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没食子酸表没食子儿茶素酯对野生型和氨苄青霉素诱导的菌株的抗生物膜效应。

Antibiofilm Effects of Epigallocatechin Gallate Against Wild-Type and Ampicillin-Induced Strains.

机构信息

College of Life Science and Technology, Wuhan Polytechnic University, Wuhan, China.

College of Food Science and Engineering, Wuhan Polytechnic University, Wuhan, China.

出版信息

Foodborne Pathog Dis. 2022 Feb;19(2):136-142. doi: 10.1089/fpd.2021.0042. Epub 2021 Nov 2.

Abstract

is an opportunistic pathogen associated with nosocomial infections and foodborne diseases. The resistance and biofilm formation of have been a great concern. In this study a multidrug-resistant strain 012 was exposed to a lethal dose of ampicillin (10 mg/mL, 2.5-fold minimal bactericidal concentration) for 24 h at 37°C. After resuscitation and isolation, five variant isolates were selected and subjected to ampicillin induction by repeatedly streaking on ampicillin-containing plates (10 mg/mL) for at least three times. In biofilm formation assays by using crystal violet staining, we found that the variant strains had enhanced biofilm-forming abilities. (-)-epigallocatechin-3-gallate (EGCG) at a minimum inhibitory concentration (MIC) (256 μg/mL) significantly reduced the biofilm formation of all variant strains and the wild-type strain ( < 0.01). Sub-MIC of EGCG (128 μg/mL) suppressed the biofilms of wild-type and two variants. However, it stimulated the biofilms of the other three variants. The antibiofilm effects of EGCG against the wild-type strain were further confirmed by confocal laser scanning microscopy. Scanning electron microscopy revealed that EGCG induced variants to form more fibrous structures. Our results revealed that a lethal dose of antibiotic exposure increased antibiotic resistance and biofilm formation of . EGCG may be used as a promising antibiofilm agent to prevent the biofilm formation in the food industry. However, the sub-MIC of EGCG is not effective and will not be applied.

摘要

是一种机会性病原体,与医院感染和食源性疾病有关。 的耐药性和生物膜形成一直是人们关注的焦点。在这项研究中,将一株多药耐药 012 株在 37°C 下用氨苄西林(10mg/mL,最小杀菌浓度的 2.5 倍)进行了 24 小时的致死剂量处理。复苏和分离后,选择了五个变体分离株,并通过在含有氨苄西林的平板(10mg/mL)上反复划线进行氨苄西林诱导,至少进行了三次。通过结晶紫染色进行生物膜形成测定,我们发现变异株具有增强的生物膜形成能力。(-)-表没食子儿茶素-3-没食子酸酯(EGCG)在最小抑制浓度(MIC)(256μg/mL)时显著降低了所有变体和野生型菌株的生物膜形成( < 0.01)。亚 MIC 的 EGCG(128μg/mL)抑制了野生型和两种变体的生物膜。然而,它刺激了另外三种变体的生物膜。EGCG 对野生型菌株的抗生物膜作用通过共聚焦激光扫描显微镜进一步得到证实。扫描电子显微镜显示,EGCG 诱导变体形成更多纤维状结构。我们的研究结果表明,抗生素的致死剂量暴露增加了 的抗生素耐药性和生物膜形成。EGCG 可能被用作一种有前途的抗生物膜剂,以防止食品工业中 的生物膜形成。然而,亚 MIC 的 EGCG 无效,不会被应用。

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