Amplification Methods Bias Metagenomic Libraries of Uncultured Single-Stranded and Double-Stranded DNA Viruses

ABSTRACT Investigation of viruses in the environment often requires the amplification of viral DNA before sequencing of viral metagenomes. In this study, two of the most widely used amplification methods, the linker amplified shotgun library (LASL) and multiple displacement amplification (MDA) methods, were applied to a sample from the seawater surface. Viral DNA was extracted from viruses concentrated by tangential flow filtration and amplified by these two methods. 454 pyrosequencing was used to read the metagenomic sequences from different libraries. The resulting taxonomic classifications of the viruses, their functional assignments, and assembly patterns differed substantially depending on the amplification method. Only double-stranded DNA viruses were retrieved from the LASL, whereas most sequences in the MDA library were from single-stranded DNA viruses, and double-stranded DNA viral sequences were minorities. Thus, the two amplification methods reveal different aspects of viral diversity.

[1]  Roger S Lasken,et al.  Mechanism of chimera formation during the Multiple Displacement Amplification reaction , 2007 .

[2]  Kyoung-Ho Kim,et al.  Metagenomic Analysis of the Viral Communities in Fermented Foods , 2010, Applied and Environmental Microbiology.

[3]  Florent E. Angly,et al.  Power law rank-abundance models for marine phage communities. , 2007, FEMS microbiology letters.

[4]  Peter Salamon,et al.  Viral and microbial community dynamics in four aquatic environments , 2010, The ISME Journal.

[5]  C. Jeon,et al.  Amplification of Uncultured Single-Stranded DNA Viruses from Rice Paddy Soil , 2008, Applied and Environmental Microbiology.

[6]  G. Church,et al.  Sequencing genomes from single cells by polymerase cloning , 2006, Nature Biotechnology.

[7]  Florent E. Angly,et al.  Viral diversity and dynamics in an infant gut. , 2008, Research in microbiology.

[8]  Tao Zhang,et al.  RNA Viral Community in Human Feces: Prevalence of Plant Pathogenic Viruses , 2005, PLoS biology.

[9]  J. Steward Purification of viruses by centrifugation , 2015 .

[10]  M. Weinbauer,et al.  Manual of Aquatic Viral Ecology , 2010 .

[11]  K. Eric Wommack,et al.  Assembly of Viral Metagenomes from Yellowstone Hot Springs , 2008, Applied and Environmental Microbiology.

[12]  Robert D. Finn,et al.  Pfam: clans, web tools and services , 2005, Nucleic Acids Res..

[13]  M. Weinbauer Ecology of prokaryotic viruses. , 2004, FEMS microbiology reviews.

[14]  Florent E. Angly,et al.  Biodiversity and biogeography of phages in modern stromatolites and thrombolites , 2008, Nature.

[15]  Eoin L. Brodie,et al.  Environmental Whole-Genome Amplification To Access Microbial Populations in Contaminated Sediments , 2006, Applied and Environmental Microbiology.

[16]  M. Breitbart,et al.  Method for discovering novel DNA viruses in blood using viral particle selection and shotgun sequencing. , 2005, BioTechniques.

[17]  H. Jeske,et al.  Rolling circle amplification revolutionizes diagnosis and genomics of geminiviruses. , 2006, Journal of virological methods.

[18]  Yan Wei Lim,et al.  Metagenomic analysis of viruses in reclaimed water. , 2009, Environmental microbiology.

[19]  P. Salamon,et al.  Metagenomic Analyses of an Uncultured Viral Community from Human Feces , 2003, Journal of bacteriology.

[20]  B. Andresen,et al.  Genomic analysis of uncultured marine viral communities , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Weizhong Li,et al.  Analysis and comparison of very large metagenomes with fast clustering and functional annotation , 2009, BMC Bioinformatics.

[22]  Shawn W. Polson,et al.  Unraveling the viral tapestry (from inside the capsid out) , 2011, The ISME Journal.

[23]  Florent E. Angly,et al.  The Marine Viromes of Four Oceanic Regions , 2006, PLoS biology.

[24]  Curtis A Suttle,et al.  Metagenomic Analysis of Coastal RNA Virus Communities , 2006, Science.

[25]  M. Breitbart,et al.  Discovery of a Novel Single-Stranded DNA Virus from a Sea Turtle Fibropapilloma by Using Viral Metagenomics , 2008, Journal of Virology.

[26]  Antonio Quesada,et al.  High Diversity of the Viral Community from an Antarctic Lake , 2009, Science.

[27]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[28]  Danielle M. Winget,et al.  Filtration-based methods for the collection of viral concentrates from large water samples , 2010 .

[29]  Owen White,et al.  The TIGRFAMs database of protein families , 2003, Nucleic Acids Res..

[30]  C. Suttle Viruses in the sea , 2005, Nature.

[31]  Dhritiman Ghosh,et al.  Metagenomic Characterization of Chesapeake Bay Virioplankton , 2007, Applied and Environmental Microbiology.

[32]  Ying Gao,et al.  Bioinformatics Applications Note Sequence Analysis Cd-hit Suite: a Web Server for Clustering and Comparing Biological Sequences , 2022 .

[33]  P. Salamon,et al.  Diversity and population structure of a near–shore marine–sediment viral community , 2004, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[34]  Peter Salamon,et al.  Metagenomic and Small-Subunit rRNA Analyses Reveal the Genetic Diversity of Bacteria, Archaea, Fungi, and Viruses in Soil , 2007, Applied and Environmental Microbiology.

[35]  S. Kravitz,et al.  CAMERA: A Community Resource for Metagenomics , 2007, PLoS biology.

[36]  S. Hino TTV, a new human virus with single stranded circular DNA genome , 2002, Reviews in medical virology.

[37]  R. Edwards,et al.  Viral metagenomics , 2005, Nature Reviews Microbiology.

[38]  C. Jeon,et al.  Development of microbial genome-probing microarrays using digital multiple displacement amplification of uncultivated microbial single cells. , 2008, Environmental science & technology.

[39]  Darren A. Natale,et al.  The COG database: an updated version includes eukaryotes , 2003, BMC Bioinformatics.

[40]  P. Hugenholtz,et al.  Multiple displacement amplification compromises quantitative analysis of metagenomes , 2010, Nature Methods.