Unbiased metagenomic sequencing complements specific routine diagnostic methods and increases chances to detect rare viral strains

被引:29
作者
Lewandowska, Dagmara W. [1 ]
Zagordi, Osvaldo [1 ]
Zbinden, Andrea [1 ]
Schuurmans, Mace M. [2 ]
Schreiber, Peter [3 ]
Geissberger, Fabienne-Desiree [1 ]
Huder, Jon B. [1 ]
Boeni, Juerg [1 ]
Benden, Christian [2 ]
Mueller, Nicolas J. [1 ,3 ]
Trkola, Alexandra [1 ]
Huber, Michael [1 ]
机构
[1] Univ Zurich, Inst Med Virol, CH-8057 Zurich, Switzerland
[2] Univ Zurich Hosp, Div Pulm Med, CH-8091 Zurich, Switzerland
[3] Univ Zurich Hosp, Div Infect Dis & Hosp Epidemiol, CH-8091 Zurich, Switzerland
关键词
Next generation sequencing; PCR; Metagenomic; Virus diagnostic; Enterovirus; Rhinovirus; TORQUE-TENO VIRUS; NUCLEIC-ACID AMPLIFICATION; RESPIRATORY-TRACT; HUMAN POLYOMAVIRUS; DNA VIRUSES; ENTEROVIRUS; IDENTIFICATION; IMMUNOSUPPRESSION; DISEASE; RHINOVIRUSES;
D O I
10.1016/j.diagmicrobio.2015.06.017
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Multiplex PCR assays for respiratory viruses are widely used in routine diagnostics, as they are highly sensitive, rapid, and cost effective. However, depending on the assay system, cross-reactivity between viruses that share a high sequence homology as well as detection of rare virus isolates with sequence variations can be problematic. Virus sequence-independent metagenomic high-throughput sequencing allows for accurate detection of all virus species in a given sample, as we demonstrate here for human Enterovirus and Rhinovirus in a lung transplant patient While early in infection a commercial PCR assay recorded Rhinovirus, high-throughput sequencing correctly identified human Enterovirus C104 as the source of infection, highlighting the potential of the technology and the benefit of applying open assay formats in complex diagnostic situations. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 138
页数:6
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