Optimized Extraction, Identification and Anti-Biofilm Action of Wu Wei Zi ( Fructus Schisandrae Chinensis ) Extracts against Vibrio parahaemolyticus

• Published in: Molecules (Basel, Switzerland) Switzerland), 2023-02, Vol.28 (5), p.2268
• Main Authors: Zhang, Zongyi, Zhao, Yanan, Cai, Jing, Wang, Tong, Song, Yujie, Lu, Jingyi, Du, Hairuo, Wang, Wenfang, Zhao, Yan, Guo, Lei
• Format: Article
• Language: English
• Subjects: anti-biofilm; antibacterial; Antibiotics; Antiinfectives and antibacterials; Bacteria; Bacterial infections; Biofilms; Cell membranes; Cholecystokinin; Deoxyribonucleic acid; DNA; Drug resistance; Ethanol; extraction optimization; Foodborne pathogens; Gastroenteritis; High performance liquid chromatography; Liquid chromatography; Minimum inhibitory concentration; Pathogenicity; Pathogens; Plant extracts; Polysaccharides; Public health; Response surface methodology; Schisandra; Schisandra chinensis; Seafood; Spectrophotometry; Variables; Vibrio parahaemolyticus; Vibrio parahaemolyticus - genetics; Wu Wei; Wu Wei Zi
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28052268

The pathogenicity of foodborne is a major concern for global public health. This study aimed to optimize the liquid-solid extraction of Wu Wei Zi extracts (WWZE) against , identify its main components, and investigate the anti-biofilm action. The extraction conditions optimized by the single-factor test and response surface methodology were ethanol concentration of 69%, temperature at 91 °C, time of 143 min, and liquid-solid ratio of 20:1 mL/g. After high performance liquid chromatography (HPLC) analysis, it was found that the main active ingredients of WWZE were schisandrol A, schisandrol B, schisantherin A, schisanhenol, and schisandrin A-C. The minimum inhibitory concentration (MIC) of WWZE, schisantherin A, and schisandrol B measured by broth microdilution assay was 1.25, 0.625, and 1.25 mg/mL, respectively, while the MIC of the other five compounds was higher than 2.5 mg/mL, indicating that schisantherin A and schizandrol B were the main antibacterial components of WWZE. Crystal violet, Coomassie brilliant blue, Congo red plate, spectrophotometry, and Cell Counting Kit-8 (CCK-8) assays were used to evaluate the effect of WWZE on the biofilm of . The results showed that WWZE could exert its dose-dependent potential to effectively inhibit the formation of biofilm and clear mature biofilm by significantly destroying the cell membrane integrity of , inhibiting the synthesis of intercellular polysaccharide adhesin (PIA), extracellular DNA secretion, and reducing the metabolic activity of biofilm. This study reported for the first time the favorable anti-biofilm effect of WWZE against , which provides a basis for deepening the application of WWZE in the preservation of aquatic products.