RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing

被引:5
|
作者
Brinkmann, Annika [1 ,2 ]
Uddin, Steven [1 ,2 ]
Ulm, Sophie-Luisa [1 ,2 ]
Pape, Katharina [1 ,2 ]
Foerster, Sophie [1 ,2 ]
Enan, Khalid [3 ]
Nourlil, Jalal [4 ]
Krause, Eva [1 ,2 ]
Schaade, Lars [1 ,2 ]
Michel, Janine [1 ,2 ]
Nitsche, Andreas [1 ,2 ]
机构
[1] WHO, Highly Pathogen Viruses, Ctr Biol Threats & Special Pathogens, Reference Lab SARS CoV 2,Robert Koch Inst, Berlin, Germany
[2] WHO, Collaborating Ctr Emerging Infect & Biol Threats, Robert Koch Inst, Berlin, Germany
[3] Minist Higher Educ & Sci Res, Khartoum, Sudan
[4] Pasteur Inst Morocco, Casablanca, Morocco
来源
PLOS ONE | 2022年 / 17卷 / 03期
关键词
HUMAN METAPNEUMOVIRUS; INFLUENZA; INFECTIONS; PNEUMONIA; SARS;
D O I
10.1371/journal.pone.0264855
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Since December 2019 the world has been facing the outbreak of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Identification of infected patients and discrimination from other respiratory infections have so far been accomplished by using highly specific real-time PCRs. Here we present a rapid multiplex approach (RespiCoV), combining highly multiplexed PCRs and MinION sequencing suitable for the simultaneous screening for 41 viral and five bacterial agents related to respiratory tract infections, including the human coronaviruses NL63, HKU1, OC43, 229E, Middle East respiratory syndrome coronavirus, SARS-CoV, and SARS-CoV-2. RespiCoV was applied to 150 patient samples with suspected SARS-CoV-2 infection and compared with specific real-time PCR. Additionally, several respiratory tract pathogens were identified in samples tested positive or negative for SARS-CoV-2. Finally, RespiCoV was experimentally compared to the commercial RespiFinder 2SMART multiplex screening assay (PathoFinder, The Netherlands).
引用
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页数:11
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