Characterization of a Novel Double-Stranded RNA Virus from Phytophthora pluvialis in New Zealand

• Published in: Viruses Vol. 14; no. 2; p. 247
• Main Authors: Xu, Zhi, Khalifa, Mahmoud E, Frampton, Rebekah A, Smith, Grant R, McDougal, Rebecca L, MacDiarmid, Robin M, Kalamorz, Falk
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26.01.2022; MDPI
• Subjects: Amino Acid Sequence; Amino acids; DNA-directed RNA polymerase; Double Stranded RNA Viruses - classification; Double Stranded RNA Viruses - genetics; Double-stranded RNA; dsRNA; Flowers & plants; Genome, Viral - genetics; Genomes; Genotype; Genotypes; Geographical distribution; New Zealand; Open Reading Frames; Pathogens; Phylogenetics; Phylogeny; Phytophthora - virology; Phytophthora pluvialis; qPCR; RNA polymerase; RNA viruses; RNA, Viral - genetics; RNA-Dependent RNA Polymerase - genetics; RNA-directed RNA polymerase; Species Specificity; virus; Viruses; New Zealand; St Louis Missouri; United States > US; New Zealand; dsRNA; Phytophthora pluvialis; qPCR; virus
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v14020247

A new dsRNA virus from the oomycete has been characterized and designated as Phytophthora pluvialis RNA virus 1 (PplRV1). The genome of the PplRV1 reference genome is 6742 bp that encodes two predicted open reading frames (ORFs). ORF1 and ORF2 overlap by a 47 nt "slippery" frameshift sequence. ORF1 encodes a putative protein of unknown function. ORF2 shows high similarity to the RNA-dependent RNA polymerase (RdRp) of other dsRNA viruses. Phylogenetic analysis of the putative PplRV1 RdRp and its most closely related viruses showed PplRV1 is distinct from other known viruses (below 33% amino acid similarity), which indicates this virus may belong to a new virus family. Analyses of the geographical distribution of PplRV1 in relation to two genetically distinct classes of its host revealed two corresponding genotypes of the PplRV1 (termed a and b), which share 92.3% nt identity. The reference genome for the second genotype is 6760 bp long and a prediction of its genetic organization shows three ORFs, with ORF2 being split into two ORFs, ORF2a and ORF2b, that is conserved in seven of eleven genotype b isolates. Additionally, a quick and simple diagnostic method using qPCR has been developed, which is suitable for large scale screens to identify PplRV1 in .