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Evaluation of SARS-CoV-2 genome detection by real-time PCR assay using pooled specimens

Objective: To evaluate SARS-CoV-2 genome detection using pooled samples by RT-qPCR assay, compared to individual samples. Method: At first all samples were tested individually using two commercial methods targeting ORF1ab, NP and E genes. Then, four experimental groups of samples were pooled and eva...

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Detalles Bibliográficos
Autores principales: Tavakoli, Forough, Yavarian, Jila, Shafiei Jandaghi, Nazanin Zahra, Sadeghi, Kaveh, Ghavami, Nastaran, Salimi, Vahid, Mokhtari-Azad, Talat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090217/
https://www.ncbi.nlm.nih.gov/pubmed/35586148
http://dx.doi.org/10.2217/fvl-2021-0014
Descripción
Sumario:Objective: To evaluate SARS-CoV-2 genome detection using pooled samples by RT-qPCR assay, compared to individual samples. Method: At first all samples were tested individually using two commercial methods targeting ORF1ab, NP and E genes. Then, four experimental groups of samples were pooled and evaluated using the same detection methods. Findings: Compared to the individual sample testing, the sample pooling conserved the sensitivity of the detection in all groups of pooled samples when the Ct value in single test was lower than 33. Conclusion: Specimen pooling may fail to detect positive samples with high Ct values. However, in scarcity of reagents or in population surveys, it could be considered as an alternative method in low prevalence settings.