The Spread of SARS-CoV-2 Omicron Variant in CALABRIA: A Spatio-Temporal Report of Viral Genome Evolution

Author:

Veneziano Claudia12,Marascio Nadia3ORCID,De Marco Carmela12ORCID,Quaresima Barbara12ORCID,Biamonte Flavia12ORCID,Trecarichi Enrico Maria45ORCID,Santamaria Gianluca1ORCID,Quirino Angela35,Torella Daniele15ORCID,Quattrone Aldo6,Matera Giovanni35,Torti Carlo45ORCID,De Filippo Caterina5,Costanzo Francesco Saverio125ORCID,Viglietto Giuseppe15

Affiliation:

1. Department of Experimental and Clinical Medicine, “Magna Graecia” University of Catanzaro, 88100 Catanzaro, Italy

2. Interdepartmental Center of Services (CIS), Molecular Genomics and Pathology, “Magna Græcia” University of Catanzaro, 88100 Catanzaro, Italy

3. Department of Health Sciences, “Magna Graecia” University of Catanzaro, 88100 Catanzaro, Italy

4. Department of Medical and Surgical Sciences, “Magna Graecia” University of Catanzaro, 88100 Catanzaro, Italy

5. “Mater Domini” University Hospital of Catanzaro, 88100 Catanzaro, Italy

6. Neuroscience Research Center, “Magna Graecia” University of Catanzaro, 88100 Catanzaro, Italy

Abstract

We investigated the evolution of SARS-CoV-2 spread in Calabria, Southern Italy, in 2022. A total of 272 RNA isolates from nasopharyngeal swabs of individuals infected with SARS-CoV-2 were sequenced by whole genome sequencing (N = 172) and/or Sanger sequencing (N = 100). Analysis of diffusion of Omicron variants in Calabria revealed the prevalence of 10 different sub-lineages (recombinant BA.1/BA.2, BA.1, BA.1.1, BA.2, BA.2.9, BA.2.10, BA.2.12.1, BA.4, BA.5, BE.1). We observed that Omicron spread in Calabria presented a similar trend as in Italy, with some notable exceptions: BA.1 disappeared in April in Calabria but not in the rest of Italy; recombinant BA.1/BA.2 showed higher frequency in Calabria (13%) than in the rest of Italy (0.02%); BA.2.9, BA.4 and BA.5 emerged in Calabria later than in other Italian regions. In addition, Calabria Omicron presented 16 non-canonical mutations in the S protein and 151 non-canonical mutations in non-structural proteins. Most non-canonical mutations in the S protein occurred mainly in BA.5 whereas non-canonical mutations in non-structural or accessory proteins (ORF1ab, ORF3a, ORF8 and N) were identified in BA.2 and BA.5 sub-lineages. In conclusion, the data reported here underscore the importance of monitoring the entire SARS-CoV-2 genome.

Funder

University Magna Graecia, Department of Experimental and Clinical Medicine

Interdepartmental Center of Services (CIS), Molecular Genomics and Pathology, Magna Græcia University of Catanzaro, Italy

Regione Calabria

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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