Double-stranded RNA virus in Korean Isolate IH-2 of Trichomonas vaginalis

  • Kim, Jong-Wook (Department of Biochemistry, Inha Research Institute for Medical Sciences, College of Medicine, Inha University) ;
  • Chung, Pyung-Rim (Department of Parasitology College of Medicine, Inha University) ;
  • Hwang, Myung-Ki (Department of Parasitology College of Medicine, Inha University) ;
  • Choi, Eun-Young (Department of Biochemistry, College of Medicine, Inha University)
  • Published : 2007.06.30

Abstract

In this study, we describe Korean isolates of Trichomonas vaginalis infected with double-stranded (ds) RNA virus (TVV). One T. vaginalis isolate infected with TVV IH-2 evidenced weak pathogenicity in the mouse assay coupled with the persistent presence of a dsRNA, thereby indicating a hypovirulence effect of dsRNA in T. vaginalis. Cloning and sequence analysis results revealed that the genomic dsRNA of TVV IH-2 was 4,647 bp in length and evidenced a sequence identity of 80% with the previously-described TVV 1-1 and 1-5, but only a 42% identity with TVV 2-1 and 3 isolates. It harbored 2 overlapping open reading frames of the putative capsid protein and dsRNA-dependent RNA polymerase (RdRp). As previously observed in the TVV isolates 1-1 and 1-5, a conserved ribosomal slip-page heptamer (CCUUUUU) and its surrounding sequence context within the consensus 14-nt overlap implied the gene expression of a capsid protein-RdRp fusion protein, occurring as the result of a potential ribosomal frameshift event. The phylogenetic analysis of RdRp showed that the Korean TVV If-2 isolate formed a compact group with TVV 1-1 and 1-5 isolates, which was divergent from TVV 2-1, 3 and other viral isolates classified as members of the Giardiavirus genus.

Keywords

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