Wang Xiaoxin, Lu Huifang, Feng Zhou, Cao Jie, Fang Chao, Xu Xianming, Zhao Liping, Shen Jian
Key Laboratory of Systems Biomedicine (Ministry of Education), Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong UniversityShanghai, China.
State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong UniversityShanghai, China.
Front Microbiol. 2017 Jul 11;8:1242. doi: 10.3389/fmicb.2017.01242. eCollection 2017.
Human breast milk is recognized as one of multiple important sources of commensal bacteria for infant gut. Previous studies searched for the bacterial strains shared between breast milk and infant feces by isolating bacteria and performing strain-level bacterial genotyping, but only limited number of milk bacteria were identified to colonize infant gut, including bacteria from , , , and /. Here, to identify the breast milk bacteria capable of colonizing gut without the interference of bacteria of origins other than the milk or the necessity to analyze infant feces, normal chow-fed germ-free mice were orally inoculated with the breast milk collected from a mother 2 days after vaginal delivery. According to 16S rRNA gene-based denaturant gradient gel electrophoresis and Illumina sequencing, bacteria at >1% abundance in the milk inoculum were only (56.0%) and (37.4%), but in the feces of recipient mice were (80.3 ± 2.3%), (10.0 ± 2.6 %), (7.6 ± 1.6%), and (2.1 ± 0.5%) that were previously shown as dominant bacterial genera in the meconium of C-section-delivered human babies; the abundance of anaerobic gut-associated bacteria, , , , , and , was 0.01-1% in the milk inoculum and 0.003-0.01% in mouse feces; the abundance of spp. was below the detection limit of Illumina sequencing in the milk but at 0.003-0.01% in mouse feces. The human breast milk microbiota-associated mouse model may be used to identify additional breast milk bacteria that potentially colonize infant gut.
人乳被认为是婴儿肠道共生细菌的多个重要来源之一。以往的研究通过分离细菌并进行菌株水平的细菌基因分型,寻找母乳和婴儿粪便中共享的细菌菌株,但仅鉴定出有限数量的母乳细菌定殖于婴儿肠道,包括来自、、、和/的细菌。在此,为了鉴定能够在不受到除母乳之外其他来源细菌干扰或无需分析婴儿粪便的情况下定殖于肠道的母乳细菌,对正常喂食普通饲料的无菌小鼠口服接种从一位母亲阴道分娩后2天采集的母乳。根据基于16S rRNA基因的变性梯度凝胶电泳和Illumina测序,接种物中丰度>1%的细菌仅为(56.0%)和(37.4%),但在受体小鼠粪便中为(80.3±2.3%)、(10.0±2.6%)、(7.6±1.6%)和(2.1±0.5%),这些细菌先前在剖宫产分娩的人类婴儿胎粪中显示为优势细菌属;肠道厌氧相关细菌、、、、和在接种物中的丰度为0.01 - 1%,在小鼠粪便中的丰度为0.003 - 0.01%;spp.在母乳中的丰度低于Illumina测序的检测限,但在小鼠粪便中的丰度为0.003 - 0.01%。人乳微生物群相关小鼠模型可用于鉴定其他可能定殖于婴儿肠道的母乳细菌。