Cargando…
Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle
The Asian longhorned beetle ( Anoplophoraglabripennis ) is an invasive, wood-boring pest that thrives in the heartwood of deciduous tree species. A large impediment faced by A . glabripennis as it feeds on woody tissue is lignin, a highly recalcitrant biopolymer that reduces access to sugars and oth...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762729/ https://www.ncbi.nlm.nih.gov/pubmed/24023907 http://dx.doi.org/10.1371/journal.pone.0073827 |
_version_ | 1782282920826765312 |
---|---|
author | Scully, Erin D. Geib, Scott M. Hoover, Kelli Tien, Ming Tringe, Susannah G. Barry, Kerrie W. Glavina del Rio, Tijana Chovatia, Mansi Herr, Joshua R. Carlson, John E. |
author_facet | Scully, Erin D. Geib, Scott M. Hoover, Kelli Tien, Ming Tringe, Susannah G. Barry, Kerrie W. Glavina del Rio, Tijana Chovatia, Mansi Herr, Joshua R. Carlson, John E. |
author_sort | Scully, Erin D. |
collection | PubMed |
description | The Asian longhorned beetle ( Anoplophoraglabripennis ) is an invasive, wood-boring pest that thrives in the heartwood of deciduous tree species. A large impediment faced by A . glabripennis as it feeds on woody tissue is lignin, a highly recalcitrant biopolymer that reduces access to sugars and other nutrients locked in cellulose and hemicellulose. We previously demonstrated that lignin, cellulose, and hemicellulose are actively deconstructed in the beetle gut and that the gut harbors an assemblage of microbes hypothesized to make significant contributions to these processes. While lignin degrading mechanisms have been well characterized in pure cultures of white rot basidiomycetes, little is known about such processes in microbial communities associated with wood-feeding insects. The goals of this study were to develop a taxonomic and functional profile of a gut community derived from an invasive population of larval A . glabripennis collected from infested host trees and to identify genes that could be relevant for the digestion of woody tissue and nutrient acquisition. To accomplish this goal, we taxonomically and functionally characterized the A . glabripennis midgut microbiota through amplicon and shotgun metagenome sequencing and conducted a large-scale comparison with the metagenomes from a variety of other herbivore-associated communities. This analysis distinguished the A. glabripennis larval gut metagenome from the gut communities of other herbivores, including previously sequenced termite hindgut metagenomes. Genes encoding enzymes were identified in the A . glabripennis gut metagenome that could have key roles in woody tissue digestion including candidate lignin degrading genes (laccases, dye-decolorizing peroxidases, novel peroxidases and β-etherases), 36 families of glycoside hydrolases (such as cellulases and xylanases), and genes that could facilitate nutrient recovery, essential nutrient synthesis, and detoxification. This community could serve as a reservoir of novel enzymes to enhance industrial cellulosic biofuels production or targets for novel control methods for this invasive and highly destructive insect. |
format | Online Article Text |
id | pubmed-3762729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37627292013-09-10 Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle Scully, Erin D. Geib, Scott M. Hoover, Kelli Tien, Ming Tringe, Susannah G. Barry, Kerrie W. Glavina del Rio, Tijana Chovatia, Mansi Herr, Joshua R. Carlson, John E. PLoS One Research Article The Asian longhorned beetle ( Anoplophoraglabripennis ) is an invasive, wood-boring pest that thrives in the heartwood of deciduous tree species. A large impediment faced by A . glabripennis as it feeds on woody tissue is lignin, a highly recalcitrant biopolymer that reduces access to sugars and other nutrients locked in cellulose and hemicellulose. We previously demonstrated that lignin, cellulose, and hemicellulose are actively deconstructed in the beetle gut and that the gut harbors an assemblage of microbes hypothesized to make significant contributions to these processes. While lignin degrading mechanisms have been well characterized in pure cultures of white rot basidiomycetes, little is known about such processes in microbial communities associated with wood-feeding insects. The goals of this study were to develop a taxonomic and functional profile of a gut community derived from an invasive population of larval A . glabripennis collected from infested host trees and to identify genes that could be relevant for the digestion of woody tissue and nutrient acquisition. To accomplish this goal, we taxonomically and functionally characterized the A . glabripennis midgut microbiota through amplicon and shotgun metagenome sequencing and conducted a large-scale comparison with the metagenomes from a variety of other herbivore-associated communities. This analysis distinguished the A. glabripennis larval gut metagenome from the gut communities of other herbivores, including previously sequenced termite hindgut metagenomes. Genes encoding enzymes were identified in the A . glabripennis gut metagenome that could have key roles in woody tissue digestion including candidate lignin degrading genes (laccases, dye-decolorizing peroxidases, novel peroxidases and β-etherases), 36 families of glycoside hydrolases (such as cellulases and xylanases), and genes that could facilitate nutrient recovery, essential nutrient synthesis, and detoxification. This community could serve as a reservoir of novel enzymes to enhance industrial cellulosic biofuels production or targets for novel control methods for this invasive and highly destructive insect. Public Library of Science 2013-09-04 /pmc/articles/PMC3762729/ /pubmed/24023907 http://dx.doi.org/10.1371/journal.pone.0073827 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Scully, Erin D. Geib, Scott M. Hoover, Kelli Tien, Ming Tringe, Susannah G. Barry, Kerrie W. Glavina del Rio, Tijana Chovatia, Mansi Herr, Joshua R. Carlson, John E. Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title | Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title_full | Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title_fullStr | Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title_full_unstemmed | Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title_short | Metagenomic Profiling Reveals Lignocellulose Degrading System in a Microbial Community Associated with a Wood-Feeding Beetle |
title_sort | metagenomic profiling reveals lignocellulose degrading system in a microbial community associated with a wood-feeding beetle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762729/ https://www.ncbi.nlm.nih.gov/pubmed/24023907 http://dx.doi.org/10.1371/journal.pone.0073827 |
work_keys_str_mv | AT scullyerind metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT geibscottm metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT hooverkelli metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT tienming metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT tringesusannahg metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT barrykerriew metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT glavinadelriotijana metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT chovatiamansi metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT herrjoshuar metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle AT carlsonjohne metagenomicprofilingrevealslignocellulosedegradingsysteminamicrobialcommunityassociatedwithawoodfeedingbeetle |