Cargando…

Decreases in average bacterial community rRNA operon copy number during succession

Trait-based studies can help clarify the mechanisms driving patterns of microbial community assembly and coexistence. Here, we use a trait-based approach to explore the importance of rRNA operon copy number in microbial succession, building on prior evidence that organisms with higher copy numbers r...

Descripción completa

Detalles Bibliográficos
Autores principales: Nemergut, Diana R, Knelman, Joseph E, Ferrenberg, Scott, Bilinski, Teresa, Melbourne, Brett, Jiang, Lin, Violle, Cyrille, Darcy, John L, Prest, Tiffany, Schmidt, Steven K, Townsend, Alan R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029226/
https://www.ncbi.nlm.nih.gov/pubmed/26565722
http://dx.doi.org/10.1038/ismej.2015.191
_version_ 1782454480992731136
author Nemergut, Diana R
Knelman, Joseph E
Ferrenberg, Scott
Bilinski, Teresa
Melbourne, Brett
Jiang, Lin
Violle, Cyrille
Darcy, John L
Prest, Tiffany
Schmidt, Steven K
Townsend, Alan R
author_facet Nemergut, Diana R
Knelman, Joseph E
Ferrenberg, Scott
Bilinski, Teresa
Melbourne, Brett
Jiang, Lin
Violle, Cyrille
Darcy, John L
Prest, Tiffany
Schmidt, Steven K
Townsend, Alan R
author_sort Nemergut, Diana R
collection PubMed
description Trait-based studies can help clarify the mechanisms driving patterns of microbial community assembly and coexistence. Here, we use a trait-based approach to explore the importance of rRNA operon copy number in microbial succession, building on prior evidence that organisms with higher copy numbers respond more rapidly to nutrient inputs. We set flasks of heterotrophic media into the environment and examined bacterial community assembly at seven time points. Communities were arrayed along a geographic gradient to introduce stochasticity via dispersal processes and were analyzed using 16 S rRNA gene pyrosequencing, and rRNA operon copy number was modeled using ancestral trait reconstruction. We found that taxonomic composition was similar between communities at the beginning of the experiment and then diverged through time; as well, phylogenetic clustering within communities decreased over time. The average rRNA operon copy number decreased over the experiment, and variance in rRNA operon copy number was lowest both early and late in succession. We then analyzed bacterial community data from other soil and sediment primary and secondary successional sequences from three markedly different ecosystem types. Our results demonstrate that decreases in average copy number are a consistent feature of communities across various drivers of ecological succession. Importantly, our work supports the scaling of the copy number trait over multiple levels of biological organization, ranging from cells to populations and communities, with implications for both microbial ecology and evolution.
format Online
Article
Text
id pubmed-5029226
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50292262016-09-21 Decreases in average bacterial community rRNA operon copy number during succession Nemergut, Diana R Knelman, Joseph E Ferrenberg, Scott Bilinski, Teresa Melbourne, Brett Jiang, Lin Violle, Cyrille Darcy, John L Prest, Tiffany Schmidt, Steven K Townsend, Alan R ISME J Original Article Trait-based studies can help clarify the mechanisms driving patterns of microbial community assembly and coexistence. Here, we use a trait-based approach to explore the importance of rRNA operon copy number in microbial succession, building on prior evidence that organisms with higher copy numbers respond more rapidly to nutrient inputs. We set flasks of heterotrophic media into the environment and examined bacterial community assembly at seven time points. Communities were arrayed along a geographic gradient to introduce stochasticity via dispersal processes and were analyzed using 16 S rRNA gene pyrosequencing, and rRNA operon copy number was modeled using ancestral trait reconstruction. We found that taxonomic composition was similar between communities at the beginning of the experiment and then diverged through time; as well, phylogenetic clustering within communities decreased over time. The average rRNA operon copy number decreased over the experiment, and variance in rRNA operon copy number was lowest both early and late in succession. We then analyzed bacterial community data from other soil and sediment primary and secondary successional sequences from three markedly different ecosystem types. Our results demonstrate that decreases in average copy number are a consistent feature of communities across various drivers of ecological succession. Importantly, our work supports the scaling of the copy number trait over multiple levels of biological organization, ranging from cells to populations and communities, with implications for both microbial ecology and evolution. Nature Publishing Group 2016-05 2015-11-13 /pmc/articles/PMC5029226/ /pubmed/26565722 http://dx.doi.org/10.1038/ismej.2015.191 Text en Copyright © 2016 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Nemergut, Diana R
Knelman, Joseph E
Ferrenberg, Scott
Bilinski, Teresa
Melbourne, Brett
Jiang, Lin
Violle, Cyrille
Darcy, John L
Prest, Tiffany
Schmidt, Steven K
Townsend, Alan R
Decreases in average bacterial community rRNA operon copy number during succession
title Decreases in average bacterial community rRNA operon copy number during succession
title_full Decreases in average bacterial community rRNA operon copy number during succession
title_fullStr Decreases in average bacterial community rRNA operon copy number during succession
title_full_unstemmed Decreases in average bacterial community rRNA operon copy number during succession
title_short Decreases in average bacterial community rRNA operon copy number during succession
title_sort decreases in average bacterial community rrna operon copy number during succession
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029226/
https://www.ncbi.nlm.nih.gov/pubmed/26565722
http://dx.doi.org/10.1038/ismej.2015.191
work_keys_str_mv AT nemergutdianar decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT knelmanjosephe decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT ferrenbergscott decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT bilinskiteresa decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT melbournebrett decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT jianglin decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT viollecyrille decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT darcyjohnl decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT presttiffany decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT schmidtstevenk decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession
AT townsendalanr decreasesinaveragebacterialcommunityrrnaoperoncopynumberduringsuccession