The gut microbiota plays a protective role in the host defence against pneumococcal pneumonia

被引:670
作者
Schuijt, Tim J. [1 ,2 ,3 ]
Lankelma, Jacqueline M. [1 ]
Scicluna, Brendon P. [1 ]
e Melo, Felipe de Sousa [1 ]
Roelofs, Joris J. T. H. [4 ]
de Boer, J. Daan [1 ]
Hoogendijk, Arjan J. [1 ]
de Beer, Regina [1 ]
de Vos, Alex [1 ]
Belzer, Clara [5 ]
de Vos, Willem M. [5 ,6 ]
van der Poll, Tom [1 ,2 ]
Wiersinga, W. Joost [1 ,2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Ctr Expt & Mol Med, Meibergdreef 9,Room G2-130, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Med, Div Infect Dis, Meibergdreef 9,Room G2-130, NL-1105 AZ Amsterdam, Netherlands
[3] Diakonessen Hosp, Dept Clin Chem Hematol & Immunol, Utrecht, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Pathol, Meibergdreef 9,Room G2-130, NL-1105 AZ Amsterdam, Netherlands
[5] Wageningen Univ, Microbiol Lab, NL-6700 AP Wageningen, Netherlands
[6] Univ Helsinki, Dept Bacteriol & Immunol, Helsinki, Finland
关键词
INTESTINAL MICROBIOTA; BACTERIAL; SEPSIS; INFECTION; RESPONSES; RECOVERY; YOUNG; LUNG;
D O I
10.1136/gutjnl-2015-309728
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Pneumonia accounts for more deaths than any other infectious disease worldwide. The intestinal microbiota supports local mucosal immunity and is increasingly recognised as an important modulator of the systemic immune system. The precise role of the gut microbiota in bacterial pneumonia, however, is unknown. Here, we investigate the function of the gut microbiota in the host defence against Streptococcus pneumoniae infections. Design We depleted the gut microbiota in C57BL/6 mice and subsequently infected them intranasally with S. pneumoniae. We then performed survival and faecal microbiota transplantation (FMT) experiments and measured parameters of inflammation and alveolar macrophage whole-genome responses. Results We found that the gut microbiota protects the host during pneumococcal pneumonia, as reflected by increased bacterial dissemination, inflammation, organ damage and mortality in microbiota-depleted mice compared with controls. FMT in gut microbiota-depleted mice led to a normalisation of pulmonary bacterial counts and tumour necrosis factor-alpha and interleukin-10 levels 6 h after pneumococcal infection. Whole-genome mapping of alveolar macrophages showed upregulation of metabolic pathways in the absence of a healthy gut microbiota. This upregulation correlated with an altered cellular responsiveness, reflected by a reduced responsiveness to lipopolysaccharide and lipoteichoic acid. Compared with controls, alveolar macrophages derived from gut microbiota-depleted mice showed a diminished capacity to phagocytose S. pneumoniae. Conclusions This study identifies the intestinal microbiota as a protective mediator during pneumococcal pneumonia. The gut microbiota enhances primary alveolar macrophage function. Novel therapeutic strategies could exploit the gut-lung axis in bacterial infections.
引用
收藏
页码:575 / 583
页数:9
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