Pyrrole-2-carboxylic acid inhibits biofilm formation and suppresses the virulence of Listeria monocytogenes.

IF 2.6 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yuxi Yue, Kai Zhong, Yanping Wu, Hong Gao
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引用次数: 0

Abstract

Bacterial adhesion and biofilm formation of Listeria monocytogenes on food-contact surfaces result in serious safety concerns. This study aimed to explore the antibiofilm efficacy of pyrrole-2-carboxylic acid (PCA) against L. monocytogenes. Crystal violet staining assay demonstrated that PCA reduced the biofilm biomass of L. monocytogenes. The 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide reduction and flow cytometric assays indicated that PCA attenuated the metabolic activity of L. monocytogenes biofilm together with a decrease in viability. Morphologic observations revealed that PCA exposure collapsed the biofilm architecture. PCA administration of 0.75 mg ml-1 decreased the excretion of extracellular DNA, protein and polysaccharide by 48.58%, 61.60% and 75.63%, respectively. PCA failed to disperse the mature biofilm, even at 1.5 mg ml-1. However, PCA suppressed L. monocytogenes adhesion on common food-contact surfaces. Additionally, PCA exposure suppressed the hemolytic activity of L. monocytogenes. These findings suggested that PCA might serve as an alternative antibiofilm agent to control L. monocytogenes contamination.

吡咯-2-羧酸抑制生物膜的形成并抑制单核增生李斯特菌的毒力。
单核细胞增生李斯特菌在食品接触表面的粘附和生物膜形成引起了严重的安全问题。本研究旨在探讨吡咯-2-羧酸(PCA)对单核增生乳杆菌的抗菌效果。结晶紫染色表明,PCA降低了单核增生乳杆菌的生物膜生物量。2,3-二-(2-甲氧基-4-硝基-5-巯基)- 2h -四氮唑-5-羧基苯胺还原和流式细胞术分析表明,PCA降低了单核增生乳杆菌生物膜的代谢活性,并降低了生物膜的活力。形态学观察显示PCA暴露使生物膜结构崩溃。0.75 mg ml-1 PCA组细胞外DNA、蛋白质和多糖的排泄量分别减少48.58%、61.60%和75.63%。PCA即使在1.5 mg ml-1的浓度下也不能分散成熟的生物膜。然而,PCA抑制了单核增生乳杆菌在常见食物接触表面的粘附。此外,PCA暴露抑制了单核增生乳杆菌的溶血活性。这些结果提示PCA可以作为一种替代的抗生物膜剂来控制单核增生乳杆菌的污染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biofouling
Biofouling 生物-海洋与淡水生物学
CiteScore
5.00
自引率
7.40%
发文量
57
审稿时长
1.7 months
期刊介绍: Biofouling is an international, peer-reviewed, multi-discliplinary journal which publishes original articles and mini-reviews and provides a forum for publication of pure and applied work on protein, microbial, fungal, plant and animal fouling and its control, as well as studies of all kinds on biofilms and bioadhesion. Papers may be based on studies relating to characterisation, attachment, growth and control on any natural (living) or man-made surface in the freshwater, marine or aerial environments, including fouling, biofilms and bioadhesion in the medical, dental, and industrial context. Specific areas of interest include antifouling technologies and coatings including transmission of invasive species, antimicrobial agents, biological interfaces, biomaterials, microbiologically influenced corrosion, membrane biofouling, food industry biofilms, biofilm based diseases and indwelling biomedical devices as substrata for fouling and biofilm growth, including papers based on clinically-relevant work using models that mimic the realistic environment in which they are intended to be used.
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