Hydroxyapatite-Mediated Separation of Double-Stranded DNA, Single-Stranded DNA, and RNA Genomes from Natural Viral Assemblages

被引:51
|
作者
Andrews-Pfannkoch, Cynthia [2 ]
Fadrosh, Douglas W. [1 ]
Thorpe, Joyce [2 ]
Williamson, Shannon J. [1 ]
机构
[1] J Craig Venter Inst, San Diego, CA 92121 USA
[2] J Craig Venter Inst, Rockville, MD 20850 USA
基金
美国国家科学基金会;
关键词
OCEAN SAMPLING EXPEDITION; METAGENOMIC CHARACTERIZATION; PHOTOSYNTHESIS GENES; VIRUSES; SEA; COMMUNITIES; SEQUENCE;
D O I
10.1128/AEM.00204-10
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Metagenomics can be used to determine the diversity of complex, often unculturable, viral communities with various nucleic acid compositions. Here, we report the use of hydroxyapatite chromatography to efficiently fractionate double-stranded DNA (dsDNA), single-stranded DNA (ssDNA), dsRNA, and ssRNA genomes from known bacteriophages. Linker-amplified shotgun libraries were constructed to generate sequencing reads from each hydroxyapatite fraction. Greater than 90% of the reads displayed significant similarity to the expected genomes at the nucleotide level. These methods were applied to marine viruses collected from the Chesapeake Bay and the Dry Tortugas National Park. Isolated nucleic acids were fractionated using hydroxyapatite chromatography followed by linker-amplified shotgun library construction and sequencing. Taxonomic analysis demonstrated that the majority of environmental sequences, regardless of their source nucleic acid, were most similar to dsDNA viruses, reflecting the bias of viral metagenomic sequence databases.
引用
收藏
页码:5039 / 5045
页数:7
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