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      Primer selection impacts specific population abundances but not community dynamics in a monthly time‐series 16S rRNA gene amplicon analysis of coastal marine bacterioplankton

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          Summary

          Primers targeting the 16S small subunit ribosomal RNA marker gene, used to characterize bacterial and archaeal communities, have recently been re‐evaluated for marine planktonic habitats. To investigate whether primer selection affects the ecological interpretation of bacterioplankton populations and community dynamics, amplicon sequencing with four primer sets targeting several hypervariable regions of the 16S rRNA gene was conducted on both mock communities constructed from cloned 16S rRNA genes and a time‐series of DNA samples from the temperate coastal Santa Barbara Channel. Ecological interpretations of community structure (delineation of depth and seasonality, correlations with environmental factors) were similar across primer sets, while population dynamics varied. We observed substantial differences in relative abundances of taxa known to be poorly resolved by some primer sets, such as Thaumarchaeota and SAR11, and unexpected taxa including Roseobacter clades. Though the magnitude of relative abundances of common OTUs differed between primer sets, the relative abundances of the OTUs were nonetheless strongly correlated. We do not endorse one primer set but rather enumerate strengths and weaknesses to facilitate selection appropriate to a system or experimental goal. While 16S rRNA gene primer bias suggests caution in assessing quantitative population dynamics, community dynamics appear robust across studies using different primers.

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          Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.

          Although the applicability of small subunit ribosomal RNA (16S rRNA) sequences for bacterial classification is now well accepted, the general use of these molecules has been hindered by the technical difficulty of obtaining their sequences. A protocol is described for rapidly generating large blocks of 16S rRNA sequence data without isolation of the 16S rRNA or cloning of its gene. The 16S rRNA in bulk cellular RNA preparations is selectively targeted for dideoxynucleotide-terminated sequencing by using reverse transcriptase and synthetic oligodeoxynucleotide primers complementary to universally conserved 16S rRNA sequences. Three particularly useful priming sites, which provide access to the three major 16S rRNA structural domains, routinely yield 800-1000 nucleotides of 16S rRNA sequence. The method is evaluated with respect to accuracy, sensitivity to modified nucleotides in the template RNA, and phylogenetic usefulness, by examination of several 16S rRNAs whose gene sequences are known. The relative simplicity of this approach should facilitate a rapid expansion of the 16S rRNA sequence collection available for phylogenetic analyses.
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            Microbial population structures in the deep marine biosphere.

            The analytical power of environmental DNA sequences for modeling microbial ecosystems depends on accurate assessments of population structure, including diversity (richness) and relative abundance (evenness). We investigated both aspects of population structure for microbial communities at two neighboring hydrothermal vents by examining the sequences of more than 900,000 microbial small-subunit ribosomal RNA amplicons. The two vent communities have different population structures that reflect local geochemical regimes. Descriptions of archaeal diversity were nearly exhaustive, but despite collecting an unparalleled number of sequences, statistical analyses indicated additional bacterial diversity at every taxonomic level. We predict that hundreds of thousands of sequences will be necessary to capture the vast diversity of microbial communities, and that different patterns of evenness for both high- and low-abundance taxa may be important in defining microbial ecosystem dynamics.
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              Experimental insights into the importance of aquatic bacterial community composition to the degradation of dissolved organic matter

              Bacteria play a central role in the cycling of carbon, yet our understanding of the relationship between the taxonomic composition and the degradation of dissolved organic matter (DOM) is still poor. In this experimental study, we were able to demonstrate a direct link between community composition and ecosystem functioning in that differently structured aquatic bacterial communities differed in their degradation of terrestrially derived DOM. Although the same amount of carbon was processed, both the temporal pattern of degradation and the compounds degraded differed among communities. We, moreover, uncovered that low-molecular-weight carbon was available to all communities for utilisation, whereas the ability to degrade carbon of greater molecular weight was a trait less widely distributed. Finally, whereas the degradation of either low- or high-molecular-weight carbon was not restricted to a single phylogenetic clade, our results illustrate that bacterial taxa of similar phylogenetic classification differed substantially in their association with the degradation of DOM compounds. Applying techniques that capture the diversity and complexity of both bacterial communities and DOM, our study provides new insight into how the structure of bacterial communities may affect processes of biogeochemical significance.
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                Author and article information

                Contributors
                emma.wear@flbs.umt.edu
                Journal
                Environ Microbiol
                Environ. Microbiol
                10.1111/(ISSN)1462-2920
                EMI
                Environmental Microbiology
                John Wiley and Sons Inc. (Hoboken )
                1462-2912
                1462-2920
                06 April 2018
                August 2018
                : 20
                : 8 , Special Issue on Marine Microbes ( doiID: 10.1111/emi.2018.20.issue-8 )
                : 2709-2726
                Affiliations
                [ 1 ] Department of Ecology Evolution and Marine Biology and Marine Science Institute; University of California Santa Barbara CA 93106 USA
                [ 2 ] Center for Microbial Oceanography: Research and Education; Department of Oceanography and Sea Grant College Program University of Hawai‘i at Mānoa Honolulu HI 96822 USA
                [ 3 ]Present address: Flathead Lake Biological Station; University of Montana Polson MT 59860 USA
                Author notes
                [*] [* ]For correspondence. E‐mail: emma.wear@ 123456flbs.umt.edu ; Tel. (406) 982‐3301; Fax (406) 982‐3201.
                Author information
                http://orcid.org/0000-0002-4811-5363
                http://orcid.org/0000-0002-2387-2886
                http://orcid.org/0000-0003-2525-3496
                Article
                EMI14091
                10.1111/1462-2920.14091
                6175402
                29521439
                128019e3-e873-4ea8-aaba-f9ac9b1ddc3b
                © 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 22 November 2017
                : 02 March 2018
                : 03 March 2018
                Page count
                Figures: 5, Tables: 2, Pages: 18, Words: 12484
                Funding
                Funded by: National Aeronautics and Space Administration Biodiversity and Ecological Forecasting program
                Award ID: NNX14AR62A
                Award ID: NNX12AO13H
                Funded by: Bureau of Ocean and Energy Management Ecosystem Studies program
                Award ID: MC15AC00006
                Funded by: National Oceanic and Atmospheric Administration
                Award ID: N/A
                Funded by: Santa Barbara Channel Marine Biodiversity Observation Network
                Funded by: NASA Earth and Space Science Fellowship Program
                Funded by: National Science Foundation Award
                Award ID: OCE‐0850857
                Funded by: NASA Postdoctoral Fellowship
                Funded by: NSF
                Award ID: OCE‐1232779
                Funded by: NIH Shared Instrumentation
                Award ID: 1S10OD010786‐01
                Funded by: Division of Ocean Sciences
                Funded by: Bureau of Ocean and Energy Management
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                emi14091
                August 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.0 mode:remove_FC converted:08.10.2018

                Microbiology & Virology
                Microbiology & Virology

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