期刊论文详细信息
BMC Microbiology
Gut microbiota characteristics in mice with antibiotic-associated diarrhea
article
Shao, Haoqing1  Zhang, Chenyang1  Xiao, Nenqun3  Tan, Zhoujin2 
[1]School of Traditional Chinese Medicine, Hunan University of Chinese Medicine
[2]Hunan Key Laboratory of TCM Prescription and Syndromes Translational Medicine
[3]School of Pharmaceutical Science, Hunan University of Chinese Medicine
[4]School of Medicine, Hunan University of Chinese Medicine
关键词: Gut microbiota;    Antibiotic-associated diarrhea;    Gentamicin;    Cefradine;    Enterococcus;    Clostridium;    16S rRNA gene sequencing;   
DOI  :  10.1186/s12866-020-01999-x
学科分类:放射科、核医学、医学影像
来源: BioMed Central
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【 摘 要 】
Antibiotic-associated diarrhea (AAD), defined as diarrhea that occurs in association with the administration of antibiotics and without another clear etiology, is one of the most common adverse drug events of antibiotics therapy. We established a diarrhea model induced by gentamycin and cefradine to investigate the microbiota characteristics in the intestinal lumen of mice with AAD and provide insights into noteworthy bacteria related to gentamicin and cefradine-associated diarrhea. The number of OTUs in the model group and the normal group was 983 and 2107, respectively, and 872 identical OTUs were shared between two groups. Species richness and species diversity of intestinal microbe were altered by antibiotics administration. PCoA showed a clear separation between AAD and health control. The dominant phyla of AAD mice were Firmicutes (52.63%) and Proteobacteria (46.37%). Among the genus with top 20 abundance, the relative abundance of 7 genera, Ruminococcus, Blautia, Enterococcus, Eubacterium, Clostridium, Coprococcus, and Aerococcus, were enriched in the model group. Based upon the LEfSe analysis, Enterococcus, Eubacterium, Ruminococcus, and Blautia were identified as potential biomarkers for AAD. The bacterial diversity of the intestinal lumen was diminished after gentamicin and cefradine administration. The alterations in the abundance and composition of gut microbiota further led to the dysfunction of gut microbiota. More specifically, gentamicin and cefradine significantly increased the abundance of the opportunistic pathogens, of which Enterococcus and Clostridium were the most prominent and most worthy of attention.
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