Next-generation and whole-genome sequencing in the diagnostic clinical microbiology laboratory

被引:109
作者
Dunne, W. M., Jr. [1 ,2 ,3 ]
Westblade, L. F. [2 ]
Ford, B. [2 ]
机构
[1] BioMarieux Inc, Durham, NC 27712 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[3] Duke Univ, Dept Pediat, Sch Med, Durham, NC 27706 USA
关键词
RESISTANT STAPHYLOCOCCUS-AUREUS; URINARY-TRACT-INFECTION; HUMAN SKIN MICROBIOME; INTESTINAL MICROBIOTA; BACTERIAL DIVERSITY; GUT MICROBIOMES; DISEASE; IDENTIFICATION; SPECIMENS; NASAL;
D O I
10.1007/s10096-012-1641-7
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The identification and/or prediction of the antimicrobial resistance of microorganisms in clinical materials solely by molecular means in the diagnostic microbiology laboratory is not novel. However, the ability to sequence multitudes of bacterial genomes and deliver and interpret the resultant sequence information in near "real-time" is the basis of next-generation sequencing (NGS) technologies. There have been numerous applications and successes of NGS applications in the clinical and public health domain. However, none have, as yet, delivered perhaps the most sought after application, i.e., the generation of microbial sequence data for "real-time" patient management. In this review, we discuss the use of NGS and whole-genome sequencing (WGS) of microorganisms as a logical next step for the routine diagnosis of infection and the prediction of antimicrobial susceptibility in the clinical microbiology laboratory.
引用
收藏
页码:1719 / 1726
页数:8
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