Department of Internal Medicine, King Fahd Hospital of the University, Alkhobar, Imam Abdulrahman bin Faisal University, Dammam, 31441, Saudi Arabia.
Earle A Chiles Research Institute, Robert W. Franz Cancer Center, Portland, Oregon, OR, 97213, USA.
BMC Gastroenterol. 2023 Jul 28;23(1):258. doi: 10.1186/s12876-023-02904-2.
BACKGROUND: Crohn's diseases and ulcerative colitis, both of which are chronic immune-mediated disorders of the gastrointestinal tract are major contributors to the overarching Inflammatory bowel diseases. It has become increasingly evident that the pathological processes of IBDs results from interactions between genetic and environmental factors, which can skew immune responses against normal intestinal flora. METHODS: The aim of this study is to assess and analyze the taxa diversity and relative abundances in CD and UC in the Saudi population. We utilized a sequencing strategy that targets all variable regions in the 16 S rRNA gene using the Swift Amplicon 16 S rRNA Panel on Illumina NovaSeq 6000. RESULTS: The composition of stool 16 S rRNA was analyzed from 219 patients with inflammatory bowel disease and from 124 healthy controls. We quantified the abundance of microbial communities to examine any significant differences between subpopulations of samples. At the genus level, two genera in particular, Veillonella and Lachnoclostridium showed significant association with CD versus controls. There were significant differences between subjects with CD versus UC, with the top differential genera spanning Akkermansia, Harryflintia, Maegamonas and Phascolarctobacterium. Furthermore, statistically significant taxa diversity in microbiome composition was observed within the UC and CD groups. CONCLUSIONS: In conclusion we have shown that there are significant differences in gut microbiota between UC, CD and controls in a Saudi Arabian inflammatory bowel disease cohort. This reinforces the need for further studies in large populations that are ethnically and geographically diverse. In addition, our results show the potential to develop classifiers that may have add additional richness of context to clinical diagnosis of UC and CD with larger inflammatory bowel disease cohorts.
背景:克罗恩病和溃疡性结肠炎均为胃肠道慢性免疫介导性疾病,是炎症性肠病的主要病因。越来越多的证据表明,IBD 的病理过程是由遗传和环境因素相互作用引起的,这些因素可能会使免疫反应对正常肠道菌群产生偏差。
方法:本研究旨在评估和分析沙特人群中 CD 和 UC 中的分类多样性和相对丰度。我们利用靶向 16S rRNA 基因所有可变区的测序策略,在 Illumina NovaSeq 6000 上使用 Swift Amplicon 16S rRNA 试剂盒进行测序。
结果:从 219 例炎症性肠病患者和 124 例健康对照者的粪便 16S rRNA 中分析了粪便 16S rRNA 的组成。我们量化了微生物群落的丰度,以检查样本亚群之间是否存在任何显著差异。在属水平上,有两个属,即韦荣球菌属和lachnoclostridium 与 CD 对照相比具有显著相关性。CD 与 UC 患者之间存在显著差异,差异最大的分类群跨越阿克曼氏菌、哈里弗林蒂亚菌、马加蒙菌和 Phascolarctobacterium。此外,在 UC 和 CD 组中观察到微生物组成的分类多样性存在显著差异。
结论:总之,我们已经表明,在沙特阿拉伯炎症性肠病队列中,UC、CD 和对照组之间的肠道微生物群存在显著差异。这进一步证明需要在具有种族和地理多样性的大人群中进行进一步研究。此外,我们的结果表明,有可能开发出分类器,这些分类器可能会为更大的炎症性肠病队列的 UC 和 CD 的临床诊断提供更多的上下文丰富度。
BMC Gastroenterol. 2023-7-28
BMC Microbiol. 2023-11-11
Inflamm Bowel Dis. 2023-7-5
Microbiol Spectr. 2022-6-29
World J Gastroenterol. 2018-4-7
Gastroenterology. 2019-12-5
Gut Microbes. 2025-12
Saudi J Gastroenterol. 2025-5-1
Therap Adv Gastroenterol. 2024-11-20
Biology (Basel). 2022-2-16
Indian J Microbiol. 2022-3
Metabolites. 2021-7-27
AMB Express. 2021-8-16
Appl Microbiol Biotechnol. 2021-8
J Gastroenterol Hepatol. 2021-10
Nutr Metab (Lond). 2020-10-22