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The Role of Subgenomic RNA in Discordant Results From Reverse Transcription-Polymerase Chain Reaction Tests for COVID-19.
Toppings, Noah B; Oberding, Lisa K; Lin, Yi-Chan; Evans, David; Pillai, Dylan R.
  • Toppings NB; From the Department of Microbiology, Immunology, and Infectious Diseases (Toppings, Pillai), University of Calgary, Calgary, Alberta, Canada.
  • Oberding LK; From the Department of Pathology and Laboratory Medicine (Oberding, Pillai), University of Calgary, Calgary, Alberta, Canada.
  • Lin YC; From the Department of Medical Microbiology & Immunology and Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Alberta, Canada (Lin, Evans).
  • Evans D; From the Department of Medical Microbiology & Immunology and Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Alberta, Canada (Lin, Evans).
  • Pillai DR; From the Department of Microbiology, Immunology, and Infectious Diseases (Toppings, Pillai), University of Calgary, Calgary, Alberta, Canada.
Arch Pathol Lab Med ; 146(7): 805-813, 2022 07 01.
Article in English | MEDLINE | ID: covidwho-1912033
ABSTRACT
CONTEXT.­ Reverse transcription-polymerase chain reaction (RT-PCR) is the standard method of diagnosing COVID-19. An inconclusive test result occurs when 1 RT-PCR target is positive for SARS-CoV-2 and 1 RT-PCR target is negative for SARS-CoV-2 within the same sample. An inconclusive result generally requires retesting. One reason why a sample may yield an inconclusive result is that one target is at a higher concentration than another target. OBJECTIVE.­ To understand the role of subgenomic RNA transcripts in discordant results from RT-PCR tests for COVID-19. DESIGN.­ A panel of 6 droplet digital PCR assays was designed to quantify the ORF1, E-gene, and N-gene of SARS-CoV-2. This panel was used to quantify viral cultures of SARS-CoV-2 that were harvested during the eclipse phase and at peak infectivity. Eleven clinical nasopharyngeal swabs were also tested with this panel. RESULTS.­ In culture, infected cells showed higher N-gene/ORF1 copy ratios than culture supernatants. The same trends in the relative abundance of copies across different targets observed in infected cells were observed in clinical samples, although trends were more pronounced in infected cells. CONCLUSIONS.­ This study showed that a greater copy number of N-gene relative to E-gene and ORF1 transcripts could potentially explain inconclusive results for some RT-PCR tests on low viral load samples. The use of N-gene RT-PCR target(s) as opposed to ORF1 targets for routine testing is supported by these data.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Arch Pathol Lab Med Year: 2022 Document Type: Article Affiliation country: Arpa.2021-0630-SA

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Arch Pathol Lab Med Year: 2022 Document Type: Article Affiliation country: Arpa.2021-0630-SA