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Metabarcoding using multiplexed markers increases species detection in complex zooplankton communities
Metabarcoding combines DNA barcoding with high‐throughput sequencing, often using one genetic marker to understand complex and taxonomically diverse samples. However, species‐level identification depends heavily on the choice of marker and the selected primer pair, often with a trade‐off between suc...
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Published in: | Evolutionary applications 2018-12, Vol.11 (10), p.1901-1914 |
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description | Metabarcoding combines DNA barcoding with high‐throughput sequencing, often using one genetic marker to understand complex and taxonomically diverse samples. However, species‐level identification depends heavily on the choice of marker and the selected primer pair, often with a trade‐off between successful species amplification and taxonomic resolution. We present a versatile metabarcoding protocol for biomonitoring that involves the use of two barcode markers (COI and 18S) and four primer pairs in a single high‐throughput sequencing run, via sample multiplexing. We validate the protocol using a series of 24 mock zooplanktonic communities incorporating various levels of genetic variation. With the use of a single marker and single primer pair, the highest species recovery was 77%. With all three COI fragments, we detected 62%–83% of species across the mock communities, while the use of the 18S fragment alone resulted in the detection of 73%–75% of species. The species detection level was significantly improved to 89%–93% when both markers were used. Furthermore, multiplexing did not have a negative impact on the proportion of reads assigned to each species and the total number of species detected was similar to when markers were sequenced alone. Overall, our metabarcoding approach utilizing two barcode markers and multiple primer pairs per barcode improved species detection rates over a single marker/primer pair by 14% to 35%, making it an attractive and relatively cost‐effective method for biomonitoring natural zooplankton communities. We strongly recommend combining evolutionary independent markers and, when necessary, multiple primer pairs per marker to increase species detection (i.e., reduce false negatives) in metabarcoding studies. |
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With all three COI fragments, we detected 62%–83% of species across the mock communities, while the use of the 18S fragment alone resulted in the detection of 73%–75% of species. The species detection level was significantly improved to 89%–93% when both markers were used. Furthermore, multiplexing did not have a negative impact on the proportion of reads assigned to each species and the total number of species detected was similar to when markers were sequenced alone. Overall, our metabarcoding approach utilizing two barcode markers and multiple primer pairs per barcode improved species detection rates over a single marker/primer pair by 14% to 35%, making it an attractive and relatively cost‐effective method for biomonitoring natural zooplankton communities. We strongly recommend combining evolutionary independent markers and, when necessary, multiple primer pairs per marker to increase species detection (i.e., reduce false negatives) in metabarcoding studies.</description><identifier>ISSN: 1752-4571</identifier><identifier>EISSN: 1752-4571</identifier><identifier>DOI: 10.1111/eva.12694</identifier><identifier>PMID: 30459837</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>18S ; Biomonitoring ; cytochrome c oxidase subunit I ; Deoxyribonucleic acid ; DNA ; DNA barcoding ; DNA sequencing ; Genetic diversity ; Genetic markers ; metabarcoding ; multigene ; multiple primer pairs ; Original ; Species ; Zooplankton</subject><ispartof>Evolutionary applications, 2018-12, Vol.11 (10), p.1901-1914</ispartof><rights>2018 McGill University. published by John Wiley & Sons Ltd</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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J.</creatorcontrib><creatorcontrib>Abbott, Cathryn L.</creatorcontrib><creatorcontrib>Cristescu, Melania E.</creatorcontrib><title>Metabarcoding using multiplexed markers increases species detection in complex zooplankton communities</title><title>Evolutionary applications</title><addtitle>Evol Appl</addtitle><description>Metabarcoding combines DNA barcoding with high‐throughput sequencing, often using one genetic marker to understand complex and taxonomically diverse samples. However, species‐level identification depends heavily on the choice of marker and the selected primer pair, often with a trade‐off between successful species amplification and taxonomic resolution. We present a versatile metabarcoding protocol for biomonitoring that involves the use of two barcode markers (COI and 18S) and four primer pairs in a single high‐throughput sequencing run, via sample multiplexing. 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We strongly recommend combining evolutionary independent markers and, when necessary, multiple primer pairs per marker to increase species detection (i.e., reduce false negatives) in metabarcoding studies.</description><subject>18S</subject><subject>Biomonitoring</subject><subject>cytochrome c oxidase subunit I</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA barcoding</subject><subject>DNA sequencing</subject><subject>Genetic diversity</subject><subject>Genetic markers</subject><subject>metabarcoding</subject><subject>multigene</subject><subject>multiple primer pairs</subject><subject>Original</subject><subject>Species</subject><subject>Zooplankton</subject><issn>1752-4571</issn><issn>1752-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kUtPxCAUhYnR-Bhd-AdMEze6mLGUAtONiTG-kjFu1C2hcBnRtlRoff16GWecqIksuIT7cXIPB6FdnI5wXEfwIkc4Y0W-gjYxp9kwpxyv_jhvoK0QHtOUpYxk62iDpDktxoRvInMNnSylV07bZpr0YbbXfdXZtoI30Ekt_RP4kNhGeZABQhJaUDZWDR2ozrom9hLl6tmD5MO5tpLNU-e-7uq-sV2Et9GakVWAnUUdoLvzs9vTy-Hk5uLq9GQyVDQt8mEhVc6pBJwbKBkrSKlVpqjmGcdYGlMSo6k2XEuJiTbEACZESs3GzBRcUzJAx3Pdti9r0AqazstKtN5GH-_CSSt-dxr7IKbuRbCM4JyzKHCwEPDuuYfQidoGBVX0BK4PIsOEUYr5OI_o_h_00fW-ifZmFB7T-MVppA7nlPIuBA9mOQxOxSw9EdMTX-lFdu_n9EvyO64IHM2BV1vB-_9K4uz-ZC75CQzNqGQ</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Zhang, Guang K.</creator><creator>Chain, Frédéric J. 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J. ; Abbott, Cathryn L. ; Cristescu, Melania E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5094-9ac475ae14feb6693bdc2c5d72711affb3fd5df7daa13df3fe133aad686f97d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>18S</topic><topic>Biomonitoring</topic><topic>cytochrome c oxidase subunit I</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA barcoding</topic><topic>DNA sequencing</topic><topic>Genetic diversity</topic><topic>Genetic markers</topic><topic>metabarcoding</topic><topic>multigene</topic><topic>multiple primer pairs</topic><topic>Original</topic><topic>Species</topic><topic>Zooplankton</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Guang K.</creatorcontrib><creatorcontrib>Chain, Frédéric J. J.</creatorcontrib><creatorcontrib>Abbott, Cathryn L.</creatorcontrib><creatorcontrib>Cristescu, Melania E.</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley-Blackwell Open Access Backfiles (Open Access)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evolutionary applications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Guang K.</au><au>Chain, Frédéric J. J.</au><au>Abbott, Cathryn L.</au><au>Cristescu, Melania E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabarcoding using multiplexed markers increases species detection in complex zooplankton communities</atitle><jtitle>Evolutionary applications</jtitle><addtitle>Evol Appl</addtitle><date>2018-12</date><risdate>2018</risdate><volume>11</volume><issue>10</issue><spage>1901</spage><epage>1914</epage><pages>1901-1914</pages><issn>1752-4571</issn><eissn>1752-4571</eissn><abstract>Metabarcoding combines DNA barcoding with high‐throughput sequencing, often using one genetic marker to understand complex and taxonomically diverse samples. However, species‐level identification depends heavily on the choice of marker and the selected primer pair, often with a trade‐off between successful species amplification and taxonomic resolution. We present a versatile metabarcoding protocol for biomonitoring that involves the use of two barcode markers (COI and 18S) and four primer pairs in a single high‐throughput sequencing run, via sample multiplexing. We validate the protocol using a series of 24 mock zooplanktonic communities incorporating various levels of genetic variation. With the use of a single marker and single primer pair, the highest species recovery was 77%. With all three COI fragments, we detected 62%–83% of species across the mock communities, while the use of the 18S fragment alone resulted in the detection of 73%–75% of species. The species detection level was significantly improved to 89%–93% when both markers were used. Furthermore, multiplexing did not have a negative impact on the proportion of reads assigned to each species and the total number of species detected was similar to when markers were sequenced alone. Overall, our metabarcoding approach utilizing two barcode markers and multiple primer pairs per barcode improved species detection rates over a single marker/primer pair by 14% to 35%, making it an attractive and relatively cost‐effective method for biomonitoring natural zooplankton communities. We strongly recommend combining evolutionary independent markers and, when necessary, multiple primer pairs per marker to increase species detection (i.e., reduce false negatives) in metabarcoding studies.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>30459837</pmid><doi>10.1111/eva.12694</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-0854-4040</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 18S Biomonitoring cytochrome c oxidase subunit I Deoxyribonucleic acid DNA DNA barcoding DNA sequencing Genetic diversity Genetic markers metabarcoding multigene multiple primer pairs Original Species Zooplankton |
title | Metabarcoding using multiplexed markers increases species detection in complex zooplankton communities |
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