类固醇对哮喘病毒性恶化期间和健康小鼠微生物组的改变。

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Kazuma Yagi, Alexander D Ethridge, Nicole R Falkowski, Yvonne J Huang, Srikanth Elesela, Gary B Huffnagle, Nicholas W Lukacs, Wendy Fonseca, Nobuhiro Asai
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引用次数: 0

摘要

本研究评估了病毒加重哮喘反应与肺部类固醇治疗和非肺部类固醇治疗如何结合免疫反应改变微生物组,并得出了惊人的数据。总体研究结果表明,虽然类固醇治疗过敏性动物减轻了呼吸道合胞病毒(RSV)引起的气道功能恶化和粘液分泌过多的严重程度,但IL-17A的表达却出现了局部增加。对肺部和肠道微生物组的分析表明,氟替卡松(FLUT)治疗会进一步改变RSV恶化的差异。利用元基因组推断软件 PICRUSt2,我们能够预测肠道微生物组变化所产生的代谢物谱与多种代谢途径存在显著差异,并与氟替卡松(FLUT)或不氟替卡松(FLUT)的特定治疗相关。重要的是,通过测量血浆代谢物,我们的数据表明,慢性过敏原暴露、RSV 恶化和 FLUT 治疗都会引起显著变化。代谢物的变化来自宿主和微生物途径。为了了解气道类固醇本身是否会改变肺和肠道微生物组以及宿主对 RSV 感染的反应,在感染 RSV 之前用 FLUT 治疗了天真动物。在感染 RSV 之前使用 FLUT 的天真动物表现出了与微生物组改变和 PICRUSt2 元基因组推断分析相对应的疾病加重。总之,这些发现为确定严重病毒性加重过敏性疾病与微生物组变化之间的重要相关性奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiome modifications by steroids during viral exacerbation of asthma and in healthy mice.

In the present studies, the assessment of how viral exacerbation of asthmatic responses with and without pulmonary steroid treatment alters the microbiome in conjunction with immune responses presents striking data. The overall findings identify that although steroid treatment of allergic animals diminished the severity of the respiratory syncytial virus (RSV)-induced exacerbation of airway function and mucus hypersecretion, there were local increases in IL-17 expression. Analysis of the lung and gut microbiome suggested that there are differences in RSV exacerbation that are further altered by fluticasone (FLUT) treatment. Using metagenomic inference software, PICRUSt2, we were able to predict that the metabolite profile produced by the changed gut microbiome was significantly different with multiple metabolic pathways and associated with specific treatments with or without FLUT. Importantly, measuring plasma metabolites in an unbiased manner, our data indicate that there are significant changes associated with chronic allergen exposure, RSV exacerbation, and FLUT treatment that are reflective of responses to the disease and treatment. In addition, the changes in metabolites appeared to have contributions from both host and microbial pathways. To understand if airway steroids on their own altered lung and gut microbiome along with host responses to RSV infection, naïve animals were treated with lung FLUT before RSV infection. The naïve animals treated with FLUT before RSV infection demonstrated enhanced disease that corresponded to an altered microbiome and the related PICRUSt2 metagenomic inference analysis. Altogether, these findings set the foundation for identifying important correlations of severe viral exacerbated allergic disease with microbiome changes and the relationship of host metabolome with a potential for early life pulmonary steroid influence on subsequent viral-induced disease.NEW & NOTEWORTHY These studies outline a novel finding that airway treatment with fluticasone, a commonly used inhaled steroid, has significant effects on not only the local lung environment but also on the mucosal microbiome, which may have significant disease implications. The findings further provide data to support that pulmonary viral exacerbations of asthma with or without steroid treatment alter the lung and gut microbiome, which have an impact on the circulating metabolome that likely alters the trajectory of disease progression.

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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