Different culture media and purification methods unveil the core proteome of Propionibacterium freudenreichii-derived extracellular vesicles.

microLife Pub Date : 2023-01-01 DOI:10.1093/femsml/uqad029
Vinícius de Rezende Rodovalho, Brenda Silva Rosa da Luz, Aurélie Nicolas, Julien Jardin, Valérie Briard-Bion, Edson Luiz Folador, Anderson Rodrigues Santos, Gwénaël Jan, Yves Le Loir, Vasco Ariston de Carvalho Azevedo, Éric Guédon
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引用次数: 1

Abstract

Bacterial extracellular vesicles (EVs) are natural lipidic nanoparticles implicated in intercellular communication. Although EV research focused mainly on pathogens, the interest in probiotic-derived EVs is now rising. One example is Propionibacterium freudenreichii, which produces EVs with anti-inflammatory effects on human epithelial cells. Our previous study with P. freudenreichii showed that EVs purified by size exclusion chromatography (SEC) displayed variations in protein content according to bacterial growth conditions. Considering these content variations, we hypothesized that a comparative proteomic analysis of EVs recovered in different conditions would elucidate whether a representative vesicular proteome existed, possibly providing a robust proteome dataset for further analysis. Therefore, P. freudenreichii was grown in two culture media, and EVs were purified by sucrose density gradient ultracentrifugation (UC). Microscopic and size characterization confirmed EV purification, while shotgun proteomics unveiled that they carried a diverse set of proteins. A comparative analysis of the protein content of UC- and SEC-derived EVs, isolated from cultures either in UF (cow milk ultrafiltrate medium) or YEL (laboratory yeast extract lactate medium), showed that EVs from all these conditions shared 308 proteins. This EV core proteome was notably enriched in proteins related to immunomodulation. Moreover, it showed distinctive features, including highly interacting proteins, compositional biases for some specific amino acids, and other biochemical parameters. Overall, this work broadens the toolset for the purification of P. freudenreichii-derived EVs, identifies a representative vesicular proteome, and enumerates conserved features in vesicular proteins. These results hold the potential for providing candidate biomarkers of purification quality, and insights into the mechanisms of EV biogenesis and cargo sorting.

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不同的培养基和纯化方法揭示了弗氏丙酸杆菌来源的细胞外囊泡的核心蛋白质组。
细菌细胞外囊泡(EVs)是参与细胞间通讯的天然脂质纳米颗粒。虽然电动汽车的研究主要集中在病原体上,但对益生菌衍生的电动汽车的兴趣正在上升。一个例子是弗氏丙酸杆菌,它产生的ev对人上皮细胞具有抗炎作用。我们之前对弗氏假单胞菌的研究表明,通过大小排斥层析(SEC)纯化的ev蛋白含量根据细菌生长条件的不同而变化。考虑到这些含量变化,我们假设对不同条件下恢复的ev进行比较蛋白质组学分析将阐明是否存在具有代表性的囊泡蛋白质组,可能为进一步分析提供一个强大的蛋白质组数据集。因此,在两种培养基中培养弗氏假单胞菌,并采用蔗糖密度梯度超离心(UC)纯化ev。显微镜和大小表征证实了EV的纯化,而鸟枪蛋白质组学揭示了它们携带了多种蛋白质。对比分析UC-和sec衍生的EVs的蛋白质含量,分别从UF(牛奶超滤培养基)和YEL(实验室酵母提取物乳酸培养基)培养基中分离,结果表明,所有这些条件下的EVs共有308种蛋白质。该EV核心蛋白质组显著富集与免疫调节相关的蛋白质。此外,它还显示出一些独特的特征,包括高度相互作用的蛋白质、某些特定氨基酸的组成偏差和其他生化参数。总的来说,这项工作拓宽了纯化弗氏假单胞菌衍生的ev的工具集,鉴定了一个具有代表性的囊泡蛋白质组,并列举了囊泡蛋白的保守特征。这些结果有可能提供纯化质量的候选生物标志物,并深入了解EV生物发生和货物分选的机制。
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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