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Effect of storage temperatures simulating transport conditions of nasopharyngeal swabs on the results of a chemiluminescence immunoassay (CLIA) to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen.
Kanta, Poonam; Ghosh, Arnab; Goyal, Kapil; Kaur, Ramandeep; Baluni, Manjari; Sircar, Shubhankar; Kumar, Vikas; Kumar, Krishan; Vijay, Neetu; Singh, Mini P.
Afiliación
  • Kanta P; Department of Virology, PGIMER, Chandigarh, India.
  • Ghosh A; Department of Virology, PGIMER, Chandigarh, India.
  • Goyal K; Department of Virology, PGIMER, Chandigarh, India.
  • Kaur R; Department of Virology, PGIMER, Chandigarh, India.
  • Baluni M; Department of Virology, PGIMER, Chandigarh, India.
  • Sircar S; Department of Virology, PGIMER, Chandigarh, India.
  • Kumar V; Department of Virology, PGIMER, Chandigarh, India.
  • Kumar K; Department of Virology, PGIMER, Chandigarh, India.
  • Vijay N; Indian Council of Medical Research (ICMR), Department of Health Research, New Delhi, India.
  • Singh MP; Department of Virology, PGIMER, Chandigarh, India. Electronic address: minipsingh@gmail.com.
Indian J Med Microbiol ; 44: 100379, 2023.
Article en En | MEDLINE | ID: mdl-37356827
ABSTRACT

PURPOSE:

Chemiluminescence Immunoassay (CLIA) is high throughput, rapid diagnostic test which has recently come up for the detection of SARS-CoV-2 antigen. The present study evaluated performance of CLIA antigen test in nasopharyngeal swab samples stored at different temperatures for 7 days to simulate the transport conditions and transit time across the country from remote peripheral laboratories to central facilities. MATERIALS AND

METHODS:

Limit of detection (LOD), sensitivity and specificity of VITROS® SARS-CoV-2 antigen assay was determined using Real-time reverse transcriptase PCR (rRT-PCR) confirmed SARS-CoV-2 positive and negative samples. To detect the effect of storage temperatures on VITROS ®SARS-CoV-2 antigen results, samples were stored at 4 â€‹°C, 25 â€‹°C & 37 â€‹°C for 7 days followed by detection of SARS-CoV-2 nucleocapsid antigen and compared with N-gene rRT-PCR.

RESULTS:

The VITROS® SARS-CoV-2 antigen test was found to have a sensitivity and specificity of 78.9% and 100% respectively with high sensitivity of 88.1% for samples with Ct â€‹< â€‹30. The LOD of VITROS assay was equivalent to 3800 copies of RNA per reactions as compared to 72 copies per reaction for rRT-PCR. We observed that more than 80% of samples with <30 Ct values could be detected by VITROS SARS-CoV-2 antigen assay at day 7 even when stored at 37 â€‹°C. For samples with Ct values between 26 and 30, on day 7 the positivity rate of N-antigen at 4 â€‹°C was 90.9% and 37 â€‹°C was 63.6%.

CONCLUSIONS:

CLIA testing can be carried out for the detection of SARS-CoV-2 N-protein in NP-swab samples transported in cold chain even with 7 days transit time, particularly for Ct â€‹< â€‹30 samples which represents cases with higher transmissibility. As drop in positivity for VITROS assay was lower as compared to rRT-PCR on day 7 in cold chain-maintained samples, the assay can be useful to screen samples received from remote peripheral areas before performing rRT-PCR.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Indian J Med Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Indian J Med Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: India
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