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Ubiquity and diversity of heterotrophic bacterial nasA genes in diverse marine environments
Nitrate uptake by heterotrophic bacteria plays an important role in marine N cycling. However, few studies have investigated the diversity of environmental nitrate assimilating bacteria (NAB). In this study, the diversity and biogeographical distribution of NAB in several global oceans and particula...
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Published in: | PloS one 2015-02, Vol.10 (2), p.e0117473 |
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description | Nitrate uptake by heterotrophic bacteria plays an important role in marine N cycling. However, few studies have investigated the diversity of environmental nitrate assimilating bacteria (NAB). In this study, the diversity and biogeographical distribution of NAB in several global oceans and particularly in the western Pacific marginal seas were investigated using both cultivation and culture-independent molecular approaches. Phylogenetic analyses based on 16S rRNA and nasA (encoding the large subunit of the assimilatory nitrate reductase) gene sequences indicated that the cultivable NAB in South China Sea belonged to the α-Proteobacteria, γ-Proteobacteria and CFB (Cytophaga-Flavobacteria-Bacteroides) bacterial groups. In all the environmental samples of the present study, α-Proteobacteria, γ-Proteobacteria and Bacteroidetes were found to be the dominant nasA-harboring bacteria. Almost all of the α-Proteobacteria OTUs were classified into three Roseobacter-like groups (I to III). Clone library analysis revealed previously underestimated nasA diversity; e.g. the nasA gene sequences affiliated with β-Proteobacteria, ε-Proteobacteria and Lentisphaerae were observed in the field investigation for the first time, to the best of our knowledge. The geographical and vertical distributions of seawater nasA-harboring bacteria indicated that NAB were highly diverse and ubiquitously distributed in the studied marginal seas and world oceans. Niche adaptation and separation and/or limited dispersal might mediate the NAB composition and community structure in different water bodies. In the shallow-water Kueishantao hydrothermal vent environment, chemolithoautotrophic sulfur-oxidizing bacteria were the primary NAB, indicating a unique nitrate-assimilating community in this extreme environment. In the coastal water of the East China Sea, the relative abundance of Alteromonas and Roseobacter-like nasA gene sequences responded closely to algal blooms, indicating that NAB may be active participants contributing to the bloom dynamics. Our statistical results suggested that salinity, temperature and nitrate may be some of the key environmental factors controlling the composition and dynamics of the marine NAB communities. |
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However, few studies have investigated the diversity of environmental nitrate assimilating bacteria (NAB). In this study, the diversity and biogeographical distribution of NAB in several global oceans and particularly in the western Pacific marginal seas were investigated using both cultivation and culture-independent molecular approaches. Phylogenetic analyses based on 16S rRNA and nasA (encoding the large subunit of the assimilatory nitrate reductase) gene sequences indicated that the cultivable NAB in South China Sea belonged to the α-Proteobacteria, γ-Proteobacteria and CFB (Cytophaga-Flavobacteria-Bacteroides) bacterial groups. In all the environmental samples of the present study, α-Proteobacteria, γ-Proteobacteria and Bacteroidetes were found to be the dominant nasA-harboring bacteria. Almost all of the α-Proteobacteria OTUs were classified into three Roseobacter-like groups (I to III). Clone library analysis revealed previously underestimated nasA diversity; e.g. the nasA gene sequences affiliated with β-Proteobacteria, ε-Proteobacteria and Lentisphaerae were observed in the field investigation for the first time, to the best of our knowledge. The geographical and vertical distributions of seawater nasA-harboring bacteria indicated that NAB were highly diverse and ubiquitously distributed in the studied marginal seas and world oceans. Niche adaptation and separation and/or limited dispersal might mediate the NAB composition and community structure in different water bodies. In the shallow-water Kueishantao hydrothermal vent environment, chemolithoautotrophic sulfur-oxidizing bacteria were the primary NAB, indicating a unique nitrate-assimilating community in this extreme environment. In the coastal water of the East China Sea, the relative abundance of Alteromonas and Roseobacter-like nasA gene sequences responded closely to algal blooms, indicating that NAB may be active participants contributing to the bloom dynamics. Our statistical results suggested that salinity, temperature and nitrate may be some of the key environmental factors controlling the composition and dynamics of the marine NAB communities.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0117473</identifier><identifier>PMID: 25647610</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algae ; Algal blooms ; Alphaproteobacteria - genetics ; Aquatic ecosystems ; Bacteria ; Bacteria - enzymology ; Bacteria - genetics ; Bacterial genetics ; Bacteroidetes - genetics ; Biodiversity ; Biogeochemistry ; Carbon ; Chemical analysis ; China ; Coastal environments ; Coastal waters ; Communities ; Community structure ; Cultivation ; Deoxyribonucleic acid ; Dispersal ; DNA ; DNA, Bacterial - genetics ; Environmental factors ; Environmental science ; Eutrophication ; Flavobacterium ; Gene expression ; Gene Library ; Gene sequencing ; Genes ; Genes, Bacterial ; Genomes ; Genomics ; Heterotrophic bacteria ; Heterotrophic Processes ; Hydrothermal plumes ; Hydrothermal vent ecosystems ; Laboratories ; Marine environment ; Microorganisms ; Molecular chains ; Nitrate reductase ; Nitrate Reductase - genetics ; Nitrates ; Oceans ; Oceans and Seas ; Offshore structures ; Oxidation ; Phylogeny ; Protein Subunits - genetics ; Proteobacteria ; Proteobacteria - genetics ; Relative abundance ; Rivers ; RNA ; RNA, Ribosomal, 16S - genetics ; rRNA 16S ; Seawater ; Seawater - microbiology ; Statistical analysis ; Statistical methods ; Sulfur ; Water analysis ; Water quality</subject><ispartof>PloS one, 2015-02, Vol.10 (2), p.e0117473</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Jiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Jiang et al 2015 Jiang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-3d01dadf47723aff1644b7ec1d3b156c22779ec136aaa2854a93c8b8fec034d03</citedby><cites>FETCH-LOGICAL-c692t-3d01dadf47723aff1644b7ec1d3b156c22779ec136aaa2854a93c8b8fec034d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1656452109/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1656452109?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,44588,53789,53791,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25647610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hong, Yiguo</contributor><creatorcontrib>Jiang, Xuexia</creatorcontrib><creatorcontrib>Dang, Hongyue</creatorcontrib><creatorcontrib>Jiao, Nianzhi</creatorcontrib><title>Ubiquity and diversity of heterotrophic bacterial nasA genes in diverse marine environments</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Nitrate uptake by heterotrophic bacteria plays an important role in marine N cycling. However, few studies have investigated the diversity of environmental nitrate assimilating bacteria (NAB). In this study, the diversity and biogeographical distribution of NAB in several global oceans and particularly in the western Pacific marginal seas were investigated using both cultivation and culture-independent molecular approaches. Phylogenetic analyses based on 16S rRNA and nasA (encoding the large subunit of the assimilatory nitrate reductase) gene sequences indicated that the cultivable NAB in South China Sea belonged to the α-Proteobacteria, γ-Proteobacteria and CFB (Cytophaga-Flavobacteria-Bacteroides) bacterial groups. In all the environmental samples of the present study, α-Proteobacteria, γ-Proteobacteria and Bacteroidetes were found to be the dominant nasA-harboring bacteria. Almost all of the α-Proteobacteria OTUs were classified into three Roseobacter-like groups (I to III). Clone library analysis revealed previously underestimated nasA diversity; e.g. the nasA gene sequences affiliated with β-Proteobacteria, ε-Proteobacteria and Lentisphaerae were observed in the field investigation for the first time, to the best of our knowledge. The geographical and vertical distributions of seawater nasA-harboring bacteria indicated that NAB were highly diverse and ubiquitously distributed in the studied marginal seas and world oceans. Niche adaptation and separation and/or limited dispersal might mediate the NAB composition and community structure in different water bodies. In the shallow-water Kueishantao hydrothermal vent environment, chemolithoautotrophic sulfur-oxidizing bacteria were the primary NAB, indicating a unique nitrate-assimilating community in this extreme environment. In the coastal water of the East China Sea, the relative abundance of Alteromonas and Roseobacter-like nasA gene sequences responded closely to algal blooms, indicating that NAB may be active participants contributing to the bloom dynamics. Our statistical results suggested that salinity, temperature and nitrate may be some of the key environmental factors controlling the composition and dynamics of the marine NAB communities.</description><subject>Algae</subject><subject>Algal blooms</subject><subject>Alphaproteobacteria - genetics</subject><subject>Aquatic ecosystems</subject><subject>Bacteria</subject><subject>Bacteria - enzymology</subject><subject>Bacteria - genetics</subject><subject>Bacterial genetics</subject><subject>Bacteroidetes - genetics</subject><subject>Biodiversity</subject><subject>Biogeochemistry</subject><subject>Carbon</subject><subject>Chemical analysis</subject><subject>China</subject><subject>Coastal environments</subject><subject>Coastal waters</subject><subject>Communities</subject><subject>Community structure</subject><subject>Cultivation</subject><subject>Deoxyribonucleic acid</subject><subject>Dispersal</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>Environmental factors</subject><subject>Environmental science</subject><subject>Eutrophication</subject><subject>Flavobacterium</subject><subject>Gene expression</subject><subject>Gene Library</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Heterotrophic bacteria</subject><subject>Heterotrophic Processes</subject><subject>Hydrothermal plumes</subject><subject>Hydrothermal vent ecosystems</subject><subject>Laboratories</subject><subject>Marine environment</subject><subject>Microorganisms</subject><subject>Molecular chains</subject><subject>Nitrate reductase</subject><subject>Nitrate Reductase - genetics</subject><subject>Nitrates</subject><subject>Oceans</subject><subject>Oceans and Seas</subject><subject>Offshore structures</subject><subject>Oxidation</subject><subject>Phylogeny</subject><subject>Protein Subunits - genetics</subject><subject>Proteobacteria</subject><subject>Proteobacteria - genetics</subject><subject>Relative abundance</subject><subject>Rivers</subject><subject>RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>rRNA 16S</subject><subject>Seawater</subject><subject>Seawater - microbiology</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Sulfur</subject><subject>Water analysis</subject><subject>Water quality</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl2L1DAUhoso7rr6D0QLguDFjPlqOr0RhsWPgYUFdb3xIpwmaZuhk8wm6eD-e1Onu0xBQXrRnPR5T96cvln2EqMlpiV-v3WDt9Av987qJcK4ZCV9lJ3jipIFJ4g-PlmfZc9C2CJU0BXnT7MzUnBWcozOs583tbkdTLzLwapcmYP2Yaxck3c6au-id_vOyLwGmUoDfW4hrPNWWx1yYyeJznfgjdW5tgfjnd1pG8Pz7EkDfdAvpvdFdvPp4_fLL4ur68-by_XVQvKKxAVVCCtQDStLQqFpMGesLrXEita44JKQsqxSSTkAkFXBoKJyVa8aLRFlCtGL7PWx7753QUxzCQLzdMuCYFQlYnMklIOt2HuT3N4JB0b82XC-FeCjkb0WuEBSkQJwnRxVpE4LznnRKC4rApinXh-m04Z6p5VMN_XQz5rOv1jTidYdBKO4YGi0-2Zq4N3toEP8h-WJaiG5MrZJfwLkzgQp1owUVckpG6nlX6j0KL0zMiWjMWl_Jng3EyQm6l-xhSEEsfn29f_Z6x9z9u0J22noYxdcP0TjbJiD7AhK70LwunmYHEZiDPb9NMQYbDEFO8lenU79QXSfZPobgIr0kw</recordid><startdate>20150203</startdate><enddate>20150203</enddate><creator>Jiang, Xuexia</creator><creator>Dang, Hongyue</creator><creator>Jiao, Nianzhi</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150203</creationdate><title>Ubiquity and diversity of heterotrophic bacterial nasA genes in diverse marine environments</title><author>Jiang, Xuexia ; Dang, Hongyue ; Jiao, Nianzhi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-3d01dadf47723aff1644b7ec1d3b156c22779ec136aaa2854a93c8b8fec034d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Algae</topic><topic>Algal blooms</topic><topic>Alphaproteobacteria - genetics</topic><topic>Aquatic ecosystems</topic><topic>Bacteria</topic><topic>Bacteria - enzymology</topic><topic>Bacteria - genetics</topic><topic>Bacterial genetics</topic><topic>Bacteroidetes - genetics</topic><topic>Biodiversity</topic><topic>Biogeochemistry</topic><topic>Carbon</topic><topic>Chemical analysis</topic><topic>China</topic><topic>Coastal environments</topic><topic>Coastal waters</topic><topic>Communities</topic><topic>Community structure</topic><topic>Cultivation</topic><topic>Deoxyribonucleic acid</topic><topic>Dispersal</topic><topic>DNA</topic><topic>DNA, Bacterial - genetics</topic><topic>Environmental factors</topic><topic>Environmental science</topic><topic>Eutrophication</topic><topic>Flavobacterium</topic><topic>Gene expression</topic><topic>Gene Library</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Genes, Bacterial</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Heterotrophic bacteria</topic><topic>Heterotrophic Processes</topic><topic>Hydrothermal plumes</topic><topic>Hydrothermal vent ecosystems</topic><topic>Laboratories</topic><topic>Marine environment</topic><topic>Microorganisms</topic><topic>Molecular chains</topic><topic>Nitrate reductase</topic><topic>Nitrate Reductase - 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However, few studies have investigated the diversity of environmental nitrate assimilating bacteria (NAB). In this study, the diversity and biogeographical distribution of NAB in several global oceans and particularly in the western Pacific marginal seas were investigated using both cultivation and culture-independent molecular approaches. Phylogenetic analyses based on 16S rRNA and nasA (encoding the large subunit of the assimilatory nitrate reductase) gene sequences indicated that the cultivable NAB in South China Sea belonged to the α-Proteobacteria, γ-Proteobacteria and CFB (Cytophaga-Flavobacteria-Bacteroides) bacterial groups. In all the environmental samples of the present study, α-Proteobacteria, γ-Proteobacteria and Bacteroidetes were found to be the dominant nasA-harboring bacteria. Almost all of the α-Proteobacteria OTUs were classified into three Roseobacter-like groups (I to III). Clone library analysis revealed previously underestimated nasA diversity; e.g. the nasA gene sequences affiliated with β-Proteobacteria, ε-Proteobacteria and Lentisphaerae were observed in the field investigation for the first time, to the best of our knowledge. The geographical and vertical distributions of seawater nasA-harboring bacteria indicated that NAB were highly diverse and ubiquitously distributed in the studied marginal seas and world oceans. Niche adaptation and separation and/or limited dispersal might mediate the NAB composition and community structure in different water bodies. In the shallow-water Kueishantao hydrothermal vent environment, chemolithoautotrophic sulfur-oxidizing bacteria were the primary NAB, indicating a unique nitrate-assimilating community in this extreme environment. In the coastal water of the East China Sea, the relative abundance of Alteromonas and Roseobacter-like nasA gene sequences responded closely to algal blooms, indicating that NAB may be active participants contributing to the bloom dynamics. Our statistical results suggested that salinity, temperature and nitrate may be some of the key environmental factors controlling the composition and dynamics of the marine NAB communities.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25647610</pmid><doi>10.1371/journal.pone.0117473</doi><oa>free_for_read</oa></addata></record> |
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subjects | Algae Algal blooms Alphaproteobacteria - genetics Aquatic ecosystems Bacteria Bacteria - enzymology Bacteria - genetics Bacterial genetics Bacteroidetes - genetics Biodiversity Biogeochemistry Carbon Chemical analysis China Coastal environments Coastal waters Communities Community structure Cultivation Deoxyribonucleic acid Dispersal DNA DNA, Bacterial - genetics Environmental factors Environmental science Eutrophication Flavobacterium Gene expression Gene Library Gene sequencing Genes Genes, Bacterial Genomes Genomics Heterotrophic bacteria Heterotrophic Processes Hydrothermal plumes Hydrothermal vent ecosystems Laboratories Marine environment Microorganisms Molecular chains Nitrate reductase Nitrate Reductase - genetics Nitrates Oceans Oceans and Seas Offshore structures Oxidation Phylogeny Protein Subunits - genetics Proteobacteria Proteobacteria - genetics Relative abundance Rivers RNA RNA, Ribosomal, 16S - genetics rRNA 16S Seawater Seawater - microbiology Statistical analysis Statistical methods Sulfur Water analysis Water quality |
title | Ubiquity and diversity of heterotrophic bacterial nasA genes in diverse marine environments |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T13%3A13%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ubiquity%20and%20diversity%20of%20heterotrophic%20bacterial%20nasA%20genes%20in%20diverse%20marine%20environments&rft.jtitle=PloS%20one&rft.au=Jiang,%20Xuexia&rft.date=2015-02-03&rft.volume=10&rft.issue=2&rft.spage=e0117473&rft.pages=e0117473-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0117473&rft_dat=%3Cgale_plos_%3EA425976349%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c692t-3d01dadf47723aff1644b7ec1d3b156c22779ec136aaa2854a93c8b8fec034d03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1656452109&rft_id=info:pmid/25647610&rft_galeid=A425976349&rfr_iscdi=true |