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生物膜形成过程中[具体物质]与[具体物质]之间相互作用的体外分析。 (你提供的原文中“and”前后缺少具体内容)

In Vitro Analysis of Interactions Between and During Biofilm Formation.

作者信息

Scaffo Julia, Lima Rayssa Durães, Dobrotka Cameron, Ribeiro Tainara A N, Pereira Renata F A, Sachs Daniela, Ferreira Rosana B R, Aguiar-Alves Fabio

机构信息

Molecular Epidemiology and Biotechnology Laboratory, Fluminense Federal University, Niteroi 24241-000, Brazil.

Postgraduate Program in Sciences Applied to Health Products, Fluminense Federal University, Niteroi 24241-000, Brazil.

出版信息

Antibiotics (Basel). 2025 May 14;14(5):504. doi: 10.3390/antibiotics14050504.

Abstract

UNLABELLED

and are classified as ESKAPE pathogens that present a significant challenge to treatment due to their increased resistance to a considerable number of antimicrobial agents. Background/Objective Biofilms exacerbate treatment challenges by providing enhanced antimicrobial and environmental protection. Mixed-species biofilms further complicate treatment options through numerous complex interspecies interactions, leading to potentially severe adverse clinical outcomes.

METHODS

This study assessed the interaction between clinical and isolates during biofilm formation using microplate biofilm formation assays, scanning electron microscopy, and confocal microscopy.

RESULTS

We identified a competitive relationship between and , where both pathogens exhibited a reduction in biofilm formation during mixed-species biofilms compared with monocultures, although outcompeted . Furthermore, we found that the cell-free conditioned media (CFCM) of significantly reduced the biofilms. Using fractioned CFCM, we identified that the anti-staphylococcal activity of the >10 kDa fraction was almost identical to the non-fractioned CFCM. Our confocal microscopy results suggest that CFCM depolarize membranes and reduces the biofilm burden.

CONCLUSIONS

These findings contribute to our understanding of the mechanisms underlying the interactions between these pathogens, suggesting that there is an antagonistic relationship between and in a biofilm setting.

摘要

未标记

[病原体名称1]和[病原体名称2]被归类为ESKAPE病原体,由于它们对大量抗菌药物的耐药性增加,给治疗带来了重大挑战。背景/目的 生物膜通过提供增强的抗菌和环境保护加剧了治疗挑战。混合物种生物膜通过众多复杂的种间相互作用使治疗选择更加复杂,导致潜在的严重不良临床结果。

方法

本研究使用微孔板生物膜形成试验、扫描电子显微镜和共聚焦显微镜评估了临床[病原体名称1]和[病原体名称2]分离株在生物膜形成过程中的相互作用。

结果

我们确定了[病原体名称1]和[病原体名称2]之间的竞争关系,与单培养相比,在混合物种生物膜形成过程中,两种病原体的生物膜形成均减少,尽管[病原体名称1]胜过[病原体名称2]。此外,我们发现[病原体名称1]的无细胞条件培养基(CFCM)显著减少了[病原体名称2]的生物膜。使用分级CFCM,我们发现分子量大于10 kDa的级分的抗葡萄球菌活性与未分级的CFCM几乎相同。我们的共聚焦显微镜结果表明,[病原体名称1]的CFCM使[病原体名称2]的膜去极化并减轻了生物膜负担。

结论

这些发现有助于我们理解这些病原体之间相互作用的潜在机制,表明在生物膜环境中[病原体名称1]和[病原体名称2]之间存在拮抗关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd5c/12108489/11d2845c5f79/antibiotics-14-00504-g001.jpg

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