Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands

Author:

Warwick-Dugdale Joanna12,Solonenko Natalie3,Moore Karen2,Chittick Lauren3,Gregory Ann C.3,Allen Michael J.12,Sullivan Matthew B.34,Temperton Ben2

Affiliation:

1. Plymouth Marine Laboratory, Plymouth, Devon, United Kingdom

2. School of Biosciences, University of Exeter, Exeter, Devon, United Kingdom

3. Department of Microbiology, Ohio State University, Columbus, OH, United States of America

4. Civil, Environmental and Geodetic Engineering, Ohio State University, Columbus, OH, United States of America

Abstract

Marine viruses impact global biogeochemical cycles via their influence on host community structure and function, yet our understanding of viral ecology is constrained by limitations in host culturing and a lack of reference genomes and ‘universal’ gene markers to facilitate community surveys. Short-read viral metagenomic studies have provided clues to viral function and first estimates of global viral gene abundance and distribution, but their assemblies are confounded by populations with high levels of strain evenness and nucleotide diversity (microdiversity), limiting assembly of some of the most abundant viruses on Earth. Such features also challenge assembly across genomic islands containing niche-defining genes that drive ecological speciation. These populations and features may be successfully captured by single-virus genomics and fosmid-based approaches, at least in abundant taxa, but at considerable cost and technical expertise. Here we established a low-cost, low-input, high throughput alternative sequencing and informatics workflow to improve viral metagenomic assemblies using short-read and long-read technology. The ‘VirION’ (Viral, long-read metagenomics via MinION sequencing) approach was first validated using mock communities where it was found to be as relatively quantitative as short-read methods and provided significant improvements in recovery of viral genomes. We then then applied VirION to the first metagenome from a natural viral community from the Western English Channel. In comparison to a short-read only approach, VirION: (i) increased number and completeness of assembled viral genomes; (ii) captured abundant, highly microdiverse virus populations, and (iii) captured more and longer genomic islands. Together, these findings suggest that VirION provides a high throughput and cost-effective alternative to fosmid and single-virus genomic approaches to more comprehensively explore viral communities in nature.

Funder

Bermuda Institute of Ocean Sciences as part of the BIOS-SCOPE program

Royal Society and the Natural Environment Research Council

NERC Great Western Four+ (GW4+) Doctoral Training Partnership PhD

Gordon and Betty Moore Foundation

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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