Samara Jumana, Moossavi Shirin, Alshaikh Belal, Ortega Van A, Pettersen Veronika Kuchařová, Ferdous Tahsin, Hoops Suzie L, Soraisham Amuchou, Vayalumkal Joseph, Dersch-Mills Deonne, Gerber Jeffrey S, Mukhopadhyay Sagori, Puopolo Karen, Tompkins Thomas A, Knights Dan, Walter Jens, Amin Harish, Arrieta Marie-Claire
Department of Physiology and Pharmacology, Snyder Institute for Chronic Diseases, University of Calgary, Calgary, AB, Canada; Department of Pediatrics, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada; International Microbiome Centre, University of Calgary, Calgary, AB, Canada; Health Sciences Centre, Winnipeg, MB, Canada.
Department of Physiology and Pharmacology, Snyder Institute for Chronic Diseases, University of Calgary, Calgary, AB, Canada; Department of Pediatrics, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada; International Microbiome Centre, University of Calgary, Calgary, AB, Canada; Microbiome and Microbial Ecology Interest Group (MMEIG), Universal Scientific Education and Research Network (USERN), Calgary, Canada.
Cell Host Microbe. 2022 May 11;30(5):696-711.e5. doi: 10.1016/j.chom.2022.04.005.
Probiotics are increasingly administered to premature infants to prevent necrotizing enterocolitis and neonatal sepsis. However, their effects on gut microbiome assembly and immunity are poorly understood. Using a randomized intervention trial in extremely premature infants, we tested the effects of a probiotic product containing four strains of Bifidobacterium species autochthonous to the infant gut and one Lacticaseibacillus strain on the compositional and functional trajectory of microbiome. Daily administration of the mixture accelerated the transition into a mature, term-like microbiome with higher stability and species interconnectivity. Besides infant age, Bifidobacterium strains and stool metabolites were the best predictors of microbiome maturation, and structural equation modeling confirmed probiotics as a major determinant for the trajectory of microbiome assembly. Bifidobacterium-driven microbiome maturation was also linked to an anti-inflammatory intestinal immune milieu. This demonstrates that Bifidobacterium strains are ecosystem engineers that lead to an acceleration of microbiome maturation and immunological consequences in extremely premature infants.
益生菌越来越多地用于早产儿,以预防坏死性小肠结肠炎和新生儿败血症。然而,它们对肠道微生物群组装和免疫的影响却知之甚少。通过对极早产儿进行随机干预试验,我们测试了一种含有四种婴儿肠道原生双歧杆菌菌株和一种乳酸乳杆菌菌株的益生菌产品对微生物群组成和功能轨迹的影响。每日服用该混合物可加速向成熟、足月样微生物群的转变,具有更高的稳定性和物种互连性。除了婴儿年龄外,双歧杆菌菌株和粪便代谢物是微生物群成熟的最佳预测指标,结构方程模型证实益生菌是微生物群组装轨迹的主要决定因素。双歧杆菌驱动的微生物群成熟也与抗炎性肠道免疫环境有关。这表明双歧杆菌菌株是生态系统工程师,可加速极早产儿的微生物群成熟并产生免疫后果。