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Microbiological Survey of the Human Gastric Ecosystem Using Culturing and Pyrosequencing Methods

机译:利用培养和焦磷酸测序方法对人胃生态系统进行微生物学调查

摘要

Stomach mucosa biopsies and gastric juices samples of 12 healthy persons were analysed by culturing in selective- and non-selective-rich media. Microbial DNA from four mucosal samples was also amplified by nested PCR using universal bacterial primers, and the 16S rDNA amplicons pyrosequenced. The total number of cultivable microorganisms recovered from the samples ranged from 102 to 104 cfu/g or ml. The isolates were identified at the species level by PCR amplification and sequencing of the 16S rDNA. Isolates belonged mainly to four genera; Propionibacterium, Lactobacillus, Streptococcus and Staphylococcus. A total of 15,622 high-quality 16S rDNA sequence reads were obtained by pyrosequencing from the four mucosal samples. Sequence analysis grouped the reads into 59 families and 69 genera, revealing wide bacterial diversity. Considerable differences in the composition of the gastric microbiota were observed among the subjects, although in all samples the most abundant operational taxonomic units belonged to Streptococcus, Propionibacterium and Lactobacillus. Comparison of the stomach microbiota with that present in other parts of the human gastrointestinal tract revealed distinctive microbial communities. This is the first study in which a combination of culture and culture-independent techniques has been used to explore the bacterial diversity of the human stomach. © 2013 Springer Science+Business Media New York.
机译:通过在富含选择性和非选择性富集培养基中培养,对12位健康人的胃黏膜活检和胃液样品进行了分析。还使用通用细菌引物通过巢式PCR扩增了四个粘膜样品中的微生物DNA,并对16S rDNA扩增子进行了焦磷酸测序。从样品中回收的可培养微生物总数为102至104 cfu / g或ml。通过16S rDNA的PCR扩增和测序在物种水平上鉴定出分离株。分离株主要属于四个属。丙酸杆菌,乳杆菌,链球菌和葡萄球菌。通过焦磷酸测序从四个粘膜样品中获得了总计15,622个高质量16S rDNA序列读数。序列分析将这些读数分为59个家族和69个属,揭示了广泛的细菌多样性。在受试者之间观察到胃微生物群组成的显着差异,尽管在所有样品中,最丰富的操作分类单位属于链球菌,丙酸杆菌和乳杆菌。胃微生物群与人胃肠道其他部位的微生物群的比较显示出独特的微生物群落。这是第一项研究,其中结合了文化和文化独立技术来探索人胃中细菌的多样性。 ©2013纽约Springer Science + Business Media。

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