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Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo
The kakapo is a critically endangered, herbivorous parrot endemic to New Zealand. The kakapo hindgut hosts a dense microbial community of low taxonomic diversity, typically dominated by Escherichia fergusonii, and has proven to be a remarkably stable ecosystem, displaying little variation in core me...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970201/ https://www.ncbi.nlm.nih.gov/pubmed/29802288 http://dx.doi.org/10.1038/s41598-018-26484-4 |
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author | Waite, David W. Dsouza, Melissa Sekiguchi, Yuji Hugenholtz, Philip Taylor, Michael W. |
author_facet | Waite, David W. Dsouza, Melissa Sekiguchi, Yuji Hugenholtz, Philip Taylor, Michael W. |
author_sort | Waite, David W. |
collection | PubMed |
description | The kakapo is a critically endangered, herbivorous parrot endemic to New Zealand. The kakapo hindgut hosts a dense microbial community of low taxonomic diversity, typically dominated by Escherichia fergusonii, and has proven to be a remarkably stable ecosystem, displaying little variation in core membership over years of study. To elucidate mechanisms underlying this robustness, we performed 16S rRNA gene-based co-occurrence network analysis to identify potential interactions between E. fergusonii and the wider bacterial community. Genomic and metagenomic sequencing were employed to facilitate interpretation of potential interactions observed in the network. E. fergusonii maintained very few correlations with other members of the microbiota, and isolates possessed genes for the generation of energy from a wide range of carbohydrate sources, including plant fibres such as cellulose. We surmise that this dominant microorganism is abundant not due to ecological interaction with other members of the microbiota, but its ability to metabolise a wide range of nutrients in the gut. This research represents the first concerted effort to understand the functional roles of the kakapo microbiota, and leverages metagenomic data to contextualise co-occurrence patterns. By combining these two techniques we provide a means for studying the diversity-stability hypothesis in the context of bacterial ecosystems. |
format | Online Article Text |
id | pubmed-5970201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59702012018-05-30 Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo Waite, David W. Dsouza, Melissa Sekiguchi, Yuji Hugenholtz, Philip Taylor, Michael W. Sci Rep Article The kakapo is a critically endangered, herbivorous parrot endemic to New Zealand. The kakapo hindgut hosts a dense microbial community of low taxonomic diversity, typically dominated by Escherichia fergusonii, and has proven to be a remarkably stable ecosystem, displaying little variation in core membership over years of study. To elucidate mechanisms underlying this robustness, we performed 16S rRNA gene-based co-occurrence network analysis to identify potential interactions between E. fergusonii and the wider bacterial community. Genomic and metagenomic sequencing were employed to facilitate interpretation of potential interactions observed in the network. E. fergusonii maintained very few correlations with other members of the microbiota, and isolates possessed genes for the generation of energy from a wide range of carbohydrate sources, including plant fibres such as cellulose. We surmise that this dominant microorganism is abundant not due to ecological interaction with other members of the microbiota, but its ability to metabolise a wide range of nutrients in the gut. This research represents the first concerted effort to understand the functional roles of the kakapo microbiota, and leverages metagenomic data to contextualise co-occurrence patterns. By combining these two techniques we provide a means for studying the diversity-stability hypothesis in the context of bacterial ecosystems. Nature Publishing Group UK 2018-05-25 /pmc/articles/PMC5970201/ /pubmed/29802288 http://dx.doi.org/10.1038/s41598-018-26484-4 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Waite, David W. Dsouza, Melissa Sekiguchi, Yuji Hugenholtz, Philip Taylor, Michael W. Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title | Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title_full | Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title_fullStr | Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title_full_unstemmed | Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title_short | Network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
title_sort | network-guided genomic and metagenomic analysis of the faecal microbiota of the critically endangered kakapo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970201/ https://www.ncbi.nlm.nih.gov/pubmed/29802288 http://dx.doi.org/10.1038/s41598-018-26484-4 |
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