Lung and gut microbiota are altered by hyperoxia and contribute to oxygen-induced lung injury in mice

被引:103
作者
Ashley, Shanna L. [1 ]
Sjoding, Michael W. [1 ,2 ,3 ]
Popova, Antonia P. [4 ]
Cui, Tracy X. [4 ]
Hoostal, Matthew J. [5 ]
Schmidt, Thomas M. [5 ,6 ]
Branton, William R. [1 ]
Dieterle, Michael G. [5 ,6 ]
Falkowski, Nicole R. [1 ]
Baker, Jennifer M. [1 ,6 ]
Hinkle, Kevin J. [1 ]
Konopka, Kristine E. [7 ]
Erb-Downward, John R. [1 ]
Huffnagle, Gary B. [1 ,6 ,8 ,9 ]
Dickson, Robert P. [1 ,3 ,6 ]
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Div Pulm & Crit Care Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Computat Med & Bioinformat, Ann Arbor, MI USA
[3] Michigan Ctr Integrat Res Crit Care, Ann Arbor, MI 48104 USA
[4] Univ Michigan, Sch Med, Dept Pediat, Div Pediat Pulmonol, Ann Arbor, MI USA
[5] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USA
[6] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI USA
[8] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[9] Univ Michigan, Mary H Weiser Food Allergy Ctr, Ann Arbor, MI 48109 USA
关键词
RESPIRATORY-DISTRESS-SYNDROME; INFLAMMATORY RESPONSE; BACTERIA; PERMEABILITY; PNEUMONIA; INCREASES; MORTALITY; TOXICITY; CATALASE; VIRULENT;
D O I
10.1126/scitranslmed.aau9959
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inhaled oxygen, although commonly administered to patients with respiratory disease, causes severe lung injury in animals and is associated with poor clinical outcomes in humans. The relationship between hyperoxia, lung and gut microbiota, and lung injury is unknown. Here, we show that hyperoxia conferred a selective relative growth advantage on oxygen-tolerant respiratory microbial species (e.g., Staphylococcus aureus) as demonstrated by an observational study of critically ill patients receiving mechanical ventilation and experiments using neonatal and adult mouse models. During exposure of mice to hyperoxia, both lung and gut bacterial communities were altered, and these communities contributed to oxygen-induced lung injury. Disruption of lung and gut microbiota preceded lung injury, and variation in microbial communities correlated with variation in lung inflammation. Germ-free mice were protected from oxygen-induced lung injury, and systemic antibiotic treatment selectively modulated the severity of oxygen-induced lung injury in conventionally housed animals. These results suggest that inhaled oxygen may alter lung and gut microbial communities and that these communities could contribute to lung injury.
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页数:15
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