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SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection
Rapid onsite whole-genome sequencing of two suspected severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) N gene diagnostic escape samples revealed a previously unreported N gene point mutation at genome position 29195. Because the G29195T mutation occurs within a region probed by a commonl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754125/ https://www.ncbi.nlm.nih.gov/pubmed/35019683 http://dx.doi.org/10.1128/spectrum.02223-21 |
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author | Ko, Karrie K. K. Abdul Rahman, Nurdyana Binte Tan, Shireen Yan Ling Chan, Kenneth X. L. Goh, Sui Sin Sim, James Heng Chiak Lim, Kun Lee Tan, Wan Loo Chan, Kian Sing Oon, Lynette L. E. Nagarajan, Niranjan Suphavilai, Chayaporn |
author_facet | Ko, Karrie K. K. Abdul Rahman, Nurdyana Binte Tan, Shireen Yan Ling Chan, Kenneth X. L. Goh, Sui Sin Sim, James Heng Chiak Lim, Kun Lee Tan, Wan Loo Chan, Kian Sing Oon, Lynette L. E. Nagarajan, Niranjan Suphavilai, Chayaporn |
author_sort | Ko, Karrie K. K. |
collection | PubMed |
description | Rapid onsite whole-genome sequencing of two suspected severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) N gene diagnostic escape samples revealed a previously unreported N gene point mutation at genome position 29195. Because the G29195T mutation occurs within a region probed by a commonly referenced U.S. CDC N gene reverse transcription (RT)-PCR assay, we hypothesize that the G29195T mutation rendered the N gene target of a proprietary commercial assay undetectable. The putative diagnostic escape G29195T mutation demonstrates the need for nearly real-time surveillance, as emergence of a novel SARS-CoV-2 variant with the potential to escape diagnostic tests continues to be a threat. IMPORTANCE Accurate diagnostic detection of SARS-CoV-2 currently depends on the large-scale deployment of RT-PCR assays. SARS-CoV-2 RT-PCR assays target predetermined regions in the viral genomes by complementary binding of primers and probes to nucleic acid sequences in the clinical samples. Potential diagnostic escapes, such as those of clinical samples harboring the G29195T mutation, may result in false-negative SARS-CoV-2 RT-PCR results. The rapid detection and sharing of potential diagnostic escapes are essential for diagnostic laboratories and manufacturers around the world, to optimize their assays as SARS-CoV-2 continues to evolve. |
format | Online Article Text |
id | pubmed-8754125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87541252022-01-24 SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection Ko, Karrie K. K. Abdul Rahman, Nurdyana Binte Tan, Shireen Yan Ling Chan, Kenneth X. L. Goh, Sui Sin Sim, James Heng Chiak Lim, Kun Lee Tan, Wan Loo Chan, Kian Sing Oon, Lynette L. E. Nagarajan, Niranjan Suphavilai, Chayaporn Microbiol Spectr Observation Rapid onsite whole-genome sequencing of two suspected severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) N gene diagnostic escape samples revealed a previously unreported N gene point mutation at genome position 29195. Because the G29195T mutation occurs within a region probed by a commonly referenced U.S. CDC N gene reverse transcription (RT)-PCR assay, we hypothesize that the G29195T mutation rendered the N gene target of a proprietary commercial assay undetectable. The putative diagnostic escape G29195T mutation demonstrates the need for nearly real-time surveillance, as emergence of a novel SARS-CoV-2 variant with the potential to escape diagnostic tests continues to be a threat. IMPORTANCE Accurate diagnostic detection of SARS-CoV-2 currently depends on the large-scale deployment of RT-PCR assays. SARS-CoV-2 RT-PCR assays target predetermined regions in the viral genomes by complementary binding of primers and probes to nucleic acid sequences in the clinical samples. Potential diagnostic escapes, such as those of clinical samples harboring the G29195T mutation, may result in false-negative SARS-CoV-2 RT-PCR results. The rapid detection and sharing of potential diagnostic escapes are essential for diagnostic laboratories and manufacturers around the world, to optimize their assays as SARS-CoV-2 continues to evolve. American Society for Microbiology 2022-01-12 /pmc/articles/PMC8754125/ /pubmed/35019683 http://dx.doi.org/10.1128/spectrum.02223-21 Text en Copyright © 2022 Ko et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observation Ko, Karrie K. K. Abdul Rahman, Nurdyana Binte Tan, Shireen Yan Ling Chan, Kenneth X. L. Goh, Sui Sin Sim, James Heng Chiak Lim, Kun Lee Tan, Wan Loo Chan, Kian Sing Oon, Lynette L. E. Nagarajan, Niranjan Suphavilai, Chayaporn SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title | SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title_full | SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title_fullStr | SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title_full_unstemmed | SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title_short | SARS-CoV-2 N Gene G29195T Point Mutation May Affect Diagnostic Reverse Transcription-PCR Detection |
title_sort | sars-cov-2 n gene g29195t point mutation may affect diagnostic reverse transcription-pcr detection |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754125/ https://www.ncbi.nlm.nih.gov/pubmed/35019683 http://dx.doi.org/10.1128/spectrum.02223-21 |
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