4.7 Article

Optimized RNA-Silencing Strategies for Rice Ragged Stunt Virus Resistance in Rice

Journal

PLANTS-BASEL
Volume 10, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/plants10102008

Keywords

RNA-silencing; virus resistance; RRSV; rice

Categories

Funding

  1. Laboratoire Mixte International LMI RICE
  2. CGIAR Research Program (CRP) on rice agri-food systems (RICE, 2017-2022)
  3. IRD (Institut de Recherche pour le Developpement, France) PhD fellowship

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Rice ragged stunt virus (RRSV) is a destructive virus in the rice culture areas of South and Far-Eastern Asia, for which no genetic resistance has been identified. Chemical treatments are currently used, but RNA-silencing approaches have been developed as resistance strategies. While miRNA-based strategies targeting viral genomes did not achieve efficient resistance against RRSV, siRNA-based strategies targeting viral fragments showed efficient and environmentally friendly resistance in transgenic rice plants.
Rice ragged stunt virus (RRSV) is one of the most damaging viruses of the rice culture area in south and far-eastern Asia. To date, no genetic resistance has been identified and only expensive and non-environmentally friendly chemical treatments are deployed to fight this important disease. Non-chemical approaches based on RNA-silencing have been developed as resistance strategies against viruses. Here, we optimized classical miRNA and siRNA-based strategies to obtain efficient and durable resistance to RRSV. miRNA-based strategies are involved in producing artificial miRNA (amiR) targeting viral genomes in plants. Classically, only one amiR is produced from a single construct. We demonstrated for the first time that two amiRs targeting conserved regions of RRSV genomes could be transgenically produced in Nicotiana benthamiana and in rice for a single precursor. Transgenic rice plants producing either one or two amiR were produced. Despite efficient amiR accumulations, miRNA-based strategies with single or double amiRs failed to achieve efficient RRSV resistance in transformed rice plants. This suggests that this strategy may not be adapted to RRSV, which could rapidly evolve to counteract them. Another RNA-silencing-based method for viral resistance concerns producing several viral siRNAs targeting a viral fragment. These viral siRNAs are produced from an inverted repeat construct carrying the targeted viral fragment. Here, we optimized the inverted repeat construct using a chimeric fragment carrying conserved sequences of three different RRSV genes instead of one. Of the three selected homozygous transgenic plants, one failed to accumulate the expected siRNA. The two other ones accumulated siRNAs from either one or three fragments. A strong reduction of RRSV symptoms was observed only in transgenic plants expressing siRNAs. We consequently demonstrated, for the first time, an efficient and environmentally friendly resistance to RRSV in rice based on the siRNA-mediated strategy.

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