tetano
Editor, Senior Moderator
Virus Res
. 2020 Sep 23;198170.
doi: 10.1016/j.virusres.2020.198170. Online ahead of print.
Signal hotspot mutations in SARS-CoV-2 genomes evolve as the virus spreads and actively replicates in different parts of the world
Stefanie Weber[SUP] 1 [/SUP], Christina Ramirez[SUP] 2 [/SUP], Walter Doerfler[SUP] 3 [/SUP]
Affiliations
Abstract
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) was first identified in Wuhan, China late in 2019. Nine months later (Sept. 18, 2020), the virus has infected > 30 million people world-wide and caused > 944.000 (3.15 %) fatalities in 220 countries and territories. Research on the genetics of the SARS-CoV-2 genome, its mutants and their penetrance can aid future defense strategies. By analyzing sequence data deposited between December 2019 and end of May 2020, we have compared nucleotide sequences of 570 SARS-CoV-2 genomes from China, Europe, the US, and India to the sequence of the Wuhan isolate. During world-wide spreading among human populations, at least 10 distinct hotspot mutations had been selected and found in up to > 80 % of viral genomes. Many of these mutations led to amino acid exchanges in replication-relevant viral proteins. Mutations in the SARS-CoV-2 genome would also impinge upon the secondary structure of the viral RNA molecule and its repertoire of interactions with essential cellular and viral proteins. The increasing frequency of SARS-CoV-2 mutation hotspots might select for dangerous viral pathogens. Alternatively, in a 29.900 nucleotide-genome, there might be a limit to the number of mutable and selectable sites which, when exhausted, could prove disadvantageous to viral survival. The speed, at which novel SARS-CoV-2 mutants are selected and dispersed around the world, could pose problems for the development of vaccines and therapeutics.
Keywords: Consequences for secondary and tertiary structures of viral RNA; Impact on replication-relevant viral proteins; Questions about immunogenesis and vaccine development; Selection of viral hotspot mutations; Sequence comparisons between 570 viral genomes to Wuhan isolate; Severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2).
. 2020 Sep 23;198170.
doi: 10.1016/j.virusres.2020.198170. Online ahead of print.
Signal hotspot mutations in SARS-CoV-2 genomes evolve as the virus spreads and actively replicates in different parts of the world
Stefanie Weber[SUP] 1 [/SUP], Christina Ramirez[SUP] 2 [/SUP], Walter Doerfler[SUP] 3 [/SUP]
Affiliations
- PMID: 32979477
- DOI: 10.1016/j.virusres.2020.198170
Abstract
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) was first identified in Wuhan, China late in 2019. Nine months later (Sept. 18, 2020), the virus has infected > 30 million people world-wide and caused > 944.000 (3.15 %) fatalities in 220 countries and territories. Research on the genetics of the SARS-CoV-2 genome, its mutants and their penetrance can aid future defense strategies. By analyzing sequence data deposited between December 2019 and end of May 2020, we have compared nucleotide sequences of 570 SARS-CoV-2 genomes from China, Europe, the US, and India to the sequence of the Wuhan isolate. During world-wide spreading among human populations, at least 10 distinct hotspot mutations had been selected and found in up to > 80 % of viral genomes. Many of these mutations led to amino acid exchanges in replication-relevant viral proteins. Mutations in the SARS-CoV-2 genome would also impinge upon the secondary structure of the viral RNA molecule and its repertoire of interactions with essential cellular and viral proteins. The increasing frequency of SARS-CoV-2 mutation hotspots might select for dangerous viral pathogens. Alternatively, in a 29.900 nucleotide-genome, there might be a limit to the number of mutable and selectable sites which, when exhausted, could prove disadvantageous to viral survival. The speed, at which novel SARS-CoV-2 mutants are selected and dispersed around the world, could pose problems for the development of vaccines and therapeutics.
Keywords: Consequences for secondary and tertiary structures of viral RNA; Impact on replication-relevant viral proteins; Questions about immunogenesis and vaccine development; Selection of viral hotspot mutations; Sequence comparisons between 570 viral genomes to Wuhan isolate; Severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2).