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      Outer membrane vesicles secreted by pathogenic and nonpathogenic Bacteroides fragilis represent different metabolic activities

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          Abstract

          Numerous studies are devoted to the intestinal microbiota and intercellular communication maintaining homeostasis. In this regard, vesicles secreted by bacteria represent one of the most popular topics for research. For example, the outer membrane vesicles (OMVs) of Bacteroides fragilis play an important nutritional role with respect to other microorganisms and promote anti-inflammatory effects on immune cells. However, toxigenic B. fragilis (ETBF) contributes to bowel disease, even causing colon cancer. If nontoxigenic B. fragilis (NTBF) vesicles exert a beneficial effect on the intestine, it is likely that ETBF vesicles can be utilized for potential pathogenic implementation. To confirm this possibility, we performed comparative proteomic HPLC-MS/MS analysis of vesicles isolated from ETBF and NTBF. Furthermore, we performed, for the first time, HPLC-MS/MS and GS-MS comparative metabolomic analysis for the vesicles isolated from both strains with subsequent reconstruction of the vesicle metabolic pathways. We utilized fluxomic experiments to validate the reconstructed biochemical reaction activities and finally observed considerable difference in the vesicle proteome and metabolome profiles. Compared with NTBF OMVs, metabolic activity of ETBF OMVs provides their similarity to micro reactors that are likely to be used for long-term persistence and implementing pathogenic potential in the host.

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          The microbiome and innate immunity.

          The intestinal microbiome is a signalling hub that integrates environmental inputs, such as diet, with genetic and immune signals to affect the host's metabolism, immunity and response to infection. The haematopoietic and non-haematopoietic cells of the innate immune system are located strategically at the host-microbiome interface. These cells have the ability to sense microorganisms or their metabolic products and to translate the signals into host physiological responses and the regulation of microbial ecology. Aberrations in the communication between the innate immune system and the gut microbiota might contribute to complex diseases.
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            The evolution of cooperation within the gut microbiota

            Cooperative phenotypes are considered central to the functioning of microbial communities in many contexts, including communication via quorum sensing, biofilm formation, antibiotic resistance, and pathogenesis 1-5 . The human intestine houses a dense and diverse microbial community critical to health 1,2,4-9 , yet we know little about cooperation within this important ecosystem. Here we experimentally test for evolved cooperation within the Bacteroidales, the dominant Gram-negative bacteria of the human intestine. We show that during growth on certain dietary polysaccharides, the model member Bacteroides thetaiotaomicron exhibits only limited cooperation. Although this organism digests these polysaccharides extracellularly, mutants lacking this ability are outcompeted. In contrast, we discovered a dedicated cross-feeding enzyme system in the prominent gut symbiont Bacteroides ovatus, which digests polysaccharide at a cost to itself but at a benefit to another species. Using in vitro systems and gnotobiotic mouse colonization models, we find that extracellular digestion of inulin increases the fitness of B.ovatus due to reciprocal benefits when it feeds other gut species such as Bacteroides vulgatus. This is a rare example of naturally-evolved cooperation between microbial species. Our study reveals both the complexity and importance of cooperative phenotypes within the mammalian intestinal microbiota.
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              Probiotics function mechanistically as delivery vehicles for neuroactive compounds: Microbial endocrinology in the design and use of probiotics.

              Mark Lyte (2011)
              I hypothesize here that the ability of probiotics to synthesize neuroactive compounds provides a unifying microbial endocrinology-based mechanism to explain the hitherto incompletely understood action of commensal microbiota that affect the host's gastrointestinal and psychological health. Once ingested, probiotics enter an interactive environment encompassing microbiological, immunological, and neurophysiological components. By utilizing a trans-disciplinary framework known as microbial endocrinology, mechanisms that would otherwise not be considered become apparent since any candidate would need to be shared among all three components. The range of neurochemicals produced by probiotics includes neurochemicals for which receptor-based targets on immune and neuronal elements (intestinal and extra-intestinal) have been well characterized. Production of neurochemicals by probiotics therefore allows for their consideration as delivery vehicles for neuroactive compounds. This unifying microbial endocrinology-based hypothesis, which may facilitate the selection and design of probiotics for clinical use, also highlights the largely unrecognized role of neuroscience in understanding how microbes may influence health. Copyright © 2011 WILEY Periodicals, Inc.
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                Author and article information

                Contributors
                natazaha@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                10 July 2017
                10 July 2017
                2017
                : 7
                : 5008
                Affiliations
                [1 ]GRID grid.465277.5, , Federal Research and Clinical Centre of Physical-Chemical Medicine Federal Medical Biological Agency, ; Malaya Pirogovskaya str., 1a, Moscow, 119435 Russian Federation
                [2 ]ISNI 0000000092721542, GRID grid.18763.3b, , Moscow Institute of Physics and Technology, ; Institutskiy Pereulok 9, Dolgoprudny, 141700 Russian Federation
                [3 ]ISNI 0000 0001 2289 6897, GRID grid.15447.33, Research Resource Center Molecular and Cell Technologies, , Saint-Petersburg State University, ; Universitetskaya nab. 7-9, Saint-Petersburg, 199034 Russian Federation
                [4 ]Analytical Phytochemistry Laboratory, Komarov Botanical Institute, Prof. Popov Street 2, Saint-Petersburg, 197376 Russia
                [5 ]ISNI 0000 0004 0440 1573, GRID grid.418853.3, , Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, ; Miklukho-Maklaya str. 16/10, Moscow 117997, Russian Federation, Moscow, Russia
                [6 ]ISNI 0000 0001 2192 9124, GRID grid.4886.2, Lab of Genome Structural Organization, Institute of Cytology, , Russian Academy of Sciences, ; Saint Petersburg, Russia
                [7 ]ISNI 0000 0000 9795 6893, GRID grid.32495.39, Institute of Nanobiotechnologies, , Peter the Great St. Petersburg Polytechnic University, ; Saint Petersburg, Russia
                [8 ]ISNI 0000 0001 2192 9124, GRID grid.4886.2, Microbial viruses laboratory, , Research Center of Biotechnology RAS, ; Moscow, Russian Federation
                Author information
                http://orcid.org/0000-0003-4473-587X
                Article
                5264
                10.1038/s41598-017-05264-6
                5503946
                28694488
                3389d192-9912-4a1f-83ff-c674db8dd341
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 23 January 2017
                : 25 May 2017
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