缺铁和高铁饮食对 SARS-CoV-2 肺部感染和疾病的影响

Agnes Carolin, David Frazer, Kexin Yan, Cameron R. Bishop, Bing Tang, Wilson Nguyen, Sheridan L. Helman, Jay Horvat, Thibaut Larcher, Daniel J. Rawle, Andreas Suhrbier
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引用次数: 0

摘要

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的冠状病毒病 2019(COVID-19)的严重程度往往取决于一系列合并症。大量文献表明,缺铁和铁超载可能会导致感染、炎症和疾病严重程度的增加,但直接的因果关系一直难以确定。在此,我们通过喂食低铁和高铁饮食来产生缺铁和铁负荷的 C57BL/6J 小鼠,并以正常铁饮食的小鼠作为对照。所有小鼠都感染了原代 omicron XXB SARS-CoV-2 分离物,并通过组织学、免疫组化和 RNA-Seq 分析了肺部炎症反应。与对照组相比,缺铁小鼠的肺部病毒载量和组织病理学无明显变化,而含铁小鼠的肺部病毒载量和组织病理学则略有减少,但变化明显。转录变化不大,但说明缺铁小鼠与对照组、铁负荷小鼠与对照组的炎症特征都普遍失调。其中一些变化可能与有害结果有关,而另一些变化则被认为是有益的。因此,与饮食相关的缺铁或铁超载会诱发炎症特征的适度改变,但组织病理学上无法检测到明显的疾病恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of iron deficient and high iron diets on SARS-CoV-2 lung infection and disease
The severity of Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is often dictated by a range of comorbidities. A considerable literature suggests iron deficiency and iron overload may contribute to increased infection, inflammation and disease severity, although direct causal relationships have been difficult to establish. Here we generate iron deficient and iron loaded C57BL/6J mice by feeding low and high iron diets, with mice on a normal iron diet representing controls. All mice were infected with a primary omicron XXB SARS-CoV-2 isolate and lung inflammatory responses were analyzed by histology, immunohistochemistry and RNA-Seq. Compared with controls, iron deficient mice showed no significant changes in lung viral loads or histopathology, whereas, iron loaded mice showed slightly, but significantly, reduced lung viral loads and histopathology. Transcriptional changes were modest, but illustrated widespread dysregulation of inflammation signatures for both iron deficient vs. controls, and iron loaded vs. controls. Some of these changes could be associated with detrimental outcomes, whereas others would be viewed as beneficial. Diet-associated iron deficiency or overload thus induced modest modulations of inflammatory signatures, but no significant histopathologically detectable disease exacerbations.
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