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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Response of Core Microbial Consortia to Chronic Hydrocarbon Contaminations in Coastal Sediment Habitats</title><author><name sortKey="Jeanbille, Mathilde" sort="Jeanbille, Mathilde" uniqKey="Jeanbille M" first="Mathilde" last="Jeanbille">Mathilde Jeanbille</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Gury, Jerome" sort="Gury, Jerome" uniqKey="Gury J" first="Jérôme" last="Gury">Jérôme Gury</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Duran, Robert" sort="Duran, Robert" uniqKey="Duran R" first="Robert" last="Duran">Robert Duran</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Tronczynski, Jacek" sort="Tronczynski, Jacek" uniqKey="Tronczynski J" first="Jacek" last="Tronczynski">Jacek Tronczynski</name><affiliation><nlm:aff id="aff2"><institution>Laboratoire Biogéochimie des Contaminants Organiques, Unité Biogéochimie et Ecotoxicologie, Département Ressources Biologiques et Environnement, Ifremer Centre Atlantique</institution><country>Nantes, France</country></nlm:aff></affiliation></author><author><name sortKey="Agogue, Helene" sort="Agogue, Helene" uniqKey="Agogue H" first="Hélène" last="Agogué">Hélène Agogué</name><affiliation><nlm:aff id="aff3"><institution>Littoral, Environnement et Sociétés, UMR 7266 Centre National de la Recherche Scientifique – Université de La Rochelle</institution><country>La Rochelle, France</country></nlm:aff></affiliation></author><author><name sortKey="Ben Said, Olfa" sort="Ben Said, Olfa" uniqKey="Ben Said O" first="Olfa" last="Ben Saïd">Olfa Ben Saïd</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff4"><institution>Laboratoire de Bio-surveillance de l’Environnement, Faculté des Sciences de Bizerte</institution><country>Zarzouna, Tunisie</country></nlm:aff></affiliation></author><author><name sortKey="Ghiglione, Jean Francois" sort="Ghiglione, Jean Francois" uniqKey="Ghiglione J" first="Jean-François" last="Ghiglione">Jean-François Ghiglione</name><affiliation><nlm:aff id="aff5"><institution>Laboratoire d’Océanographie Microbienne, Sorbonne Universités, UMR 7621, Centre National de la Recherche Scientifique-University Pierre and Marie Curie</institution><country>Banyuls sur mer, France</country></nlm:aff></affiliation></author><author><name sortKey="Auguet, Jean Christophe" sort="Auguet, Jean Christophe" uniqKey="Auguet J" first="Jean-Christophe" last="Auguet">Jean-Christophe Auguet</name><affiliation><nlm:aff id="aff6"><institution>Marine Biodiversity, Exploitation and Conservation, UMR Centre National de la Recherche Scientifique 9190</institution><country>Montpellier, France</country></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">27790213</idno><idno type="pmc">5061854</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061854</idno><idno type="RBID">PMC:5061854</idno><idno type="doi">10.3389/fmicb.2016.01637</idno><date when="2016">2016</date><idno type="wicri:Area/Pmc/Corpus">000215</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Response of Core Microbial Consortia to Chronic Hydrocarbon Contaminations in Coastal Sediment Habitats</title><author><name sortKey="Jeanbille, Mathilde" sort="Jeanbille, Mathilde" uniqKey="Jeanbille M" first="Mathilde" last="Jeanbille">Mathilde Jeanbille</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Gury, Jerome" sort="Gury, Jerome" uniqKey="Gury J" first="Jérôme" last="Gury">Jérôme Gury</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Duran, Robert" sort="Duran, Robert" uniqKey="Duran R" first="Robert" last="Duran">Robert Duran</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation></author><author><name sortKey="Tronczynski, Jacek" sort="Tronczynski, Jacek" uniqKey="Tronczynski J" first="Jacek" last="Tronczynski">Jacek Tronczynski</name><affiliation><nlm:aff id="aff2"><institution>Laboratoire Biogéochimie des Contaminants Organiques, Unité Biogéochimie et Ecotoxicologie, Département Ressources Biologiques et Environnement, Ifremer Centre Atlantique</institution><country>Nantes, France</country></nlm:aff></affiliation></author><author><name sortKey="Agogue, Helene" sort="Agogue, Helene" uniqKey="Agogue H" first="Hélène" last="Agogué">Hélène Agogué</name><affiliation><nlm:aff id="aff3"><institution>Littoral, Environnement et Sociétés, UMR 7266 Centre National de la Recherche Scientifique – Université de La Rochelle</institution><country>La Rochelle, France</country></nlm:aff></affiliation></author><author><name sortKey="Ben Said, Olfa" sort="Ben Said, Olfa" uniqKey="Ben Said O" first="Olfa" last="Ben Saïd">Olfa Ben Saïd</name><affiliation><nlm:aff id="aff1"><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff4"><institution>Laboratoire de Bio-surveillance de l’Environnement, Faculté des Sciences de Bizerte</institution><country>Zarzouna, Tunisie</country></nlm:aff></affiliation></author><author><name sortKey="Ghiglione, Jean Francois" sort="Ghiglione, Jean Francois" uniqKey="Ghiglione J" first="Jean-François" last="Ghiglione">Jean-François Ghiglione</name><affiliation><nlm:aff id="aff5"><institution>Laboratoire d’Océanographie Microbienne, Sorbonne Universités, UMR 7621, Centre National de la Recherche Scientifique-University Pierre and Marie Curie</institution><country>Banyuls sur mer, France</country></nlm:aff></affiliation></author><author><name sortKey="Auguet, Jean Christophe" sort="Auguet, Jean Christophe" uniqKey="Auguet J" first="Jean-Christophe" last="Auguet">Jean-Christophe Auguet</name><affiliation><nlm:aff id="aff6"><institution>Marine Biodiversity, Exploitation and Conservation, UMR Centre National de la Recherche Scientifique 9190</institution><country>Montpellier, France</country></nlm:aff></affiliation></author></analytic><series><title level="j">Frontiers in Microbiology</title><idno type="eISSN">1664-302X</idno><imprint><date when="2016">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Traditionally, microbial surveys investigating the effect of chronic anthropogenic pressure such as polyaromatic hydrocarbons (PAHs) contaminations consider just the alpha and beta diversity and ignore the interactions among the different taxa forming the microbial community. Here, we investigated the ecological relationships between the three domains of life (i.e., <italic>Bacteria, Archaea</italic>, and <italic>Eukarya</italic>) using 454 pyrosequencing on the 16S rRNA and 18S rRNA genes from chronically impacted and pristine sediments, along the coasts of the Mediterranean Sea (Gulf of Lion, Vermillion coast, Corsica, Bizerte lagoon and Lebanon) and the French Atlantic Ocean (Bay of Biscay and English Channel). Our approach provided a robust ecological framework for the partition of the taxa abundance distribution into 859 core Operational taxonomic units (OTUs) and 6629 satellite OTUs. OTUs forming the core microbial community showed the highest sensitivity to changes in environmental and contaminant variations, with salinity, latitude, temperature, particle size distribution, total organic carbon (TOC) and PAH concentrations as main drivers of community assembly. The core communities were dominated by <italic>Gammaproteobacteria</italic> and <italic>Deltaproteobacteria</italic> for <italic>Bacteria</italic>, by <italic>Thaumarchaeota, Bathyarchaeota</italic> and <italic>Thermoplasmata</italic> for <italic>Archaea</italic> and <italic>Metazoa</italic> and <italic>Dinoflagellata</italic> for <italic>Eukarya</italic>. In order to find associations among microorganisms, we generated a co-occurrence network in which PAHs were found to impact significantly the potential predator – prey relationship in one microbial consortium composed of ciliates and <italic>Actinobacteria</italic>. Comparison of network topological properties between contaminated and non-contaminated samples showed substantial differences in the network structure and indicated a higher vulnerability to environmental perturbations in the contaminated sediments.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Acosta Gonzalez, A" uniqKey="Acosta Gonzalez A">A. Acosta-González</name></author><author><name sortKey="Rossell M Ra, R" uniqKey="Rossell M Ra R">R. Rosselló-Móra</name></author><author><name sortKey="Marques, S" uniqKey="Marques S">S. Marqués</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Albert, R" uniqKey="Albert R">R. Albert</name></author><author><name sortKey="Jeong, H" uniqKey="Jeong H">H. Jeong</name></author><author><name sortKey="Barabasi, A L" uniqKey="Barabasi A">A.-L. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Front Microbiol</journal-id><journal-id journal-id-type="iso-abbrev">Front Microbiol</journal-id><journal-id journal-id-type="publisher-id">Front. Microbiol.</journal-id><journal-title-group><journal-title>Frontiers in Microbiology</journal-title></journal-title-group><issn pub-type="epub">1664-302X</issn><publisher><publisher-name>Frontiers Media S.A.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">27790213</article-id><article-id pub-id-type="pmc">5061854</article-id><article-id pub-id-type="doi">10.3389/fmicb.2016.01637</article-id><article-categories><subj-group subj-group-type="heading"><subject>Microbiology</subject><subj-group><subject>Original Research</subject></subj-group></subj-group></article-categories><title-group><article-title>Response of Core Microbial Consortia to Chronic Hydrocarbon Contaminations in Coastal Sediment Habitats</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Jeanbille</surname><given-names>Mathilde</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/334042/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Gury</surname><given-names>Jérôme</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/358233/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Duran</surname><given-names>Robert</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/90111/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Tronczynski</surname><given-names>Jacek</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Agogué</surname><given-names>Hélène</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/358606/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Ben Saïd</surname><given-names>Olfa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Ghiglione</surname><given-names>Jean-François</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/204627/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Auguet</surname><given-names>Jean-Christophe</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref><xref ref-type="author-notes" rid="fn001"><sup>*</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/192804/overview"></uri></contrib></contrib-group><aff id="aff1"><sup>1</sup><institution>Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 Centre National de la Recherche Scientifique – Université de Pau et des Pays de L’Adour</institution><country>Pau, France</country></aff><aff id="aff2"><sup>2</sup><institution>Laboratoire Biogéochimie des Contaminants Organiques, Unité Biogéochimie et Ecotoxicologie, Département Ressources Biologiques et Environnement, Ifremer Centre Atlantique</institution><country>Nantes, France</country></aff><aff id="aff3"><sup>3</sup><institution>Littoral, Environnement et Sociétés, UMR 7266 Centre National de la Recherche Scientifique – Université de La Rochelle</institution><country>La Rochelle, France</country></aff><aff id="aff4"><sup>4</sup><institution>Laboratoire de Bio-surveillance de l’Environnement, Faculté des Sciences de Bizerte</institution><country>Zarzouna, Tunisie</country></aff><aff id="aff5"><sup>5</sup><institution>Laboratoire d’Océanographie Microbienne, Sorbonne Universités, UMR 7621, Centre National de la Recherche Scientifique-University Pierre and Marie Curie</institution><country>Banyuls sur mer, France</country></aff><aff id="aff6"><sup>6</sup><institution>Marine Biodiversity, Exploitation and Conservation, UMR Centre National de la Recherche Scientifique 9190</institution><country>Montpellier, France</country></aff><author-notes><fn fn-type="edited-by"><p>Edited by: <italic>Guillermina Hernandez-Raquet, Institut National de la Recherche Agronomique, France</italic></p></fn><fn fn-type="edited-by"><p>Reviewed by: <italic>Marlis Reich, University of Bremen, Germany; Michael Seeger, Federico Santa María Technical University, Chile</italic></p></fn><corresp id="fn001">*Correspondence: <italic>Jean-Christophe Auguet, <email xlink:type="simple">jean-christophe.auguet@cnrs.fr</email></italic></corresp><fn fn-type="other" id="fn002"><p>This article was submitted to Systems Microbiology, a section of the journal Frontiers in Microbiology</p></fn></author-notes><pub-date pub-type="epub"><day>13</day><month>10</month><year>2016</year></pub-date><pub-date pub-type="collection"><year>2016</year></pub-date><volume>7</volume><elocation-id>1637</elocation-id><history><date date-type="received"><day>13</day><month>5</month><year>2016</year></date><date date-type="accepted"><day>30</day><month>9</month><year>2016</year></date></history><permissions><copyright-statement>Copyright © 2016 Jeanbille, Gury, Duran, Tronczynski, Agogué, Ben Saïd, Ghiglione and Auguet.</copyright-statement><copyright-year>2016</copyright-year><copyright-holder>Jeanbille, Gury, Duran, Tronczynski, Agogué, Ben Saïd, Ghiglione and Auguet</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>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) or licensor 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.</license-p></license></permissions><abstract><p>Traditionally, microbial surveys investigating the effect of chronic anthropogenic pressure such as polyaromatic hydrocarbons (PAHs) contaminations consider just the alpha and beta diversity and ignore the interactions among the different taxa forming the microbial community. Here, we investigated the ecological relationships between the three domains of life (i.e., <italic>Bacteria, Archaea</italic>, and <italic>Eukarya</italic>) using 454 pyrosequencing on the 16S rRNA and 18S rRNA genes from chronically impacted and pristine sediments, along the coasts of the Mediterranean Sea (Gulf of Lion, Vermillion coast, Corsica, Bizerte lagoon and Lebanon) and the French Atlantic Ocean (Bay of Biscay and English Channel). Our approach provided a robust ecological framework for the partition of the taxa abundance distribution into 859 core Operational taxonomic units (OTUs) and 6629 satellite OTUs. OTUs forming the core microbial community showed the highest sensitivity to changes in environmental and contaminant variations, with salinity, latitude, temperature, particle size distribution, total organic carbon (TOC) and PAH concentrations as main drivers of community assembly. The core communities were dominated by <italic>Gammaproteobacteria</italic> and <italic>Deltaproteobacteria</italic> for <italic>Bacteria</italic>, by <italic>Thaumarchaeota, Bathyarchaeota</italic> and <italic>Thermoplasmata</italic> for <italic>Archaea</italic> and <italic>Metazoa</italic> and <italic>Dinoflagellata</italic> for <italic>Eukarya</italic>. In order to find associations among microorganisms, we generated a co-occurrence network in which PAHs were found to impact significantly the potential predator – prey relationship in one microbial consortium composed of ciliates and <italic>Actinobacteria</italic>. Comparison of network topological properties between contaminated and non-contaminated samples showed substantial differences in the network structure and indicated a higher vulnerability to environmental perturbations in the contaminated sediments.</p></abstract><kwd-group><kwd>co-occurrence network</kwd><kwd>core community</kwd><kwd>microbial consortia</kwd><kwd>PAH</kwd><kwd>chronic contamination</kwd><kwd>coastal sediment</kwd></kwd-group><funding-group><award-group><funding-source id="cn001">Ministère de l’Education Nationale, de l’Enseignement Supérieur et de la Recherche<named-content content-type="fundref-id">10.13039/501100004793</named-content></funding-source></award-group><award-group><funding-source id="cn002">Institut National des Sciences de l’Univers, Centre National de la Recherche Scientifique<named-content content-type="fundref-id">10.13039/501100004617</named-content></funding-source></award-group><award-group><funding-source id="cn003">Agence Nationale de la Recherche<named-content content-type="fundref-id">10.13039/501100001665</named-content></funding-source></award-group></funding-group><counts><fig-count count="7"></fig-count><table-count count="2"></table-count><equation-count count="0"></equation-count><ref-count count="98"></ref-count><page-count count="13"></page-count><word-count count="0"></word-count></counts></article-meta></front><body><sec><title>Introduction</title><p>Marine sediments cover more than two-thirds of the Earth’s surface. Microorganisms play a central role in global biogeochemical cycling within these habitats (<xref rid="B58" ref-type="bibr">Nealson, 1997</xref>; <xref rid="B73" ref-type="bibr">Reed and Martiny, 2013</xref>), but also in the biodegradation of undesirable compounds (<xref rid="B95" ref-type="bibr">Wiatrowski and Barkay, 2005</xref>; <xref rid="B21" ref-type="bibr">Fernández-Luqueño et al., 2010</xref>). Yet, the immense complexity of microbial communities have prevented the precise description of the species involved in these processes and how microbial communities respond to common contaminants such as polyaromatic hydrocarbons (PAHs; <xref rid="B62" ref-type="bibr">Nogales et al., 2011</xref>). These questions are particularly relevant in the coastal ecosystems, which support numerous human activities exerting considerable anthropogenic pressures. Hydrocarbon pollution constitutes the most significant of these pressures, as it is estimated to represent worldwide between 1.3 and 8.8 millions tons of discharge per year (<xref rid="B63" ref-type="bibr">Oil in the Sea III, 2003</xref>). Estimations of oil discharge in the Mediterranean sea (<xref rid="B19" ref-type="bibr">European Environment Agency, 2006</xref>) show that a major part of this pollution is of chronic origin.</p><p>The response of microbial communities to chronic inputs of PAHs (<xref rid="B62" ref-type="bibr">Nogales et al., 2011</xref>; <xref rid="B87" ref-type="bibr">Sun et al., 2012</xref>, <xref rid="B88" ref-type="bibr">2013</xref>; <xref rid="B1" ref-type="bibr">Acosta-González et al., 2013</xref>; <xref rid="B77" ref-type="bibr">Sauret et al., 2015</xref>) has received little attention compared to the effect of acute contaminations (<xref rid="B33" ref-type="bibr">Head et al., 2006</xref>; <xref rid="B82" ref-type="bibr">Stauffert et al., 2013</xref>, <xref rid="B81" ref-type="bibr">2014a</xref>,<xref rid="B83" ref-type="bibr">b</xref>; <xref rid="B37" ref-type="bibr">Kimes et al., 2014</xref>; <xref rid="B38" ref-type="bibr">King et al., 2015</xref>). Although no general trend has emerged yet, sediments chronically impacted by PAHs evidenced contrasted variations in bacterial alpha diversity (<xref rid="B61" ref-type="bibr">Nogales et al., 2007</xref>; <xref rid="B67" ref-type="bibr">Paissé et al., 2008</xref>; <xref rid="B96" ref-type="bibr">Zhang et al., 2008</xref>; <xref rid="B68" ref-type="bibr">Païssé et al., 2010</xref>; <xref rid="B75" ref-type="bibr">Rosano-Hernández et al., 2012</xref>; <xref rid="B87" ref-type="bibr">Sun et al., 2012</xref>, <xref rid="B88" ref-type="bibr">2013</xref>), and in community composition, with <italic>Deltaproteobacteria</italic> and <italic>Gammaproteobacteria</italic> as dominant taxa (<xref rid="B67" ref-type="bibr">Paissé et al., 2008</xref>; <xref rid="B96" ref-type="bibr">Zhang et al., 2008</xref>; <xref rid="B6" ref-type="bibr">Ben Said et al., 2010</xref>; <xref rid="B88" ref-type="bibr">Sun et al., 2013</xref>). As compared to bacteria, only poor attention is paid nowadays to the response of archaea and eukaryotes to hydrocarbons inputs (<xref rid="B33" ref-type="bibr">Head et al., 2006</xref>; <xref rid="B14" ref-type="bibr">Dias et al., 2011</xref>; <xref rid="B83" ref-type="bibr">Stauffert et al., 2014b</xref>).</p><p>All the studies investigating the response of microbial communities to hydrocarbon contaminations have focused mainly on the abundance of taxa found in individual samples (i.e., alpha diversity) or on the turnover of taxa among site (i.e., beta diversity). However, the different species inhabiting any particular habitat interact with each other through flows of matter, energy or information, forming complex ecological networks and these interactions may be more important for ecosystem functioning than richness or abundance (<xref rid="B57" ref-type="bibr">Montoya et al., 2006</xref>). Hence, in addition to its alpha and beta diversity facets, biodiversity encompass also the ecological relationships (i.e., direct or indirect interactions) among taxa (<xref rid="B65" ref-type="bibr">Olesen et al., 2007</xref>). While plant and macro-organism ecologists have investigated ecological networks for long times (<xref rid="B16" ref-type="bibr">Dunne et al., 2002a</xref>,<xref rid="B17" ref-type="bibr">b</xref>; <xref rid="B57" ref-type="bibr">Montoya et al., 2006</xref>), the recent interest of microbial ecologists for this kind of approach have permitted to ascertain the functional role, the trophic interactions or the ecological niche of uncultured microorganisms (<xref rid="B11" ref-type="bibr">Chaffron et al., 2010</xref>; <xref rid="B84" ref-type="bibr">Steele et al., 2011</xref>; <xref rid="B4" ref-type="bibr">Barberán et al., 2012</xref>; <xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>).</p><p>Here we used network analyses in order to explore microbial co-occurrences between the three domains of life in coastal sediments bearing chronic hydrocarbon inputs. We tested the hypothesis of: (i) the existence of core microbial Operational taxonomic units (OTUs) that respond to chronic hydrocarbon contaminations and (ii) an impact of chronic PAH contaminations on the topology of microbial networks. We used 454 pyrosequencing on the 16S rRNA and 18S rRNA genes from coastal sediment microbial communities sampled in chronically impacted and pristine sediments, along the coasts of the Mediterranean Sea and the French Atlantic Ocean.</p></sec><sec sec-type="materials|methods" id="s1"><title>Materials and Methods</title><sec><title>Study Sites and Sampling</title><p>Forty-two sediment samples were collected in different sites along the Mediterranean and the Atlantic French coasts (<bold>Figure <xref ref-type="fig" rid="F1">1</xref></bold>, Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S1</xref>). An <italic>a priori</italic> contamination criterion was determined according to the vicinity of potential input of hydrocarbons, like urbanized areas, industrial activities, industrial or recreational shipping activities. According to this criterion, contaminated and non-contaminated surface sediment samples (1–2 cm) were collected within each site. Non-contaminated samples were collected at least 2 km away from contaminated sites. Sites from Le Havre (samples MA1 and MA2), Lorient (GC1 and GC2), La Rochelle (LR1), Port-Vendres (PV1 to PV3), Thau lagoon (M5 and M6), Toulon (M3 and M4), Beirut (L1 and L2), Bizerte (BI1) and Ajaccio (M1 and M2) were subjected to industrial activities and industrial shipping (<bold>Figure <xref ref-type="fig" rid="F1">1</xref></bold>). Sites from Banyuls-sur-Mer (BA1 et BA4) and Quiberon (GC1) were subjected to recreational shipping activities. Finally, GC6 and GC7 samples were collected in the same location before (August 1999) and after (July 2000) the Erika oil spill, which occurred in December 1999.</p><fig id="F1" position="float"><label>FIGURE 1</label><caption><p><bold>Map of the 42 sediments sampling stations.</bold> Within each location <italic>a priori</italic> non-contaminated sites are in light gray and <italic>a priori</italic> contaminated sites in black (i.e., contamination criterion defined before sampling). The <italic>x-</italic> and <italic>y-</italic>axes stand for decimal longitude and latitude, respectively.</p></caption><graphic xlink:href="fmicb-07-01637-g001"></graphic></fig><p>Samples were frozen immediately and transported at -18°C to the laboratory, where they were conserved at -80°C until further analysis. Salinity, temperature, particle size distribution (PSD, % < 63 μm), total organic carbon content (%TOC) and PAH concentrations were different among sites (Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S1</xref>). PSD was measured using laser diffraction, according to <xref rid="B3" ref-type="bibr">Azoury et al. (2013)</xref> and %TOC was determined according to <xref rid="B90" ref-type="bibr">Tronczynski et al. (2005)</xref>, on the decarbonated sediment samples by flash combustion (900–1000°C) with thermal conductivity detection (TCD). PSD was not determined for Bizerte samples, two samples from Lebanon and samples from La Rochelle. %TOC was not determined for two samples from Lebanon, one from the Gulf of Lion, three from Corsica and two samples from La Rochelle (Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S1</xref>). PAH analyses were processed according to <xref rid="B82" ref-type="bibr">Stauffert et al. (2013)</xref> using Gas-Chromatography coupled to Mass-Spectrometry (GC-MS). As PAH concentrations were significantly correlated (rho > 0.75, <italic>p</italic> < 0.05), we were able to calculate PAH sums and compare them with several Sediment Quality Guidelines (SQG, <xref rid="B7" ref-type="bibr">Buchman, 2008</xref>): PEL (Probable Effect Low), ERL (Effect Range Low) and T50 (50% toxicity concentration). Two PAH diagnosis ratios [phenanthrene/anthracene (P/A) and fluoranthene/pyrene (F/P)] were considered in order to evaluate the source of contamination across sites. Fluoranthene and phenanthrene are found in fossil fuels and are therefore petrogenic PAHs, while anthracene and pyrene are produced during combustions and are pyrogenic PAHs. Values below 10 and above 1 for P/A and F/P, respectively, were shown to indicate a pyrogenic source of PAHs (<xref rid="B8" ref-type="bibr">Budzinski et al., 1997</xref>).</p></sec><sec><title>Molecular Methods and Sequence Processing</title><p>Total genomic DNA was extracted from 250 mg of sediment samples using the PowerSoil DNA isolation kit (MO-BIO Laboratories Inc.). PCR amplifications were performed using primers 27f (5′-AGRGTTTGATCMTGGCTCAG-3′) and 519r (5′-GTNTTACNGCGGCKGCTG-3′) targeting the V1–V3 region of the bacterial 16S rRNA gene (<xref rid="B94" ref-type="bibr">Weisburg et al., 1991</xref>), primers 344f (3′-ACGGGGYGCAGCAGGCGCGA-5′) and 915r (3′-GTGCTCCCCCGCCAATTCCT-5′) targeting the V3–V4 region of the archaeal 16S rRNA gene (<xref rid="B72" ref-type="bibr">Raskin et al., 1994</xref>) and primers 1560f (3′-TGGTGCATGGCCGTTCTTAGT-5′) and 2035r (3′-CATCTAAGGGCATCACAGACC-5′) targeting the VR4 region of the eukaryotic 18S rRNA gene (<xref rid="B32" ref-type="bibr">Hardy et al., 2010</xref>). Pyrosequencing was performed at Mr. DNA – Molecular Research (Shallowater, TX, USA), using a Roche 454 GS-FLX Titanium instrument (Roche, NJ, USA). Pyrosequencing resulted in 693687, 290816, and 110044 raw reads for bacterial, archaeal and eukaryotic datasets, respectively, (Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S2</xref>). Raw reads from the three datasets were independently quality-based, trimmed, and aligned on the May 2013 Greengenes reference alignment for prokaryotes (<xref rid="B54" ref-type="bibr">McDonald et al., 2012</xref>) and SILVA 119 database for eukaryotes (<xref rid="B71" ref-type="bibr">Quast et al., 2013</xref>). Chimera were subsequently detected and eliminated using UCHIME (<xref rid="B18" ref-type="bibr">Edgar et al., 2011</xref>). All statistical analyses were performed on a random subsample of 3238, 829 and 804 sequences for bacterial, archaeal and eukaryotic datasets, respectively, corresponding to the smaller number of sequences per sample in the datasets, after trimming and quality processing. OTUs were clustered at a 90% identity threshold following the Mothur 454 Standard Operating Procedure (<xref rid="B78" ref-type="bibr">Schloss et al., 2009</xref>) with few modifications. The 90% threshold for OTUs is close to the taxonomic level of the family (<xref rid="B39" ref-type="bibr">Konstantinidis and Tiedje, 2007</xref>). This threshold was used to get sufficiently abundant OTUs for correlation analysis (i.e., enough occurrence and abundance to get statistically robust Spearman correlations). Another advantage of using this threshold is to circumvent potential taxonomic misclassifications due to sequencing anomalies (<xref rid="B4" ref-type="bibr">Barberán et al., 2012</xref>; <xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>). This resulted in 6034 bacterial OTUs, 680 archaeal OTUs and 774 eukaryotic OTUs. Taxonomic classification of each OTU was performed using the May 2013 Greengenes reference alignment for prokaryotes (<xref rid="B54" ref-type="bibr">McDonald et al., 2012</xref>) and the SILVA 119 database for eukaryotes (<xref rid="B71" ref-type="bibr">Quast et al., 2013</xref>). A representative sequence (i.e., the closest sequence of all other sequences) for each OTU was selected and a phylogenetic tree was reconstructed for each domain of life using the ARB software (<xref rid="B50" ref-type="bibr">Ludwig et al., 2004</xref>). Bacterial, archaeal and eukaryotic base frequency ARB filters were applied to exclude highly variable positions before sequences were added using the ARB parsimony insertion tool to the May 2013 Greengenes and SILVA 119 backbone trees, for prokaryotes and eukaryotes, respectively. Resulting phylogenetic trees were exported and used to run UniFrac weighted matrix calculation for each domain of life (<xref rid="B49" ref-type="bibr">Lozupone et al., 2006</xref>). Weighted UniFrac distance matrices were further used in beta-diversity analysis. We used PERMANOVA based on 1000 permutations (<xref rid="B53" ref-type="bibr">McArdle and Anderson, 2001</xref>) with function Adonis of the vegan package in R (<xref rid="B64" ref-type="bibr">Oksanen et al., 2013</xref>) to assess the source of variation in the weighted UniFrac matrices. Each dataset encompass the 42 samples of this study. The complete dataset was deposited in the NCBI Sequence Read Archive (SRA) database under study Accession no SRP063723.</p></sec><sec><title>Statistical Analysis</title><p>Taking independently the Atlantic and Mediterranean regions (see Results), contaminated and non-contaminated site groups were defined by calculating and plotting Euclidean distances based on 11 PAHs as a dendrogram based on hierarchical ascendant classification (HAC, Supplementary Figure <xref ref-type="supplementary-material" rid="SM1">S1</xref>). Mean total PAH concentrations between contaminated and non-contaminated sites from each geographic region (i.e., Atlantic and Mediterranean regions) were compared using the Wilcoxon–Mann–Whitney <italic>U</italic> test.</p><p>Collinearities in independent environmental variables were tested before running permutational Manova (PERMANOVA), species abundance distribution (SAD) and network analysis. Variables with collinearity up to 0.75 were grouped together, and proxies were used as explanatory variables. Fluroranthene was the representative predictor for 10 other PAH (i.e., Fluorene, Pyrene, Anthracene, Benz[<italic>a</italic>]anthracene, Benzo[<italic>a</italic>]pyrene, Benzo[<italic>g,h,i</italic>]Perylene, Chrysene, Dibenz[<italic>a,h</italic>]Anthracene, Indeno[1,2,3,<italic>c-d</italic>]Pyrene and Phenanthrene) and salinity for latitude and temperature (Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S3</xref>). Salinity and fluoranthene concentration were log transformed, and F/P ratio was squared transformed to improve the linearity and homoscedasticity of residuals.</p><p>The OTU abundance table was used to examine the SAD patterns of each OTU and partition the SAD into core and satellite microbial OTUs. For this purpose, the index of dispersion for each OTU was calculated as the ratio of the variance to the mean abundance (VMR) multiplied by the occurrence. This index was used to model whether lineages follow a Poisson distribution (i.e., stochastic distribution), falling between the 2.5 and 97.5% confidence interval of the χ<sup>2</sup> distribution (<xref rid="B41" ref-type="bibr">Krebs, 1999</xref>).</p></sec><sec><title>Co-occurrence Network Analysis</title><p>Associations between bacterial, archaeal and eukaryotic OTUs were inferred from an undirected co-occurrence network. Pairwise score between 90% core OTUs were computed using Spearman’s rank correlations. Only co-occurrences corresponding to correlations with a coefficient (rho) > 0.6 and a statistical significance (<italic>P</italic>-value) < 0.001 were considered for further analysis. Non-random co-occurrence patterns were tested with the checkerboard score (<italic>C</italic>-score) under a null model preserving site frequencies (<xref rid="B85" ref-type="bibr">Stone and Roberts, 1990</xref>; <xref rid="B29" ref-type="bibr">Gotelli and McCabe, 2002</xref>). A <italic>C</italic>-score calculated for each pair of microbial OTUs was compared with the <italic>C</italic>-score computed for 5000 randomly assembled null matrices. In order to avoid biases affecting raw <italic>C</italic>-score values (i.e., OTU number, abundance…), the standardized effect size (SES) was calculated (<xref rid="B80" ref-type="bibr">Sridhar et al., 2012</xref>). Because the <italic>C</italic>-score is an inverse indicator of the frequency of co-occurrence, positive SES values indicate less co-occurrence than expected by chance (i.e., predominance of segregation within communities) and <italic>vice versa</italic> for negative values (i.e., predominance of facilitation). If co-occurrences were not different from what was expected by chance, values of SES should fall between -2 and 2.</p><p>The network was visualized with the Gephi software (<xref rid="B5" ref-type="bibr">Bastian et al., 2009</xref>). Nodes represented prokaryotic and eukaryotic OTUs at 90% identity and edges represented the significant correlations between them. Network characterization for comparisons between contaminated and uncontaminated sediments was performed using a set of overall network topological indices (i.e., average node connectivity, average path length, average clustering coefficient and modularity; <xref rid="B60" ref-type="bibr">Newman, 2003</xref>). After module detection, each module was represented by its singular value decomposition (SVD) of abundance profile by using module eigengene analysis (<xref rid="B42" ref-type="bibr">Langfelder and Horvath, 2007</xref>). Module response to environmental and contaminant parameters was assessed by correlations between module eigengenes and environmental factors.</p><p>All analyses were run using the R packages vegan (<xref rid="B64" ref-type="bibr">Oksanen et al., 2013</xref>), igraph (<xref rid="B12" ref-type="bibr">Csardi and Nepusz, 2006</xref>) and WGCNA packages (<xref rid="B43" ref-type="bibr">Langfelder and Horvath, 2008</xref>).</p></sec></sec><sec><title>Results and Discussion</title><sec><title>Variation in Environmental Parameters and PAH Concentrations</title><p>Particle size distribution, %TOC, salinity, and temperature averages of the water column were significantly greater in the Mediterranean sites than in the Atlantic sites (Supplementary Figure <xref ref-type="supplementary-material" rid="SM1">S2</xref>). The salinity, temperature, and latitude gradients were highly correlated (Spearman rho = -0.82, <italic>p</italic>-value = 0.001, Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S3</xref>). Because of the important environmental heterogeneity among the sediments from the two regions, we analyzed the PAHs contamination gradient in both regions individually. PAHs concentrations were strongly correlated to each other (rho > 0.75, <italic>p</italic> < 0.05, Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S3</xref>). In order to compare the PAH concentrations to the Sediment Quality Guidelines thresholds (SQG; <xref rid="B7" ref-type="bibr">Buchman, 2008</xref>), which are available for 9 PAHs among the 11 PAHs of our dataset, the sums of these 9 PAHs concentrations (Σ PAH<sub>9</sub>) and of the corresponding SQGs were calculated (i.e., for fluoranthene, pyrene, anthracene, benz[<italic>a</italic>]anthracene, benzo[<italic>a</italic>]pyrene, chrysene, dibenz[<italic>a,h</italic>]anthracene, fluorene, phenanthrene; <bold>Figure <xref ref-type="fig" rid="F2">2</xref></bold>). The SQG used are the following: PEL, ERL, which are low trigger concentrations and T50 (50% toxicity concentration) values.</p><fig id="F2" position="float"><label>FIGURE 2</label><caption><p><bold>Boxplots presenting the sum of 9 PAH concentrations (Σ PAH<sub>9</sub>, μg/kg DW: fluoranthene, pyrene, anthracene, benz[<italic>a</italic>]anthracene, benzo[<italic>a</italic>]pyrene, chrysene, dibenz[<italic>a,h</italic>]anthracene, fluorene, phenanthrene) in sediment samples from the Mediterranean Sea and Atlantic Ocean.</bold> Plotted thresholds (full line) correspond to Sediment Quality Guidelines: Probable Effect Level (PEL), Effect Range Low (ERL), and 50% toxicity concentration (T50). Within the Atlantic and the Mediterranean Sea subsets, the means of Σ PAH<sub>9</sub> are significantly different between contaminated and non-contaminated samples (<italic>p</italic> < 0.001, Wilcoxon–Mann–Whitney test).</p></caption><graphic xlink:href="fmicb-07-01637-g002"></graphic></fig><p>The HAC analysis confirmed the <italic>a priori</italic> classification (i.e., pre-sampling classification) for most of the samples, and particularly for Mediterranean samples (Supplementary Figure <xref ref-type="supplementary-material" rid="SM1">S1</xref>). <bold>Figure <xref ref-type="fig" rid="F2">2</xref></bold> shows the differences of mean Σ PAH<sub>9</sub> concentrations between Mediterranean and Atlantic regions. Contaminated samples determined using the HAC analysis exhibited significantly higher mean PAH concentrations in both Mediterranean and Atlantic regions (<bold>Figure <xref ref-type="fig" rid="F2">2</xref></bold>). However, the difference between contaminated and non-contaminated samples was much greater in the Mediterranean sites. When comparing mean Σ PAH<sub>9</sub> concentrations, PEL, ERL, and T50 separated Mediterranean contaminated sites from non-contaminated sites, while only PEL could be a threshold between contaminated and non-contaminated Atlantic sites (<bold>Figure <xref ref-type="fig" rid="F2">2</xref></bold>). SQGs were originally defined regarding macrofauna ecotoxicological assays (<xref rid="B7" ref-type="bibr">Buchman, 2008</xref>), and little is known about their reliability for the determination of PAHs toxicity on microorganisms (<xref rid="B87" ref-type="bibr">Sun et al., 2012</xref>). However, bacterial community structure from chronically contaminated estuarine sediment was previously found to respond to low trigger concentrations (<xref rid="B87" ref-type="bibr">Sun et al., 2012</xref>). These structure modifications were mainly related to change in core OTU abundances (<xref rid="B88" ref-type="bibr">Sun et al., 2013</xref>).</p><p>We used diagnosis ratios of PAH concentrations (i.e., fluoranthene to pyrene (F/P) and phenanthrene to anthracene (P/A)) to get an indication of the dominant source of contamination by PAHs (i.e., pyrogenic versus petrogenic; <xref rid="B8" ref-type="bibr">Budzinski et al., 1997</xref>; <xref rid="B59" ref-type="bibr">Neff et al., 2005</xref>). Most of the samples, from both the Mediterranean and the Atlantic regions, exhibited P/A values lower than 10 and F/P values above 1, indicating a pyrogenic contamination (Supplementary Figure <xref ref-type="supplementary-material" rid="SM1">S3</xref>, Supplementary Table <xref ref-type="supplementary-material" rid="SM1">S1</xref>). In contrast, none of the sites exhibited clear petrogenic contamination according to these ratios. PAHs derived from combustion in coastal sediments occurs through atmospheric deposition (<xref rid="B46" ref-type="bibr">Lipiatou et al., 1997</xref>; <xref rid="B28" ref-type="bibr">Golomb et al., 2001</xref>), which constitutes a chronic PAH input since the Industrial Revolution (<xref rid="B45" ref-type="bibr">Lima et al., 2003</xref>; <xref rid="B3" ref-type="bibr">Azoury et al., 2013</xref>). Considering the diagnosis ratios, we could therefore infer that the samples analyzed here were thus facing mainly chronic contamination by pyrolytic PAHs.</p></sec><sec><title>Partitioning the Core and Satellite Communities</title><p>Traditionally in macro-ecology, the SAD in spatially or temporally separated sites can be divided into two groups: the core species/taxa, which are widely distributed and generally abundant, and the satellite species/taxa, which mostly occur in low abundance and at a reduced number of sites (<xref rid="B31" ref-type="bibr">Hanski, 1982</xref>; <xref rid="B52" ref-type="bibr">Magurran and Henderson, 2003</xref>; <xref rid="B92" ref-type="bibr">Ulrich and Zalewski, 2006</xref>). Previous studies showed that this division of the SAD was not artifactual and demonstrated that environmental factors shaped the relative abundance of the core species/taxa, whereas random dispersal mostly explained satellite species/taxa community assembly (<xref rid="B52" ref-type="bibr">Magurran and Henderson, 2003</xref>; <xref rid="B92" ref-type="bibr">Ulrich and Zalewski, 2006</xref>; <xref rid="B51" ref-type="bibr">Magurran, 2007</xref>). The concept has been reinforced in subsequent studies, which suggested that relevant aspects of the SAD could be overlooked without such a partition (<xref rid="B91" ref-type="bibr">Ulrich and Ollik, 2004</xref>; <xref rid="B30" ref-type="bibr">Gray et al., 2005</xref>; <xref rid="B15" ref-type="bibr">Dolan et al., 2009</xref>). Despite a growing number of surveys interested by rare or core communities in microbial ecology (<xref rid="B25" ref-type="bibr">Galand et al., 2009</xref>; <xref rid="B69" ref-type="bibr">Pedrós-Alió, 2012</xref>; <xref rid="B36" ref-type="bibr">Hugoni et al., 2013</xref>; <xref rid="B10" ref-type="bibr">Cariveau et al., 2014</xref>), the mechanistic framework developed by <xref rid="B52" ref-type="bibr">Magurran and Henderson (2003)</xref> to partition the SAD has been very rarely used (<xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>).</p><p>For this purpose, 7488 microbial OTUs (6034 bacteria, 680 archaea, and 774 eukaryotes OTUs at 90% cutoff) from the 42 sediments sampled in this study were analyzed in an abundance-<italic>vs.</italic>-occurrence plot (<bold>Figure <xref ref-type="fig" rid="F3">3A</xref></bold>). In agreement with one of the most robust trend in macro-ecology (<xref rid="B26" ref-type="bibr">Gaston et al., 2000</xref>), we found a significant and positive relationship between the mean abundance and the occurrence. However, due to a high number of OTUs, the typical discontinuity that separates core from satellite OTUs was not appreciable (<bold>Figure <xref ref-type="fig" rid="F3">3A</xref></bold>). In order to partition the SAD, we compared the index of dispersion for each OTU to a model assuming a stochastic distribution (Poisson model) falling between the 2.5% and 97.5% confidence limit of the χ<sup>2</sup> distribution (<xref rid="B41" ref-type="bibr">Krebs, 1999</xref>). Overall, 859 OTUs (11% of the initial number of OTUs) were found to form the core microbial community of coastal sediments (<bold>Figure <xref ref-type="fig" rid="F3">3B</xref></bold>). They represented 80% of the reads. In contrast, the remaining 89% of the OTUs fell below the 2.5% confidence limit line, indicating random distribution through sediment samples (<bold>Figure <xref ref-type="fig" rid="F3">3B</xref></bold>). The ranking abundance plot confirmed that this method represent a tractable and reproducible approach to partition the SAD of microbial communities (<bold>Figure <xref ref-type="fig" rid="F3">3B</xref></bold>). It also highlights the fact that the definition of core or satellite OTUs should not be only based on abundance or occurrence/permanence but on both, as suggested by <xref rid="B35" ref-type="bibr">Hubbell (2001)</xref>.</p><fig id="F3" position="float"><label>FIGURE 3</label><caption><p><bold>Species abundance distribution (SAD) pattern of microbial OTUs in the 42 libraries analyzed. (A)</bold> Occurrence of OTU (number of studies in which a given OTU was found) plotted against its average abundance across these studies. The dotted line depicts the positive correlation between abundance and occurrence. Black and gray dots represent core and satellite OTUs, respectively. <bold>(B)</bold> Occurrence of each microbial OTU plotted against its dispersion index. The line depicts the 2.5% confidence limit of the χ<sup>2</sup> distribution: lineages falling bellow this line follow a Poisson distribution and are randomly dispersed in space. A rank abundance plot of all the OTUs is represented in order to indicate the ranking of the core OTUs.</p></caption><graphic xlink:href="fmicb-07-01637-g003"></graphic></fig></sec><sec><title>Composition and Sensitivity of Core and Satellite Community Members to Environmental Parameters and Hydrocarbon Contamination</title><p>Core and satellite community compositions were found to differ significantly for the three domains of life (<bold>Figure <xref ref-type="fig" rid="F4">4</xref></bold>). A high percentage of satellite OTUs remained unclassified at the phylum level, particularly for eukaryotes with more than 50% of the OTU that could not be affiliated to any taxa. For bacteria, the core community was dominated by OTUs belonging to the <italic>Gammaproteobacteria</italic> (16% of the total abundance) and <italic>Deltaproteobacteria</italic> (9%), which are known to be dominant clades in marine sediments (both contaminated and pristine) and to encompass a large number of hydrocarbon-degrader strains (<xref rid="B67" ref-type="bibr">Paissé et al., 2008</xref>; <xref rid="B96" ref-type="bibr">Zhang et al., 2008</xref>; <xref rid="B74" ref-type="bibr">Rojo, 2009</xref>; <xref rid="B40" ref-type="bibr">Kostka et al., 2011</xref>; <xref rid="B1" ref-type="bibr">Acosta-González et al., 2013</xref>; <xref rid="B88" ref-type="bibr">Sun et al., 2013</xref>). The dominance of <italic>Deltaproteobacteria</italic> OTUs within the core community is in agreement with results found along a pollution gradient in estuarine sediments (<xref rid="B88" ref-type="bibr">Sun et al., 2013</xref>). This class includes most of the sulfate-reducing genera, which play a crucial role in the anaerobic degradation of organic matter (<xref rid="B44" ref-type="bibr">Leloup et al., 2009</xref>), but also in hydrocarbon degradation (<xref rid="B86" ref-type="bibr">Suárez-Suárez et al., 2011</xref>; <xref rid="B81" ref-type="bibr">Stauffert et al., 2014a</xref>). Archaeal core community was the most divergent from the satellite community, with domination by OTUs belonging to the <italic>Thaumarchaeota, Bathyarchaeota</italic> and <italic>Thermoplasmata</italic> (<bold>Figure <xref ref-type="fig" rid="F4">4</xref></bold>). The latter groups, which represented 22 and 14% of total abundance, respectively, were found to be part of the core microbiota in a meta-analysis regrouping more than 200 sediment studies (<xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>). Both archaeal groups seemed to form specific consortia in sediment ecosystems, suggesting a potentially relevant trophic connection related to the degradation of aromatic compounds and detrital proteins (<xref rid="B47" ref-type="bibr">Lloyd et al., 2013</xref>; <xref rid="B55" ref-type="bibr">Meng et al., 2014</xref>; <xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>). In contrast, distribution and potential functions of the <italic>Parvarchaeota</italic> (previously known as <italic>Haloarchaea</italic>), which represented 64% of the total abundance in the archaeal satellite community, are currently unknown.</p><fig id="F4" position="float"><label>FIGURE 4</label><caption><p><bold>Relative abundance of the different microbial taxa in core and satellite groups at the taxonomic level of the class.</bold> Only Classes belonging to Phyla representing more than 5% of total relative abundance were represented. The whole taxonomy of both core and satellite OTUs is available in .csv files within the Supplementary Material.</p></caption><graphic xlink:href="fmicb-07-01637-g004"></graphic></fig><p>For eukaryote a large proportion of the OTUs of the core and satellite communities remained unclassified (i.e., 25% and 57%, respectively), highlighting our ignorance about eukaryotic communities inhabiting coastal sediments. With a growing number of environmental surveys investigating the structure and diversity of eukaryotic communities using the 18S rDNA gene and NGS (next generation sequencing), this result underpinned the urge for the development of eukaryotic taxonomy databases similar to those for prokaryotes. The remaining OTUs were dominated both in the core and satellite communities by members of the <italic>Holozoa</italic> kingdom and the <italic>Alveolata</italic> superphylum with 45 and 18% of the total abundance, respectively.</p><p>We conducted PERMANOVA analyses in order to identify whether the core or the satellite community would show the highest sensitivity to changes in environmental and contaminant variables (<bold>Table <xref ref-type="table" rid="T1">1</xref></bold>). As expected, we observed a strong filtering effect on the most abundant and frequent OTUs forming the core community, with salinity (associated with latitude and temperature) representing the main environmental parameters driving the community composition. %TOC and particle size distribution (% > 63 μm) together explained an additional 10% of the variance in community composition, while fluoranthene explained only 2% of this variance. The response to the measured predictors was weak for the OTUs forming the satellite community, with only 2% of the overall variance explained by salinity. This result may indicate a minimal influence of satellite OTUs on biogeochemical cycles as previously postulated (<xref rid="B27" ref-type="bibr">Gobet et al., 2012</xref>), and contrary to core OTUs that are thought to contribute actively to the biomass and the nutrient cycling within the community (<xref rid="B9" ref-type="bibr">Campbell et al., 2011</xref>; <xref rid="B24" ref-type="bibr">Gaidos et al., 2011</xref>; <xref rid="B69" ref-type="bibr">Pedrós-Alió, 2012</xref>). However, <italic>Gammaproteobacteria</italic> and <italic>Deltaproteobacteria</italic>, which encompass many species able to degrade hydrocarbons (<xref rid="B70" ref-type="bibr">Prince et al., 2010</xref>), were found in similar proportions in the rare and core communities (<bold>Figure <xref ref-type="fig" rid="F4">4</xref></bold>), suggesting the potential role of the rare benthic biosphere in hydrocarbon degradation. Bacterial hydrocarbon-degraders, such as <italic>Cycloclasticus</italic>, were depicted as members of the rare community in non-polluted environment, and became dominant in the presence of hydrocarbon contamination (<xref rid="B89" ref-type="bibr">Teira et al., 2007</xref>; <xref rid="B76" ref-type="bibr">Sauret et al., 2014</xref>). This fluctuating state of specialized taxa from the rare community could facilitate the adaptation of the whole community to chronic hydrocarbon contamination. Overall, despite the predominant response of the core community to environmental changes, we cannot exclude the potentially central role of members of the rare community in chronically hydrocarbon-polluted sediments.</p><table-wrap id="T1" position="float"><label>Table 1</label><caption><p>Results of the PERMANOVA analysis for the estimation of the relative contribution of environmental parameters to the phylogenetic community composition of the core and satellite microbial communities.</p></caption><table frame="hsides" rules="groups" cellspacing="5" cellpadding="5"><thead><tr><th valign="top" align="left" rowspan="1" colspan="1">PERMANOVA (<italic>n</italic> = 32)</th><th valign="top" align="left" rowspan="1" colspan="1">Core</th><th valign="top" align="left" rowspan="1" colspan="1">Satellite</th></tr></thead><tbody><tr><td valign="top" align="left" rowspan="1" colspan="1">Fluoranthene</td><td valign="top" align="left" rowspan="1" colspan="1">2%<sup>∗</sup></td><td valign="top" align="left" rowspan="1" colspan="1"></td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Phenanthrene/Anthracene (P/A)</td><td valign="top" align="left" rowspan="1" colspan="1"></td><td valign="top" align="left" rowspan="1" colspan="1"></td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Fluoranthene to pyrene (F/P)</td><td valign="top" align="left" rowspan="1" colspan="1"></td><td valign="top" align="left" rowspan="1" colspan="1"></td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Salinity</td><td valign="top" align="left" rowspan="1" colspan="1">11%<sup>∗∗∗</sup></td><td valign="top" align="left" rowspan="1" colspan="1">2%<sup>∗</sup></td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Particle size distribution (% > 63 μm)</td><td valign="top" align="left" rowspan="1" colspan="1">5%<sup>∗∗</sup></td><td valign="top" align="left" rowspan="1" colspan="1"></td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">% Total Organic Carbon</td><td valign="top" align="left" rowspan="1" colspan="1">5%<sup>∗∗</sup></td><td valign="top" align="left" rowspan="1" colspan="1"></td></tr></tbody></table><table-wrap-foot><attrib><italic>Fluoranthene was a proxy for 10 other PAH (i.e., fluoranthene, pyrene, anthracene, benz[<italic>a</italic>]anthracene, benzo[<italic>a</italic>]pyrene, chrysene, dibenz[<italic>a,h</italic>]anthracene, fluorene, phenanthrene), salinity for latitude and temperature. <sup>∗</sup><italic>p</italic> < 0.05, <sup>∗∗</sup><italic>p</italic> < 0.01, <sup>∗∗∗</sup><italic>p</italic> < 0.001.</italic></attrib></table-wrap-foot></table-wrap></sec><sec><title>Response of Microbial Consortia and Network Properties to PAH Contaminations</title><p>As illustrated by recent studies, microbial co-occurrence patterns can help to unveil ecologically meaningful interactions between taxa (<xref rid="B34" ref-type="bibr">Horner-Devine et al., 2007</xref>; <xref rid="B84" ref-type="bibr">Steele et al., 2011</xref>; <xref rid="B22" ref-type="bibr">Fillol et al., 2016</xref>) and network properties can be used to study community stability in altered conditions (<xref rid="B98" ref-type="bibr">Zhou et al., 2011</xref>; <xref rid="B13" ref-type="bibr">Deng et al., 2012</xref>; <xref rid="B20" ref-type="bibr">Faust and Raes, 2012</xref>; <xref rid="B88" ref-type="bibr">Sun et al., 2013</xref>). To get a first insight in the potential microbial consortia affected by PAH contaminations and the potential effect of these contaminants on the core community integrity, we constructed a co-occurrence network based on strong and significant Spearman correlations. The dataset containing core OTUs was filtered for optimizing network sensitivity and specificity. The final network included 131 nodes and 566 edges (<bold>Figure <xref ref-type="fig" rid="F5">5</xref></bold>). We used the SES of the <italic>C</italic>-score metric to assess the existence of non-random co-occurrence patterns in the network (<xref rid="B29" ref-type="bibr">Gotelli and McCabe, 2002</xref>; <xref rid="B34" ref-type="bibr">Horner-Devine et al., 2007</xref>; <xref rid="B48" ref-type="bibr">López et al., 2013</xref>). We observed a SES value of 2.56 (<italic>P</italic> < 0.001, <italic>C</italic>-score<sub>norm</sub> = 0.88) indicating non-random network structure. The network was largely dominated by bacterial OTUs, which represented 76% of the nodes (<bold>Figure <xref ref-type="fig" rid="F5">5</xref></bold>). <italic>Eukarya</italic> and <italic>Archaea</italic> represented 15 and 9% of the nodes, respectively. Correlations between domains were common within the network although intra-domain connections tended to be more numerous. These co-occurrences might reflect OTUs performing similarly or harboring complementary functions, but they may also be caused by shared preferred environmental conditions (<xref rid="B84" ref-type="bibr">Steele et al., 2011</xref>; <xref rid="B13" ref-type="bibr">Deng et al., 2012</xref>). Network approaches showed that co-occurring OTUs are often organized into groups, or modules, of functional significance (<xref rid="B11" ref-type="bibr">Chaffron et al., 2010</xref>; <xref rid="B4" ref-type="bibr">Barberán et al., 2012</xref>; <xref rid="B93" ref-type="bibr">Vick-Majors et al., 2014</xref>). Modularity analysis revealed a complex structure composed of 11 modules (<bold>Figure <xref ref-type="fig" rid="F6">6A</xref></bold>). Modules are groups of highly connected OTUs within the group but with very few connections outside the group. <bold>Figure <xref ref-type="fig" rid="F6">6B</xref></bold> shows the response of modules to environment changes, as assessed by means of correlations between modules and environmental parameters. Five of the 11 modules detected were significantly correlated with the environmental parameters measured in this study (<bold>Figure <xref ref-type="fig" rid="F6">6B</xref></bold>). Modules 1, 2, and 6 were correlated to salinity (and associated latitude and temperature), confirming the strong effect of these variables on microbial consortia. In agreement with previous works (<xref rid="B11" ref-type="bibr">Chaffron et al., 2010</xref>; <xref rid="B23" ref-type="bibr">Freilich et al., 2010</xref>; <xref rid="B20" ref-type="bibr">Faust and Raes, 2012</xref>), modules could be considered as ecological and/or functional niches as suggested by modules 1, 2 and 6, which represented low salinity/high latitude and high salinity/low latitude sub-networks, respectively. Module 5 was the only microbial consortium responding (negatively) to fluoranthene and associated PAH concentrations, indicating that PAH contaminations might have a negative impact on the members of this module. This module was composed of four eukaryotic and two bacterial OTUs connected by an unusual number of negative correlations between OTUs belonging to <italic>Actinobacteria</italic> and OTUs belonging to the <italic>Alveolata</italic> taxa (<bold>Figure <xref ref-type="fig" rid="F7">7</xref></bold>), suggesting predator – prey relationships (<xref rid="B20" ref-type="bibr">Faust and Raes, 2012</xref>). This assumption is in agreement with the fact that Alveolates, and more particularly Ciliates, feed on a variety of prey but that many ciliate groups are bacterivores (<xref rid="B56" ref-type="bibr">Meng et al., 2012</xref>).</p><fig id="F5" position="float"><label>FIGURE 5</label><caption><p><bold>Co-occurrence OTU network based on correlation analysis.</bold> Each node denotes a microbial OTU 90%. Node size is proportional to the degree (i.e., the number of links from this node to any other node) and node color denotes taxonomic classification. Edge lines between nodes represent significant co-occurrence relationships. Edge size indicates the strength of Spearman correlation among nodes.</p></caption><graphic xlink:href="fmicb-07-01637-g005"></graphic></fig><fig id="F6" position="float"><label>FIGURE 6</label><caption><p><bold>(A)</bold> Same network as in <bold>Figure <xref ref-type="fig" rid="F5">5</xref></bold>, but modules are indicated. Modules significantly related to environmental parameters are colored in black. <bold>(B)</bold> The correlations between module eigengenes and environmental traits in the core community network. Only module significantly related to environmental parameters and contaminants are shown. The color of each plot indicates the correlation between corresponding module eigengene and environmental trait. Red color means highly positive correlation and green color means highly negative correlation. The numbers in each plot are the correlation coefficient (r) and significance (p) in parentheses. Correlations with <italic>p</italic> > 0.05 are in bold.</p></caption><graphic xlink:href="fmicb-07-01637-g006"></graphic></fig><fig id="F7" position="float"><label>FIGURE 7</label><caption><p><bold>Co-occurrence OTU network for module 5.</bold> Edge size indicates the number of connections (degree). Node size is proportional to the degree (i.e., the number of links from this node to any other node) and node color denotes taxonomic classification. Edge lines between nodes represent significant co-occurrences relationships. Values indicated Spearman correlations.</p></caption><graphic xlink:href="fmicb-07-01637-g007"></graphic></fig><p>Comparing network properties and overall topology can be used to study community stability/vulnerability in altered conditions. In order to assess the influence of hydrocarbon contaminants on network properties, we split the core OTU abundance table based on the classification provided by the HAC (Supplementary Figure <xref ref-type="supplementary-material" rid="SM1">S2</xref>) and constructed separated microbial networks for non-contaminated and contaminated sediment communities (<bold>Table <xref ref-type="table" rid="T2">2</xref></bold>). Non-contaminated and contaminated networks were generated for the whole dataset and for each region (i.e., Mediterranean and Atlantic) in order to limit the influence of environmental variables (i.e., salinity, temperature, latitude, PSD and %TOC, which were significantly different between Mediterranean and Atlantic regions). Network comparisons are commonly achieved by calculating the average for each node of four network indices (i) connectivity or degree distribution, which represent the number of edges of a node toward other nodes; (ii) path length, which is the shortest path between two nodes; (iii) the clustering coefficient, which describes how well a node is connected to its neighbors; (iv) modularity, a measure of the structuration of the network into modules (<xref rid="B13" ref-type="bibr">Deng et al., 2012</xref>). <bold>Table <xref ref-type="table" rid="T2">2</xref></bold> showed that the three pairs of networks calculated here presented the typical topology for microbial networks (<xref rid="B11" ref-type="bibr">Chaffron et al., 2010</xref>; <xref rid="B84" ref-type="bibr">Steele et al., 2011</xref>; <xref rid="B4" ref-type="bibr">Barberán et al., 2012</xref>; <xref rid="B13" ref-type="bibr">Deng et al., 2012</xref>): scale-free (i.e., node connectivity distribution not different from a power law model, data not shown), small-world (clustering coefficient ranging from 0.56 to 0.89 and average path from 2.22 to 2.75) and modular (modularity ranging from 0.72 to 0.86). Overall and except for the Atlantic samples, significant differences between contaminated and non-contaminated networks were detected in terms of average connectivity, average shortest path and average clustering coefficient (<bold>Table <xref ref-type="table" rid="T2">2</xref></bold>). These results indicated that hydrocarbon contaminations might have a significant and negative effect on the interactions among microbial taxa in coastal sediments. Indeed, the higher values for average shortest path in contaminated networks may imply lower efficiency and speed in the transmission of information, energy or material in the system, potentially altering the response of the microbial community to environmental perturbations (<xref rid="B97" ref-type="bibr">Zhou et al., 2010</xref>; <xref rid="B13" ref-type="bibr">Deng et al., 2012</xref>). In addition, the lower connectivity and lower average clustering coefficient in contaminated networks may make the networks less resistant to change (<xref rid="B2" ref-type="bibr">Albert et al., 2000</xref>; <xref rid="B57" ref-type="bibr">Montoya et al., 2006</xref>). This may also indicate a potential perturbation of the network and the loss of important community members. A lower clustering coefficient is indeed an indication of the loss of highly connected nodes (i.e., hubs), which have been related to the concept of keystone species (<xref rid="B66" ref-type="bibr">Paine, 1969</xref>; <xref rid="B84" ref-type="bibr">Steele et al., 2011</xref>). Such keystone species loss could cause a greater fragility of the network, which ultimately could lead to its fragmentation and to secondary extinctions of species relying on the hubs (<xref rid="B79" ref-type="bibr">Solé and Montoya, 2001</xref>).</p><table-wrap id="T2" position="float"><label>Table 2</label><caption><p>Topological properties of the networks generated for core communities in contaminated and non-contaminated samples.</p></caption><table frame="hsides" rules="groups" cellspacing="5" cellpadding="5"><thead><tr><th valign="top" align="left" rowspan="1" colspan="1">Network properties</th><th valign="top" align="center" rowspan="1" colspan="1">Ctot-prist</th><th valign="top" align="center" rowspan="1" colspan="1">Ctot-cont</th><th valign="top" align="center" rowspan="1" colspan="1">Cmed-prist</th><th valign="top" align="center" rowspan="1" colspan="1">Cmed-cont</th><th valign="top" align="center" rowspan="1" colspan="1">Catl-prist</th><th valign="top" align="center" rowspan="1" colspan="1">Catl-cont</th></tr></thead><tbody><tr><td valign="top" align="left" rowspan="1" colspan="1">N° of original OTUs</td><td valign="top" align="center" rowspan="1" colspan="1">322</td><td valign="top" align="center" rowspan="1" colspan="1">312</td><td valign="top" align="center" rowspan="1" colspan="1">216</td><td valign="top" align="center" rowspan="1" colspan="1">197</td><td valign="top" align="center" rowspan="1" colspan="1">167</td><td valign="top" align="center" rowspan="1" colspan="1">166</td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">N° of OTU in the network</td><td valign="top" align="center" rowspan="1" colspan="1">126</td><td valign="top" align="center" rowspan="1" colspan="1">133</td><td valign="top" align="center" rowspan="1" colspan="1">98</td><td valign="top" align="center" rowspan="1" colspan="1">99</td><td valign="top" align="center" rowspan="1" colspan="1">76</td><td valign="top" align="center" rowspan="1" colspan="1">78</td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Average Degree (connectivity)</td><td valign="top" align="center" rowspan="1" colspan="1">9.2<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">8.6<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">6.8<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">5.1<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">5</td><td valign="top" align="center" rowspan="1" colspan="1">5.1</td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Average clustering coefficient</td><td valign="top" align="center" rowspan="1" colspan="1">0.89<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">0.74<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">0.62<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">0.56<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">0.64</td><td valign="top" align="center" rowspan="1" colspan="1">0.63</td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Modularity</td><td valign="top" align="center" rowspan="1" colspan="1">0.86</td><td valign="top" align="center" rowspan="1" colspan="1">0.84</td><td valign="top" align="center" rowspan="1" colspan="1">0.74</td><td valign="top" align="center" rowspan="1" colspan="1">0.72</td><td valign="top" align="center" rowspan="1" colspan="1">0.73</td><td valign="top" align="center" rowspan="1" colspan="1">0.75</td></tr><tr><td valign="top" align="left" rowspan="1" colspan="1">Average shortest path (geodesic distance)</td><td valign="top" align="center" rowspan="1" colspan="1">1.31<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">1.75<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">1.22<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">1.70<sup>a</sup></td><td valign="top" align="center" rowspan="1" colspan="1">1.24</td><td valign="top" align="center" rowspan="1" colspan="1">1.25</td></tr></tbody></table><table-wrap-foot><attrib><italic>Ctot, Cmed and Catl stand for whole data set, Mediterranean samples, Atlantic samples, respectively. Prist and cont stand for pristine and contaminated samples. <sup>a</sup>Significant difference (<italic>P</italic> < 0.001) between values from non contaminated and contaminated networks.</italic></attrib></table-wrap-foot></table-wrap><p>Altogether, these results suggested that hydrocarbon contaminations might have altered the microbial network in coastal sediments, rendering the microbial communities inhabiting these habitats more vulnerable to environmental perturbations.</p></sec></sec><sec><title>Author Contributions</title><p>J-CA, JG, and RD conceived and designed the study. MJ ran the experiments. J-CA and MJ ran the data analysis. J-FG, JT, OB, and HA provided sediment samples, chemical and physical data. J-CA and MJ prepared the manuscript.</p></sec><sec><title>Conflict of Interest Statement</title><p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p></sec></body><back><fn-group><fn fn-type="financial-disclosure"><p><bold>Funding.</bold> This work was supported by a Ph.D. grant from the French Ministry of Higher Education and Research to MJ, by the CNRS INSU EC2CO “Microbien” and “ECODYN” program project INTERMIC and the Agence Nationale de la Recherche (ANR) project EUREKA (ANR-14-CE02-0004).</p></fn></fn-group><sec sec-type="supplementary material"><title>Supplementary Material</title><p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="http://journal.frontiersin.org/article/10.3389/fmicb.2016.01637">http://journal.frontiersin.org/article/10.3389/fmicb.2016.01637</ext-link></p><supplementary-material content-type="local-data" id="SM1"><media xlink:href="Data_Sheet_1.CSV"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="SM2"><media xlink:href="Data_Sheet_2.CSV"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="SM3"><media xlink:href="Data_Sheet_3.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></sec><ref-list><title>References</title><ref id="B1"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Acosta-González</surname><given-names>A.</given-names></name><name><surname>Rosselló-Móra</surname><given-names>R.</given-names></name><name><surname>Marqués</surname><given-names>S.</given-names></name></person-group> (<year>2013</year>). <article-title>Characterization of the anaerobic microbial community in oil-polluted subtidal sediments: aromatic biodegradation potential after the Prestige oil spill.</article-title><source><italic>Environ. 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