Anti-pathogenic methods
The present disclosure teaches the protection of plants and human and non-human subjects from pathogens. The present disclosure enables a multivalent approach to inhibiting pathogen infection in plant and human and non-human animal subjects and to ameliorate damage to susceptible subjects.
1. A method for treating fungal pathogen infection of a subject, said method comprising providing cells of said subject with a Class I defensin, wherein the Class I defensin has a mature domain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 85, 3, 6, 12, 24, 27, 36, 39 and 45, and a permeabilizing defensin having a mature domain selected from the group consisting of NaDI, TPP3, PhD1A, PhD2, NoD173, SEQ ID NOs: 3, 6, 12, 24, 70, 71 and 72, wherein the Class I defensin and the permeabilizing defensin are not the same.
2. The method of claim 1 , wherein the subject is a plant.
3. The method of claim 2 , wherein the Class I defensin and permeabilizing defensin are produced by a genetically modified plant cell or both defensins are applied topically to the plant or via the plant's root system or as a seed coating or as a surface spray.
4. The method of claim 1 , further comprising providing the cell of said subject with a proteinase inhibitor or precursor form thereof.
5. The method of claim 1 , wherein the fungal pathogen is selected from the group consisting of Fusarium graminearum, Colletotrichum graminicola, Leptosphaeria maculans, Alternaria brassicicola, Alternaria alternata, Aspergillus nidulans, Botrytis cinerea, Cercospora beticola, Cercospora zeae maydis, Cochliobolus heterostrophus, Exserohilum turcicum, Fusarium culmorum, Fusarium oxysporum, Fusarium solani, Fusarium pseudograminearum, Fusarium verticilloides, Gaeumannomyces graminis var. tritici, Plasmodiophora brassicae, Sclerotinia sclerotiorum, Stenocarpella maydis, Thielaviopsis basicola, Verticillium dahliae, Ustilago zeae, Puccinia sorghi, Macrophomina phaseolina, Phialophora gregata, Diaporthe phaseolorum, Cercospora sojina, Phytophthora sojae, Rhizoctonia solani, Phakopsora pachyrhizi, Alternaria macrospora, Cercospora gossypina, Phoma exigua, Puccinia schedonnardii, Puccinia cacabata, Phymatotrichopsis omnivora, Fusarium avenaceum, Alternaria brassicae, Alternaria raphani, Erysiphe graminis, Septoria tritici, Septoria nodorum, Mycosphaerella zeae, Rhizoctonia cerealis, Ustilago tritici, Puccinia graminis, Puccinia triticina, Tilletia indica, Tilletia caries, and Tilletia controversa, Aspergillus niger, Candida, Cryptococcus, Trichophyton interdigitale and Trichophyton rubrum.
6. The method of claim 2 , wherein the plant is a crop plant selected from the group consisting of a forage crop, oilseed crop, grain crop, fruit crop, vegetable crop, fiber crop, spice crop, nut crop, turf crop, sugar crop, beverage crop and a forest crop.
7. The method of claim 6 , wherein the crop plant is selected from the group consisting of soybean, canola, corn, cotton and wheat.
8. The method of claim 2 , wherein the Class I defensin and permeabilizing defensin are applied as a seed coating.
9. The method of claim 1 , wherein the subject is a human or non-human animal.
10. The method of claim 9 , wherein the Class I defensin and permeabilizing defensin are applied topically to the human or non-human subject.
11. The method of claim 1 , wherein the Class I defensin has a mature domain selected from the group consisting of SEQ ID NOs:6, 12, 24, 27, 36 and 45, and the permeabilizing defensin has a mature domain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs:6, 12, 24 and 70.
12. The method of claim 4 , wherein the proteinase inhibitor is a cystatin.
13. The method of claim 5 , wherein the Fusarium oxysporum is selected from the group consisting of Fusarium oxysporum f. sp. vasinfectum, Fusarium oxysporum f. sp. dianthi and Fusarium oxysporum f. sp. lycopersici.