Microbial Contamination in Next Generation Sequencing: Implications for Sequence-Based Analysis of Clinical Samples

被引:123
作者
Strong, Michael J. [1 ,2 ]
Xu, Guorong [3 ]
Morici, Lisa [4 ]
Bon-Durant, Sandra Splinter [5 ]
Baddoo, Melody [1 ,2 ]
Lin, Zhen [1 ,2 ]
Fewell, Claire [1 ,2 ]
Taylor, Christopher M. [6 ,7 ]
Flemington, Erik K. [1 ,2 ]
机构
[1] Tulane Univ, Dept Pathol, New Orleans, LA 70118 USA
[2] Tulane Univ, Tulane Canc Ctr, New Orleans, LA 70118 USA
[3] Univ Calif San Diego, Dept Genom Med, San Diego, CA 92103 USA
[4] Tulane Univ, Dept Microbiol & Immunol, New Orleans, LA 70118 USA
[5] Univ Wisconsin, Ctr Biotechnol, Madison, WI 53705 USA
[6] Louisiana State Univ, Sch Med, Dept Microbiol Immunol & Parasitol, New Orleans, LA USA
[7] Childrens Hosp New Orleans, Res Inst Children, New Orleans, LA USA
关键词
EPSTEIN-BARR-VIRUS; CHINESE PATIENTS; NIH-CQV; RNA; DISCOVERY; ORIGIN;
D O I
10.1371/journal.ppat.1004437
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The high level of accuracy and sensitivity of next generation sequencing for quantifying genetic material across organismal boundaries gives it tremendous potential for pathogen discovery and diagnosis in human disease. Despite this promise, substantial bacterial contamination is routinely found in existing human-derived RNA-seq datasets that likely arises from environmental sources. This raises the need for stringent sequencing and analysis protocols for studies investigating sequence-based microbial signatures in clinical samples.
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页数:6
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