来自毒性巴西褐藻的胞外囊泡能诱导先天性细胞中TLR4和dectin-1的表达,并促进Th1/Th17反应的增强。

IF 5.5 1区 农林科学 Q1 IMMUNOLOGY
Virulence Pub Date : 2024-12-01 Epub Date: 2024-03-21 DOI:10.1080/21505594.2024.2329573
Bruno Montanari Borges, Monique Gama de Santana, Nycolas Willian Preite, Valéria de Lima Kaminski, Gabriel Trentin, Fausto Almeida, Flávio Vieira Loures
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引用次数: 0

摘要

细胞外囊泡(EVs)是一种膜封闭的纳米颗粒,可运输多种生物大分子,并参与真菌疾病病理生理学相关的重要机制和功能。副球孢子菌病(PCM)的主要致病菌--巴西副球孢子菌的 EVs 可调节巨噬细胞的免疫反应。在这项研究中,我们评估了从肉芽肿病灶中分离出的毒性巴西副球孢子菌 EVs 蛋白质组,并比较了它们与动物通过前从真菌中分离出的 EVs(对照 EVs)在挑战巨噬细胞和树突状细胞(DCs)时的免疫调节能力。蛋白质组显示,与对照 EVs 相比,毒性 EVs 有更多的毒力因子,如 GP43、蛋白 14-3-3、GAPDH,以及在 PCM 中从未描述过的毒力因子,如天冬氨肽酶和 SidJ 类似物。在巨噬细胞和树突状细胞(DC)中,病毒性细胞外囊泡诱导的 TLR4 和 Dectin-1 表达高于对照 EV。相反,毒性细胞外小泡诱导的 TLR2 表达较低。此外,毒力EVs诱导的CD80、CD86和TNF-α表达量较低,但促进的IL-6和IL-10表达量较高,这表明从毒力巴西酵母中分离出的EVs促进了较温和的DC和巨噬细胞成熟。在这里,我们发现毒力真菌的EVs刺激了更高频率的Th1/Tc1、Th17和Treg细胞,这为真菌胞外囊泡的研究提供了新的视角。综上所述,我们的研究结果表明,巴西鹅膏菌利用其细胞外囊泡作为毒力包,操纵免疫系统,从而产生较温和的免疫反应,帮助真菌逃避免疫系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular vesicles from virulent P. brasiliensis induce TLR4 and dectin-1 expression in innate cells and promote enhanced Th1/Th17 response.

Extracellular vesicles (EVs) are membrane-enclosed nanoparticles that transport several biomolecules and are involved in important mechanisms and functions related to the pathophysiology of fungal diseases. EVs from Paracoccidioides brasiliensis, the main causative agent of Paracoccidioidomycosis (PCM), modulate the immune response of macrophages. In this study, we assessed the EVs proteome from a virulent P. brasiliensis isolated from granulomatous lesions and compared their immunomodulatory ability with EVs isolated from the fungus before the animal passage (control EVs) when challenging macrophages and dendritic cells (DCs). Proteome showed that virulent EVs have a higher abundance of virulence factors such as GP43, protein 14-3-3, GAPDH, as well as virulence factors never described in PCM, such as aspartyl aminopeptidase and a SidJ analogue compared with control EVs. Virulent extracellular vesicles induced higher expression of TLR4 and Dectin-1 than control EVs in macrophages and dendritic cells (DCs). In opposition, a lower TLR2 expression was induced by virulent EVs. Additionally, virulent EVs induced lower expression of CD80, CD86 and TNF-α, but promoted a higher expression of IL-6 and IL-10, suggesting that EVs isolated from virulent P. brasiliensis-yeast promote a milder DCs and macrophage maturation. Herein, we showed that EVs from virulent fungi stimulated a higher frequency of Th1/Tc1, Th17, and Treg cells, which gives new insights into fungal extracellular vesicles. Taken together, our results suggest that P. brasiliensis utilizes its EVs as virulence bags that manipulate the immune system in its favour, creating a milder immune response and helping with fungal evasion from the immune system.

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来源期刊
Virulence
Virulence IMMUNOLOGY-MICROBIOLOGY
CiteScore
9.20
自引率
1.90%
发文量
123
审稿时长
6-12 weeks
期刊介绍: Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication. Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.
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