Aix Marseille Université, URMITE, UM63, CNRS 7278, IRD 198, INSERM 1095, 13005, Marseille, France.
Eur J Clin Microbiol Infect Dis. 2013 Nov;32(11):1471-81. doi: 10.1007/s10096-013-1900-2. Epub 2013 Jun 2.
The rebirth of bacterial culture has been highlighted successively by environmental microbiologists, the design of axenic culture for intracellular bacteria in clinical microbiology, and, more recently, by human gut microbiota studies. Indeed, microbial culturomics (large scale of culture conditions with the identification of colonies by MALDI-TOF or 16S rRNA) allowed to culture 32 new bacterial species from only four stool samples studied. We performed culturomics in comparison with pyrosequencing 16S rRNA targeting the V6 region on an anorexia nervosa stool sample because this clinical condition has never been explored before by culture, while its composition has been observed to be atypical by metagenomics. We tested 88 culture conditions generating 12,700 different colonies identifying 133 bacterial species, with 19 bacterial species never isolated from the human gut before, including 11 new bacterial species for which the genome has been sequenced. These 11 new bacterial species isolated from a single stool sample allow to extend more significantly the repertoire in comparison to the bacterial species validated by the rest of the world during the last 2 years. Pyrosequencing indicated a dramatic discrepancy with the culturomics results, with only 23 OTUs assigned to the species level overlapping (17 % of the culturomics results). Most of the sequences assigned to bacteria detected only by pyrosequencing belonged to Ruminococcaceae, Lachnospiraceae, and Erysipelotrichaceae constituted by strictly anaerobic species, indicating the future route for culturomics. This study revealed new bacterial species participating significantly to the extension of the gut microbiota repertoire, which is the first step before being able to connect the bacterial composition with the geographic or clinical status.
细菌培养的复兴已先后被环境微生物学家、临床微生物学中用于培养胞内细菌的无菌培养以及最近的人类肠道微生物组研究所强调。事实上,微生物培养组学(大量的培养条件,通过 MALDI-TOF 或 16S rRNA 鉴定菌落)仅从 4 个研究的粪便样本中就培养出了 32 个新的细菌物种。我们在厌食症粪便样本上进行了培养组学研究,与靶向 V6 区的焦磷酸测序 16S rRNA 进行了比较,因为这种临床情况以前从未通过培养进行过探索,而其组成通过宏基因组学观察到是非典型的。我们测试了 88 种培养条件,生成了 12700 个不同的菌落,鉴定出 133 种细菌,其中有 19 种细菌以前从未从人类肠道中分离出来,包括 11 种新的细菌,其基因组已经测序。从单个粪便样本中分离出的这 11 种新细菌与过去 2 年来世界其他地区验证的细菌物种相比,更显著地扩展了菌群谱。焦磷酸测序与培养组学结果存在显著差异,只有 23 个 OTU 被分配到种水平重叠(占培养组学结果的 17%)。大多数仅通过焦磷酸测序分配给细菌的序列属于 Ruminococcaceae、Lachnospiraceae 和 Erysipelotrichaceae,这些科由严格的厌氧菌组成,这表明了培养组学的未来方向。这项研究揭示了参与扩展肠道微生物群谱的新细菌物种,这是能够将细菌组成与地理或临床状况联系起来的第一步。