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Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities

Viruses are the most abundant biological entities on Earth and play key roles in host ecology, evolution, and horizontal gene transfer. Despite recent progress in viral metagenomics, the inherent genetic complexity of virus populations still poses technical difficulties for recovering complete virus...

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Autores principales: Beaulaurier, John, Luo, Elaine, Eppley, John M., Uyl, Paul Den, Dai, Xiaoguang, Burger, Andrew, Turner, Daniel J., Pendelton, Matthew, Juul, Sissel, Harrington, Eoghan, DeLong, Edward F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111524/
https://www.ncbi.nlm.nih.gov/pubmed/32075851
http://dx.doi.org/10.1101/gr.251686.119
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author Beaulaurier, John
Luo, Elaine
Eppley, John M.
Uyl, Paul Den
Dai, Xiaoguang
Burger, Andrew
Turner, Daniel J.
Pendelton, Matthew
Juul, Sissel
Harrington, Eoghan
DeLong, Edward F.
author_facet Beaulaurier, John
Luo, Elaine
Eppley, John M.
Uyl, Paul Den
Dai, Xiaoguang
Burger, Andrew
Turner, Daniel J.
Pendelton, Matthew
Juul, Sissel
Harrington, Eoghan
DeLong, Edward F.
author_sort Beaulaurier, John
collection PubMed
description Viruses are the most abundant biological entities on Earth and play key roles in host ecology, evolution, and horizontal gene transfer. Despite recent progress in viral metagenomics, the inherent genetic complexity of virus populations still poses technical difficulties for recovering complete virus genomes from natural assemblages. To address these challenges, we developed an assembly-free, single-molecule nanopore sequencing approach, enabling direct recovery of complete virus genome sequences from environmental samples. Our method yielded thousands of full-length, high-quality draft virus genome sequences that were not recovered using standard short-read assembly approaches. Additionally, our analyses discriminated between populations whose genomes had identical direct terminal repeats versus those with circularly permuted repeats at their termini, thus providing new insight into native virus reproduction and genome packaging. Novel DNA sequences were discovered, whose repeat structures, gene contents, and concatemer lengths suggest they are phage-inducible chromosomal islands, which are packaged as concatemers in phage particles, with lengths that match the size ranges of co-occurring phage genomes. Our new virus sequencing strategy can provide previously unavailable information about the genome structures, population biology, and ecology of naturally occurring viruses and viral parasites.
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spelling pubmed-71115242020-04-03 Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities Beaulaurier, John Luo, Elaine Eppley, John M. Uyl, Paul Den Dai, Xiaoguang Burger, Andrew Turner, Daniel J. Pendelton, Matthew Juul, Sissel Harrington, Eoghan DeLong, Edward F. Genome Res Method Viruses are the most abundant biological entities on Earth and play key roles in host ecology, evolution, and horizontal gene transfer. Despite recent progress in viral metagenomics, the inherent genetic complexity of virus populations still poses technical difficulties for recovering complete virus genomes from natural assemblages. To address these challenges, we developed an assembly-free, single-molecule nanopore sequencing approach, enabling direct recovery of complete virus genome sequences from environmental samples. Our method yielded thousands of full-length, high-quality draft virus genome sequences that were not recovered using standard short-read assembly approaches. Additionally, our analyses discriminated between populations whose genomes had identical direct terminal repeats versus those with circularly permuted repeats at their termini, thus providing new insight into native virus reproduction and genome packaging. Novel DNA sequences were discovered, whose repeat structures, gene contents, and concatemer lengths suggest they are phage-inducible chromosomal islands, which are packaged as concatemers in phage particles, with lengths that match the size ranges of co-occurring phage genomes. Our new virus sequencing strategy can provide previously unavailable information about the genome structures, population biology, and ecology of naturally occurring viruses and viral parasites. Cold Spring Harbor Laboratory Press 2020-03 /pmc/articles/PMC7111524/ /pubmed/32075851 http://dx.doi.org/10.1101/gr.251686.119 Text en © 2020 Beaulaurier et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Method
Beaulaurier, John
Luo, Elaine
Eppley, John M.
Uyl, Paul Den
Dai, Xiaoguang
Burger, Andrew
Turner, Daniel J.
Pendelton, Matthew
Juul, Sissel
Harrington, Eoghan
DeLong, Edward F.
Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title_full Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title_fullStr Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title_full_unstemmed Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title_short Assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
title_sort assembly-free single-molecule sequencing recovers complete virus genomes from natural microbial communities
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111524/
https://www.ncbi.nlm.nih.gov/pubmed/32075851
http://dx.doi.org/10.1101/gr.251686.119
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