| Literature DB >> 33229462 |
Alexandra Popa1, Jakob-Wendelin Genger1, Michael D Nicholson2,3,4, Thomas Penz1, Daniela Schmid5, Stephan W Aberle6, Benedikt Agerer1, Alexander Lercher1, Lukas Endler7, Henrique Colaço1, Mark Smyth1, Michael Schuster1, Miguel L Grau8, Francisco Martínez-Jiménez8, Oriol Pich8, Wegene Borena9, Erich Pawelka10, Zsofia Keszei1, Martin Senekowitsch1, Jan Laine1, Judith H Aberle6, Monika Redlberger-Fritz6, Mario Karolyi10, Alexander Zoufaly10, Sabine Maritschnik5, Martin Borkovec5, Peter Hufnagl5, Manfred Nairz11, Günter Weiss11, Michael T Wolfinger12,13, Dorothee von Laer9, Giulio Superti-Furga1,14, Nuria Lopez-Bigas8,15, Elisabeth Puchhammer-Stöckl6, Franz Allerberger5, Franziska Michor2,3,4,16,17,18, Christoph Bock1,19, Andreas Bergthaler20.
Abstract
Superspreading events shaped the coronavirus disease 2019 (COVID-19) pandemic, and their rapid identification and containment are essential for disease control. Here, we provide a national-scale analysis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) superspreading during the first wave of infections in Austria, a country that played a major role in initial virus transmissions in Europe. Capitalizing on Austria's well-developed epidemiological surveillance system, we identified major SARS-CoV-2 clusters during the first wave of infections and performed deep whole-genome sequencing of more than 500 virus samples. Phylogenetic-epidemiological analysis enabled the reconstruction of superspreading events and charts a map of tourism-related viral spread originating from Austria in spring 2020. Moreover, we exploited epidemiologically well-defined clusters to quantify SARS-CoV-2 mutational dynamics, including the observation of low-frequency mutations that progressed to fixation within the infection chain. Time-resolved virus sequencing unveiled viral mutation dynamics within individuals with COVID-19, and epidemiologically validated infector-infectee pairs enabled us to determine an average transmission bottleneck size of 103 SARS-CoV-2 particles. In conclusion, this study illustrates the power of combining epidemiological analysis with deep viral genome sequencing to unravel the spread of SARS-CoV-2 and to gain fundamental insights into mutational dynamics and transmission properties.Entities:
Year: 2020 PMID: 33229462 DOI: 10.1126/scitranslmed.abe2555
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956