International Journal of Infectious Diseases (Jan 2022)

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

  • 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

Journal volume & issue
Vol. 114
pp. 112 – 114

Abstract

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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.

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