Abstract

Antiviral RNA silencing/interference (RNAi) of negative-strand (-) RNA plant viruses (NSVs) has been studied less than for single-stranded, positive-sense (+)RNA plant viruses. From the latter, genomic and subgenomic mRNA molecules are targeted by RNAi. However, genomic RNA strands from plant NSVs are generally wrapped tightly within viral nucleocapsid (N) protein to form ribonucleoproteins (RNPs), the core unit for viral replication, transcription and movement. In this study, the targeting of the NSV tospoviral genomic RNA and mRNA molecules by antiviral RNA-induced silencing complexes (RISC) was investigated, in vitro and in planta. RISC fractions isolated from tospovirus-infected N. benthamiana plants specifically cleaved naked, purified tospoviral genomic RNAs in vitro, but not genomic RNAs complexed with viral N protein. In planta RISC complexes, activated by a tobacco rattle virus (TRV) carrying tospovirus NSs or Gn gene fragments, mainly targeted the corresponding viral mRNAs and hardly genomic (viral and viral-complementary strands) RNA assembled into RNPs. In contrast, for the (+)ssRNA cucumber mosaic virus (CMV), RISC complexes, activated by TRV carrying CMV 2a or 2b gene fragments, targeted CMV genomic RNA. Altogether, the results indicated that antiviral RNAi primarily targets tospoviral mRNAs whilst their genomic RNA is well protected in RNPs against RISC-mediated cleavage. Considering the important role of RNPs in the replication cycle of all NSVs, the findings made in this study are likely applicable to all viruses belonging to this group.

Highlights

  • Plants have evolved different layers of defense against pathogen invasions [1,2,3]

  • We hypothesized that the viral RNP structure would protect the viral genomic RNA from cleavage by host antiviral RNA-induced silencing complexes (RISC)

  • Since viral mRNAs do not associate with N protein into RNPs, we expected that RISC would likely target the viral mRNA

Read more

Summary

Introduction

Plants have evolved different layers of defense against pathogen invasions [1,2,3]. One of the first layers involves cell-surface immune receptors that recognize pathogen associated molecular patterns (PAMPs) and induce pattern triggered immunity (PTI). Plants evolved intracellular immune receptors that recognize pathogen effectors and induce effector triggered immunity (ETI). This ongoing battle is commonly presented in a zigzag model [1]. DsRNA is recognized and processed by Dicer-like (DCL) proteins of the host plant into small interfering RNA (siRNA) duplexes of 21–24 nt in size [8,9]. These are loaded into an RNA-induced silencing complex (RISCs), containing a core Argonaute effector [11]. Fractions of plants infected with TBSV P19 mutants, but not from those infected with the wild-type virus, contained the RNAi-associated ssRNA-specific ribonucleases [12]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

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