Abstract

BackgroundRice dwarf virus (RDV), a plant reovirus, is mainly transmitted by the green rice leafhopper, Nephotettix cincticeps, in a persistent-propagative manner. Plant reoviruses are thought to replicate and assemble within cytoplasmic structures called viroplasms. Nonstructural protein Pns4 of RDV, a phosphoprotein, is localized around the viroplasm matrix and forms minitubules in insect vector cells. However, the functional role of Pns4 minitubules during viral infection in insect vector is still unknown yet.MethodsRNA interference (RNAi) system targeting Pns4 gene of RDV was conducted. Double-stranded RNA (dsRNA) specific for Pns4 gene was synthesized in vitro, and introduced into cultured leafhopper cells by transfection or into insect body by microinjection. The effects of the knockdown of Pns4 expression due to RNAi induced by synthesized dsRNA from Pns4 gene on viral replication and spread in cultured cells and insect vector were analyzed using immunofluorescence, western blotting or RT-PCR assays.ResultsIn cultured leafhopper cells, the knockdown of Pns4 expression due to RNAi induced by synthesized dsRNA from Pns4 gene strongly inhibited the formation of minitubules, preventing the accumulation of viroplasms and efficient viral infection in insect vector cells. RNAi induced by microinjection of dsRNA from Pns4 gene significantly reduced the viruliferous rate of N. cincticeps. Furthermore, it also strongly inhibited the formation of minitubules and viroplasms, preventing efficient viral spread from the initially infected site in the filter chamber of intact insect vector.ConclusionsPns4 of RDV is essential for viral infection and replication in insect vector. It may directly participate in the functional role of viroplasm for viral replication and assembly of progeny virions during viral infection in leafhopper vector.

Highlights

  • Rice dwarf virus (RDV), a plant reovirus, is mainly transmitted by the green rice leafhopper, Nephotettix cincticeps, in a persistent-propagative manner

  • RNA interference (RNAi) induced by dsPns4 inhibits the replication and infection of RDV in cultured insect vector cells In order to investigate the functional role of Pns4 of RDV, the RNAi activity induced by double-stranded RNA (dsRNA) specific for the Pns4 gene was examined in cultured leafhopper cells

  • Northern blot assay demonstrated that small interfering RNAs (siRNAs) approximately 21 nt in length from dsPns4 and dsRNAs specific for the green fluorescence protein (dsGFP) treatments were detected (Fig. 1a), indicating that RNAi induced by dsRNAs was active in cultured leafhopper cells

Read more

Summary

Introduction

Rice dwarf virus (RDV), a plant reovirus, is mainly transmitted by the green rice leafhopper, Nephotettix cincticeps, in a persistent-propagative manner. Nonstructural protein Pns of RDV, a phosphoprotein, is localized around the viroplasm matrix and forms minitubules in insect vector cells. Rice dwarf virus (RDV), a phytoreovirus in the family Reoviridae, is mainly transmitted by the leafhopper vector, Nephotettix cincticeps, in a persistent-propagative manner [5]. The functions of nonstructural proteins in the insect vector have been determined using continuous cell cultures derived from N. cincticeps. Pns and Pns aggregate together to form the viroplasm matrix for viral replication and progeny virions assembly [22]. Our recent report shows that Pns of RDV is a principal regulator for viral replication and infection in its insect vector [23]. Whether the formation of the Pns minitubule is essential for viral replication and infection in insect vector cells is undetermined yet

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.