Carolin Agnes, Frazer David, Yan Kexin, Bishop Cameron R, Tang Bing, Nguyen Wilson, Helman Sheridan L, Horvat Jay, Larcher Thibaut, Rawle Daniel J, Suhrbier Andreas
Inflammation Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Molecular Nutrition, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Front Microbiol. 2024 Sep 4;15:1441495. doi: 10.3389/fmicb.2024.1441495. eCollection 2024.
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/6 J mice by feeding standard low and high iron diets, with mice on a normal iron diet representing controls. All mice were infected with a primary SARS-CoV-2 omicron XBB 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.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)的严重程度通常由一系列合并症决定。大量文献表明,缺铁和铁过载可能导致感染增加、炎症和疾病严重程度加重,尽管难以确定直接的因果关系。
在这里,我们通过喂食标准的低铁和高铁饮食来培育缺铁和铁过载的C57BL/6 J小鼠,以正常铁饮食的小鼠作为对照。所有小鼠均感染了一种主要的SARS-CoV-2奥密克戎XBB毒株,并通过组织学、免疫组织化学和RNA测序分析肺部炎症反应。
与对照组相比,缺铁小鼠的肺部病毒载量和组织病理学无显著变化,而铁过载小鼠的肺部病毒载量和组织病理学有轻微但显著的降低。转录变化不大,但表明缺铁组与对照组、铁过载组与对照组之间炎症特征存在广泛的失调。其中一些变化可能与有害结果相关,而其他变化则被视为有益的。
因此,饮食相关的缺铁或铁过载会引起炎症特征的适度调节,但不会导致组织病理学上可检测到的明显疾病加重。