Metagenomics for pathogen detection in public health

被引:158
作者
Miller, Ruth R. [1 ]
Montoya, Vincent [2 ]
Gardy, Jennifer L. [1 ]
Patrick, David M. [1 ]
Tang, Patrick [2 ,3 ]
机构
[1] Univ British Columbia, Fac Med, UBC Sch Populat & Publ Hlth, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 2B5, Canada
[3] British Columbia Ctr Dis Control, Publ Hlth Microbiol & Reference Lab, Vancouver, BC V5Z 2B4, Canada
来源
GENOME MEDICINE | 2013年 / 5卷
关键词
HUMAN MICROBIOME; CLOSTRIDIUM-DIFFICILE; ESCHERICHIA-COLI; GUT MICROBIOTA; DNA VIRUS; SEQUENCE; GENOME; IDENTIFICATION; PCR; DIVERSITY;
D O I
10.1186/gm485
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Traditional pathogen detection methods in public health infectious disease surveillance rely upon the identification of agents that are already known to be associated with a particular clinical syndrome. The emerging field of metagenomics has the potential to revolutionize pathogen detection in public health laboratories by allowing the simultaneous detection of all microorganisms in a clinical sample, without a priori knowledge of their identities, through the use of next-generation DNA sequencing. A single metagenomics analysis has the potential to detect rare and novel pathogens, and to uncover the role of dysbiotic microbiomes in infectious and chronic human disease. Making use of advances in sequencing platforms and bioinformatics tools, recent studies have shown that metagenomics can even determine the whole-genome sequences of pathogens, allowing inferences about antibiotic resistance, virulence, evolution and transmission to be made. We are entering an era in which more novel infectious diseases will be identified through metagenomics-based methods than through traditional laboratory methods. The impetus is now on public health laboratories to integrate metagenomics techniques into their diagnostic arsenals.
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页数:14
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