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与坏死性小肠结肠炎发展相关的早产儿肠道微生物模式。

Preterm infant gut microbial patterns related to the development of necrotizing enterocolitis.

作者信息

Lindberg Tristan P, Caimano Melissa J, Hagadorn James I, Bennett Erin M, Maas Kendra, Brownell Elizabeth A, Matson Adam P

机构信息

Division of Neonatology, Connecticut Children's Medical Center, Hartford, CT, USA.

University of Connecticut School of Medicine, Farmington, CT, USA.

出版信息

J Matern Fetal Neonatal Med. 2020 Feb;33(3):349-358. doi: 10.1080/14767058.2018.1490719. Epub 2018 Jul 18.

Abstract

To define gut microbial patterns in preterm infants with and without necrotizing enterocolitis (NEC) and to characterize clinical factors related to the composition of the preterm intestinal microbiome. Fecal samples were collected at one-week intervals from infants with gestational ages <30 weeks at a single level IV neonatal intensive care unit. Using 16S rRNA gene sequencing, the composition and diversity of microbiota were determined in samples collected from five NEC infants and five matched controls. Hierarchical linear regression was used to identify clinical factors related to microbial diversity and specific bacterial signatures. Low levels of diversity were demonstrated in samples obtained from all preterm infants and antibiotic exposure further decreased diversity among both NEC cases and controls. Fecal microbial composition differed between NEC cases and controls, with a greater abundance of and bacteria belonging to the class among NEC infants. Control infants demonstrated a greater abundance of bacteria belonging to the phylum . These findings indicate that an association exists between intestinal and NEC, and strengthens the notion that an overly exuberant response to Gram-negative products, particularly lipopolysaccharide, in the preterm intestine is involved in NEC pathogenesis. Cumulative exposure to antibiotics corresponded to a reduction in microbial diversity in both NEC cases and controls.

摘要

确定患有和未患有坏死性小肠结肠炎(NEC)的早产儿的肠道微生物模式,并描述与早产肠道微生物群组成相关的临床因素。在一家单一的IV级新生儿重症监护病房,对孕周<30周的婴儿每隔一周采集粪便样本。使用16S rRNA基因测序,确定从5例NEC婴儿和5例匹配对照采集的样本中微生物群的组成和多样性。采用分层线性回归来确定与微生物多样性和特定细菌特征相关的临床因素。所有早产儿样本的多样性水平较低,抗生素暴露进一步降低了NEC病例和对照的多样性。NEC病例和对照的粪便微生物组成不同,NEC婴儿中属于 类的 和细菌丰度更高。对照婴儿中属于 门的细菌丰度更高。这些发现表明肠道 与NEC之间存在关联,并强化了这样一种观念,即早产儿肠道对革兰氏阴性产物,特别是脂多糖的过度活跃反应参与了NEC的发病机制。NEC病例和对照中抗生素的累积暴露都与微生物多样性的降低相对应。

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