Abstract

A total of 101 papaya ringspot virus-W (PRSV-W) isolates were collected from five different cucurbit hosts in six counties of Oklahoma during the 2016–2018 growing seasons. The coat protein (CP) coding region of these isolates was amplified by reverse transcription-polymerase chain reaction, and 370 clones (3–5 clones/isolate) were sequenced. Phylogenetic analysis revealed three phylogroups while host, location, and collection time of isolates had minimal impact on grouping pattern. When CP gene sequences of these isolates were compared with sequences of published PRSV isolates (both P and W strains), they clustered into four phylogroups based on geographical location. Oklahoman PRSV-W isolates formed one of the four distinct major phylogroups. The permutation-based tests, including Ks, Ks *, Z *, Snn, and neutrality tests, indicated significant genetic differentiation and polymorphisms among PRSV-W populations in Oklahoma. The selection analysis confirmed that the CP gene is undergoing purifying selection. The mutation frequencies among all PRSV-W isolates were within the range of 1 × 10−3. The substitution mutations in 370 clones of PRSV-W isolates showed a high proportion of transition mutations, which gave rise to higher GC content. The N-terminal region of the CP gene mostly contained the variable sites with numerous mutational hotspots, while the core region was highly conserved.

Highlights

  • Papaya ringspot virus (PRSV), a single-stranded, positive-sense RNA virus, belongs to the family Potyviridae and genus Potyvirus

  • We evaluated mutation frequency and its pattern within individual clones of papaya ringspot virus-W (PRSV-W) isolates collected from different regions of Oklahoma

  • The complete coat protein (CP) gene of these isolates was amplified by reverse transcription-polymerase chain reaction (RT-PCR), and the expected size DNA bands were gel-purified

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Summary

Introduction

Papaya ringspot virus (PRSV), a single-stranded, positive-sense RNA virus, belongs to the family Potyviridae and genus Potyvirus. The site-directed mutagenesis study in recombinant viruses showed that lysine amino acid (aa) at position 27 in NIa-Pro determines the host specificity in PRSV-P, as a single aa change at that position from lysine to aspartic acid can change the host range of PRSV-P to non-papaya-infecting [4]. PRSV particles are non-enveloped, flexuous, and filamentous rods about 680–900 nm in length and 12–15 nm in diameter. They are transmitted by several aphid species in a non-persistent, non-circulative manner [5,6]. PRSV has a linear single-stranded and positive-sense RNA (+ssRNA) genome that is approximately

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