SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a pandemic. Diagnostic testing for SARS-CoV-2 has continuously been challenged due to several variants with diverse spike (S) and nucleocapsid (N) protein mutations []. SARS-CoV-2 variant proliferation potentially affects N prot...
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2022
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oai:doaj.org-article:38d454027a0c4adeb2e5f1ea07400fdc2021-11-30T04:14:31ZSARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance1201-971210.1016/j.ijid.2021.11.006https://doaj.org/article/38d454027a0c4adeb2e5f1ea07400fdc2022-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1201971221008535https://doaj.org/toc/1201-9712Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a pandemic. Diagnostic testing for SARS-CoV-2 has continuously been challenged due to several variants with diverse spike (S) and nucleocapsid (N) protein mutations []. SARS-CoV-2 variant proliferation potentially affects N protein-targeted rapid antigen testing. In this study, rapid antigen and reverse transcription PCR (RT-PCR) tests were performed simultaneously in patients with suspected coronavirus disease 2019 (COVID-19). Direct whole genome sequencing was performed to determine the N protein variations, and the viral assemblies were uploaded to GISAID. The genomes were then compared with those of global virus strains from GISAID. These isolates belonged to the B.1.1.7 variant, exhibiting several amino acid substitutions, including D3L, R203K, G204R, and S235F N protein mutations. The T135I mutation was also identified in one variant case in which the rapid antigen test and RT-PCR test were discordantly negative and positive, respectively. These findings suggest that the variants undetected by the Panbio COVID-19 rapid antigen test may be due to the T135I mutation in the N protein, posing a potential diagnostic risk for commercially available antigen tests. Hence, we recommend concomitant paired rapid antigen tests and molecular diagnostic methods to detect SARS-CoV-2. False-negative results could be rapidly corrected using confirmatory RT-PCR results to prevent future COVID-19 outbreaks.Ming-Jr JianHsing-Yi ChungChih-Kai ChangJung-Chung LinKuo-Ming YehChien-Wen ChenDe-Yu LinFeng-Yee ChangKuo-Sheng HungCherng-Lih PerngHung-Sheng ShangElsevierarticleCOVID-19SARS-CoV-2Rapid antigen testB.1.1.7 variantN proteinInfectious and parasitic diseasesRC109-216ENInternational Journal of Infectious Diseases, Vol 114, Iss , Pp 112-114 (2022) |
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COVID-19 SARS-CoV-2 Rapid antigen test B.1.1.7 variant N protein Infectious and parasitic diseases RC109-216 |
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COVID-19 SARS-CoV-2 Rapid antigen test B.1.1.7 variant N protein Infectious and parasitic diseases RC109-216 Ming-Jr Jian Hsing-Yi Chung Chih-Kai Chang Jung-Chung Lin Kuo-Ming Yeh Chien-Wen Chen De-Yu Lin Feng-Yee Chang Kuo-Sheng Hung Cherng-Lih Perng Hung-Sheng Shang SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
description |
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a pandemic. Diagnostic testing for SARS-CoV-2 has continuously been challenged due to several variants with diverse spike (S) and nucleocapsid (N) protein mutations []. SARS-CoV-2 variant proliferation potentially affects N protein-targeted rapid antigen testing. In this study, rapid antigen and reverse transcription PCR (RT-PCR) tests were performed simultaneously in patients with suspected coronavirus disease 2019 (COVID-19). Direct whole genome sequencing was performed to determine the N protein variations, and the viral assemblies were uploaded to GISAID. The genomes were then compared with those of global virus strains from GISAID. These isolates belonged to the B.1.1.7 variant, exhibiting several amino acid substitutions, including D3L, R203K, G204R, and S235F N protein mutations. The T135I mutation was also identified in one variant case in which the rapid antigen test and RT-PCR test were discordantly negative and positive, respectively. These findings suggest that the variants undetected by the Panbio COVID-19 rapid antigen test may be due to the T135I mutation in the N protein, posing a potential diagnostic risk for commercially available antigen tests. Hence, we recommend concomitant paired rapid antigen tests and molecular diagnostic methods to detect SARS-CoV-2. False-negative results could be rapidly corrected using confirmatory RT-PCR results to prevent future COVID-19 outbreaks. |
format |
article |
author |
Ming-Jr Jian Hsing-Yi Chung Chih-Kai Chang Jung-Chung Lin Kuo-Ming Yeh Chien-Wen Chen De-Yu Lin Feng-Yee Chang Kuo-Sheng Hung Cherng-Lih Perng Hung-Sheng Shang |
author_facet |
Ming-Jr Jian Hsing-Yi Chung Chih-Kai Chang Jung-Chung Lin Kuo-Ming Yeh Chien-Wen Chen De-Yu Lin Feng-Yee Chang Kuo-Sheng Hung Cherng-Lih Perng Hung-Sheng Shang |
author_sort |
Ming-Jr Jian |
title |
SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
title_short |
SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
title_full |
SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
title_fullStr |
SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
title_full_unstemmed |
SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance |
title_sort |
sars-cov-2 variants with t135i nucleocapsid mutations may affect antigen test performance |
publisher |
Elsevier |
publishDate |
2022 |
url |
https://doaj.org/article/38d454027a0c4adeb2e5f1ea07400fdc |
work_keys_str_mv |
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