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Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease.

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TLDR
Understanding the interaction of the microbiota with pathogens and the immune system will provide critical insight into the pathogenesis of disease and the development of strategies to prevent and treat inflammatory disease.
Abstract
The intestinal tract of mammals is colonized by a large number of microorganisms including trillions of bacteria that are referred to collectively as the gut microbiota. These indigenous microorganisms have co-evolved with the host in a symbiotic relationship. In addition to metabolic benefits, symbiotic bacteria provide the host with several functions that promote immune homeostasis, immune responses, and protection against pathogen colonization. The ability of symbiotic bacteria to inhibit pathogen colonization is mediated via several mechanisms including direct killing, competition for limited nutrients, and enhancement of immune responses. Pathogens have evolved strategies to promote their replication in the presence of the gut microbiota. Perturbation of the gut microbiota structure by environmental and genetic factors increases the risk of pathogen infection, promotes the overgrowth of harmful pathobionts, and the development of inflammatory disease. Understanding the interaction of the microbiota with pathogens and the immune system will provide critical insight into the pathogenesis of disease and the development of strategies to prevent and treat inflammatory disease.

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Journal ArticleDOI

The microbiome and cancer.

TL;DR: Next‐generation sequencing technology has permitted a thorough exploration of microbiomes such as that of the human gut, enabling observation of taxonomic and metabolomic relationships between the microbiome and cancer.
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Oral microbiomes: more and more importance in oral cavity and whole body

TL;DR: Oral microbiomes play an important role in the human microbial community and human health, and the use of recently developed molecular methods has greatly expanded the knowledge of the composition and function of the oral microbiome in health and disease.
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Cytokine Networks in the Pathophysiology of Inflammatory Bowel Disease.

TL;DR: The progression of IBD from the perspective of remodeling of cytokine networks is discussed, placing well-established and under-studied cytokine modules in the context of cellular interactions, their dynamic regulation in late stages of disease and their current and potential use in the clinic.
References
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Journal ArticleDOI

Interleukin-22 regulates the complement system to promote resistance against pathobionts after pathogen-induced intestinal damage.

TL;DR: A critical role for interleukin-22 (IL-22) is reported in systemic protection against bacterial pathobionts that translocate into the circulation after infection with the pathogen Clostridium difficile.
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Molecular analysis of faecal and duodenal samples reveals significantly higher prevalence and numbers of Pseudomonas aeruginosa in irritable bowel syndrome.

TL;DR: This study shows that P. aeruginosa is detected more frequently and at higher levels in IBS patients than in healthy subjects, suggesting its potential role in the pathophysiology of IBS.
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Gram-positive bacteria are held at a distance in the colon mucus by the lectin-like protein ZG16

TL;DR: The function of ZG16 reveals a mechanism for keeping bacteria further away from the host colon epithelium and is important for a safe normal host-bacteria symbiosis.
Journal ArticleDOI

IL-22 controls iron-dependent nutritional immunity against systemic bacterial infections

TL;DR: A previously unrecognized host defense mechanism regulated by IL-22 that relies on the induction of hemopexin to limit heme availability to bacteria, leading to suppression of bacterial growth during systemic infections is revealed.
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