Epidemiology of Severe Acute Respiratory Syndrome Coronavirus 2 Emergence Amidst Community-Acquired Respiratory Viruses

Author:

Leuzinger Karoline12,Roloff Tim34,Gosert Rainer1,Sogaard Kirstin34,Naegele Klaudia1,Rentsch Katharina5,Bingisser Roland6,Nickel Christian H6,Pargger Hans7,Bassetti Stefano8,Bielicki Julia9,Khanna Nina10ORCID,Tschudin Sutter Sarah10,Widmer Andreas10,Hinic Vladimira4,Battegay Manuel10,Egli Adrian34,Hirsch Hans H1210ORCID

Affiliation:

1. Clinical Virology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland

2. Transplantation and Clinical Virology, Department of Biomedicine, University of Basel, Basel, Switzerland

3. Applied Microbiology Research, Laboratory Medicine, Department of Biomedicine, University of Basel, Basel, Switzerland

4. Clinical Bacteriology and Mycology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland

5. Clinical Chemistry, Laboratory Medicine, University Hospital Basel, Basel, Switzerland

6. Emergency Medicine, University Hospital Basel, Basel, Switzerland

7. Intensive Care Unit, University Hospital Basel, Basel, Switzerland

8. Internal Medicine, University Hospital Basel, Basel, Switzerland

9. Pediatric Infectious Diseases and Hospital Epidemiology, University Children’s Hospital Basel, Basel, Switzerland

10. Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland

Abstract

Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in China as the cause of coronavirus disease 2019 in December 2019 and reached Europe by late January 2020, when community-acquired respiratory viruses (CARVs) are at their annual peak. We validated the World Health Organization (WHO)–recommended SARS-CoV-2 assay and analyzed the epidemiology of SARS-CoV-2 and CARVs. Methods Nasopharyngeal/oropharyngeal swabs (NOPS) from 7663 patients were prospectively tested by the Basel S-gene and WHO-based E-gene (Roche) assays in parallel using the Basel N-gene assay for confirmation. CARVs were prospectively tested in 2394 NOPS by multiplex nucleic acid testing, including 1816 (75%) simultaneously for SARS-CoV-2. Results The Basel S-gene and Roche E-gene assays were concordant in 7475 cases (97.5%) including 825 (11%) SARS-CoV-2 positives. In 188 (2.5%) discordant cases, SARS-CoV-2 loads were significantly lower than in concordant positive ones and confirmed in 105 (1.4%). Adults were more frequently SARS-CoV-2 positive, whereas children tested more frequently CARV positive. CARV coinfections with SARS-CoV-2 occurred in 1.8%. SARS-CoV-2 replaced CARVs within 3 weeks, reaching 48% of all detected respiratory viruses followed by rhinovirus/enterovirus (13%), influenza virus (12%), coronavirus (9%), respiratory syncytial virus (6%), and metapneumovirus (6%). Conclusions Winter CARVs were dominant during the early SARS-CoV-2 pandemic, impacting infection control and treatment decisions, but were rapidly replaced, suggesting competitive infection. We hypothesize that preexisting immune memory and innate immune interference contribute to the different SARS-CoV-2 epidemiology among adults and children.

Funder

Clinical Virology Division

Clinical Bacteriology and Mycology Division, Laboratory Medicine, University Hospital Basel

Department of Biomedicine, University of Basel

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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