Department of Gastroenterology, All India Institute of Medical Sciences, New Delhi, India.
School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
J Gastroenterol. 2016 Jul;51(7):660-71. doi: 10.1007/s00535-016-1193-1. Epub 2016 Mar 19.
The disease profile in the Indian population provides a unique opportunity for studying the host microbiome interaction in both infectious (amebiasis) and autoimmune diseases like inflammatory bowel disease (IBD) from a similar environment and genetic background. Analysis of fecal samples from untreated amebic liver abscess (ALA) patients, Entamoeba histolytica (Eh)-negative and -positive asymptomatic individuals, and pus samples from naive ALA patients revealed a significant reduction in Lactobacillus in asymptomatic individuals (Eh +ve) and ALA patients. Two anaerobic genera, namely Bacteroides and Peptostreptococcus, were detected in naive ALA pus samples. Analysis of fecal samples from amoebic colitis patients showed a significant decline in population of Bacteroides, Clostridium coccoides and leptum subgroup, Lactobacillus, Campylobacter, and Eubacterium, whereas a significant increase in Bifidobacterium was observed. Mucosa-associated bacterial flora analysis from IBD patients and healthy controls revealed a significant difference in concentration of bacteria among predominating and subdominating genera between ulcerative colitis (UC), Crohn's disease (CD) patients, and controls. In contrast to the mucosal studies, we found a significant increase in lactobacilli population in fecal samples of active UC patients. Another study revealed a significant decrease of Clostridium coccoides and leptum clusters in fecal samples of active UC patients along with decreased concentrations of fecal SCFAs, especially of n-butyrate, iso-butyrate, and acetate. We therefore found similar perturbations in gut microbiome in both infectious and autoimmune diseases, indicating inflammation to be the major driver for changes in gut microbiome.
印度人群的疾病谱为研究感染性疾病(阿米巴病)和自身免疫性疾病(如炎症性肠病)中的宿主微生物组相互作用提供了独特的机会,因为这些疾病具有相似的环境和遗传背景。对未经治疗的阿米巴性肝脓肿(ALA)患者、Eh 阴性和阳性无症状个体的粪便样本以及来自无经验性 ALA 患者的脓液样本进行分析,结果显示无症状个体(Eh+ve)和 ALA 患者中乳酸杆菌数量明显减少。在无经验性 ALA 脓液样本中检测到两种厌氧菌属,即拟杆菌属和消化链球菌属。对阿米巴结肠炎患者的粪便样本进行分析,结果显示拟杆菌属、梭菌 coccoides 和 leptum 亚群、乳酸杆菌、弯曲菌和真杆菌的数量显著下降,而双歧杆菌的数量显著增加。对 IBD 患者和健康对照者的黏膜相关细菌菌群进行分析,结果显示溃疡性结肠炎(UC)、克罗恩病(CD)患者和对照组之间优势属和亚优势属的细菌浓度存在显著差异。与黏膜研究不同,我们发现活跃性 UC 患者粪便样本中的乳酸杆菌数量显著增加。另一项研究显示,活跃性 UC 患者粪便样本中的梭菌 coccoides 和 leptum 簇显著减少,粪便中 SCFAs 的浓度,特别是丁酸、异丁酸和乙酸降低。因此,我们发现感染性和自身免疫性疾病中肠道微生物组存在相似的紊乱,表明炎症是肠道微生物组变化的主要驱动因素。