ddPCR: a more accurate tool for SARS-CoV-2 detection in low viral load specimens
Quantitative real time PCR (RT-PCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, due to the low viral load specimens and the limitations of RT-PCR, significant numbers of false negative reports are inevitable, which results in failure to timely diagnose, cut off...
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Published in | Emerging microbes & infections Vol. 9; no. 1; pp. 1259 - 1268 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Taylor & Francis
01.01.2020
Taylor & Francis Ltd Taylor & Francis Group |
Subjects | |
Online Access | Get full text |
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Abstract | Quantitative real time PCR (RT-PCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, due to the low viral load specimens and the limitations of RT-PCR, significant numbers of false negative reports are inevitable, which results in failure to timely diagnose, cut off transmission, and assess discharge criteria. To improve this situation, an optimized droplet digital PCR (ddPCR) was used for detection of SARS-CoV-2, which showed that the limit of detection of ddPCR is significantly lower than that of RT-PCR. We further explored the feasibility of ddPCR to detect SARS-CoV-2 RNA from 77 patients, and compared with RT-PCR in terms of the diagnostic accuracy based on the results of follow-up survey. 26 patients of COVID-19 with negative RT-PCR reports were reported as positive by ddPCR. The sensitivity, specificity, PPV, NPV, negative likelihood ratio (NLR) and accuracy were improved from 40% (95% CI: 27-55%), 100% (95% CI: 54-100%), 100%, 16% (95% CI: 13-19%), 0.6 (95% CI: 0.48-0.75) and 47% (95% CI: 33-60%) for RT-PCR to 94% (95% CI: 83-99%), 100% (95% CI: 48-100%), 100%, 63% (95% CI: 36-83%), 0.06 (95% CI: 0.02-0.18), and 95% (95% CI: 84-99%) for ddPCR, respectively. Moreover, 6/14 (42.9%) convalescents were detected as positive by ddPCR at 5-12 days post discharge. Overall, ddPCR shows superiority for clinical diagnosis of SARS-CoV-2 to reduce the false negative reports, which could be a powerful complement to the RT-PCR. |
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AbstractList | Quantitative real time PCR (RT-PCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, due to the low viral load specimens and the limitations of RT-PCR, significant numbers of false negative reports are inevitable, which results in failure to timely diagnose, cut off transmission, and assess discharge criteria. To improve this situation, an optimized droplet digital PCR (ddPCR) was used for detection of SARS-CoV-2, which showed that the limit of detection of ddPCR is significantly lower than that of RT-PCR. We further explored the feasibility of ddPCR to detect SARS-CoV-2 RNA from 77 patients, and compared with RT-PCR in terms of the diagnostic accuracy based on the results of follow-up survey. 26 patients of COVID-19 with negative RT-PCR reports were reported as positive by ddPCR. The sensitivity, specificity, PPV, NPV, negative likelihood ratio (NLR) and accuracy were improved from 40% (95% CI: 27–55%), 100% (95% CI: 54–100%), 100%, 16% (95% CI: 13–19%), 0.6 (95% CI: 0.48–0.75) and 47% (95% CI: 33–60%) for RT-PCR to 94% (95% CI: 83–99%), 100% (95% CI: 48–100%), 100%, 63% (95% CI: 36–83%), 0.06 (95% CI: 0.02–0.18), and 95% (95% CI: 84–99%) for ddPCR, respectively. Moreover, 6/14 (42.9%) convalescents were detected as positive by ddPCR at 5–12 days post discharge. Overall, ddPCR shows superiority for clinical diagnosis of SARS-CoV-2 to reduce the false negative reports, which could be a powerful complement to the RT-PCR. Quantitative real time PCR (RT-PCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, due to the low viral load specimens and the limitations of RT-PCR, significant numbers of false negative reports are inevitable, which results in failure to timely diagnose, cut off transmission, and assess discharge criteria. To improve this situation, an optimized droplet digital PCR (ddPCR) was used for detection of SARS-CoV-2, which showed that the limit of detection of ddPCR is significantly lower than that of RT-PCR. We further explored the feasibility of ddPCR to detect SARS-CoV-2 RNA from 77 patients, and compared with RT-PCR in terms of the diagnostic accuracy based on the results of follow-up survey. 26 patients of COVID-19 with negative RT-PCR reports were reported as positive by ddPCR. The sensitivity, specificity, PPV, NPV, negative likelihood ratio (NLR) and accuracy were improved from 40% (95% CI: 27-55%), 100% (95% CI: 54-100%), 100%, 16% (95% CI: 13-19%), 0.6 (95% CI: 0.48-0.75) and 47% (95% CI: 33-60%) for RT-PCR to 94% (95% CI: 83-99%), 100% (95% CI: 48-100%), 100%, 63% (95% CI: 36-83%), 0.06 (95% CI: 0.02-0.18), and 95% (95% CI: 84-99%) for ddPCR, respectively. Moreover, 6/14 (42.9%) convalescents were detected as positive by ddPCR at 5-12 days post discharge. Overall, ddPCR shows superiority for clinical diagnosis of SARS-CoV-2 to reduce the false negative reports, which could be a powerful complement to the RT-PCR.Quantitative real time PCR (RT-PCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, due to the low viral load specimens and the limitations of RT-PCR, significant numbers of false negative reports are inevitable, which results in failure to timely diagnose, cut off transmission, and assess discharge criteria. To improve this situation, an optimized droplet digital PCR (ddPCR) was used for detection of SARS-CoV-2, which showed that the limit of detection of ddPCR is significantly lower than that of RT-PCR. We further explored the feasibility of ddPCR to detect SARS-CoV-2 RNA from 77 patients, and compared with RT-PCR in terms of the diagnostic accuracy based on the results of follow-up survey. 26 patients of COVID-19 with negative RT-PCR reports were reported as positive by ddPCR. The sensitivity, specificity, PPV, NPV, negative likelihood ratio (NLR) and accuracy were improved from 40% (95% CI: 27-55%), 100% (95% CI: 54-100%), 100%, 16% (95% CI: 13-19%), 0.6 (95% CI: 0.48-0.75) and 47% (95% CI: 33-60%) for RT-PCR to 94% (95% CI: 83-99%), 100% (95% CI: 48-100%), 100%, 63% (95% CI: 36-83%), 0.06 (95% CI: 0.02-0.18), and 95% (95% CI: 84-99%) for ddPCR, respectively. Moreover, 6/14 (42.9%) convalescents were detected as positive by ddPCR at 5-12 days post discharge. Overall, ddPCR shows superiority for clinical diagnosis of SARS-CoV-2 to reduce the false negative reports, which could be a powerful complement to the RT-PCR. |
Author | Suo, Tao Hu, Wenjia Ullah, Hafiz Zhang, Qi Xu, Ke Lan, Ke Wang, Xin Huang, Zhixiang Chen, Tielong Guo, Dong Feng, Jiangpeng Chen, Yu Yang, Yang Liu, Yingle Liu, Xinjin Liu, Yuan Zhang, Qiuhan Sajid, Muhanmmad Deng, Liping Xiong, Yong Chen, Guozhong Guo, Ming Liu, Fang |
Author_xml | – sequence: 1 givenname: Tao surname: Suo fullname: Suo, Tao organization: State Key Laboratory of Virology, Renmin Hospital, Wuhan University – sequence: 2 givenname: Xinjin surname: Liu fullname: Liu, Xinjin organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 3 givenname: Jiangpeng surname: Feng fullname: Feng, Jiangpeng organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 4 givenname: Ming surname: Guo fullname: Guo, Ming organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 5 givenname: Wenjia surname: Hu fullname: Hu, Wenjia organization: Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 6 givenname: Dong surname: Guo fullname: Guo, Dong organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 7 givenname: Hafiz surname: Ullah fullname: Ullah, Hafiz organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 8 givenname: Yang surname: Yang fullname: Yang, Yang organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 9 givenname: Qiuhan surname: Zhang fullname: Zhang, Qiuhan organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 10 givenname: Xin surname: Wang fullname: Wang, Xin organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 11 givenname: Muhanmmad surname: Sajid fullname: Sajid, Muhanmmad organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 12 givenname: Zhixiang surname: Huang fullname: Huang, Zhixiang organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 13 givenname: Liping surname: Deng fullname: Deng, Liping organization: Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 14 givenname: Tielong surname: Chen fullname: Chen, Tielong organization: Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 15 givenname: Fang surname: Liu fullname: Liu, Fang organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 16 givenname: Ke surname: Xu fullname: Xu, Ke organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 17 givenname: Yuan surname: Liu fullname: Liu, Yuan organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 18 givenname: Qi orcidid: 0000-0003-2868-1816 surname: Zhang fullname: Zhang, Qi organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 19 givenname: Yingle surname: Liu fullname: Liu, Yingle organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 20 givenname: Yong orcidid: 0000-0003-0678-4064 surname: Xiong fullname: Xiong, Yong email: yongxiong64@163.com organization: Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 21 givenname: Guozhong surname: Chen fullname: Chen, Guozhong email: guozhongch6389@163.com organization: State Key Laboratory of Virology, Renmin Hospital, Wuhan University – sequence: 22 givenname: Ke surname: Lan fullname: Lan, Ke email: klan@whu.edu.cn organization: Frontier Science Center for Immunology and Metabolism, Wuhan University – sequence: 23 givenname: Yu orcidid: 0000-0003-1300-4652 surname: Chen fullname: Chen, Yu email: chenyu@whu.edu.cn organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32438868$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Betacoronavirus - genetics clinical detection Coronavirus Infections - diagnosis COVID-19 droplet digital PCR false negative False Negative Reactions Humans Limit of Detection Pandemics Pneumonia, Viral - diagnosis Real-Time Polymerase Chain Reaction - methods RNA, Viral - genetics RT-PCR SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Viral Load - methods |
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Title | ddPCR: a more accurate tool for SARS-CoV-2 detection in low viral load specimens |
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