A metagenome of a full-scale microbial community carrying out enhanced biological phosphorus removal
Enhanced biological phosphorus removal (EBPR) is widely used for removal of phosphorus from wastewater. In this study, a metagenome (18.2 Gb) was generated using Illumina sequencing from a full-scale EBPR plant to study the community structure and genetic potential. Quantitative fluorescence in situ...
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description | Enhanced biological phosphorus removal (EBPR) is widely used for removal of phosphorus from wastewater. In this study, a metagenome (18.2 Gb) was generated using Illumina sequencing from a full-scale EBPR plant to study the community structure and genetic potential. Quantitative fluorescence
in situ
hybridization (qFISH) was applied as an independent method to evaluate the community structure. The results were in qualitative agreement, but a DNA extraction bias against gram positive bacteria using standard extraction protocols was identified, which would not have been identified without the use of qFISH. The genetic potential for community function showed enrichment of genes involved in phosphate metabolism and biofilm formation, reflecting the selective pressure of the EBPR process. Most contigs in the assembled metagenome had low similarity to genes from currently sequenced genomes, underlining the need for more reference genomes of key EBPR species. Only the genome of ‘
Candidatus
Accumulibacter’, a genus of phosphorus-removing organisms, was closely enough related to the species present in the metagenome to allow for detailed investigations. Accumulibacter accounted for only 4.8% of all bacteria by qFISH, but the depth of sequencing enabled detailed insight into their microdiversity in the full-scale plant. Only 15% of the reads matching Accumulibacter had a high similarity (>95%) to the sequenced Accumulibacter clade IIA strain UW-1 genome, indicating the presence of some microdiversity. The differences in gene complement between the Accumulibacter clades were limited to genes for extracellular polymeric substances and phage-related genes, suggesting a selective pressure from phages on the Accumulibacter diversity. |
doi_str_mv | 10.1038/ismej.2011.176 |
format | Article |
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in situ
hybridization (qFISH) was applied as an independent method to evaluate the community structure. The results were in qualitative agreement, but a DNA extraction bias against gram positive bacteria using standard extraction protocols was identified, which would not have been identified without the use of qFISH. The genetic potential for community function showed enrichment of genes involved in phosphate metabolism and biofilm formation, reflecting the selective pressure of the EBPR process. Most contigs in the assembled metagenome had low similarity to genes from currently sequenced genomes, underlining the need for more reference genomes of key EBPR species. Only the genome of ‘
Candidatus
Accumulibacter’, a genus of phosphorus-removing organisms, was closely enough related to the species present in the metagenome to allow for detailed investigations. Accumulibacter accounted for only 4.8% of all bacteria by qFISH, but the depth of sequencing enabled detailed insight into their microdiversity in the full-scale plant. Only 15% of the reads matching Accumulibacter had a high similarity (>95%) to the sequenced Accumulibacter clade IIA strain UW-1 genome, indicating the presence of some microdiversity. The differences in gene complement between the Accumulibacter clades were limited to genes for extracellular polymeric substances and phage-related genes, suggesting a selective pressure from phages on the Accumulibacter diversity.</description><identifier>ISSN: 1751-7362</identifier><identifier>EISSN: 1751-7370</identifier><identifier>DOI: 10.1038/ismej.2011.176</identifier><identifier>PMID: 22170425</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Bacteria - classification ; Bacteria - genetics ; Bacteria - metabolism ; Biofilms ; Biomedical and Life Sciences ; Community structure ; Deoxyribonucleic acid ; DNA ; DNA, Bacterial - genetics ; Ecology ; Evolutionary Biology ; Fluorescence ; Fluorescence in situ hybridization ; Genomes ; Gram-positive bacteria ; Hybridization ; In Situ Hybridization, Fluorescence ; Life Sciences ; Metabolism ; Metagenome ; Microbial Ecology ; Microbial Genetics and Genomics ; Microbiology ; Original ; original-article ; Phages ; Phosphate ; Phosphorus ; Phosphorus - metabolism ; Phosphorus removal ; Plant communities ; RNA, Ribosomal, 16S - genetics ; RNA, Ribosomal, 16S - metabolism ; Sequence Analysis, DNA ; Sewage - microbiology ; Waste Disposal, Fluid ; Waste water ; Waste Water - microbiology</subject><ispartof>The ISME Journal, 2012-06, Vol.6 (6), p.1094-1106</ispartof><rights>International Society for Microbial Ecology 2012</rights><rights>Copyright Nature Publishing Group Jun 2012</rights><rights>Copyright © 2012 International Society for Microbial Ecology 2012 International Society for Microbial Ecology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-2221f85bc4d98468a16d90a37c3e6699a0ffff6688f942608e524c9a842764ce3</citedby><cites>FETCH-LOGICAL-c557t-2221f85bc4d98468a16d90a37c3e6699a0ffff6688f942608e524c9a842764ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358022/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358022/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22170425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albertsen, Mads</creatorcontrib><creatorcontrib>Hansen, Lea Benedicte Skov</creatorcontrib><creatorcontrib>Saunders, Aaron Marc</creatorcontrib><creatorcontrib>Nielsen, Per Halkjær</creatorcontrib><creatorcontrib>Nielsen, Kåre Lehmann</creatorcontrib><title>A metagenome of a full-scale microbial community carrying out enhanced biological phosphorus removal</title><title>The ISME Journal</title><addtitle>ISME J</addtitle><addtitle>ISME J</addtitle><description>Enhanced biological phosphorus removal (EBPR) is widely used for removal of phosphorus from wastewater. In this study, a metagenome (18.2 Gb) was generated using Illumina sequencing from a full-scale EBPR plant to study the community structure and genetic potential. Quantitative fluorescence
in situ
hybridization (qFISH) was applied as an independent method to evaluate the community structure. The results were in qualitative agreement, but a DNA extraction bias against gram positive bacteria using standard extraction protocols was identified, which would not have been identified without the use of qFISH. The genetic potential for community function showed enrichment of genes involved in phosphate metabolism and biofilm formation, reflecting the selective pressure of the EBPR process. Most contigs in the assembled metagenome had low similarity to genes from currently sequenced genomes, underlining the need for more reference genomes of key EBPR species. Only the genome of ‘
Candidatus
Accumulibacter’, a genus of phosphorus-removing organisms, was closely enough related to the species present in the metagenome to allow for detailed investigations. Accumulibacter accounted for only 4.8% of all bacteria by qFISH, but the depth of sequencing enabled detailed insight into their microdiversity in the full-scale plant. Only 15% of the reads matching Accumulibacter had a high similarity (>95%) to the sequenced Accumulibacter clade IIA strain UW-1 genome, indicating the presence of some microdiversity. The differences in gene complement between the Accumulibacter clades were limited to genes for extracellular polymeric substances and phage-related genes, suggesting a selective pressure from phages on the Accumulibacter diversity.</description><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - metabolism</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Community structure</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>Ecology</subject><subject>Evolutionary Biology</subject><subject>Fluorescence</subject><subject>Fluorescence in situ hybridization</subject><subject>Genomes</subject><subject>Gram-positive bacteria</subject><subject>Hybridization</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Metagenome</subject><subject>Microbial Ecology</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Original</subject><subject>original-article</subject><subject>Phages</subject><subject>Phosphate</subject><subject>Phosphorus</subject><subject>Phosphorus - metabolism</subject><subject>Phosphorus removal</subject><subject>Plant communities</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>RNA, Ribosomal, 16S - metabolism</subject><subject>Sequence Analysis, DNA</subject><subject>Sewage - microbiology</subject><subject>Waste Disposal, Fluid</subject><subject>Waste water</subject><subject>Waste Water - microbiology</subject><issn>1751-7362</issn><issn>1751-7370</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkctr3DAQxkVpaNK01x6LoJdevNHDluRLIYS-IJBLehZaeezVosdWsgP730fbTZe0RDBIML_5NDMfQh8oWVHC1ZUrAbYrRihdUSleoQsqO9pILsnr01uwc_S2lC0hnRRCvkHnjFFJWtZdoOEaB5jNBDEFwGnEBo-L902xxgMOzua0dsZjm0JYopv32Jqc9y5OOC0zhrgx0cKA1y75NLlahXebVGrkpeAMIT0Y_w6djcYXeP90X6Jf377e3_xobu--_7y5vm1s18m5YbWtUXVr2w69aoUyVAw9MVxaDkL0vSFjPUIoNfYtE0RBx1rbG9UyKVoL_BJ9OerulnWAwUKcs_F6l10wea-TcfrfTHQbPaUHzXmnCGNV4POTQE6_FyizDq5Y8N5ESEvRlLDK0Zbyin76D92mJcc6XqUoF4IxchBcHam6x1IyjKdmKNEHA_UfA_XBQF0NrAUfn49wwv86VoGrI1BqKk6Qn__7ouQjnBGoeQ</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Albertsen, Mads</creator><creator>Hansen, Lea Benedicte Skov</creator><creator>Saunders, Aaron Marc</creator><creator>Nielsen, Per Halkjær</creator><creator>Nielsen, Kåre Lehmann</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20120601</creationdate><title>A metagenome of a full-scale microbial community carrying out enhanced biological phosphorus removal</title><author>Albertsen, Mads ; Hansen, Lea Benedicte Skov ; Saunders, Aaron Marc ; Nielsen, Per Halkjær ; Nielsen, Kåre Lehmann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c557t-2221f85bc4d98468a16d90a37c3e6699a0ffff6688f942608e524c9a842764ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Bacteria - 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In this study, a metagenome (18.2 Gb) was generated using Illumina sequencing from a full-scale EBPR plant to study the community structure and genetic potential. Quantitative fluorescence
in situ
hybridization (qFISH) was applied as an independent method to evaluate the community structure. The results were in qualitative agreement, but a DNA extraction bias against gram positive bacteria using standard extraction protocols was identified, which would not have been identified without the use of qFISH. The genetic potential for community function showed enrichment of genes involved in phosphate metabolism and biofilm formation, reflecting the selective pressure of the EBPR process. Most contigs in the assembled metagenome had low similarity to genes from currently sequenced genomes, underlining the need for more reference genomes of key EBPR species. Only the genome of ‘
Candidatus
Accumulibacter’, a genus of phosphorus-removing organisms, was closely enough related to the species present in the metagenome to allow for detailed investigations. Accumulibacter accounted for only 4.8% of all bacteria by qFISH, but the depth of sequencing enabled detailed insight into their microdiversity in the full-scale plant. Only 15% of the reads matching Accumulibacter had a high similarity (>95%) to the sequenced Accumulibacter clade IIA strain UW-1 genome, indicating the presence of some microdiversity. The differences in gene complement between the Accumulibacter clades were limited to genes for extracellular polymeric substances and phage-related genes, suggesting a selective pressure from phages on the Accumulibacter diversity.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>22170425</pmid><doi>10.1038/ismej.2011.176</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria - classification Bacteria - genetics Bacteria - metabolism Biofilms Biomedical and Life Sciences Community structure Deoxyribonucleic acid DNA DNA, Bacterial - genetics Ecology Evolutionary Biology Fluorescence Fluorescence in situ hybridization Genomes Gram-positive bacteria Hybridization In Situ Hybridization, Fluorescence Life Sciences Metabolism Metagenome Microbial Ecology Microbial Genetics and Genomics Microbiology Original original-article Phages Phosphate Phosphorus Phosphorus - metabolism Phosphorus removal Plant communities RNA, Ribosomal, 16S - genetics RNA, Ribosomal, 16S - metabolism Sequence Analysis, DNA Sewage - microbiology Waste Disposal, Fluid Waste water Waste Water - microbiology |
title | A metagenome of a full-scale microbial community carrying out enhanced biological phosphorus removal |
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