生物
微生物学
空肠弯曲杆菌
16S核糖体RNA
弯曲杆菌
细菌
基因组
实时聚合酶链反应
致病菌
聚合酶链反应
肠道菌群
基因组
粪便
细菌遗传学
核糖体RNA
基因
遗传学
大肠杆菌
免疫学
作者
Teemu Rinttilä,Anna Kassinen,Erja Malinen,Lotta Krogius,Airi Palva
标识
DOI:10.1111/j.1365-2672.2004.02409.x
摘要
The microbiota of the human intestinal tract constitutes a complex ecosystem. We report the design and optimization of an extensive set of 16S rDNA-targeted species- and group-specific primers for more accurate quantification of bacteria from faecal samples with real-time PCR.A linear range of quantification between 0.1-10 pg and 10 ng of specific target genome was obtained, which corresponds to detection of ca 30-4500 to 1.9 x 10(6)-6.0 x 10(6) target bacterial genomes. Functionality of the assays was confirmed by quantification of target bacterial DNA from faecal DNA preparations of healthy volunteers and irritable bowel syndrome (IBS) patients. Additionally, spiking of faecal preparations with Helicobacter pylori, Clostridium difficile or Campylobacter jejuni was used to confirm the accurate and sensitive quantification.Real-time PCR is a very sensitive and precise technique for an extensive quantitative evaluation of gut microbiota and is feasible for detection of human pathogens from faecal samples.To design and optimize an extensive set of real-time PCR assays targeting a large group of predominant and pathogenic GI microbial species for further use in updating the current knowledge of the putative role of gut microbiota in health and disease.
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