Evaluation of semiochemical toxicity to houseflies and stable flies (Diptera: Muscidae)

BACKGROUND: The housefly, Musca domestica L., and stable fly, Stomoxys calcitrans (L.) are cosmopolitan pests of both farm and home environments. Houseflies have been shown to be resistant to a variety of insecticides, and new chemistries are slow to emerge on the market. Toxicities of selected semiochemicals with molecular structures indicative of insecticidal activity were determined against adults from an insecticide‐susceptible laboratory strain of houseflies. The three most active semiochemicals were also evaluated against recently colonized housefly and stable fly strains. RESULTS: Nineteen semiochemicals classified as aliphatic alcohols, terpenoids, ketones and carboxylic esters showed toxicity to houseflies and stable flies. Rosalva (LC₅₀ = 25.98 µg cm^?2) followed by geranyl acetone and citronellol (LC₅₀ = 49.97 and 50.02 µg cm^?2) were identified as the most toxic compounds to houseflies. Permethrin was up to 144‐fold more toxic than rosalva on the susceptible strain. However, it was only 35‐fold more toxic to the insecticide‐tolerant field strain. The compounds generated high toxicity to stable flies, with LC₅₀ values ranging from 16.30 to 40.41 µg cm^?2. CONCLUSION: Quantification of LC₅₀ values of rosalva, citronellol and geranyl acetone against susceptible housefly and field‐collected housefly and stable fly strains showed that semiochemicals could serve as potent insecticides for fly control programs. Copyright © 2010 Society of Chemical Industry     

Ecdysone metabolism by soluble enzymes from three species of diptera and its inhibition by the insect growth regulator TH-6040

Homogenates of larvae, pupae, and adults of house flies (Musca domestica L.), flesh flies (Sarcophaga bullata Parker), and blow flies (Phormia regina (Meigen)) have been examined for enzymes which convert α- and β-ecdysone to apolar products. Most of the activity was found in the soluble fraction from house flies and flesh flies but none of the blow fly fractions was active. Two enzymes seem to be involved in the ecdysone metabolism, one requiring NADPH and the other functioning without this cofactor. The product of the latter enzyme is thought to be the 3-dehydro-ecdysone. This product is further converted to the 3α-hydroxy isomer of ecdysone by the NADPH-requiring enzyme. On feeding the insect growth regulator TH-6040 (1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)-urea) to larvae at dietary levels ranging from 0.3 to 10 ppm, the activity of the enzyme producing the 3-dehydro product is reduced by 20 to 82%. It is suggested that the growth regulator exerts its effect on pupal-adult ecdysis through its inhibition of ecdysone metabolism.     

Insecticidal properties of monoterpenoid derivatives to the house fly (diptera: Muscidae) and red flour beetle (coleoptera: Tenebrionidae)

Monoterpenoid derivatives were synthesized and their insecticidal activities were evaluated against red flour beetles, Tribolium castaneum (Herbst), in fumigant bioassays and against house flies Musca domestica (L.) in topical, fumigant, and ovicidal bioassays. Acetate derivatives and haloacetate derivatives were compared with each other, and with the parent monoterpenoid to determine structure-activity relationships. Acetate derivatives were more active than the propionate derivatives of cyclic monoterpenoids in the topical, fumigant, and ovicidal bioassays. Pivalates were topically more insecticidal than acetates to adult house flies, while the acetates had the greater ovicidal activity. Acetates and pivalates were more effective than haloacetates in the topical, red flour beetle fumigation and ovicidal bioassays. Fluoroacetates of cyclic monoterpenoids were the most effective house fly fumigants, followed by acetates, and trichloroacetates. Several derivatives were produced that displayed enhanced activity relative to the parent alcohols or phenols.     

Insecticidal potency of novel compounds on multiple insect species of medical and veterinary importance

BACKGROUND: Vector‐borne diseases continue to present significant threats to human, animal and plant health. Mosquitoes, houseflies, sand flies and stable flies are well‐known vectors of several human and animal pathogens. The toxicity of selected semiochemicals with molecular structures indicative of insecticidal activity was determined against these insect species with the aim of developing novel insecticides toxic to multiple insect species. RESULTS: Three semiochemicals, namely beta‐damascone, cyclemone A and melafleur, showed remarkable toxicity to three mosquitoes, Aedes aegypti L., Ae. albopictus (Skuse) and Anopheles quadrimaculatus Say, the housefly, Musca domestica L., the stable fly, Stomoxys calcitrans L., and the sand fly, Lutzomyia shannoni (Dyar). The chemicals were equally toxic to several field‐collected permethrin‐tolerant housefly strains. When formulated as 500 mL L^?1 emulsifiable concentrates, the chemicals demonstrated stability and toxicity on filter paper and camouflage military fabrics, with persistence up to 8 days under laboratory conditions. The chemicals were equally effective under field conditions when evaluated on unpainted plywood panels, although a higher dosage was required under field conditions to achieve similar efficacy. CONCLUSION: Laboratory quantification of LC₅₀ values and field efficacy of three semiochemicals as formulated compounds on mosquitoes, houseflies, stable flies and sand flies showed that these semiochemicals could serve as potent insecticides for multiple insect species. Copyright © 2010 Society of Chemical Industry     

A test for repellency to non-biting flies and a comparison of repellents using Musca domestica L.

A system for testing the effect of a repellent against nonbiting flies attracted to man was developed for Musca domestica L. and Musca vetustissima Walk., and was used to compare the repellency of a range of chemicals against the former. Both arms of one person were simultaneously exposed to large numbers of the test insect in a cage, with repellent applied to a 45 cm² area on one arm, and the solvent to an identical area on the other arm. By varying the dose of repellent, a dose-to-repellency relationship was established and evaluated using probit analysis to determine 50% (RD₅₀) and 90% (RD₉₀) repellency. Both values were required to characterise a repellent. Greatest uniformity of results was obtained with even illumination of the cages from above and exclusion of side lighting. RD₅₀ and RD₉₀ values were not affected by prior exposure of the flies in a cage and did not change with time. Of the repellents tested, dipropyl isocinchomeronate was the most effective against M. domestica. The repellent effect of mixtures of the compounds was tested against M. domestica and was less than expected by summation of the components acting alone, suggesting that to minimise the total dose of chemical applied to skin, single compounds are preferable to mixtures.     

Microsomal metabolism of juvenile hormone analogs in the house fly,Musca domestica L.

Of six juvenile hormone analogs of the alkyl 3,7,11-trimethyl-2,4-dodecadienate type, only the isopropyl ester was strongly morphogenic in the house fly, Musca domestica L. In vitro assays revealed that house fly microsomes contain B-esterases as well as oxidases which metabolize such analogs. However, these esterases did not hydrolyze the isopropyl ester, ZR-515. Enzymes prepared from larvae, pupae, and adults were all active and there was evidence that in the late larval stage the esterase activity was cyclic, showing a minimum in the early third instar and a maximum a few hours later. When microsomes from two susceptible and two resistant house fly strains were compared for metabolic activity against the juvenile hormone analogs, those from the resistant strains were 1.3 to 20 × higher in oxidase activity but there was no difference in esterase activity. The oxidative metabolism of two analogs ZR-515 and 512 was greatly enhanced when the flies were induced with phenobarbital but there was no enhancement in metabolism of three of the remaining analogs and only a slight enhancement of a fourth. It is concluded that the insecticidal action of ZR-515 is largely due to its stability in the presence of the house fly esterases.     

Toxicity of spinosad to susceptible and resistant strains of house flies,Musca domestica

The toxicity of spinosad, a new insecticide derived from the bacterium Saccharopolyspora spinosa, was evaluated against susceptible and resistant strains of house fly (Musca domestica L.). Spinosad was highly toxic to house flies based on 72-h LD₅₀ values and the symptoms of poisoning were consistent with a neurotoxic mechanism of action. Spinosad was relatively slow acting, with the maximum toxicity noted at 72 h. Piperonyl butoxide and S,S,S,-tribu-tylphosphorotrithioate synergized the toxicity of spinosad by 3·0- and 1·8-fold, respectively, while diethyl maleate had no significant effect. These results suggest that there is a small degree of monooxygenase-mediated spinosad detoxification in house flies, while hydrolases may be only minimally important and glutathione transferases may have no role. There were no substantial levels of cross-resistance detected, except in the LPR strain where a low 4·3-fold cross-resistance was observed. The cyclodiene-resistant OCR strain was 2·7-fold more sensitive to spinosad than the susceptible strain (CS). These results suggest that cross-resistance may not be a limiting factor for the use of spinosad against house flies. © 1998 Society of Chemical Industry     

Stereochemical basis for the insecticidal activity of carbamoylated and acylated pyrazolines

Methyl 3-(4-chlorophenyl)-1-[N-(4-chlorophenyl)carbamoyl]-4-methyl-2-pyrazoline-4-carboxylate was converted to corresponding (1R)- and (1S)-phenethyl esters via its carboxylic acid and acid chloride at the C-4 atom to separate the diastereomers. Their configurations were confirmed by X-ray analysis. Both isomers of the (1R)methylbenzyl ester were subjected to transesterification with sodium methoxide to obtain enantiomers of the starting methyl ester. Their insecticidal activity was measured against American cockroaches (Periplaneta americana (L.)) by injection and against house flies (Musca domestica L.) by topical application under various synergistic conditions with metabolic inhibitors. The activity values of the four α-methylbenzyl esters and the R-isomer of the starting methyl ester were similar. The S-enantiomer of the methyl ester was about 10 and 100 times more active than the R-isomer against the cockroach and the fly, respectively. Some N-arylacetyl and N-aryloxyacetyl derivatives of the starting N-(4-chlorophenyl)carbamoyl compound gave very low activity. Conformation-energy profiles for some compounds suggested that the conformation of substituents on the N-1 atom in the pyrazoline ring has a specific role for the potential insecticidal effects.     

Structure—activity relationship for some substituted dialkyl vinyl phosphates

The biological activity against the house fly, Musca domestica L., is reported for a series of dialkyl 2-bromo-1-(2,4-dichlorophenyl)vinyl phosphates. Maximum activity and the lowest degree of synergism with piperonyl butoxide were found with the dimethyl ester. Good activity was also shown by the diethyl ester. Both these compounds, used at the same dose, inhibited fly-head acetylcholinesterase. Compounds with longer alkyl chains were less effective and did not inhibit acetylcholinesterase.     

Interaction between the factor delaying penetration of insecticides and the desethylation mechanism of resistance in organophosphorus-resistant houseflies

The desethylation (gene a) and penetration delaying (pen) factors of resistance to organophosphorus insecticides isolated by genetical methods from the diazinon-selected SKA strain of houseflies (Musca domestica L.) were inbred into a strain whose resistance was compared with that of flies with single factors of resistance and the SKA strain. Pen alone decreases kill marginally, and gene a alone raises LD₅₀ to 1·4–48 times that of susceptible flies, depending on the insecticide. The two factors together increase resistance greatly to many organophosphorus insecticides (up to 5–10 times or more to diazinon, malathion-ethyl and chlorthion-ethyl than of flies with gene a only) indicating that the two factors interact. Interaction is greater against the thionates than the corresponding phosphates, probably because pen delays entry of thionates more than of the corresponding phosphates. The role in resistance of each factor when hetero-and homo-zygous, and the reasons for interaction, are discussed.     

An electrophysiological investigation of the susceptible (cooper) and resistant (kdr; super-kdr) strains of the adult housefly,Musca domestica L

The electrical activity of abdominal nerves of the housefly, Musca domestica L., was used as a bioassay to study nerve sensitivity to DDT and deltamethrin in susceptible (Cooper) and resistant (kdr, super-kdr) strains. By this technique the resistant strains were less sensitive (approximately 10 000-fold) than Cooper, but the bioassay could not distinguish between super-kdr and kdr in their responses to either compound and so could not account for the greater resistance shown by flies with super-kdr above kdr flies when these insecticides are applied topically. Although factors other than nerve insensitivity may be involved, the compounds were applied to the preparation in aqueous saline solutions at, or close to, their solubility limits and this could have masked differences in responses of nerves from the resistant strains.     

Enhancement of dye-sensitized phototoxicity to house fly larvae in vivo by dietary ascorbate,diazabicyclooctane, and other additives

Several reagents reported to be singlet oxygen quenchers and/or radical scavengers and to be protectants against photooxidative damage to isolated systems in vitro were examined, in vivo, for protective effect on the larvae of the house fly (Musca domestica L.; Diptera:Muscidae). A standardized erythrosine-sensitized phototoxic test procedure was used. β-Carotene appeared to show some protective effect. Other dietary additives exhibited no measurable degree of protection to the larvae in vitro; on the contrary, mortality increased in the presence of butylated hydroxytoluene, ascorbate, and diazabicyclooctane.     

Multiple Resistance in the Larger House Fly Musca domestica in Germany

Populations of the housefly Musca domestica isolated from farms in different German districts with strong resistance problems were compared to laboratory strains with varying resistance spectra. Resistance against pyrethroids, organophosphates and carbamates was tested using impregnated filter papers, and by topical application using a susceptible housefly strain (origin WHO) for comparison. The multi-resistant fly strains tested had a strong resistance against these insecticide groups, ranging from 37- to >10000-fold for organophosphates and 150- to >6600-fold for pyrethroids. The constituent enantiomer pairs of the α-cyano-pyrethroid cyfluthrin were tested, as was beta-cyfluthrin. With respect to multi-resistant fly strains, the isomers II and IV had the best activity, with LD₅₀ values of 0·012 and 0·014 μg per fly, respectively. In addition, different groups of insect growth regulators (juvenile hormone analogues, chitin synthesis inhibitors and one triazine derivative) were tested in a special larvicidal test. The chitin synthesis inhibitors were quite effective against multi-resistant M. domestica strains except for one strain with strong resistance against chitin synthesis inhibitors, developed after extensive treatments with benzoylphenylureas for several years. The fly strains tested were not resistant against cyromazine. Additionally, the insecticides were combined with the synergists piperonyl butoxide, tributylphosphorotrithioate (DEF) and Cibacron blue and tested against the fly strain with the strongest resistance spectrum (‘Grimm’) in comparison to the susceptible strain (‘WHO-N’). Piperonyl butoxide had the greatest effect on the efficacy of cyfluthrin followed by Cibacron blue and DEF. In a parallel investigation with susceptible and resistant house fly strains, different enzyme activities related with resistance mechanisms were tested, e.g. glutathione S-transferase (3·5-fold) and mixed-function oxidase (2·3-fold). Implications of these results for management of insecticide resistance in M. domestica are discussed.     

Determining the source of house flies (Musca domestica) using stable isotope analysis

BACKGROUND: Intensive livestock units frequently produce flies in large numbers that, on migration, cause nuisance to the occupants of neighbouring dwellings. The resolution of such problems is often reliant on the unequivocal identification of the origin of the flies, particularly when several potential sources exist. This study evaluated stable isotope analysis as a method for differentiating adult houseflies (Musca domestica) on the basis of their dietary history so as to determine their likely source. RESULTS: Flies were reared in the laboratory on several substrates, including chicken and cattle manure, laboratory diet and household vegetable waste. Different fly parts (wings, heads and legs) and whole flies were analysed immediately after eclosion and after 10 days. The δ¹³C and δ¹⁵N values for adults that had developed on each diet type were highly distinct. Both isotopic ratios altered markedly after maintaining the flies for 10 days on a diet of cane sugar solution. CONCLUSIONS: Stable isotope analysis readily differentiated flies that had developed on a range of substrates. The technique, therefore, shows potential to be employed to determine the likely source of various nuisance insects, and to contribute to the abatement of such problems. Copyright © 2011 Society of Chemical Industry     

Genetic and biochemical mechanisms limiting fipronil toxicity in the LPR strain of house fly,Musca domestica

Fipronil is a new insecticide which exerts its toxic action by interacting with the insect GABA-gated chloride channel. Previous studies have shown that cyclodiene-resistant insects have low to moderate levels of cross-resistance to fipronil, while other resistant strains are usually susceptible. In contrast, we recently found a strain (LPR) of house fly (Musca domestica L) with 15-fold cross-resistance to fipronil that was not associated with cyclodiene resistance. Fipronil cross-resistance in LPR was inherited as an intermediately dominant, autosomal, multigenic trait. [¹⁴C]Fipronil was observed to penetrate into LPR flies more slowly than into susceptible flies. S,S,S-tributylphosphorotrithioate and diethyl maleate pretreatment did not reduce the level of fipronil cross-resistance, while piperonyl butoxide resulted in a slight decrease. These results indicate that decreased penetration and monooxygenase-mediated detoxification may be mechanisms contributing to fipronil cross-resistance in the LPR strain. © 1999 Society of Chemical Industry     

DDT and pyrethroids: Receptor binding in relation to knockdown resistance (kdr) in the house fly

The nature of target site or knockdown resistance (kdr) to DDT and pyrethroids was studied by investigating specific binding of [14_C] DDT and [14_C] cis-permethrin to the previously established membrane receptors from the heads of susceptible (sbo) and resistant (kdr) strains of the house fly, Musca domestica L. In vivo studies showed the heads from sbo flies bound two to three times more DDT than those from kdr flies at all doses tested. Reduced binding was also observed in kdr flies in in vitro [14_C] DDT binding assays. Scatchard analysis indicated that kdr flies have the same affinity but fewer receptors per milligram protein in the CNS than sbo flies. Assays with [14_C] cis-permethrin also showed binding was much reduced in kdr flies in comparison with sbo flies. Based on these results, the nature of the target site insensitivity of kdr flies may relate to their having a reduced number of receptors for the insecticides.     

Insecticidal activity of the pyrethrins and related compounds. IX. 5-benzyl-3-furylmethyl 2,2-dimethylcyciopropanecarboxylates with non-ethylenic substituents at position 3 on the cyclopropane ring

The insecticidal activities against houseflies (Musca domestica L.) and mustard beetles (Phaedon cochleariae Fab.) of 29 new 5-benzyl-3-furylmethyl 2,2-dimethyl-cyclopropane-carboxylates are compared with those of the corresponding chrysanthe-mate (bioresmethrin) to assess the influence of non-ethylenic and isobutenyl substituents at position 3 of the cyclopropane ring. Of the new groups investigated, only 3-methoxyiminomethyl gives equal or enhanced activity; 3-(2-furyl) esters are moderately effective, but 3-phenyl and 3-alkoxycarbonyl compounds show weak activity. A 3-(2,2,2-trihaloethyl) compound was more active than compounds with other saturated groups, such as isobutyl.     

Nicotinoid and pyrethroid insecticide resistance in houseflies (Diptera: Muscidae) collected from Florida dairies

BACKGROUND: The housefly, Musca domestica L., continues to be a major pest of confined livestock operations. Houseflies have developed resistance to most chemical classes, and new chemistries for use in animal agriculture are increasingly slow to emerge. Five adult housefly strains from four Florida dairy farms were evaluated for resistance to four insecticides (beta‐cyfluthrin, permethrin, imidacloprid and nithiazine). RESULTS: Significant levels of tolerance were found in most field strains to all insecticides, and in some cases substantial resistance was apparent (as deduced from comparison with prior published results). At the LC₉₀ level, greater than 20‐fold resistance was found in two of the fly strains for permethrin and one fly strain for imidacloprid. Beta‐cyfluthrin LC₉₀ resistance ratios exceeded tenfold resistance in three fly strains. The relatively underutilized insecticide nithiazine had the lowest resistance ratios; however, fourfold LC₉₀ resistance was observed in one southern Florida fly strain. Farm insecticide use and its impact on resistance selection in Florida housefly populations are discussed. CONCLUSION: Housefly resistance to pyrethroids is widespread in Florida. Imidacloprid resistance is emerging, and tolerance was observed to both imidacloprid and nithiazine. If these insecticides are to retain efficacy, producer use must be restrained. Copyright © 2009 Society of Chemical Industry     

Quantitative structure-activity study of insecticidal 2-methoxy-5-(substituted-phenyl)-1, 3, 2-oxazaphospholidine 2-sulfides against Musca domestica L. by topical application

The quantitative relationship between the structure of 2-methoxy-5-(substituted-phenyl)-1, 3, 2-oxazaphospholidine 2-sulfides (5-PMOS) and their insecticidal activity against the house fly. Musca domestica L., was analyzed using reported physicochemical parameters and regression analysis. The electronic nature of the substituent on the phenyl group of 5-PMOS has the most significant effect on the activity, followed by hydrophobic and steric effects; the optimum value of Σρ is zero and the more hydrophobic the substituents on the phenyl group, the higher the insecticidal activity. The plots of observed pLD₅₀, values against calculated pLD₅₀ values for compounds having substituents in the ortho-position deviated downwards from those of compounds having substituents at the meta and/or para positions. This ortho-effect, which reduces the insecticidal activity of compounds having substituents at the ortho-position, was expressed by a dummy parameter D, which has the value 2 for di-ortho-substituted derivatives, 1 for mono-ortho-substituted derivatives and zero for others. Thus, the highest activity was obtained for 2-methoxy-5-phenyl-1, 3, 2-oxazaphospholidine 2-sulfide, and the activity was decreased by the introduction of any substituents on the phenyl group.     

Naturally occurring cyanohydrins,analogues and derivatives as potential insecticides

Several naturally occurring cyanohydrins were tested for fumigation toxicity to two insect species, the house fly (Musca domestica L) and the lesser grain borer (Rhyzopertha dominica (F)). Synthetic analogues of these compounds were tested as well. Most of the cyanohydrins tested were more toxic as fumigants to M domestica and R dominica than chloropicrin; some compounds were nearly as toxic as dichlorvos. Naturally occurring cyanohydrins were among the most toxic tested. © 2000 Society of Chemical Industry