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LuNER: Multiplexed SARS-CoV-2 detection in clinical swab and wastewater samples.
Stahl, Elizabeth C; Gopez, Allan R; Tsuchida, Connor A; Fan, Vinson B; Moehle, Erica A; Witkowsky, Lea B; Hamilton, Jennifer R; Lin-Shiao, Enrique; McElroy, Matthew; McDevitt, Shana L; Ciling, Alison; Tsui, C Kimberly; Pestal, Kathleen; Gildea, Holly K; Keller, Amanda; Sylvain, Iman A; Williams, Clara; Hirsh, Ariana; Ehrenberg, Alexander J; Kantor, Rose; Metzger, Matthew; Nelson, Kara L; Urnov, Fyodor D; Ringeisen, Bradley R; Giannikopoulos, Petros; Doudna, Jennifer A.
  • Stahl EC; University of California, Berkeley, Berkeley, CA, United States of America.
  • Gopez AR; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Tsuchida CA; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Fan VB; University of California, Berkeley, Berkeley, CA, United States of America.
  • Moehle EA; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Witkowsky LB; University of California, Berkeley, Berkeley, CA, United States of America.
  • Hamilton JR; University of California, Berkeley, Berkeley, CA, United States of America.
  • Lin-Shiao E; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • McElroy M; University of California, Berkeley, Berkeley, CA, United States of America.
  • McDevitt SL; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Ciling A; University of California, Berkeley, Berkeley, CA, United States of America.
  • Tsui CK; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Pestal K; University of California, Berkeley, Berkeley, CA, United States of America.
  • Gildea HK; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Keller A; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Sylvain IA; University of California, Berkeley, Berkeley, CA, United States of America.
  • Williams C; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Hirsh A; University of California, Berkeley, Berkeley, CA, United States of America.
  • Ehrenberg AJ; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Kantor R; University of California, Berkeley, Berkeley, CA, United States of America.
  • Metzger M; University of California, Berkeley, Berkeley, CA, United States of America.
  • Nelson KL; University of California, Berkeley, Berkeley, CA, United States of America.
  • Urnov FD; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Ringeisen BR; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Giannikopoulos P; Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, United States of America.
  • Doudna JA; University of California, Berkeley, Berkeley, CA, United States of America.
PLoS One ; 16(11): e0258263, 2021.
Article in English | MEDLINE | ID: covidwho-1700786
ABSTRACT
Clinical and surveillance testing for the SARS-CoV-2 virus relies overwhelmingly on RT-qPCR-based diagnostics, yet several popular assays require 2-3 separate reactions or rely on detection of a single viral target, which adds significant time, cost, and risk of false-negative results. Furthermore, multiplexed RT-qPCR tests that detect at least two SARS-CoV-2 genes in a single reaction are typically not affordable for large scale clinical surveillance or adaptable to multiple PCR machines and plate layouts. We developed a RT-qPCR assay using the Luna Probe Universal One-Step RT-qPCR master mix with publicly available primers and probes to detect SARS-CoV-2 N gene, E gene, and human RNase P (LuNER) to address these shortcomings and meet the testing demands of a university campus and the local community. This cost-effective test is compatible with BioRad or Applied Biosystems qPCR machines, in 96 and 384-well formats, with or without sample pooling, and has a detection sensitivity suitable for both clinical reporting and wastewater surveillance efforts.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ribonuclease P / Wastewater / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2021 Document Type: Article Affiliation country: Journal.pone.0258263

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ribonuclease P / Wastewater / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2021 Document Type: Article Affiliation country: Journal.pone.0258263