Bayesian reconstruction of SARS-CoV-2 transmissions highlights substantial proportion of negative serial intervals

The serial interval is a key epidemiological measure that quantifies the time between the onset of symptoms in an infector-infectee pair. It indicates how quickly new generations of cases appear, thus informing on the speed of an epidemic. Estimating the serial interval requires to identify pairs of...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Epidemics 2023-09, Vol.44, p.100713-100713, Article 100713
Hauptverfasser: Geismar, Cyril, Nguyen, Vincent, Fragaszy, Ellen, Shrotri, Madhumita, Navaratnam, Annalan M.D., Beale, Sarah, Byrne, Thomas E., Fong, Wing Lam Erica, Yavlinsky, Alexei, Kovar, Jana, Hoskins, Susan, Braithwaite, Isobel, Aldridge, Robert W., Hayward, Andrew C., White, Peter J., Jombart, Thibaut, Cori, Anne
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The serial interval is a key epidemiological measure that quantifies the time between the onset of symptoms in an infector-infectee pair. It indicates how quickly new generations of cases appear, thus informing on the speed of an epidemic. Estimating the serial interval requires to identify pairs of infectors and infectees. Yet, most studies fail to assess the direction of transmission between cases and assume that the order of infections - and thus transmissions - strictly follows the order of symptom onsets, thereby imposing serial intervals to be positive. Because of the long and highly variable incubation period of SARS-CoV-2, this may not always be true (i.e an infectee may show symptoms before their infector) and negative serial intervals may occur. This study aims to estimate the serial interval of different SARS-CoV-2 variants whilst accounting for negative serial intervals. This analysis included 5 842 symptomatic individuals with confirmed SARS-CoV-2 infection amongst 2 579 households from September 2020 to August 2022 across England & Wales. We used a Bayesian framework to infer who infected whom by exploring all transmission trees compatible with the observed dates of symptoms, based on a wide range of incubation period and generation time distributions compatible with estimates reported in the literature. Serial intervals were derived from the reconstructed transmission pairs, stratified by variants. We estimated that 22% (95% credible interval (CrI) 8–32%) of serial interval values are negative across all VOC. The mean serial interval was shortest for Omicron BA5 (2.02 days, 1.26–2.84) and longest for Alpha (3.37 days, 2.52–4.04). This study highlights the large proportion of negative serial intervals across SARS-CoV-2 variants. Because the serial interval is widely used to estimate transmissibility and forecast cases, these results may have critical implications for epidemic control. [Display omitted] •This study reconstructed transmission chains from thousands of cases in the UK.•1 in 5 transmission events had negative SI.•The SI was characterised for all major SARS-CoV-2 VOCs.•The SARS-COV-2 SI consistently shortened since the Alpha variant.
ISSN:1755-4365
1878-0067
DOI:10.1016/j.epidem.2023.100713