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培育囊性纤维化相关多微生物生物膜以探究群落表型。

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes.

机构信息

Département de Biologie, Université de Sherbrooke.

Département de Biologie, Université de Sherbrooke;

出版信息

J Vis Exp. 2024 Apr 19(206). doi: 10.3791/66785.

Abstract

Most in vitro models lack the capacity to fully probe bacterial phenotypes emerging from the complex interactions observed in real-life environments. This is particularly true in the context of hard-to-treat, chronic, and polymicrobial biofilm-based infections detected in the airways of individuals living with cystic fibrosis (CF), a multiorgan genetic disease. While multiple microbiome studies have defined the microbial compositions detected in the airway of people with CF (pwCF), no in vitro models thus far have fully integrated critical CF-relevant lung features. Therefore, a significant knowledge gap exists in the capacity to investigate the mechanisms driving the pathogenesis of mixed species CF lung infections. Here, we describe a recently developed four-species microbial community model, including Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus sanguinis, and Prevotella melaninogenica grown in CF-like conditions. Through the utilization of this system, clinically relevant phenotypes such as antimicrobial recalcitrance of several pathogens were observed and explored at the molecular level. The usefulness of this in vitro model resides in its standardized workflow that can facilitate the study of interspecies interactions in the context of chronic CF lung infections.

摘要

大多数体外模型缺乏充分探究真实环境中复杂相互作用所产生的细菌表型的能力。在治疗难度大、慢性和多微生物生物膜为基础的气道感染方面尤其如此,这些感染在囊性纤维化 (CF) 患者的气道中被检测到。CF 是一种多器官遗传疾病。虽然多项微生物组研究已经确定了在 CF 患者气道中检测到的微生物组成,但迄今为止还没有任何体外模型完全整合了关键的 CF 相关肺特征。因此,在研究混合物种 CF 肺部感染的发病机制方面存在着很大的知识差距。在这里,我们描述了一种最近开发的四物种微生物群落模型,包括铜绿假单胞菌、金黄色葡萄球菌、血链球菌和黑色素普雷沃氏菌,在 CF 样条件下生长。通过利用该系统,我们观察到了几种病原体的抗菌抗性等临床相关表型,并在分子水平上进行了探讨。该体外模型的有用之处在于其标准化的工作流程,可以促进在慢性 CF 肺部感染背景下研究种间相互作用。

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