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      Coral microbiome database: Integration of sequences reveals high diversity and relatedness of coral‐associated microbes

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      1 , 2 , , 3 ,
      Environmental Microbiology Reports
      John Wiley & Sons, Inc.

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          Summary

          Coral‐associated microorganisms are thought to play a fundamental role in the health and ecology of corals, but understanding of specific coral–microbial interactions are lacking. In order to create a framework to examine coral–microbial specificity, we integrated and phylogenetically compared 21,100 SSU rRNA gene Sanger‐produced sequences from bacteria and archaea associated with corals from previous studies, and accompanying host, location and publication metadata, to produce the Coral Microbiome Database. From this database, we identified 39 described and candidate phyla of Bacteria and two Archaea phyla associated with corals, demonstrating that corals are one of the most phylogenetically diverse animal microbiomes. Secondly, this new phylogenetic resource shows that certain microorganisms are indeed specific to corals, including evolutionary distinct hosts. Specifically, we identified 2–37 putative monophyletic, coral‐specific sequence clusters within bacterial genera associated with the greatest number of coral species ( Vibrio, Endozoicomonas and Ruegeria) as well as functionally relevant microbial taxa (“ Candidatus Amoebophilus ”, “Candidatus Nitrosopumilus” and under recognized cyanobacteria). This phylogenetic resource provides a framework for more targeted studies of corals and their specific microbial associates, which is timely given the escalated need to understand the role of the coral microbiome and its adaptability to changing ocean and reef conditions.

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          Diversity, structure and convergent evolution of the global sponge microbiome

          Sponges (phylum Porifera) are early-diverging metazoa renowned for establishing complex microbial symbioses. Here we present a global Porifera microbiome survey, set out to establish the ecological and evolutionary drivers of these host–microbe interactions. We show that sponges are a reservoir of exceptional microbial diversity and major contributors to the total microbial diversity of the world's oceans. Little commonality in species composition or structure is evident across the phylum, although symbiont communities are characterized by specialists and generalists rather than opportunists. Core sponge microbiomes are stable and characterized by generalist symbionts exhibiting amensal and/or commensal interactions. Symbionts that are phylogenetically unique to sponges do not disproportionally contribute to the core microbiome, and host phylogeny impacts complexity rather than composition of the symbiont community. Our findings support a model of independent assembly and evolution in symbiont communities across the entire host phylum, with convergent forces resulting in analogous community organization and interactions.
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            Distinctive Gut Microbiota of Honey Bees Assessed Using Deep Sampling from Individual Worker Bees

            Surveys of 16S rDNA sequences from the honey bee, Apis mellifera, have revealed the presence of eight distinctive bacterial phylotypes in intestinal tracts of adult worker bees. Because previous studies have been limited to relatively few sequences from samples pooled from multiple hosts, the extent of variation in this microbiota among individuals within and between colonies and locations has been unclear. We surveyed the gut microbiota of 40 individual workers from two sites, Arizona and Maryland USA, sampling four colonies per site. Universal primers were used to amplify regions of 16S ribosomal RNA genes, and amplicons were sequenced using 454 pyrotag methods, enabling analysis of about 330,000 bacterial reads. Over 99% of these sequences belonged to clusters for which the first blastn hits in GenBank were members of the known bee phylotypes. Four phylotypes, one within Gammaproteobacteria (corresponding to “Candidatus Gilliamella apicola”) one within Betaproteobacteria (“Candidatus Snodgrassella alvi”), and two within Lactobacillus, were present in every bee, though their frequencies varied. The same typical bacterial phylotypes were present in all colonies and at both sites. Community profiles differed significantly among colonies and between sites, mostly due to the presence in some Arizona colonies of two species of Enterobacteriaceae not retrieved previously from bees. Analysis of Sanger sequences of rRNA of the Snodgrassella and Gilliamella phylotypes revealed that single bees contain numerous distinct strains of each phylotype. Strains showed some differentiation between localities, especially for the Snodgrassella phylotype.
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              Coral-associated bacteria and their role in the biogeochemical cycling of sulfur.

              Marine bacteria play a central role in the degradation of dimethylsulfoniopropionate (DMSP) to dimethyl sulfide (DMS) and acrylic acid, DMS being critical to cloud formation and thereby cooling effects on the climate. High concentrations of DMSP and DMS have been reported in scleractinian coral tissues although, to date, there have been no investigations into the influence of these organic sulfur compounds on coral-associated bacteria. Two coral species, Montipora aequituberculata and Acropora millepora, were sampled and their bacterial communities were characterized by both culture-dependent and molecular techniques. Four genera, Roseobacter, Spongiobacter, Vibrio, and Alteromonas, which were isolated on media with either DMSP or DMS as the sole carbon source, comprised the majority of clones retrieved from coral mucus and tissue 16S rRNA gene clone libraries. Clones affiliated with Roseobacter sp. constituted 28% of the M. aequituberculata tissue libraries, while 59% of the clones from the A. millepora libraries were affiliated with sequences related to the Spongiobacter genus. Vibrio spp. were commonly isolated from DMS and acrylic acid enrichments and were also present in 16S rRNA gene libraries from coral mucus, suggesting that under "normal" environmental conditions, they are a natural component of coral-associated communities. Genes homologous to dddD, and dddL, previously implicated in DMSP degradation, were also characterized from isolated strains, confirming that bacteria associated with corals have the potential to metabolize this sulfur compound when present in coral tissues. Our results demonstrate that DMSP, DMS, and acrylic acid potentially act as nutrient sources for coral-associated bacteria and that these sulfur compounds are likely to play a role in structuring bacterial communities in corals, with important consequences for the health of both corals and coral reef ecosystems.
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                Author and article information

                Contributors
                megan.huggett@newcastle.edu.au
                aapprill@whoi.edu
                Journal
                Environ Microbiol Rep
                Environ Microbiol Rep
                10.1111/(ISSN)1758-2229
                EMI4
                Environmental Microbiology Reports
                John Wiley & Sons, Inc. (Hoboken, USA )
                1758-2229
                20 September 2018
                June 2019
                : 11
                : 3 , Special Issue on Ecophysiology of Aquatic Microbes ( doiID: 10.1111/emi4.2019.11.issue-3 )
                : 372-385
                Affiliations
                [ 1 ] School of Environmental and Life Sciences University of Newcastle Ourimbah NSW, 2258 Australia
                [ 2 ] School of Science Edith Cowan University Joondalup WA Australia
                [ 3 ] Marine Chemistry and Geochemistry Department Woods Hole Oceanographic Institution Woods Hole MA USA
                Author notes
                [*] [* ]E‐mail megan.huggett@ 123456newcastle.edu.au ; Tel. +61 2 4348 4025; Fax +61 2 4349 4404; E‐mail aapprill@ 123456whoi.edu ; Tel. 01‐508‐289‐2649; Fax 01‐508‐457‐2164.
                Author information
                https://orcid.org/0000-0002-3401-0704
                https://orcid.org/0000-0002-4249-2977
                Article
                EMI412686
                10.1111/1758-2229.12686
                7379671
                30094953
                cb3c1c4b-216c-4b38-9e89-bca5602f0823
                © 2018 The Authors. Environmental Microbiology Reports published by Society for Applied Microbiology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 17 January 2018
                : 04 August 2018
                Page count
                Figures: 8, Tables: 0, Pages: 14, Words: 7509
                Funding
                Funded by: NSF , open-funder-registry 10.13039/100000001;
                Award ID: OCE‐1233612
                Award ID: OCE‐1736288
                Funded by: Edith Cowan University , open-funder-registry 10.13039/501100001798;
                Categories
                Brief Report
                Brief Reports
                Custom metadata
                2.0
                June 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.5 mode:remove_FC converted:24.07.2020

                Microbiology & Virology
                Microbiology & Virology

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