| Literature DB >> 33643253 |
Alberto A Amarilla1, Naphak Modhiran1,2, Yin Xiang Setoh1, Nias Y G Peng1, Julian D J Sng1, Benjamin Liang1, Christopher L D McMillan1, Morgan E Freney1, Stacey T M Cheung1, Keith J Chappell1,2,3, Alexander A Khromykh1,3, Paul R Young1,2,3, Daniel Watterson1,2,3.
Abstract
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.Entities:
Keywords: SARS-CoV-2; coronaviruses; immuno-plaque assay (iPA); viral quantification
Year: 2021 PMID: 33643253 PMCID: PMC7906992 DOI: 10.3389/fmicb.2021.625136
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640