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Cycle Threshold (Ct) Values of SARS-CoV-2 Detected with the GeneXpert ® System and a Mutation Associated with Different Target Gene Failure.

Authors :
Yamashita K
Taniguchi T
Niizeki N
Nagao Y
Suzuki A
Toguchi A
Takebayashi S
Ishikawa J
Nagura O
Furuhashi K
Iwaizumi M
Maekawa M
Source :
Current issues in molecular biology [Curr Issues Mol Biol] 2023 May 07; Vol. 45 (5), pp. 4124-4134. Date of Electronic Publication: 2023 May 07.
Publication Year :
2023

Abstract

SARS-CoV-2 nucleic acid detection tests enable rapid virus detection; however, it is challenging to identify genotypes to comprehend the local epidemiology and infection routes in real-time qRT-PCR. At the end of June 2022, our hospital experienced an in-hospital cluster of COVID-19. When examined using the GeneXpert <superscript>®</superscript> System, the cycle threshold (Ct) value of the N2 region of the nucleocapsid gene of SARS-CoV-2 was approximately 10 cycles higher than that of the envelope gene. Sanger sequencing revealed a G29179T mutation in the primer and probe binding sites. A review of past test results revealed differences in Ct values in 21 of 345 SARS-CoV-2-positive patients, of which 17 cases were cluster-related and 4 were not. Including these 21 cases, 36 cases in total were selected for whole-genome sequencing (WGS). The viral genomes in the cluster-related cases were identified as BA.2.10, and those in the non-cluster cases were closely related and classified as being downstream of BA.2.10 and other lineages. Although WGS can provide comprehensive information, its use is limited in various laboratory settings. A measurement platform reporting and comparing Ct values of different target genes can improve test accuracy, enhance our understanding of infection spread, and be applied to the quality control of reagents.

Details

Language :
English
ISSN :
1467-3045
Volume :
45
Issue :
5
Database :
MEDLINE
Journal :
Current issues in molecular biology
Publication Type :
Academic Journal
Accession number :
37232731
Full Text :
https://doi.org/10.3390/cimb45050262