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      Sporulation capability and amylosome conservation among diverse human colonic and rumen isolates of the keystone starch‐degrader Ruminococcus bromii

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          Summary

          Ruminococcus bromii is a dominant member of the human colonic microbiota that plays a ‘keystone’ role in degrading dietary resistant starch. Recent evidence from one strain has uncovered a unique cell surface ‘amylosome’ complex that organizes starch‐degrading enzymes. New genome analysis presented here reveals further features of this complex and shows remarkable conservation of amylosome components between human colonic strains from three different continents and a R. bromii strain from the rumen of Australian cattle. These R. bromii strains encode a narrow spectrum of carbohydrate active enzymes (CAZymes) that reflect extreme specialization in starch utilization. Starch hydrolysis products are taken up mainly as oligosaccharides, with only one strain able to grow on glucose. The human strains, but not the rumen strain, also possess transporters that allow growth on galactose and fructose. R. bromii strains possess a full complement of sporulation and spore germination genes and we demonstrate the ability to form spores that survive exposure to air. Spore formation is likely to be a critical factor in the ecology of this nutritionally highly specialized bacterium, which was previously regarded as ‘non‐sporing’, helping to explain its widespread occurrence in the gut microbiota through the ability to transmit between hosts.

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          The comprehensive antibiotic resistance database.

          The field of antibiotic drug discovery and the monitoring of new antibiotic resistance elements have yet to fully exploit the power of the genome revolution. Despite the fact that the first genomes sequenced of free living organisms were those of bacteria, there have been few specialized bioinformatic tools developed to mine the growing amount of genomic data associated with pathogens. In particular, there are few tools to study the genetics and genomics of antibiotic resistance and how it impacts bacterial populations, ecology, and the clinic. We have initiated development of such tools in the form of the Comprehensive Antibiotic Research Database (CARD; http://arpcard.mcmaster.ca). The CARD integrates disparate molecular and sequence data, provides a unique organizing principle in the form of the Antibiotic Resistance Ontology (ARO), and can quickly identify putative antibiotic resistance genes in new unannotated genome sequences. This unique platform provides an informatic tool that bridges antibiotic resistance concerns in health care, agriculture, and the environment.
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            PROSITE, a protein domain database for functional characterization and annotation

            PROSITE consists of documentation entries describing protein domains, families and functional sites, as well as associated patterns and profiles to identify them. It is complemented by ProRule, a collection of rules based on profiles and patterns, which increases the discriminatory power of these profiles and patterns by providing additional information about functionally and/or structurally critical amino acids. PROSITE is largely used for the annotation of domain features of UniProtKB/Swiss-Prot entries. Among the 983 (DNA-binding) domains, repeats and zinc fingers present in Swiss-Prot (release 57.8 of 22 September 2009), 696 (∼70%) are annotated with PROSITE descriptors using information from ProRule. In order to allow better functional characterization of domains, PROSITE developments focus on subfamily specific profiles and a new profile building method giving more weight to functionally important residues. Here, we describe AMSA, an annotated multiple sequence alignment format used to build a new generation of generalized profiles, the migration of ScanProsite to Vital-IT, a cluster of 633 CPUs, and the adoption of the Distributed Annotation System (DAS) to facilitate PROSITE data integration and interchange with other sources. The latest version of PROSITE (release 20.54, of 22 September 2009) contains 1308 patterns, 863 profiles and 869 ProRules. PROSITE is accessible at: http://www.expasy.org/prosite/.
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              Impact of diet and individual variation on intestinal microbiota composition and fermentation products in obese men.

              There is growing interest in understanding how diet affects the intestinal microbiota, including its possible associations with systemic diseases such as metabolic syndrome. Here we report a comprehensive and deep microbiota analysis of 14 obese males consuming fully controlled diets supplemented with resistant starch (RS) or non-starch polysaccharides (NSPs) and a weight-loss (WL) diet. We analyzed the composition, diversity and dynamics of the fecal microbiota on each dietary regime by phylogenetic microarray and quantitative PCR (qPCR) analysis. In addition, we analyzed fecal short chain fatty acids (SCFAs) as a proxy of colonic fermentation, and indices of insulin sensitivity from blood samples. The diet explained around 10% of the total variance in microbiota composition, which was substantially less than the inter-individual variance. Yet, each of the study diets induced clear and distinct changes in the microbiota. Multiple Ruminococcaceae phylotypes increased on the RS diet, whereas mostly Lachnospiraceae phylotypes increased on the NSP diet. Bifidobacteria decreased significantly on the WL diet. The RS diet decreased the diversity of the microbiota significantly. The total 16S ribosomal RNA gene signal estimated by qPCR correlated positively with the three major SCFAs, while the amount of propionate specifically correlated with the Bacteroidetes. The dietary responsiveness of the individual's microbiota varied substantially and associated inversely with its diversity, suggesting that individuals can be stratified into responders and non-responders based on the features of their intestinal microbiota.
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                Author and article information

                Contributors
                h.flint@abdn.ac.uk
                Journal
                Environ Microbiol
                Environ. Microbiol
                10.1111/(ISSN)1462-2920
                EMI
                Environmental Microbiology
                John Wiley and Sons Inc. (Hoboken )
                1462-2912
                1462-2920
                07 December 2017
                January 2018
                : 20
                : 1 , Thematic Issue: Life of Microbes in rhizosphere ( doiID: 10.1111/emi.2018.20.issue-1 )
                : 324-336
                Affiliations
                [ 1 ] Microbiology Group The Rowett Institute, University of Aberdeen Aberdeen UK
                [ 2 ] Department of Biomolecular Sciences The Weizmann Institute of Science Rehovot Israel
                [ 3 ] AgResearch Limited, Grasslands Research Centre, Palmerston North 4442 New Zealand
                [ 4 ] School of Agriculture and Food Sciences The University of Queensland QLD St Lucia, Australia
                [ 5 ] Queensland Alliance for Agriculture and Food Innovation The University of Queensland QLD St Lucia, Australia
                [ 6 ] Department of Agriculture and Fisheries Agri‐Science Queensland Brisbane QLD Australia
                [ 7 ] Department of Microbiology and Immunology University of Michigan Medical School Ann Arbor MI USA
                [ 8 ] Hospital Cantonal “Padre Alberto Buffoni”, Avenida 3 de Julio y Victor Villegas Quininde Esmeraldas Province Ecuador
                [ 9 ] The Gut Health and Food Safety Institute Strategic Programme, Institute of Food Research Norwich UK
                [ 10 ]Present address: Faculty of Natural Sciences, Ben‐Gurion University of the Negev Beer‐Sheva 8499000 Israel
                Author notes
                [*] [* ]For correspondence. E‐mail: h.flint@ 123456abdn.ac.uk ; Tel: 00441224712751; Fax +441224 438699.
                Author information
                http://orcid.org/0000-0001-5099-8495
                Article
                EMI14000
                10.1111/1462-2920.14000
                5814915
                29159997
                30138a24-feff-4d44-abbc-58a5d4c84627
                © 2017 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 September 2017
                : 25 October 2017
                : 16 November 2017
                Page count
                Figures: 6, Tables: 1, Pages: 13, Words: 8336
                Funding
                Funded by: BBSRC
                Award ID: BB/L009951/1
                Funded by: Scottish Government Food, Land and People program
                Funded by: Israel Science Foundation
                Award ID: 1349/13
                Award ID: 1339/13
                Funded by: United States‐Israel Binational Science Foundation (BSF)
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                emi14000
                January 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.2.2 mode:remove_FC converted:16.02.2018

                Microbiology & Virology
                Microbiology & Virology

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