An RNAi-Based Control of Fusarium graminearum Infections Through Spraying of Long dsRNAs Involves a Plant Passage and Is Controlled by the Fungal Silencing Machinery.

Meeting the increasing food and energy demands of a growing population will require the development of ground-breaking strategies that promote sustainable plant production. Host-induced gene silencing has shown great potential for controlling pest and diseases in crop plants. However, while delivery of inhibitory noncoding double-stranded (ds)RNA by transgenic expression is a promising concept, it requires the generation of transgenic crop plants which may cause substantial delay for application strategies depending on the transformability and genetic stability of the crop plant species. Using the agronomically important barley-Fusarium graminearum pathosystem, we alternatively demonstrate that a spray application of a long noncoding dsRNA (791 nt CYP3-dsRNA), which targets the three fungal cytochrome P450 lanosterol C-14α-demethylases, required for biosynthesis of fungal ergosterol, inhibits fungal growth in the directly sprayed (local) as well as the non-sprayed (distal) parts of detached leaves. Unexpectedly, efficient spray-induced control of fungal infections in the distal tissue involved passage of CYP3-dsRNA via the plant vascular system and processing into small interfering (si)RNAs by fungal DICER-LIKE 1 (FgDCL-1) after uptake by the pathogen. We discuss important consequences of this new finding on future RNA-based disease control strategies. Given the ease of design, high specificity, and applicability to diverse pathogens, the use of target-specific dsRNA as an anti-fungal agent offers unprecedented potential as a new plant protection strategy

(A-E) The fungal silencing machinery is required for efficient SIGS in distal leaf parts.

<p><b>(A,B)</b> The fungal <i>dicer-like-1</i> mutant Fg-IFA65_Δdcl-1 heavily infected barley leaves despite a prior spray-treatment with <i>CYP3</i>-dsRNA. Photographs were taken at 6 dpi. <b>(C)</b> Gene-specific qPCR analysis of <i>CYP51A</i>, <i>CYP51B</i>, and <i>CYP51C</i> transcripts in the wild type Fg-IFA65 and the mutant Fg-IFA65_Δdcl-1 at 6 dpi in the distal, semi-systemic leaf areas. <b>(D)</b> Inhibition of <i>CYP51</i> gene expression upon <i>CYP3</i>-dsRNA treatment of axenically grown Fg-IFA65_- Bars represent mean values ±SDs of three independent sample collections. The reduction in <i>CYP51</i> expression in samples treated with <i>CYP3</i>-dsRNA compared with mock-treated controls was statistically significant (*P < 0.05, **P < 0.01; Student´s t test). <b>(E-G)</b> Profiling of <i>CYP3</i>-dsRNA-derived sRNAs in axenically grown Fg-IFA65. (E) Scaffold of the 791 nt long <i>CYP3</i>-dsRNA. The fragments of <i>CYP51</i> genes are indicated. (F,G) Total sRNAs were isolated from axenically-cultured Fg-IFA65. sRNA reads of fungal sRNAs from untreated (F) and <i>CYP3</i>-dsRNA-treated (G) fungal cultures are mapped to the sequence of <i>CYP3</i>-dsRNA.</p

(A,B) Defense-related salicylate- and jasmonate-responsive genes are not induced by <i>CYP3</i>-dsRNA.

<p>Detached second leaves of three-week-old barley were sprayed with 20 ng μL^-1 <i>CYP3</i>-dsRNA or TE (control), respectively, and 48 h later drop-inoculated with Fg-IFA65. Leaves were harvested 6 dpi and analyzed for gene expression by qPCR: <b>(A)</b> <i>Pathogenesis-related</i> 1 (<i>HvPR1</i>) and <b>(B)</b> <i>S-adenosyl-l-methionine</i>:<i>jasmonic acid carboxyl methyltransferase</i> (<i>HvJMT</i>). Both genes are highly responsive to Fg-IFA65 but not to <i>CYP3</i>-dsRNA or TE treatment. Please note that a combined treatment of <i>CYP3</i>-dsRNA followed by Fg-IFA65 48 h later also did not induce these marker genes, which shows independently that fungal development on <i>CYP3</i>-dsRNA-treated leaves is strongly inhibited.</p

(A-E) The fungal silencing machinery is required for efficient SIGS in distal leaf parts.

<p><b>(A,B)</b> The fungal <i>dicer-like-1</i> mutant Fg-IFA65_Δdcl-1 heavily infected barley leaves despite a prior spray-treatment with <i>CYP3</i>-dsRNA. Photographs were taken at 6 dpi. <b>(C)</b> Gene-specific qPCR analysis of <i>CYP51A</i>, <i>CYP51B</i>, and <i>CYP51C</i> transcripts in the wild type Fg-IFA65 and the mutant Fg-IFA65_Δdcl-1 at 6 dpi in the distal, semi-systemic leaf areas. <b>(D)</b> Inhibition of <i>CYP51</i> gene expression upon <i>CYP3</i>-dsRNA treatment of axenically grown Fg-IFA65_- Bars represent mean values ±SDs of three independent sample collections. The reduction in <i>CYP51</i> expression in samples treated with <i>CYP3</i>-dsRNA compared with mock-treated controls was statistically significant (*P < 0.05, **P < 0.01; Student´s t test). <b>(E-G)</b> Profiling of <i>CYP3</i>-dsRNA-derived sRNAs in axenically grown Fg-IFA65. (E) Scaffold of the 791 nt long <i>CYP3</i>-dsRNA. The fragments of <i>CYP51</i> genes are indicated. (F,G) Total sRNAs were isolated from axenically-cultured Fg-IFA65. sRNA reads of fungal sRNAs from untreated (F) and <i>CYP3</i>-dsRNA-treated (G) fungal cultures are mapped to the sequence of <i>CYP3</i>-dsRNA.</p

(A,B) Northern gel blot analysis of <i>CYP3</i>-dsRNA and <i>CYP3</i>-dsRNA-derived siRNA accumulation in local and distal (semi-systemic) barley leaf areas.

<p><b>(A)</b> Detection of 791 nt long <i>CYP3</i>-dsRNA precursor in pooled leaf tissue from non-infected leaves using [α-32P]-dCTP labeled <i>CYP3</i>-dsRNA as probe. Local (L) and distal (semi-systemic [S]) leaf segments were sampled separately at the indicated times after spraying with <i>CYP3-</i>dsRNA. No signal was detected in samples from TE-sprayed plants. <b>(B)</b> Recording <i>CYP3</i>-dsRNA-derived small RNAs in local and distal (semi-systemic) leaf areas using [α-32P]-dCTP labeled <i>CYP3</i>-dsRNA as probe. In this experiment, small RNAs could not be detected in distal (non-sprayed) tissues. siRNA generated <i>in vitro</i> by a commercial Dicer preparation from <i>CYP3</i>-dsRNA was used as positive control. No signal was detected in samples from TE-sprayed plants. Ethidium bromide-stained rRNA served as the loading control. Signals originate from the same membrane but different exposure times.</p

(A-J) Confocal laser scanning microscopy of ATTO 488-labeled <i>CYP3</i>-dsRNA_A488 in locally sprayed barley leaves.

<p><b>(A-C)</b> Detection of <i>CYP3</i>-dsRNA_A488 (green) in xylem vessels of vascular bundles 24 h after spraying. <b>(D-G)</b> Longitudinal sections reveal uptake of <i>CYP3</i>-dsRNA_A488 by cells of the phloem tissue at 24 h after spraying. SE, sieve element; CC, companion cell; SP, sieve plate; PPC, phloem parenchyma cell; MC, mesophyll cell. The red cells result from the autofluorescence of chloroplasts (F,G). <b>(H-J)</b> Leaf hair cells (trichome), stomata, germinating spores (GS) and fungal hyphae strongly accumulated <i>CYP3</i>-dsRNA_A488. Fungal hyphae (IF) are stained with chitin-specific dye WGA-Alexa Fluor 594 (red) 24 h after inoculation. EC, epidermal cells. RNA signals in germinated conidia are marked by arrow heads. Scale bars 100 μm (A-H), 20 μm (F), and 10 μm (J).</p