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Gut microbiota and Clostridium difficile infections

机译:肠道菌群和艰难梭菌感染

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Clostridium difficile infections (CDI) are the first cause of healthcare associated diarrhea in both Europe and the USA, causing between 15,000 and 30,000 deaths annually. Over the age of 65, antibiotic treatments are the two main risk factors of developing CDI. Fecal microbiota transplantation has a major role to play in managing these infections. Gut microbiota dysbiosis associated with CDI has been now comprehensively analyzed. Elderly individuals, patients treated with antibiotics or proton pump inhibitors have a dramatically decreased level of gut microbiota diversity as well as undergoing structural changes in taxa composition. In addition to this decreased diversity, patients with CDI present an increase in species belonging to Proteobacteria and a decrease in Clostridiales Incertae Sedis XI, and some commensal bacteria as Ruminococcaceae , Lachnospiraceae or Bifidobacterium longum for patients with CDI, caused by the 027 ribotype. Fecal microbiota transplantation is followed by a reestablishment of diversity, an increase in Firmicutes and Bacteroidetes and a decrease in Proteobacteria, Enterobacteriaceae and Streptoccaceae . Most of the studies are performed using metagenomics and sometimes yield contradictory results. Large studies, including culture dependent techniques and metagenomics using optimized extraction protocols to limit biases should be designed in order to comprehensively highlight the gut microbiota dysbiosis and consider specific microbiome-based therapeutic approaches.
机译:艰难梭菌感染(CDI)是在欧洲和美国引起的与医疗保健相关的腹泻的首要原因,每年造成15,000至30,000例死亡。 65岁以上,抗生素治疗是发展CDI的两个主要危险因素。粪便菌群移植在控制这些感染中起着重要作用。现已全面分析了与CDI相关的肠道菌群失调。老年人,接受抗生素或质子泵抑制剂治疗的患者肠道菌群多样性水平显着降低,并且分类单元的结构发生变化。除了这种减少的多样性外,CDI患者还表现出属于Proteobacteria的物种增加,而不育梭状芽胞杆菌(Clostridiales Incertae Sedis XI)的减少,以及由027核糖体引起的CDI患者的一些常见细菌如Ruminococcaceae,Lachnospiraceae或long Bifidobacterium longum。粪便菌群移植后,多样性得以恢复,硬毛菌和拟杆菌的数量增加,变形杆菌,肠杆菌科和链球菌科的数量减少。大多数研究使用宏基因组学进行,有时会产生矛盾的结果。应设计大型研究,包括依赖培养物的技术和使用优化的提取方案来限制偏倚的宏基因组学,以全面突出肠道菌群的营养不良,并考虑基于微生物组的特定治疗方法。

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