Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA

被引:55
作者
Lee, Jean Y. H. [1 ,2 ]
Best, Nickala [3 ]
McAuley, Julie [1 ]
Porter, Jessica L. [1 ]
Seemann, Torsten [1 ,4 ]
Schultz, Mark B. [4 ]
Sait, Michelle [4 ]
Orlando, Nicole [4 ]
Mercoulia, Karolina [4 ]
Ballard, Susan A. [4 ]
Druce, Julian [5 ]
Tran, Thomas [5 ]
Catton, Mike G. [5 ]
Pryor, Melinda J. [6 ]
Cui, Huanhuan L. [6 ]
Luttick, Angela [6 ]
McDonald, Sean [3 ]
Greenhalgh, Arran [3 ]
Kwong, Jason C. [1 ,7 ]
Sherry, Norelle L. [4 ,7 ]
Graham, Maryza [8 ]
Hoang, Tuyet [1 ,4 ]
Herisse, Marion [1 ]
Pidot, Sacha J. [1 ]
Williamson, Deborah A. [1 ,4 ,9 ]
Howden, Benjamin P. [1 ,4 ,7 ]
Monk, Ian R. [1 ]
Stinear, Timothy P. [1 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Peter Doherty Inst Infect & Immun, Melbourne, Vic, Australia
[2] Monash Hlth, Dept Infect Dis, Clayton, Vic, Australia
[3] GenWorks Pty Ltd, Thebarton, SA, Australia
[4] Univ Melbourne, Peter Doherty Inst Infect & Immun, Publ Hlth Lab, Microbiol Diagnost Unit, Melbourne, Vic, Australia
[5] Peter Doherty Inst Infect & Immun, Victorian Infect Dis Reference Lab Melbourne Hlth, Melbourne, Vic, Australia
[6] 360Biolabs, Melbourne, Vic, Australia
[7] Austin Hlth, Dept Infect Dis, Heidelberg, Vic, Australia
[8] Monash Hlth, Dept Microbiol, Clayton, Vic, Australia
[9] Melbourne Hlth, Melbourne, Vic, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
nasopharyngeal swabs; RT-LAMP; SARS-CoV-2; universal transport media;
D O I
10.1099/jmm.0.001238
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction. The SARS-CoV-2 pandemic of 2020 has resulted in unparalleled requirements for RNA extraction kits and enzymes required for virus detection, leading to global shortages. This has necessitated the exploration of alternative diagnostic options to alleviate supply chain issues. Aim. To establish and validate a reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for the detection of SARS-CoV-2 from nasopharyngeal swabs. Methodology. We used a commercial RT-LAMP mastermix from OptiGene in combination with a primer set designed to detect the CDC N1 region of the SARS-CoV-2 nucleocapsid (N) gene. A single-tube, single-step fluorescence assay was implemented whereby 1 mu l of universal transport medium (UTM) directly from a nasopharyngeal swab could be used as template, bypassing the requirement for RNA purification. Amplification and detection could be conducted in any thermocycler capable of holding 65 degrees C for 30 min and measure fluorescence in the FAM channel at 1 min intervals. Results. Assay evaluation by assessment of 157 clinical specimens previously screened by E-gene RT-qPCR revealed assay sensitivity and specificity of 87 and 100%, respectively. Results were fast, with an average time-to-positive (Tp) for 93 clinical samples of 14 min (sd +/- 7 min). Using dilutions of SARS-CoV-2 virus spiked into UTM, we also evaluated assay performance against FDA guidelines for implementation of emergency-use diagnostics and established a limit-of-detection of 54 Tissue Culture Infectious Dose 50 per ml (TCID50 ml(-1)), with satisfactory assay sensitivity and specificity. A comparison of 20 clinical specimens between four laboratories showed excellent interlaboratory concordance; performing equally well on three different, commonly used thermocyclers, pointing to the robustness of the assay. Conclusion. With a simplified workflow, The N1 gene Single Tube Optigene LAMP assay (N1-STOP-LAMP) is a powerful, scalable option for specific and rapid detection of SARS-CoV-2 and an additional resource in the diagnostic armamentarium against COVID-19.
引用
收藏
页码:1169 / 1178
页数:10
相关论文
共 36 条
[1]   Open for outbreaks [J].
不详 .
NATURE BIOTECHNOLOGY, 2020, 38 (04) :377-377
[2]  
[Anonymous], 2020, RAPID COLORIMETRIC D
[3]  
[Anonymous], 2020, J MOL DIAGNOSTICS
[4]  
Arnold C, 2020, NAT MED
[5]   Development of a reverse transcription-loop-mediated isothermal amplification as a rapid early-detection method for novel SARS-CoV-2 [J].
Baek, Yun Hee ;
Um, Jihye ;
Antigua, Khristine Joy C. ;
Park, Ji-Hyun ;
Kim, Yeonjae ;
Oh, Sol ;
Kim, Young-il ;
Choi, Won-Suk ;
Kim, Seong Gyu ;
Jeong, Ju Hwan ;
Chin, Bum Sik ;
Nicolas, Halcyon Dawn G. ;
Ahn, Ji-Young ;
Shin, Kyeong Seob ;
Choi, Young Ki ;
Park, Jun-Sun ;
Song, Min-Suk .
EMERGING MICROBES & INFECTIONS, 2020, 9 (01) :998-1007
[6]  
Bhadra S., 2020, BIORXIV
[7]   CRISPR-Cas12-based detection of SARS-CoV-2 [J].
Broughton, James P. ;
Deng, Xianding ;
Yu, Guixia ;
Fasching, Clare L. ;
Servellita, Venice ;
Singh, Jasmeet ;
Miao, Xin ;
Streithorst, Jessica A. ;
Granados, Andrea ;
Sotomayor-Gonzalez, Alicia ;
Zorn, Kelsey ;
Gopez, Allan ;
Hsu, Elaine ;
Gu, Wei ;
Miller, Steve ;
Pan, Chao-Yang ;
Guevara, Hugo ;
Wadford, Debra A. ;
Chen, Janice S. ;
Chiu, Charles Y. .
NATURE BIOTECHNOLOGY, 2020, 38 (07) :870-+
[8]   Isolation and rapid sharing of the 2019 novel coronavirus (SAR-CoV-2) from the first patient diagnosed with COVID-19 in Australia [J].
Caly, Leon ;
Druce, Julian ;
Roberts, Jason ;
Bond, Katherine ;
Tran, Thomas ;
Kostecki, Renata ;
Yoga, Yano ;
Naughton, William ;
Taiaroa, George ;
Seemann, Torsten ;
Schultz, Mark B. ;
Howden, Benjamin P. ;
Korman, Tony M. ;
Lewin, Sharon R. ;
Williamson, Deborah A. ;
Catton, Mike G. .
MEDICAL JOURNAL OF AUSTRALIA, 2020, 212 (10) :459-462
[9]  
Center for Disease Control, 2020, 2019 NOV COR 2019 NC
[10]  
Centre for Disease Control, 2020, REAL TIM RT PCR PAN