Insecticide Resistance Action Committee

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The Insecticide Resistance Action Committee (IRAC) was formed in 1984 and works as a specialist technical group of the industry association CropLife to be able to provide a coordinated industry response to prevent or delay the development of insecticide resistance in insect, mite and nematode pests. IRAC strives to facilitate communication and education on insecticide and traits resistance as well as to promote the development and facilitate the implementation of insecticide resistance management strategies. [1]

Contents

IRAC is recognised by the Food and Agriculture Organization (FAO) and the World Health Organization (WHO) of the United Nations as an advisory body on matters pertaining to insecticide resistance. [2]

Pesticideresistance.org is a database financed by IRAC, US Department of Agriculture, and others. [3]

Sponsors

IRAC's sponsors are: ADAMA, BASF, Bayer CropScience, Corteva, FMC, Mitsui Chemicals, Nihon Nohyaku, Sumitomo Chemical, Syngenta and UPL. [4]

Mode of action classification

IRAC publishes an insecticide mode of action (MoA) classification that lists most common insecticides and acaricides and recommends that "successive generations of a pest should not be treated with compounds from the same MoA Group". [5] [6] IRAC assigns a mode of action (MoA) to an insecticide, based on sufficient scientific data. [7] They then update the mode of action (MoA) classification. [5] Several insecticides and classes of insecticide may act through the same mode of action. [8]

Classes of Insecticide

If an insecticide is successful, follow-on insecticides, based on the chemical structure of the first in class (prototype) insecticide, may be developed either by the original company or by competitors. Sought after are insecticides which have improved properties or which kill different orders or species of insect. The resulting classes of insecticides are named by IRAC after common usage has been established, although alternative names may be found in the scientific literature.

Table of modes of action and classes of insecticide

In the table the number of insecticides listed in each class is given, and an example of each class. The number of insecticides in the IRAC class listing as of 2024 is given in column Nr (A). The number in the Compendium of Pesticide Common Names [9] (insecticide + acaricide) is given in column Nr (B), although the name given there to the class historically is often different to the IRAC class name.

IRAC
code
Mode of actionClassNr (A)Nr (B)Example
1 A Acetylcholinesterase (AChE) inhibitors Carbamates 2652 Carbofuran
1 B Acetylcholinesterase (AChE) inhibitors Organophosphates 66171 Chlorpyrifos
2 A GABA-gated chloride channel blockers Cyclodiene organochlorines 217 Endosulfan
2 B GABA-gated chloride channel blockers Phenylpyrazoles (Fiproles)27 Fipronil
3 A Sodium channel modulators Pyrethroids, Pyrethrins 4384 Permethrin
3 B Sodium channel modulators DDT, Methoxychlor 220 DDT
4 A Nicotinic acetylcholine receptor (nAChR) competitive modulators Neonicotinoids 711 Imidacloprid
4 B Nicotinic acetylcholine receptor (nAChR) competitive modulators Nicotine 11 Nicotine
4 C Nicotinic acetylcholine receptor (nAChR) competitive modulatorsSulfoximines11 Sulfoxaflor
4 D Nicotinic acetylcholine receptor (nAChR) competitive modulatorsButenolides11 Flupyradifurone
4 E Nicotinic acetylcholine receptor (nAChR) competitive modulatorsMesoionics33Triflumezopyrim
4 F Nicotinic acetylcholine receptor (nAChR) competitive modulatorsPyridylidenes11Flupyrimin
5 Nicotinic acetylcholine receptor (nAChR) allosteric modulators - Site ISpinosyns22 Spinosad
6 Glutamate-gated chloride channel (GluCl) allosteric modulators Avermectins, Milbemycins 410 Abamectin
7 A Juvenile hormone receptor modulators Juvenile hormone analogues 37 Methoprene
7 B Juvenile hormone receptor modulators Fenoxycarb 11 Fenoxycarb
7 C Juvenile hormone receptor modulators Pyriproxyfen 11 Pyriproxyfen
8 AMiscellaneous non-specific (multi-site) inhibitorsAlkyl halides> 310 1,3-dichloropropene
8 BMiscellaneous non-specific (multi-site) inhibitors Chloropicrin 11 Chloropicrin
8 CMiscellaneous non-specific (multi-site) inhibitorsFluorides25 Sulfuryl fluoride
8 DMiscellaneous non-specific (multi-site) inhibitorsBorates52 Boric acid
8 EMiscellaneous non-specific (multi-site) inhibitors Tartar emetic 10 Tartar emetic
8 FMiscellaneous non-specific (multi-site) inhibitors Methyl isothiocyanate generators32 Dazomet
9 B Chordotonal Organ TRPV Channel Modulatorspyridine azomethine derivatives22 Pymetrozine
9 D Chordotonal Organ TRPV Channel ModulatorsPyropenes11Afidopyropen
10 AMite growth inhibitors affecting CHS1 Clofentezine, Diflovidazin, Hexythiazox35Clofentezine
10 BMite growth inhibitors affecting CHS1 Etoxazole 11 Etoxazole
11 AMicrobial disruptors of insect midgut membranes Bacillus thuringiensis and the insecticidal proteins they produce4n.a.n.a.
11 BMicrobial disruptors of insect midgut membranes Bacillus sphaericus 1n.a.n.a.
12 AInhibitors of mitochondrial ATP synthase Diafenthiuron 11 Diafenthiuron
12 BInhibitors of mitochondrial ATP synthase Organotin miticides38 Cyhexatin
12 CInhibitors of mitochondrial ATP synthase Propargite 14 Propargite
12 DInhibitors of mitochondrial ATP synthase Tetradifon 12 Tetradifon
13 Uncouplers of oxidative phosphorylation via disruption of the proton gradientPyrroles, Dinitrophenols, Sulfluramid 38 Chlorfenapyr
14 Nicotinic acetylcholine receptor (nAChR) channel blockers Nereistoxin analogues45 Thiocyclam
15Inhibitors of chitin biosynthesis affecting CHS1 Benzoylureas 1115 Lufenuron
16Inhibitors of chitin biosynthesis, type 1 Buprofezin 11 Buprofezin
17 Moulting disruptor, Dipteran Cyromazine 11 Cyromazine
18 Ecdysone receptor agonists Diacylhydrazines 46 Tebufenozide
19 Octopamine receptor agonists Amitraz 17 Amitraz
20 A Mitochondrial complex III electron transport inhibitors – Qo site Hydramethylnon 11 Hydramethylnon
20 B Mitochondrial complex III electron transport inhibitors – Qo siteAcequinocyl11Acequinocyl
20 C Mitochondrial complex III electron transport inhibitors – Qo siteFluacrypyrim14Fluacrypyrim
20 D Mitochondrial complex III electron transport inhibitors – Qo siteBifenazate11Bifenazate
21 A Mitochondrial complex I electron transport inhibitors METI acaricides and insecticides69 Tebufenpyrad
21 B Mitochondrial complex I electron transport inhibitors Rotenone 11 Rotenone
22 AVoltage-dependent sodium channel blockers Oxadiazines11 Indoxacarb
22 BVoltage-dependent sodium channel blockers Semicarbazones11 Metaflumizone
23Inhibitors of acetyl-CoA carboxylase Tetronic and Tetramic acid derivatives56 Spirotetramat
24 A Mitochondrial complex IV electron transport inhibitors Phosphides43 Phosphine
24 B Mitochondrial complex IV electron transport inhibitors Cyanides33 Sodium cyanide
25 A Mitochondrial complex II electron transport inhibitors Beta-ketonitrile derivatives26Cyenopyrafen
25 B Mitochondrial complex II electron transport inhibitors Carboxanilides11Pyflubumide
28 Ryanodine receptor modulators Diamides 519 Chlorantraniliprole
29 Chordotonal organ nicotinamidase inhibitors Flonicamid 12 Flonicamid
30 GABA-gated chloride channel allosteric modulatorsMeta-diamides, Isoxazolines 315 Broflanilide
31 Baculoviruses Granuloviruses (GVs), Nucleopolyhedroviruses (NPVs)4n.a. Cydia pomonella GV
32 Nicotinic Acetylcholine Receptor (nAChR) Allosteric Modulators - Site II GS-omega/kappa HXTX-Hv1a peptide 1n.a. GS-omega/kappa HXTX-Hv1a peptide
33 Calcium‐activated potassium channel (KCa2) modulatorsAcynonapyr11Acynonapyr
34 Mitochondrial complex III electron transport inhibitors – Qi site Flometoquin11Flometoquin
35 RNA Interference mediated target suppressorsLedprona12Ledprona
36 Chordotonal organ modulators – undefined target sitePyridazine pyrazolecarboxamides11Dimpropyridaz
37Vesicular acetylcholine transporter (VAChT) inhibitorOxazosulfyl11Oxazosulfyl
UNCompounds of unknown or uncertain MoAmany various classes1083Benzoximate
UNB Bacterial agents (non-Bt) of unknown or uncertain MoAclass not defined2n.a. Wolbachie pipientis (Zap)
UNE Botanical essence including synthetic, extracts and unrefined oils with unknown or uncertain MoAclass not defined5n.a. neem oil
UNF Fungal agents of unknown or uncertain MoAclass not defined6n.a. Beauveria bassiana strains
UNMNon-specific mechanical and physical disruptorsclass not defined3n.a. Mineral Oil
UNPPeptides of unknown or uncertain MoAno examplesnonen.a.no examples
UNV Viral agents (non-baculovirus) of unknown or uncertain MoAno examplesnonen.a.no examples

See also

Further reading

Related Research Articles

<span class="mw-page-title-main">Insecticide</span> Pesticide used against insects

Insecticides are pesticides used to kill insects. They include ovicides and larvicides used against insect eggs and larvae, respectively. The major use of insecticides is in agriculture, but they are also used in home and garden settings, industrial buildings, for vector control, and control of insect parasites of animals and humans.

<span class="mw-page-title-main">Pesticide resistance</span> Decreased effectiveness of a pesticide on a pest

Pesticide resistance describes the decreased susceptibility of a pest population to a pesticide that was previously effective at controlling the pest. Pest species evolve pesticide resistance via natural selection: the most resistant specimens survive and pass on their acquired heritable changes traits to their offspring. If a pest has resistance then that will reduce the pesticide's efficacy – efficacy and resistance are inversely related.

<span class="mw-page-title-main">Carbamate</span> Chemical group (>N–C(=O)–O–)

In organic chemistry, a carbamate is a category of organic compounds with the general formula R2NC(O)OR and structure >N−C(=O)−O−, which are formally derived from carbamic acid. The term includes organic compounds, formally obtained by replacing one or more of the hydrogen atoms by other organic functional groups; as well as salts with the carbamate anion H2NCOO.

<span class="mw-page-title-main">Benzoylurea insecticide</span> Class of insecticide

Benzoylureas (BPUs) are chemical derivatives of N-benzoyl-N-phenylurea, which are used as insecticides. They do not directly kill the insect, but disrupt moulting and egg hatch, and thus act as insect growth regulators. They act by inhibiting chitin synthase, preventing the formation of chitin in the insect's body.

<span class="mw-page-title-main">Spinosad</span> Insecticide

Spinosad is an insecticide based on chemical compounds found in the bacterial species Saccharopolyspora spinosa. The genus Saccharopolyspora was discovered in 1985 in isolates from crushed sugarcane. The bacteria produce yellowish-pink aerial hyphae, with bead-like chains of spores enclosed in a characteristic hairy sheath. This genus is defined as aerobic, Gram-positive, nonacid-fast actinomycetes with fragmenting substrate mycelium. S. spinosa was isolated from soil collected inside a nonoperational sugar mill rum still in the Virgin Islands. Spinosad is a mixture of chemical compounds in the spinosyn family that has a generalized structure consisting of a unique tetracyclic ring system attached to an amino sugar (D-forosamine) and a neutral sugar (tri-Ο-methyl-L-rhamnose). Spinosad is relatively nonpolar and not easily dissolved in water.

<span class="mw-page-title-main">Cyhalothrin</span> Synthetic pyrethroid used as insecticide

Cyhalothrin is an organic compound that, in specific isomeric forms, is used as a pesticide. It is a pyrethroid, a class of synthetic insecticides that mimic the structure and properties of the naturally occurring insecticide pyrethrin which is present in the flowers of Chrysanthemum cinerariifolium. Pyrethroids, such as cyhalothrin, are often preferred as an active ingredient in agricultural insecticides because they are more cost-effective and longer acting than natural pyrethrins. λ-and γ-cyhalothrin are now used to control insects and spider mites in crops including cotton, cereals, potatoes and vegetables.

In enzymology, a chitin synthase is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">Cyfluthrin</span> Chemical compound

Cyfluthrin is a pyrethroid insecticide and common household pesticide. It is a complex organic compound and the commercial product is sold as a mixture of isomers. Like most pyrethroids, it is highly toxic to fish and invertebrates, but it is far less toxic to humans. It is generally supplied as a 10–25% liquid concentrate for commercial use and is diluted prior to spraying onto agricultural crops and outbuildings.

The milbemycins are a group of macrolides chemically related to the avermectins and were first isolated in 1972 from Streptomyces hygroscopicus. They are used in veterinary medicine as antiparasitic agents against worms, ticks and fleas. They also show insecticidal and acaricidal activity.

<i>Tuta absoluta</i> Pest worm of tomato, potato, and others

Tuta absoluta or Phthorimaea absoluta is a species of moth in family Gelechiidae known by the common names South American tomato pinworm, tomato leafminer, tomato pinworm and South American tomato moth. It is well known as a serious pest of tomato crops in Europe, Africa, western Asia and South and Central America, with larvae causing up to 100% loss if not effectively controlled.

CropLife International is an international trade association of agrochemical companies founded in 2001. It was previously known as Global Crop Protection Federation and started out as International Group of National Associations of Manufacturers of Agrochemical Products in 1967. Its members include the world's largest agricultural biotechnology and agricultural pesticide businesses namely BASF, Bayer CropScience, Corteva, FMC Corp., Sumitomo Chemical and Syngenta. The international body combines several national-level or continent-wide organisations, each one having the same goals but differing according to local language and custom.

An insect growth regulator (IGR) is a chemical insecticide that kills insects indirectly by disrupting their life cycles. The term was initially proposed to describe the effects of juvenile hormone analogs. Although the term "insect growth disruptor" more accurately describes the actions of IGRs, it did not become widely used. IGRs encompass chemical classes with three modes of action : juvenile hormone analogs, chitin synthesis inhibitors, and ecdysone receptor agonists.

<span class="mw-page-title-main">Diamide insecticides</span> Class of insecticide

Diamide insecticides are a class of insecticides, active mainly against lepidoptera (caterpillars), which act on the insect ryanodine receptor. They are diamides of either phthalic acid or anthranilic acid, with various appropriate further substitutions.

<span class="mw-page-title-main">Cyantraniliprole</span> Chemical compound used as an insecticide.

Cyantraniliprole is an insecticide of the diamide class. It shows strong activity and lepidoptera (caterpillars), and since it shows systemic activity it is also active against sucking pests such as aphids and whitefly.

<span class="mw-page-title-main">Etoxazole</span> Chemical compound

Etoxazole is a narrow spectrum systemic acaricide used to combat spider mites. It targets a variety of mites in the egg, larvae and nymph stages however not the adult stage. It also exhibits insecticidal activity towards aphids, the green rice leafhopper and diamondback moth. The mode of action has been shown to inhibit chitin synthase (IRAC group 10B). Resistance due to its high efficacy and cross resistance when used with other acaricides are both of concern similar to was seen in the fast development of cross resistance in the previous generation of acaricides. The LC50 for resistant mite strains has been observed over 100,000 times greater than that of susceptible strains. Thus resistance management strategies are important in order to limit the increase of etoxazole resistant mite strains.

<span class="mw-page-title-main">Chlorantraniliprole</span> Chemical compound

Chlorantraniliprole is an insecticide of the diamide class used for insects found on fruit and vegetable crops as well as ornamental plants.

<span class="mw-page-title-main">Nereistoxin</span> Chemical compound

Nereistoxin is a natural product identified in 1962 as the toxic organic compound N,N-dimethyl-1,2-dithiolan-4-amine. It had first been isolated in 1934 from the marine annelid Lumbriconereis heteropoda and acts by blocking the nicotinic acetylcholine receptor. Researchers at Takeda in Japan investigated it as a possible insecticide. They subsequently developed a number of derivatives that were commercialised, including those with the ISO common names bensultap, cartap, thiocyclam and thiosultap.

<span class="mw-page-title-main">Broflanilide</span> Chemical compound

Broflanilide is a complex, polycyclic, organohalogen insecticide which provides a novel mode of action (MoA).

<span class="mw-page-title-main">Flupyradifurone</span> Chemical compound

Flupyradifurone is a systemic butenolide insecticide developed by Bayer CropScience under the name Sivanto. Flupyradifurone protects crops from sap-feeding pests such as aphids and is safer for non-target organisms compared to other insecticides. Sivanto was launched in 2014 since it obtained its first commercial registration in central America. Insecticide Resistance Action Committee (IRAC) classified Flupyradifurone as 4D subset (butenolide) and it is the first pesticide in the butenolide category. It was approved by European Union in 2015.

<span class="mw-page-title-main">Pymetrozine</span> Chemical compound

Pymetrozine is an insecticide in the pyridine-azomethine chemical class, primarily utilized for controlling homopteran pests, such as aphids and whiteflies, in agricultural settings. Its mode of action selectively targets the feeding behavior of sap-feeding insects, causing them to cease feeding soon after ingestion. This unique mechanism limits its impact on non-target organisms, including beneficial insects. Pymetrozine has been extensively used on rice, potatoes, a wide variety of vegetable brassica crops and various other crops as an alternative to organophosphorus pesticides.

References

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  2. Insecticide Resistance Action Committee (April 2007). "Resistance Management for Sustainable Agriculture and Improved Public Health" (PDF). Croplife.
  3. "Arthropod Pesticide Resistance Database". Michigan State University. Retrieved 2024-12-10.
  4. "IRAC / Our sponsors". IRAC. Retrieved 4 December 2024.
  5. 1 2 "Interactive MoA Classification". Insecticide Resistance Action Committee. 2020-09-16. Retrieved 2021-04-01.
  6. Sparks, Thomas C.; Nauen, Ralf (2015). "IRAC: Mode of action classification and insecticide resistance management". Pesticide Biochemistry and Physiology. 121. Elsevier BV: 122–128. doi: 10.1016/j.pestbp.2014.11.014 . ISSN   0048-3575.
  7. "Mode of Action Team". Insecticide Resistance Action Committee. Retrieved 5 December 2024.
  8. Sparks, Thomas C.; Crossthwaite, Andrew J.; Nauen, Ralf; Banba, Shinichi; et al. (2020). "Insecticides, biologics and nematicides: Updates to IRAC's mode of action classification - a tool for resistance management". Pesticide Biochemistry and Physiology. 167: 104587. doi: 10.1016/j.pestbp.2020.104587 .
  9. "Classification of Pesticides". BCPC: Compendium of Pesticide Common Names. Retrieved 5 December 2024.