Venzon Mericien, Bernard-Raichon Lucie, Klein Jon, Axelrad Jordan E, Zhang Chenzhen, Hussey Grant A, Sullivan Alexis P, Casanovas-Massana Arnau, Noval Maria G, Valero-Jimenez Ana M, Gago Juan, Putzel Gregory, Pironti Alejandro, Wilder Evan, Thorpe Lorna E, Littman Dan R, Dittmann Meike, Stapleford Kenneth A, Shopsin Bo, Torres Victor J, Ko Albert I, Iwasaki Akiko, Cadwell Ken, Schluter Jonas
Vilcek Institute of Graduate Biomedical Sciences, New York University Grossman School of Medicine, New York, NY, USA.
Kimmel Center for Biology and Medicine at the Skirball Institute, New York University Grossman School of Medicine, New York, NY, USA.
bioRxiv. 2022 Mar 2:2021.07.15.452246. doi: 10.1101/2021.07.15.452246.
The microbial populations in the gut microbiome have recently been associated with COVID-19 disease severity. However, a causal impact of the gut microbiome on COVID-19 patient health has not been established. Here we provide evidence that gut microbiome dysbiosis is associated with translocation of bacteria into the blood during COVID-19, causing life-threatening secondary infections. Antibiotics and other treatments during COVID-19 can potentially confound microbiome associations. We therefore first demonstrate in a mouse model that SARS-CoV-2 infection can induce gut microbiome dysbiosis, which correlated with alterations to Paneth cells and goblet cells, and markers of barrier permeability. Comparison with stool samples collected from 96 COVID-19 patients at two different clinical sites also revealed substantial gut microbiome dysbiosis, paralleling our observations in the animal model. Specifically, we observed blooms of opportunistic pathogenic bacterial genera known to include antimicrobial-resistant species in hospitalized COVID-19 patients. Analysis of blood culture results testing for secondary microbial bloodstream infections with paired microbiome data obtained from these patients indicates that bacteria may translocate from the gut into the systemic circulation of COVID-19 patients. These results are consistent with a direct role for gut microbiome dysbiosis in enabling dangerous secondary infections during COVID-19.
肠道微生物群中的微生物种群最近被认为与新冠肺炎疾病的严重程度有关。然而,肠道微生物群对新冠肺炎患者健康的因果影响尚未得到证实。在此,我们提供证据表明,肠道微生物群失调与新冠肺炎期间细菌向血液中的易位有关,会导致危及生命的继发性感染。新冠肺炎期间使用的抗生素和其他治疗方法可能会混淆微生物群的关联。因此,我们首先在小鼠模型中证明,新冠病毒感染可诱导肠道微生物群失调,这与潘氏细胞和杯状细胞的改变以及屏障通透性标志物相关。对来自两个不同临床地点的96名新冠肺炎患者粪便样本的比较也显示出明显的肠道微生物群失调,这与我们在动物模型中的观察结果一致。具体而言,我们在住院的新冠肺炎患者中观察到已知包含耐药菌的机会致病菌属大量繁殖。对这些患者进行的继发性微生物血流感染血培养结果分析以及配对的微生物群数据表明,细菌可能从肠道易位到新冠肺炎患者的体循环中。这些结果与肠道微生物群失调在新冠肺炎期间引发危险的继发性感染中所起的直接作用一致。
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