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spyder, a new method for in silico design and assessment of 16S rRNA gene primers for molecular microbial ecology
Abstract Molecular microbial ecology studies are heavily reliant on ‘Universal’ 16S rRNA gene primers for elucidating microbial community structure and composition, and yet primer design and optimization is often overlooked. Primers that exhibit minor biases due to primer–template mismatches can sub...
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Published in: | FEMS microbiology letters 2011-07, Vol.320 (2), p.152-159 |
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creator | Thomas, Matthew C. Thomas, Dallas K. Selinger, L. Brent Inglis, G. Douglas |
description | Abstract
Molecular microbial ecology studies are heavily reliant on ‘Universal’ 16S rRNA gene primers for elucidating microbial community structure and composition, and yet primer design and optimization is often overlooked. Primers that exhibit minor biases due to primer–template mismatches can substantially alter the pool of amplicons from a community DNA sample, resulting in inaccurate conclusions. As a result, it is important that primers are critically evaluated against the most comprehensive data sets available before commencing molecular microbial community studies. We present a user-friendly, multi-platform (e.g. Windows, Linux, Mac) method named spyder for the in silico design and assessment of 16S rRNA gene primers. The method utilizes the Ribosomal Database Project's Probe Match feature coupled with a compact program (available at http://people.uleth.ca/~selibl/Spyder/Spyder.html) that aligns and identifies mismatches between primers and templates. To demonstrate the value of spyder, we assessed commonly used ‘Universal’ and phyla-specific primers and identified primer modifications that improved the coverage of target organisms by 5–42% as well as removed excessive degeneracies. |
doi_str_mv | 10.1111/j.1574-6968.2011.02302.x |
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Molecular microbial ecology studies are heavily reliant on ‘Universal’ 16S rRNA gene primers for elucidating microbial community structure and composition, and yet primer design and optimization is often overlooked. Primers that exhibit minor biases due to primer–template mismatches can substantially alter the pool of amplicons from a community DNA sample, resulting in inaccurate conclusions. As a result, it is important that primers are critically evaluated against the most comprehensive data sets available before commencing molecular microbial community studies. We present a user-friendly, multi-platform (e.g. Windows, Linux, Mac) method named spyder for the in silico design and assessment of 16S rRNA gene primers. The method utilizes the Ribosomal Database Project's Probe Match feature coupled with a compact program (available at http://people.uleth.ca/~selibl/Spyder/Spyder.html) that aligns and identifies mismatches between primers and templates. To demonstrate the value of spyder, we assessed commonly used ‘Universal’ and phyla-specific primers and identified primer modifications that improved the coverage of target organisms by 5–42% as well as removed excessive degeneracies.</description><identifier>ISSN: 0378-1097</identifier><identifier>EISSN: 1574-6968</identifier><identifier>DOI: 10.1111/j.1574-6968.2011.02302.x</identifier><identifier>PMID: 21554380</identifier><identifier>CODEN: FMLED7</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>16S rRNA gene ; Algorithms ; Amino Acid Sequence ; bacteria ; Bacteriology ; Base Sequence ; Biological and medical sciences ; Communities ; Community structure ; Computational Biology - methods ; Computer-Aided Design ; Databases, Nucleic Acid ; Deoxyribonucleic acid ; Design ; Design analysis ; Design optimization ; DNA ; DNA Primers ; Ecological monitoring ; Environmental Microbiology ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Genes, Bacterial ; Microbiology ; Microorganisms ; Miscellaneous ; Molecular Sequence Data ; primer design ; Primers ; ribosomal database project ; RNA, Ribosomal, 16S - genetics ; rRNA 16S ; Sequence Alignment ; Software ; universal</subject><ispartof>FEMS microbiology letters, 2011-07, Vol.320 (2), p.152-159</ispartof><rights>2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved 2011</rights><rights>FEMS Microbiology Letters © 2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. No claim to original Canadian government works</rights><rights>2015 INIST-CNRS</rights><rights>FEMS Microbiology Letters © 2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. No claim to original Canadian government works.</rights><rights>2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5032-77ea2bad1d4c3b0e7a4043565ec3e8c0056392c20ae9d0fab648f2cc56c73de43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24245548$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21554380$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomas, Matthew C.</creatorcontrib><creatorcontrib>Thomas, Dallas K.</creatorcontrib><creatorcontrib>Selinger, L. Brent</creatorcontrib><creatorcontrib>Inglis, G. Douglas</creatorcontrib><title>spyder, a new method for in silico design and assessment of 16S rRNA gene primers for molecular microbial ecology</title><title>FEMS microbiology letters</title><addtitle>FEMS Microbiol Lett</addtitle><description>Abstract
Molecular microbial ecology studies are heavily reliant on ‘Universal’ 16S rRNA gene primers for elucidating microbial community structure and composition, and yet primer design and optimization is often overlooked. Primers that exhibit minor biases due to primer–template mismatches can substantially alter the pool of amplicons from a community DNA sample, resulting in inaccurate conclusions. As a result, it is important that primers are critically evaluated against the most comprehensive data sets available before commencing molecular microbial community studies. We present a user-friendly, multi-platform (e.g. Windows, Linux, Mac) method named spyder for the in silico design and assessment of 16S rRNA gene primers. The method utilizes the Ribosomal Database Project's Probe Match feature coupled with a compact program (available at http://people.uleth.ca/~selibl/Spyder/Spyder.html) that aligns and identifies mismatches between primers and templates. To demonstrate the value of spyder, we assessed commonly used ‘Universal’ and phyla-specific primers and identified primer modifications that improved the coverage of target organisms by 5–42% as well as removed excessive degeneracies.</description><subject>16S rRNA gene</subject><subject>Algorithms</subject><subject>Amino Acid Sequence</subject><subject>bacteria</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Communities</subject><subject>Community structure</subject><subject>Computational Biology - methods</subject><subject>Computer-Aided Design</subject><subject>Databases, Nucleic Acid</subject><subject>Deoxyribonucleic acid</subject><subject>Design</subject><subject>Design analysis</subject><subject>Design optimization</subject><subject>DNA</subject><subject>DNA Primers</subject><subject>Ecological monitoring</subject><subject>Environmental Microbiology</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Bacterial</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>Miscellaneous</subject><subject>Molecular Sequence Data</subject><subject>primer design</subject><subject>Primers</subject><subject>ribosomal database project</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>rRNA 16S</subject><subject>Sequence Alignment</subject><subject>Software</subject><subject>universal</subject><issn>0378-1097</issn><issn>1574-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkl1rFDEUhoModlv9CxIQ6U1nPPmYTObCi1KsCquCH9chmzmzZpmZbJMd2v33ZrprBUU8NzlwnvdAzvsSQhmULNfrTcmqWhaqUbrkwFgJXAAv7x6RxcPgMVmAqHXBoKlPyGlKGwCQHNRTcsJZVUmhYUFu0nbfYryglo54Swfc_Qgt7UKkfqTJ994F2mLy65HasaU2JUxpwHFHQ0eZ-krjl0-XdI0j0m30A8Z0Lx5Cj27qbe68i2HlbU_RhT6s98_Ik872CZ8f3zPy_frtt6v3xfLzuw9Xl8vCVSB4Uddo-cq2rJVOrABrK0GKSlXoBGoHUCnRcMfBYtNCZ1dK6o47VylXixalOCPnh73bGG4mTDsz-OSw7-2IYUqmASlrWQn1X1LXrFFSSZ7Jl3-QmzDFMX_DZAMqrbWEJlMvjtS0GrA182Fs3JtfV8_AqyNgk7N9F-3ofPrNSS4zqTP35sDd-h73D3MGZk6B2ZjZbDObbeYUmPsUmDtz_XE5d1kvDvowbf-hLv5Si5_osLKr</recordid><startdate>201107</startdate><enddate>201107</enddate><creator>Thomas, Matthew C.</creator><creator>Thomas, Dallas K.</creator><creator>Selinger, L. 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Psychology</topic><topic>Genes, Bacterial</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>Miscellaneous</topic><topic>Molecular Sequence Data</topic><topic>primer design</topic><topic>Primers</topic><topic>ribosomal database project</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>rRNA 16S</topic><topic>Sequence Alignment</topic><topic>Software</topic><topic>universal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, Matthew C.</creatorcontrib><creatorcontrib>Thomas, Dallas K.</creatorcontrib><creatorcontrib>Selinger, L. Brent</creatorcontrib><creatorcontrib>Inglis, G. 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Brent</au><au>Inglis, G. Douglas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>spyder, a new method for in silico design and assessment of 16S rRNA gene primers for molecular microbial ecology</atitle><jtitle>FEMS microbiology letters</jtitle><addtitle>FEMS Microbiol Lett</addtitle><date>2011-07</date><risdate>2011</risdate><volume>320</volume><issue>2</issue><spage>152</spage><epage>159</epage><pages>152-159</pages><issn>0378-1097</issn><eissn>1574-6968</eissn><coden>FMLED7</coden><abstract>Abstract
Molecular microbial ecology studies are heavily reliant on ‘Universal’ 16S rRNA gene primers for elucidating microbial community structure and composition, and yet primer design and optimization is often overlooked. Primers that exhibit minor biases due to primer–template mismatches can substantially alter the pool of amplicons from a community DNA sample, resulting in inaccurate conclusions. As a result, it is important that primers are critically evaluated against the most comprehensive data sets available before commencing molecular microbial community studies. We present a user-friendly, multi-platform (e.g. Windows, Linux, Mac) method named spyder for the in silico design and assessment of 16S rRNA gene primers. The method utilizes the Ribosomal Database Project's Probe Match feature coupled with a compact program (available at http://people.uleth.ca/~selibl/Spyder/Spyder.html) that aligns and identifies mismatches between primers and templates. To demonstrate the value of spyder, we assessed commonly used ‘Universal’ and phyla-specific primers and identified primer modifications that improved the coverage of target organisms by 5–42% as well as removed excessive degeneracies.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21554380</pmid><doi>10.1111/j.1574-6968.2011.02302.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 16S rRNA gene Algorithms Amino Acid Sequence bacteria Bacteriology Base Sequence Biological and medical sciences Communities Community structure Computational Biology - methods Computer-Aided Design Databases, Nucleic Acid Deoxyribonucleic acid Design Design analysis Design optimization DNA DNA Primers Ecological monitoring Environmental Microbiology Escherichia coli - genetics Fundamental and applied biological sciences. Psychology Genes, Bacterial Microbiology Microorganisms Miscellaneous Molecular Sequence Data primer design Primers ribosomal database project RNA, Ribosomal, 16S - genetics rRNA 16S Sequence Alignment Software universal |
title | spyder, a new method for in silico design and assessment of 16S rRNA gene primers for molecular microbial ecology |
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