Publication:
Respiratory Syncytial Virus in Adult Patients at a Tertiary Care Hospital in Germany: Clinical Features and Molecular Epidemiology of the Fusion Protein in the Severe Respiratory Season of 2022/2023

dc.contributor.authorHönemann, Mario
dc.contributor.authorMaier, Melanie
dc.contributor.authorFrille, Armin
dc.contributor.authorThiem, Stephanie
dc.contributor.authorBergs, Sandra
dc.contributor.authorWilliams, Thomas C
dc.contributor.authorMas-Lloret, Vicente
dc.contributor.authorLübbert, Christoph
dc.contributor.authorPietsch, Corinna
dc.date.accessioned2025-03-24T10:25:31Z
dc.date.available2025-03-24T10:25:31Z
dc.date.issued2024-06-12
dc.description.abstractFollowing an interseasonal rise in mainly pediatric respiratory syncytial virus (RSV) cases in Germany in 2021, an exceptionally high number of adult cases was observed in the subsequent respiratory season of 2022/2023. The aim of this study was to compare the clinical presentation of RSV infections in the pre- and post-SARS-CoV-2 pandemic periods. Additionally, the local epidemiology of the RSV fusion protein was analyzed at a molecular genetic and amino acid level. RSV detections in adults peaked in calendar week 1 of 2023, 8 weeks earlier than the earliest peak observed in the three pre-pandemic seasons. Although the median age of the adult patients was not different (66.5 vs. 65 years), subtle differences between both periods regarding comorbidities and the clinical presentation of RSV cases were noted. High rates of comorbidities prevailed; however, significantly lower numbers of patients with a history of lung transplantation (p = 0.009), chronic kidney disease (p = 0.013), and immunosuppression (p = 0.038) were observed in the 2022/2023 season. In contrast, significantly more lower respiratory tract infections (p < 0.001), in particular in the form of pneumonia (p = 0.015) and exacerbations of obstructive lung diseases (p = 0.008), were detected. An ICU admission was noted for 23.7% of all patients throughout the study period. Sequence analysis of the fusion protein gene revealed a close phylogenetic relatedness, regardless of the season of origin. However, especially for RSV-B, an accumulation of amino acid point substitutions was noted, including in antigenic site Ø. The SARS-CoV-2 pandemic had a tremendous impact on the seasonality of RSV, and the introduction of new vaccination and immunization strategies against RSV warrants further epidemiologic studies of this important pathogen.
dc.description.peerreviewed
dc.description.sponsorshipThe authors acknowledge the support from Leipzig University for open-access publishing. A. Frille was supported by the postdoctoral fellowship “MetaRot program” (clinician scientist program) from the Federal Ministry of Education and Research (BMBF), Germany (FKZ 01EO1501, IFB Adiposity Diseases), a research grant from the “Mitteldeutsche Gesellschaft für Pneumologie (MDGP) e.V.” (2018-MDGP-PA-002), a junior research grant from the Medical Faculty, Leipzig University (934100-012), a graduate fellowship from the “Novartis Foundation”, and the “PETictCAC” project (ERAPerMed_324), which was funded with tax funds based on the budget passed by the Saxon State Parliament (Germany) under the frame of ERA PerMed (Horizon 2020 Research and Innovation Framework Programme of the European Commission Research Directorate-General, Grant Agreement No. 779282).
dc.format.number6
dc.format.page943
dc.format.volume16
dc.identifier.citationHönemann M, Maier M, Frille A, Thiem S, Bergs S, Williams TC, Mas V, Lübbert C, Pietsch C. Respiratory Syncytial Virus in Adult Patients at a Tertiary Care Hospital in Germany: Clinical Features and Molecular Epidemiology of the Fusion Protein in the Severe Respiratory Season of 2022/2023. Viruses. 2024 Jun 12;16(6):943.
dc.identifier.doi10.3390/v16060943
dc.identifier.e-issn1999-4915
dc.identifier.journalViruses
dc.identifier.pubmedID38932235
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26561
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/779282/EU
dc.relation.publisherversionhttps://doi.org/10.3390/v16060943
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)
dc.repisalud.institucionISCIII
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectRSV
dc.subjectFusion protein
dc.subjectMolecular epidemiology
dc.subjectRespiratory infections
dc.subjectRespiratory viruses
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshCOVID-19
dc.subject.meshFemale
dc.subject.meshGermany
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshMolecular Epidemiology
dc.subject.meshPhylogeny
dc.subject.meshRespiratory Syncytial Virus Infections
dc.subject.meshRespiratory Syncytial Virus, Human
dc.subject.meshRespiratory Tract Infections
dc.subject.meshSARS-CoV-2
dc.subject.meshSeasons
dc.subject.meshTertiary Care Centers
dc.subject.meshViral Fusion Proteins
dc.subject.meshYoung Adult
dc.titleRespiratory Syncytial Virus in Adult Patients at a Tertiary Care Hospital in Germany: Clinical Features and Molecular Epidemiology of the Fusion Protein in the Severe Respiratory Season of 2022/2023
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscoverycdaece7c-45bc-4988-bb11-429e0b25402b
relation.isPublisherOfPublication30293a55-0e53-431f-ae8c-14ab01127be9
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Table S1: Primers used for RSV (F gene) sequencing, Table S2: Reagent composition for RSV-A sequencing (first PCR), Table S3: Reagent composition for RSV-B sequencing (first PCR), Table S4: Cycling conditions for RSV sequencing (first PCR), Table S5: Reagent composition for RSV-A sequencing (nested PCR), Table S6: Reagent composition for RSV-B sequencing (nested PCR), Table S7: Cycling conditions for RSV sequencing (nested PCR), Table S8: RSV-A reference sequences by Goya et al., Table S9: RSV-B reference sequences by Goya et al., Table S10: Amino acid residues of antigenic sites Ø–V, Table S11: Co-infecting pathogens, Table S12: Study population and clinical features of RSV cases in the 2021/2022 and 2022/2023 seasons, Figure S1: Molecular phylogenetic analysis of the RSV-A F gene by the maximum likelihood method, Figure S2: Molecular phylogenetic analysis of the RSV-B F gene by the maximum likelihood method.