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      Same, same but different: symbiotic bacterial associations in GBR sponges

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          Abstract

          Symbioses in marine sponges involve diverse consortia of microorganisms that contribute to the health and ecology of their hosts. The microbial communities of 13 taxonomically diverse Great Barrier Reef (GBR) sponge species were assessed by DGGE and 16S rRNA gene sequencing to determine intra and inter species variation in bacterial symbiont composition. Microbial profiling revealed communities that were largely conserved within different individuals of each species with intra species similarity ranging from 65–100%. 16S rRNA gene sequencing revealed that the communities were dominated by Proteobacteria, Chloroflexi, Acidobacteria, Actinobacteria, Nitrospira, and Cyanobacteria. Sponge-associated microbes were also highly host-specific with no operational taxonomic units (OTUs) common to all species and the most ubiquitous OTU found in only 5 of the 13 sponge species. In total, 91% of the OTUs were restricted to a single sponge species. However, GBR sponge microbes were more closely related to other sponge-derived bacteria than they were to environmental communities with sequences falling within 50 of the 173 previously defined sponge-(or sponge-coral) specific sequence clusters (SC). These SC spanned the Acidobacteria, Actinobacteria, Proteobacteria, Bacteroidetes, Chloroflexi, Cyanobacteria, Gemmatimonadetes, Nitrospira , and the Planctomycetes-Verrucomicrobia-Chlamydiae superphylum. The number of sequences assigned to these sponge-specific clusters across all species ranged from 0 to 92%. No relationship between host phylogeny and symbiont communities were observed across the different sponge orders, although the highest level of similarity was detected in two closely related Xestospongia species. This study identifies the core microbial inhabitants in a range of GBR sponges thereby providing the basis for future studies on sponge symbiotic function and research aiming to predict how sponge holobionts will respond to environmental perturbation.

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          Beyond the Venn diagram: the hunt for a core microbiome.

          Discovering a core microbiome is important for understanding the stable, consistent components across complex microbial assemblages. A core is typically defined as the suite of members shared among microbial consortia from similar habitats, and is represented by the overlapping areas of circles in Venn diagrams, in which each circle contains the membership of the sample or habitats being compared. Ecological insight into core microbiomes can be enriched by 'omics approaches that assess gene expression, thereby extending the concept of the core beyond taxonomically defined membership to community function and behaviour. Parameters defined by traditional ecology theory, such as composition, phylogeny, persistence and connectivity, will also create a more complex portrait of the core microbiome and advance understanding of the role of key microorganisms and functions within and across ecosystems. © 2011 Society for Applied Microbiology and Blackwell Publishing Ltd.
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            Bellerophon: a program to detect chimeric sequences in multiple sequence alignments.

            Bellerophon is a program for detecting chimeric sequences in multiple sequence datasets by an adaption of partial treeing analysis. Bellerophon was specifically developed to detect 16S rRNA gene chimeras in PCR-clone libraries of environmental samples but can be applied to other nucleotide sequence alignments. Bellerophon is available as an interactive web server at http://foo.maths.uq.edu.au/~huber/bellerophon.pl
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              Genomic insights into the marine sponge microbiome.

              Marine sponges (phylum Porifera) often contain dense and diverse microbial communities, which can constitute up to 35% of the sponge biomass. The genome of one sponge, Amphimedon queenslandica, was recently sequenced, and this has provided new insights into the origins of animal evolution. Complementary efforts to sequence the genomes of uncultivated sponge symbionts have yielded the first glimpse of how these intimate partnerships are formed. The remarkable microbial and chemical diversity of the sponge-microorganism association, coupled with its postulated antiquity, makes sponges important model systems for the study of metazoan host-microorganism interactions, and their evolution, as well as for enabling access to biotechnologically important symbiont-derived natural products. In this Review, we discuss our current understanding of the interactions between marine sponges and their microbial symbiotic consortia, and highlight recent insights into these relationships from genomic studies.
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                Author and article information

                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbio.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                02 November 2012
                18 January 2013
                2012
                : 3
                : 444
                Affiliations
                [1] 1Australian Institute of Marine Science Townsville, QLD, Australia
                [2] 2Northern Australian Marine Research Alliance, Arafura Timor Research Facility Darwin Brinkin, NT, Australia
                [3] 3Research Institute for the Environment and Livelihoods, Charles Darwin University Casuarina, NT, Australia
                [4] 4Australian Centre for Ecogenomics, University of Queensland Brisbane, QLD, Australia
                [5] 5Centre for Microbial Innovation, School of Biological Sciences, The University of Auckland Auckland, New Zealand
                [6] 6Department of Fisheries, Government of Western Australia North Beach, WA, Australia
                [7] 7Marine Ecology Research Centre, School of Environment, Science and Engineering, Southern Cross University Lismore, NSW, Australia
                Author notes

                Edited by: Karla B. Heidelberg, University of Southern California, USA

                Reviewed by: Susannah G. Tringe, DOE Joint Genome Institute, USA; Spencer V. Nyholm, University of Connecticut, USA

                *Correspondence: N. S. Webster, Australian Institute of Marine Science, PMB 3, Townsville Mail Centre, QLD 4810, Australia. e-mail: n.webster@ 123456aims.gov.au

                This article was submitted to Frontiers in Aquatic Microbiology, a specialty of Frontiers in Microbiology.

                Article
                10.3389/fmicb.2012.00444
                3548243
                23346080
                46f51a72-3605-45ec-95b0-1789df5268c1
                Copyright © 2013 Webster, Luter, Soo, Botté, Simister, Abdo and Whalan.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 17 October 2012
                : 31 December 2012
                Page count
                Figures: 5, Tables: 4, Equations: 0, References: 64, Pages: 11, Words: 7090
                Categories
                Microbiology
                Original Research Article

                Microbiology & Virology
                diversity,great barrier reef,microorganism,sponge,symbiont
                Microbiology & Virology
                diversity, great barrier reef, microorganism, sponge, symbiont

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