An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2

被引:39
作者
Amarilla, Alberto A. [1 ]
Modhiran, Naphak [1 ,2 ]
Setoh, Yin Xiang [1 ,4 ]
Peng, Nias Y. G. [1 ]
Sng, Julian D. J. [1 ]
Liang, Benjamin [1 ]
McMillan, Christopher L. D. [1 ]
Freney, Morgan E. [1 ]
Cheung, Stacey T. M. [1 ]
Chappell, Keith J. [1 ,2 ,3 ]
Khromykh, Alexander A. [1 ,3 ]
Young, Paul R. [1 ,2 ,3 ]
Watterson, Daniel [1 ,2 ,3 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld, Australia
[2] Univ Queensland, Australian Inst Biotechnol & Nanotechnol, St Lucia, Qld, Australia
[3] Univ Queensland, Australian Infect Dis Res Ctr, St Lucia, Qld, Australia
[4] Natl Environm Agcy, Environm Hlth Inst, Singapore, Singapore
关键词
coronaviruses; SARS-CoV-2; immuno-plaque assay (iPA); viral quantification; CORONAVIRUS; SPIKE; NEUTRALIZATION; GLYCOPROTEIN; ANTIBODIES; RECEPTOR; DOMAIN; CELLS;
D O I
10.3389/fmicb.2021.625136
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has been identified as the causative agent of coronavirus disease 2019 and is capable of human-to-human transmission and rapid global spread. The rapid emergence and global spread of SARS-CoV-2 has encouraged the establishment of a rapid, sensitive, and reliable viral detection and quantification methodology. Here, we present an alternative assay, termed immuno-plaque assay (iPA), which utilizes a combination of plaque assay and immunofluorescence techniques. We have extensively optimized the conditions for SARS-CoV-2 infection and demonstrated the great flexibility of iPA detection using several antibodies and dual-probing with two distinct epitope-specific antibodies. In addition, we showed that iPA could be utilized for ultra-high-throughput viral titration and neutralization assay within 24 h and is amenable to a 384-well format. These advantages will significantly accelerate SARS-CoV-2 research outcomes during this pandemic period.
引用
收藏
页数:17
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