Wang Yunwei, Hoenig Jeanette D, Malin Kathryn J, Qamar Sanaa, Petrof Elaine O, Sun Jun, Antonopoulos Dionysios A, Chang Eugene B, Claud Erika C
Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
ISME J. 2009 Aug;3(8):944-54. doi: 10.1038/ismej.2009.37. Epub 2009 Apr 16.
Neonatal necrotizing enterocolitis (NEC) is an inflammatory intestinal disorder affecting preterm infants. Intestinal bacteria have an important function; however no causative pathogen has been identified. The purpose of this study was to determine if there are differences in microbial patterns that may be critical to the development of this disease. Fecal samples from 20 preterm infants, 10 with NEC and 10 matched controls (including 4 twin pairs) were obtained from patients in a single site level III neonatal intensive care unit. Bacterial DNA from individual fecal samples was PCR-amplified and subjected to terminal restriction fragment length polymorphism analysis and library sequencing of the 16S rRNA gene to characterize diversity and structure of the enteric microbiota. The distribution of samples from NEC patients distinctly clustered separately from controls. Intestinal bacterial colonization in all preterm infants was notable for low diversity. Patients with NEC had even less diversity, an increase in abundance of Gammaproteobacteria, a decrease in other bacteria species, and had received a higher mean number of previous days of antibiotics. Our results suggest that NEC is associated with severe lack of microbiota diversity that may accentuate the impact of single dominant microorganisms favored by empiric and widespread use of antibiotics.
新生儿坏死性小肠结肠炎(NEC)是一种影响早产儿的炎症性肠道疾病。肠道细菌具有重要作用;然而,尚未确定致病病原体。本研究的目的是确定微生物模式是否存在差异,这些差异可能对该疾病的发展至关重要。从一家三级新生儿重症监护病房的患者中获取了20名早产儿的粪便样本,其中10名患有NEC,10名作为匹配对照(包括4对双胞胎)。对各个粪便样本中的细菌DNA进行PCR扩增,并对16S rRNA基因进行末端限制性片段长度多态性分析和文库测序,以表征肠道微生物群的多样性和结构。NEC患者的样本分布与对照组明显分开聚类。所有早产儿的肠道细菌定植均以低多样性为特征。NEC患者的多样性更低,γ-变形菌丰度增加,其他细菌种类减少,并且之前接受抗生素治疗的平均天数更多。我们的结果表明,NEC与微生物群多样性严重缺乏有关,这可能会加剧经验性和广泛使用抗生素所青睐的单一优势微生物的影响。