Change of Intestinal Microbiota in Mice Model of Bronchopulmonary Dysplasia
Abstract Background: Gut microbiota has been proposed to be related to the pathogenesis of pulmonary diseases such as asthma and lung cancer, according to the gut-lung axis. However, little is known about the relationship between broncho-pulmonary dysplasia (BPD) and gut microbiota. This study was designed to investigate the changes of gut microbiota in neonatal mice with BPD. Methods: BPD model was induced through exposure to high concentration of oxygen. HE staining was utilized to determine the modeling efficiency. Stool samples were collected from the distal colon for the sequencing of V3-V4 regions of 16S rRNA, in order to analyze the gut microbiota diversity.Results: BPD models were established in this study. Alpha diversity indicated that there were no statistical differences in the abundance of gut microbiota between model group and control group. On day 14, there were statistical differences in the genetic diversity between two groups (p<0.05). Beta diversity analysis showed that there were statistical differences in the gut microbiota on day 14 (R=0.368, p=0.021). Line discriminant analysis (LDA) showed that there were 22 markers with statistical differences on day 14 (p<0.05), while those on day 7 and 21 were 3 and 4, respectively. Functional prediction analysis showed that the top 3 metabolic pathways were signal transduction (PFDR=0.037), glycan biosynthesis and metabolism (PFDR=0.032), and metabolism of terpenoids and polyketides (PFDR=0.049). Conclusions: BPD mice showed disorder of gut microbiota, which may involve with specific metabolic pathways in the early stage. In the presence of intestinal maturity in mice, the differences of the gut microbiota between the two groups would gradually disappear.