Willing Ben, Halfvarson Jonas, Dicksved Johan, Rosenquist Magnus, Järnerot Gunnar, Engstrand Lars, Tysk Curt, Jansson Janet K
Department of Microbiology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Inflamm Bowel Dis. 2009 May;15(5):653-60. doi: 10.1002/ibd.20783.
Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD).
To reduce variations in exposure during establishment of the gut flora and the influence of genotype, we studied the mucosa-associated microbiota of monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD. DNA was extracted from biopsies collected from 5 locations between the ileum and rectum. Bacterial 16S ribosomal RNA genes were amplified and community composition assessed by terminal-restriction fragment length polymorphism, cloning and sequencing, and quantitative real-time polymerase chain reaction (PCR).
The microbial compositions at all biopsy locations for each individual were similar, regardless of disease state, but there were differences between individuals. In particular, individuals with predominantly ileal CD had a dramatically lower abundance (P < 0.001) of Faecalibacterium prausnitzii and increased abundance (P < 0.03) of Escherichia coli compared to healthy co-twins and those with CD localized in the colon. This dysbiosis was significantly correlated to the disease phenotype rather than genotype.
The reduced abundance of F. prausnitzii and increased abundance of E. coli are indicative of an ileal CD phenotype, distinct from colonic CD, and the relative abundances of these specific bacterial populations are promising biomarker candidates for differential diagnosis of CD and eventually customized treatment.
无关个体之间肠道微生物群组成存在巨大个体差异,这使得识别导致克罗恩病(CD)的生态失调的具体方面具有挑战性。
为了减少肠道菌群建立过程中暴露的差异以及基因型的影响,我们研究了同卵双胞胎中患CD不一致(n = 6)或一致(n = 4)的个体的黏膜相关微生物群。从回肠和直肠之间的5个位置采集的活检组织中提取DNA。扩增细菌16S核糖体RNA基因,并通过末端限制性片段长度多态性、克隆和测序以及定量实时聚合酶链反应(PCR)评估群落组成。
每个个体所有活检部位的微生物组成相似,与疾病状态无关,但个体之间存在差异。特别是,与健康的双胞胎和结肠型CD患者相比,主要为回肠型CD的个体中普拉梭菌的丰度显著降低(P < 0.001),大肠杆菌的丰度增加(P < 0.03)。这种生态失调与疾病表型而非基因型显著相关。
普拉梭菌丰度降低和大肠杆菌丰度增加表明为回肠型CD表型,与结肠型CD不同,这些特定细菌种群的相对丰度有望成为CD鉴别诊断以及最终定制治疗的生物标志物候选物。