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      Potential false-negative nucleic acid testing results for Severe Acute Respiratory Syndrome Coronavirus 2 from thermal inactivation of samples with low viral loads

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          Abstract

          Background

          Corona Virus Disease-2019 (COVID-19) has spread widely throughout the world since the end of 2019. Nucleic acid testing (NAT) has played an important role in patient diagnosis and management of COVID-19. In some circumstances, thermal inactivation at 56 °C has been recommended to inactivate Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) before NAT. However, this procedure could theoretically disrupt nucleic acid integrity of this single-stranded RNA virus and cause false negatives in real-time polymerase chain reaction (RT-PCR) tests.

          Methods

          We investigated whether thermal inactivation could affect the results of viral NAT. We examined the effects of thermal inactivation on the quantitative RT-PCR results of SARS-CoV-2 particularly with regard to the rates of false-negative results for specimens carrying low viral loads. We additionally investigated the effects of different specimen types, sample preservation times and a chemical inactivation approach on NAT.

          Results

          Our work showed increased Ct values in specimens from diagnosed COVID-19 patients in RT-PCR tests after thermal incubation. Moreover, about half of the weak-positive samples (7 of 15 samples, 46.7%) were RT-PCR negative after heat inactivation in at least one parallel testing. The use of guanidinium-based lysis for preservation of these specimens had a smaller impact on RT-PCR results with fewer false negatives (2 of 15 samples, 13.3%) and significantly less increase in Ct values than heat inactivation.

          Conclusion

          Thermal inactivation adversely affected the efficiency of RT-PCR for SARS-CoV-2 detection. Given the limited applicability associated with chemical inactivators, other approaches to ensure the overall protection of laboratory personnel need consideration.

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          Most cited references9

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          Stability and inactivation of SARS coronavirus

          The SARS-coronavirus (SARS-CoV) is a newly emerged, highly pathogenic agent that caused over 8,000 human infections with nearly 800 deaths between November 2002 and September 2003. While direct person-to-person transmission via respiratory droplets accounted for most cases, other modes have not been ruled out. Faecal shedding is common and prolonged and has caused an outbreak in Hong Kong. We studied the stability of SARS-CoV under different conditions, both in suspension and dried on surfaces, in comparison with other human-pathogenic viruses, including human coronavirus HCoV-229E. In suspension, HCoV-229E gradually lost its infectivity completely while SARS-CoV retained its infectivity for up to 9 days; in the dried state, survival times were 24 h versus 6 days. Thermal inactivation at 56°C was highly effective in the absence of protein, reducing the virus titre to below detectability; however, the addition of 20% protein exerted a protective effect resulting in residual infectivity. If protein-containing solutions are to be inactivated, heat treatment at 60°C for at least 30 min must be used. Different fixation procedures, e.g. for the preparation of immunofluorescence slides, as well as chemical means of virus inactivation commonly used in hospital and laboratory settings were generally found to be effective. Our investigations confirm that it is possible to care for SARS patients and to conduct laboratory scientific studies on SARS-CoV safely. Nevertheless, the agent’s tenacity is considerably higher than that of HCoV-229E, and should SARS re-emerge, increased efforts need to be devoted to questions of environmental hygiene.
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            Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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              Is Open Access

              Heat inactivation of the Middle East respiratory syndrome coronavirus

              The culture supernatants of the emerging Middle East respiratory syndrome coronavirus (MERS-CoV) were submitted to three temperatures over time and tested for infectivity by TCID50 method on Vero E6 cells. At 56°C, almost 25 minutes were necessary to reduce the initial titre by 4 log10. Increasing temperature to 65°C had a strong negative effect on viral infectivity as virucidy dropped significantly to 1 minute. On the contrary, no significant decrease in titre was observed after 2 hours at 25°C. These data might be useful in establishing biosafety measures in laboratories against MERS-CoV.
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                Author and article information

                Contributors
                Journal
                Clin Chem
                Clin. Chem
                clinchem
                Clinical Chemistry
                Oxford University Press
                0009-9147
                1530-8561
                04 April 2020
                04 April 2020
                : hvaa091
                Affiliations
                [h1 ]National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences , P. R. China
                [h2 ]Graduate School, Chinese Academy of Medical Sciences, Peking Union Medical College , Beijing, China
                [h3 ] Beijing Engineering Research Center of Laboratory Medicine , Beijing Hospital, Beijing, China
                [h4 ] Institute for Infectious Disease and Endemic Disease Control , Beijing Center for Disease Prevention and Control, Beijing, China
                [h5 ] Research Centre for Preventive Medicine of Beijing , Beijing, China
                [h6 ]School of Public Health, Capital Medical University , Beijing, China
                [h7 ]Department of Clinical Laboratory, Beijing Hospital , National Center of Gerontology, Beijing, China
                Author notes

                Yang Pan and Luyao Long contributed equally to the work.

                To whom correspondence may be addressed. Email: rensimei4162@ 123456bjhmoh.cn (Simei Ren), or bjcdcxm@ 123456126.com (Quanyi Wang). National Center for Clinical Laboratories, Beijing Hospital, No.1 Dahua Road, Dongdan, Beijing 100730, P. R. China; Fax: +86-010-65132968; or No.16 Heping Li Middle St, Beijing 100013, P. R. China; Fax: +86-010-64407122.
                Article
                hvaa091
                10.1093/clinchem/hvaa091
                7184485
                32246822
                66891a5d-4b8b-43b2-bec8-13aa53a36d5e
                © 2020 American Association for Clinical Chemistry

                This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model ( https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 06 March 2020
                : 20 March 2020
                : 23 March 2020
                Page count
                Pages: 24
                Categories
                Article
                Custom metadata
                accepted-manuscript
                PAP

                covid-19,sars-cov-2,thermal inactivation,nucleic acid test,rt-pcr,false negative

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