Cargando…

Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil

Microorganisms that degrade cellulose utilize extracellular reactions that yield free by-products which can promote interactions with noncellulolytic organisms. We hypothesized that these interactions determine the ecological and physiological traits governing the fate of cellulosic carbon (C) in so...

Descripción completa

Detalles Bibliográficos
Autores principales: Wilhelm, Roland C., Pepe-Ranney, Charles, Weisenhorn, Pamela, Lipton, Mary, Buckley, Daniel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8545098/
https://www.ncbi.nlm.nih.gov/pubmed/33402535
http://dx.doi.org/10.1128/mBio.03099-20
_version_ 1784589949119496192
author Wilhelm, Roland C.
Pepe-Ranney, Charles
Weisenhorn, Pamela
Lipton, Mary
Buckley, Daniel H.
author_facet Wilhelm, Roland C.
Pepe-Ranney, Charles
Weisenhorn, Pamela
Lipton, Mary
Buckley, Daniel H.
author_sort Wilhelm, Roland C.
collection PubMed
description Microorganisms that degrade cellulose utilize extracellular reactions that yield free by-products which can promote interactions with noncellulolytic organisms. We hypothesized that these interactions determine the ecological and physiological traits governing the fate of cellulosic carbon (C) in soil. We performed comparative genomics with genome bins from a shotgun metagenomic-stable isotope probing experiment to characterize the attributes of cellulolytic and noncellulolytic taxa accessing (13)C from cellulose. We hypothesized that cellulolytic taxa would exhibit competitive traits that limit access, while noncellulolytic taxa would display greater metabolic dependency, such as signatures of adaptive gene loss. We tested our hypotheses by evaluating genomic traits indicative of competitive exclusion or metabolic dependency, such as antibiotic production, growth rate, surface attachment, biomass degrading potential, and auxotrophy. The most (13)C-enriched taxa were cellulolytic Cellvibrio (Gammaproteobacteria) and Chaetomium (Ascomycota), which exhibited a strategy of self-sufficiency (prototrophy), rapid growth, and competitive exclusion via antibiotic production. Auxotrophy was more prevalent in cellulolytic Actinobacteria than in cellulolytic Proteobacteria, demonstrating differences in dependency among cellulose degraders. Noncellulolytic taxa that accessed (13)C from cellulose (Planctomycetales, Verrucomicrobia, and Vampirovibrionales) were also more dependent, as indicated by patterns of auxotrophy and (13)C labeling (i.e., partial labeling or labeling at later stages). Major (13)C-labeled cellulolytic microbes (e.g., Sorangium, Actinomycetales, Rhizobiales, and Caulobacteraceae) possessed adaptations for surface colonization (e.g., gliding motility, hyphae, attachment structures) signifying the importance of surface ecology in decomposing particulate organic matter. Our results demonstrated that access to cellulosic C was accompanied by ecological trade-offs characterized by differing degrees of metabolic dependency and competitive exclusion.
format Online
Article
Text
id pubmed-8545098
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-85450982021-10-27 Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil Wilhelm, Roland C. Pepe-Ranney, Charles Weisenhorn, Pamela Lipton, Mary Buckley, Daniel H. mBio Research Article Microorganisms that degrade cellulose utilize extracellular reactions that yield free by-products which can promote interactions with noncellulolytic organisms. We hypothesized that these interactions determine the ecological and physiological traits governing the fate of cellulosic carbon (C) in soil. We performed comparative genomics with genome bins from a shotgun metagenomic-stable isotope probing experiment to characterize the attributes of cellulolytic and noncellulolytic taxa accessing (13)C from cellulose. We hypothesized that cellulolytic taxa would exhibit competitive traits that limit access, while noncellulolytic taxa would display greater metabolic dependency, such as signatures of adaptive gene loss. We tested our hypotheses by evaluating genomic traits indicative of competitive exclusion or metabolic dependency, such as antibiotic production, growth rate, surface attachment, biomass degrading potential, and auxotrophy. The most (13)C-enriched taxa were cellulolytic Cellvibrio (Gammaproteobacteria) and Chaetomium (Ascomycota), which exhibited a strategy of self-sufficiency (prototrophy), rapid growth, and competitive exclusion via antibiotic production. Auxotrophy was more prevalent in cellulolytic Actinobacteria than in cellulolytic Proteobacteria, demonstrating differences in dependency among cellulose degraders. Noncellulolytic taxa that accessed (13)C from cellulose (Planctomycetales, Verrucomicrobia, and Vampirovibrionales) were also more dependent, as indicated by patterns of auxotrophy and (13)C labeling (i.e., partial labeling or labeling at later stages). Major (13)C-labeled cellulolytic microbes (e.g., Sorangium, Actinomycetales, Rhizobiales, and Caulobacteraceae) possessed adaptations for surface colonization (e.g., gliding motility, hyphae, attachment structures) signifying the importance of surface ecology in decomposing particulate organic matter. Our results demonstrated that access to cellulosic C was accompanied by ecological trade-offs characterized by differing degrees of metabolic dependency and competitive exclusion. American Society for Microbiology 2021-01-05 /pmc/articles/PMC8545098/ /pubmed/33402535 http://dx.doi.org/10.1128/mBio.03099-20 Text en Copyright © 2021 Wilhelm et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Wilhelm, Roland C.
Pepe-Ranney, Charles
Weisenhorn, Pamela
Lipton, Mary
Buckley, Daniel H.
Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title_full Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title_fullStr Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title_full_unstemmed Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title_short Competitive Exclusion and Metabolic Dependency among Microorganisms Structure the Cellulose Economy of an Agricultural Soil
title_sort competitive exclusion and metabolic dependency among microorganisms structure the cellulose economy of an agricultural soil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8545098/
https://www.ncbi.nlm.nih.gov/pubmed/33402535
http://dx.doi.org/10.1128/mBio.03099-20
work_keys_str_mv AT wilhelmrolandc competitiveexclusionandmetabolicdependencyamongmicroorganismsstructurethecelluloseeconomyofanagriculturalsoil
AT peperanneycharles competitiveexclusionandmetabolicdependencyamongmicroorganismsstructurethecelluloseeconomyofanagriculturalsoil
AT weisenhornpamela competitiveexclusionandmetabolicdependencyamongmicroorganismsstructurethecelluloseeconomyofanagriculturalsoil
AT liptonmary competitiveexclusionandmetabolicdependencyamongmicroorganismsstructurethecelluloseeconomyofanagriculturalsoil
AT buckleydanielh competitiveexclusionandmetabolicdependencyamongmicroorganismsstructurethecelluloseeconomyofanagriculturalsoil