1. Use of 16S rRNA Gene-Targeted Group-Specific Primers for Real-Time PCR Analysis of Predominant Bacteria in Mouse Feces
- Author
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Jing Zhang, Zi-Chun Hua, Liangqiang He, Bingya Yang, Yunwen Yang, Xuerui Zhang, Xian-Jie Huang, and Mang-Kun Chen
- Subjects
Male ,Firmicutes ,Gut flora ,Real-Time Polymerase Chain Reaction ,Applied Microbiology and Biotechnology ,Microbiology ,Feces ,Mice ,RNA, Ribosomal, 16S ,Methods ,Animals ,Tenericutes ,Bacteria ,Ecology ,biology ,Verrucomicrobia ,Bacteroidetes ,Ribosomal RNA ,biology.organism_classification ,16S ribosomal RNA ,Gastrointestinal Microbiome ,Gastrointestinal Tract ,Mice, Inbred C57BL ,Proteobacteria ,Food Science ,Biotechnology - Abstract
Mouse models are widely used for studying gastrointestinal (GI) tract-related diseases. It is necessary and important to develop a new set of primers to monitor the mouse gut microbiota. In this study, 16S rRNA gene-targeted group-specific primers for Firmicutes , Actinobacteria , Bacteroidetes , Deferribacteres , “ Candidatus Saccharibacteria,” Verrucomicrobia , Tenericutes , and Proteobacteria were designed and validated for quantification of the predominant bacterial species in mouse feces by real-time PCR. After confirmation of their accuracy and specificity by high-throughput sequencing technologies, these primers were applied to quantify the changes in the fecal samples from a trinitrobenzene sulfonic acid-induced colitis mouse model. Our results showed that this approach efficiently predicted the occurrence of colitis, such as spontaneous chronic inflammatory bowel disease in transgenic mice. The set of primers developed in this study provides a simple and affordable method to monitor changes in the intestinal microbiota at the phylum level.
- Published
- 2015