Division of Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, UCSF Benioff Children's Hospital, University of California, San Francisco.
Blood Systems Research Institute.
J Pediatr Gastroenterol Nutr. 2019 Jan;68(1):30-36. doi: 10.1097/MPG.0000000000002140.
We examined the fecal virome and bacterial community composition of children with Crohn disease (CD), ulcerative colitis (UC), and healthy controls to test the hypothesis that unique patterns of viral organisms and/or presence of bacterial pathogens may be identified that could contribute to the pathogenesis of pediatric inflammatory bowel disease (IBD).
Fecal samples from 24 children (mean 12.2 years) with CD (n = 7) or UC (n = 5) and similar aged controls (n = 12) were processed to determine individual viromes. Viral sequences were identified through translated protein sequence similarity search. Bacterial microbiota were determined by sequencing of the V4 region of the 16S rRNA gene.
Only a few human viruses were detected, so virome analyses focused on bacterial viruses. The relative abundance of Caudovirales was greater than that of Microviridae phages in both IBD and healthy controls. Caudovirales phages were more abundant in CD (mean 80.8%) than UC (48.8%) (P = 0.05) but not controls. The richness of viral strains in Microviridae but not Caudovirales was higher in controls than CD (P = 0.05) but not UC cases. No other measure of phage abundance, richness, or Shannon diversity showed significant difference between the 2 IBD and control groups. Bacterial microbiota analysis revealed that IBD diagnosis, albumin, hemoglobin, erythrocyte sedimentation rate, and probiotic supplementation correlated to the composition of gut bacterial microbiota.
Minor patterns in gut virome and bacterial community composition distinguish pediatric IBD patients from healthy controls. Probiotics are associated with bacterial microbiota composition. These exploratory results need confirmation in larger studies.
我们检测了克罗恩病(CD)、溃疡性结肠炎(UC)患儿以及健康对照者的粪便病毒组和细菌群落组成,以验证以下假说,即可能存在独特的病毒群和/或细菌病原体,从而有助于阐明儿童炎症性肠病(IBD)的发病机制。
对 24 名儿童(平均年龄 12.2 岁)的粪便样本进行处理,以确定个体病毒组,这些儿童包括 CD(n=7)或 UC(n=5)患儿以及相似年龄的健康对照者(n=12)。通过翻译蛋白序列相似性搜索鉴定病毒序列。通过 16S rRNA 基因 V4 区测序确定细菌微生物组。
仅检测到少数几种人类病毒,因此病毒组分析集中于细菌病毒。Caudovirales 的相对丰度大于 IBD 和健康对照者 Microviridae 噬菌体。Caudovirales 噬菌体在 CD(平均 80.8%)中的丰度高于 UC(48.8%)(P=0.05),但在对照组中并非如此。Microviridae 噬菌体的病毒株丰富度在对照组中高于 CD(P=0.05),但在 UC 病例中并非如此。噬菌体丰度、丰富度或 Shannon 多样性的其他衡量指标在 2 种 IBD 和对照组之间均无显著差异。细菌微生物组分析显示,IBD 诊断、白蛋白、血红蛋白、红细胞沉降率和益生菌补充与肠道细菌微生物组的组成相关。
肠道病毒组和细菌群落组成的细微差异可将儿科 IBD 患者与健康对照者区分开来。益生菌与细菌微生物组组成相关。这些探索性结果需要在更大的研究中得到证实。