Background: Potyviridae is the largest plant infecting family under the monophyletic group Riboviria, infects many of the food, fodder and ornamental crops. Due to the higher mutation and recombination rate, potyvirids are evolving rapidly, adapting to the environmental chaos and expanding their hosts. Virus control measures are need to be updated as the economic importance of potyvirids is massive. microRNAs (miRNAs) are well known for their functional importance in eukaryotes and many viruses. Regardless of its biogenesis, whether canonical or noncanonical, microRNA centric antivirus approaches attract the researchers to the hopeful future of nextgeneration broad-spectrum antiviral measures. Methods: In this study, we predicted and screened banana bract mosaic virus (BBrMV) encoding miRNAs by computation approaches and their targets on banana transcriptome using plant small RNA target analysis server (psRNAtarget). The target gene functions were annotated by Blast2GO. The predicted BBrMV miRNAs were experimentally screened by stem-loop RT-PCR. Results: The results showed that, among the predicted BBrMV miRNAs, miRNA2 is conserved throughout BBrMV isolates and has multiple virus-specific target transcripts. In addition, primary experimental validation for the predicted miRNAs revealed that miRNA2 exists in the BBrMV infected banana leaf samples. Conclusions: The existence of BBrMV miRNA2 is confirmed by stem-loop RT-PCR followed by cloning and sequencing. The presence of miRNA of Potyviridae is rarely addressed and would definitely spread the hope to understand the virus infectious cycle. Our report would also help to better understand and manipulate potyviral infections.
BackgroundThe tmRNA (transfer messenger RNA), encoded by ssrA gene, is involved in rescuing of stalled ribosomes by a process called trans-translation. Additionally, regions of the ssrA gene act as recognition sites for various integrases. Variations in ssrA genes were widely reported among the members of Enterobacteriaceae, but the functional relevance in the course of evolution are not well understood. In this study, we investigated the horizontal gene transfer of tmRNA among the members of Enterobacteriaceae.
Methods and ResultsHorizontal gene transfer in tmRNA was found by predicting recombination signals in the tmRNA belong to Enterobacteriaceae using recombination detection program (RDP5). Our results revealed 7 recombination signals in tmRNA among different species. We further showed that the recombination signals was more in the domains present in the 3' end than the domains in the 5' end of tmRNA. Of note, the mRNA region, which codes for the peptide tag was reported in many recombination signals.Further, members belonging to genera Yersinia, Erwinia, Dickeya, and Enterobacter were highly represented in the recombination signatures.
ConclusionsTaken together, our results revealed a high level of recombination among speci c regions of tmRNA of Enterobacteriaceae and suggest the possible role of recombination in the diversi cation of SsrA function in proteolysis and other pathways.
We have analysed the genome sequence of Wuhan poty-like virus 1 (WuPLV1), reported as an unclassified RNA virus in GenBank (Accession no: KX884573.1). Based on the polyprotein sequence identity (ranging from 55.2 to 71.1%), with classifiable members of the Macluravirus genus of the plant virus family Potyviridae, we suggest that WuPLV1 represents a possible new species of Macluravirus, although the virus was isolated from the Chinese land snail Mastigeulota kiangsinensis, which is not known to be a host or vector of macluraviruses.
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