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极低出生体重儿粪便细菌预测代谢途径分布:与新生儿重症监护病房生长不良的潜在关系。

Predicted Metabolic Pathway Distributions in Stool Bacteria in Very-Low-Birth-Weight Infants: Potential Relationships with NICU Faltered Growth.

机构信息

College of Nursing, University of South Florida, Tampa, FL 33612, USA.

Department of Anthropology, University of South Florida, Tampa, FL 33620, USA.

出版信息

Nutrients. 2020 May 8;12(5):1345. doi: 10.3390/nu12051345.

Abstract

Many very-low-birth-weight (VLBW) infants experience growth faltering in early life despite adequate nutrition. Early growth patterns can affect later neurodevelopmental and anthropometric potentials. The role of the dysbiotic gut microbiome in VLBW infant growth is unknown. Eighty-four VLBW infants were followed for six weeks after birth with weekly stool collection. DNA was extracted from samples and the V4 region of the 16S rRNA gene was sequenced with Illumina MiSeq. A similar microbiota database from full-term infants was used for comparing gut microbiome and predicted metabolic pathways. The class Gammaproteobacteria increased or remained consistent over time in VLBW infants. Out of 228 metabolic pathways that were significantly different between term and VLBW infants, 133 pathways were significantly lower in VLBW infants. Major metabolic differences in their gut microbiome included pathways involved in decreased glycan biosynthesis and metabolism, reduced biosynthetic capacity, interrupted amino acid metabolism, changes that could result in increased infection susceptibility, and many other system deficiencies. Our study reveals poor postnatal growth in a VLBW cohort who had dysbiotic gut microbiota and differences in predicted metabolic pathways compared to term infants. The gut microbiota in VLBW infants likely plays an important role in postnatal growth.

摘要

许多极低出生体重(VLBW)婴儿尽管接受了充足的营养,但在生命早期仍会出现生长迟缓。早期的生长模式会影响后期的神经发育和人体测量学潜力。肠道微生物组失调在 VLBW 婴儿生长中的作用尚不清楚。84 名 VLBW 婴儿在出生后 6 周内每周收集一次粪便进行随访。从样本中提取 DNA,并使用 Illumina MiSeq 对 16S rRNA 基因的 V4 区进行测序。使用来自足月婴儿的类似微生物组数据库来比较肠道微生物组和预测的代谢途径。在 VLBW 婴儿中,类肠杆菌属(Gammaproteobacteria)随着时间的推移而增加或保持一致。在足月婴儿和 VLBW 婴儿之间存在显著差异的 228 条代谢途径中,有 133 条在 VLBW 婴儿中显著降低。其肠道微生物组的主要代谢差异包括参与糖生物合成和代谢减少、生物合成能力降低、氨基酸代谢中断的途径,这些变化可能导致感染易感性增加和许多其他系统缺陷。我们的研究揭示了 VLBW 队列中存在的不良的产后生长情况,这些婴儿的肠道微生物组失调,与足月婴儿相比,预测的代谢途径也存在差异。VLBW 婴儿的肠道微生物组可能在产后生长中发挥重要作用。

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