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PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities
Phylogeny is a powerful tool that can be incorporated into quantitative descriptions of community diversity, yet its use has been limited largely due to the difficulty in constructing phylogenies which incorporate the wide genomic diversity of microbial communities. Here, we describe the development...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973285/ https://www.ncbi.nlm.nih.gov/pubmed/36645293 http://dx.doi.org/10.1128/mbio.03455-22 |
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author | Huang, Xinyang Erickson, David L. Meng, Jianghong |
author_facet | Huang, Xinyang Erickson, David L. Meng, Jianghong |
author_sort | Huang, Xinyang |
collection | PubMed |
description | Phylogeny is a powerful tool that can be incorporated into quantitative descriptions of community diversity, yet its use has been limited largely due to the difficulty in constructing phylogenies which incorporate the wide genomic diversity of microbial communities. Here, we describe the development of a web portal, PhyloPlus, which enables users to generate customized phylogenies that may be applied to any bacterial or archaeal communities. We demonstrate the power of phylogeny by comparing metrics that employ phylogeny with those that do not when applied to data sets from two metagenomic studies (fermented food, n = 58; human microbiome, n = 60). This example shows how inclusion of all bacterial species identified by taxonomic classifiers (Kraken2 and Kaiju) made the phylogeny perfectly congruent to the corresponding classification outputs. Our phylogeny-based approach also enabled the construction of more constrained null models which (i) shed light into community structure and (ii) minimize potential inflation of type I errors. Construction of such null models allowed for the observation of under-dispersion in 44 (75.86%) food samples, with the metacommunity defined as bacteria that were found in different food matrices. We also observed that closely related species with high abundance and uneven distribution across different sites could potentially exaggerate the dissimilarity between phylogenetically similar communities if they were measured using traditional species-based metrics (P(adj.) = 0.003), whereas this effect was mitigated by incorporating phylogeny (P(adj.) = 1). In summary, our tool can provide additional insights into microbial communities of interest and facilitate the use of phylogeny-based approaches in metagenomic analyses. |
format | Online Article Text |
id | pubmed-9973285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99732852023-03-01 PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities Huang, Xinyang Erickson, David L. Meng, Jianghong mBio Research Article Phylogeny is a powerful tool that can be incorporated into quantitative descriptions of community diversity, yet its use has been limited largely due to the difficulty in constructing phylogenies which incorporate the wide genomic diversity of microbial communities. Here, we describe the development of a web portal, PhyloPlus, which enables users to generate customized phylogenies that may be applied to any bacterial or archaeal communities. We demonstrate the power of phylogeny by comparing metrics that employ phylogeny with those that do not when applied to data sets from two metagenomic studies (fermented food, n = 58; human microbiome, n = 60). This example shows how inclusion of all bacterial species identified by taxonomic classifiers (Kraken2 and Kaiju) made the phylogeny perfectly congruent to the corresponding classification outputs. Our phylogeny-based approach also enabled the construction of more constrained null models which (i) shed light into community structure and (ii) minimize potential inflation of type I errors. Construction of such null models allowed for the observation of under-dispersion in 44 (75.86%) food samples, with the metacommunity defined as bacteria that were found in different food matrices. We also observed that closely related species with high abundance and uneven distribution across different sites could potentially exaggerate the dissimilarity between phylogenetically similar communities if they were measured using traditional species-based metrics (P(adj.) = 0.003), whereas this effect was mitigated by incorporating phylogeny (P(adj.) = 1). In summary, our tool can provide additional insights into microbial communities of interest and facilitate the use of phylogeny-based approaches in metagenomic analyses. American Society for Microbiology 2023-01-16 /pmc/articles/PMC9973285/ /pubmed/36645293 http://dx.doi.org/10.1128/mbio.03455-22 Text en Copyright © 2023 Huang 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 Huang, Xinyang Erickson, David L. Meng, Jianghong PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title | PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title_full | PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title_fullStr | PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title_full_unstemmed | PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title_short | PhyloPlus: a Universal Tool for Phylogenetic Interrogation of Metagenomic Communities |
title_sort | phyloplus: a universal tool for phylogenetic interrogation of metagenomic communities |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973285/ https://www.ncbi.nlm.nih.gov/pubmed/36645293 http://dx.doi.org/10.1128/mbio.03455-22 |
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