Yao Caiqing, Zhang Yu, You Lijun, E Jingjing, Wang Junguo
College of Food Science, Shanxi Normal University, Taiyuan, 030031, China.
School of Food Science and Engineering, Bohai University, Liaoning, 121013, China.
BMC Microbiol. 2025 Apr 29;25(1):258. doi: 10.1186/s12866-025-03985-7.
Due to the heterogeneity of the human gut environment, the gut microbiota is complex and diverse, and has been insufficiently explored. In this study, one fresh fecal sample was cultured using 12 commercial or modified media and incubation of culture plates anaerobically and aerobically, the conventional experienced colony picking (ECP) was first used to isolate the colonies and obtain pure culture strains. On this basis, all the colonies grown on the culture plates were collected for culture-enriched metagenomic sequencing (CEMS), and the original sample was also subjected to direct culture-independent metagenomic sequencing (CIMS), the study compared the effects of three methods for analyzing the microbiota contained in the sample. It was found that compared with CEMS, conventional ECP failed to detect a large proportion of strains grown in culture media, resulting in missed detection of culturable microorganisms in the gut. Microbes identified by CEMS and CIMS showed a low degree of overlap (18% of species), whereas species identified by CEMS and CIMS alone accounted for 36.5% and 45.5%, respectively. It suggests that both culture-dependent and culture-independent approaches are essential in revealing gut microbial diversity. Moreover, based on the CEMS results, growth rate index (GRiD) values for various strains on different media were calculated to predict the optimal medium for bacterial growth; this method can be used to design new media for intestinal microbial isolation, promote the recovery of specific microbiota, and obtain new insights into the human microbiome diversity. This is among the first studies on CEMS of the human gut microbiota.
由于人类肠道环境的异质性,肠道微生物群复杂多样,尚未得到充分研究。在本研究中,使用12种商业或改良培养基对一份新鲜粪便样本进行培养,并在厌氧和好氧条件下孵育培养平板,首先采用传统经验菌落挑选(ECP)方法分离菌落并获得纯培养菌株。在此基础上,收集培养平板上生长的所有菌落进行培养富集宏基因组测序(CEMS),同时对原始样本进行直接免培养宏基因组测序(CIMS),该研究比较了三种分析样本中微生物群方法的效果。结果发现,与CEMS相比,传统的ECP未能检测到在培养基中生长的大部分菌株,导致肠道中可培养微生物的漏检。通过CEMS和CIMS鉴定的微生物重叠度较低(物种的18%),而仅通过CEMS和CIMS鉴定的物种分别占36.5%和45.5%。这表明依赖培养和不依赖培养的方法对于揭示肠道微生物多样性都至关重要。此外,基于CEMS结果,计算了不同菌株在不同培养基上的生长速率指数(GRiD)值,以预测细菌生长的最佳培养基;该方法可用于设计新的肠道微生物分离培养基,促进特定微生物群的恢复,并获得对人类微生物组多样性的新认识。这是关于人类肠道微生物群CEMS的首批研究之一。