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Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches

BACKGROUND: Gut microbiomes, such as the rumen, greatly influence host nutrition due to their feed energy-harvesting capacity. We investigated temporal ecological interactions facilitating energy harvesting at the fresh perennial ryegrass (PRG)-biofilm interface in the rumen using an in sacco approa...

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Autores principales: Huws, Sharon A., Edwards, Joan E., Lin, Wanchang, Rubino, Francesco, Alston, Mark, Swarbreck, David, Caim, Shabhonam, Stevens, Pauline Rees, Pachebat, Justin, Won, Mi-Young, Oyama, Linda B., Creevey, Christopher J., Kingston-Smith, Alison H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215763/
https://www.ncbi.nlm.nih.gov/pubmed/34154659
http://dx.doi.org/10.1186/s40168-021-01087-w
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author Huws, Sharon A.
Edwards, Joan E.
Lin, Wanchang
Rubino, Francesco
Alston, Mark
Swarbreck, David
Caim, Shabhonam
Stevens, Pauline Rees
Pachebat, Justin
Won, Mi-Young
Oyama, Linda B.
Creevey, Christopher J.
Kingston-Smith, Alison H.
author_facet Huws, Sharon A.
Edwards, Joan E.
Lin, Wanchang
Rubino, Francesco
Alston, Mark
Swarbreck, David
Caim, Shabhonam
Stevens, Pauline Rees
Pachebat, Justin
Won, Mi-Young
Oyama, Linda B.
Creevey, Christopher J.
Kingston-Smith, Alison H.
author_sort Huws, Sharon A.
collection PubMed
description BACKGROUND: Gut microbiomes, such as the rumen, greatly influence host nutrition due to their feed energy-harvesting capacity. We investigated temporal ecological interactions facilitating energy harvesting at the fresh perennial ryegrass (PRG)-biofilm interface in the rumen using an in sacco approach and prokaryotic metatranscriptomic profiling. RESULTS: Network analysis identified two distinct sub-microbiomes primarily representing primary (≤ 4 h) and secondary (≥ 4 h) colonisation phases and the most transcriptionally active bacterial families (i.e Fibrobacteriaceae, Selemondaceae and Methanobacteriaceae) did not interact with either sub-microbiome, indicating non-cooperative behaviour. Conversely, Prevotellaceae had most transcriptional activity within the primary sub-microbiome (focussed on protein metabolism) and Lachnospiraceae within the secondary sub-microbiome (focussed on carbohydrate degradation). Putative keystone taxa, with low transcriptional activity, were identified within both sub-microbiomes, highlighting the important synergistic role of minor bacterial families; however, we hypothesise that they may be ‘cheating’ in order to capitalise on the energy-harvesting capacity of other microbes. In terms of chemical cues underlying transition from primary to secondary colonisation phases, we suggest that AI-2-based quorum sensing plays a role, based on LuxS gene expression data, coupled with changes in PRG chemistry. CONCLUSIONS: In summary, we show that fresh PRG-attached prokaryotes are resilient and adapt quickly to changing niches. This study provides the first major insight into the complex temporal ecological interactions occurring at the plant-biofilm interface within the rumen. The study also provides valuable insights into potential plant breeding strategies for development of the utopian plant, allowing optimal sustainable production of ruminants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01087-w.
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spelling pubmed-82157632021-06-23 Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches Huws, Sharon A. Edwards, Joan E. Lin, Wanchang Rubino, Francesco Alston, Mark Swarbreck, David Caim, Shabhonam Stevens, Pauline Rees Pachebat, Justin Won, Mi-Young Oyama, Linda B. Creevey, Christopher J. Kingston-Smith, Alison H. Microbiome Research BACKGROUND: Gut microbiomes, such as the rumen, greatly influence host nutrition due to their feed energy-harvesting capacity. We investigated temporal ecological interactions facilitating energy harvesting at the fresh perennial ryegrass (PRG)-biofilm interface in the rumen using an in sacco approach and prokaryotic metatranscriptomic profiling. RESULTS: Network analysis identified two distinct sub-microbiomes primarily representing primary (≤ 4 h) and secondary (≥ 4 h) colonisation phases and the most transcriptionally active bacterial families (i.e Fibrobacteriaceae, Selemondaceae and Methanobacteriaceae) did not interact with either sub-microbiome, indicating non-cooperative behaviour. Conversely, Prevotellaceae had most transcriptional activity within the primary sub-microbiome (focussed on protein metabolism) and Lachnospiraceae within the secondary sub-microbiome (focussed on carbohydrate degradation). Putative keystone taxa, with low transcriptional activity, were identified within both sub-microbiomes, highlighting the important synergistic role of minor bacterial families; however, we hypothesise that they may be ‘cheating’ in order to capitalise on the energy-harvesting capacity of other microbes. In terms of chemical cues underlying transition from primary to secondary colonisation phases, we suggest that AI-2-based quorum sensing plays a role, based on LuxS gene expression data, coupled with changes in PRG chemistry. CONCLUSIONS: In summary, we show that fresh PRG-attached prokaryotes are resilient and adapt quickly to changing niches. This study provides the first major insight into the complex temporal ecological interactions occurring at the plant-biofilm interface within the rumen. The study also provides valuable insights into potential plant breeding strategies for development of the utopian plant, allowing optimal sustainable production of ruminants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01087-w. BioMed Central 2021-06-21 /pmc/articles/PMC8215763/ /pubmed/34154659 http://dx.doi.org/10.1186/s40168-021-01087-w Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Huws, Sharon A.
Edwards, Joan E.
Lin, Wanchang
Rubino, Francesco
Alston, Mark
Swarbreck, David
Caim, Shabhonam
Stevens, Pauline Rees
Pachebat, Justin
Won, Mi-Young
Oyama, Linda B.
Creevey, Christopher J.
Kingston-Smith, Alison H.
Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title_full Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title_fullStr Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title_full_unstemmed Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title_short Microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
title_sort microbiomes attached to fresh perennial ryegrass are temporally resilient and adapt to changing ecological niches
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215763/
https://www.ncbi.nlm.nih.gov/pubmed/34154659
http://dx.doi.org/10.1186/s40168-021-01087-w
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