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Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin

The rapid development of methicillin-resistant Staphylococcus aureus (MRSA) drug resistance and the formation of biofilms seriously challenge the clinical application of classic antibiotics. Extracts of the traditional herb Chenopodium ambrosioides L. were found to have strong antibiofilm activity a...

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Autores principales: He, Xinlong, Zhang, Wenwen, Cao, Qingchao, Li, Yinyue, Bao, Guangyu, Lin, Tao, Bao, Jiaojiao, Chang, Caiwang, Yang, Changshui, Yin, Yi, Xu, Jiahui, Ren, Zhenyu, Jin, Yingshan, Lu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769653/
https://www.ncbi.nlm.nih.gov/pubmed/36354319
http://dx.doi.org/10.1128/spectrum.02782-22
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author He, Xinlong
Zhang, Wenwen
Cao, Qingchao
Li, Yinyue
Bao, Guangyu
Lin, Tao
Bao, Jiaojiao
Chang, Caiwang
Yang, Changshui
Yin, Yi
Xu, Jiahui
Ren, Zhenyu
Jin, Yingshan
Lu, Feng
author_facet He, Xinlong
Zhang, Wenwen
Cao, Qingchao
Li, Yinyue
Bao, Guangyu
Lin, Tao
Bao, Jiaojiao
Chang, Caiwang
Yang, Changshui
Yin, Yi
Xu, Jiahui
Ren, Zhenyu
Jin, Yingshan
Lu, Feng
author_sort He, Xinlong
collection PubMed
description The rapid development of methicillin-resistant Staphylococcus aureus (MRSA) drug resistance and the formation of biofilms seriously challenge the clinical application of classic antibiotics. Extracts of the traditional herb Chenopodium ambrosioides L. were found to have strong antibiofilm activity against MRSA, but their mechanism of action remains poorly understood. This study was designed to investigate the antibacterial and antibiofilm activities against MRSA of flavonoids identified from C. ambrosioides L. in combination with classic antibiotics, including ceftazidime, erythromycin, levofloxacin, penicillin G, and vancomycin. Liquid chromatography-mass spectrometry (LC-MS) was used to analyze the nonvolatile chemical compositions. Reverse transcription (RT)-PCR was used to investigate potential multitargets of flavonoids based on global transcriptional responses of virulence and antibiotic resistance. A synergistic antibacterial and biofilm-inhibiting activity of the alcoholic extract of the ear of C. ambrosioides L. in combination with penicillin G was observed against MRSA, which proved to be closely related to the interaction of the main components of kaempferol rhamnosides with quercetin. In regard to the mechanism, the increased sensitivity of MRSA to penicillin G was shown to be related to the downregulation of penicillinase with SarA as a potential drug target, while the antibiofilm activity was mainly related to downregulation of various virulence factors involved in the initial and mature stages of biofilm development, with SarA and/or σB as drug targets. This study provides a theoretical basis for further exploration of the medicinal activity of kaempferol rhamnosides and quercetin and their application in combination with penicillin G against MRSA biofilm infection. IMPORTANCE In this study, the synergistic antibacterial and antibiofilm effects of the traditional herb C. ambrosioides L. and the classic antibiotic penicillin G on MRSA provide a potential strategy to deal with the rapid development of MRSA antibiotic resistance. This study also provides a theoretical basis for further optimizing the combined effect of kaempferol rhamnosides, quercetin, and penicillin G and exploring anti-MRSA biofilm infection research with SarA and σB as drug targets.
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spelling pubmed-97696532022-12-22 Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin He, Xinlong Zhang, Wenwen Cao, Qingchao Li, Yinyue Bao, Guangyu Lin, Tao Bao, Jiaojiao Chang, Caiwang Yang, Changshui Yin, Yi Xu, Jiahui Ren, Zhenyu Jin, Yingshan Lu, Feng Microbiol Spectr Research Article The rapid development of methicillin-resistant Staphylococcus aureus (MRSA) drug resistance and the formation of biofilms seriously challenge the clinical application of classic antibiotics. Extracts of the traditional herb Chenopodium ambrosioides L. were found to have strong antibiofilm activity against MRSA, but their mechanism of action remains poorly understood. This study was designed to investigate the antibacterial and antibiofilm activities against MRSA of flavonoids identified from C. ambrosioides L. in combination with classic antibiotics, including ceftazidime, erythromycin, levofloxacin, penicillin G, and vancomycin. Liquid chromatography-mass spectrometry (LC-MS) was used to analyze the nonvolatile chemical compositions. Reverse transcription (RT)-PCR was used to investigate potential multitargets of flavonoids based on global transcriptional responses of virulence and antibiotic resistance. A synergistic antibacterial and biofilm-inhibiting activity of the alcoholic extract of the ear of C. ambrosioides L. in combination with penicillin G was observed against MRSA, which proved to be closely related to the interaction of the main components of kaempferol rhamnosides with quercetin. In regard to the mechanism, the increased sensitivity of MRSA to penicillin G was shown to be related to the downregulation of penicillinase with SarA as a potential drug target, while the antibiofilm activity was mainly related to downregulation of various virulence factors involved in the initial and mature stages of biofilm development, with SarA and/or σB as drug targets. This study provides a theoretical basis for further exploration of the medicinal activity of kaempferol rhamnosides and quercetin and their application in combination with penicillin G against MRSA biofilm infection. IMPORTANCE In this study, the synergistic antibacterial and antibiofilm effects of the traditional herb C. ambrosioides L. and the classic antibiotic penicillin G on MRSA provide a potential strategy to deal with the rapid development of MRSA antibiotic resistance. This study also provides a theoretical basis for further optimizing the combined effect of kaempferol rhamnosides, quercetin, and penicillin G and exploring anti-MRSA biofilm infection research with SarA and σB as drug targets. American Society for Microbiology 2022-11-10 /pmc/articles/PMC9769653/ /pubmed/36354319 http://dx.doi.org/10.1128/spectrum.02782-22 Text en Copyright © 2022 He et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
He, Xinlong
Zhang, Wenwen
Cao, Qingchao
Li, Yinyue
Bao, Guangyu
Lin, Tao
Bao, Jiaojiao
Chang, Caiwang
Yang, Changshui
Yin, Yi
Xu, Jiahui
Ren, Zhenyu
Jin, Yingshan
Lu, Feng
Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title_full Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title_fullStr Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title_full_unstemmed Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title_short Global Downregulation of Penicillin Resistance and Biofilm Formation by MRSA Is Associated with the Interaction between Kaempferol Rhamnosides and Quercetin
title_sort global downregulation of penicillin resistance and biofilm formation by mrsa is associated with the interaction between kaempferol rhamnosides and quercetin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769653/
https://www.ncbi.nlm.nih.gov/pubmed/36354319
http://dx.doi.org/10.1128/spectrum.02782-22
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