Introduction and Characteristics of SARS-CoV-2 in North-East of Romania During the First COVID-19 Outbreak

• Published in: Frontiers in microbiology Vol. 12; p. 654417
• Main Authors: Lobiuc, Andrei, Dimian, Mihai, Gheorghita, Roxana, Sturdza, Olga Adriana Caliman, Covasa, Mihai
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 07-07-2021
• Subjects: coronavirus; Microbiology; mutations; NSP3; ORF7; phylogeny; routes
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2021.654417

Romania officially declared its first Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) case on February 26, 2020. The first and largest coronavirus disease 2019 (COVID-19) outbreak in Romania was recorded in Suceava, North-East region of the country, and originated at the Suceava regional county hospital. Following sheltering-in-place measures, infection rates decreased, only to rise again after relaxation of measures. This study describes the spread of SARS-CoV-2 in Suceava and other parts of Romania and analyses the mutations and their association with clinical manifestation of the disease during the period of COVID-19 outbreak. Sixty-two samples were sequenced
via
high-throughput platform and screened for variants. For selected mutations, putative biological significance was assessed, and their effects on disease severity. Phylogenetic analysis was conducted on Romanian genomes (
n
= 112) and on sequences originating from Europe, United Kingdom, Africa, Asia, South, and North America (
n
= 876). The results indicated multiple introduction events for SARS-CoV-2 in Suceava, mainly from Italy, Spain, United Kingdom, and Russia although some sequences were also related to those from the Czechia, Belgium, and France. Most Suceava genomes contained mutations common to European lineages, such as A20268G, however, approximately 10% of samples were missing such mutations, indicating a possible different arrival route. While overall genome regions ORF1ab, S, and ORF7 were subject to most mutations, several recurring mutations such as A105V were identified, and these were mainly present in severe forms of the disease. Non-synonymous mutations, such as T987N (Thr987Asn in NSP3a domain), associated with changes in a protein responsible for decreasing viral tethering in human host were also present. Patients with diabetes and hypertension exhibited higher risk ratios (RR) of acquiring severe forms of the disease and these were mainly related to A105V mutation. This study identified the arrival routes of SARS-CoV-2 in Romania and revealed potential associations between the SARS-CoV-2 genomic organization circulating in the country and the clinical manifestation of COVID-19 disease.