Estimating and mitigating amplification bias in qualitative and quantitative arthropod metabarcoding
Amplicon based metabarcoding promises rapid and cost-efficient analyses of species composition. However, it is disputed whether abundance estimates can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem, but...
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description | Amplicon based metabarcoding promises rapid and cost-efficient analyses of species composition. However, it is disputed whether abundance estimates can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem, but come with considerable increases in workload and cost. Here, we analyze multilocus datasets of diverse arthropod communities, to evaluate whether amplification bias can be countered by (
1
) targeting loci with highly degenerate primers or conserved priming sites, (
2
) increasing PCR template concentration, (
3
) reducing PCR cycle number or (
4
) avoiding locus specific amplification by directly sequencing genomic DNA. Amplification bias is reduced considerably by degenerate primers or targeting amplicons with conserved priming sites. Surprisingly, a reduction of PCR cycles did not have a strong effect on amplification bias. The association of taxon abundance and read count was actually less predictable with fewer cycles. Even a complete exclusion of locus specific amplification did not exclude bias. Copy number variation of the target loci may be another explanation for read abundance differences between taxa, which would affect amplicon based and PCR free methods alike. As read abundance biases are taxon specific and predictable, the application of correction factors allows abundance estimates. |
doi_str_mv | 10.1038/s41598-017-17333-x |
format | Article |
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1
) targeting loci with highly degenerate primers or conserved priming sites, (
2
) increasing PCR template concentration, (
3
) reducing PCR cycle number or (
4
) avoiding locus specific amplification by directly sequencing genomic DNA. Amplification bias is reduced considerably by degenerate primers or targeting amplicons with conserved priming sites. Surprisingly, a reduction of PCR cycles did not have a strong effect on amplification bias. The association of taxon abundance and read count was actually less predictable with fewer cycles. Even a complete exclusion of locus specific amplification did not exclude bias. Copy number variation of the target loci may be another explanation for read abundance differences between taxa, which would affect amplicon based and PCR free methods alike. As read abundance biases are taxon specific and predictable, the application of correction factors allows abundance estimates.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-017-17333-x</identifier><identifier>PMID: 29247210</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/158/2464 ; 631/158/670 ; Abundance ; Animals ; Arthropods ; Arthropods - genetics ; Bias ; Copy number ; DNA Copy Number Variations - genetics ; DNA Primers - genetics ; DNA sequencing ; Gene Amplification - genetics ; High-Throughput Nucleotide Sequencing - methods ; Humanities and Social Sciences ; multidisciplinary ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Primers ; Science ; Science (multidisciplinary) ; Species composition ; Taxa</subject><ispartof>Scientific reports, 2017-12, Vol.7 (1), p.17668-12, Article 17668</ispartof><rights>The Author(s) 2017</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-dfe7153b643fd3eee2d397e87a22150a948ad3305fb0c3e08c52819d4696590f3</citedby><cites>FETCH-LOGICAL-c540t-dfe7153b643fd3eee2d397e87a22150a948ad3305fb0c3e08c52819d4696590f3</cites><orcidid>0000-0001-7493-2159</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732254/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732254/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29247210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krehenwinkel, Henrik</creatorcontrib><creatorcontrib>Wolf, Madeline</creatorcontrib><creatorcontrib>Lim, Jun Ying</creatorcontrib><creatorcontrib>Rominger, Andrew J.</creatorcontrib><creatorcontrib>Simison, Warren B.</creatorcontrib><creatorcontrib>Gillespie, Rosemary G.</creatorcontrib><title>Estimating and mitigating amplification bias in qualitative and quantitative arthropod metabarcoding</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Amplicon based metabarcoding promises rapid and cost-efficient analyses of species composition. However, it is disputed whether abundance estimates can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem, but come with considerable increases in workload and cost. Here, we analyze multilocus datasets of diverse arthropod communities, to evaluate whether amplification bias can be countered by (
1
) targeting loci with highly degenerate primers or conserved priming sites, (
2
) increasing PCR template concentration, (
3
) reducing PCR cycle number or (
4
) avoiding locus specific amplification by directly sequencing genomic DNA. Amplification bias is reduced considerably by degenerate primers or targeting amplicons with conserved priming sites. Surprisingly, a reduction of PCR cycles did not have a strong effect on amplification bias. The association of taxon abundance and read count was actually less predictable with fewer cycles. Even a complete exclusion of locus specific amplification did not exclude bias. Copy number variation of the target loci may be another explanation for read abundance differences between taxa, which would affect amplicon based and PCR free methods alike. 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Wolf, Madeline ; Lim, Jun Ying ; Rominger, Andrew J. ; Simison, Warren B. ; Gillespie, Rosemary G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-dfe7153b643fd3eee2d397e87a22150a948ad3305fb0c3e08c52819d4696590f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>631/158/2464</topic><topic>631/158/670</topic><topic>Abundance</topic><topic>Animals</topic><topic>Arthropods</topic><topic>Arthropods - genetics</topic><topic>Bias</topic><topic>Copy number</topic><topic>DNA Copy Number Variations - genetics</topic><topic>DNA Primers - genetics</topic><topic>DNA sequencing</topic><topic>Gene Amplification - genetics</topic><topic>High-Throughput Nucleotide Sequencing - methods</topic><topic>Humanities and Social Sciences</topic><topic>multidisciplinary</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Primers</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Species composition</topic><topic>Taxa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krehenwinkel, Henrik</creatorcontrib><creatorcontrib>Wolf, Madeline</creatorcontrib><creatorcontrib>Lim, Jun Ying</creatorcontrib><creatorcontrib>Rominger, Andrew J.</creatorcontrib><creatorcontrib>Simison, Warren B.</creatorcontrib><creatorcontrib>Gillespie, Rosemary G.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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 Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krehenwinkel, Henrik</au><au>Wolf, Madeline</au><au>Lim, Jun Ying</au><au>Rominger, Andrew J.</au><au>Simison, Warren B.</au><au>Gillespie, Rosemary G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estimating and mitigating amplification bias in qualitative and quantitative arthropod metabarcoding</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2017-12-15</date><risdate>2017</risdate><volume>7</volume><issue>1</issue><spage>17668</spage><epage>12</epage><pages>17668-12</pages><artnum>17668</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Amplicon based metabarcoding promises rapid and cost-efficient analyses of species composition. However, it is disputed whether abundance estimates can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem, but come with considerable increases in workload and cost. Here, we analyze multilocus datasets of diverse arthropod communities, to evaluate whether amplification bias can be countered by (
1
) targeting loci with highly degenerate primers or conserved priming sites, (
2
) increasing PCR template concentration, (
3
) reducing PCR cycle number or (
4
) avoiding locus specific amplification by directly sequencing genomic DNA. Amplification bias is reduced considerably by degenerate primers or targeting amplicons with conserved priming sites. Surprisingly, a reduction of PCR cycles did not have a strong effect on amplification bias. The association of taxon abundance and read count was actually less predictable with fewer cycles. Even a complete exclusion of locus specific amplification did not exclude bias. Copy number variation of the target loci may be another explanation for read abundance differences between taxa, which would affect amplicon based and PCR free methods alike. As read abundance biases are taxon specific and predictable, the application of correction factors allows abundance estimates.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29247210</pmid><doi>10.1038/s41598-017-17333-x</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7493-2159</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/158/2464 631/158/670 Abundance Animals Arthropods Arthropods - genetics Bias Copy number DNA Copy Number Variations - genetics DNA Primers - genetics DNA sequencing Gene Amplification - genetics High-Throughput Nucleotide Sequencing - methods Humanities and Social Sciences multidisciplinary Polymerase chain reaction Polymerase Chain Reaction - methods Primers Science Science (multidisciplinary) Species composition Taxa |
title | Estimating and mitigating amplification bias in qualitative and quantitative arthropod metabarcoding |
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