Re-examination of nepovirus polyprotein cleavage sites highlights the diverse specificities and evolutionary relationships of nepovirus 3C-like proteases

• Published in: Archives of virology Vol. 167; no. 12; pp. 2529 - 2543
• Main Author: Sanfaçon, Hélène
• Format: Journal Article
• Language: English
• Published: Vienna Springer Vienna 01.12.2022; Springer Nature B.V
• Subjects: Amino acids; Biomedical and Life Sciences; Biomedicine; Endopeptidases - genetics; Genomes; Infectious Diseases; Medical Microbiology; Nepovirus - genetics; Original; Original Article; Peptide Hydrolases - genetics; Peptide Hydrolases - metabolism; Phylogenetics; Phylogeny; Polyproteins; Polyproteins - chemistry; Proteinase; Proteins; RNA polymerase; RNA viruses; RNA, Viral - chemistry; RNA, Viral - genetics; Secoviridae - genetics; Taxonomy; Viral Proteins - metabolism; Virology; Viruses
• ISSN: 0304-8608; 1432-8798
• DOI: 10.1007/s00705-022-05564-x

Plant-infecting viruses of the genus Nepovirus (subfamily Comovirinae , family Secoviridae , order Picornavirales ) are bipartite positive-strand RNA viruses with each genomic RNA encoding a single large polyprotein. The RNA1-encoded 3C-like protease cleaves the RNA1 polyprotein at five sites and the RNA2 polyprotein at two or three sites, depending on the nepovirus. The specificity of nepovirus 3C-like proteases is notoriously diverse, making the prediction of cleavage sites difficult. In this study, the position of nepovirus cleavage sites was systematically re-evaluated using alignments of the RNA1 and RNA2 polyproteins, phylogenetic relationships of the proteases, and sequence logos to examine specific preferences for the P6 to P1’ positions of the cleavage sites. Based on these analyses, the positions of previously elusive cleavage sites, notably the 2a-MP cleavage sites of subgroup B nepoviruses, are now proposed. Distinct nepovirus protease clades were identified, each with different cleavage site specificities, mostly determined by the nature of the amino acid at the P1 and P1’ positions of the cleavage sites, as well as the P2 and P4 positions. The results will assist the prediction of cleavage sites for new nepoviruses and help refine the taxonomy of nepoviruses. An improved understanding of the specificity of nepovirus 3C-like proteases can also be used to investigate the cleavage of plant proteins by nepovirus proteases and to understand their adaptation to a broad range of hosts.