Knockdown of capsid protein encoding novel ATPase domain inhibits genome packaging in potato leafroll virus

• Published in: 3 Biotech 2022-03, Vol.12 (3), p.66-66, Article 66
• Main Authors: Kumar, Jitesh, Kumar, Ravi Ranjan, Das, Dilip Kumar, Mohanty, Auroshikha, Rajani, Kumari, Kumari, Namaste, Kumar, Vinod, Kumar, Sunil, Kumbhar, Bajarang Vasant, Ranjan, Tushar
• Format: Article
• Language: English
• Subjects: Adenosine triphosphatase; Agriculture; Assembly; Binding; Bioinformatics; Biomaterials; Biotechnology; Cancer Research; Capsid protein; Chemistry; Chemistry and Materials Science; CP gene; CP protein; Gene expression; Genomes; Molecular docking; Molecular machines; Original; Original Article; Packaging; Plant viruses; Polerovirus; Polypeptides; Potatoes; Protein composition; Proteins; RNA-mediated interference; siRNA; Solanum tuberosum; Stem Cells; Viruses
• ISSN: 2190-572X; 2190-5738
• DOI: 10.1007/s13205-021-03085-z

Potato leafroll virus (PLRV) uses powerful molecular machines to package its genome into a viral capsid employing ATP as fuel. Although, recent bioinformatics and structural studies have revealed detailed mechanism of DNA packaging, little is known about the mechanochemistry of genome packaging in small plant viruses such as PLRV. We have identified a novel P-loop-containing ATPase domain with two Walker A-like motifs, two arginine fingers, and two sensor motifs distributed throughout the polypeptide chain of PLRV capsid protein (CP). The composition and arrangement of the ATP binding and hydrolysis domain of PLRV CP is unique and rarely reported. The discovery of the system sheds new light on the mechanism of viral genome packaging, regulation of viral assembly process, and evolution of plant viruses. Here, we used the RNAi approach to suppress CP gene expression, which in turn prevented PLRV genome packaging and assembly in Solanum tuberosum cv. Khufri Ashoka. Potato plants agroinfiltrated with siRNA constructs against the CP with ATPase domain exhibited no rolling symptoms upon PLRV infection, indicating that the silencing of CP gene expression is an efficient method for generating PLRV-resistant potato plants. In addition, molecular docking study reveals that the PLRV CP protein has ATP-binding pocket at the interface of each monomer. This further confirms that knockdown of the CP harboring ATP-binding domain could hamper the process of viral genome packaging and assembly. Moreover, our findings provide a robust approach to generate PLRV-resistant potato plants, which can be further extended to other species. Finally, we propose a new mechanism of genome packaging and assembly in plant viruses.