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Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter
Targeting sequencing to genes involved in key environmental processes, i.e., ecofunctional genes, provides an opportunity to sample nature's gene guilds to greater depth and help link community structure to process-level outcomes. Vastly different approaches have been implemented for sequence p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775264/ https://www.ncbi.nlm.nih.gov/pubmed/24062736 http://dx.doi.org/10.3389/fmicb.2013.00279 |
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author | Penton, C. Ryan Johnson, Timothy A. Quensen, John F. Iwai, Shoko Cole, James R. Tiedje, James M. |
author_facet | Penton, C. Ryan Johnson, Timothy A. Quensen, John F. Iwai, Shoko Cole, James R. Tiedje, James M. |
author_sort | Penton, C. Ryan |
collection | PubMed |
description | Targeting sequencing to genes involved in key environmental processes, i.e., ecofunctional genes, provides an opportunity to sample nature's gene guilds to greater depth and help link community structure to process-level outcomes. Vastly different approaches have been implemented for sequence processing and, ultimately, for taxonomic placement of these gene reads. The overall quality of next generation sequence analysis of functional genes is dependent on multiple steps and assumptions of unknown diversity. To illustrate current issues surrounding amplicon read processing we provide examples for three ecofunctional gene groups. A combination of in silico, environmental and cultured strain sequences was used to test new primers targeting the dioxin and dibenzofuran degrading genes dxnA1, dbfA1, and carAa. The majority of obtained environmental sequences were classified into novel sequence clusters, illustrating the discovery value of the approach. For the nitrite reductase step in denitrification, the well-known nirK primers exhibited deficiencies in reference database coverage, illustrating the need to refine primer-binding sites and/or to design multiple primers, while nirS primers exhibited bias against five phyla. Amino acid-based OTU clustering of these two N-cycle genes from soil samples yielded only 114 unique nirK and 45 unique nirS genus-level groupings, likely a reflection of constricted primer coverage. Finally, supervised and non-supervised OTU analysis methods were compared using the nifH gene of nitrogen fixation, with generally similar outcomes, but the clustering (non-supervised) method yielded higher diversity estimates and stronger site-based differences. High throughput amplicon sequencing can provide inexpensive and rapid access to nature's related sequences by circumventing the culturing barrier, but each unique gene requires individual considerations in terms of primer design and sequence processing and classification. |
format | Online Article Text |
id | pubmed-3775264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37752642013-09-23 Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter Penton, C. Ryan Johnson, Timothy A. Quensen, John F. Iwai, Shoko Cole, James R. Tiedje, James M. Front Microbiol Microbiology Targeting sequencing to genes involved in key environmental processes, i.e., ecofunctional genes, provides an opportunity to sample nature's gene guilds to greater depth and help link community structure to process-level outcomes. Vastly different approaches have been implemented for sequence processing and, ultimately, for taxonomic placement of these gene reads. The overall quality of next generation sequence analysis of functional genes is dependent on multiple steps and assumptions of unknown diversity. To illustrate current issues surrounding amplicon read processing we provide examples for three ecofunctional gene groups. A combination of in silico, environmental and cultured strain sequences was used to test new primers targeting the dioxin and dibenzofuran degrading genes dxnA1, dbfA1, and carAa. The majority of obtained environmental sequences were classified into novel sequence clusters, illustrating the discovery value of the approach. For the nitrite reductase step in denitrification, the well-known nirK primers exhibited deficiencies in reference database coverage, illustrating the need to refine primer-binding sites and/or to design multiple primers, while nirS primers exhibited bias against five phyla. Amino acid-based OTU clustering of these two N-cycle genes from soil samples yielded only 114 unique nirK and 45 unique nirS genus-level groupings, likely a reflection of constricted primer coverage. Finally, supervised and non-supervised OTU analysis methods were compared using the nifH gene of nitrogen fixation, with generally similar outcomes, but the clustering (non-supervised) method yielded higher diversity estimates and stronger site-based differences. High throughput amplicon sequencing can provide inexpensive and rapid access to nature's related sequences by circumventing the culturing barrier, but each unique gene requires individual considerations in terms of primer design and sequence processing and classification. Frontiers Media S.A. 2013-09-17 /pmc/articles/PMC3775264/ /pubmed/24062736 http://dx.doi.org/10.3389/fmicb.2013.00279 Text en Copyright © 2013 Penton, Johnson, Quensen, Iwai, Cole and Tiedje. http://creativecommons.org/licenses/by/3.0/ 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. |
spellingShingle | Microbiology Penton, C. Ryan Johnson, Timothy A. Quensen, John F. Iwai, Shoko Cole, James R. Tiedje, James M. Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title | Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title_full | Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title_fullStr | Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title_full_unstemmed | Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title_short | Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
title_sort | functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775264/ https://www.ncbi.nlm.nih.gov/pubmed/24062736 http://dx.doi.org/10.3389/fmicb.2013.00279 |
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