Pathogens (Jul 2022)

From Alpha to Delta—Genetic Epidemiology of SARS-CoV-2 (hCoV-19) in Southern Poland

  • Emilia Morawiec,
  • Maria Miklasińska-Majdanik,
  • Jolanta Bratosiewicz-Wąsik,
  • Robert D. Wojtyczka,
  • Denis Swolana,
  • Ireneusz Stolarek,
  • Michał Czerwiński,
  • Aleksandra Skubis-Sikora,
  • Magdalena Samul,
  • Agnieszka Polak,
  • Celina Kruszniewska-Rajs,
  • Adam Pudełko,
  • Marek Figlerowicz,
  • Anna Bednarska-Czerwińska,
  • Tomasz J. Wąsik

DOI
https://doi.org/10.3390/pathogens11070780
Journal volume & issue
Vol. 11, no. 7
p. 780

Abstract

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In Poland, the first case of SARS-CoV-2 infection was confirmed in March 2020. Since then, many circulating virus lineages fueled rapid pandemic waves which inflicted a severe burden on the Polish healthcare system. Some of these lineages were associated with increased transmissibility and immune escape. Mutations in the viral spike protein, which is responsible for host cell recognition and serves as the primary target for neutralizing antibodies, are of particular importance. We investigated the molecular epidemiology of the SARS-CoV-2 clades circulating in Southern Poland from February 2021 to August 2021. The 921 whole-genome sequences were used for variant identification, spike mutation, and phylogenetic analyses. The Pango B.1.1.7 was the dominant variant (n = 730, 89.68%) from March 2021 to July 2021. In July 2021, the B.1.1.7 was displaced by the B.1.617.2 lineage with 66.66% in July 2021 and 92.3% in August 2021 frequencies, respectively. Moreover, our results were compared with the sequencing available on the GISAID platform for other regions of Poland, the Czech Republic, and Slovakia. The analysis showed that the dominant variant in the analyzed period was B.1.1.7 in all countries and Southern Poland (Silesia). Interestingly, B.1.1.7 was replaced by B.1.617.2 earlier in Southern Poland than in the rest of the country. Moreover, in the Czech Republic and Slovakia, AY lineages were predominant at that time, contrary to the Silesia region.

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