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通过核糖体DNA序列分析研究人类结肠生物群。

Human colonic biota studied by ribosomal DNA sequence analysis.

作者信息

Wilson K H, Blitchington R B

机构信息

Infectious Diseases Section, VA Medical Center, Durham, NC 27705, USA.

出版信息

Appl Environ Microbiol. 1996 Jul;62(7):2273-8. doi: 10.1128/aem.62.7.2273-2278.1996.

Abstract

Human colonic biota is a complex microbial ecosystem that serves as a host defense. Unlike most microbial ecosystems, its composition has been studied extensively by relatively efficient culture methods. We have compared an established culture-based method with direct amplification and partial sequencing of cloned 16S rRNA genes from a human fecal specimen. Nine cycles of PCR were also compared with 35 cycles. Colonies and cloned amplicons were classified by comparing their ribosomal DNA (rDNA; DNA coding for rRNA) sequences with rDNA sequences of known phylogeny. Quantitative culture recovered 58% of the microscopic count. The 48 colonies identified gave 21 rDNA sequences; it was estimated that 72% of the rDNA sequences from the total population of culturable cells would match these 21 sampled sequences (72% coverage). Fifty 9-cycle clones gave 27 sequences and 59% coverage of cloned rDNAs. Thirty-nine rDNAs cloned after 35 cycles of PCR gave 13 sequences for 74% coverage. Thus, the representation of the ecosystem after 35 cycles of PCR was distorted and lacked diversity. However, when the number of temperature cycles was minimized, biodiversity was preserved, and there was good agreement between culturing bacteria and sampling rDNA directly.

摘要

人类结肠生物群是一个作为宿主防御的复杂微生物生态系统。与大多数微生物生态系统不同,其组成已通过相对有效的培养方法进行了广泛研究。我们将一种既定的基于培养的方法与从人类粪便标本中直接扩增和部分测序克隆的16S rRNA基因进行了比较。还比较了9个PCR循环与35个循环。通过将菌落和克隆扩增子的核糖体DNA(rDNA;编码rRNA的DNA)序列与已知系统发育的rDNA序列进行比较来进行分类。定量培养回收了显微镜计数的58%。鉴定出的48个菌落产生了21个rDNA序列;据估计,可培养细胞总数的rDNA序列中有72%与这21个采样序列匹配(覆盖率72%)。50个9循环克隆产生了27个序列,克隆rDNA的覆盖率为59%。35个PCR循环后克隆的39个rDNA产生了13个序列,覆盖率为74%。因此,35个PCR循环后生态系统的代表性被扭曲且缺乏多样性。然而,当温度循环次数减到最少时,生物多样性得以保留,并且培养细菌与直接采样rDNA之间有很好的一致性。

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