Departments of Biological Sciences, and Pharmacology and Therapeutics, Inflammation Research Network, University of Calgary, 2500 University Dr. N.W, Calgary, T2N 1N4, Canada.
Institute of Digestive Health Research, INSERM UMR1220, Université Toulouse Paul Sabatier, Toulouse, France.
J Biomed Sci. 2019 Jan 3;26(1):1. doi: 10.1186/s12929-018-0495-4.
Gut microbiota interacting with an intact mucosal surface are key to the maintenance of homeostasis and health. This review discusses the current state of knowledge of the biofilm mode of growth of these microbiota communities, and how in turn their disruptions may cause disease. Beyond alterations of relative microbial abundance and diversity, the aim of the review is to focus on the disruptions of the microbiota biofilm structure and function, the dispersion of commensal bacteria, and the mechanisms whereby these dispersed commensals may become pathobionts. Recent findings have linked iron acquisition to the expression of virulence factors in gut commensals that have become pathobionts. Causal studies are emerging, and mechanisms common to enteropathogen-induced disruptions, as well as those reported for Inflammatory Bowel Disease and colo-rectal cancer are used as examples to illustrate the great translational potential of such research. These new observations shed new light on our attempts to develop new therapies that are able to protect and restore gut microbiota homeostasis in the many disease conditions that have been linked to microbiota dysbiosis.
肠道微生物群与完整的黏膜表面相互作用是维持体内平衡和健康的关键。本文讨论了这些微生物群落生物膜生长模式的现有知识状态,以及它们的破坏如何导致疾病。除了相对微生物丰度和多样性的改变外,本综述的目的还在于关注微生物群落生物膜结构和功能的破坏、共生菌的分散,以及这些分散的共生菌如何成为条件致病菌的机制。最近的研究发现,铁的获取与肠道共生菌中毒力因子的表达有关,这些共生菌已经成为条件致病菌。因果关系研究正在出现,与肠道病原体引起的破坏共同的机制,以及报道的炎症性肠病和结直肠癌被用来作为例子来说明这种研究的巨大转化潜力。这些新的观察结果为我们开发新疗法提供了新的思路,这些新疗法能够在与微生物失调相关的许多疾病中保护和恢复肠道微生物群的体内平衡。