IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center, Milan, Italy.
Department of Biomedical Sciences, Humanitas University, Milan, Italy.
United European Gastroenterol J. 2019 Oct;7(8):999-1007. doi: 10.1177/2050640619876787. Epub 2019 Sep 27.
The association of intestinal dysbiosis with the pathogenesis of inflammatory bowel disease has been well established. Besides bacteria, microbiota comprises yeasts, archaea, protists and viruses, neglected actors in inflammatory bowel disease-associated microbiota. In the past, a great limitation in studying microbiota composition was the low sensitivity of sequencing technologies and that few computational approaches were sufficient to thoroughly analyse the whole microbiome. However, new cutting-edge technologies in nucleic acid sequencing, -omics analysis and the innovative statistics and bioinformatics pipelines made possible more sensitive and accurate metagenomics, ultimately identifying novel players in intestinal inflammation, including prokaryotic and eukaryotic viruses, that together form the gut virome. The discovery of peculiar inflammatory bowel disease-associated microbial strains will not only shed new light on inflammatory bowel disease aetiogenesis, they may also support the development of novel therapeutic strategies not merely treating symptoms, but precisely counteracting the primary cause of chronic intestinal inflammation.
肠道菌群失调与炎症性肠病的发病机制密切相关。除了细菌,微生物群还包括真菌、古菌、原生动物和病毒,这些都是炎症性肠病相关微生物群中被忽视的因素。过去,研究微生物群组成的一个主要限制因素是测序技术的灵敏度低,而且很少有计算方法足以彻底分析整个微生物组。然而,核酸测序、组学分析以及创新的统计和生物信息学管道的新技术使得更敏感和准确的宏基因组学成为可能,最终确定了肠道炎症的新参与者,包括原核生物和真核生物病毒,它们共同构成了肠道病毒组。发现特殊的炎症性肠病相关微生物菌株不仅将为炎症性肠病的发病机制提供新的线索,还可能支持新的治疗策略的发展,这些策略不仅可以治疗症状,还可以针对慢性肠道炎症的主要原因进行精确的对抗。