Abstract
The first case of SARS-CoV-2 in Basel, Switzerland was detected on February 26th 2020. We present a phylogenetic study to explore viral introduction and evolution during the exponential early phase of the local COVID-19 outbreak from February 26th until March 23rd. We sequenced SARS-CoV-2 naso-oropharyngeal swabs from 746 positive tests that were performed at the University Hospital Basel during the study period. We successfully generated 468 high quality genomes from unique patients and called variants with our COVID-19 Pipeline (COVGAP), and analysed viral genetic diversity using PANGOLIN taxonomic lineages. To identify introduction and dissemination events we incorporated global SARS-CoV-2 genomes and inferred a time-calibrated phylogeny. Epidemiological data from patient questionnaires was used to facilitate the interpretation of phylogenetic observations. The early outbreak in Basel was dominated by lineage B.1 (83·6%), detected first on March 2nd, although the first sample identified belonged to B.1.1. Within B.1, 68·2% of our samples fall within a clade defined by the SNP C15324T (‘Basel cluster’), including 157 identical sequences at the root of the ‘Basel cluster’, some of which we can specifically trace to regional spreading events. We infer the origin of B.1-C15324T to mid-February in our tri-national region. The other genomes map broadly over the global phylogenetic tree, showing several introduction events from and/or dissemination to other regions of the world via travellers. Family transmissions can also be traced in our data. A single lineage variant dominated the outbreak in the Basel area while other lineages, such as the first (B.1.1), did not propagate. A mass gathering event was the predominant initial source of cases, with travel returners and family transmissions to a lesser extent. We highlight the importance of adding specific questions to epidemiological questionnaires, to obtain data on attendance of large gatherings and their locations, as well as travel history, to effectively identify routes of transmissions in up-coming outbreaks. This phylogenetic analysis in concert with epidemiological and contact tracing data, allows connection and interpretation of events, and can inform public health interventions.Trial Registration: ClinicalTrials.gov NCT04351503.
Highlights
The COVID-19 pandemic rapidly spread around the globe during the first six months of 2020
COVID-19 was first reported in December 2019 in Wuhan, China, and has spread around the globe since
The most common tool for tracking and containing the spread of the disease-causing virus–SARS-CoV-2 –are classical epidemiology and contact tracing, which collapse under too high case burdens as seen in this pandemic
Summary
The COVID-19 pandemic rapidly spread around the globe during the first six months of 2020. Due to the accumulation of mutations, phylogenetic analysis of SARS-CoV-2 is becoming more granular over time [14], providing increasing resolution of transmission dynamics and events. The first sample within the Basel cluster, from March 2nd, was from a patient residing in Central Switzerland, who was transferred to a care facility in Basel-City where six further people tested positive between March 5th and March 17th with identical viral genomes. The second sample within the Basel cluster was from a patient diagnosed on March 3rd, who had attended a religious event in Alsace, France, that took place between February 17th and 21st. One other patient, who tested positive on March 9th but had symptoms 14 days prior to testing, had an identical viral genome and had attended this event. Several other positively tested patients, from whom we could not successfully sequence virus genomes, attended this event
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