SwabExpress: An end-to-end protocol for extraction-free COVID-19 testing.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
29 Apr 2021
Historique:
pubmed: 9 6 2020
medline: 9 6 2020
entrez: 9 6 2020
Statut: epublish

Résumé

The urgent need for massively scaled clinical testing for SARS-CoV-2, along with global shortages of critical reagents and supplies, has necessitated development of streamlined laboratory testing protocols. Conventional nucleic acid testing for SARS-CoV-2 involves collection of a clinical specimen with a nasopharyngeal swab in transport medium, nucleic acid extraction, and quantitative reverse transcription PCR (RT-qPCR) (1). As testing has scaled across the world, the global supply chain has buckled, rendering testing reagents and materials scarce (2). To address shortages, we developed SwabExpress, an end-to-end protocol developed to employ mass produced anterior nares swabs and bypass the requirement for transport media and nucleic acid extraction. We evaluated anterior nares swabs, transported dry and eluted in low-TE buffer as a direct-to-RT-qPCR alternative to extraction-dependent viral transport media. We validated our protocol of using heat treatment for viral activation and added a proteinase K digestion step to reduce amplification interference. We tested this protocol across archived and prospectively collected swab specimens to fine-tune test performance. After optimization, SwabExpress has a low limit of detection at 2-4 molecules/uL, 100% sensitivity, and 99.4% specificity when compared side-by-side with a traditional RT-qPCR protocol employing extraction. On real-world specimens, SwabExpress outperforms an automated extraction system while simultaneously reducing cost and hands-on time. SwabExpress is a simplified workflow that facilitates scaled testing for COVID-19 without sacrificing test performance. It may serve as a template for the simplification of PCR-based clinical laboratory tests, particularly in times of critical shortages during pandemics.

Sections du résumé

BACKGROUND BACKGROUND
The urgent need for massively scaled clinical testing for SARS-CoV-2, along with global shortages of critical reagents and supplies, has necessitated development of streamlined laboratory testing protocols. Conventional nucleic acid testing for SARS-CoV-2 involves collection of a clinical specimen with a nasopharyngeal swab in transport medium, nucleic acid extraction, and quantitative reverse transcription PCR (RT-qPCR) (1). As testing has scaled across the world, the global supply chain has buckled, rendering testing reagents and materials scarce (2). To address shortages, we developed SwabExpress, an end-to-end protocol developed to employ mass produced anterior nares swabs and bypass the requirement for transport media and nucleic acid extraction.
METHODS METHODS
We evaluated anterior nares swabs, transported dry and eluted in low-TE buffer as a direct-to-RT-qPCR alternative to extraction-dependent viral transport media. We validated our protocol of using heat treatment for viral activation and added a proteinase K digestion step to reduce amplification interference. We tested this protocol across archived and prospectively collected swab specimens to fine-tune test performance.
RESULTS RESULTS
After optimization, SwabExpress has a low limit of detection at 2-4 molecules/uL, 100% sensitivity, and 99.4% specificity when compared side-by-side with a traditional RT-qPCR protocol employing extraction. On real-world specimens, SwabExpress outperforms an automated extraction system while simultaneously reducing cost and hands-on time.
CONCLUSION CONCLUSIONS
SwabExpress is a simplified workflow that facilitates scaled testing for COVID-19 without sacrificing test performance. It may serve as a template for the simplification of PCR-based clinical laboratory tests, particularly in times of critical shortages during pandemics.

Identifiants

pubmed: 32511368
doi: 10.1101/2020.04.22.056283
pmc: PMC7263496
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : K24 AI150991
Pays : United States
Organisme : NHGRI NIH HHS
ID : RM1 HG010461
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007044
Pays : United States

Commentaires et corrections

Type : UpdateIn

Auteurs

Sanjay Srivatsan (S)

Department of Genome Sciences, University of Washington, Seattle WA, USA.

Sarah Heidl (S)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Brian Pfau (B)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Beth K Martin (BK)

Department of Genome Sciences, University of Washington, Seattle WA, USA.

Peter D Han (PD)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Weizhi Zhong (W)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Katrina van Raay (K)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Evan McDermot (E)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Jordan Opsahl (J)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Luis Gamboa (L)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Nahum Smith (N)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Melissa Truong (M)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Shari Cho (S)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Kaitlyn A Barrow (KA)

Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle WA, USA.

Lucille M Rich (LM)

Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle WA, USA.

Jeremy Stone (J)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Caitlin R Wolf (CR)

Department of Allergy and Infectious Disease, University of Washington, Seattle WA, USA.

Denise J McCulloch (DJ)

Department of Allergy and Infectious Disease, University of Washington, Seattle WA, USA.

Ashley E Kim (AE)

Department of Allergy and Infectious Disease, University of Washington, Seattle WA, USA.

Elisabeth Brandstetter (E)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Sarah L Sohlberg (SL)

Department of Allergy and Infectious Disease, University of Washington, Seattle WA, USA.

Misja Ilcisin (M)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Rachel E Geyer (RE)

Department of Family Medicine, University of Washington, Seattle, Washington, USA.

Wei Chen (W)

Department of Genome Sciences, University of Washington, Seattle WA, USA.

Jase Gehring (J)

Department of Genome Sciences, University of Washington, Seattle WA, USA.

Sriram Kosuri (S)

Octant, Inc. Emeryville CA, USA.
Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles CA, USA.

Trevor Bedford (T)

Department of Genome Sciences, University of Washington, Seattle WA, USA.
Brotman Baty Institute For Precision Medicine, Seattle WA, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Mark J Rieder (MJ)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Deborah A Nickerson (DA)

Department of Genome Sciences, University of Washington, Seattle WA, USA.
Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Helen Y Chu (HY)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.
Department of Allergy and Infectious Disease, University of Washington, Seattle WA, USA.

Eric Q Konnick (EQ)

Brotman Baty Institute For Precision Medicine, Seattle WA, USA.
Department of Laboratory Medicine and Pathology, Seattle WA, USA.

Jason S Debley (JS)

Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle WA, USA.

Jay Shendure (J)

Department of Genome Sciences, University of Washington, Seattle WA, USA.
Brotman Baty Institute For Precision Medicine, Seattle WA, USA.
Howard Hughes Medical Institute. Seattle WA, USA.

Christina M Lockwood (CM)

Department of Genome Sciences, University of Washington, Seattle WA, USA.
Brotman Baty Institute For Precision Medicine, Seattle WA, USA.
Department of Laboratory Medicine and Pathology, Seattle WA, USA.

Lea M Starita (LM)

Department of Genome Sciences, University of Washington, Seattle WA, USA.
Brotman Baty Institute For Precision Medicine, Seattle WA, USA.

Classifications MeSH