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      Compositional and Quantitative Insights Into Bacterial and Archaeal Communities of South Pacific Deep-Sea Sponges (Demospongiae and Hexactinellida)

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          Abstract

          In the present study, we profiled bacterial and archaeal communities from 13 phylogenetically diverse deep-sea sponge species (Demospongiae and Hexactinellida) from the South Pacific by 16S rRNA-gene amplicon sequencing. Additionally, the associated bacteria and archaea were quantified by real-time qPCR. Our results show that bacterial communities from the deep-sea sponges are mostly host-species specific similar to what has been observed for shallow-water demosponges. The archaeal deep-sea sponge community structures are different from the bacterial community structures in that they are almost completely dominated by a single family, which are the ammonia-oxidizing genera within the Nitrosopumilaceae. Remarkably, the archaeal communities are mostly specific to individual sponges (rather than sponge-species), and this observation applies to both hexactinellids and demosponges. Finally, archaeal 16s gene numbers, as detected by quantitative real-time PCR, were up to three orders of magnitude higher than in shallow-water sponges, highlighting the importance of the archaea for deep-sea sponges in general.

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          Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities.

          mothur aims to be a comprehensive software package that allows users to use a single piece of software to analyze community sequence data. It builds upon previous tools to provide a flexible and powerful software package for analyzing sequencing data. As a case study, we used mothur to trim, screen, and align sequences; calculate distances; assign sequences to operational taxonomic units; and describe the alpha and beta diversity of eight marine samples previously characterized by pyrosequencing of 16S rRNA gene fragments. This analysis of more than 222,000 sequences was completed in less than 2 h with a laptop computer.
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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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              Assessing the complex sponge microbiota: core, variable and species-specific bacterial communities in marine sponges.

              Marine sponges are well known for their associations with highly diverse, yet very specific and often highly similar microbiota. The aim of this study was to identify potential bacterial sub-populations in relation to sponge phylogeny and sampling sites and to define the core bacterial community. 16S ribosomal RNA gene amplicon pyrosequencing was applied to 32 sponge species from eight locations around the world's oceans, thereby generating 2567 operational taxonomic units (OTUs at the 97% sequence similarity level) in total and up to 364 different OTUs per sponge species. The taxonomic richness detected in this study comprised 25 bacterial phyla with Proteobacteria, Chloroflexi and Poribacteria being most diverse in sponges. Among these phyla were nine candidate phyla, six of them found for the first time in sponges. Similarity comparison of bacterial communities revealed no correlation with host phylogeny but a tropical sub-population in that tropical sponges have more similar bacterial communities to each other than to subtropical sponges. A minimal core bacterial community consisting of very few OTUs (97%, 95% and 90%) was found. These microbes have a global distribution and are probably acquired via environmental transmission. In contrast, a large species-specific bacterial community was detected, which is represented by OTUs present in only a single sponge species. The species-specific bacterial community is probably mainly vertically transmitted. It is proposed that different sponges contain different bacterial species, however, these bacteria are still closely related to each other explaining the observed similarity of bacterial communities in sponges in this and previous studies. This global analysis represents the most comprehensive study of bacterial symbionts in sponges to date and provides novel insights into the complex structure of these unique associations.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                24 April 2020
                2020
                : 11
                : 716
                Affiliations
                [1] 1RD3 Marine Symbioses, GEOMAR Helmholtz Centre for Ocean Research Kiel , Kiel, Germany
                [2] 2Institute for Chemistry and Biology of the Marine Environment (ICBM), University of Oldenburg , Oldenburg, Germany
                [3] 3German Center for Marine Biodiversity Research, Senckenberg Research Institute , Wilhelmshaven, Germany
                [4] 4National Institute of Water and Atmospheric Research , Ltd., Auckland, New Zealand
                [5] 5National Institute of Water and Atmospheric Research , Ltd., Wellington, New Zealand
                [6] 6Department of Earth and Environmental Sciences, Paleontology & Geobiology, Ludwig-Maximilians-Universität München , Munich, Germany
                [7] 7GeoBio-Center, Ludwig-Maximilians-Universität München , Munich, Germany
                [8] 8Bayerische Staatssammlung für Paläontologie und Geologie , Munich, Germany
                [9] 9Christian-Albrecht University of Kiel , Kiel, Germany
                [10] 10Helmholtz Institute for Functional Marine Biodiversity at the University of Oldenburg (HIFMB) , Oldenburg, Germany
                Author notes

                Edited by: Zhiyong Li, Shanghai Jiao Tong University, China

                Reviewed by: Nicole De Voogd, Naturalis Biodiversity Center, Netherlands; Marco J. L. Coolen, Curtin University, Australia; Lu Fan, Southern University of Science and Technology, China

                *Correspondence: Ute Hentschel, uhentschel@ 123456geomar.de

                This article was submitted to Microbial Symbioses, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2020.00716
                7193145
                32390977
                7bc8e641-c782-482d-b455-c50d38083150
                Copyright © 2020 Steinert, Busch, Bayer, Kodami, Arbizu, Kelly, Mills, Erpenbeck, Dohrmann, Wörheide, Hentschel and Schupp.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 23 October 2019
                : 27 March 2020
                Page count
                Figures: 6, Tables: 4, Equations: 0, References: 78, Pages: 16, Words: 0
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                16s rrna amplicons,archaea,bacteria,demospongiae,hexactinellida,porifera,quantitative real-time pcr (qpcr),south pacific ocean

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