Investigation of gut microbiome changes in type 1 diabetic mellitus rats based on high-throughput sequencing

Biomed Pharmacother. 2020 Apr:124:109873. doi: 10.1016/j.biopha.2020.109873. Epub 2020 Jan 24.

Abstract

The incidence of type 1 diabetes mellitus (T1DM) is increasing year by year, gut microbiota is considered to be closely related to the occurrence and development of T1DM in recent years. In this study, Sprague Dawley (SD) rats were intraperitoneally injected with 75mg/kg streptozotocin to establish T1DM model, fecal samples were collected and DNA were extracted, 16S rRNA microbial gene clone library were constructed, and lastly high-throughput sequencing and bioinformatics analysis were performed. The results showed that the abundances of pathogenic bacteria such as Ruminococcaceae, Shigella, Enterococcus, Streptococcus, Rothia and Alistipes associated with infection and inflammation in T1DM rats were up-regulated, while the abundances of beneficial bacteria such as Lactobacillus, Faecalitalea, Butyricicoccus and Allobaculum were reduced. Among them, Butyricicoccus and Allobaculum protect intestinal barrier function by producing short-chain fatty acids. This study suggests that intestinal inflammation and reduction of short chain fatty acids (SCFAs) caused by the imbalance of gut microbiota are crucial to the pathogenesis of T1DM.

Keywords: 16S rRNA sequencing; Analysis of correlation; Changes in abundance; Gut microbiome; Type 1 diabetes mellitus.

MeSH terms

  • Animals
  • Bacteria / isolation & purification
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / microbiology
  • Diabetes Mellitus, Experimental / physiopathology*
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / microbiology
  • Diabetes Mellitus, Type 1 / physiopathology*
  • Fatty Acids, Volatile / metabolism
  • Gastrointestinal Microbiome*
  • High-Throughput Nucleotide Sequencing
  • Inflammation / genetics
  • Inflammation / microbiology
  • Inflammation / pathology*
  • Male
  • RNA, Ribosomal, 16S
  • Rats
  • Rats, Sprague-Dawley
  • Streptozocin

Substances

  • Fatty Acids, Volatile
  • RNA, Ribosomal, 16S
  • Streptozocin