| Literature DB >> 34035246 |
Ramesh Yelagandula1, Aleksandr Bykov2, Alexander Vogt3, Robert Heinen1,2,4, Ezgi Özkan2, Marcus Martin Strobl1, Juliane Christina Baar1, Kristina Uzunova1,2,4, Bence Hajdusits2, Darja Kordic2, Erna Suljic5, Amina Kurtovic-Kozaric5, Sebija Izetbegovic5, Justine Schaeffer6,7, Peter Hufnagl6, Alexander Zoufaly8,9, Tamara Seitz8, Manuela Födinger9,10, Franz Allerberger6, Alexander Stark2,11, Luisa Cochella12, Ulrich Elling13.
Abstract
The COVID-19 pandemic has demonstrated the need for massively-parallel, cost-effective tests monitoring viral mical">spread. Here we present SARSeq, saliva analysis by RNA sequencing, a method to detect <mical">span class="Species">SARS-CoV-2 and other respiratory viruses on tens of thousands of samples in parallel. SARSeq relies on next generation sequencing of multiple amplicons generated in a multiplexed RT-PCR reaction. Two-dimensional, unique dual indexing, using four indices per sample, enables unambiguous and scalable assignment of reads to individual samples. We calibrate SARSeq on SARS-CoV-2 synthetic RNA, virions, and hundreds of human samples of various types. Robustness and sensitivity were virtually identical to quantitative RT-PCR. Double-blinded benchmarking to gold standard quantitative-RT-PCR performed by human diagnostics laboratories confirms this high sensitivity. SARSeq can be used to detect Influenza A and B viruses and human rhinovirus in parallel, and can be expanded for detection of other pathogens. Thus, SARSeq is ideally suited for differential diagnostic of infections during a pandemic.Entities:
Year: 2021 PMID: 34035246 DOI: 10.1038/s41467-021-22664-5
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919