Background
Macadamia nut, also known as macadamia nut, is a macadamia plant originally produced in Australia, not only has higher economic value, but also has good nutritional value and medicinal value, and is vegetatively reputed as the king of dried fruit. The macadimia nuts have more diseases and insect pests, more than 30 diseases and more than 300 insect pests, and the more serious diseases include damping off, root rot, flower blight, anthracnose, ulceration and gray mold. Wherein the gray mold damages the top parts of newly-extracted young leaves and inflorescences of the macadamia nut tree body, fine-spot water-immersed spots appear after the newly-extracted leaves are damaged, the whole diseased leaves become black along with the development of the disease course, and a layer of gray green powder is grown on the surfaces of the newly-extracted leaves and branches to cause the newly-extracted leaves and the branches to die; after the inflorescence is damaged, the top of the inflorescence cannot grow normally and is dried up, and the healthy growth and yield of the macadimia nuts are seriously influenced. At present, the pesticide preparation for preventing and treating the gray mold of the macadimia nuts is less, the macadimia nut gray mold has serious resistance to common pesticides, and the application dose and the application frequency of the pesticides are generally increased to achieve better prevention and treatment effects when fruit growers prevent and treat the diseases, so that the prevention and treatment cost is increased, and the pesticide residue of the macadimia nuts can be increased.
The fluxapyroxad is a latest generation succinate dehydrogenase inhibitor bactericide discovered and developed by the Prov. Chengdu, and is marketed in 2017, and the fluxapyroxad inhibits the respiration of pathogenic fungi by inhibiting succinate dehydrogenase in a tricarboxylic acid cycle during the mitochondrial respiration of the pathogenic fungi, so that the energy metabolism is blocked, the growth of the pathogenic fungi is inhibited, and the pathogenic fungi die. Has the advantages of high efficiency, broad spectrum, low toxicity and the like, and can prevent and treat various diseases including gray mold, brown spot, leaf spot, sclerotinia rot and gibberellic disease. Like other bactericides, the fluxapyroxad has a single action site, and pathogenic bacteria are easy to generate drug resistance if a large amount of single dosage is applied for a long time. The fluxapyroxad is compounded with other medicaments with different action mechanisms and no cross resistance, and has important significance for protecting the medicaments and delaying the drug resistance of pathogenic bacteria.
The information disclosed in this background section is only for enhancement of understanding of the general background of the invention and should not be taken as an acknowledgement or any form of suggestion that this information forms the prior art already known to a person skilled in the art.
Disclosure of Invention
The invention aims to provide a medicament composition for preventing and treating macadimia nut gray mold, so as to overcome the defects that the cost for preventing and treating the macadimia nut gray mold is high, pesticide residues of macadimia nuts are high due to large-dose application of pesticides, and pathogenic bacteria are easy to generate drug resistance due to long-term large-dose single-dose application of epoxiconazole hydroxylamine.
In order to achieve the purpose, the invention provides a medicament composition for preventing and treating macadimia nut gray mold, which is prepared by compounding the active ingredients of fluxapyroxad with orysastrobin, pyraoxystrobin or mandipropamid.
Preferably, the mass ratio of the fluxapyroxad to the orysastrobin is 1-40: 40-1.
Preferably, the mass ratio of the fluxapyroxad to the pyraoxystrobin is 1-15: 60-1.
Preferably, the mass ratio of the fluxapyroxad to the mandipropamid is 1-25: 100-1.
Compared with the prior art, the invention has the following beneficial effects:
(1) the pharmaceutical composition for preventing and treating the gray mold of the macadimia nuts consists of the active ingredients with different action mechanisms, can effectively slow down the drug resistance of the gray mold of the macadimia nuts, and reduces the drug resistance risk caused by the single use of the epoxiconazole hydroxylamine.
The pesticide composition for preventing and treating the gray mold of the macadimia nuts has obvious synergy when binary compounding is carried out, has good prevention and treatment effect on the gray mold of the macadimia nuts, can reduce the pesticide application dose and the pesticide application frequency, reduces the prevention and treatment cost, lightens the pressure of pesticides on the environment, and reduces pesticide residues.
Detailed Description
The following detailed description of specific embodiments of the invention is provided, but it should be understood that the scope of the invention is not limited to the specific embodiments.
Examples: indoor bioactivity test after compounding of epoxiconazole acyl hydroxylamine
Reagent to be tested: 99.0 percent of fluxapyroxad technical, 98 percent of orysastrobin technical, 96 percent of pyraoxystrobin technical and 93 percent of mandipropamid technical, wherein the technical materials are all sold in the market.
Test germs: pathogenic bacteria of gray mold of macadamia nut
The test method comprises the following steps:
1. dissolving the raw materials in ethanol, diluting with 0.1% Tween-80, respectively preparing single mother liquor, setting multiple groups of ratios, and setting 5-6 gradient mass concentrations of each single agent and each group of mixture according to equal ratio method;
2. firstly, quantitatively adding a pre-melted PDA culture medium into a sterile conical flask under the aseptic condition, quantitatively sucking liquid medicines from low concentration to high concentration in sequence, respectively adding into the conical flasks, and fully shaking. Then, the mixture was poured into 4 dishes 9cm in diameter in equal amounts to prepare drug-containing plates, and blank controls containing only ethanol and 0.1% Tween-80 were added to the plates, and 3 treatments were repeated for each treatment.
3. Under the aseptic condition, punching the edges of bacterial colonies of the gray mold pathogenic bacteria of the macadimia nuts by using a sterilization puncher with the diameter of 5mm to prepare bacterial cakes with the diameter of 5 mm; inoculating the fungus cake in the center of the medicated plate with the hypha facing upwards, covering with a dish, and culturing at 25 deg.C in an incubator.
4. When the diameter of the blank control colony is more than 2/3 of the diameter of the culture dish, measuring the diameter of the colony by a caliper, vertically measuring the diameter of each colony by a cross method once, taking the average value, calculating the hypha growth inhibition rate of each treatment, carrying out regression analysis on the logarithm value of the medicament concentration and the hypha growth inhibition rate value by DPS software, calculating the EC50 of each treatment medicament, and calculating the cotoxicity coefficient (CTC value) of the mixture according to the Sun Yunpei method.
Hypha growth inhibition ratio (%) = [ (blank control colony diameter-5) - (medicament treatment colony diameter-5) ]/[ (blank control colony diameter-5) ] × 100;
measured virulence index (ATI) = (standard agent EC 50/test agent EC 50) × 100;
theoretical virulence index (TTI) = a agent virulence index x percent of a in the mixture + B agent virulence index x percent of B in the mixture;
co-toxicity coefficient (CTC) = [ measured toxicity index (ATI)/theoretical toxicity index of the mixture (TTI) ] × 100.
Criteria are divided according to joint action:
the co-toxicity coefficient (CTC) is more than or equal to 120 and shows a synergistic effect; the co-toxicity coefficient (CTC) is less than or equal to 80, and the antagonism is shown; 80< co-toxicity coefficient (CTC) <120 showed additive effect.
The results of the experiments are shown in tables 1-3.
TABLE 1 indoor bioactivity determination of the complex formulation of fluxapyroxad and orysastrobin on the pathogenic bacteria of gray mold of macadamia nut
Name and proportion of the medicament
|
EC50(mg/L)
|
ATI
|
TTI
|
CTC
|
Fluxapyroxad acyl hydroxylamine
|
0.52
|
100
|
--
|
--
|
Oxidofenamid
|
3.29
|
15.81
|
--
|
--
|
Fluxapyroxad 1: oxidofenamid 40
|
1.93
|
26.94
|
17.86
|
150.87
|
Fluxapyroxad 1: orysastrobin 30
|
1.38
|
37.68
|
18.52
|
203.45
|
Fluxapyroxad 1: oxidofenamid 20
|
1.02
|
50.98
|
19.81
|
257.29
|
Fluxapyroxad 1: oxidofenamid 15
|
0.77
|
67.53
|
21.07
|
320.55
|
Fluxapyroxad 1: oxidofenamid 10
|
0.54
|
96.30
|
23.46
|
410.48
|
Fluxapyroxad 1: oxidofenamid 5
|
0.63
|
82.54
|
29.84
|
276.63
|
Fluxapyroxad 1: oxidofenamid 1
|
0.56
|
92.86
|
57.90
|
160.37
|
Fluxapyroxad 5: oxidofenamid 1
|
0.41
|
126.83
|
85.97
|
147.53
|
Fluxapyroxad 10: oxidofenamid 1
|
0.24
|
216.67
|
92.35
|
234.62
|
Fluxapyroxad 15: oxidofenamid 1
|
0.15
|
346.67
|
94.74
|
365.92
|
Fluxapyroxad 20: oxidofenamid 1
|
0.23
|
226.09
|
95.99
|
235.53
|
Fluxapyroxad 30: oxidofenamid 1
|
0.31
|
167.74
|
97.28
|
172.42
|
Fluxapyroxad 40: oxidofenamid 1
|
0.40
|
130.00
|
97.95
|
132.73 |
As shown in Table 1, after the fluxapyroxad and the orysastrobin are compounded, the mass ratio of the fluxapyroxad to the orysastrobin is 1-40: the co-toxicity coefficient to the pathogenic bacteria of the gray mold of the macadimia nuts is more than 120 within the range of 40-1, and particularly, the mass ratio of the two is 1: when the dosage is 10, the co-toxicity coefficient reaches 410.48, and the synergistic effect is most obvious.
TABLE 2 indoor bioactivity assay of complex formulation of fluxapyroxad and pyraoxystrobin on pathogenic bacteria of gray mold of macadamia nut
Name and proportion of the medicament
|
EC50(mg/L)
|
ATI
|
TTI
|
CTC
|
Fluxapyroxad acyl hydroxylamine
|
0.52
|
100
|
--
|
--
|
Pyraoxystrobin
|
5.23
|
9.94
|
--
|
--
|
Fluxapyroxad 1: pyraoxystrobin 60
|
2.11
|
26.64
|
11.42
|
215.82
|
Fluxapyroxad 1: pyraoxystrobin 50
|
1.78
|
29.21
|
11.71
|
249.51
|
Fluxapyroxad 1: pyraoxystrobin 40
|
1.52
|
34.21
|
12.14
|
281.82
|
Fluxapyroxad 1: pyraoxystrobin 30
|
0.92
|
56.52
|
12.85
|
439.94
|
Fluxapyroxad 1: pyraoxystrobin 20
|
1.07
|
48.60
|
14.23
|
314.49
|
Fluxapyroxad 1: pyraoxystrobin 10
|
0.83
|
62.65
|
18.13
|
345.57
|
Fluxapyroxad 1: pyraoxystrobin 1
|
0.52
|
100.00
|
54.97
|
181.91
|
Fluxapyroxad 3: pyraoxystrobin 1
|
0.34
|
152.94
|
77.49
|
197.33
|
Fluxapyroxad 5: pyraoxystrobin 1
|
0.24
|
216.67
|
84.99
|
254.93
|
Fluxapyroxad 7: pyraoxystrobin 1
|
0.35
|
148.57
|
88.754
|
167.42
|
Fluxapyroxad 9: pyraoxystrobin 1
|
0.43
|
120.93
|
90.99
|
132.90
|
Fluxapyroxad 12: pyraoxystrobin 1
|
0.27
|
192.59
|
93.07
|
206.93
|
Fluxapyroxad 15: pyraoxystrobin 1
|
0.19
|
273.68
|
94.37
|
290.01 |
As shown in Table 2, after the fluxapyroxad and the pyraoxystrobin are compounded, the mass ratio of the fluxapyroxad to the pyraoxystrobin is 1-15: the co-toxicity coefficient to the pathogenic bacteria of the gray mold of the macadimia nuts is more than 120 within the range of 60-1, and particularly, the mass ratio of the pathogenic bacteria to the gray mold of the macadimia nuts is 1: at 30 hours, the co-toxicity coefficient reaches 439.94, and the synergistic effect is most obvious.
TABLE 3 indoor bioactivity assay of complex pairs of Oxyfluorazole and mandipropamid on the pathogenic bacteria of gray mold of macadamia nut
Name and proportion of the medicament
|
EC50(mg/L)
|
ATI
|
TTI
|
CTC
|
Fluxapyroxad acyl hydroxylamine
|
0.52
|
100
|
--
|
--
|
Mandipropamid
|
32.57
|
1.60
|
--
|
--
|
Fluxapyroxad 1: mandipropamid 100
|
13.24
|
3.93
|
2.57
|
152.77
|
Fluxapyroxad 1: mandipropamid 90
|
8.85
|
5.88
|
2.68
|
219.41
|
Fluxapyroxad 1: mandipropamid 70
|
6.36
|
8.18
|
2.98
|
274.13
|
Fluxapyroxad 1: mandipropamid 50
|
3.47
|
14.99
|
3.53
|
425.00
|
Fluxapyroxad 1: mandipropamid 30
|
5.19
|
10.02
|
4.77
|
210.01
|
Fluxapyroxad 1: mandipropamid 10
|
2.71
|
19.19
|
10.54
|
182.01
|
Fluxapyroxad 1: mandipropamid 1
|
0.75
|
69.33
|
50.80
|
136.49
|
Pyraflufen-ethyl 4: mandipropamid 1
|
0.28
|
185.71
|
80.32
|
231.22
|
Fluxapyroxad 8: mandipropamid 1
|
0.37
|
140.54
|
89.07
|
157.79
|
Fluxapyroxad 12: mandipropamid 1
|
0.31
|
167.74
|
92.43
|
181.48
|
Pyraflufen-ethyl 16: mandipropamid 1
|
0.26
|
200.00
|
94.21
|
212.29
|
Fluxapyroxad 20: mandipropamid 1
|
0.20
|
26.00
|
95.31
|
272.78
|
Fluxapyroxad 25: mandipropamid 1
|
0.17
|
305.88
|
96.22
|
317.91 |
As shown in Table 3, after the fluxapyroxad and the mandipropamid are compounded, the mass ratio of the fluxapyroxad to the mandipropamid is 1-25: the cotoxicity coefficient to the pathogenic bacteria of the gray mold of the macadimia nuts is more than 120 within the range of 100-1, and particularly, the mass ratio of the pathogenic bacteria to the gray mold of the macadimia nuts is 1: at 50, the co-toxicity coefficient reaches 425.00, and the synergistic effect is most obvious.
The foregoing descriptions of specific exemplary embodiments of the present invention have been presented for purposes of illustration and description. It is not intended to limit the invention to the precise form disclosed, and obviously many modifications and variations are possible in light of the above teaching. The exemplary embodiments were chosen and described in order to explain certain principles of the invention and its practical application to enable one skilled in the art to make and use various exemplary embodiments of the invention and various alternatives and modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the claims and their equivalents.