| Literature DB >> 34877674 |
Matthew M Hernandez1, Radhika Banu1, Ana S Gonzalez-Reiche2, Adriana van de Guchte2, Zenab Khan2, Paras Shrestha1, Liyong Cao1, Feng Chen1, Huanzhi Shi1, Ayman Hanna1, Hala Alshammary3, Shelcie Fabre1, Angela Amoako3, Ajay Obla2, Bremy Alburquerque2,4, Luz Helena Patiño5, Juan David Ramírez5, Robert Sebra2,6,7,8, Melissa R Gitman1, Michael D Nowak1, Carlos Cordon-Cardo1, Ted E Schutzbank9, Viviana Simon1,3,10,11, Harm van Bakel2,6, Emilia Mia Sordillo1, Alberto E Paniz-Mondolfi1.
Abstract
The coronavirus disease 2019 (COVID-19) pandemic has sparked the rapid development of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) diagnostics. However, emerging variants pose the risk for target dropout and false-negative results secondary to primer/probe binding site (PBS) mismatches. The Agena MassARRAY® SARS-CoV-2 Panel combines reverse-transcription polymerase chain reaction and matrix-assisted laser desorption/ionization time-of-flight mass-spectrometry to probe for five targets across N and ORF1ab genes, which provides a robust platform to accommodate PBS mismatches in divergent viruses. Herein, we utilize a deidentified data set of 1262 SARS-CoV-2-positive specimens from Mount Sinai Health System (New York City) from December 2020 to April 2021 to evaluate target results and corresponding sequencing data. Overall, the level of PBS mismatches was greater in specimens with target dropout. Of specimens with N3 target dropout, 57% harbored an A28095T substitution that is highly specific for the Alpha (B.1.1.7) variant of concern. These data highlight the benefit of redundancy in target design and the potential for target performance to illuminate the dynamics of circulating SARS-CoV-2 variants.Entities:
Keywords: B.1.1.7; MALDI-TOF; RT-PCR; SARS-CoV-2; diagnostic; dropout; variants
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Year: 2021 PMID: 34877674 PMCID: PMC8854350 DOI: 10.1002/jmv.27510
Source DB: PubMed Journal: J Med Virol ISSN: 0146-6615 Impact factor: 20.693