WO2017121809A1 - Use of active substances for controlling virus infection in plants - Google Patents

Use of active substances for controlling virus infection in plants Download PDF

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Publication number
WO2017121809A1
WO2017121809A1 PCT/EP2017/050583 EP2017050583W WO2017121809A1 WO 2017121809 A1 WO2017121809 A1 WO 2017121809A1 EP 2017050583 W EP2017050583 W EP 2017050583W WO 2017121809 A1 WO2017121809 A1 WO 2017121809A1
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WIPO (PCT)
Prior art keywords
plants
group
virus
substituted
formula
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PCT/EP2017/050583
Other languages
French (fr)
Inventor
Rachel Baltz
David Bernier
Florence JAY-BRIOUDES
Thomas Knobloch
Maxime Vitel
Olivier Voinnet
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Bayer Cropscience Aktiengesellschaft
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Application filed by Bayer Cropscience Aktiengesellschaft filed Critical Bayer Cropscience Aktiengesellschaft
Priority to EA201891591A priority Critical patent/EA034906B1/en
Priority to US16/069,194 priority patent/US20190053490A1/en
Priority to EP17701804.1A priority patent/EP3402333B1/en
Priority to CN201780006565.2A priority patent/CN108471747B/en
Priority to CA3011340A priority patent/CA3011340A1/en
Priority to JP2018536281A priority patent/JP6960927B2/en
Priority to KR1020187023350A priority patent/KR20180100680A/en
Priority to AU2017206952A priority patent/AU2017206952B2/en
Priority to MX2018008721A priority patent/MX381520B/en
Priority to BR112018014308-1A priority patent/BR112018014308A2/en
Priority to ES17701804T priority patent/ES2764800T3/en
Priority to UAA201808474A priority patent/UA122707C2/en
Priority to CONC2018/0008451A priority patent/CO2018008451A2/en
Priority to PL17701804T priority patent/PL3402333T3/en
Publication of WO2017121809A1 publication Critical patent/WO2017121809A1/en

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G7/00—Botany in general
    • A01G7/06—Treatment of growing trees or plants, e.g. for preventing decay of wood, for tingeing flowers or wood, for prolonging the life of plants
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
    • C07D305/02—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D305/10—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having one or more double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Definitions

  • the present invention relates to the use of active substances for stimulating the natural defense mechanism of plants against viruses in order to control virus infections in plants and to methods for controlling virus infections in plants.
  • the present invention also pertains to the use of active substances for activating the RNA-interference-based natural defense mechanism (also designated herein as RNA-silencing-based natural defense mechanism) of plants against viruses.
  • RNA-interference-based natural defense mechanism also designated herein as RNA-silencing-based natural defense mechanism
  • Plant viruses are responsible for major crop damages around the world. Indeed, some virus families, such as the Potyviridae, cause critical yield losses both in developed and emerging countries, conflicting with the ever-increasing food demand. To limit virus infections and spread, disease management is mainly conducted via prevention, as curative treatments are not or poorly efficient.
  • WO2011/030816 teaches the use of certain ascorbic acid derivatives to control certain plan viruses.
  • WO2012/016048 provides for the use of azide-modified biomolecules as antiviral agents, including against plant viruses.
  • WO2014/050894 teaches the use of other ascorbic acid related compounds to control plant viruses.
  • RNA silencing plays a major part in this balance by dynamically linking developmental programs and environmental stress responses to gene expression changes through transcriptional gene silencing (TGS) and post-transcriptional gene silencing (PTGS).
  • TGS transcriptional gene silencing
  • PTGS post-transcriptional gene silencing
  • Disease resistance in plants relies on preformed barriers, toxic secondary metabolites and inducible defense mechanisms.
  • pathogen recognition plants often initiate hypersensitive response, leading to cell death at the infection site and preventing the pathogen from spreading.
  • pathogen detection triggers various inducible systemic defenses, in parts of the plant distant from the primary infection site. This process, known as Systemic Acquired Resistance (SAR), is effective in many plant species. The resistance achieved is long-lasting and effective against subsequent infections by a broad range of pathogens e.g. fungi, bacteria and viruses.
  • SAR Systemic Acquired Resistance
  • the Strobilurin class of fungicides comprises a variety of synthetic plant-protecting compounds with broad-spectrum.
  • the strobilurin Pyraclostrobin has been demonstrated to enhance the resistance of tobacco against infection by either tobacco mosaic virus (TMV) or the wildfire pathogen Pseudomonas syringae pv tabaci (Herms et al., Plant Physiology 2002, 130: 120- 127).
  • TMV tobacco mosaic virus
  • Pseudomonas syringae pv tabaci Herms et al., Plant Physiology 2002, 130: 120- 127.
  • Pyraclostrobin was also able to enhance TMV resistance in NahG transgenic tobacco plants unable to accumulate significant amounts of the endogenous salicylic acid.
  • Pyraclostrobin enhances TMV resistance in tobacco either by acting downstream of Salicylic Acid (SA) in the SA signaling mechanism or by functioning independently of SA.
  • SA Salicylic Acid
  • RNA silencing is a mechanism that directly defends plant host cells against exogenous nucleic acids, including viruses and transposable elements. This defense is triggered by double-stranded RNA (dsRNA), derived from amplification of invasive nucleic acids, which is processed by the host into small interfering RNAs (siRNAs) that are 20-24 nucleotides (nt) in size. These siRNAs are then used to guide the silencing of the viral or transposable element RNA or DNA through PTGS or TGS, respectively.
  • dsRNA double-stranded RNA
  • siRNAs small interfering RNAs
  • RNA silencing is then a potent antiviral mechanism whereby small interfering siRNAs processed by the enzyme Dicer from viral double-stranded RNA replication intermediates are loaded into ARGON AUTE effector proteins and turned back onto the invader's RNA genome to induce its degradation.
  • This innate immune response is remarkably versatile because, being solely programmed by structural and nucleotide-sequence genomic features, it can respond to virtually any plant virus (Shimura et al., 2011, Biochimica et Biophysica Acta 1809: 601-612).
  • RNA silencing Attesting the importance of RNA silencing in plant defense, plants impaired in siRNA production or activity are hyper-susceptible to phytoviruses, and conversely many viruses have evolved suppressors of RNAi in order to maintain virulence (Voinnet O. et al, Nature Review Microbiology 2013 Nov;l l(l l):745-60).
  • Figure 1 illustrates the qPCR analysis of the SUL mRNA relative levels in SUC-SUL plants seven days after treatment with DMSO only or DFPM, normalized to EXP10. Error bars represent standard deviation from three independent experiments.
  • Figure 2 represents the average number of infection foci at five days post-infection on inoculated leaves. Error bars represent standard deviation from twelve plants.
  • Figure 3 illustrates the RT-qPCR analyses on HcPro mRNA accumulation in systemic tissues at six days post-infection. Error bars represent standard deviation from three independent PCR results.
  • (Ci-C6)alkyl refers to a branched- or straight-chain alkyl group containing from 1 to 6 carbon atoms.
  • Representative examples of (Ci-Ce)alkyl include methyl, ethyl, n-propyl, i-propyl and the different butyl, pentyl or hexyl isomers.
  • halogen refers to a fluorine, chlorine, iodine or bromine atom.
  • (Ci-C6)haloalkyl refers to a (Ci-Ce)alkyl group, as defined above, wherein at least one hydrogen atom is replaced with a halogen atom.
  • Representative examples of (Ci-C 6 )haloalkyl include -CF 3 ,- CH 2 C1 and -CH 2 -CF 3 .
  • (Ci-C6)cyanoalkyl refers to a (Ci-Ce)alkyl group, as defined above, wherein at least one hydrogen atom is replaced with a cyano group.
  • (C3-C6)cycloalkyl refers to a saturated monocyclic alkyl radical wherein the cyclic framework has 3 to 6 carbon atoms.
  • Representative examples of "(C3- C6)cycloalkyl” include cyclopropyl, cyclobutyl and cyclopentyl.
  • azabicycloalkyl refers to a fully saturated monovalent radical containing from 5 and up to 10 carbon atoms and a nitrogen atom in a bicyclic ring.
  • Representative examples of "azabicycloalkyl” include azabicyclo[3.1.0]hexyl, azabicyclo[2.2.1]heptyl and azabicyclo[2.2.2]octyl.
  • any hydrogen on the designated atom or group can be replaced with a substituent (up to and including that every hydrogen is replaced with a substituent) provided that the normal valency of the designated atom or group is not exceeded and that the substitution results in a stable compound.
  • active substance designates a compound of formula (I) as described herein or any mixtures thereof.
  • compounds of formula (I) as disclosed herein are suitable for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses. Therefore, the compounds of formula (I) as disclosed herein may be useful for controlling viral diseases in plants.
  • control or “controlling” as used herein designates a preventive or curative control.
  • the present invention relates to a method for controlling viral diseases in plants, more specifically to a method for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses.
  • the method comprises applying to the plants one or more compounds of formula (I):
  • Rl is a phenyl that may be substituted with one or more halogens, preferably chlorine and bromine;
  • - R2 is a -NR'R" group wherein :
  • R' and R" are independently selected from the group consisting of (Ci- Ce)alkyl (preferably methyl, ethyl and n-propyl) and (C3-Ce)cycloalkyl (preferably c- pentyl), or
  • R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine, or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of halogen, (Ci-Ce)alkyl and (Ci-Ce)cyanoalkyl, or
  • the active substance is a compound of formula (I) wherein
  • Rl is a phenyl substituted with one or two halogens independently chosen from chlorine or bromine ;
  • - R2 is a -NR'R" group wherein :
  • R' and R" are independently selected from the group consisting of methyl, ethyl, n-propyl and cyclopentyl, or
  • - R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of methyl, fluorine and cyanoethyl, or - R' and R" together with the nitrogen atom to which they are attached form an azabicyclo[3.1.0]hexyl substituted with a (Ci-C6)haloalkyl, such as a trifluoromethyl.
  • the active substance is a compound of formula (I) wherein :
  • Rl is selected from the group consisting of 3-chlorophenyl, 4-chlorophenyl, 4- bromophenyl, 2,3-dichlorophenyl and 3,4-dichlorophenyl ; and/or
  • R2 is selected from the group consisting of -NEt2, -N(n-Pr)2, -N(c-pentyl)Me, piperidin-l-yl, pyrrolidin-l-yl, N-morpholino, 4,4-difluoropiperidin-l-yl, , 4-(2- cyanoethyl)-piperazin- l-yl, 2,6-dimethylmorpholin-4-yl and 6-(trifluoromethyl)-3- azabicyclo[3.1.0]hex-3-yl.
  • the active substance is a compound of formula (I) wherein Rl and R2 are selected such as to provide the specific compounds disclosed herein below in table 1.
  • the active substance is a compound of formula (I) wherein :
  • Rl is 3,4-dichlorophenyl and R2 is 4,4-difluoropiperidinyl-l-yl ; or
  • Rl is 3,4-dichlorophenyl and R2 is piperidin-l-yl ; or
  • Rl is 4-bromophenyl and R2 is piperidin- l-yl.
  • DFPM rapidly downregulates ABA-dependent gene expression in plant and also inhibits ABA- induced stomatal closure. DFPM also stimulates expression of plant defense-related genes including PHYTOALEXIN DEFICIENT4 (PAD4)- and ENHANCED DISEASE SUSCEPTIBILITY 1 (EDS 1) (Kim et al., Current Biology 201 1, 21, 1 1 :990-997).
  • PHYTOALEXIN DEFICIENT4 PAD4
  • ENHANCED DISEASE SUSCEPTIBILITY 1 EDS 1
  • 5-Arylfuran-2-thioamides of formula (I) may be suitably prepared :
  • An effective amount of active substance is typically applied to the plants.
  • the effective amount of active substance which is applied to the plants will depend on various factors, such as the nature of the active substance, the formulation, the plants being targeted (plants nature and plants part), the application method, the purpose of the treatment (prophylactic or therapeutic) and the virus being targeted.
  • the amount applied to the plants may suitably range from 0.01 to 5 kg ha, or from 0.1 to 3 kg ha, or from 0.5 to 2 kg ha.
  • the active substance is applied to the plants.
  • plants as used herein include plants and parts thereof, such as the aerial and/or subterraneous parts of the plants as well as the harvested material.
  • Subterraneous plants parts include root, rhizomes, tubers, suckers, slips, seeds and seed.
  • the aerial plant parts include stem, bark, shoot, leaf, flower, fruits, fruiting bodies, stalk, needles and branches.
  • the active substance may be efficiently applied to the root, rhizomes, tubers, suckers, slips, seeds, seed, stem, bark, shoot, leaf, flower, fruits, fruiting bodies, stalk, needles, branches, harvested material of the plants.
  • the method for controlling viral diseases in plants comprises applying the disclosed active substance to the plants' habitat and/or store.
  • the active substance can be efficiently applied to a large variety of plants. It may be applied to plants of the varieties which are commercially available or in use. However, plant varieties are also understood as meaning plants with novel traits which have been bred either by traditional breeding, by mutagenesis or with the aid of recombinant DNA techniques and/or to plants which can be obtained by traditional breeding and optimization methods or else by biotechnological and genetic engineering methods or by combinations of these methods; this includes the transgenic plants and the plants which are capable or not of being protected by Plant Breeders' Rights.
  • the active substance may also be efficiently applied to genetically modified organisms (GMOs).
  • GMOs genetically modified organisms
  • Genetically modified plants are plants in which a heterologous gene has been stably integrated into the genome.
  • the expression "heterologous gene” essentially means a gene which has been provided or assembled outside the plants and, when introduced into the nuclear, chloroplastic or mitochondrial genome, imparts novel or improved agronomic or other properties to the transformed plant by expressing a protein or polypeptide of interest or by down regulating or silencing another gene which is present in the plant, or other genes which are present in the plant (using, for example, antisense technology, cosuppression technology or RNAi technology [RNA interference]).
  • a heterologous gene that is located in the genome is also called a transgene.
  • transgene that is defined by its particular location in the plant genome is referred to as a transformation event, or transgenic event.
  • All plants which have genetic material which imparts, to these plants, especially advantageous, useful traits (whether obtained by breeding and/or by biotechnology) may be treated by the disclosed method.
  • Plants and plant varieties which can likewise be treated in accordance with the invention are those plants which are resistant to one or more abiotic stress factors.
  • Abiotic stress conditions can include, for example, drought, chill and heat conditions, osmotic stress, water-logging, elevated soil salt content, elevated exposure to minerals, ozone conditions, high-light conditions, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients or the avoidance of shade.
  • Plants and plant varieties which can likewise be treated in accordance with the invention are those plants which are characterized by enhanced yield characteristics.
  • Enhanced yield in these palm plants can be the result of, for example, improved plant physiology, improved plant growth and improved plant development, such as water utilization efficiency, water retention efficiency, improved nitrogen utilization, improved carbon assimilation, improved photosynthesis, increased germination efficiency and modified maturation.
  • the yield can furthermore be influenced by improved plant architecture (under stress conditions and under nonstress conditions), among which early flowering, flowering control for the production of hybrid seed, seedling vigour, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, number of seeds per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence, and lodging resistance.
  • Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and oil composition, nutritional value, reduction in antinutritional compounds, improved processability and improved storability.
  • Plants which can likewise be treated in accordance with the invention are hybrid plants that already express the characteristics of heterosis, or hybrid vigour, which generally results in higher yield, higher vigour, better health and better resistance to biotic and abiotic stress factors.
  • Such plants are typically generated by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent).
  • the hybrid seed is typically harvested from the male-sterile plants and sold to growers.
  • Male-sterile plants can sometimes (for example in maize) be generated by detasseling (i.e. the mechanical removal of the male reproductive organs or the male flowers); however, more typically, male sterility is the result of genetic determinants in the plant genome.
  • cytoplasmic male sterility have been described for example for Brassica species (WO 1992/005251, WO 1995/009910, WO 1998/27806, WO 2005/002324, WO 2006/021972 and US 6,229,072).
  • male-sterile plants can also be obtained by plant biotechnology methods, such as genetic engineering.
  • a particularly advantageous means for generating male-sterile plants is described in WO 89/10396, in which, for example, a ribonuclease such as a barnase is selectively expressed in the tapetum cells in the stamens. The fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar (for example WO 1991/002069).
  • the active substance is particularly suitable for controlling viral diseases in the following plants: cotton, flax, grapevine, fruit, vegetables, such as Rosaceae sp. (for example pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds and peaches, and soft fruits such as strawberries), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp.
  • Rosaceae sp. for example pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds and peaches, and soft fruits such as strawberries
  • Rosaceae sp. for example pome fruits such as apples and pears, but also stone fruits such as
  • Rubiaceae sp. for example coffee
  • Theaceae sp. Sterculiceae sp.
  • Rutaceae sp. for example lemons, oranges and grapefruit
  • Solanaceae sp. for example tomatoes
  • Liliaceae sp. for example lettuce
  • Umbelliferae sp. for example lettuce
  • Alliaceae sp. for example leek, onion
  • peas for example peas
  • major crop plants such as Gramineae sp. (for example maize, turf, cereals such as wheat, rye, rice, barley, oats, millet and triticale), Asteraceae sp. (for example sunflower), Brassicaceae sp. (for example white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes, and oilseed rape, mustard, horseradish and cress), Fabacae sp. (for example bean, peanuts), Papilionaceae sp. (for example soya bean), Solanaceae sp. (for example potatoes), Chenopodiaceae sp. (for example sugar beet, fodder beet, swiss chard, beetroot); useful plants and ornamental plants for gardens and wooded areas; and genetically modified varieties of each of these plants.
  • the active substance is suitable for controlling viral diseases in vegetables.
  • the active substance is particularly suitable for controlling viruses of the following families or genus: Caulimoviridae, Geminiviridae, Bromoviridae, Closteroviridae, Comoviridae Potyviridae, Sequiviridae, Tombusviridae, Rhabdoviridae, Bunyaviridae, Partitiviridae, Rheoviridae, Capillovirus, Carlavirus, Enamovirus, Furovirus, Hordeivirus, Idaeovirus, Luteovirus, Marafivirus, Potexvirus, Sobemovirus, Tenuivirus, Tobamovirus, Tobravirus, Trichovirus, Tymovirus and Umbravirus.
  • the active substance is used for controlling viruses of the following species : Turnip mosaic virus, turnip crinkle virus, bean pod mottle virus, cauliflower mosaic virus, tobacco mosaic virus, tomato bushy stunt virus, rice ragged stunt virus, cucumber mosaic virus, barley yellow dwarf virus, beet yellows virus, lettuce yellows virus,ariae mosaic virus, peanut stunt virus and potato virus Y.
  • the active substance can be applied to the plants in any suitable forms.
  • the active substance may be applied in the form of a suspension, e.g. water- or oil-based suspension, emulsion, solution, powder such as wettable powder, foam, paste, granules, microparticles, aerosols or microencapsulations.
  • Suitable formulations can be prepared in conventional manners.
  • the formulations comprising the active substance may be ready-for-use compositions, i.e. compositions that can be directly applied to the plants by a suitable device, or they may be in the form of commercial concentrates which have to be diluted prior to use.
  • the formulations may comprise the active substance alone or in combination with other active substances such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, further fungicides, growth-regulating substances, herbicides, safeners and/or fertilizers.
  • the active substance or formulations comprising thereof may be applied to the plants in any customary manners, e.g. watering, spraying, dusting, atomizing.
  • the active substance may be directly or indirectly applied to the plants, the environment, the habitat and/or the store.
  • the active substance can be injected into or below the bark, poured or sprayed around the plant onto the ground (soil, sandy soil, gravelly soil, rocky soil, loamy soil or mixed soil).
  • a further type of application is the spraying onto the plant and its plant parts.
  • the active substance composition can be admixed to the ground material (soil, sandy soil, gravelly soil, rocky soil, loamy soil or mixed soil) and/or to the seeds.
  • the active substance can be applied to the irrigation system, either in dry or else in liquid form.
  • the active substance is preferably applied to the plants by spraying.
  • the present invention also relates to the use of compounds of formula (I) as disclosed herein for controlling viral diseases in plants, more specifically for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses.
  • the plants and/or viruses are as disclosed above.
  • the compounds of formula (I) stimulate the RNA-silencing-based defense mechanism of the plants through an increase in small RNA production.
  • the ability of the compounds of formula (I) to increase small RNA production can also be used in genetically modified plants transformed with an RNAi construct designed to improve agronomic traits and/or to provide resistance against pathogens (e.g. bacteria, fungi), resistance against insect/pest and/or stress tolerance. Therefore, the present invention also relates to the use of one or more compounds of formula (I) to improve agronomic traits and/or to provide resistance against pathogens, resistance against insect/pest and/or stress tolerance in genetically modified plants transformed with an RNAi construct through enhancement of small RNA production.
  • the present invention also relates to a compound of formula (I) and/or a composition comprising thereof, wherein the compound of formula (I) is as follows:
  • Rl is a phenyl substituted with one or more halogens, preferably chlorine and bromine;
  • - R2 is a -NR'R" group wherein :
  • R' and R" are independently selected from the group consisting of (Ci- Ce)alkyl (preferably methyl, ethyl and n-propyl) and (C3-Ce)cycloalkyl (preferably c- pentyl), or
  • - R' and R" together with the nitrogen atom to which they are attached form an azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl, preferably an azabicyclo[3.1.0]hexyl that may be substituted with a (Ci-C6)haloalkyl.
  • the compound is a compound of formula (I) wherein :
  • Rl is a phenyl substituted with one or two halogens independently chosen from chlorine or bromine ;
  • - R2 is a -NR'R" group wherein :
  • R' and R" are independently selected from the group consisting of methyl, ethyl, n-propyl and cyclopentyl, or
  • the compound is a compound of formula (I) wherein :
  • Rl is 3,4-dichlorophenyl ;
  • R2 is selected from the group consisting of - ⁇ 3 ⁇ 4, -N(n-Pr)2, -N(c-pentyl)Me, 4,4- difluoropiperidin-l-yl, 2,6-dimethylmorpholin-4-yl and 6-(trifluoromefhyl)-3- azabicyclo[3.1.0]hex-3-yl.
  • composition of the present invention typically comprises, in addition to the compound of formula (I), one or more acceptable carriers, in particular one or more agriculturally acceptable carriers.
  • a carrier is a natural or synthetic, organic or inorganic substance with which the active ingredients are mixed or combined for better applicability, in particular for better application to plants, plant parts or seeds.
  • the carrier which may be solid or liquid, is generally inert.
  • suitable solid carriers include, but are not limited to, ammonium salts, natural rock flours, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and synthetic rock flours, such as finely divided silica, alumina and silicates.
  • suitable solid carriers include, but are not limited to, crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, synthetic granules of inorganic and organic flours and granules of organic material such as paper, sawdust, coconut shells, maize cobs and tobacco stalks.
  • suitable liquid carriers include, but are not limited to, water, polar and nonpolar organic chemical liquids, for example from the classes of aromatic and nonaromatic hydrocarbons (such as cyclohexane, paraffins, alkylbenzenes, xylene, toluene alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride), alcohols and polyols (which may optionally also be substituted, etherified and or esterified, such as butanol or glycol), ketones (such as acetone, methyl ethyl ketone, methyl isobutyl ketone cyclohexanone), esters (including fats and oils) and (poly)ethers, unsubstituted and substituted amines, amides (such as dimethylformamide),lactams (such as N-alkylpyrrolidones) and lac
  • the carrier may also be a liquefied gaseous extender, i.e. liquid which is gaseous at standard temperature and under standard pressure, for example aerosol propellants such as halohydrocarbons, butane, propane, nitrogen and carbon dioxide.
  • a liquefied gaseous extender i.e. liquid which is gaseous at standard temperature and under standard pressure
  • aerosol propellants such as halohydrocarbons, butane, propane, nitrogen and carbon dioxide.
  • compositions may further comprise one or more acceptable auxiliaries which are customary for formulating compositions (e.g. agrochemical compositions), such as one or more surfactants.
  • suitable surfactants include emulsifiers and/or foam formers, dispersants or wetting agents having ionic or nonionic properties, or mixtures thereof.
  • Examples thereof are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene and/or propylene oxide with fatty alcohols, fatty acids or fatty amines (polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers), substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyl taurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty esters of polyols, and derivatives of compounds containing sulphates, sulphonates and phosphates, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, protein hydroly sates, lignosulph
  • auxiliaries which are customary for formulating agrochemical compositions include water repellent, siccatives, binder (adhesive, tackifier, fixing agent, such as carboxymethylcellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, natural phospholipids such as cephalins and lecithins and synthetic phospholipids, polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose), thickeners, stabilizers (e.g.
  • dyes or pigments such as inorganic pigments, e.g. iron oxide, titanium oxide and Prussian Blue ; organic dyes, e.g. alizarin, azo and metal phthalocyanine dyes), antifoams (e.g. silicone antifoams and magnesium stearate), preservatives (e.g.
  • dichlorophene and benzyl alcohol hemiformal secondary thickeners (cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica), stickers, gibberellins and processing auxiliaries, mineral and vegetable oils, perfumes, waxes and nutrients (including trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc), protective colloids, thixotropic substances, penetrants, sequestering agents and complex formers.
  • the choice of the carriers and/or auxiliaries will depend on the intended mode of application of the composition and/or on the physical properties of the active ingredient(s).
  • RNAi also acts as an antiviral response in mammals.
  • the compounds of formula (I) can be used for stimulating the natural defense mechanism of mammals against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of mammals against viruses.
  • the present invention also relates to compounds of formula (I) as disclosed herein for use as a medicament, in particular for use in the treatment or prevention of a viral infection.
  • the compound of formula (I) as disclosed herein may be used in a method for treating or preventing a viral infection in mammals which comprises administrating to a mammal in need thereof an effective amount of a compound of formula (I) as disclosed herein.
  • the term "mammals” as used herein includes humans.
  • the plants' RNA silencing pathway can be easily monitored with certain artificially-created reporter plants called the "SUC-SUL Arabidopsis reporter plants" (Dunoyer et al., Nat. Genet. 37, 1356-1360, 2005).
  • the SUC-SUL Arabidopsis reporter plants are transgenic plants expressing an inverted-repeat (IR) double-stranded RNA designed to target the SULPHUR (SUL) transcript in the vasculature under the control of the SUC2 promoter (Truernit et al, Planta 196(3), 564-570, 1995). Once expressed, the dsRNA is processed into small interfering RNAs directing non-cell autonomous post-transcriptional gene silencing of the SULPHUR transcript, in turn causing vein-centered chlorosis. Since the observed chlorosis results from the silencing of the SULPHUR transcript, an expansion of the chlorosis, observable directly on the plants, is correlated with an intensification of the RNA silencing pathway at the molecular level.
  • IR inverted-repeat
  • SUL SULPHUR
  • DMSO dimethylsulfoxide
  • EC emulsifiable concentrate
  • Results are shown in table 1 below.
  • Treatment with 300 ppm of DFPM [5-(3,4- dichlorophenyl)furan-2-yl]-piperidine-l-ylmethanethione) and analogues thereof led to a significant increase in the percentage of chlorosis confirming the activity of the active substance as putative robust enhancers of RNA silencing.
  • the active substances identified for their ability to increase the surface and intensity of the chlorotic zone were then tested, in a second step, on some AtSUC2-GFP reporter plants, which are specifically reporting the activity of the SUC2 promoter (Wright et al., Plant Physiol. 131, 1555-1565, 2003).
  • Table 1 evaluation of DFPM (compound ID No. 3) and analogs thereof on SUC-SUL reporter plants. The level of chlorosis of mock treated plant reached 10%.
  • Example 2 Confirmation of the molecular effect of the silencing modulators
  • DFPM RNAi machinery enhancing effect of DFPM on the RNAi machinery has been validated at the phenotypic and molecular levels.
  • the plant aerial tissues were collected and analyzed molecularly using state-of-the-art methodologies.
  • Example 3 Antiviral efficacy of silencing modulators on Arabidopsis
  • the Turnip mosaic virus belongs to the Potyviridae, the largest family of known plant viruses. This virus infects a wide range of plants, in particular Brassicaceae. TuMV genome consists of a positive- sense single-stranded RNA molecule (+ ssRNA).
  • the antiviral efficacy of DFMP was tested with a fluorescently-tagged potyvirus (TuMV-GFP) in order to specifically pinpoint when and where the effect of the molecules is induced during virus primary infection, as well as its local or systemic spread.
  • Virus titers were measured by qPCR and/or virus protein accumulation on Western blot analyses and by counting the number of primary infection foci under UV light in the case of the TuMV-GFP.
  • DFPM leads to a clear reduction of the accumulation of virus titers five days-post-infection on the Arabidopsis plants.
  • a strong reduction of virus accumulation was consistently observed with TuMV-GFP both on inoculated leaves ( Figure 2) and on systemic tissues upon treatment with DFPM, as measured by the reduction of the accumulation of the TuMV-derived HcPro mRNA levels ( Figure 3).
  • TCV Turnip crinkle virus
  • CaMV Cauliflower mosaic virus
  • the TCV belongs to the Tombusviridae family and infects various types of plant species including the common plant models A. thaliana and N. benthamiana. Its genome is another example of +strand RNA virus.
  • the CaMV belongs to the Caulimoviridae family. It infects mostly Brassicaceae such as turnip and cabbage, but is also able to infect A. thaliana. CaMV consists of a double-stranded DNA molecule.
  • DFPM treatment at lOOppm lead to a strong reduction of virus accumulation both on inoculated leaves and on systemic tissues, as measured by the reduction of the accumulation of the TCV- derived P38 mRNA and CaMV-derived P6 mRNA.
  • the Bean pod mottle virus is a plant pathogenic virus of the family Comoviridae. This virus infects legumes and more particularly soybean.
  • BPMV genome consists of a bipartite positive-sense single- stranded RNA molecule (+ ssRNA).
  • BPMV-GFP fluorescently-tagged comoviruss
  • Soybean plants were sprayed with 100 or 200ppm of DFPM and emulsifiable concentrate (EC) Premix one day before to infect the plants with the BPMV-GFP virus. Twelve replicates were used for each condition. DFPM lead to a clear reduction of the number of plants showing BPMV symptoms and a clear reduction of the BPMV fluorescence on soybean seven days-post- infection on soybean (Table 2).
  • Table 2 Reduction of BMPV symptoms and fluorescence upon treatment with DFPM at 100 and 200 ppm.

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Abstract

The use of specific active substances, alone or in combination, for controlling virus infections in plants and a method for using said specific active substances for controlling said virus infections in the field of plant protection and the protection of materials are disclosed.

Description

Use of active substances for controlling virus infection in plants
TECHNICAL FIELD
The present invention relates to the use of active substances for stimulating the natural defense mechanism of plants against viruses in order to control virus infections in plants and to methods for controlling virus infections in plants. The present invention also pertains to the use of active substances for activating the RNA-interference-based natural defense mechanism (also designated herein as RNA-silencing-based natural defense mechanism) of plants against viruses. BACKGROUND
Plant viruses are responsible for major crop damages around the world. Indeed, some virus families, such as the Potyviridae, cause critical yield losses both in developed and emerging countries, conflicting with the ever-increasing food demand. To limit virus infections and spread, disease management is mainly conducted via prevention, as curative treatments are not or poorly efficient.
Several compounds have been identified for trying to control plant viruses. WO2011/030816 teaches the use of certain ascorbic acid derivatives to control certain plan viruses. WO2012/016048 provides for the use of azide-modified biomolecules as antiviral agents, including against plant viruses. WO2014/050894 teaches the use of other ascorbic acid related compounds to control plant viruses.
Plants have evolved to continuously cope with threats using their available resources and balancing them between growth or defense against biotic and abiotic threats. RNA silencing plays a major part in this balance by dynamically linking developmental programs and environmental stress responses to gene expression changes through transcriptional gene silencing (TGS) and post-transcriptional gene silencing (PTGS). Disease resistance in plants relies on preformed barriers, toxic secondary metabolites and inducible defense mechanisms. Upon pathogen recognition, plants often initiate hypersensitive response, leading to cell death at the infection site and preventing the pathogen from spreading. In addition, pathogen detection triggers various inducible systemic defenses, in parts of the plant distant from the primary infection site. This process, known as Systemic Acquired Resistance (SAR), is effective in many plant species. The resistance achieved is long-lasting and effective against subsequent infections by a broad range of pathogens e.g. fungi, bacteria and viruses.
The Strobilurin class of fungicides comprises a variety of synthetic plant-protecting compounds with broad-spectrum. In 2002, the strobilurin Pyraclostrobin has been demonstrated to enhance the resistance of tobacco against infection by either tobacco mosaic virus (TMV) or the wildfire pathogen Pseudomonas syringae pv tabaci (Herms et al., Plant Physiology 2002, 130: 120- 127). Pyraclostrobin was also able to enhance TMV resistance in NahG transgenic tobacco plants unable to accumulate significant amounts of the endogenous salicylic acid. Pyraclostrobin enhances TMV resistance in tobacco either by acting downstream of Salicylic Acid (SA) in the SA signaling mechanism or by functioning independently of SA. The latter assumption is the more likely because, in infiltrated leaves, Pyraclostrobin did not cause the accumulation of SA-inducible pathogenesis-related (PR)-l proteins that often are used as conventional molecular markers for SA-induced disease resistance. Application of strobilurins is described either alone (WO 01/82701) or in mixture with metiram (WO 2007/104669).
Among the plant defense responses to phytoviruses, the antiviral RNA silencing pathway is the broadest defense system affecting both the local and the systemic accumulation of a wide range of viruses. RNA silencing is a mechanism that directly defends plant host cells against exogenous nucleic acids, including viruses and transposable elements. This defense is triggered by double-stranded RNA (dsRNA), derived from amplification of invasive nucleic acids, which is processed by the host into small interfering RNAs (siRNAs) that are 20-24 nucleotides (nt) in size. These siRNAs are then used to guide the silencing of the viral or transposable element RNA or DNA through PTGS or TGS, respectively.
RNA silencing is then a potent antiviral mechanism whereby small interfering siRNAs processed by the enzyme Dicer from viral double-stranded RNA replication intermediates are loaded into ARGON AUTE effector proteins and turned back onto the invader's RNA genome to induce its degradation. This innate immune response is remarkably versatile because, being solely programmed by structural and nucleotide-sequence genomic features, it can respond to virtually any plant virus (Shimura et al., 2011, Biochimica et Biophysica Acta 1809: 601-612). Attesting the importance of RNA silencing in plant defense, plants impaired in siRNA production or activity are hyper-susceptible to phytoviruses, and conversely many viruses have evolved suppressors of RNAi in order to maintain virulence (Voinnet O. et al, Nature Review Microbiology 2013 Nov;l l(l l):745-60).
Although certain compounds have been identified in the past as potential inducers of certain plant defense mechanisms against viruses, there remains a need to provide active substances suitable for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the broad non-specific RNA-silencing-based defense mechanism of plants against viruses in order to control viral diseases in plants.
FIGURES
Figure 1 illustrates the qPCR analysis of the SUL mRNA relative levels in SUC-SUL plants seven days after treatment with DMSO only or DFPM, normalized to EXP10. Error bars represent standard deviation from three independent experiments.
Figure 2 represents the average number of infection foci at five days post-infection on inoculated leaves. Error bars represent standard deviation from twelve plants. Figure 3 illustrates the RT-qPCR analyses on HcPro mRNA accumulation in systemic tissues at six days post-infection. Error bars represent standard deviation from three independent PCR results. DEFINITIONS
The term "(Ci-C6)alkyl" as used herein refers to a branched- or straight-chain alkyl group containing from 1 to 6 carbon atoms. Representative examples of (Ci-Ce)alkyl include methyl, ethyl, n-propyl, i-propyl and the different butyl, pentyl or hexyl isomers.
The term "halogen" as used herein refers to a fluorine, chlorine, iodine or bromine atom.
The term "(Ci-C6)haloalkyl" as used herein refers to a (Ci-Ce)alkyl group, as defined above, wherein at least one hydrogen atom is replaced with a halogen atom. Representative examples of (Ci-C6)haloalkyl include -CF3,- CH2C1 and -CH2-CF3.
The term "(Ci-C6)cyanoalkyl" as used herein refers to a (Ci-Ce)alkyl group, as defined above, wherein at least one hydrogen atom is replaced with a cyano group.
The term "(C3-C6)cycloalkyl" as used herein refers to a saturated monocyclic alkyl radical wherein the cyclic framework has 3 to 6 carbon atoms. Representative examples of "(C3- C6)cycloalkyl" include cyclopropyl, cyclobutyl and cyclopentyl.
The term "azabicycloalkyl" as used herein refers to a fully saturated monovalent radical containing from 5 and up to 10 carbon atoms and a nitrogen atom in a bicyclic ring. Representative exemples of "azabicycloalkyl" include azabicyclo[3.1.0]hexyl, azabicyclo[2.2.1]heptyl and azabicyclo[2.2.2]octyl.
The expression "may be substituted" as used herein (e.g. a phenyl that may be substituted), means that the substitution is optional and therefore includes both unsubstituted and substituted atoms or groups (e.g. unsubstituted and substituted phenyl). When an atom or group is substituted, any hydrogen on the designated atom or group can be replaced with a substituent (up to and including that every hydrogen is replaced with a substituent) provided that the normal valency of the designated atom or group is not exceeded and that the substitution results in a stable compound.
The term "active substance" as used herein designates a compound of formula (I) as described herein or any mixtures thereof.
DETAILED DESCRIPTION
It has now been found that compounds of formula (I) as disclosed herein are suitable for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses. Therefore, the compounds of formula (I) as disclosed herein may be useful for controlling viral diseases in plants. The term "control" or "controlling" as used herein designates a preventive or curative control.
Accordingly, the present invention relates to a method for controlling viral diseases in plants, more specifically to a method for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses. The method comprises applying to the plants one or more compounds of formula (I):
Figure imgf000005_0001
wherein
- Rl is a phenyl that may be substituted with one or more halogens, preferably chlorine and bromine;
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of (Ci- Ce)alkyl (preferably methyl, ethyl and n-propyl) and (C3-Ce)cycloalkyl (preferably c- pentyl), or
- R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine, or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of halogen, (Ci-Ce)alkyl and (Ci-Ce)cyanoalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl, preferably azabicyclo[3.1.0]hexyl that may be substituted with a (Ci-C6)haloalkyl. some embodiments, the active substance is a compound of formula (I) wherein
- Rl is a phenyl substituted with one or two halogens independently chosen from chlorine or bromine ; and/or
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of methyl, ethyl, n-propyl and cyclopentyl, or
- R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of methyl, fluorine and cyanoethyl, or - R' and R" together with the nitrogen atom to which they are attached form an azabicyclo[3.1.0]hexyl substituted with a (Ci-C6)haloalkyl, such as a trifluoromethyl.
In some preferred embodiments, the active substance is a compound of formula (I) wherein :
- Rl is selected from the group consisting of 3-chlorophenyl, 4-chlorophenyl, 4- bromophenyl, 2,3-dichlorophenyl and 3,4-dichlorophenyl ; and/or
R2 is selected from the group consisting of -NEt2, -N(n-Pr)2, -N(c-pentyl)Me, piperidin-l-yl, pyrrolidin-l-yl, N-morpholino, 4,4-difluoropiperidin-l-yl, , 4-(2- cyanoethyl)-piperazin- l-yl, 2,6-dimethylmorpholin-4-yl and 6-(trifluoromethyl)-3- azabicyclo[3.1.0]hex-3-yl.
In some embodiments, the active substance is a compound of formula (I) wherein Rl and R2 are selected such as to provide the specific compounds disclosed herein below in table 1. In some preferred embodiments, the active substance is a compound of formula (I) wherein :
Rl is 3,4-dichlorophenyl and R2 is 4,4-difluoropiperidinyl-l-yl ; or
Rl is 3,4-dichlorophenyl and R2 is piperidin-l-yl ; or
Rl is 4-bromophenyl and R2 is piperidin- l-yl.
Compound of formula (I) wherein Rl is 3,4-dichlorophenyl and R2 is piperidin-l-yl is known as DFPM [5-(3,4-Dichlorophenyl)Furan-2-yl]-Piperidin- l-ylMethanethione.
DFPM rapidly downregulates ABA-dependent gene expression in plant and also inhibits ABA- induced stomatal closure. DFPM also stimulates expression of plant defense-related genes including PHYTOALEXIN DEFICIENT4 (PAD4)- and ENHANCED DISEASE SUSCEPTIBILITY 1 (EDS 1) (Kim et al., Current Biology 201 1, 21, 1 1 :990-997).
5-Arylfuran-2-thioamides of formula (I) may be suitably prepared :
- either from 5-arylfuran-2-carboxaldehydes and amines by a Wilgerodt-Kindler reaction, as disclosed in Fedorovich, Ganushchak, Karpyak, Obushchak, Lesyuk, Russian Journal of Organic Chemistry 2007 , 43(8), 1 190-1 195 Γ10.1 134/S10704280070801801
- or via thionation (using classical methods such as treatment with phosphorus pentasulfide or Lawesson reagent, see e.g. "Thionation reactions of Lawesson's reagents" : Cava, Levinson, Tetrahedron 1985, 41(22), 5061-5087 rl0.1016/S0040-4020(01)96753-5l) of the corresponding 5-arylfuran-2-carboxamides, which in turn are readily obtained by literature- known methods (see e.g. Drizin, Gregg, et al, Bioorganic & Medicinal Chemistry 2008, 16(12), 6379-6386 [10.1016/j.bmc.2008.05.003l ; Gargano, Perspicace, et al, European Journal of Medicinal Chemistry 2014, 87, 203-219 rl0.1016/i.eimech.2014.09.06H). An effective amount of active substance is typically applied to the plants. The effective amount of active substance which is applied to the plants will depend on various factors, such as the nature of the active substance, the formulation, the plants being targeted (plants nature and plants part), the application method, the purpose of the treatment (prophylactic or therapeutic) and the virus being targeted. The amount applied to the plants may suitably range from 0.01 to 5 kg ha, or from 0.1 to 3 kg ha, or from 0.5 to 2 kg ha.
As indicated above, the active substance is applied to the plants. The term "plants" as used herein include plants and parts thereof, such as the aerial and/or subterraneous parts of the plants as well as the harvested material. Subterraneous plants parts include root, rhizomes, tubers, suckers, slips, seeds and seed. The aerial plant parts include stem, bark, shoot, leaf, flower, fruits, fruiting bodies, stalk, needles and branches. Thus, the active substance may be efficiently applied to the root, rhizomes, tubers, suckers, slips, seeds, seed, stem, bark, shoot, leaf, flower, fruits, fruiting bodies, stalk, needles, branches, harvested material of the plants. In alternative embodiments, the method for controlling viral diseases in plants comprises applying the disclosed active substance to the plants' habitat and/or store.
The active substance can be efficiently applied to a large variety of plants. It may be applied to plants of the varieties which are commercially available or in use. However, plant varieties are also understood as meaning plants with novel traits which have been bred either by traditional breeding, by mutagenesis or with the aid of recombinant DNA techniques and/or to plants which can be obtained by traditional breeding and optimization methods or else by biotechnological and genetic engineering methods or by combinations of these methods; this includes the transgenic plants and the plants which are capable or not of being protected by Plant Breeders' Rights.
The active substance may also be efficiently applied to genetically modified organisms (GMOs). Genetically modified plants are plants in which a heterologous gene has been stably integrated into the genome. The expression "heterologous gene" essentially means a gene which has been provided or assembled outside the plants and, when introduced into the nuclear, chloroplastic or mitochondrial genome, imparts novel or improved agronomic or other properties to the transformed plant by expressing a protein or polypeptide of interest or by down regulating or silencing another gene which is present in the plant, or other genes which are present in the plant (using, for example, antisense technology, cosuppression technology or RNAi technology [RNA interference]). A heterologous gene that is located in the genome is also called a transgene. A transgene that is defined by its particular location in the plant genome is referred to as a transformation event, or transgenic event. All plants which have genetic material which imparts, to these plants, especially advantageous, useful traits (whether obtained by breeding and/or by biotechnology) may be treated by the disclosed method.
Plants and plant varieties which can likewise be treated in accordance with the invention are those plants which are resistant to one or more abiotic stress factors. Abiotic stress conditions can include, for example, drought, chill and heat conditions, osmotic stress, water-logging, elevated soil salt content, elevated exposure to minerals, ozone conditions, high-light conditions, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients or the avoidance of shade.
Plants and plant varieties which can likewise be treated in accordance with the invention are those plants which are characterized by enhanced yield characteristics. Enhanced yield in these palm plants can be the result of, for example, improved plant physiology, improved plant growth and improved plant development, such as water utilization efficiency, water retention efficiency, improved nitrogen utilization, improved carbon assimilation, improved photosynthesis, increased germination efficiency and modified maturation. The yield can furthermore be influenced by improved plant architecture (under stress conditions and under nonstress conditions), among which early flowering, flowering control for the production of hybrid seed, seedling vigour, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, number of seeds per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence, and lodging resistance. Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and oil composition, nutritional value, reduction in antinutritional compounds, improved processability and improved storability.
Plants which can likewise be treated in accordance with the invention are hybrid plants that already express the characteristics of heterosis, or hybrid vigour, which generally results in higher yield, higher vigour, better health and better resistance to biotic and abiotic stress factors. Such plants are typically generated by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent). The hybrid seed is typically harvested from the male-sterile plants and sold to growers. Male-sterile plants can sometimes (for example in maize) be generated by detasseling (i.e. the mechanical removal of the male reproductive organs or the male flowers); however, more typically, male sterility is the result of genetic determinants in the plant genome. In this case, in particular when seed is the desired product which is to be harvested from the hybrid plants, it is typically useful to ensure that male fertility in hybrid plants which contain the genetic determinants responsible for male sterility is fully restored. This can be achieved by ensuring that the male parents have appropriate fertility restorer genes which are capable of restoring male fertility in hybrid plants which contain the genetic determinants responsible for male sterility. Genetic determinants for male sterility can be located in the cytoplasm. Examples of cytoplasmic male sterility (CMS) have been described for example for Brassica species (WO 1992/005251, WO 1995/009910, WO 1998/27806, WO 2005/002324, WO 2006/021972 and US 6,229,072). However, genetic determinants for male sterility may also be located in the nuclear genome. Male-sterile plants can also be obtained by plant biotechnology methods, such as genetic engineering. A particularly advantageous means for generating male-sterile plants is described in WO 89/10396, in which, for example, a ribonuclease such as a barnase is selectively expressed in the tapetum cells in the stamens. The fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar (for example WO 1991/002069).
The active substance is particularly suitable for controlling viral diseases in the following plants: cotton, flax, grapevine, fruit, vegetables, such as Rosaceae sp. (for example pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds and peaches, and soft fruits such as strawberries), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp. (for example banana trees and plantations), Rubiaceae sp. (for example coffee), Theaceae sp., Sterculiceae sp., Rutaceae sp. (for example lemons, oranges and grapefruit); Solanaceae sp. (for example tomatoes), Liliaceae sp., Asteraceae sp. (for example lettuce), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp. (for example cucumber), Alliaceae sp. (for example leek, onion), Papilionaceae sp. (for example peas); major crop plants, such as Gramineae sp. (for example maize, turf, cereals such as wheat, rye, rice, barley, oats, millet and triticale), Asteraceae sp. (for example sunflower), Brassicaceae sp. (for example white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes, and oilseed rape, mustard, horseradish and cress), Fabacae sp. (for example bean, peanuts), Papilionaceae sp. (for example soya bean), Solanaceae sp. (for example potatoes), Chenopodiaceae sp. (for example sugar beet, fodder beet, swiss chard, beetroot); useful plants and ornamental plants for gardens and wooded areas; and genetically modified varieties of each of these plants.
More specifically, the active substance is suitable for controlling viral diseases in vegetables. The active substance is particularly suitable for controlling viruses of the following families or genus: Caulimoviridae, Geminiviridae, Bromoviridae, Closteroviridae, Comoviridae Potyviridae, Sequiviridae, Tombusviridae, Rhabdoviridae, Bunyaviridae, Partitiviridae, Rheoviridae, Capillovirus, Carlavirus, Enamovirus, Furovirus, Hordeivirus, Idaeovirus, Luteovirus, Marafivirus, Potexvirus, Sobemovirus, Tenuivirus, Tobamovirus, Tobravirus, Trichovirus, Tymovirus and Umbravirus.
Preferably, the active substance is used for controlling viruses of the following species : Turnip mosaic virus, turnip crinkle virus, bean pod mottle virus, cauliflower mosaic virus, tobacco mosaic virus, tomato bushy stunt virus, rice ragged stunt virus, cucumber mosaic virus, barley yellow dwarf virus, beet yellows virus, lettuce yellows virus, maise mosaic virus, peanut stunt virus and potato virus Y.
The active substance can be applied to the plants in any suitable forms. For example, the active substance may be applied in the form of a suspension, e.g. water- or oil-based suspension, emulsion, solution, powder such as wettable powder, foam, paste, granules, microparticles, aerosols or microencapsulations. Suitable formulations can be prepared in conventional manners. The formulations comprising the active substance may be ready-for-use compositions, i.e. compositions that can be directly applied to the plants by a suitable device, or they may be in the form of commercial concentrates which have to be diluted prior to use.
The formulations may comprise the active substance alone or in combination with other active substances such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, further fungicides, growth-regulating substances, herbicides, safeners and/or fertilizers. The active substance or formulations comprising thereof may be applied to the plants in any customary manners, e.g. watering, spraying, dusting, atomizing. The active substance may be directly or indirectly applied to the plants, the environment, the habitat and/or the store. For example, the active substance can be injected into or below the bark, poured or sprayed around the plant onto the ground (soil, sandy soil, gravelly soil, rocky soil, loamy soil or mixed soil). A further type of application is the spraying onto the plant and its plant parts. In dry form, the active substance composition can be admixed to the ground material (soil, sandy soil, gravelly soil, rocky soil, loamy soil or mixed soil) and/or to the seeds. The active substance can be applied to the irrigation system, either in dry or else in liquid form. The active substance is preferably applied to the plants by spraying.
The present invention also relates to the use of compounds of formula (I) as disclosed herein for controlling viral diseases in plants, more specifically for stimulating the natural defense mechanism of plants against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of plants against viruses. The plants and/or viruses are as disclosed above.
The compounds of formula (I) stimulate the RNA-silencing-based defense mechanism of the plants through an increase in small RNA production. Advantageously, the ability of the compounds of formula (I) to increase small RNA production can also be used in genetically modified plants transformed with an RNAi construct designed to improve agronomic traits and/or to provide resistance against pathogens (e.g. bacteria, fungi), resistance against insect/pest and/or stress tolerance. Therefore, the present invention also relates to the use of one or more compounds of formula (I) to improve agronomic traits and/or to provide resistance against pathogens, resistance against insect/pest and/or stress tolerance in genetically modified plants transformed with an RNAi construct through enhancement of small RNA production.
The present invention also relates to a compound of formula (I) and/or a composition comprising thereof, wherein the compound of formula (I) is as follows:
Figure imgf000011_0001
wherein
- Rl is a phenyl substituted with one or more halogens, preferably chlorine and bromine;
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of (Ci- Ce)alkyl (preferably methyl, ethyl and n-propyl) and (C3-Ce)cycloalkyl (preferably c- pentyl), or
- R' and R" together with the nitrogen atom to which they are attached form a substituted piperidine or morpholine, wherein said substituted piperidine or morpholine is substituted with one or more substituents selected from the group consisting of halogen and (Ci-Ce)alkyl, or
- R' and R" together with the nitrogen atom to which they are attached form an azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl, preferably an azabicyclo[3.1.0]hexyl that may be substituted with a (Ci-C6)haloalkyl.
In some embodiments, the compound is a compound of formula (I) wherein :
- Rl is a phenyl substituted with one or two halogens independently chosen from chlorine or bromine ; and/or
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of methyl, ethyl, n-propyl and cyclopentyl, or
- R' and R" together with the nitrogen atom to which they are attached form a substituted piperidine or morpholine, wherein said substituted piperidine or morpholine is substituted with one or more substituents selected from the group consisting of methyl and fluorine,
- R' and R" together with the nitrogen atom to which they are attached form an azabicyclo[3.1.0]hexyl substituted with a (Ci-C6)haloalkyl, such as a trifluoromethyl. In some preferred embodiments, the compound is a compound of formula (I) wherein :
Rl is 3,4-dichlorophenyl ; and/or
R2 is selected from the group consisting of -Νί¾, -N(n-Pr)2, -N(c-pentyl)Me, 4,4- difluoropiperidin-l-yl, 2,6-dimethylmorpholin-4-yl and 6-(trifluoromefhyl)-3- azabicyclo[3.1.0]hex-3-yl.
The composition of the present invention typically comprises, in addition to the compound of formula (I), one or more acceptable carriers, in particular one or more agriculturally acceptable carriers.
A carrier is a natural or synthetic, organic or inorganic substance with which the active ingredients are mixed or combined for better applicability, in particular for better application to plants, plant parts or seeds. The carrier, which may be solid or liquid, is generally inert.
Examples of suitable solid carriers include, but are not limited to, ammonium salts, natural rock flours, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and synthetic rock flours, such as finely divided silica, alumina and silicates. Examples of typically useful solid carriers for preparing granules include, but are not limited to, crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, synthetic granules of inorganic and organic flours and granules of organic material such as paper, sawdust, coconut shells, maize cobs and tobacco stalks.
Examples of suitable liquid carriers include, but are not limited to, water, polar and nonpolar organic chemical liquids, for example from the classes of aromatic and nonaromatic hydrocarbons (such as cyclohexane, paraffins, alkylbenzenes, xylene, toluene alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride), alcohols and polyols (which may optionally also be substituted, etherified and or esterified, such as butanol or glycol), ketones (such as acetone, methyl ethyl ketone, methyl isobutyl ketone cyclohexanone), esters (including fats and oils) and (poly)ethers, unsubstituted and substituted amines, amides (such as dimethylformamide),lactams (such as N-alkylpyrrolidones) and lactones, sulphones and sulphoxides (such as dimethyl sulphoxide). The carrier may also be a liquefied gaseous extender, i.e. liquid which is gaseous at standard temperature and under standard pressure, for example aerosol propellants such as halohydrocarbons, butane, propane, nitrogen and carbon dioxide.
The composition may further comprise one or more acceptable auxiliaries which are customary for formulating compositions (e.g. agrochemical compositions), such as one or more surfactants. Examples of suitable surfactants include emulsifiers and/or foam formers, dispersants or wetting agents having ionic or nonionic properties, or mixtures thereof. Examples thereof are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene and/or propylene oxide with fatty alcohols, fatty acids or fatty amines (polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers), substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyl taurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty esters of polyols, and derivatives of compounds containing sulphates, sulphonates and phosphates, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, protein hydroly sates, lignosulphite waste liquors and methylcellulose. A surfactant is typically used when the active ingredient and/or the carrier is insoluble in water and the application is made with water. Then, the amount of surfactants typically ranges from 5 to 40 % by weight of the composition.
Further examples of auxiliaries which are customary for formulating agrochemical compositions include water repellent, siccatives, binder (adhesive, tackifier, fixing agent, such as carboxymethylcellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, natural phospholipids such as cephalins and lecithins and synthetic phospholipids, polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose), thickeners, stabilizers (e.g. cold stabilizers, preservatives, antioxidants, light stabilizers, or other agents which improve chemical and/or physical stability), dyes or pigments (such as inorganic pigments, e.g. iron oxide, titanium oxide and Prussian Blue ; organic dyes, e.g. alizarin, azo and metal phthalocyanine dyes), antifoams (e.g. silicone antifoams and magnesium stearate), preservatives (e.g. dichlorophene and benzyl alcohol hemiformal), secondary thickeners (cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica), stickers, gibberellins and processing auxiliaries, mineral and vegetable oils, perfumes, waxes and nutrients (including trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc), protective colloids, thixotropic substances, penetrants, sequestering agents and complex formers. The choice of the carriers and/or auxiliaries will depend on the intended mode of application of the composition and/or on the physical properties of the active ingredient(s).
As previously mentioned, plants are known to use the RNA silencing pathway to fend off invading viruses. In mammals, until the recent findings of Y. Li et al. and P. V. Maillard et al. (Y. Li et al., Science, 342: 231-234, 2013 ; P. V. Maillard et al., Science, 342: 235-238, 2013), scientists could only evidence the gene-regulatory role of RNAi. Now, Y. Li et al. and P. V. Maillard et al. have evidenced that RNAi also acts as an antiviral response in mammals. Hence, the compounds of formula (I) can be used for stimulating the natural defense mechanism of mammals against viruses, in particular for stimulating the RNA-silencing-based defense mechanism of mammals against viruses.
Therefore, the present invention also relates to compounds of formula (I) as disclosed herein for use as a medicament, in particular for use in the treatment or prevention of a viral infection.
The compound of formula (I) as disclosed herein may be used in a method for treating or preventing a viral infection in mammals which comprises administrating to a mammal in need thereof an effective amount of a compound of formula (I) as disclosed herein. The term "mammals" as used herein includes humans.
The present invention is explained in greater detail with the aid of the examples which follow. EXAMPLES Example 1 : Identification of modulators of plant's silencing machinery - use of SUC-SUL reporter plants
The plants' RNA silencing pathway can be easily monitored with certain artificially-created reporter plants called the "SUC-SUL Arabidopsis reporter plants" (Dunoyer et al., Nat. Genet. 37, 1356-1360, 2005).
The SUC-SUL Arabidopsis reporter plants are transgenic plants expressing an inverted-repeat (IR) double-stranded RNA designed to target the SULPHUR (SUL) transcript in the vasculature under the control of the SUC2 promoter (Truernit et al, Planta 196(3), 564-570, 1995). Once expressed, the dsRNA is processed into small interfering RNAs directing non-cell autonomous post-transcriptional gene silencing of the SULPHUR transcript, in turn causing vein-centered chlorosis. Since the observed chlorosis results from the silencing of the SULPHUR transcript, an expansion of the chlorosis, observable directly on the plants, is correlated with an intensification of the RNA silencing pathway at the molecular level.
Five days post-germination A. thaliana seedlings (n=6) were sprayed with different solutions containing 300 ppm of an active molecule according to the invention, with dimethylsulfoxide (DMSO) 5 % and a standard emulsifiable concentrate (EC) premix formulation (6 seedlings/test). Four repetitions were performed for each molecule. Control plants were treated with DMSO only (mock treated plants). The effects of the treatments on the SUC-SUL reporter plants were assessed 14 days after treatment under trans-illumination and digitally recorded with a stereo-microscope by measuring the surface and intensity of the chlorotic zone (percentage of chlorosis). Two independent experiments were carried out in order to estimate the average percentage of chlorosis for each molecule. Results are shown in table 1 below. Treatment with 300 ppm of DFPM ([5-(3,4- dichlorophenyl)furan-2-yl]-piperidine-l-ylmethanethione) and analogues thereof led to a significant increase in the percentage of chlorosis confirming the activity of the active substance as putative robust enhancers of RNA silencing. In order to discard molecules acting straightly on the promoter and not on the RNA silencing machinery, the active substances identified for their ability to increase the surface and intensity of the chlorotic zone were then tested, in a second step, on some AtSUC2-GFP reporter plants, which are specifically reporting the activity of the SUC2 promoter (Wright et al., Plant Physiol. 131, 1555-1565, 2003).
Figure imgf000015_0001
Figure imgf000015_0002
Table 1 : evaluation of DFPM (compound ID No. 3) and analogs thereof on SUC-SUL reporter plants. The level of chlorosis of mock treated plant reached 10%. Example 2 : Confirmation of the molecular effect of the silencing modulators
The enhancing effect of DFPM on the RNAi machinery has been validated at the phenotypic and molecular levels. Four-week-old SUC-SUL Arabidopsis plants at rosette stage were sprayed with DFPM at 200 ppm. Seven days after treatment, it was shown that DFMP induced a clear expansion of the RNAi-dependent vein-centered chlorotic phenotype, which was not observed with DMSO only (mock control). The plant aerial tissues were collected and analyzed molecularly using state-of-the-art methodologies. The visual expansion of the chlorosis correlated with reductions in SUL transcript levels, as analyzed by real-time qRT-PCR (Figure 1), as well as reductions in SUL protein levels quantifiable on Western blot analyses. Furthermore, these effects were associated with an over-accumulation of both SUL 21-nt and 24-nt long siRNAs derived from the transgenic SUL. Altogether, these data support that DFPM induces the plant's RNAi pathway.
Example 3 : Antiviral efficacy of silencing modulators on Arabidopsis The Turnip mosaic virus (TuMV) belongs to the Potyviridae, the largest family of known plant viruses. This virus infects a wide range of plants, in particular Brassicaceae. TuMV genome consists of a positive- sense single-stranded RNA molecule (+ ssRNA). The antiviral efficacy of DFMP was tested with a fluorescently-tagged potyvirus (TuMV-GFP) in order to specifically pinpoint when and where the effect of the molecules is induced during virus primary infection, as well as its local or systemic spread.
Arabidopsis plants were sprayed with 100 or 200 ppm of DFMP 3 days before infecting the plants with the TuMV-GFP virus. Virus titers were measured by qPCR and/or virus protein accumulation on Western blot analyses and by counting the number of primary infection foci under UV light in the case of the TuMV-GFP.
DFPM leads to a clear reduction of the accumulation of virus titers five days-post-infection on the Arabidopsis plants. A strong reduction of virus accumulation was consistently observed with TuMV-GFP both on inoculated leaves (Figure 2) and on systemic tissues upon treatment with DFPM, as measured by the reduction of the accumulation of the TuMV-derived HcPro mRNA levels (Figure 3).
Similar results were obtained with DFPM with the unrelated viruses Turnip crinkle virus (TCV,) and Cauliflower mosaic virus (CaMV). The TCV belongs to the Tombusviridae family and infects various types of plant species including the common plant models A. thaliana and N. benthamiana. Its genome is another example of +strand RNA virus. The CaMV belongs to the Caulimoviridae family. It infects mostly Brassicaceae such as turnip and cabbage, but is also able to infect A. thaliana. CaMV consists of a double-stranded DNA molecule.
DFPM treatment at lOOppm lead to a strong reduction of virus accumulation both on inoculated leaves and on systemic tissues, as measured by the reduction of the accumulation of the TCV- derived P38 mRNA and CaMV-derived P6 mRNA.
Example 4 : Antiviral efficacy of silencing modulators on Soybean plants
The Bean pod mottle virus (BPMV) is a plant pathogenic virus of the family Comoviridae. This virus infects legumes and more particularly soybean. BPMV genome consists of a bipartite positive-sense single- stranded RNA molecule (+ ssRNA). The antiviral efficacy of silencing enhancers was tested with a fluorescently-tagged comoviruss (BPMV-GFP) in order to specifically pinpoint when and where the effect of the molecules is induced during virus primary infection, local or systemic spread.
Soybean plants were sprayed with 100 or 200ppm of DFPM and emulsifiable concentrate (EC) Premix one day before to infect the plants with the BPMV-GFP virus. Twelve replicates were used for each condition. DFPM lead to a clear reduction of the number of plants showing BPMV symptoms and a clear reduction of the BPMV fluorescence on soybean seven days-post- infection on soybean (Table 2).
Figure imgf000017_0001
Table 2: Reduction of BMPV symptoms and fluorescence upon treatment with DFPM at 100 and 200 ppm.

Claims

Claims:
A method for controlling viral diseases in plants, which comprises applying to the plants at least one compound of formula (I) :
Figure imgf000018_0001
- Rl is a phenyl that may be substituted with one or more halogens ;
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of (Ci-Ce)alkyl and (C3-C6)cycloalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine, or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of halogen, (Ci- Ce)alkyl and (Ci-Ce)cyanoalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form an azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl.
2. The method according to claim 1, wherein Rl is selected from the group consisting of 3-chlorophenyl, 4-chlorophenyl, 4-bromophenyl, 2,3-dichlorophenyl and 3,4- dichlorophenyl.
The method according to claim 1 or 2 wherein R2 is selected from the group consisting
Figure imgf000018_0002
of -NEt2, -N(n-Pr)2, -N(c-pentyl)Me, piperidin-l-yl, pyrrolidin-l-yl, N-morpholino,
4,4-difluoropiperidin- 1 -yl, 4-(2-cyanoethyl)-piperazin- 1 -yl, 2,6-dimethylmorpholin-4-yl and 6-(trifluoromethyl)-3-azabicyclo[3.1.0]hex-3-yl. The method according to anyone of claims 1 to 3, wherein the control is based on a stimulation of the natural defense mechanism of plants against viruses.
The method according to claim 4, wherein the natural defense mechanism of plants against viruses is a RNA-silencing based plant defense mechanism.
The method according to anyone of the preceding claims, wherein said method is a preventive method.
The method according to anyone of the preceding claims, wherein said plants are selected from the group consisting of cotton, flax, grapevine, fruit, vegetables, crop plants, ornamental plants for gardens and wooded area and genetically modified varieties of each of these plants.
The method according to anyone of the preceding claims, wherein said plants are selected from the group consisting of Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp., Rubiaceae sp., Theaceae sp., Sterculiceae sp., Rutaceae sp. ; Solanaceae sp., Liliaceae sp., Asteraceae sp., Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Alliaceae sp., Papilionaceae sp., Asteraceae sp., Brassicaceae sp., Fabacae sp. , Papilionaceae sp. , Solanaceae sp. and Chenopodiaceae sp..
The method according to anyone of the preceding claims, wherein said viruses are selected from the group consisting of the following families or genus: Caulimoviridae, Geminiviridae, Bromoviridae, Closteroviridae, Comoviridae Potyviridae, Sequiviridae, Tombusviridae, Rhabdoviridae, Bunyaviridae, Partitiviridae, Rheoviridae, Capillovirus, Carlavirus, Enamovirus, Furovirus, Hordeivirus, Idaeovirus, Luteovirus, Marafivirus, Potexvirus, Sobemovirus, Tenuivirus, Tobamovirus, Tobravirus, Trichovirus, Tymovirus and Umbravirus.
The method according to anyone of the preceding claims, wherein said viruses are selected from the group consisting of Turnip mosaic virus, turnip crinkle virus, bean pod mottle virus, cauliflower mosaic virus, tobacco mosaic virus, tomato bushy stunt virus, rice ragged stunt virus, cucumber mosaic virus, barley yellow dwarf virus, beet yellows virus, lettuce yellows virus, maise mosaic virus, peanut stunt virus and potato virus Y.
11. The method according to anyone of the preceding claims, wherein the compound of formula (I) is applied by spraying to the plants.
12. The method according to anyone of the preceding claims, wherein the compound of formula (I) is applied to the plants in an amount ranging from 0.01 to 5kg ha.
13. Use of a compound of formula (I) as defined in claim 1, 2 or 3 for stimulating the natural defense mechanism of plants against viruses.
14. Use according to claim 13 for stimulating the RNA-silencing-based plant defense mechanism.
15. Use of a compound of formula (I) as defined in claim 1, 2 or 3 to improve agronomic traits and/or to provide resistance against pathogens, insect, pest and/or to provide stress tolerance in genetically modified plants transformed with an RNAi construct.
16. A compound of formula (I) :
Figure imgf000020_0001
wherein
- Rl is a phenyl substituted with one or more halogens ;
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of (Ci-C6)alkyl and (C3-C6)cycloalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form a substituted piperidine or morpholine, wherein said substituted piperidine or morpholine is substituted with one or more substituents selected from the group consisting of halogen and (Ci-C6)alkyl, or
- R' and R" together with the nitrogen atom to which they are attached form an azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl.
17. A compound of formula (I)
Figure imgf000021_0001
(I) wherein
- Rl is a phenyl that may be substituted with one or more halogens ;
- R2 is a -NR'R" group wherein :
- R' and R" are independently selected from the group consisting of (Ci-Ce)alkyl and (C3-C6)cycloalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocycle chosen from pyrrolidine, piperidine, morpholine, or piperazine, wherein said heterocycle may be substituted with one or more substituents selected from the group consisting of halogen, (Ci- Ce)alkyl and (Ci-Ce)cyanoalkyl, or
- R' and R" together with the nitrogen atom to which they are attached form an azabicycloalkyl that may be substituted with a (Ci-C6)haloalkyl ; s a medicament.
PCT/EP2017/050583 2016-01-13 2017-01-12 Use of active substances for controlling virus infection in plants WO2017121809A1 (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102746282A (en) * 2011-04-21 2012-10-24 中国农业大学 N-5-substituted phenyl-2-furoyl compounds, preparation method and application thereof
EP2902387A1 (en) * 2012-09-27 2015-08-05 Nippon Soda Co., Ltd. Ascorbic acid-related compound and anti-plant-virus agent

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005007141A2 (en) * 2003-07-11 2005-01-27 Proteologics, Inc. Ubiquitin ligase inhibitors and methods related thereto
US8642660B2 (en) * 2007-12-21 2014-02-04 The University Of Rochester Method for altering the lifespan of eukaryotic organisms
WO2011047129A1 (en) * 2009-10-15 2011-04-21 Southern Research Institute Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
WO2011097607A1 (en) * 2010-02-08 2011-08-11 Southern Research Institute Anti-viral treatment and assay to screen for anti-viral agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102746282A (en) * 2011-04-21 2012-10-24 中国农业大学 N-5-substituted phenyl-2-furoyl compounds, preparation method and application thereof
EP2902387A1 (en) * 2012-09-27 2015-08-05 Nippon Soda Co., Ltd. Ascorbic acid-related compound and anti-plant-virus agent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
I. S. FEDOROVICH ET AL: "Thioamides from 5-arylfurfural and monosubstituted piperazine derivatives (Wilgerodt-Kindler reaction)", RUSSIAN JOURNAL OF ORGANIC CHEMISTRY., vol. 43, no. 8, 1 August 2007 (2007-08-01), US, pages 1190 - 1195, XP055260243, ISSN: 1070-4280, DOI: 10.1134/S1070428007080180 *

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