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Estimation of viral richness from shotgun metagenomes using a frequency count approach

BACKGROUND: Viruses are important drivers of ecosystem functions, yet little is known about the vast majority of viruses. Viral shotgun metagenomics enables the investigation of broad ecological questions in phage communities. One ecological characteristic is species richness, which is the number of...

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Autores principales: Allen, Heather K, Bunge, John, Foster, James A, Bayles, Darrell O, Stanton, Thaddeus B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869190/
https://www.ncbi.nlm.nih.gov/pubmed/24451229
http://dx.doi.org/10.1186/2049-2618-1-5
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author Allen, Heather K
Bunge, John
Foster, James A
Bayles, Darrell O
Stanton, Thaddeus B
author_facet Allen, Heather K
Bunge, John
Foster, James A
Bayles, Darrell O
Stanton, Thaddeus B
author_sort Allen, Heather K
collection PubMed
description BACKGROUND: Viruses are important drivers of ecosystem functions, yet little is known about the vast majority of viruses. Viral shotgun metagenomics enables the investigation of broad ecological questions in phage communities. One ecological characteristic is species richness, which is the number of different species in a community. Viruses do not have a phylogenetic marker analogous to the bacterial 16S rRNA gene with which to estimate richness, and so contig spectra are employed to measure the number of virus taxa in a given community. A contig spectrum is generated from a viral shotgun metagenome by assembling the random sequence reads into groups of sequences that overlap (contigs) and counting the number of sequences that group within each contig. Current tools available to analyze contig spectra to estimate phage richness are limited by relying on rank-abundance data. RESULTS: We present statistical estimates of virus richness from contig spectra. The program CatchAll (http://www.northeastern.edu/catchall/) was used to analyze contig spectra in terms of frequency count data rather than rank-abundance, thus enabling formal statistical analyses. Also, the influence of potentially spurious low-frequency counts on richness estimates was minimized by two methods, empirical and statistical. The results show greater estimates of viral richness than previous calculations in nearly all environments analyzed, including swine feces and reclaimed fresh water. CONCLUSIONS: CatchAll yielded consistent estimates of richness across viral metagenomes from the same or similar environments. Additionally, analysis of pooled viral metagenomes from different environments via mixed contig spectra resulted in greater richness estimates than those of the component metagenomes. Using CatchAll to analyze contig spectra will improve estimations of richness from viral shotgun metagenomes, particularly from large datasets, by providing statistical measures of richness.
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spelling pubmed-38691902013-12-30 Estimation of viral richness from shotgun metagenomes using a frequency count approach Allen, Heather K Bunge, John Foster, James A Bayles, Darrell O Stanton, Thaddeus B Microbiome Research BACKGROUND: Viruses are important drivers of ecosystem functions, yet little is known about the vast majority of viruses. Viral shotgun metagenomics enables the investigation of broad ecological questions in phage communities. One ecological characteristic is species richness, which is the number of different species in a community. Viruses do not have a phylogenetic marker analogous to the bacterial 16S rRNA gene with which to estimate richness, and so contig spectra are employed to measure the number of virus taxa in a given community. A contig spectrum is generated from a viral shotgun metagenome by assembling the random sequence reads into groups of sequences that overlap (contigs) and counting the number of sequences that group within each contig. Current tools available to analyze contig spectra to estimate phage richness are limited by relying on rank-abundance data. RESULTS: We present statistical estimates of virus richness from contig spectra. The program CatchAll (http://www.northeastern.edu/catchall/) was used to analyze contig spectra in terms of frequency count data rather than rank-abundance, thus enabling formal statistical analyses. Also, the influence of potentially spurious low-frequency counts on richness estimates was minimized by two methods, empirical and statistical. The results show greater estimates of viral richness than previous calculations in nearly all environments analyzed, including swine feces and reclaimed fresh water. CONCLUSIONS: CatchAll yielded consistent estimates of richness across viral metagenomes from the same or similar environments. Additionally, analysis of pooled viral metagenomes from different environments via mixed contig spectra resulted in greater richness estimates than those of the component metagenomes. Using CatchAll to analyze contig spectra will improve estimations of richness from viral shotgun metagenomes, particularly from large datasets, by providing statistical measures of richness. BioMed Central 2013-02-04 /pmc/articles/PMC3869190/ /pubmed/24451229 http://dx.doi.org/10.1186/2049-2618-1-5 Text en Copyright © 2013 Allen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Allen, Heather K
Bunge, John
Foster, James A
Bayles, Darrell O
Stanton, Thaddeus B
Estimation of viral richness from shotgun metagenomes using a frequency count approach
title Estimation of viral richness from shotgun metagenomes using a frequency count approach
title_full Estimation of viral richness from shotgun metagenomes using a frequency count approach
title_fullStr Estimation of viral richness from shotgun metagenomes using a frequency count approach
title_full_unstemmed Estimation of viral richness from shotgun metagenomes using a frequency count approach
title_short Estimation of viral richness from shotgun metagenomes using a frequency count approach
title_sort estimation of viral richness from shotgun metagenomes using a frequency count approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869190/
https://www.ncbi.nlm.nih.gov/pubmed/24451229
http://dx.doi.org/10.1186/2049-2618-1-5
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