tetano
Editor, Senior Moderator
Virol J
. 2022 Apr 11;19(1):67.
doi: 10.1186/s12985-022-01793-3.
Establishment and evaluation of a quadruple quantitative real-time PCR assay for simultaneous detection of human coronavirus subtypes
Mengchuan Zhao[SUP] #[/SUP][SUP] 1 2 [/SUP], Yi Xu[SUP] #[/SUP][SUP] 3 [/SUP], Dijun Zhang[SUP] 4 [/SUP], Guixia Li[SUP] 2 [/SUP], Huixia Gao[SUP] 3 [/SUP], Xianping Zeng[SUP] 4 [/SUP], Yanqing Tie[SUP] 5 [/SUP], Yong Wu[SUP] 4 [/SUP], Erhei Dai[SUP] 6 [/SUP], Zhishan Feng[SUP] 7 8 [/SUP]
Affiliations
Abstract
Background: The newly discovered severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and four seasonal human coronaviruses (HCoVs) (HCoV-229E, HCoV-OC43, HCoV-NL63 and HCoV-HKU1) still circulate worldwide. The early clinical symptoms of SARS-CoV-2 and seasonal HCoV infections are similar, so rapid and accurate identification of the subtypes of HCoVs is crucial for early diagnosis, early treatment, prevention and control of these infections. However, current multiplex molecular diagnostic techniques for HCoV subtypes including SARS-CoV-2 are limited.
Methods: We designed primers and probes specific for the S and N genes of SARS-CoV-2, the N gene of severe acute respiratory syndrome coronavirus (SARS-CoV), and the ORF1ab gene of four seasonal HCoVs, as well as the human B2M gene product. We developed and optimized a quadruple quantitative real-time PCR assay (qq-PCR) for simultaneous detection of SARS-CoV-2, SARS-CoV and four seasonal HCoVs. This assay was further tested for specificity and sensitivity, and validated using 184 clinical samples.
Results: The limit of detection of the qq-PCR assay was in the range 2.5 × 10[SUP]1[/SUP] to 6.5 × 10[SUP]1[/SUP] copies/μL for each gene and no cross-reactivity with other common respiratory viruses was observed. The intra-assay and inter-assay coefficients of variation were 0.5-2%. The qq-PCR assay had a 91.9% sensitivity and 100.0% specificity for SARS-CoV-2 and a 95.7% sensitivity and 100% specificity for seasonal HCoVs, using the approved commercial kits as the reference. Compared to the commercial kits, total detection consistency was 98.4% (181/184) for SARS-CoV-2 and 98.6% (142/144) for seasonal HCoVs.
Conclusion: With the advantages of sensitivity, specificity, rapid detection, cost-effectiveness, and convenience, this qq-PCR assay has potential for clinical use for rapid discrimination between SARS-CoV-2, SARS-CoV and seasonal HCoVs.
Keywords: Coronavirus; Quadruple quantitative real-time PCR; SARS-CoV-2; Subtypes.
. 2022 Apr 11;19(1):67.
doi: 10.1186/s12985-022-01793-3.
Establishment and evaluation of a quadruple quantitative real-time PCR assay for simultaneous detection of human coronavirus subtypes
Mengchuan Zhao[SUP] #[/SUP][SUP] 1 2 [/SUP], Yi Xu[SUP] #[/SUP][SUP] 3 [/SUP], Dijun Zhang[SUP] 4 [/SUP], Guixia Li[SUP] 2 [/SUP], Huixia Gao[SUP] 3 [/SUP], Xianping Zeng[SUP] 4 [/SUP], Yanqing Tie[SUP] 5 [/SUP], Yong Wu[SUP] 4 [/SUP], Erhei Dai[SUP] 6 [/SUP], Zhishan Feng[SUP] 7 8 [/SUP]
Affiliations
- PMID: 35410305
- DOI: 10.1186/s12985-022-01793-3
Abstract
Background: The newly discovered severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and four seasonal human coronaviruses (HCoVs) (HCoV-229E, HCoV-OC43, HCoV-NL63 and HCoV-HKU1) still circulate worldwide. The early clinical symptoms of SARS-CoV-2 and seasonal HCoV infections are similar, so rapid and accurate identification of the subtypes of HCoVs is crucial for early diagnosis, early treatment, prevention and control of these infections. However, current multiplex molecular diagnostic techniques for HCoV subtypes including SARS-CoV-2 are limited.
Methods: We designed primers and probes specific for the S and N genes of SARS-CoV-2, the N gene of severe acute respiratory syndrome coronavirus (SARS-CoV), and the ORF1ab gene of four seasonal HCoVs, as well as the human B2M gene product. We developed and optimized a quadruple quantitative real-time PCR assay (qq-PCR) for simultaneous detection of SARS-CoV-2, SARS-CoV and four seasonal HCoVs. This assay was further tested for specificity and sensitivity, and validated using 184 clinical samples.
Results: The limit of detection of the qq-PCR assay was in the range 2.5 × 10[SUP]1[/SUP] to 6.5 × 10[SUP]1[/SUP] copies/μL for each gene and no cross-reactivity with other common respiratory viruses was observed. The intra-assay and inter-assay coefficients of variation were 0.5-2%. The qq-PCR assay had a 91.9% sensitivity and 100.0% specificity for SARS-CoV-2 and a 95.7% sensitivity and 100% specificity for seasonal HCoVs, using the approved commercial kits as the reference. Compared to the commercial kits, total detection consistency was 98.4% (181/184) for SARS-CoV-2 and 98.6% (142/144) for seasonal HCoVs.
Conclusion: With the advantages of sensitivity, specificity, rapid detection, cost-effectiveness, and convenience, this qq-PCR assay has potential for clinical use for rapid discrimination between SARS-CoV-2, SARS-CoV and seasonal HCoVs.
Keywords: Coronavirus; Quadruple quantitative real-time PCR; SARS-CoV-2; Subtypes.