Cargando…

Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms

Wood decomposer fungi are grouped by how they extract sugars from lignocellulose. Brown rot fungi selectively degrade cellulose and hemicellulose, leaving lignin intact, and white rot fungi degrade all components. Many trees are susceptible to both rot types, giving carbon in Earth’s woody biomass,...

Descripción completa

Detalles Bibliográficos
Autores principales: Haq, Irshad Ul, Hillmann, Benjamin, Moran, Molly, Willard, Samuel, Knights, Dan, Fixen, Kathryn R., Schilling, Jonathan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723729/
https://www.ncbi.nlm.nih.gov/pubmed/37938255
http://dx.doi.org/10.1038/s43705-022-00108-5
_version_ 1784844251960442880
author Haq, Irshad Ul
Hillmann, Benjamin
Moran, Molly
Willard, Samuel
Knights, Dan
Fixen, Kathryn R.
Schilling, Jonathan S.
author_facet Haq, Irshad Ul
Hillmann, Benjamin
Moran, Molly
Willard, Samuel
Knights, Dan
Fixen, Kathryn R.
Schilling, Jonathan S.
author_sort Haq, Irshad Ul
collection PubMed
description Wood decomposer fungi are grouped by how they extract sugars from lignocellulose. Brown rot fungi selectively degrade cellulose and hemicellulose, leaving lignin intact, and white rot fungi degrade all components. Many trees are susceptible to both rot types, giving carbon in Earth’s woody biomass, specifically lignin, a flexible fate that is affected not only by the fungal decomposition mechanism but also the associated microbial community. However, little is understood about how rot type may influence the microbial community in decaying wood. In this study, we quantified bacterial communities associated with Fomes fomentarius (white rot) and Fomitopsis betulina (brown rot) found on a shared tree host species, birch (Betula papyrifera). We collected 25 wood samples beneath sporocarps  of F. fomentarius (n = 13) and F. betulina (n = 12) on standing dead trees, and coupled microbial DNA sequencing with chemical signatures of rot type (pH and lignin removal). We found that bacterial communities for both fungi were dominated by Proteobacteria, a commonly reported association. However, rot type exerted significant influence on less abundant taxa in ways that align logically with fungal traits. Amplicon sequence variants (ASVs) were enriched in Firmicutes in white-rotted wood, and were enriched in Alphaproteobacteria, Actinobacteria and Acidobacteria in lower pH brown rot. Our results suggest that wood decomposer strategies may exert significant selection effects on bacteria, or vice versa, among less-abundant taxa that have been overlooked when using abundance as the only measure of influence.
format Online
Article
Text
id pubmed-9723729
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-97237292023-01-04 Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms Haq, Irshad Ul Hillmann, Benjamin Moran, Molly Willard, Samuel Knights, Dan Fixen, Kathryn R. Schilling, Jonathan S. ISME Commun Article Wood decomposer fungi are grouped by how they extract sugars from lignocellulose. Brown rot fungi selectively degrade cellulose and hemicellulose, leaving lignin intact, and white rot fungi degrade all components. Many trees are susceptible to both rot types, giving carbon in Earth’s woody biomass, specifically lignin, a flexible fate that is affected not only by the fungal decomposition mechanism but also the associated microbial community. However, little is understood about how rot type may influence the microbial community in decaying wood. In this study, we quantified bacterial communities associated with Fomes fomentarius (white rot) and Fomitopsis betulina (brown rot) found on a shared tree host species, birch (Betula papyrifera). We collected 25 wood samples beneath sporocarps  of F. fomentarius (n = 13) and F. betulina (n = 12) on standing dead trees, and coupled microbial DNA sequencing with chemical signatures of rot type (pH and lignin removal). We found that bacterial communities for both fungi were dominated by Proteobacteria, a commonly reported association. However, rot type exerted significant influence on less abundant taxa in ways that align logically with fungal traits. Amplicon sequence variants (ASVs) were enriched in Firmicutes in white-rotted wood, and were enriched in Alphaproteobacteria, Actinobacteria and Acidobacteria in lower pH brown rot. Our results suggest that wood decomposer strategies may exert significant selection effects on bacteria, or vice versa, among less-abundant taxa that have been overlooked when using abundance as the only measure of influence. Nature Publishing Group UK 2022-03-30 /pmc/articles/PMC9723729/ /pubmed/37938255 http://dx.doi.org/10.1038/s43705-022-00108-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Haq, Irshad Ul
Hillmann, Benjamin
Moran, Molly
Willard, Samuel
Knights, Dan
Fixen, Kathryn R.
Schilling, Jonathan S.
Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title_full Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title_fullStr Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title_full_unstemmed Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title_short Bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
title_sort bacterial communities associated with wood rot fungi that use distinct decomposition mechanisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723729/
https://www.ncbi.nlm.nih.gov/pubmed/37938255
http://dx.doi.org/10.1038/s43705-022-00108-5
work_keys_str_mv AT haqirshadul bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT hillmannbenjamin bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT moranmolly bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT willardsamuel bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT knightsdan bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT fixenkathrynr bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms
AT schillingjonathans bacterialcommunitiesassociatedwithwoodrotfungithatusedistinctdecompositionmechanisms