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      Microbial metal‐sulfide oxidation in inactive hydrothermal vent chimneys suggested by metagenomic and metaproteomic analyses

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          Summary

          Metal‐sulfides are wide‐spread in marine benthic habitats. At deep‐sea hydrothermal vents, they occur as massive sulfide chimneys formed by mineral precipitation upon mixing of reduced vent fluids with cold oxygenated sea water. Although microorganisms inhabiting actively venting chimneys and utilizing compounds supplied by the venting fluids are well studied, only little is known about microorganisms inhabiting inactive chimneys. In this study, we combined 16S rRNA gene‐based community profiling of sulfide chimneys from the Manus Basin (SW Pacific) with radiometric dating, metagenome ( n = 4) and metaproteome ( n = 1) analyses. Our results shed light on potential lifestyles of yet poorly characterized bacterial clades colonizing inactive chimneys. These include sulfate‐reducing Nitrospirae and sulfide‐oxidizing Gammaproteobacteria dominating most of the inactive chimney communities. Our phylogenetic analysis attributed the gammaproteobacterial clades to the recently described Woeseiaceae family and the SSr‐clade found in marine sediments around the world. Metaproteomic data identified these Gammaproteobacteria as autotrophic sulfide‐oxidizers potentially facilitating metal‐sulfide dissolution via extracellular electron transfer. Considering the wide distribution of these gammaproteobacterial clades in marine environments such as hydrothermal vents and sediments, microbially accelerated neutrophilic mineral oxidation might be a globally relevant process in benthic element cycling and a considerable energy source for carbon fixation in marine benthic habitats.

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          Most cited references81

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          Extracellular electron transfer via microbial nanowires.

          Microbes that can transfer electrons to extracellular electron acceptors, such as Fe(iii) oxides, are important in organic matter degradation and nutrient cycling in soils and sediments. Previous investigations on electron transfer to Fe(iii) have focused on the role of outer-membrane c-type cytochromes. However, some Fe(iii) reducers lack c-cytochromes. Geobacter species, which are the predominant Fe(iii) reducers in many environments, must directly contact Fe(iii) oxides to reduce them, and produce monolateral pili that were proposed, on the basis of the role of pili in other organisms, to aid in establishing contact with the Fe(iii) oxides. Here we report that a pilus-deficient mutant of Geobacter sulfurreducens could not reduce Fe(iii) oxides but could attach to them. Conducting-probe atomic force microscopy revealed that the pili were highly conductive. These results indicate that the pili of G. sulfurreducens might serve as biological nanowires, transferring electrons from the cell surface to the surface of Fe(iii) oxides. Electron transfer through pili indicates possibilities for other unique cell-surface and cell-cell interactions, and for bioengineering of novel conductive materials.
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            Swarm v2: highly-scalable and high-resolution amplicon clustering

            Previously we presented Swarm v1, a novel and open source amplicon clustering program that produced fine-scale molecular operational taxonomic units (OTUs), free of arbitrary global clustering thresholds and input-order dependency. Swarm v1 worked with an initial phase that used iterative single-linkage with a local clustering threshold (d), followed by a phase that used the internal abundance structures of clusters to break chained OTUs. Here we present Swarm v2, which has two important novel features: (1) a new algorithm for d = 1 that allows the computation time of the program to scale linearly with increasing amounts of data; and (2) the new fastidious option that reduces under-grouping by grafting low abundant OTUs (e.g., singletons and doubletons) onto larger ones. Swarm v2 also directly integrates the clustering and breaking phases, dereplicates sequencing reads with d = 0, outputs OTU representatives in fasta format, and plots individual OTUs as two-dimensional networks.
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              Geomicrobiology of deep-sea hydrothermal vents.

              During the cycling of seawater through the earth's crust along the mid-ocean ridge system, geothermal energy is transferred into chemical energy in the form of reduced inorganic compounds. These compounds are derived from the reaction of seawater with crustal rocks at high temperatures and are emitted from warm (
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                Author and article information

                Contributors
                meier@microbial-ecology.net
                ameyerdi@mpi-bremen.de
                Journal
                Environ Microbiol
                Environ. Microbiol
                10.1111/(ISSN)1462-2920
                EMI
                Environmental Microbiology
                John Wiley & Sons, Inc. (Hoboken, USA )
                1462-2912
                1462-2920
                21 January 2019
                February 2019
                : 21
                : 2 ( doiID: 10.1111/emi.2019.21.issue-2 )
                : 682-701
                Affiliations
                [ 1 ] Max Planck Institute for Marine Microbiology Celsiusstrasse 1, 28359, Bremen Germany
                [ 2 ] MARUM – Center for Marine Environmental Sciences, Petrology of the Ocean Crust group University of Bremen Leobener Str., 28359, Bremen Germany
                [ 3 ] Institute of Pharmacy Ernst‐Moritz‐Arndt‐University Friedrich‐Ludwig‐Jahn‐Straße 17, 17489, Greifswald Germany
                [ 4 ] Department of Earth Sciences Memorial University of Newfoundland 40 Arctic Ave, Saint John's NL, A1B 3X7 Canada
                [ 5 ] GEOMAR Helmholtz Centre for Ocean Research Wischhofstraße 1‐3, 24148, Kiel Germany
                Author notes
                [*] [* ]For correspondence. E‐mail meier@ 123456microbial-ecology.net ; Tel. +43 1 427776636. E‐mail ameyerdi@ 123456mpi-bremen.de ; Tel. +49 421 2028 941; Fax +49 421 2028 580
                [†]

                Present address: Division of Microbial Ecology, Department of Microbiology and Ecosystem Science, Research Network Chemistry meets Microbiology, University of Vienna, Althanstrasse 14, 1180, Vienna, Austria.

                Author information
                https://orcid.org/0000-0001-8286-9073
                https://orcid.org/0000-0002-7213-3596
                Article
                EMI14514
                10.1111/1462-2920.14514
                6850669
                30585382
                f9f04a68-16ab-4310-aad7-9ed63cc9526f
                © 2018 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 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
                : 31 August 2018
                : 17 December 2018
                : 19 December 2018
                Page count
                Figures: 6, Tables: 2, Pages: 20, Words: 14754
                Funding
                Funded by: Deutsche Forschungsgemeinschaft , open-funder-registry 10.13039/501100001659;
                Funded by: Max‐Planck‐Gesellschaft , open-funder-registry 10.13039/501100004189;
                Funded by: Max Planck Society , open-funder-registry 10.13039/501100004189;
                Funded by: German Research Foundation , open-funder-registry 10.13039/501100001659;
                Award ID: SO216
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                February 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.1 mode:remove_FC converted:12.11.2019

                Microbiology & Virology
                Microbiology & Virology

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