Metagenomic analysis of human diarrhea: Viral detection and discovery

被引:262
作者
Finkbeiner, Stacy R. [1 ,2 ,3 ]
Allred, Adam F. [1 ,2 ,3 ]
Tarr, Phillip I. [4 ]
Klein, Eileen J. [5 ]
Kirkwood, Carl D. [6 ]
Wang, David [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Microbiol & Mol Pathol, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Dept Immunol, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[4] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[5] Childrens Hosp & Reg Med Ctr, Dept Emergency Med, Seattle, WA USA
[6] Royal Childrens Hosp, Enter Virus Res Grp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
关键词
D O I
10.1371/journal.ppat.1000011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Worldwide, approximately 1.8 million children die from diarrhea annually, and millions more suffer multiple episodes of nonfatal diarrhea. On average, in up to 40% of cases, no etiologic agent can be identified. The advent of metagenomic sequencing has enabled systematic and unbiased characterization of microbial populations; thus, metagenomic approaches have the potential to define the spectrum of viruses, including novel viruses, present in stool during episodes of acute diarrhea. The detection of novel or unexpected viruses would then enable investigations to assess whether these agents play a causal role in human diarrhea. In this study, we characterized the eukaryotic viral communities present in diarrhea specimens from 12 children by employing a strategy of "micro-mass sequencing'' that entails minimal starting sample quantity (< 100 mg stool), minimal sample purification, and limited sequencing ( 384 reads per sample). Using this methodology we detected known enteric viruses as well as multiple sequences from putatively novel viruses with only limited sequence similarity to viruses in GenBank.
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页数:9
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