METHOD FOR CONTROLLING FUSARIUM OXYSPORUM F. SP. CUBENSE TROPICAL RACE 4

Abstract

The present disclosure provides a method for controlling Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4). The present disclosure mainly aims to solve the problem of effectively inhibiting the Foc TR4, but the existing fungicides cannot effectively inhibit the Foc TR4 without damage to banana plants. By treating with the fungicide disclosed by the present disclosure, the growth of the Foc TR4 can be limited, and there is no adverse effect on banana plants.

Claims

1. A method for controlling Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4), comprising: preparing an agrochemical agent, wherein the agrochemical agent includes a compound xerucitrinin A.

2. The method according to claim 1, wherein the agrochemical agent for controlling Foc TR4 further comprises an agricultural-pharmacologically acceptable adjuvant.

3. The method according to claim 1, wherein the agrochemical agent for controlling Foc TR4 further comprises other agrochemical agents for controlling Foc TR4.

4. The method according to claim 1, wherein the agrochemical agent for controlling Foc TR4 is in a pharmaceutical dosage form selected from the group consisting of a wettable powder, a water dispersible granule, a suspension and an emulsifiable concentrate.

5. The method according to claim 1, wherein a concentration of the compound xerucitrinin A in the agrochemical agent for controlling Foc TR4 is 3 mM.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] FIG. 1 illustrates a Fe-binding function of compound xerucitrinin A;

[0016] FIG. 2 illustrates an effect of compound xerucitrinin A on spores of Foc TR4. (A to C) Normal spores of Foc TR4; (D to F) spores of Foc TR4 treated with 3 mM compound xerucitrinin A;

[0017] FIG. 3 illustrates effects of compounds xerucitrinin A (XcA) and 8-hydroxyquinoline (8HQ) on the growth of banana seedlings at inhibitory concentrations.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0018] In order to specifically clarify the means and implementation effects used in the present disclosure, the present disclosure will be further described below in conjunction with examples and drawings.

Example 1

[0019] Chrome azurol S (CAS) agar plate, namely the siderophore screening medium consisting of 1 mL of 20% glucose solution, 3 mL of 10% casein, 100 μL of 1 mmoL/L CaCl.sub.2), 2 mL of 1 mmoL/L MgSO.sub.4, 100 mL of H.sub.2O, and 1.8 g of agar, was heated, and supplemented with 5 mL each of CAS dye solution and phosphate buffered saline (PBS) at 60° C. slowly to obtain a CAS-blue agar medium.

[0020] CAS dye solution included: 1 mmol/L CAS, 4 mmol/L hexadecyl trimethyl ammonium bromide, and 0.1 mmol/L FeCl.sub.3.

[0021] PBS (pH 6.8) included: 2.427 g of Na.sub.2HPO.sub.4.12H.sub.2O, 0.5905 g of NaH.sub.2PO.sub.4.2H.sub.2O, 0.075 g of KH.sub.2PO.sub.4, 0.250 g of NH.sub.4Cl, 0.125 g of NaCl, and 100 mL of H.sub.2O. All the above solutions were prepared with deionized water.

[0022] A sterile Oxford cup was placed in the middle of the CAS agar plate; 200 μL of 0.2 mM compound solution was pipetted into the Oxford cup using a sterile pipette tip, and let stand for 12 h to observe whether there was a siderophore zone around the Oxford cup.

[0023] The results show that the compound xerucitrinin A has a Fe-binding function. The Fe-binding ability of xerucitrinin A was detected by using the CAS agar plate. As shown in FIG. 1, xerucitrinin A was added to an Oxford cup and let stand for 3 h, and a siderophore zone appeared around the Oxford cup, indicating that xerucitrinin A has a Fe-binding ability. The growth of Foc TR4 is inhibited by binding Fe.

Example 2

[0024] XcA (the compound xerucitrinin A) at a final concentration of 3 mM was added to Gauze's Medium #1, and the filtered spore suspension of Foc was added, with a final spore concentration of 1×10.sup.7 spores/mL. The control treatment was implemented by treating with the same volume of sterile water. The spore suspension was cultured at 28° C. in the dark for 24 h. The spores of Foc were collected and fixed in a 2.5% (v/v) glutaraldehyde solution at 4° C. overnight. The fixed spores were rinsed twice with 0.1 mol/L PBS (pH 7.4), dehydrated gradiently with 30%, 50%, 70%, 80%, 90%, 95%, and 100% ethanol solutions for 20 min, dried and subjected to gold spraying. The spore morphology of Foc TR4 was observed under a scanning electron microscope.

[0025] The results show that the addition of 3 mM xerucitrinin A in the Gauze's Medium #1 can change the spore morphology of Foc, cause obvious crenation on the surface of the spores of Foc, and affect the germination and growth of the spores of Foc (FIG. 2).

Example 3

[0026] XcA was dissolved in ethanol. In order to investigate the effect of XcA on the growth of Brazilian banana, 3 mM XcA was added to Gauze's Medium #1. A volume of ethanol (CK) equal to the compound concentration was added to the control. A negative control was set up, and 200 μM 8-hydroxyquinoline (8HQ) was added to the Gauze's Medium #1. Then Brazilian banana seedlings were planted in a culture plate containing the above-mentioned treated medium. Each treatment had 6 replicates (6 Brazilian banana seedlings). The culture plate containing Brazilian banana seedlings was placed in a growth chamber to grow for 10 days to observe the effect on plant growth. Each treatment continued to grow for two months, during which an equal volume of sterile water was supplemented, and the plant height, root weight and seedling weight of each treatment were determined.

[0027] The results showed that sterile water, 3 mM compound xerucitrinin A (XcA) and 200 μM 8HQ were added to the Gauze's Medium #1,respectively. Compared with the control, the 3 mM compound xerucitrinin A had no adverse effect on the growth of banana seedlings (FIG. 3).

[0028] The compound xerucitrinin A can be used as an effective additive in a fungicide for controlling Foc TR4, and has excellent application value.