Patent Application
20130190169
The present invention relates generally to a synergistically effective combination comprising, as active components, folpet (I) and epoxiconazole (II), to a method for controlling phytopathogenic fungi using a combination of folpet (I) and epoxiconazole (II), and also to compositions comprising this combination in admixture and kits comprising this combination.
The phthalimide derivative N-(trichloromethanesulfenyl)phthalimide, folpet, is a well known protective leaf-fungicide disclosed in U.S. Pat. Nos. 2,553,770; 2,553,771 and 2,553,776. Folpet was first registered as pesticide in the U.S. in 1984. It is used, inter alia, to control grapevine downy mildew, cherry leaf spot, rose mildew, rose black spot, and apple scab, and is used on berries, flowers, ornamentals, fruits and vegetables, and for seed- and plant-bed treatment. Folpet is also used as a fungicide in paints and plastics, and for treatment of internal and external structural surfaces of buildings.
The triazole derivative (2RS;3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fluorophenyl)propyl]-1H-1,2,4-triazole, epoxiconazole, its synthesis and its antifungal properties have been disclosed in U.S. Pat. Nos. 4,464,381 and 4,906,652. Epoxiconazole is a broad spectrum contact and systemic fungicide used to control powdery mildew, brown and yellow rusts, Septoria tritici and Septoria Nodorum on Winter and Spring wheat and Triticale; powdery mildew, Rhyncosporium, net blotch and brown and yellow rust on Winter and Spring barley; powdery mildew, Rhyncosporium, net blotch and brown and yellow rust on Rye; and powdery mildew on Oats.
Combinations of agricultural fungicides are typically used to broaden the spectrum of control, to minimize the doses of chemicals used and to reduce the cost of the treatment through additive effect. Combinations of agricultural fungicides can be also used to avoid or delay the risk of resistance development. In some cases, resistance can be overcome by using combinations of fungicide.
U.S. Pat. Nos. 4,464,381 and 4,906,652 further disclose a list of fungicides with which epoxiconazole may be combined, inter alia, with folpet, but do not suggest any synergism.
The present invention provides compositions and methods employing combinations of synergistically effective amounts of folpet (I) and epoxiconazole (II).
In certain embodiments, fungicidal combinations are provided, comprising folpet (I) and epoxiconazole (II) in admixture in a synergistically effective amount.
In further embodiments, methods for controlling phytopathogenic fungi are provided, wherein the phytopathogenic fungi, their habitat, plants, soil, or seed to be protected against fungal attack are treated with an effective amount of a combination, for example as admixture, as described above.
In related embodiments, methods for controlling phytopathogenic harmful fungi are provided, wherein one or more of the harmful fungi, their habitat, plants, soil, or seed to be protected are treated simultaneously or sequentially in either order, with a first amount of folpet and a second amount of epoxiconazole; wherein the first and second amounts are synergistically effective.
Also provided herein is the use of the combination of folpet (I) and epoxiconazole (II) as described above for preparing a composition or kit suitable for controlling harmful fungi.
Further embodiments of the present invention provide a fungicidal composition or kit comprising the fungicidal combination as described above and a carrier.
Within still further embodiments, a seed treated with a fungicidal combination as described above is provided.
The applicant has surprisingly found that a combination treatment based on folpet and epoxiconazole, characterized by different modes of action exhibits a considerable synergistic effect, allowing a higher fungicidal activity to be obtained than that envisaged on the basis of the activities of each of the fungicides. Such a combination further displays the advantage of having a wider range of use, and allowing the dosages of folpet and epoxiconazole to be reduced, thereby allowing effective control of numerous diseases which can cause damage to plants (or fruits or seeds thereof) of great economic interest.
Representative plants include, for example, vegetable plants, legume plants, cereal plants, fodder plants, grass plants, fiber plants, oil seed plants, field plants, garden plants, greenhouse plants, and houseplants. Cereal plants include, for example, wheat (e.g., durum wheat or common wheat), rice, corn, barley, oats, triticale and rye.
The compositions, kits, and methods described herein are distinguished by excellent activity against a broad spectrum of phytopathogenic fungi belonging to the following classes: Ascomycetes (e.g. Venturia, Podosphaera, Erysiphe, Monilinia, Uncinula, Aureobasidium, Sclerophoma), Basidiomycetes (e.g. Hemileia, Rhizoctonia, Puccinia, Coniophora, Serpula, Poria, Uromyces, Gloeophyllum, Lentinus, Coriolus, Irpex) and Fungi imperfecti (e.g. Botrytis, Helminthosporium, Rhynchosporium, Fusarium, Septoria, Cercospora, Alternaria, Pyricularia, Penocillium, Geotrichum).
Such compositions, kits, and methods are especially useful for controlling phytopathogenic fungi of cereal plants and their seeds, such as ascomycetous pseudothecial fungus, Mycosphaerella graminicola (Anamorph Septoria tritici); in certain embodiments such control is achieved using low application rates, such that a minimum total amount of active compounds applied, while retaining sufficient activity against the phytopathogenic fungi.
The active components folpet (I) and epoxiconazole (II) can be applied in admixture, for example in the form of a ready-mixed composition, as a tank mix, or may be applied separately, in any order. In certain embodiments, the compounds I and II are employed in a weight ratio that ranges from 1:1 to 20:1 of folpet (I) to epoxiconazole (II) , and in further embodiments, compounds I and II are employed in a weight ratio that ranges from 1:1 to 10:1 of folpet (I) to epoxiconazole (II).
The application rates of the mixture may vary, depending on the effect desired; in particular in agricultural crop areas, such rates may range, for example, from 25 to 2000 grams per hectare (g/ha), from 50 to 1500 g/ha, or from 100 to 1000 g/ha. When the active components are applied separately, the application rates for the compound I typically range from 10 to 1500 g/ha, from 50 to 1500 g/ha, or from 100 to 1000 g/ha; and the application rates for the compound II typically range from 10 to 500 g/ha, from 10 to 300 g/ha, or from 10 to 150 g/ha.
In the treatment of seed, the application rates of the admixture or the separate components generally range from 1 to 1000 g/100 kg of seed, from 1 to 200 g/100 kg of seed, or from 5 to 100 g/100 kg of seed.
In the control of harmful fungi which are pathogenic for plants, in particular cereal plants, the separate or joint application of the compound I and the compound II or of the mixtures of the compound I and the compound II is carried out by any suitable technique known in the art, such as spraying or dusting the seeds, the plants or the soil before or after sowing of the plants, or before or after emergence of the plants.
The invention also provides fungicidal compositions comprising as active components, folpet (I) and epoxiconazole (II) in admixture. Such compositions may comprise, in addition to the aforementioned active components, one or more additional active and/or inactive ingredients. Representative active ingredients include, for example, other microbiocides such as fungicides, insecticides, acaricides, nematicides, herbicides, plant growth regulators, and/or fertilizers. Inactive ingredients included, for example, carriers, surfactants, and other application-promoting adjuvants customarily employed in formulation technology, as well as components that facilitate storage of the composition. Suitable carriers and adjuvants can be solid or liquid and include substances ordinarily employed in formulation technology, e.g. natural or regenerated mineral substances, solvents, dispersants, wetting agents, tackifiers, thickeners, binders or fertilizers.
Compositions may be formulated in any conventional form, such as solutions, emulsions, suspensions, dusts, powders, pastes, granules, or any other technically feasible formulation. The compositions are prepared in known manner, e.g., by homogeneously mixing and/or grinding the active ingredients with extenders, e.g., liquid and solid carriers and, where appropriate, surface-active compounds.
In general, the compositions provided herein comprise from 0.01 to 90% by weight of active agent, from 0.01 to 30% agriculturally acceptable surfactant and 10 to 99.99% solid or liquid formulation inert ingredients and adjuvants. Concentrated forms of compositions generally contain from about 2 and 80%, (e.g., about 10 and 50%) by weight of active agent. Commercial products will preferably be formulated as concentrates; the end user will normally employ diluted formulations.
In another embodiment, the invention also provides a kit comprising fungicidal compositions comprising as active components, folpet (I) and epoxiconazole (II) separately. Such compositions may comprise, in addition to the aforementioned active components, one or more additional active and/or inactive ingredients as described above. The compositions for the kit may be formulated in any conventional form as described above, and prepared as described above. Thus, the kit may comprises a first container comprising folpet (I) and a carrier, and a second container comprising epoxiconazole (II) and a carrier. In general, each of the compositions for the kit comprise from 0.01 to 90% by weight of active agent, from 0.01 to 30% agriculturally acceptable surfactant and 10 to 99.99% solid or liquid formulation inert ingredients and adjuvants. Concentrated forms of compositions generally contain from about 2 and 80%, (e.g., about 10 and 50%) by weight of active agent. Commercial products will preferably be formulated as concentrates; the end user will normally employ diluted formulations. Instructions for use may also be provided with the kit.
As noted above, the compositions, kits, and methods described herein exhibit a synergistic effect. A synergistic effect exists whenever the action of a combination of active components is greater than the sum of the action of each of the components alone. Therefore, a synergistically effective amount (or an effective amount of a synergistic admixture or combination) of a fungicidal admixture or fungicidal combination is an amount that exhibits greater fungicidal activity than the sum of the fungicidal activities of the individual components.
The Wadley method is well-known method for determining whether synergy exists. In the Wadley method, synergistic activity is determined from dose response curves. With this method, the efficacy of the active ingredient (“a.i.”) is determined by comparing the degree of fungal attack on treated plants with that on untreated, similarly inoculated and incubated check plants. Each a.i. is generally tested at multiple (e.g., 6) concentrations, and dose response curves are generated. The dose response curves are used to establish the EC50 (i.e., the effective concentration of a.i. providing 50% disease control) of the individual compounds as well as of the combinations (EC50observed). The experimentally found values of the mixture at a given weight ratio are compared ith the values that would have been found were only a complementary efficacy of the components was present (EC50 (A+B)expected). The EC50 (A+B)expected is generally calculated according to Wadley (Levi et al., EPPO-Bulletin 16, 1986, 651-657) or (Wadley, F. M., U.S. Dep. Agric., Res. Adm., Bur. Entomol. And Plant Quar. ET-223, 1945, 8) as follows:
EC50(A+B)expected−(a+b)/[(a/EC50(A)observed)+b/EC50(B)observed)]
wherein a and b are the weight ratios of the compounds A and B in the mixture and the indexes (A),(B) and (A+B) refer to the observed EC50 values of the compounds A, B or the A+B mixture thereof.
The ratio EC50(A+B) expected/EC50 (A+B)observed expresses the factor of interaction level (R).
The nature of the interaction existing between fungicides used in the combination obtained from the Wadley formula is presented in the following Table 1 (Ulrich Gisi, Phytopathology, 86, 1996, 1273-1279). In the context of the present disclosure, the biological response is generally used to determine a synergistic effect.
Hereinafter, one or more embodiments of the present invention will be described in detail with reference to the following examples. However, these examples are not intended to limit the purpose and scope of this disclosure.
The strain used in this study is the reference strain Mg Refl, which is susceptible to QoI (Quinone outside Inhibitors) and DMI (demethylation inhibitor) fungicides.
This strain has been isolated from infected wheat leaves in the United Kingdom.
Pycnospores of this M. graminicola strain are transferred with a sterile spatula to Maly-Yeast Extract-Agar medium (“MYE”) and incubated at 19° C. in darkness. After 10 days of incubation, pycnospores of this strain of M. graminicola strain are scraped with a sterile scalpel at the surface of the MYE medium and transferred to a 1.5 ml Eppendorf tube containing 1 ml of 2 times concentrated Glucose-Bacto Peptone (2× GBP) liquid medium.
The pycnospores suspension of this strain is adjusted to 2×104 spores/ml in 2× GBP liquid medium.
In vitro evaluation of the sensitivity level of M. graminicola strains towards epoxiconazole and folpet used alone or in admixture
Bacto-Peptone-Glucose liquid medium (“BPG”) was autoclaved for 30 minutes at 120° C., then allowed to settle at room temperature. Folpet, epoxiconazole, or a mixture of epoxiconazole and folpet at each of the following weight ratios (epoxiconazole to folpet), were added to sterile distilled water: 1:10, 1:7.5 and 1:1. The amounts of each component are shown in the table below.
The total final concentration of active ingredient (i.e., the sum of the active ingredient concentrations) was: 0, 0.00256, 0.0128, 0.064, 0.32, 1.6, 8.0, or 40 μg a.i./ml. After homogenization, 100 pl of each solution was added to a well of a 96-well microtitre plate, with sterile distilled water without fungicide used as the control. Then, each well was seeded with 100 μl of the pycnospores suspension (2×104 pycnospores/ml) prepared in 2× BPG liquid medium. For each fungicide ratio and concentration tested, 6 replicates were tested (6 rows per strain). The microtitre plates were then incubated in the dark at 19° C. for 7 days.
The degree of mycelial growth in the liquid medium was assessed by measuring the optical density of the wells containing the spore suspensions and fungicide concentrations. The measurements were made at 0 and 7 days using a Biotek plate reader at a wavelength of 405 nm, and the XLStat-Dose software (Addinsoft) was used to capture and process the data. Then, the mean as well as the lower and higher 95% limit of confidence EC50 values of the M. graminicola strain Mg Ref 1 response to each fungicide (used alone or in a mixture) were determined.
The dose response curves were used to establish the EC50. The fungicide interactions in the mixture were calculated according to Wadley (as discussed above). The results are presented in the following Table 2.
These results demonstrate that epoxiconazole and folpet, in the various concentrations and weight ratios indicated above, exhibit a synergistic effect against M. graminicola.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IL11/00270 | 3/22/2011 | WO | 00 | 11/9/2012 |
| Number | Date | Country | |
|---|---|---|---|
| 61316024 | Mar 2010 | US | |
| 61316188 | Mar 2010 | US |
