Transforming clinical microbiology with bacterial genome sequencing

被引:526
作者
Didelot, Xavier [4 ]
Bowden, Rory [2 ,3 ,4 ]
Wilson, Daniel J. [1 ,3 ]
Peto, Tim E. A. [1 ,2 ]
Crook, Derrick W. [1 ,2 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Oxford OX3 9DU, England
[2] John Radcliffe Hosp, NIHR Oxford Biomed Res Ctr, Oxford OX3 9DU, England
[3] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[4] Univ Oxford, Dept Stat, Oxford OX1 3TG, England
关键词
DESORPTION IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY; RESISTANT STAPHYLOCOCCUS-AUREUS; MYCOBACTERIUM-TUBERCULOSIS; METHICILLIN-RESISTANT; ROUTINE IDENTIFICATION; RAPID DETECTION; EVOLUTION; GENERATION; GENE;
D O I
10.1038/nrg3226
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Whole-genome sequencing of bacteria has recently emerged as a cost-effective and convenient approach for addressing many microbiological questions. Here, we review the current status of clinical microbiology and how it has already begun to be transformed by using next-generation sequencing. We focus on three essential tasks: identifying the species of an isolate, testing its properties, such as resistance to antibiotics and virulence, and monitoring the emergence and spread of bacterial pathogens. We predict that the application of next-generation sequencing will soon be sufficiently fast, accurate and cheap to be used in routine clinical microbiology practice, where it could replace many complex current techniques with a single, more efficient workflow.
引用
收藏
页码:601 / 612
页数:12
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