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Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis

BACKGROUND: Streptococcus mutans, an important Gram-positive pathogen in dental caries, uses sortase A (SrtA) to anchor surface proteins to the bacterial cell wall, thereby promoting biofilm formation and attachment to the tooth surface. DESIGN: Based on activity-guided separation, inhibitors of S....

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Autores principales: Cho, Eunji, Hwang, Ji-Yeon, Park, Jae Sung, Oh, Daehyun, Oh, Dong-Chan, Park, Hyeung-Geun, Shin, Jongheon, Oh, Ki-Bong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225741/
https://www.ncbi.nlm.nih.gov/pubmed/35756538
http://dx.doi.org/10.1080/20002297.2022.2088937
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author Cho, Eunji
Hwang, Ji-Yeon
Park, Jae Sung
Oh, Daehyun
Oh, Dong-Chan
Park, Hyeung-Geun
Shin, Jongheon
Oh, Ki-Bong
author_facet Cho, Eunji
Hwang, Ji-Yeon
Park, Jae Sung
Oh, Daehyun
Oh, Dong-Chan
Park, Hyeung-Geun
Shin, Jongheon
Oh, Ki-Bong
author_sort Cho, Eunji
collection PubMed
description BACKGROUND: Streptococcus mutans, an important Gram-positive pathogen in dental caries, uses sortase A (SrtA) to anchor surface proteins to the bacterial cell wall, thereby promoting biofilm formation and attachment to the tooth surface. DESIGN: Based on activity-guided separation, inhibitors of S. mutans SrtA were isolated from Juniperus chinensis and identified through combined spectroscopic analysis. Further effects of isolated SrtA inhibitor on S. mutans were evaluated on bacterial aggregation, adherence and biofilm formation. RESULTS: Six compounds (1–6) were isolated from the dried heartwood of J. chinensis. A novel compound designated 3’,3”-dihydroxy-(−)-matairesinol (1) was identified, which exhibited potent inhibitory activity toward S. mutans SrtA (IC(50) = 16.1 μM) without affecting microbial viability (minimum inhibitory concentration > 300 μM). The results of subsequent bioassays using compound 1 indicated that this compound inhibits S. mutans aggregation, adhesion and biofilm formation on solid surfaces by inhibiting SrtA activity. The onset and magnitude of inhibition of adherence and biofilm formation in S. mutans treated with compound 1 at 4× the SrtA IC(50) are comparable to the behaviors of the untreated srtA-deletion mutant. CONCLUSION: Our findings suggest that small-molecule inhibitors of S. mutans SrtA may be useful for the prevention of dental plaque and treatment of dental microbial diseases.
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spelling pubmed-92257412022-06-24 Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis Cho, Eunji Hwang, Ji-Yeon Park, Jae Sung Oh, Daehyun Oh, Dong-Chan Park, Hyeung-Geun Shin, Jongheon Oh, Ki-Bong J Oral Microbiol Original Article BACKGROUND: Streptococcus mutans, an important Gram-positive pathogen in dental caries, uses sortase A (SrtA) to anchor surface proteins to the bacterial cell wall, thereby promoting biofilm formation and attachment to the tooth surface. DESIGN: Based on activity-guided separation, inhibitors of S. mutans SrtA were isolated from Juniperus chinensis and identified through combined spectroscopic analysis. Further effects of isolated SrtA inhibitor on S. mutans were evaluated on bacterial aggregation, adherence and biofilm formation. RESULTS: Six compounds (1–6) were isolated from the dried heartwood of J. chinensis. A novel compound designated 3’,3”-dihydroxy-(−)-matairesinol (1) was identified, which exhibited potent inhibitory activity toward S. mutans SrtA (IC(50) = 16.1 μM) without affecting microbial viability (minimum inhibitory concentration > 300 μM). The results of subsequent bioassays using compound 1 indicated that this compound inhibits S. mutans aggregation, adhesion and biofilm formation on solid surfaces by inhibiting SrtA activity. The onset and magnitude of inhibition of adherence and biofilm formation in S. mutans treated with compound 1 at 4× the SrtA IC(50) are comparable to the behaviors of the untreated srtA-deletion mutant. CONCLUSION: Our findings suggest that small-molecule inhibitors of S. mutans SrtA may be useful for the prevention of dental plaque and treatment of dental microbial diseases. Taylor & Francis 2022-06-14 /pmc/articles/PMC9225741/ /pubmed/35756538 http://dx.doi.org/10.1080/20002297.2022.2088937 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Eunji
Hwang, Ji-Yeon
Park, Jae Sung
Oh, Daehyun
Oh, Dong-Chan
Park, Hyeung-Geun
Shin, Jongheon
Oh, Ki-Bong
Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title_full Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title_fullStr Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title_full_unstemmed Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title_short Inhibition of Streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase A from Juniperus chinensis
title_sort inhibition of streptococcus mutans adhesion and biofilm formation with small-molecule inhibitors of sortase a from juniperus chinensis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225741/
https://www.ncbi.nlm.nih.gov/pubmed/35756538
http://dx.doi.org/10.1080/20002297.2022.2088937
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