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Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries

Longstanding questions relate to the existence of naturally distinct bacterial species and genetic approaches to distinguish them. Bacterial genomes in public databases form distinct groups, but these databases are subject to isolation and deposition biases. To avoid these biases, we compared 5,203...

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Autores principales: Olm, Matthew R., Crits-Christoph, Alexander, Diamond, Spencer, Lavy, Adi, Matheus Carnevali, Paula B., Banfield, Jillian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967389/
https://www.ncbi.nlm.nih.gov/pubmed/31937678
http://dx.doi.org/10.1128/mSystems.00731-19
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author Olm, Matthew R.
Crits-Christoph, Alexander
Diamond, Spencer
Lavy, Adi
Matheus Carnevali, Paula B.
Banfield, Jillian F.
author_facet Olm, Matthew R.
Crits-Christoph, Alexander
Diamond, Spencer
Lavy, Adi
Matheus Carnevali, Paula B.
Banfield, Jillian F.
author_sort Olm, Matthew R.
collection PubMed
description Longstanding questions relate to the existence of naturally distinct bacterial species and genetic approaches to distinguish them. Bacterial genomes in public databases form distinct groups, but these databases are subject to isolation and deposition biases. To avoid these biases, we compared 5,203 bacterial genomes from 1,457 environmental metagenomic samples to test for distinct clouds of diversity and evaluated metrics that could be used to define the species boundary. Bacterial genomes from the human gut, soil, and the ocean all exhibited gaps in whole-genome average nucleotide identities (ANI) near the previously suggested species threshold of 95% ANI. While genome-wide ratios of nonsynonymous and synonymous nucleotide differences (dN/dS) decrease until ANI values approach ∼98%, two methods for estimating homologous recombination approached zero at ∼95% ANI, supporting breakdown of recombination due to sequence divergence as a species-forming force. We evaluated 107 genome-based metrics for their ability to distinguish species when full genomes are not recovered. Full-length 16S rRNA genes were least useful, in part because they were underrecovered from metagenomes. However, many ribosomal proteins displayed both high metagenomic recoverability and species discrimination power. Taken together, our results verify the existence of sequence-discrete microbial species in metagenome-derived genomes and highlight the usefulness of ribosomal genes for gene-level species discrimination. IMPORTANCE There is controversy about whether bacterial diversity is clustered into distinct species groups or exists as a continuum. To address this issue, we analyzed bacterial genome databases and reports from several previous large-scale environment studies and identified clear discrete groups of species-level bacterial diversity in all cases. Genetic analysis further revealed that quasi-sexual reproduction via horizontal gene transfer is likely a key evolutionary force that maintains bacterial species integrity. We next benchmarked over 100 metrics to distinguish these bacterial species from each other and identified several genes encoding ribosomal proteins with high species discrimination power. Overall, the results from this study provide best practices for bacterial species delineation based on genome content and insight into the nature of bacterial species population genetics.
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spelling pubmed-69673892020-02-03 Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries Olm, Matthew R. Crits-Christoph, Alexander Diamond, Spencer Lavy, Adi Matheus Carnevali, Paula B. Banfield, Jillian F. mSystems Research Article Longstanding questions relate to the existence of naturally distinct bacterial species and genetic approaches to distinguish them. Bacterial genomes in public databases form distinct groups, but these databases are subject to isolation and deposition biases. To avoid these biases, we compared 5,203 bacterial genomes from 1,457 environmental metagenomic samples to test for distinct clouds of diversity and evaluated metrics that could be used to define the species boundary. Bacterial genomes from the human gut, soil, and the ocean all exhibited gaps in whole-genome average nucleotide identities (ANI) near the previously suggested species threshold of 95% ANI. While genome-wide ratios of nonsynonymous and synonymous nucleotide differences (dN/dS) decrease until ANI values approach ∼98%, two methods for estimating homologous recombination approached zero at ∼95% ANI, supporting breakdown of recombination due to sequence divergence as a species-forming force. We evaluated 107 genome-based metrics for their ability to distinguish species when full genomes are not recovered. Full-length 16S rRNA genes were least useful, in part because they were underrecovered from metagenomes. However, many ribosomal proteins displayed both high metagenomic recoverability and species discrimination power. Taken together, our results verify the existence of sequence-discrete microbial species in metagenome-derived genomes and highlight the usefulness of ribosomal genes for gene-level species discrimination. IMPORTANCE There is controversy about whether bacterial diversity is clustered into distinct species groups or exists as a continuum. To address this issue, we analyzed bacterial genome databases and reports from several previous large-scale environment studies and identified clear discrete groups of species-level bacterial diversity in all cases. Genetic analysis further revealed that quasi-sexual reproduction via horizontal gene transfer is likely a key evolutionary force that maintains bacterial species integrity. We next benchmarked over 100 metrics to distinguish these bacterial species from each other and identified several genes encoding ribosomal proteins with high species discrimination power. Overall, the results from this study provide best practices for bacterial species delineation based on genome content and insight into the nature of bacterial species population genetics. American Society for Microbiology 2020-01-14 /pmc/articles/PMC6967389/ /pubmed/31937678 http://dx.doi.org/10.1128/mSystems.00731-19 Text en Copyright © 2020 Olm 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
Olm, Matthew R.
Crits-Christoph, Alexander
Diamond, Spencer
Lavy, Adi
Matheus Carnevali, Paula B.
Banfield, Jillian F.
Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title_full Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title_fullStr Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title_full_unstemmed Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title_short Consistent Metagenome-Derived Metrics Verify and Delineate Bacterial Species Boundaries
title_sort consistent metagenome-derived metrics verify and delineate bacterial species boundaries
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967389/
https://www.ncbi.nlm.nih.gov/pubmed/31937678
http://dx.doi.org/10.1128/mSystems.00731-19
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