tetano
Editor, Senior Moderator
J Clin Lab Anal
. 2021 Dec 3;e24137.
doi: 10.1002/jcla.24137. Online ahead of print.
Smaller reaction volume of triplex taqman real-time reverse transcription-PCR assays for diagnosing coronavirus disease 2019
Wenxue Dong[SUP] 1 [/SUP], Xu Yang[SUP] 1 [/SUP], Jing Li[SUP] 1 [/SUP], Zhiying Zhang[SUP] 1 [/SUP], Lijun Liu[SUP] 1 [/SUP], Zhipeng Zhao[SUP] 1 2 [/SUP], Longli Kang[SUP] 1 [/SUP]
Affiliations
Abstract
Background: Coronavirus disease 2019 (COVID-19) has had a devastating impact on public health services worldwide. Currently, there are no standard remedies or therapies for COVID-19. it is important to identify and diagnose COVID-19 to control the spread. But clinical symptoms of COVID-19 are very similar to those of other respiratory viruses.
Results: As a result, the diagnosis of COVID-19 relies heavily on detecting pathogens. We established a bunch of triplex new TaqMan real-time PCR assays. Three sets of primers and probes (targeting the ORF1ab, N, and E genes, respectively) are poorly consistent with other human coronaviruses and the human influenza virus. The sensitivity of established PCR assays notices as few as 100 copies per PCR of the ORF1ab, N, and E genes. Meanwhile, standard curves concluded from constant PCR reaction all showed glorious linear correlations between Ct values and the polymer loading copy variety (correlation coefficient (R[SUP]2[/SUP] ) of ORF1ab, N, and E genes is 0.996, 0.991, and 0.998, respectively). Surveillance of RNA-based pseudovirus demonstrated that they were identified to be positive with respect to SARS-CoV-2 and that established PCR assays are achievable.
Conclusion: The assays established provide a smaller reaction volume for diagnosing COVID-19.
Keywords: COVID-19; RT-PCR; SARS-CoV-2; nucleic acid testing.
. 2021 Dec 3;e24137.
doi: 10.1002/jcla.24137. Online ahead of print.
Smaller reaction volume of triplex taqman real-time reverse transcription-PCR assays for diagnosing coronavirus disease 2019
Wenxue Dong[SUP] 1 [/SUP], Xu Yang[SUP] 1 [/SUP], Jing Li[SUP] 1 [/SUP], Zhiying Zhang[SUP] 1 [/SUP], Lijun Liu[SUP] 1 [/SUP], Zhipeng Zhao[SUP] 1 2 [/SUP], Longli Kang[SUP] 1 [/SUP]
Affiliations
- PMID: 34859916
- DOI: 10.1002/jcla.24137
Abstract
Background: Coronavirus disease 2019 (COVID-19) has had a devastating impact on public health services worldwide. Currently, there are no standard remedies or therapies for COVID-19. it is important to identify and diagnose COVID-19 to control the spread. But clinical symptoms of COVID-19 are very similar to those of other respiratory viruses.
Results: As a result, the diagnosis of COVID-19 relies heavily on detecting pathogens. We established a bunch of triplex new TaqMan real-time PCR assays. Three sets of primers and probes (targeting the ORF1ab, N, and E genes, respectively) are poorly consistent with other human coronaviruses and the human influenza virus. The sensitivity of established PCR assays notices as few as 100 copies per PCR of the ORF1ab, N, and E genes. Meanwhile, standard curves concluded from constant PCR reaction all showed glorious linear correlations between Ct values and the polymer loading copy variety (correlation coefficient (R[SUP]2[/SUP] ) of ORF1ab, N, and E genes is 0.996, 0.991, and 0.998, respectively). Surveillance of RNA-based pseudovirus demonstrated that they were identified to be positive with respect to SARS-CoV-2 and that established PCR assays are achievable.
Conclusion: The assays established provide a smaller reaction volume for diagnosing COVID-19.
Keywords: COVID-19; RT-PCR; SARS-CoV-2; nucleic acid testing.