SARS-CoV-2 variants with T135I nucleocapsid mutations may affect antigen test performance

被引:34
作者
Jian, Ming-, Jr. [1 ]
Chung, Hsing-Yi [1 ]
Chang, Chih-Kai [1 ]
Lin, Jung-Chung [2 ]
Yeh, Kuo-Ming [2 ]
Chen, Chien-Wen [3 ]
Lin, De-Yu [2 ]
Chang, Feng-Yee [2 ]
Hung, Kuo-Sheng [4 ]
Perng, Cherng-Lih [1 ]
Shang, Hung-Sheng [1 ]
机构
[1] Triserv Gen Hosp, Natl Def Med Ctr, Dept Pathol, Div Clin Pathol, 325,Sect 2,Cheng Kung Rd, Taipei 114, Taiwan
[2] Triserv Gen Hosp, Natl Def Med Ctr, Dept Med, Div Infect Dis & Trop Med, Taipei, Taiwan
[3] Triserv Gen Hosp, Natl Def Med Ctr, Dept Med, Div Pulm & Crit Care Med, Taipei, Taiwan
[4] Triserv Gen Hosp, Ctr Precis Med & Genom, Natl Def Med Ctr, Taipei, Taiwan
关键词
COVID-19; SARS-CoV-2; Rapid antigen test; B.1.1.7; variant; N protein; COVID-19;
D O I
10.1016/j.ijid.2021.11.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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. (C) 2021 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
引用
收藏
页码:112 / 114
页数:3
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