Suppr超能文献

一种用于控制乳房链球菌生物膜的生物工程改造的乳链菌肽衍生物。

A Bioengineered Nisin Derivative To Control Streptococcus uberis Biofilms.

作者信息

Pérez-Ibarreche Mariana, Field Des, Ross R Paul, Hill Colin

机构信息

APC Microbiome Ireland, University College Cork, Cork, Ireland.

School of Microbiology, University College Cork, Cork, Ireland.

出版信息

Appl Environ Microbiol. 2021 Jul 27;87(16):e0039121. doi: 10.1128/AEM.00391-21.

Abstract

Antimicrobial peptides are evolving as novel therapeutic options against the increasing problem of multidrug-resistant microorganisms, and nisin is one such avenue. However, some bacteria possess a specific nisin resistance system (NSR), which cleaves the peptide reducing its bactericidal efficacy. NSR-based resistance was identified in strains of Streptococcus uberis, a ubiquitous pathogen that causes mastitis in dairy cattle. Previous studies have demonstrated that a nisin A derivative termed nisin PV, featuring S29P and I30V, exhibits enhanced resistance to proteolytic cleavage by NSR. Our objective was to investigate the ability of this nisin derivative to eradicate and inhibit biofilms of S. uberis DPC 5344 and ATCC 700407 () using crystal violet (biomass), 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) (viability) assays, and confocal microscopy (viability and architecture). When preestablished biofilms were assessed, both peptides reduced biofilm biomass by over 60% compared to that of the untreated controls. However, a 42% higher reduction in viability was observed following treatment with nisin PV compared to that of nisin A. Accordingly, confocal microscopy analysis revealed significantly more dead cells on the biofilm upper surface and a reduced thickness following treatment with nisin PV. When biofilm inhibition was assessed, nisin PV inhibited biofilm formation and decreased viability up to 56% and 85% more than nisin A, respectively. Confocal microscopy analysis revealed a lack of biofilm for ATCC 700407 and only dead cells for DPC 5344. These results suggest that nisin PV is a promising alternative to effectively reduce the biofilm formation of strains carrying NSR. One of the four most prevalent species of bovine mastitis-causing pathogens is Its ability to form biofilms confers on the bacteria greater resistance to antibiotics, requiring higher doses to be more effective. In a bid to limit antibiotic resistance development, the need for alternative antimicrobials is paramount. Bacteriocins such as nisin represent one such alternative that could alleviate the impact of mastitis caused by However, many strains of have been shown to possess nisin resistance determinants, such as the nisin resistance protein (NSR). In this study, we demonstrate the ability of nisin and a nisin derivative termed PV that is insensitive to NSR to prevent and remove biofilms of NSR-producing strains. These findings will add new information to the antimicrobial bacteriocins and control of research fields specifically in relation to biofilms and mastitis-associated strains.

摘要

抗菌肽正逐渐成为应对多药耐药微生物这一日益严重问题的新型治疗选择,乳链菌肽就是其中之一。然而,一些细菌拥有特定的乳链菌肽抗性系统(NSR),该系统会切割这种肽,降低其杀菌效力。在乳房链球菌菌株中发现了基于NSR的抗性,乳房链球菌是一种普遍存在的病原体,可导致奶牛患乳腺炎。先前的研究表明,一种名为乳链菌肽PV的乳链菌肽A衍生物,具有S29P和I30V特征,对NSR的蛋白水解切割具有增强的抗性。我们的目标是使用结晶紫(生物量)、2,3-双-(2-甲氧基-4-硝基-5-磺基苯基)-2H-四唑-5-羧基苯胺(XTT)(活力)测定法以及共聚焦显微镜(活力和结构)来研究这种乳链菌肽衍生物根除和抑制乳房链球菌DPC 5344和ATCC 700407生物膜的能力。在评估预先形成的生物膜时,与未处理的对照相比,两种肽均使生物膜生物量减少了60%以上。然而,与乳链菌肽A相比,用乳链菌肽PV处理后观察到活力降低了42%。因此,共聚焦显微镜分析显示,用乳链菌肽PV处理后,生物膜上表面的死细胞明显更多,厚度减小。在评估生物膜抑制时,乳链菌肽PV抑制生物膜形成,并使活力分别比乳链菌肽A降低多达56%和85%。共聚焦显微镜分析显示,对于ATCC 700407没有生物膜,对于DPC 5344只有死细胞。这些结果表明,乳链菌肽PV是有效减少携带NSR菌株生物膜形成的有前途的替代物。引起牛乳腺炎的四种最常见病原体之一是[此处原文缺失具体病原体名称]。其形成生物膜的能力使细菌对抗生素具有更大的抗性,需要更高剂量才能更有效。为了限制抗生素耐药性的发展,对替代抗菌剂的需求至关重要。诸如乳链菌肽之类的细菌素就是这样一种可以减轻由[此处原文缺失具体病原体名称]引起的乳腺炎影响的替代物。然而,许多[此处原文缺失具体病原体名称]菌株已被证明具有乳链菌肽抗性决定因素,例如乳链菌肽抗性蛋白(NSR)。在本研究中,我们证明了乳链菌肽和一种对NSR不敏感的名为PV的乳链菌肽衍生物预防和去除产生NSR的[此处原文缺失具体病原体名称]菌株生物膜的能力。这些发现将为抗菌细菌素以及特别是与生物膜和[此处原文缺失具体病原体名称]乳腺炎相关菌株的控制研究领域增添新信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b2f/8315181/15589c023357/aem.00391-21-f001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验