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1.
Pest Manag Sci ; 69(11): 1280-90, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23554261

ABSTRACT

BACKGROUND: Pheromone antagonists are good disruptants of the pheromone communication in insects and, as such, have been used in mating disruption experiments. In this study, new non-fluorinated electrophilic keto derivatives structurally related to the pheromone of Cydia pomonella (codlemone) have been synthesised and tested as putative pheromone antagonists. RESULTS: Codlemone (1) was prepared in excellent stereoselectivity in a new, iterative approach involving two Horner-Wadsworth-Emmons reactions. Methyl ketone (2), keto ester (3) and diketone (4) were obtained from codlemone in straightforward approaches in good overall yields and excellent stereochemical purity (≥98% E,E). In electrophysiology, only compound 2 displayed inhibition of the antennal response to the pheromone after presaturation of the antennal receptors. Compounds 2 to 4 did not inhibit the pheromone-degrading enzyme responsible for codlemone metabolism, but mixtures of ketone 2 and diketone 4 with codlemone elicited erratic flights on males in a wind tunnel. In the field, blends of either compound (2 or 4) with the pheromone caught significantly fewer males than codlemone alone. CONCLUSION: Codlemone and the potential antagonists 2 to 4 have been synthesised in good yields and excellent stereoselectivity. These chemicals behave as pheromone antagonists of the codling moth both in the laboratory and in the field.


Subject(s)
Dodecanol/analogs & derivatives , Moths/drug effects , Moths/physiology , Sex Attractants/pharmacology , Animals , Dodecanol/antagonists & inhibitors , Dodecanol/chemical synthesis , Dodecanol/chemistry , Dodecanol/pharmacology , Female , Male , Sex Attractants/antagonists & inhibitors , Sex Attractants/chemical synthesis , Sex Attractants/chemistry
2.
J Agric Food Chem ; 57(18): 8514-9, 2009 Sep 23.
Article in English | MEDLINE | ID: mdl-19702270

ABSTRACT

A new pheromone antagonist of the codling moth Cydia pomonella is reported. Presaturation of the antennae of the insects with vapors of the antagonist (E,E)-8,10-dodecadienyl trifluoromethyl ketone, analogue of the main component of the pheromone (codlemone), resulted in lower electrophysiological responses to the pheromone relative to untreated insects. In the wind tunnel, the compound elicited a remarkable disruptive effect on all types of behavior of males flying toward a source baited with a pheromone/antagonist blend in 1:1, 1:5, and 1:10 ratios. The insects displayed erratic flights in the presence of the antagonist, as shown by their flight parameters in comparison to insects attracted to the pheromone alone. In the field, traps baited with mixtures of 1:10 codlemone/antagonist attracted considerably lower numbers of males than the natural attractant. The antagonist, however, did not inhibit the pheromone-degrading enzymes present in male antennae, suggesting that trifluoromethyl ketones are not sufficiently electrophilic to produce a stable intermediate adduct with a cysteine residue of the enzyme, a mechanism previously proposed for oxidase inhibition in insects. Overall and taking into account our previous reports and, particularly, the reduction in damage induced in maize fields by a trifluoromethyl ketone analogue of the pheromone of Sesamia nonagrioides (Sole, J.; Sans, A.; Riba, M.; Rosa, E.; Bosch, M. P.; Barrot, M.; Palencia, J.; Castella, J.; Guerrero, A. Reduction of damage by the Mediterranean corn borer, Sesamia nonagrioides , and the European corn borer, Ostrinia nubilalis , in maize fields by a trifluoromethyl ketone pheromone analog . Entomol. Exp. Appl. 2008, 126, 28-39), the antagonist might be a new candidate to consider in future strategies to control the codling moth.


Subject(s)
Ketones/pharmacology , Moths/chemistry , Pheromones/antagonists & inhibitors , Animals , Behavior, Animal/drug effects , Dodecanol/analogs & derivatives , Dodecanol/chemistry , Enzyme Inhibitors/pharmacology , Insect Control/methods , Male , Moths/enzymology , Pheromones/metabolism , Pheromones/pharmacology
3.
J Chem Ecol ; 35(7): 779-84, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19593653

ABSTRACT

Several sympatric lepidopteran species feed on maize plants, and the different components of their species-specific female sex pheromones may play a role in attracting conspecifics and/or deter heterospecific males. In this study, we analyzed the content of Mythimna unipuncta pheromone glands and tested the response of males to components of their own pheromone blend and that of Sesamia nonagrioides in the wind tunnel. Whole pheromone glands, and lures where (Z)-9-hexadecenyl acetate, Z)-11-hexadecen-1-ol or (Z)-9-hexadecenyl acetate + (Z)-11-hexadecen-1-ol were added to the major component, (Z)-11-hexadecenyl acetate, elicited significantly higher responses by M. unipuncta males than lures with main component alone, although the levels varied with concentration. In the field a rather different outcome was observed, as the addition of other compounds found in the female pheromone gland did not improve trap catch over lures with only (Z)-11-hexadecenyl acetate. The addition of (Z)-11-hexadecenal, a compound of the S. nonagrioides pheromone, to (Z)-11-hexadecenyl acetate significantly reduced attraction of M. unipuncta males both in the wind tunnel and in the field, as well as the number of sympatric clover cutworm, Discestra trifolii, under field conditions. The addition of (Z)-9-hexadecenyl acetate, a minor component of the M. unipuncta pheromone blend, reduced the number of S. nonagrioides captured in field traps that were baited with the S. nonagrioides lure. The significance of such inhibition in the reproductive isolation of sympatric species that attack maize is discussed.


Subject(s)
Lepidoptera/drug effects , Sex Attractants/pharmacology , Acetates/pharmacology , Aldehydes/pharmacology , Animals , Female , Male , Sex Attractants/chemistry , Sex Attractants/isolation & purification , Sexual Behavior, Animal
4.
Pest Manag Sci ; 63(6): 608-14, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17487881

ABSTRACT

Sesamia nonagrioides Lef. and Ostrinia nubilalis (Hübn.) are two corn borers present in the Mediterranean area that share a similar feeding habitat. The female sex pheromones of the two species consist of (Z)-11-hexadecenyl acetate, (Z)-11-hexadecen-1-ol, (Z)-11-hexadecenal and dodecyl acetate (77:8:10:5 w/w) and (Z)-11-tetradecenyl acetate and (E)-11-tetradecenyl acetate (97:3 w/w) respectively. Although the pheromones share no common components, previous work had shown the inhibition of the response by O. nubilalis males to their own pheromone owing to the presence of S. nonagrioides pheromone. In this study, the pheromone of O. nubilalis and its two components separately were shown to inhibit the attraction of S. nonagrioides males to the synthetic female pheromone in both laboratory wind-tunnel bioassay and field trapping studies. In the wind tunnel, the number of contacts of S. nonagrioides males with the source were significantly (P < 0.05) reduced by the single pheromone components of O. nubilalis. In the field, the addition of 1% of O. nubilalis pheromone significantly (P < 0.05) reduced the catches of S. nonagrioides males. The components of both pheromones also elicited electroantennographic responses from antennae of male S. nonagrioides moths. The ecological consequences and the possibilities of applying this cross-inhibition for mating disruption techniques are discussed.


Subject(s)
Moths/drug effects , Pest Control, Biological , Sex Attractants/pharmacology , Sexual Behavior, Animal/drug effects , Animals , Dose-Response Relationship, Drug , Female , Male , Moths/metabolism , Moths/physiology , Sex Attractants/administration & dosage , Sex Attractants/isolation & purification
5.
J Chem Ecol ; 32(5): 1071-84, 2006 May.
Article in English | MEDLINE | ID: mdl-16739024

ABSTRACT

Mixing the sex pheromones of the Mediterranean corn borer, Sesamia nonagrioides, and the European corn borer, Ostrinia nubilalis, results in significantly lower captures of O. nubilalis when compared to traps loaded with its pheromone alone. Rubber septa loaded with a constant concentration of the pheromone of O. nubilalis and different percentages of the S. nonagrioides pheromone (from 1 to 100%) causes dose-dependent antagonism in the field. Electroantennograms of O. nubilalis males showed high antennal responses to its own pheromone components, followed by smaller responses to the major, [(Z)-11-hexadecenyl acetate (Z11-16:Ac)], and two minor components [dodecyl acetate (12:Ac) and (Z)-11-hexadecenal (Z11-16:Ald)] of the S. nonagrioides pheromone. There was almost no response to the S. nonagrioides minor component (Z)-11-hexadecenol (Z11-16:OH). Field tests that used traps baited with the O. nubilalis pheromone plus individual components of S. nonagrioides showed that Z11-16:Ald causes the antagonism. Adding 1% Z11-16:Ald to the pheromone of O. nubilalis reduced oriented flight and pheromone source contact in the wind tunnel by 26% and 83%, respectively, and trap captures in the field by 90%. The other three pheromone components of S. nonagrioides inhibited pheromone source contact but not oriented flight of O. nubilalis males and did not inhibit capture in the field. Cross-adaptation electroantennogram suggests that Z11-16:Ald stimulates a different odor receptor neuron than the pheromone components of O. nubilalis. We conclude that Z11-16:Ald is a potent antagonist of the behavioral response of O. nubilalis.


Subject(s)
Moths/chemistry , Sex Attractants/antagonists & inhibitors , Animals , Electrophysiology , Female , Male , Moths/physiology , Olfactory Receptor Neurons , Sex Attractants/analysis , Sexual Behavior, Animal
6.
J Agric Food Chem ; 53(4): 1158-65, 2005 Feb 23.
Article in English | MEDLINE | ID: mdl-15713034

ABSTRACT

The antagonistic effect on the pheromone response and catabolism of male European corn borers, Ostrinia nubilalis, by several trifluoromethyl ketones is reported. (Z)-11-Tetradecenyl trifluoromethyl ketone (Z11-14:TFMK), the most closely related analogue of the main component of the pheromone, elicits a remarkable disruptive effect on close approach and source contact of males flying to a source baited with mixtures of the pheromone and the antagonist in 5:1 and 10:1 ratios. In this experiment, the male displayed an erratic flight track with frequent counter turns and intersections with the plume. In the field, the TFMK significantly lowered the number of males caught when mixed with the pheromone in a 10:1 ratio in comparison with the natural attractant. The compound was also a good inhibitor of the antennal esterase of the insect with a IC(50) value of 0.28 muM. The homologous (Z)-10-tridecenyl trifluoromethyl ketone, with one carbon less in the chain, also elicited an antagonistic effect in the wind tunnel, but in the field, the results were not conclusive. The effect induced was lower than the one displayed by Z11-14:TFMK including the activity as the esterase inhibitor (IC(50) value of 7.55 muM). The saturated tetradecyl trifluoromethyl ketone, tetradecyltrifluoropyruvamide, and (Z)-11-2-thiatetradecenyl trifluoromethyl ketone resulted completely inactive. The results obtained in conjunction to the previously shown low toxicity to mice by related trifluoromethyl ketones provide new important data for the putative utilization of these chemicals as new pest control agents.


Subject(s)
Behavior, Animal/drug effects , Ketones/pharmacology , Moths/physiology , Pheromones/antagonists & inhibitors , Animals , Enzyme Inhibitors/pharmacology , Esterases/antagonists & inhibitors , Insecticides , Male
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