Zhou Yanjiao, Shan Gururaj, Sodergren Erica, Weinstock George, Walker W Allan, Gregory Katherine E
The Genome Institute, Washington University, St. Louis, MO, United States of America; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, United States of America.
Cooper Medical School of Rowan University, Camden, NJ, United States of America.
PLoS One. 2015 Mar 5;10(3):e0118632. doi: 10.1371/journal.pone.0118632. eCollection 2015.
Necrotizing enterocolitis (NEC) is an inflammatory disease of the newborn bowel, primarily affecting premature infants. Early intestinal colonization has been implicated in the pathogenesis of NEC. The objective of this prospective case-control study was to evaluate differences in the intestinal microbiota between infants who developed NEC and unaffected controls prior to disease onset. We conducted longitudinal analysis of the 16S rRNA genes of 312 samples obtained from 12 NEC cases and 26 age-matched controls with a median frequency of 7 samples per subject and median sampling interval of 3 days. We found that the microbiome undergoes dynamic development during the first two months of life with day of life being the major factor contributing to the colonization process. Depending on when the infant was diagnosed with NEC (i.e. early vs. late onset), the pattern of microbial progression was different for cases and controls. The difference in the microbiota was most overt in early onset NEC cases and controls. In proximity to NEC onset, the abundances of Clostridium sensu stricto from Clostridia class were significantly higher in early onset NEC subjects comparing to controls. In late onset NEC, Escherichia/Shigella among Gammaproteobacteria, showed an increasing pattern prior to disease onset, and was significantly higher in cases than controls six days before NEC onset. Cronobacter from Gammaproteobacteria was also significantly higher in late onset NEC cases than controls 1-3 days prior to NEC onset. Thus, the specific infectious agent associated with NEC may vary by the age of infant at disease onset. We found that intravenously administered antibiotics may have an impact on the microbial diversity present in fecal material. Longitudinal analysis at multiple time points was an important strategy utilized in this study, allowing us to appreciate the dynamics of the premature infant intestinal microbiome while approaching NEC at various points.
坏死性小肠结肠炎(NEC)是一种新生儿肠道炎症性疾病,主要影响早产儿。早期肠道定植与NEC的发病机制有关。这项前瞻性病例对照研究的目的是评估患NEC的婴儿与疾病发作前未受影响的对照组之间肠道微生物群的差异。我们对从12例NEC病例和26例年龄匹配的对照中获得的312个样本的16S rRNA基因进行了纵向分析,每位受试者样本的中位频率为7个,中位采样间隔为3天。我们发现,微生物群在生命的前两个月经历动态发展,出生天数是影响定植过程的主要因素。根据婴儿被诊断为NEC的时间(即早发型与晚发型),病例组和对照组的微生物进展模式有所不同。微生物群的差异在早发型NEC病例和对照组中最为明显。在接近NEC发作时,与对照组相比,早发型NEC受试者中梭菌纲的严格意义上的梭菌丰度显著更高。在晚发型NEC中,γ-变形菌纲中的埃希氏菌属/志贺氏菌属在疾病发作前呈增加模式,在NEC发作前六天病例组中的含量显著高于对照组。在NEC发作前1 - 3天,γ-变形菌纲的阪崎肠杆菌在晚发型NEC病例中的含量也显著高于对照组。因此,与NEC相关的特定感染因子可能因疾病发作时婴儿的年龄而异。我们发现静脉注射抗生素可能会对粪便中的微生物多样性产生影响。在多个时间点进行纵向分析是本研究采用的一项重要策略,使我们能够在不同时间点接近NEC时了解早产儿肠道微生物群的动态变化。