CN108925557B - Application of acetaldehyde in preparation of nematode insecticide - Google Patents

Application of acetaldehyde in preparation of nematode insecticide Download PDF

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CN108925557B
CN108925557B CN201810714260.3A CN201810714260A CN108925557B CN 108925557 B CN108925557 B CN 108925557B CN 201810714260 A CN201810714260 A CN 201810714260A CN 108925557 B CN108925557 B CN 108925557B
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acetaldehyde
root
nematode
nematodes
knot
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CN108925557A (en
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张吉斌
邵宗泽
余晨
黄典
蔡珉敏
郑龙玉
喻子牛
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Huazhong Agricultural University
Third Institute of Oceanography SOA
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Third Institute of Oceanography SOA
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N35/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals

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Abstract

The invention discloses a volatile substance acetaldehyde with activity to root-knot nematodes. The result of the nematicidal activity measurement shows that acetaldehyde has strong contact activity, and the half lethal concentration of the acetaldehyde is EC50/6h (mg/L) =141.4 mug/ml respectively; it has fumigating activity to root-knot nematode; inhibiting the hatching of root knot nematode eggs; chemotaxis experiments show that the compound has attraction effect on root-knot nematodes. Acetaldehyde is generally used as an insect attractant and a fumigant, and has an insecticidal effect on root-knot nematodes, and an inhibition effect and an attraction effect on egg hatching are discovered for the first time.

Description

Application of acetaldehyde in preparation of nematode insecticide
Technical Field
The invention belongs to the technical field of agricultural microbiology, and particularly relates to application of acetaldehyde in preparation of a nematode pesticide.
Technical Field
Root-knot nematodes (RKNs) are proprietary root parasites that infect more than 3000 plant species worldwide, one of the most serious plant parasitic nematodes in the world, especially in tropical and subtropical agricultural areas (Korea et al 2006). Root knot nematode (Meloidogyne spp.) is an endoparasitic nematode that colonizes plant roots and belongs to the order of the Bacillales (Tylenchida), the family Heterodermaceae (Heterodermidae), the subfamily of the root knot (Meloidogyne), the genus Meloidogyne (Meloidogyne). In China, the meloidogyne incognita is the most widely distributed and most seriously harmful. Root-knot nematodes are sometimes difficult to control due to their broad host range, short life cycle, high reproduction rate, and good endoparasitic properties (Chen et al 2004).
For the prevention and treatment of root-knot nematodes, chemical agents are used as main agents, and play an important role in ensuring high and stable yield of crops. But because of the toxic residue, the chemical nematocide has serious environmental pollution and is unsafe for people and livestock in the using process. Many nematicides have been banned, many developing countries, especially in tropical or subtropical regions, where the climate is suitable for nematode activity and reproduction, perennial plants and crops grown in succession in the same plot are often very severely damaged by nematodes, and developing countries where large amounts of food are needed, which have to rely on perennial crops and crop continuous cropping, and therefore few crop rotation is used to control root-knot nematodes; the application of resistant varieties is not wide at present, firstly, the application is limited by agronomic characters, and secondly, after a disease-resistant variety is continuously planted in a region, the selection action of the disease-resistant variety changes the population of nematodes, so that the number of a few nematode types which are not resistant by the variety is increased, and the resistance is gradually lost. For the above reasons, in addition to the continued search for efficient, low-toxicity, low-residue, highly selective nematicides, new methods have also been sought ecologically, and biological control is one of them (wanningham et al 2002).
In recent years, volatile metabolites produced by microorganisms have increasingly shown potential value in plant parasitic nematode control. Many Volatile Organic Compounds (VOCs), including alcohols, aldehydes, ketones, olefins, ethers, phenols, esters, and the like, have good nematicidal activity. The volatile organic compounds have properties that are not possessed by typical nematicide: some volatile organic compounds can increase plant resistance through activation of plant defense signaling pathways; the soil permeability and volatility are good, so that the soil can directly reach pathogens, and plant diseases can be killed more effectively; microorganisms generally produce a plurality of volatile organic compounds, so that drug resistance caused by plant diseases is avoided; in addition, volatile organic compounds generally have the effect of attracting or repelling pathogenic nematodes and insects.
A number of nematicidal Volatile Organic Compounds (VOCs) have now been found, representative fumigants being halogenated hydrocarbons and thioisothiocyanates, including methyl bromide, methyl iodide, sulfuryl fluoride, dazomet, metam, 1, 3-dichloropropene, chloropicrin, calcium cyanamide, methyl isothiocyanate, dimethyldisulfide, etc. (Leugenk et al 2016). The volatile organic compounds are less studied in the area of nematode-attracting repellents, such as methyl salicylate, lauric acid, etc.
Disclosure of Invention
The invention aims to provide an application of acetaldehyde in preparing a nematode insecticide, wherein the application comprises the preparation of the insecticide, a fumigant and an attractant, and the acetaldehyde has the following chemical formula:
Figure BDA0001717071230000021
in order to achieve the purpose, the invention adopts the following technical measures:
the application process of acetaldehyde in preparing nematode pesticide includes using acetaldehyde as main effective component or one of the effective components to prepare nematode pesticide, nematode fumigant, nematode attractant or nematode egg inhibitor.
In the above application, preferably, the nematode is meloidogyne incognita.
Compared with the prior art, the invention has the following advantages:
the invention reports the induction activity of acetaldehyde to root-knot nematodes, the killing activity of acetaldehyde to root-knot nematodes and the inhibiting activity of acetaldehyde to egg hatching and fumigating for the first time, and provides new selectivity for preparing novel root-knot nematode biocontrol agents.
The nematicide prepared from acetaldehyde has the advantages of high efficiency, low toxicity, good persistence and multiple action modes.
Drawings
FIG. 1: a pesticidal profile of acetaldehyde against root knot nematodes;
wherein: a: a control group of nematodes; b: acetaldehyde treated group nematodes (24 h).
FIG. 2: acetaldehyde inhibits nematode insecticidal profiles by fumigation;
wherein: a: a control group of nematodes; b: acetaldehyde treated group nematodes (24 h).
FIG. 3 is a schematic diagram of chemotaxis experiments.
Detailed Description
The experimental procedures in the following examples are reported as conventional procedures in microbiology unless otherwise specified. The reagents or materials, if not specifically stated, are commercially available.
Example 1:
the application of acetaldehyde in preparing root-knot nematode pesticide includes the following steps:
picking nematodes from the roots of the tomatoes to infect root knots, placing the egg masses in a 96-well plate for incubation at 20 ℃, and observing the incubation condition of the root-knot nematodes; collecting larvae of the root-knot nematode J2 stage in a centrifugal tube to obtain nematode suspension; adding 200 μ L of sample into 96-well plate, adding 2 μ L of chloramphenicol (30mg/mL) and 30 head nematodes with solvent as blank control, repeating each group for 3 times, sealing with sealing film, and placing in constant temperature incubator; the experimental results were observed at 6h and 24 h.
Nematode mortality rate ═ nematode death number/test nematode number × (100)%
TABLE 1 Meloidogyne incognita killing Activity of acetaldehyde
Figure BDA0001717071230000031
Example 2:
the application of acetaldehyde in preparing the root-knot nematode fumigant comprises the following application processes:
picking nematodes from the roots of the tomatoes to infect root knots, placing the egg masses in a 96-well plate for incubation at 20 ℃, and observing the incubation condition of the root-knot nematodes; collecting larvae of the root-knot nematode J2 stage in a centrifugal tube to obtain nematode suspension; selecting one hole from a 96-hole plate, adding 200 mu L of sample, adding 2 mu L of chloramphenicol (30mg/mL) and 60-head nematode into each hole, sealing with a sealing film, and placing in a constant temperature incubator; the experimental results were observed at 6h and 24 h.
Nematode mortality rate ═ nematode death number/test nematode number × (100)%
TABLE 2 Fumigation Activity of acetaldehyde against Meloidogyne incognita
Figure BDA0001717071230000032
10mg/mL acetaldehyde fumigates the root-knot nematode, and the death rate reaches 100% in 6 hours.
Example 3:
experiment for inhibiting incubation and fumigation of southern root knot nematode eggs by acetaldehyde
Picking nematodes from the roots of the tomatoes to infect root knots, placing the egg masses in a 96-well plate for incubation at 20 ℃, and observing the incubation condition of the root-knot nematodes; collecting larvae of the root-knot nematode J2 stage in a centrifugal tube to obtain nematode suspension; selecting one hole from a 96-hole plate, adding 200 mu L of sample, adding 1 oocyst into each hole, sealing by a sealing film, and placing in a constant-temperature incubator; the experimental results were observed at 1d, 2d, and 3 d.
TABLE 3 inhibitory Effect of acetaldehyde on hatching of Meloidogyne incognita eggs
Figure BDA0001717071230000041
The 10mg/mL acetaldehyde fumigates the root-knot nematode oocysts, and can effectively inhibit the hatching of eggs.
Example 4:
the application of acetaldehyde in preparing the attractant for meloidogyne incognita comprises the following steps:
collecting the hatched root-knot nematodes in a centrifugal tube to obtain a J2 nematode suspension; preparing a sample solution, and diluting to 10mg/mL, 3mg/mL and 1 mg/mL; adding samples according to the chemotaxis experimental schematic diagram (figure 3), adding 100 heads of nematode-containing suspension at the center of the plate; sealing the flat plate by using a sealing film, placing the flat plate in a constant temperature box at 20 ℃, shading, observing for 8 hours, and counting the number of nematodes in an experimental area and a control area on two sides of the buffer area.
Chemotaxis index (c.i value) ═ number of nematodes in experimental zone-number of nematodes in control zone)/(number of nematodes in experimental zone + number of nematodes in control zone)
C.I. epsilon (0, 1) shows an attracting effect
C.I. epsilon-1, 0) shows that the composition has a repellent effect
TABLE 4 attraction of acetaldehyde to Meloidogyne incognita
Figure BDA0001717071230000042
The C.I values are all larger than 0, and acetaldehyde has attraction effect on the root-knot nematode.

Claims (1)

1. The application of acetaldehyde in preparing a preparation which has the effects of killing, luring, fumigating and inhibiting nematode eggs for southern root-knot nematodes.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102027901A (en) * 2010-12-07 2011-04-27 浙江农林大学 Adult monochamus alternatus hope attractant
CN103299999A (en) * 2013-06-26 2013-09-18 中国农业科学院植物保护研究所 Application technology of furfural serving as soil fumigant
CN104412968A (en) * 2013-09-06 2015-03-18 中国农业大学 Application of vanillic aldehyde in preparation of Meloidogyne incognita Chitwood insecticide inhibitor
CN107047621A (en) * 2017-06-14 2017-08-18 福建农林大学 Gentamicin phenylacetaldehyde mixture nematicide and preparation method thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102027901A (en) * 2010-12-07 2011-04-27 浙江农林大学 Adult monochamus alternatus hope attractant
CN103299999A (en) * 2013-06-26 2013-09-18 中国农业科学院植物保护研究所 Application technology of furfural serving as soil fumigant
CN104412968A (en) * 2013-09-06 2015-03-18 中国农业大学 Application of vanillic aldehyde in preparation of Meloidogyne incognita Chitwood insecticide inhibitor
CN107047621A (en) * 2017-06-14 2017-08-18 福建农林大学 Gentamicin phenylacetaldehyde mixture nematicide and preparation method thereof

Non-Patent Citations (5)

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Title
CAPLUS.Effect of acetaldehyde on free living soil nematodes Caenorhabditis elegans, N2- and IPE1-lines.《STN CAPLUS 摘要 159:650734》.2013, *
Effect of acetaldehyde on free living soil nematodes Caenorhabditis elegans, N2- and IPE1-lines;CAPLUS;《STN CAPLUS 摘要 159:650734》;20131231;摘要 *
Identification and Characterization of Nnematicidal Volatile Organic Compounds from Deep-Sea Virgibacillus dokdonensis MCCC 1A00493;Dian Huang et.al.;《Molecules》;20200209;第25卷(第3期);744 *
Testing the efficacy of chemicals for killing soil-inhabiting nematodes under field conditions;Christie, J. R. et.al.;《Proc. Helminthol. Soc. Wash., D.C.》;19511231(第18期);9-13 *
Threshold chemosensitivity and hypothetical chemoreceptor function of the nematode Caenorhabditis elegans;Terrill, Willliam F. et.al.;《Journal of Chemical Ecology》;19961231;第22卷(第8期);1463-1475 *

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