Key result
SARS-CoV-2 subgenomic RNAs and encoded proteins drive viral replication, immune evasion, and COVID-19 pathogenesis.
Why the study?
A comprehensive understanding of the molecular virological events and immunological features during SARS-CoV-2 replication is needed to provide targets for vaccine and drug development.
Understanding the characteristics and functions of SARS-CoV-2 subgenomic RNAs provides potential targets for vaccine and drug development.
May identify new targets for COVID-19 vaccines and antivirals; leaves open the need for clinical validation before therapeutic adoption.
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is currently widespread throughout the world, accompanied by a rising number of people infected and breakthrough infection of variants, which make the virus highly transmissible and replicable. A comprehensive understanding of the molecular virological events and induced immunological features during SARS-CoV-2 replication can provide reliable targets for vaccine and drug development. Among the potential targets, subgenomic RNAs and their encoded proteins involved in the life cycle of SARS-CoV-2 are extremely important in viral duplication and pathogenesis. Subgenomic RNAs employ a range of coping strategies to evade immune surveillance from replication to translation, which allows RNAs to synthesize quickly, encode structural proteins efficiently and complete the entire process of virus replication and assembly successfully. This review focuses on the characteristics and functions of SARS-CoV-2 subgenomic RNAs and their encoded proteins and explores in depth the role of subgenomic RNAs in the replication and infection of host cells to provide important clues to the mechanism of COVID-19 pathogenesis.
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Zhang et al. (2022) conducted a review in COVID-19. SARS-CoV-2 subgenomic RNAs was evaluated. SARS-CoV-2 subgenomic RNAs and their encoded proteins play a crucial role in viral replication, evasion of immune surveillance, and COVID-19 pathogenesis.
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