Verster Adrian J, Salerno Paige, Valls Rebecca, Barrack Kaitlyn, Price Courtney E, McClure Emily A, Madan Juliette C, O'Toole George A, Sanville Julie L, Ross Benjamin D
Department of Microbiology and Immunology, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire, USA.
Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire, USA.
mBio. 2025 Mar 12;16(3):e0342024. doi: 10.1128/mbio.03420-24. Epub 2025 Feb 13.
The healthy human infant gut microbiome undergoes stereotypical changes in taxonomic composition between birth and maturation to an adult-like stable state. During this time, extensive communication between microbiota and the host immune system contributes to health status later in life. Although there are many reported associations between microbiota compositional alterations and disease in adults, less is known about how microbiome development is altered in pediatric diseases. One pediatric disease linked to altered gut microbiota composition is cystic fibrosis (CF), a multi-organ genetic disease involving impaired chloride secretion across epithelia and heightened inflammation both in the gut and at other body sites. Here, we use shotgun metagenomics to profile the strain-level composition and developmental dynamics of the infant fecal microbiota from several CF and non-CF longitudinal cohorts spanning from birth to greater than 36 months of life. We identify a set of keystone species that define microbiota development in early life in non-CF infants but are missing or decreased in relative abundance in infants with CF, resulting in a delayed pattern of microbiota maturation, persistent entrenchment in a transitional developmental phase, and subsequent failure to attain an adult-like stable microbiota. Delayed maturation is strongly associated with cumulative antibiotic treatments, and we also detect the increased relative abundance of oral-derived bacteria and higher levels of fungi in infants with CF, features that are associated with decreased gut bacterial density. These findings suggest the potential for future directed therapies targeted at overcoming developmental delays in microbiota maturation for infants with CF.IMPORTANCEThe human gastrointestinal tract harbors a diversity of microbes that colonize upon birth and collectively contribute to host health throughout life. Infants with the disease cystic fibrosis (CF) harbor altered gut microbiota compared to non-CF counterparts, with lower levels of beneficial bacteria. How this altered population is established in infants with CF and how it develops over the first years of life is not well understood. By leveraging multiple large non-CF infant fecal metagenomic data sets and samples from a CF cohort collected prior to highly effective modulator therapy, we define microbiome maturation in infants up to 3 years of age. Our findings identify conserved age-diagnostic species in the non-CF infant microbiome that are diminished in abundance in CF counterparts that instead exhibit an enrichment of oral-derived bacteria and fungi associated with antibiotic exposure. Together, our study builds toward microbiota-targeted therapy to restore healthy microbiota dynamics in infants with CF.
健康人类婴儿的肠道微生物群在从出生到成熟为类似成人的稳定状态的过程中,其分类组成会发生典型变化。在此期间,微生物群与宿主免疫系统之间的广泛交流对日后的健康状况有重要影响。虽然有许多关于成人微生物群组成改变与疾病之间关联的报道,但对于儿科疾病中微生物组发育如何改变却知之甚少。一种与肠道微生物群组成改变有关的儿科疾病是囊性纤维化(CF),这是一种多器官遗传病,涉及上皮细胞氯化物分泌受损以及肠道和身体其他部位炎症加剧。在这里,我们使用鸟枪法宏基因组学对来自几个CF和非CF纵向队列的婴儿粪便微生物群的菌株水平组成和发育动态进行分析,这些队列涵盖从出生到36个月以上的时间段。我们确定了一组关键物种,它们定义了非CF婴儿早期生命中的微生物群发育,但在CF婴儿中缺失或相对丰度降低,导致微生物群成熟模式延迟,持续停留在过渡发育阶段,随后无法达到类似成人的稳定微生物群。成熟延迟与累积抗生素治疗密切相关,我们还检测到CF婴儿中源自口腔的细菌相对丰度增加以及真菌水平升高,这些特征与肠道细菌密度降低有关。这些发现表明,未来有可能针对CF婴儿微生物群成熟的发育延迟进行定向治疗。
重要性
人类胃肠道中栖息着各种各样的微生物,它们在出生时就开始定殖,并在整个生命过程中共同促进宿主健康。与非CF婴儿相比,患有囊性纤维化(CF)疾病的婴儿肠道微生物群发生了改变,有益细菌水平较低。目前尚不清楚这种改变的菌群在CF婴儿中是如何形成的,以及在生命的最初几年中它是如何发展的。通过利用多个大型非CF婴儿粪便宏基因组数据集以及来自CF队列且在高效调节剂治疗之前收集的样本,我们定义了3岁以下婴儿的微生物组成熟情况。我们的研究结果确定了非CF婴儿微生物组中保守的年龄诊断物种,这些物种在CF婴儿中的丰度降低,而CF婴儿中则表现出与抗生素暴露相关的源自口腔的细菌和真菌的富集。总之,我们的研究朝着以微生物群为靶点的治疗方向发展,以恢复CF婴儿的健康微生物群动态。