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芍药苷减少 /AI-2 系统控制的生物膜形成和毒力在 ……

Paeoniflorin reduce /AI-2 system-controlled biofilm formation and virulence in .

机构信息

College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China.

Key Laboratory of Molecular Pathogen and Immunology of Animal of Luoyang, Luoyang, China.

出版信息

Virulence. 2021 Dec;12(1):3062-3073. doi: 10.1080/21505594.2021.2010398.

DOI:10.1080/21505594.2021.2010398
PMID:34923916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8923065/
Abstract

(), more specifically serotype 2, is a bacterial pathogen that threatens the lives of pigs and humans. Like many other pathogens, exhibits quorum sensing (QS) system-controlled virulence factors, such as biofilm formation that complicates treatment. Therefore, impairing the QS involving LuxS/AI-2 cycle in , may be a promising alternative strategy for overcoming infections. In this study, we investigated paeoniflorin (PF), a monoterpenoid glycoside compound extracted from peony, as an inhibitor of LuxS/AI-2 system. At a sub-minimal inhibitory concentration (MIC) (1/16 MIC; 25 μg/ml), PF significantly reduced biofilm formation by through inhibition of extracellular polysaccharide (EPS) production, without affecting bacterial growth. Moreover, evidence was brought that PF reduces AI-2 activity in biofilm. Molecular docking indicated that LuxS may be the target of PF. Monitoring LuxS enzymatic activity confirmed that PF had a partial inhibitory effect. Finally, we showed that the use of PF in a mouse model can relieve infections. This study highlighted the anti-biofilm potential of PF against , and brought evidence that it may as an inhibitor of the LuxS/AI-2 system to prevent biofilm-related infections. PF can thus be used as a new type of natural biofilm inhibitor for clinical application.

摘要

(),更具体地说是血清型 2,是一种威胁猪和人类生命的细菌病原体。与许多其他病原体一样,表现出群体感应(QS)系统控制的毒力因子,例如生物膜形成,这使得治疗变得复杂。因此,削弱涉及 LuxS/AI-2 循环的 QS,可能是克服感染的一种有前途的替代策略。在这项研究中,我们研究了从牡丹中提取的单萜糖苷化合物芍药苷(PF)作为 LuxS/AI-2 系统的抑制剂。在亚最小抑制浓度(MIC)(1/16 MIC;25μg/ml)下,PF 通过抑制细胞外多糖(EPS)的产生,显著降低了通过抑制细胞外多糖(EPS)的产生而导致的生物膜形成,而不影响细菌生长。此外,有证据表明 PF 降低了生物膜中的 AI-2 活性。分子对接表明 LuxS 可能是 PF 的靶标。监测 LuxS 酶活性证实 PF 具有部分抑制作用。最后,我们表明在小鼠模型中使用 PF 可以缓解感染。这项研究强调了 PF 对生物膜的抗生物膜潜力,并提供了证据表明它可能作为 LuxS/AI-2 系统的抑制剂来预防生物膜相关感染。因此,PF 可以用作临床应用的新型天然生物膜抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/0b44f0d1ea16/KVIR_A_2010398_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/a272b54618f3/KVIR_A_2010398_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/3739ae635ed2/KVIR_A_2010398_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/46850d2a93d5/KVIR_A_2010398_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/afd5d35b0b48/KVIR_A_2010398_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/0b44f0d1ea16/KVIR_A_2010398_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/a272b54618f3/KVIR_A_2010398_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/3739ae635ed2/KVIR_A_2010398_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/46850d2a93d5/KVIR_A_2010398_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/afd5d35b0b48/KVIR_A_2010398_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/8923065/0b44f0d1ea16/KVIR_A_2010398_F0005_OC.jpg

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