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Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021.
Payen, Shannon Harger; Gorzalski, Andrew; Siao, Danielle Denise; Pandori, Mark; Verma, Subhash C; Rossetto, Cyprian C.
  • Payen SH; Department of Microbiology & Immunology, University of Nevada, Reno, 1664 North Virginia St. MS 320 Reno, NV 89557, USA; School of Medicine, University of Nevada, Reno, 1664 North Virginia St., Reno, NV 89557, USA.
  • Gorzalski A; Nevada State Public Health Laboratory, 1664 North Virginia St., Reno, NV 89557, USA.
  • Siao DD; Nevada State Public Health Laboratory, 1664 North Virginia St., Reno, NV 89557, USA.
  • Pandori M; School of Medicine, University of Nevada, Reno, 1664 North Virginia St., Reno, NV 89557, USA; Nevada State Public Health Laboratory, 1664 North Virginia St., Reno, NV 89557, USA.
  • Verma SC; Department of Microbiology & Immunology, University of Nevada, Reno, 1664 North Virginia St. MS 320 Reno, NV 89557, USA; School of Medicine, University of Nevada, Reno, 1664 North Virginia St., Reno, NV 89557, USA.
  • Rossetto CC; Department of Microbiology & Immunology, University of Nevada, Reno, 1664 North Virginia St. MS 320 Reno, NV 89557, USA; School of Medicine, University of Nevada, Reno, 1664 North Virginia St., Reno, NV 89557, USA. Electronic address: crossetto@med.unr.edu.
Infect Genet Evol ; 111: 105434, 2023 07.
Article in English | MEDLINE | ID: covidwho-2301622
ABSTRACT
In early 2020, the emergence and spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the human population quickly developed into a global pandemic. SARS-CoV-2 is the etiological agent of coronavirus disease 2019 (COVID-19) which has a broad range of respiratory illnesses. As the virus circulates, it acquires nucleotide changes. These mutations are potentially due to the inherent differences in the selection pressures within the human population compared to the original zoonotic reservoir of SARS-CoV-2 and formerly naïve humans. The acquired mutations will most likely be neutral, but some may have implications for viral transmission, disease severity, and resistance to therapies or vaccines. This is a follow-up study from our early report (Hartley et al. J Genet Genomics. 01202021;48(1)40-51) which detected a rare variant (nsp12, RdRp P323F) circulating within Nevada in mid 2020 at high frequency. The primary goals of the current study were to determine the phylogenetic relationship of the SARS-CoV-2 genomes within Nevada and to determine if there are any unusual variants within Nevada compared to the current database of SARS-CoV-2 sequences. Whole genome sequencing and analysis of SARS-CoV-2 from 425 positively identified nasopharyngeal/nasal swab specimens were performed from October 2020 to August 2021 to determine any variants that could result in potential escape from current therapeutics. Our analysis focused on nucleotide mutations that generated amino acid variations in the viral Spike (S) protein, Receptor binding domain (RBD), and the RNA-dependent RNA-polymerase (RdRp) complex. The data indicate that SARS-CoV-2 sequences from Nevada did not contain any unusual variants that had not been previously reported. Additionally, we did not detect the previously identified the RdRp P323F variant in any of the samples. This suggests that the rare variant we detected before was only able to circulate because of the stay-at-home orders and semi-isolation experience during the early months of the pandemic. IMPORTANCE SARS-COV-2 continues to circulate in the human population. In this study, SARS-CoV-2 positive nasopharyngeal/nasal swab samples were used for whole genome sequencing to determine the phylogenetic relationship of SARS-CoV-2 sequences within Nevada from October 2020 to August 2021. The resulting data is being added to a continually growing database of SARS-CoV-2 sequences that will be important for understanding the transmission and evolution of the virus as it spreads around the globe.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Etiology study / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2023 Document Type: Article Affiliation country: J.meegid.2023.105434

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Etiology study / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2023 Document Type: Article Affiliation country: J.meegid.2023.105434