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      Evidence of the simultaneous replications of active viruses in specimens positive for multiple respiratory viruses

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          ABSTRACT

          Genetic diagnostic assays for the detection of respiratory viruses sometimes show simultaneous multiple infections with low copy numbers. In such cases, the disease is considered caused by a single etiologic agent and others are nonspecific reactions and/or contaminations. Interferon-dependent interference is seen in dual infections of influenza and respiratory syncytial virus, which are the main causes of respiratory infections. Virus isolation is one of the answers in detecting other active viruses present in specimens, and the air–liquid interface culture of human bronchial/tracheal epithelial cells (HBTEC-ALI) is optimal for the isolation of respiratory viruses owing to its wide range of susceptibility. In this study, we successfully confirmed the replications of various viruses from specimens with low copy numbers and simultaneous passage of two to three viruses using HBTEC-ALI cultures, mainly including human bocavirus 1 and/or human rhinovirus.

          IMPORTANCE

          Since the pandemic of coronavirus diseases 2019, the use of real-time PCR assay has become widespread among people who were not familiar with it in virus detection. As a result, whether a high real-time PCR value in one time test indicates virus transmissibly became a complicated social problem, regardless of the difference in assays and/or amplification conditions, the time and number of diagnostic test during the time course of infection. In addition, the multiple positives in the test of respiratory viruses further add to the confusion in the interpretation of the infection. To address this issue, we performed virus isolation using pediatric SARI (severe acute respiratory infections) specimens on air–liquid interface culture of human bronchial/tracheal epithelial cell culture. The result of this study can be a strong evidence that the specimens showing positivity for multiple agents in real-time PCR tests possibly contain infectious viruses.

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          Most cited references46

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          Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR

          Background The ongoing outbreak of the recently emerged novel coronavirus (2019-nCoV) poses a challenge for public health laboratories as virus isolates are unavailable while there is growing evidence that the outbreak is more widespread than initially thought, and international spread through travellers does already occur. Aim We aimed to develop and deploy robust diagnostic methodology for use in public health laboratory settings without having virus material available. Methods Here we present a validated diagnostic workflow for 2019-nCoV, its design relying on close genetic relatedness of 2019-nCoV with SARS coronavirus, making use of synthetic nucleic acid technology. Results The workflow reliably detects 2019-nCoV, and further discriminates 2019-nCoV from SARS-CoV. Through coordination between academic and public laboratories, we confirmed assay exclusivity based on 297 original clinical specimens containing a full spectrum of human respiratory viruses. Control material is made available through European Virus Archive – Global (EVAg), a European Union infrastructure project. Conclusion The present study demonstrates the enormous response capacity achieved through coordination of academic and public laboratories in national and European research networks.
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            Duration of infectiousness and correlation with RT-PCR cycle threshold values in cases of COVID-19, England, January to May 2020

            Severe acute respiratory syndrome coronavirus 2 viral load in the upper respiratory tract peaks around symptom onset and infectious virus persists for 10 days in mild-to-moderate coronavirus disease (n = 324 samples analysed). RT-PCR cycle threshold (Ct) values correlate strongly with cultivable virus. Probability of culturing virus declines to 8% in samples with Ct > 35 and to 6% 10 days after onset; it is similar in asymptomatic and symptomatic persons. Asymptomatic persons represent a source of transmissible virus.
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              Development of Genetic Diagnostic Methods for Novel Coronavirus 2019 (nCoV-2019) in Japan

              During the emergence of novel coronavirus 2019 (nCoV) outbreak in Wuhan city, China at the end of 2019, there was movement of many airline travelers between Wuhan and Japan, suggesting that the Japanese population was at high risk of infection by the virus. Hence, we urgently developed diagnostic systems for detection of 2019 nCoV. Two nested RT-PCR and two real-time RT-PCR assays were adapted for use in Japan. As of February 8, 2020, these assays have successfully detected 25 positive cases of infection in Japan.
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                Author and article information

                Contributors
                Role: Data curationRole: InvestigationRole: MethodologyRole: Resources
                Role: InvestigationRole: Resources
                Role: InvestigationRole: MethodologyRole: ResourcesRole: Software
                Role: InvestigationRole: MethodologyRole: ResourcesRole: Software
                Role: Resources
                Role: Resources
                Role: Resources
                Role: Resources
                Role: Resources
                Role: Data curationRole: ValidationRole: VisualizationRole: Writing – review and editing
                Role: Resources
                Role: ResourcesRole: SupervisionRole: Writing – review and editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SoftwareRole: SupervisionRole: ValidationRole: VisualizationRole: Writing – original draftRole: Writing – review and editing
                Role: Editor
                Journal
                Microbiol Spectr
                Microbiol Spectr
                spectrum
                Microbiology Spectrum
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2165-0497
                January 2024
                05 December 2023
                05 December 2023
                : 12
                : 1
                : e01920-23
                Affiliations
                [1 ] Department of Virology III, National Institute of Infectious Disease; , Gakuen, Musashimurayama, Tokyo, Japan
                [2 ] Department of Pediatrics, School of Medicine, Fukushima Medical University; , Hikarigaoka, Fukushima, Japan
                [3 ] Faculty of Veterinary Medicine, Nippon Veterinary and Life Science University; , Musashino, Tokyo, Japan
                Emory University School of Medicine; , Atlanta, Georgia, USA
                Author notes
                Address correspondence to Kazuya Shirato, shirato@ 123456niid.go.jp

                The authors declare no conflict of interest.

                Author information
                https://orcid.org/0000-0002-7145-7126
                https://orcid.org/0000-0003-4955-6221
                https://orcid.org/0000-0002-3375-9799
                Article
                01920-23 spectrum.01920-23
                10.1128/spectrum.01920-23
                10783086
                38051050
                99e6a829-8462-4aae-ac0a-64e7c6aff947
                Copyright © 2023 Kawase et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 08 May 2023
                : 04 November 2023
                Page count
                supplementary-material: 2, authors: 13, Tables: 5, References: 48, Pages: 13, Words: 7430
                Funding
                Funded by: Japan Agency for Medical Research and Development (AMED);
                Award ID: 22fk0108119j0603 and 23fk0108661j0001
                Award Recipient :
                Funded by: Japan Agency for Medical Research and Development (AMED);
                Award ID: 22kf0108117j0103 and 22fk0108543j0201
                Award Recipient :
                Funded by: MEXT | Japan Society for the Promotion of Science (JSPS);
                Award ID: 20K06441
                Award Recipient :
                Categories
                Research Article
                clinical-microbiology, Clinical Microbiology
                Custom metadata
                January 2024

                respiratory virus,co-cultivation,real-time rt-pcr,hbtec-ali culture

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