S-Variant SARS-CoV-2 Lineage B1.1.7 Is Associated With Significantly Higher Viral Load in Samples Tested by TaqPath Polymerase Chain Reaction

Author:

Kidd Michael12ORCID,Richter Alex3,Best Angus4,Cumley Nicola4,Mirza Jeremy4,Percival Benita4,Mayhew Megan4,Megram Oliver4,Ashford Fiona4,White Thomas4,Moles-Garcia Emma4,Crawford Liam4,Bosworth Andrew2,Atabani Sowsan F12,Plant Tim4,McNally Alan5ORCID

Affiliation:

1. Public Health England, Birmingham, United Kingdom

2. University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom

3. Institute of Cancer and Genomic Science, College of Medical and Dental Science, University of Birmingham, Birmingham, United Kingdom

4. Clinical Immunology Service, Institute of Immunology and Immunotherapy, College of Medical and Dental Science, University of Birmingham, Birmingham, United Kingdom

5. Institute of Microbiology and Infection, College of Medical and Dental Science, University of Birmingham, Birmingham, United Kingdom

Abstract

Abstract A SARS-CoV-2 variant B1.1.7 containing mutation Δ69/70 has spread rapidly in the United Kingdom and shows an identifiable profile in ThermoFisher TaqPath RT-qPCR, S gene target failure (SGTF). We analyzed recent test data for trends and significance. Linked cycle threshold (Ct) values for respiratory samples showed that a low Ct for ORF1ab and N were clearly associated with SGTF. Significantly more SGTF samples had higher inferred viral loads between 1×107 and 1×108. Our conclusion is that patients whose samples exhibit the SGTF profile are more likely to have high viral loads, which may explain higher infectivity and rapidity of spread.

Funder

UK Department of Health and Social Care

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference13 articles.

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