Wang Fan, Yu Lingmin, Ren Yuting, Zhang Qianwen, He Shanshan, Zhao Minlei, He Zhili, Gao Qi, Chen Jianguo
Beijing YuGen Pharmaceutical Co., Ltd., Beijing, China.
YingTan City people's Hospital, Yingtan, China.
Front Microbiol. 2024 Mar 1;15:1272062. doi: 10.3389/fmicb.2024.1272062. eCollection 2024.
Viable microorganisms and a diverse microbial ecosystem found in human milk play a crucial role in promoting healthy immune system and shaping the microbial community in the infant's gut. Culturomics is a method to obtain a comprehensive repertoire of human milk microbiota. However, culturomics is an onerous procedure, and needs expertise, making it difficult to be widely implemented. Currently, there is no efficient and feasible culturomics method specifically designed for human milk microbiota yet. Therefore, the aim of this study was to develop a more efficient and feasible culturomics method specifically designed for human milk microbiota. We obtained fresh samples of human milk from healthy Chinese mothers and conducted a 27-day enrichment process using blood culture bottles. Bacterial isolates were harvested at different time intervals and cultured on four different types of media. Using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, we identified a total of 6601 colonies and successfully obtained 865 strains, representing 4 phyla, 21 genera, and 54 species. By combining CBA and MRS media, we were able to cultivate over 94.4% of bacterial species with high diversity, including species-specific microorganisms. Prolonged pre-incubation in blood culture bottles significantly increased the number of bacterial species by about 33% and improved the isolation efficiency of beneficial bacteria with low abundance in human milk. After optimization, we reduced the pre-incubation time in blood culture bottles and selected optimal picking time-points (0, 3, and 6 days) at 37°C. By testing 6601 colonies using MALDI-TOF MS, we estimated that this new protocol could obtain more than 90% of bacterial species, reducing the workload by 57.0%. In conclusion, our new culturomics strategy, which involves the combination of CBA and MRS media, extended pre-incubation enrichment, and optimized picking time-points, is a feasible method for studying the human milk microbiota. This protocol significantly improves the efficiency of culturomics and allows for the establishment of a comprehensive repertoire of bacterial species and strains in human milk.
人乳中存在的活微生物和多样的微生物生态系统在促进健康免疫系统和塑造婴儿肠道微生物群落方面发挥着关键作用。培养组学是一种获取人乳微生物群综合信息库的方法。然而,培养组学是一个繁琐的过程,需要专业知识,这使得它难以广泛实施。目前,还没有专门为人乳微生物群设计的高效可行的培养组学方法。因此,本研究的目的是开发一种专门为人乳微生物群设计的更高效可行的培养组学方法。我们从健康的中国母亲那里获取了新鲜的人乳样本,并使用血培养瓶进行了为期27天的富集过程。在不同时间间隔收集细菌分离物,并在四种不同类型的培养基上培养。使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析,我们共鉴定出6601个菌落,并成功获得865株菌株,代表4个门、21个属和54个种。通过结合CBA和MRS培养基,我们能够培养出94.4%以上具有高度多样性的细菌物种,包括特定物种的微生物。在血培养瓶中延长预培养时间显著增加了细菌物种数量约33%,并提高了人乳中低丰度有益细菌的分离效率。优化后,我们缩短了血培养瓶中的预培养时间,并选择了在37°C下的最佳挑取时间点(0、3和6天)。通过使用MALDI-TOF MS测试6601个菌落,我们估计这个新方案可以获得90%以上的细菌物种,将工作量减少57.0%。总之,我们的新培养组学策略,包括结合CBA和MRS培养基、延长预培养富集和优化挑取时间点,是一种研究人乳微生物群的可行方法。该方案显著提高了培养组学的效率,并允许建立人乳中细菌物种和菌株的综合信息库。