiofilmformationandvirulencefactorproductioninistaphylococcusaureusi
AT yulongtan hydroquinonesinhibitbiofilmformationandvirulencefactorproductioninistaphylococcusaureusi
AT jintaelee hydroquinonesinhibitbiofilmformationandvirulencefactorproductioninistaphylococcusaureusi