4.6 Article

Evaluation of SARS-CoV-2 ORF7a Deletions from COVID-19-Positive Individuals and Its Impact on Virus Spread in Cell Culture

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VIRUSES-BASEL
卷 15, 期 3, 页码 -

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MDPI
DOI: 10.3390/v15030801

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SARS-CoV-2; ORF7a; COVID-19; sgRNAs; viral fitness; B; 1; 33 lineage

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This study investigates the presence of SARS-CoV-2 ORF7a deletions in COVID-19-positive individuals. It identifies three different sizes of ORF7a deletions, which do not affect subgenomic RNA production downstream of ORF7a but result in decreased sizes of fragments associated with genes upstream of ORF7a. In silico analysis suggests that these deletions impair protein function and isolated viruses with partial ORF7a deletion exhibit reduced infectious particles after 48 hours.
The spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), causing the COVID-19 outbreak, posed a primary concern of public health worldwide. The most common changes in SARS-CoV-2 are single nucleotide substitutions, also reported insertions and deletions. This work investigates the presence of SARS-CoV-2 ORF7a deletions identified in COVID-19-positive individuals. Sequencing of SARS-CoV-2 complete genomes showed three different ORF7a size deletions (190-nt, 339-nt and 365-nt). Deletions were confirmed through Sanger sequencing. The ORF7a increment 190 was detected in a group of five relatives with mild symptoms of COVID-19, and the ORF7a increment 339 and ORF7a increment 365 in a couple of co-workers. These deletions did not affect subgenomic RNAs (sgRNA) production downstream of ORF7a. Still, fragments associated with sgRNA of genes upstream of ORF7a showed a decrease in size when corresponding to samples with deletions. In silico analysis suggests that the deletions impair protein proper function; however, isolated viruses with partial deletion of ORF7a can replicate in culture cells similarly to wild-type viruses at 24 hpi, but with less infectious particles after 48 hpi. These findings on deleted ORF7a accessory protein gene, contribute to understanding SARS-CoV-2 phenotypes such as replication, immune evasion and evolutionary fitness as well insights into the role of SARS-CoV-2_ORF7a in the mechanism of virus-host interactions.

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