Molecular analysis of jejunal, ileal, caecal and recto-sigmoidal human colonic microbiota using 16S rRNA gene libraries and terminal restriction fragment length polymorphism

生物 末端限制性片段长度多态性 拟杆菌 微生物学 脆弱类杆菌 限制性片段长度多态性 16S核糖体RNA γ蛋白杆菌 真细菌 双歧杆菌 分子生物学 遗传学 乳酸菌 基因 聚合酶链反应 细菌 抗生素
作者
Hidenori Hayashi,Rei Takahashi,Takahiro Nishi,Mitsuo Sakamoto,Yoshimi Benno
出处
期刊:Journal of Medical Microbiology [Microbiology Society]
卷期号:54 (11): 1093-1101 被引量:335
标识
DOI:10.1099/jmm.0.45935-0
摘要

Microbiota in gut contents of jejunum, ileum, caecum and recto-sigmoid colon obtained from three elderly individuals at autopsy were compared using 16S rRNA gene libraries and terminal restriction fragment length polymorphism (T-RFLP). Random clones of 16S rRNA gene sequences were isolated after PCR amplification with universal primer sets of total genomic DNA extracted from each sample of gut contents. An average of 90 randomly selected clones were partially sequenced (about 500 bp). T-RFLP analysis was performed using the 16S rRNA gene amplified from each sample. The lengths of the terminal restriction fragments were analysed after digestion with Hha I and Msp I. The jejunal and ileal microbiota consisted of simple microbial communities of streptococci, lactobacilli, ‘ Gammaproteobacteria ', the Enterococcus group and the Bacteroides group. Most of the species were facultative anaerobes or aerobes. The Clostridium coccoides group and the Clostridium leptum subgroup, which are the most predominant groups in human faeces, were not detected in samples from the upper gastrointestinal tract. The caecal microbiota was more complex than the jejunal and ileal microbiota. The C . coccoides group, the C . leptum subgroup and the Bacteroides group were detected in the caecum. The recto-sigmoidal colonic microbiota consisted of complex microbial communities, with numerous species that belonged to the C. coccoides group, the C. leptum subgroup, the Bacteroides group, ‘ Gammaproteobacteria ', the Bifidobacterium group, streptococci and lactobacilli, and included more than 26 operational taxonomic units. The results showed marked individual differences in the composition of microbiota in each region.
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