Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens
Quorum sensing (QS) plays an essential role in virulence factor production, biofilm formation, and antimicrobial resistance. As a potent QS inhibitor, hordenine can inhibit both QS and biofilm formation in Pseudomonas aeruginosa and Serratia marcescens. In this work, we tested the QS inhibitory pote...
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KeAi Communications Co., Ltd.
2021
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oai:doaj.org-article:9cee47318d7641dfa1c169303874c4f02021-11-04T04:33:34ZQuorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens2405-805X10.1016/j.synbio.2021.09.010https://doaj.org/article/9cee47318d7641dfa1c169303874c4f02021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2405805X21000624https://doaj.org/toc/2405-805XQuorum sensing (QS) plays an essential role in virulence factor production, biofilm formation, and antimicrobial resistance. As a potent QS inhibitor, hordenine can inhibit both QS and biofilm formation in Pseudomonas aeruginosa and Serratia marcescens. In this work, we tested the QS inhibitory potential of 27 hordenine analogs against QS and biofilm formation in P. aeruginosa and S. marcescens. Among the tested analogs, seven (12, 28, 27, 26, 2, 23, and 7) exhibited strong QS inhibitory activity against P. aeruginosa, five of which (12, 28, 27, 26, and 2) showed better inhibitory activity than hordenine. In addition, seven analogs (28, 12, 23, 7, 26, 2, and 27) exhibited better biofilm inhibition against P. aeruginosa than hordenine. Four analogs (7, 28, 2, and 12) showed QS inhibitory activity against S. marcescens, two of which (7 and 28) demonstrated better inhibitory activity than hordenine. Furthermore, analog 7 showed similar biofilm inhibition against S. marcescens as hordenine. Structure-activity relationship (SAR) analysis indicated that the inhibitory activities of the analogs were related to four factors, i.e., carbon chain length, presence or absence of an α,β-CC bond, amino group with/without lipophilic group, such as methyl group, and hydroxyl group in benzene ring.Yue LiuJun-Jian LiHong-Yuan LiShi-Ming DengAi-Qun JiaKeAi Communications Co., Ltd.articleHordenine analogsPseudomonas aeruginosaSerratia marcescensQuorum sensing inhibitionQSARBiofilmBiotechnologyTP248.13-248.65Biology (General)QH301-705.5ENSynthetic and Systems Biotechnology, Vol 6, Iss 4, Pp 360-368 (2021) |
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Hordenine analogs Pseudomonas aeruginosa Serratia marcescens Quorum sensing inhibition QSAR Biofilm Biotechnology TP248.13-248.65 Biology (General) QH301-705.5 |
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Hordenine analogs Pseudomonas aeruginosa Serratia marcescens Quorum sensing inhibition QSAR Biofilm Biotechnology TP248.13-248.65 Biology (General) QH301-705.5 Yue Liu Jun-Jian Li Hong-Yuan Li Shi-Ming Deng Ai-Qun Jia Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
description |
Quorum sensing (QS) plays an essential role in virulence factor production, biofilm formation, and antimicrobial resistance. As a potent QS inhibitor, hordenine can inhibit both QS and biofilm formation in Pseudomonas aeruginosa and Serratia marcescens. In this work, we tested the QS inhibitory potential of 27 hordenine analogs against QS and biofilm formation in P. aeruginosa and S. marcescens. Among the tested analogs, seven (12, 28, 27, 26, 2, 23, and 7) exhibited strong QS inhibitory activity against P. aeruginosa, five of which (12, 28, 27, 26, and 2) showed better inhibitory activity than hordenine. In addition, seven analogs (28, 12, 23, 7, 26, 2, and 27) exhibited better biofilm inhibition against P. aeruginosa than hordenine. Four analogs (7, 28, 2, and 12) showed QS inhibitory activity against S. marcescens, two of which (7 and 28) demonstrated better inhibitory activity than hordenine. Furthermore, analog 7 showed similar biofilm inhibition against S. marcescens as hordenine. Structure-activity relationship (SAR) analysis indicated that the inhibitory activities of the analogs were related to four factors, i.e., carbon chain length, presence or absence of an α,β-CC bond, amino group with/without lipophilic group, such as methyl group, and hydroxyl group in benzene ring. |
format |
article |
author |
Yue Liu Jun-Jian Li Hong-Yuan Li Shi-Ming Deng Ai-Qun Jia |
author_facet |
Yue Liu Jun-Jian Li Hong-Yuan Li Shi-Ming Deng Ai-Qun Jia |
author_sort |
Yue Liu |
title |
Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
title_short |
Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
title_full |
Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
title_fullStr |
Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
title_full_unstemmed |
Quorum sensing inhibition of hordenine analogs on Pseudomonas aeruginosa and Serratia marcescens |
title_sort |
quorum sensing inhibition of hordenine analogs on pseudomonas aeruginosa and serratia marcescens |
publisher |
KeAi Communications Co., Ltd. |
publishDate |
2021 |
url |
https://doaj.org/article/9cee47318d7641dfa1c169303874c4f0 |
work_keys_str_mv |
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_version_ |
1718445289248915456 |