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Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data
BACKGROUND: Interest in understanding the mechanisms that lead to a particular composition of the Gut Microbiota is highly increasing, due to the relationship between this ecosystem and the host health state. Particularly relevant is the study of the Relative Species Abundance (RSA) distribution, th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959352/ https://www.ncbi.nlm.nih.gov/pubmed/26821617 http://dx.doi.org/10.1186/s12859-015-0858-8 |
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author | Sala, Claudia Vitali, Silvia Giampieri, Enrico do Valle, Ìtalo Faria Remondini, Daniel Garagnani, Paolo Bersanelli, Matteo Mosca, Ettore Milanesi, Luciano Castellani, Gastone |
author_facet | Sala, Claudia Vitali, Silvia Giampieri, Enrico do Valle, Ìtalo Faria Remondini, Daniel Garagnani, Paolo Bersanelli, Matteo Mosca, Ettore Milanesi, Luciano Castellani, Gastone |
author_sort | Sala, Claudia |
collection | PubMed |
description | BACKGROUND: Interest in understanding the mechanisms that lead to a particular composition of the Gut Microbiota is highly increasing, due to the relationship between this ecosystem and the host health state. Particularly relevant is the study of the Relative Species Abundance (RSA) distribution, that is a component of biodiversity and measures the number of species having a given number of individuals. It is the universal behaviour of RSA that induced many ecologists to look for theoretical explanations. In particular, a simple stochastic neutral model was proposed by Volkov et al. relying on population dynamics and was proved to fit the coral-reefs and rain forests RSA. Our aim is to ascertain if this model also describes the Microbiota RSA and if it can help in explaining the Microbiota plasticity. RESULTS: We analyzed 16S rRNA sequencing data sampled from the Microbiota of three different animal species by Jeraldo et al. Through a clustering procedure (UCLUST), we built the Operational Taxonomic Units. These correspond to bacterial species considered at a given phylogenetic level defined by the similarity threshold used in the clustering procedure. The RSAs, plotted in the form of Preston plot, were fitted with Volkov’s model. The model fits well the Microbiota RSA, except in the tail region, that shows a deviation from the neutrality assumption. Looking at the model parameters we were able to discriminate between different animal species, giving also a biological explanation. Moreover, the biodiversity estimator obtained by Volkov’s model also differentiates the animal species and is in good agreement with the first and second order Hill’s numbers, that are common evenness indexes simply based on the fraction of individuals per species. CONCLUSIONS: We conclude that the neutrality assumption is a good approximation for the Microbiota dynamics and the observation that Volkov’s model works for this ecosystem is a further proof of the RSA universality. Moreover, the ability to separate different animals with the model parameters and biodiversity number are promising results if we think about future applications on human data, in which the Microbiota composition and biodiversity are in close relationships with a variety of diseases and life-styles. |
format | Online Article Text |
id | pubmed-4959352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49593522016-08-01 Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data Sala, Claudia Vitali, Silvia Giampieri, Enrico do Valle, Ìtalo Faria Remondini, Daniel Garagnani, Paolo Bersanelli, Matteo Mosca, Ettore Milanesi, Luciano Castellani, Gastone BMC Bioinformatics Research BACKGROUND: Interest in understanding the mechanisms that lead to a particular composition of the Gut Microbiota is highly increasing, due to the relationship between this ecosystem and the host health state. Particularly relevant is the study of the Relative Species Abundance (RSA) distribution, that is a component of biodiversity and measures the number of species having a given number of individuals. It is the universal behaviour of RSA that induced many ecologists to look for theoretical explanations. In particular, a simple stochastic neutral model was proposed by Volkov et al. relying on population dynamics and was proved to fit the coral-reefs and rain forests RSA. Our aim is to ascertain if this model also describes the Microbiota RSA and if it can help in explaining the Microbiota plasticity. RESULTS: We analyzed 16S rRNA sequencing data sampled from the Microbiota of three different animal species by Jeraldo et al. Through a clustering procedure (UCLUST), we built the Operational Taxonomic Units. These correspond to bacterial species considered at a given phylogenetic level defined by the similarity threshold used in the clustering procedure. The RSAs, plotted in the form of Preston plot, were fitted with Volkov’s model. The model fits well the Microbiota RSA, except in the tail region, that shows a deviation from the neutrality assumption. Looking at the model parameters we were able to discriminate between different animal species, giving also a biological explanation. Moreover, the biodiversity estimator obtained by Volkov’s model also differentiates the animal species and is in good agreement with the first and second order Hill’s numbers, that are common evenness indexes simply based on the fraction of individuals per species. CONCLUSIONS: We conclude that the neutrality assumption is a good approximation for the Microbiota dynamics and the observation that Volkov’s model works for this ecosystem is a further proof of the RSA universality. Moreover, the ability to separate different animals with the model parameters and biodiversity number are promising results if we think about future applications on human data, in which the Microbiota composition and biodiversity are in close relationships with a variety of diseases and life-styles. BioMed Central 2016-01-20 /pmc/articles/PMC4959352/ /pubmed/26821617 http://dx.doi.org/10.1186/s12859-015-0858-8 Text en © Sala et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sala, Claudia Vitali, Silvia Giampieri, Enrico do Valle, Ìtalo Faria Remondini, Daniel Garagnani, Paolo Bersanelli, Matteo Mosca, Ettore Milanesi, Luciano Castellani, Gastone Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title | Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title_full | Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title_fullStr | Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title_full_unstemmed | Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title_short | Stochastic neutral modelling of the Gut Microbiota’s relative species abundance from next generation sequencing data |
title_sort | stochastic neutral modelling of the gut microbiota’s relative species abundance from next generation sequencing data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959352/ https://www.ncbi.nlm.nih.gov/pubmed/26821617 http://dx.doi.org/10.1186/s12859-015-0858-8 |
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