Influenza A, Influenza B, human respiratory syncytial virus and SARSCoV-2 molecular diagnostics and epidemiology in the post COVID-19 era
Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple r...
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Published in | Respiratory research Vol. 25; no. 1; pp. 234 - 9 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
05.06.2024
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1465-993X 1465-9921 1465-993X |
DOI | 10.1186/s12931-024-02862-7 |
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Abstract | Background
The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting.
Methods
Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2.
Results
The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022.
Conclusion
The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. |
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AbstractList | The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting. Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2. The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022. The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting. Methods Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2. Results The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022. Conclusion The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. Keywords: SARS-CoV-2, Flu-A/B, HRSV, rtRT-PCR, Multiplex, Co-detections, Turnaround-time Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting. Methods Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2. Results The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022. Conclusion The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting. Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2. The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022. The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting.BACKGROUNDThe concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting.Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2.METHODSTwo time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2.The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022.RESULTSThe results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022.The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected.CONCLUSIONThe results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. Abstract Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical microbiology laboratories. Multiplexed molecular testing on automated platforms that focus on the simultaneous detection of multiple respiratory viruses in a single tube is a useful approach for current and future diagnosis of respiratory infections in the clinical setting. Methods Two time periods were included in the study: from February to April 2022, an early 2022 period, during the gradual lifting of COVID-19 prevention measures in the country, and from October 2022 to April 2023, the 2022/23 respiratory infections season. We analysed a total of 1,918 samples in the first period and 18,131 respiratory samples in the second period using a multiplex molecular assay for the simultaneous detection of Influenza A (Flu-A), Influenza B (Flu-B), Human Respiratory Syncytial Virus (HRSV) and SARS-CoV-2. Results The results from early 2022 showed a strong dominance of SARS-CoV-2 infections with 1,267/1,918 (66.1%) cases. Flu-A was detected in 30/1,918 (1.6%) samples, HRSV in 14/1,918 (0.7%) samples, and Flu-B in 2/1,918 (0.1%) samples. Flu-A/SARS-CoV-2 co-detections were observed in 11/1,267 (0.9%) samples, and HRSV/SARS-CoV-2 co-detection in 5/1,267 (0.4%) samples. During the 2022/23 winter respiratory season, SARS-CoV-2 was detected in 1,738/18,131 (9.6%), Flu-A in 628/18,131 (3.5%), Flu-B in 106/18,131 (0.6%), and HRSV in 505/18,131 (2.8%) samples. Interestingly, co-detections were present to a similar extent as in early 2022. Conclusion The results show that the multiplex molecular approach is a valuable tool for the simultaneous laboratory diagnosis of SARS-CoV-2, Flu-A/B, and HRSV in hospitalized and outpatients. Infections with Flu-A/B, and HRSV occurred shortly after the COVID-19 control measures were lifted, so a strong reoccurrence of various respiratory infections and co-detections in the post COVID-19 period was to be expected. |
ArticleNumber | 234 |
Audience | Academic |
Author | Luštrek, Manca Knap, Nataša Suljič, Alen Petrovec, Miroslav Kogoj, Rok Uršič, Tina Avšič-Županc, Tatjana Korva, Miša Cesar, Zala Virant, Monika Jevšnik |
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PublicationDecade | 2020 |
PublicationPlace | London |
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PublicationTitle | Respiratory research |
PublicationTitleAbbrev | Respir Res |
PublicationTitleAlternate | Respir Res |
PublicationYear | 2024 |
Publisher | BioMed Central BioMed Central Ltd BMC |
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References | MJ Virant (2862_CR18) 2023; 15 TK Burki (2862_CR3) 2021; 9 A Cheng (2862_CR12) 2022; 102 MC Swets (2862_CR28) 2022; 399 2862_CR21 A Kandeel (2862_CR24) 2023; 23 M Moriyama (2862_CR16) 2020; 29 P Stamm (2862_CR19) 2021; 210 T Ursic (2862_CR7) 2022; 23 LE Wee (2862_CR25) 2020; 128 N Ravi (2862_CR1) 2020; 165 TR Mercer (2862_CR2) 2021; 22 EJ Chow (2862_CR23) 2023; 21 M Xu (2862_CR5) 2013; 139 FH Varela (2862_CR20) 2021; 11 SH Kim (2862_CR10) 2022; 10 2862_CR17 HH Mostafa (2862_CR9) 2021; 59 2862_CR14 W Zhen (2862_CR15) 2022; 10 H Shuai (2862_CR22) 2022; 603 L Lansbury (2862_CR26) 2020; 81 R Ehret (2862_CR13) 2022; 299 T Almeida (2862_CR6) 2023; 5 N Zhang (2862_CR4) 2020; 92 NE Babady (2862_CR8) 2013; 13 LO Attwood (2862_CR11) 2020; 128 D Kim (2862_CR27) 2020; 323 |
References_xml | – volume: 23 start-page: 703 issue: 6 year: 2022 ident: 2862_CR7 publication-title: J Biomed Res Environ Sci doi: 10.37871/jbres1500 – volume: 59 start-page: e02955 year: 2021 ident: 2862_CR9 publication-title: J Clin Microbiol doi: 10.1128/jcm.02955-20 – volume: 10 start-page: e0039922 year: 2022 ident: 2862_CR10 publication-title: Microbiol Spectr doi: 10.1128/spectrum.00399-22 – volume: 81 start-page: 266 year: 2020 ident: 2862_CR26 publication-title: J Infect doi: 10.1016/j.jinf.2020.05.046 – volume: 22 start-page: 415 year: 2021 ident: 2862_CR2 publication-title: Nat Rev Genet doi: 10.1038/s41576-021-00360-w – ident: 2862_CR14 doi: 10.1016/j.jcv.2022.105164 – volume: 15 start-page: 1218 issue: 6 year: 2023 ident: 2862_CR18 publication-title: Viruses doi: 10.3390/v15061218 – volume: 210 start-page: 277 year: 2021 ident: 2862_CR19 publication-title: Med Microbiol Immunol doi: 10.1007/s00430-021-00720-7 – volume: 102 start-page: 115575 year: 2022 ident: 2862_CR12 publication-title: Diagn Microbiol Infect Dis doi: 10.1016/j.diagmicrobio.2021.115575 – volume: 5 start-page: 1880 issue: 9 year: 2023 ident: 2862_CR6 publication-title: Viruses doi: 10.3390/v15091880 – volume: 10 start-page: e0109021 year: 2022 ident: 2862_CR15 publication-title: Microbiol Spectr doi: 10.1128/spectrum.01090-21 – volume: 29 start-page: 83 issue: 1 year: 2020 ident: 2862_CR16 publication-title: Annu Rev Virol doi: 10.1146/annurev-virology-012420-022445 – volume: 603 start-page: 693 year: 2022 ident: 2862_CR22 publication-title: Nature doi: 10.1038/s41586-022-04442-5 – volume: 128 start-page: 104448 year: 2020 ident: 2862_CR11 publication-title: J Clin Virol doi: 10.1016/j.jcv.2020.104448 – volume: 23 start-page: 1067 year: 2023 ident: 2862_CR24 publication-title: BMC Public Health doi: 10.1186/s12889-023-15880-9 – volume: 92 start-page: 408 year: 2020 ident: 2862_CR4 publication-title: J Med Virol doi: 10.1002/jmv.25674 – volume: 11 start-page: 05007 year: 2021 ident: 2862_CR20 publication-title: J Glob Health doi: 10.7189/jogh.11.05007 – volume: 139 start-page: 118 year: 2013 ident: 2862_CR5 publication-title: Am J Clin Pathol doi: 10.1309/AJCPH7X3NLYZPHBW – volume: 399 start-page: 1463 year: 2022 ident: 2862_CR28 publication-title: Lancet doi: 10.1016/S0140-6736(22)00383-X – volume: 21 start-page: 195 year: 2023 ident: 2862_CR23 publication-title: Nat Rev Microbiol doi: 10.1038/s41579-022-00807-9 – ident: 2862_CR17 – volume: 128 start-page: 104436 year: 2020 ident: 2862_CR25 publication-title: J Clin Virol doi: 10.1016/j.jcv.2020.104436 – volume: 9 start-page: e103 year: 2021 ident: 2862_CR3 publication-title: Lancet Respir Med doi: 10.1016/S2213-2600(21)00364-7 – ident: 2862_CR21 doi: 10.1093/ofid/ofab618 – volume: 299 start-page: 114338 year: 2022 ident: 2862_CR13 publication-title: J Virol Methods doi: 10.1016/j.jviromet.2021.114338 – volume: 323 start-page: 2085 year: 2020 ident: 2862_CR27 publication-title: JAMA doi: 10.1001/jama.2020.6266 – volume: 13 start-page: 779 year: 2013 ident: 2862_CR8 publication-title: Expert Rev Mol Diagn doi: 10.1586/14737159.2013.848794 – volume: 165 start-page: 112454 year: 2020 ident: 2862_CR1 publication-title: Biosens Bioelectron doi: 10.1016/j.bios.2020.112454 |
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The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and... The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and clinical... Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for clinicians and... Abstract Background The concurrent circulation of SARS-CoV-2 with other respiratory viruses is unstoppable and represents a new diagnostic reality for... |
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SubjectTerms | Adult Aged Analysis Co-detections Coinfection - diagnosis Coinfection - epidemiology COVID-19 - diagnosis COVID-19 - epidemiology Epidemiology Female Flu-A/B Health aspects HRSV Humans Influenza Influenza A virus - genetics Influenza A virus - isolation & purification Influenza B virus - genetics Influenza B virus - isolation & purification Influenza, Human - diagnosis Influenza, Human - epidemiology Influenza, Human - virology Laboratories Male Medicine Medicine & Public Health Microbiology Middle Aged Molecular Diagnostic Techniques - methods Multiplex Pneumology/Respiratory System Prevention Respiratory Syncytial Virus Infections - diagnosis Respiratory Syncytial Virus Infections - epidemiology Respiratory Syncytial Virus, Human - genetics Respiratory Syncytial Virus, Human - isolation & purification Risk factors rtRT-PCR SARS-CoV-2 SARS-CoV-2 - genetics SARS-CoV-2 - isolation & purification Seasons Testing |
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Title | Influenza A, Influenza B, human respiratory syncytial virus and SARSCoV-2 molecular diagnostics and epidemiology in the post COVID-19 era |
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