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Early unrecognised SARS-CoV-2 introductions shaped the first pandemic wave, Sweden, 2020
Department of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Institute for Social and Preventive Medicine, University of Bern, Bern, Switzerland; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
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2024 (English)In: Eurosurveillance, ISSN 1025-496X, E-ISSN 1560-7917, Vol. 29, no 41, article id 2400021Article in journal (Refereed) Published
Abstract [en]

Background: Despite the unprecedented measures implemented globally in early 2020 to prevent the spread of SARS-CoV-2, Sweden, as many other countries, experienced a severe first wave during the COVID-19 pandemic.

Aim: We investigated the introduction and spread of SARS-CoV-2 into Sweden.MethodsWe analysed stored respiratory specimens (n = 1,979), sampled 7 February-2 April 2020, by PCR for SARS-CoV-2 and sequenced PCR-positive specimens. Sequences generated from newly detected cases and stored positive specimens February-June 2020 (n = 954) were combined with sequences (Sweden: n = 730; other countries: n = 129,913) retrieved from other sources for Nextstrain clade assignment and phylogenetic analyses.

Results: Twelve previously unrecognised SARS-CoV-2 cases were identified: the earliest was sampled on 3 March, 1 week before recognised community transmission. We showed an early influx of clades 20A and 20B from Italy (201/328, 61% of cases exposed abroad) and clades 19A and 20C from Austria (61/328, 19%). Clade 20C dominated the first wave (20C: 908/1,684, 54%; 20B: 438/1,684, 26%; 20A: 263/1,684, 16%), and 800 of 1,684 (48%) Swedish sequences formed a country-specific 20C cluster defined by a spike mutation (G24368T). At the regional level, the proportion of clade 20C sequences correlated with an earlier weighted mean date of COVID-19 deaths.

Conclusion: Community transmission in Sweden started when mitigation efforts still focused on preventing influx. This created a transmission advantage for clade 20C, likely introduced from ongoing cryptic spread in Austria. Therefore, pandemic preparedness should have a comprehensive approach, including capacity for large-scale diagnostics to allow early detection of travel-related cases and community transmission.

Place, publisher, year, edition, pages
European Centre for Disease Prevention and Control , 2024. Vol. 29, no 41, article id 2400021
Keywords [en]
COVID-19 pandemic, SARS-CoV-2, epidemiology, phylogenetics, viral respiratory tract infection
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:oru:diva-116684DOI: 10.2807/1560-7917.ES.2024.29.41.2400021ISI: 001342391500003PubMedID: 39392000Scopus ID: 2-s2.0-85206041825OAI: oai:DiVA.org:oru-116684DiVA, id: diva2:1905174
Funder
Knut and Alice Wallenberg Foundation, 2020.0182Knut and Alice Wallenberg Foundation, 2020.0241Swedish Research Council, 2021-05045Swedish Research Council, 2021-06545Konung Gustaf V:s och Drottning Victorias Frimurarestiftelse
Note

Funding:

The sequencing in the study was partially funded by the Swedish Corona Commission appointed by the government and the Pandemic Preparedness programme, SciLifeLab (no. VC-2021-0033). Magnus Gisslén was supported by the Swedish state, under an agreement between the Swedish government and the regional councils (ALF agreement ALFGBG-965885); by SciLifeLab from the Knut and Alice Wallenberg Foundation (2020.0182 & 2020.0241); by the Swedish Research Council (2021-05045 & 2021-06545); and by King Gustaf V:s and Queen Victoria’s Foundation.

 

Available from: 2024-10-11 Created: 2024-10-11 Last updated: 2025-04-01Bibliographically approved

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