ABSTRACT
RNA-targeting compounds or small interfering RNAs (siRNAs) offer a potent means for controlling viral infections. An essential prerequisite to their design depends on identifying conserved and functional viral RNA structures in cells. Techniques that probe RNA structures in situ have been developed recently including SHAPE-MaP, which has been helpful in analyzing the secondary structures of RNA. In this study, we report on the application of SHAPE-MaP to the Porcine Epidemic Diarrhoea Virus (PEDV) RNA genome to categorize different functional regions including potential quadruplex forming sequence and target sites of small interfering RNA (siRNA). Our results show that these structures can be exploited to inhibit viral proliferation and that SHAPE-MaP is an effective method to the identification of secondary structures in RNA genomes.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Section on Methods including 'SHAPE-MaP data analysis', 'PEDV RNA secondary structure modeling guided by SHAPE data', 'Identification of low SHAPE-high Shannon regions', 'Identification of high SHAPE-low Shannon regions', 'Determination of the antiviral activity of Braco-19 against PEDV by RT-qPCR' were updated with detailed descriptions and references added.