26
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Chronic Polyaromatic Hydrocarbon (PAH) Contamination Is a Marginal Driver for Community Diversity and Prokaryotic Predicted Functioning in Coastal Sediments

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Benthic microorganisms are key players in the recycling of organic matter and recalcitrant compounds such as polyaromatic hydrocarbons (PAHs) in coastal sediments. Despite their ecological importance, the response of microbial communities to chronic PAH pollution, one of the major threats to coastal ecosystems, has received very little attention. In one of the largest surveys performed so far on coastal sediments, the diversity and composition of microbial communities inhabiting both chronically contaminated and non-contaminated coastal sediments were investigated using high-throughput sequencing on the 18S and 16S rRNA genes. Prokaryotic alpha-diversity showed significant association with salinity, temperature, and organic carbon content. The effect of particle size distribution was strong on eukaryotic diversity. Similarly to alpha-diversity, beta-diversity patterns were strongly influenced by the environmental filter, while PAHs had no influence on the prokaryotic community structure and a weak impact on the eukaryotic community structure at the continental scale. However, at the regional scale, PAHs became the main driver shaping the structure of bacterial and eukaryotic communities. These patterns were not found for PICRUSt predicted prokaryotic functions, thus indicating some degree of functional redundancy. Eukaryotes presented a greater potential for their use as PAH contamination biomarkers, owing to their stronger response at both regional and continental scales.

          Related collections

          Most cited references72

          • Record: found
          • Abstract: found
          • Article: not found

          16S ribosomal DNA amplification for phylogenetic study.

          A set of oligonucleotide primers capable of initiating enzymatic amplification (polymerase chain reaction) on a phylogenetically and taxonomically wide range of bacteria is described along with methods for their use and examples. One pair of primers is capable of amplifying nearly full-length 16S ribosomal DNA (rDNA) from many bacterial genera; the additional primers are useful for various exceptional sequences. Methods for purification of amplified material, direct sequencing, cloning, sequencing, and transcription are outlined. An obligate intracellular parasite of bovine erythrocytes, Anaplasma marginale, is used as an example; its 16S rDNA was amplified, cloned, sequenced, and phylogenetically placed. Anaplasmas are related to the genera Rickettsia and Ehrlichia. In addition, 16S rDNAs from several species were readily amplified from material found in lyophilized ampoules from the American Type Culture Collection. By use of this method, the phylogenetic study of extremely fastidious or highly pathogenic bacterial species can be carried out without the need to culture them. In theory, any gene segment for which polymerase chain reaction primer design is possible can be derived from a readily obtainable lyophilized bacterial culture.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Pyrosequencing enumerates and contrasts soil microbial diversity.

            Estimates of the number of species of bacteria per gram of soil vary between 2000 and 8.3 million (Gans et al., 2005; Schloss and Handelsman, 2006). The highest estimate suggests that the number may be so large as to be impractical to test by amplification and sequencing of the highly conserved 16S rRNA gene from soil DNA (Gans et al., 2005). Here we present the use of high throughput DNA pyrosequencing and statistical inference to assess bacterial diversity in four soils across a large transect of the western hemisphere. The number of bacterial 16S rRNA sequences obtained from each site varied from 26,140 to 53,533. The most abundant bacterial groups in all four soils were the Bacteroidetes, Betaproteobacteria and Alphaproteobacteria. Using three estimators of diversity, the maximum number of unique sequences (operational taxonomic units roughly corresponding to the species level) never exceeded 52,000 in these soils at the lowest level of dissimilarity. Furthermore, the bacterial diversity of the forest soil was phylum rich compared to the agricultural soils, which are species rich but phylum poor. The forest site also showed far less diversity of the Archaea with only 0.009% of all sequences from that site being from this group as opposed to 4%-12% of the sequences from the three agricultural sites. This work is the most comprehensive examination to date of bacterial diversity in soil and suggests that agricultural management of soil may significantly influence the diversity of bacteria and archaea.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Improving indicator species analysis by combining groups of sites

                Bookmark

                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                19 August 2016
                2016
                : 7
                : 1303
                Affiliations
                [1] 1Equipe Environnement et Microbiologie, Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux, UMR 5254 CNRS - Université de Pau et des Pays de L’Adour Pau, France
                [2] 2Laboratoire Biogéochimie des Contaminants Organiques, Unité Biogéochimie et Ecotoxicologie, Département Ressources Biologiques et Environnement, Ifremer Centre Atlantique Nantes, France
                [3] 3Laboratoire d’Océanographie Microbienne, Sorbonne Universités, CNRS, Université Pierre-et-Marie-Curie, UMR 7621, Observatoire Océanologique Banyuls-sur-mer, France
                [4] 4Littoral, Environnement et Sociétés, UMR 7266 CNRS – Université de La Rochelle La Rochelle, France
                [5] 5Laboratoire de Bio-surveillance de l’Environnement, Faculté des Sciences de Bizerte Zarzouna, Tunisia
                [6] 6Laboratoire Microorganismes: Génome et Environnement, UMR 6023 CNRS – Université Blaise Pascal Aubière, France
                [7] 7Processus de Transferts et d’Echanges dans l’Environnement, EA 3819, Université de Toulon La Garde, France
                [8] 8Marine Biodiversity, Exploitation and Conservation, UMR CNRS 9190 Montpellier, France
                Author notes

                Edited by: Belinda Ferrari, University of New South Wales, Australia

                Reviewed by: Dennis A. Bazylinski, University of Nevada, Las Vegas, USA; Michelle Power, Macquarie University, Australia

                *Correspondence: Mathilde Jeanbille, mathilde.jeanbille@ 123456univ-pau.fr

                This article was submitted to Microbiotechnology, Ecotoxicology, and Bioremediation, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2016.01303
                4990537
                ac14676e-79c3-4000-9bdd-aff34f9d6e07
                Copyright © 2016 Jeanbille, Gury, Duran, Tronczynski, Ghiglione, Agogué, Saïd, Taïb, Debroas, Garnier and Auguet.

                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.

                History
                : 17 May 2016
                : 08 August 2016
                Page count
                Figures: 6, Tables: 2, Equations: 0, References: 104, Pages: 15, Words: 0
                Funding
                Funded by: Ministère de l’Education Nationale, de l’Enseignement Supérieur et de la Recherche 10.13039/501100004793
                Funded by: Institut National des Sciences de l’Univers, Centre National de la Recherche Scientifique 10.13039/501100004617
                Funded by: Agence de l’Eau Rhône Méditerranée Corse 10.13039/501100007758
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                microbial communities,pah,chronic contamination,coastal sediment,functional diversity

                Comments

                Comment on this article