methoprene and pyriproxyfen

Synthetic compounds that mimic the action of juvenile hormones (JHs) are founding members of a class of insecticides called insect growth regulators (IGRs). Like JHs, these juvenoids block metamorphosis of insect larvae to reproductive adults. Many biologically active juvenoids deviate in their chemical structure considerably from the sesquiterpenoid JHs, raising questions about the mode of action of such JH mimics. Despite the early deployment of juvenoid IGRs in the mid-1970s, their molecular effect could not be understood until recent discoveries of JH signaling through an intracellular JH receptor, namely the ligand-binding transcription factor Methoprene-tolerant (Met). Here, we briefly overview evidence defining three widely employed and chemically distinct juvenoid IGRs (methoprene, pyriproxyfen, and fenoxycarb), as agonist ligands of the JH receptor. We stress that knowledge of the target molecule is critical for using these compounds both as insecticides and as research tools.

Topics: Animals; Gene Expression Regulation, Developmental; Insecticide Resistance; Insecticides; Juvenile Hormones; Ligands; Metamorphosis, Biological; Methoprene; Phenylcarbamates; Pyridines; Structure-Activity Relationship

The efficacy of three groups of insect growth regulators, namely juvenile hormone mimics (methoprene and pyriproxyfen), chitin synthesis inhibitors (diflubenzuron and novaluron), and molting disruptor (cyromazine) was evaluated for the first time, against Aedes albopictus Skuse (Diptera: Culicidae) larvae from 14 districts in Sabah, Malaysia. The results showed that all field populations of Ae. albopictus were susceptible towards methoprene, pyriproxyfen, diflubenzuron, novaluron, and cyromazine, with resistance ratio values ranging from 0.50-0.90, 0.60-1.00, 0.67-1.17, 0.71-1.29, and 0.74-1.07, respectively. Overall, the efficacy assessment of insect growth regulators in this study showed promising outcomes and they could be further explored as an alternative to conventional insecticides.

Topics: Aedes; Animals; Diflubenzuron; Insect Vectors; Insecticides; Juvenile Hormones; Larva; Malaysia; Methoprene; Mosquito Control; Phenylurea Compounds; Pyridines

Exposure of adult mosquitoes to pyriproxyfen (PPF), an analog of insect juvenile hormone (JH), has shown promise to effectively sterilize female mosquitoes. However, the underlying mechanisms of the PPF-induced decrease in mosquito fecundity are largely unknown. We performed a comprehensive study to dissect the mode of PPF action in Aedes aegypti mosquitoes. Exposure to PPF prompted the overgrowth of primary follicles in sugar-fed Ae. aegypti females but blocked the development of primary follicles at Christopher's Stage III after blood feeding. Secondary follicles were precociously activated in PPF-treated mosquitoes. Moreover, PPF substantially altered the expression of many genes that are essential for mosquito physiology and oocyte development in the fat body and ovary. In particular, many metabolic genes were differentially expressed in response to PPF treatment, thereby affecting the mobilization and utilization of energy reserves. Furthermore, PPF treatment on the previtellogenic female adults considerably modified mosquito responses to JH and 20-hydroxyecdysone (20E), two major hormones that govern mosquito reproduction. Krüppel homolog 1, a JH-inducible transcriptional regulator, showed consistently elevated expression after PPF exposure. Conversely, PPF upregulated the expression of several key players of the 20E regulatory cascades, including HR3 and E75A, in the previtellogenic stage. After blood-feeding, the expression of these 20E response genes was significantly weaker in PPF-treated mosquitoes than the solvent-treated control groups. RNAi-mediated knockdown of the Methoprene-tolerant (Met) protein, the JH receptor, partially rescued the impaired follicular development after PPF exposure and substantially increased the hatching of the eggs produced by PPF-treated female mosquitoes. Thus, the results suggested that PPF relied on Met to exert its sterilizing effects on female mosquitoes. In summary, this study finds that PPF exposure disturbs normal hormonal responses and metabolism in Ae. aegypti, shedding light on the molecular targets and the downstream signaling pathways activated by PPF.

Topics: Aedes; Animals; Culicidae; Ecdysterone; Fat Body; Female; Glycogen; Insect Proteins; Insecticides; Juvenile Hormones; Methoprene; Ovary; Pyridines; RNA Interference; Sterilization; Triglycerides

A field study was carried out on the year-long residual activity of the insect growth regulator (IGR) pyriproxyfen (Nylar 0.5G) in comparison with methoprene (Altosid® XRP Pellets) against mosquito developmental stages in catch basins in northwestern Riverside County, southern California. Pyriproxyfen was applied at 75, 100, 125, 150, 175 g per catch basin and methoprene at 3.5 g per catch basin. A total of 80 catch basins (10 per each treatment and 20 for control) were used. Posttreatment observations of catch basins were carried out at weekly intervals, with all pupal collections reared to adults. Mosquito species composition in this study, consisting mostly of Culex species (693), was predominated by Cx. quinquefasciatus (92.8%), followed by Cx. erythrothorax (5.5%), Cx. tarsalis (1.2%), Cx. stigmatosoma (0.3%), and Cx. thriambus (0.2%). Activity of both IGRs was expressed as percent inhibition of adult emergence (% IAE). Data generated on % IAE showed that, like methoprene, pyriproxyfen provided complete control of mosquitoes at 75, 125, and 175 g per catch basin up to 50 wk posttreatment at the Riverside amusement park, whereas its activity against mosquitoes in catch basins treated with 100 g and 150 g at the Eastvale site was short-lived, up to 48 wk. Water samples, bioassayed against laboratory-reared, 4th-stage larvae of Cx. quinquefasciatus 1-2 wk after the 50-wk-long study, showed evidence of significant % IAE (∼50) by pyriproxyfen at the 2 higher rates (125 g, 175 g) used at the amusement park. In conclusion, pyriproxyfen can be used to effectively control mosquitoes in catch basins for 48-50 wk, depending on the rate of application.

Topics: Animals; California; Culex; Female; Insecticides; Larva; Male; Methoprene; Mosquito Control; Ovum; Pupa; Pyridines

The use of topical and oral therapies on pets has revolutionized the control of cat fleas, Ctenocephalides felis felis (Bouché). Herein, we tested the biological activity of two adulticides, fipronil and imidacloprid, and the insect growth regulators (IGRs), methoprene and pyriproxyfen. The LC50's of fipronil, imidacloprid, methoprene, and pyriproxyfen in larval rearing medium for second and third instars were 1.13, 0.73, 0.35, and 0.23 ppm, respectively. Combinations of imidacloprid and methoprene and pyriproxyfen were synergistic. The combination indices (CIs) at an effective dose (ED95) of imidacloprid:methoprene (Im:Meth) were 0.54, 0.44, 0.66, 0.73, and 0.62 for Im1:Meth1, Im5:Meth1, Im10:Meth1, Im20:Meth1, and Im40:Meth1, respectively. Similarly, the CIs of imidacloprid:pyriproxyfen (Im:Pyri) at an ED95 were 0.73 and 0.50 for Im1:Pyri1 and Im5:Pyri1, respectively. Combinations of fipronil:methoprene (Fip:Meth) provided variable results with Fip1:Meth1 being antagonistic (CI = 1.61). Combinations at 5:1, 10:1, and 20:1 at an ED95 were moderately synergistic. Combinations of Fip:Pyri at 1:1 were antagonistic at an ED95 with a CI of 2.87. When the combinations were reversed, neither the imidacloprid nor fipronil synergized either IGR. The dose response indices (DRI) for both Im:Meth and Im:Pyri indicate that the concentrations of the combinations could be significantly reduced and still be as effective as imidacloprid alone. Certain combinations of adulticides and IGRs were synergistic against immature fleas.

Topics: Animals; Ctenocephalides; Drug Synergism; Insect Control; Insecticides; Juvenile Hormones; Larva; Methoprene; Neonicotinoids; Nitro Compounds; Pyrazoles; Pyridines

Aerosol application of insecticides as part of an integrated pest management program is becoming more widely adopted in food facilities such as flour mills. However, the method of application and the complex structural features within a facility can impact how insecticide particles travel and settle on surfaces and therefore impact the consistency in efficacy obtained. Here we investigated how the location from which an aerosol insecticide is released impacts the spatial pattern of aerosol deposition, using efficacy against Tribolium confusum Jacquelin du Val (Coleoptera: Tenebrionidae), the confused flour beetle, as a model insects. Concrete bioassay arenas containing T. confusum adults and flour were exposed to two commercial aerosol formulations, pyrethrin + pyriproxyfen and pyrethrin + methoprene, and observed for initial adult knockdown and subsequent mortality. Aerosols were applied from one of three static locations or a fourth application comprised of multiple aerosol release points. The aerosol release position had a significant effect on T. confusum adult knockdown and mortality; both ranged from 0 to 100% depending on bioassay arena location. The multiple aerosol release positions tended to have more bioassay arenas with higher knockdown and mortality, and had a more consistent impact across all arena locations, yet there were still areas on the mill floor where little adult beetle efficacy was observed. The effect of each aerosol on T. confusum adults is a culmination of how the aerosol was applied, the distance the aerosol particles traveled, and the complexity of a milling facility.

Topics: Aerosols; Animals; Food Parasitology; Insect Control; Insecticides; Methoprene; Pyrethrins; Pyridines; Tribolium

In a field trial, pyriproxyfen (Sumilarv 0.5% G) applied at 10 g and 50 g per catch basin and S-methoprene (Altosid XR briquet 2.1%) at 1 briquet per catch basin at a local park provided 100% inhibition of adult emergence (IAE) of the test species, Culex quinquefasciatus , for the first 3 wk. The IAE dropped to 69% to 85% for pyriproxyfen and 68% for methoprene at 4 wk posttreatment. The IAE at 5 to 8 wk posttreatment, although remaining high, was overshadowed by high mortality in control catch basins. The high mortality in control could be attributed to autodissemination of pyriproxyfen by mosquitoes from treated to untreated catch basins.

Topics: Animals; California; Culex; Insecticides; Methoprene; Mosquito Control; Pyridines

Insect growth regulators (IGRs) methoprene and pyriproxyfen are widely used as topical treatments to pets or applied to the indoor environment to control cat fleas, Ctenocephalides felis (Bouché). The toxicity of methoprene, pyriproxyfen, and combinations of both IGRs to cat flea larvae was determined. The LC

Topics: Animals; Cat Diseases; Cats; Drug Synergism; Female; Flea Infestations; Insecticide Resistance; Insecticides; Juvenile Hormones; Larva; Male; Methoprene; Pyridines; Siphonaptera

The juvenile hormone analogues methoprene and pyriproxyfen were evaluated as rodent feed-through insecticides for control of immature stages of the sandfly Phlebotomus papatasi Scopoli (Diptera: Psychodidae). The development and survival of P. papatasi second-instar larvae fed faeces from Syrian hamsters, Mesocricetus auratus, that had been fed a diet containing methoprene (0, 9.788, 97.88 or 978.8 p.p.m.) or pyriproxyfen (0, 9.82, 98.2 or 982 p.p.m.) were evaluated. The faeces of methoprene-treated hamsters greatly reduced the percentage of larvae that pupated at all concentrations tested and prevented adult emergence at all but the lowest concentration (9.788 p.p.m.). Pyriproxyfen prevented both pupation and adult emergence at all concentrations tested. The results of this study suggest that a control strategy using rodent baits containing juvenile hormone analogues to control phlebotomine sandflies that live in rodent burrows and feed on rodent faeces may be possible. As rodent reservoirs and vectors of Leishmania major live in close association in many parts of the Middle East, control of the transmission of the agent of zoonotic cutaneous leishmaniasis may also be possible.

Topics: Animals; Cricetinae; Feces; Insect Control; Insecticides; Juvenile Hormones; Larva; Leishmaniasis, Cutaneous; Mesocricetus; Methoprene; Phlebotomus; Pyridines

Thirteen cats and 7 dogs living in 14 homes were treated topically with either a dinotefuran (22%, w/w)/pyriproxyfen (3.00%, w/w) (DP) or dinotefuran (4.95%, w/w)/pyriproxyfen (0.44%, w/w)/permethrin (36.08%, w/w) (DPP) topical spot-on, respectively. Twenty cats and 7 dogs living in 16 homes were treated topically with either a fipronil (9.8%, w/w)/(S)-methoprene (11.8%, w/w) or fipronil (9.8%, w/w)/(S)-methoprene (8.8%, w/w) topical spot-on (FM), respectively. All products were applied according to label directions by study investigators on day 0 and again between days 28 and 30. Flea populations on pets were assessed using visual area counts and premise flea infestations were assessed using intermittent-light flea traps on days 0, 7, 14, 21, 28-30, 40-45, and 54-60. A single application of the DP-DPP and FM formations reduced flea populations by 87.35% and 88.44%, respectively within 7 days. Following two monthly applications of either the DP-DPP or FM formulations, pet flea burdens were reduced by 95.24% and 95.47%, respectively. Flea numbers in the indoor-premises were also markedly reduced by days 54-60, with 98.05% and 96.15% reductions in intermittent-light flea trap counts in the DP-DPP or FM treatment groups, respectively.

Topics: Administration, Topical; Animals; Cat Diseases; Cats; Dog Diseases; Dogs; Flea Infestations; Florida; Guanidines; Housing; Insecticides; Methoprene; Neonicotinoids; Nitro Compounds; Permethrin; Pets; Pyrazoles; Pyridines

Juvenile hormone (JH) is a sesquiterpenoid of vital importance for insect development, yet the molecular basis of JH signaling remains obscure, mainly because a bona fide JH receptor has not been identified. Mounting evidence points to the basic helix-loop-helix (bHLH)/Per-Arnt-Sim (PAS) domain protein Methoprene-tolerant (Met) as the best JH receptor candidate. However, details of how Met transduces the hormonal signal are missing. Here, we demonstrate that Met specifically binds JH III and its biologically active mimics, methoprene and pyriproxyfen, through its C-terminal PAS domain. Substitution of individual amino acids, predicted to form a ligand-binding pocket, with residues possessing bulkier side chains reduces JH III binding likely because of steric hindrance. Although a mutation that abolishes JH III binding does not affect a Met-Met complex that forms in the absence of methoprene, it prevents both the ligand-dependent dissociation of the Met-Met dimer and the ligand-dependent interaction of Met with its partner bHLH-PAS protein Taiman. These results show that Met can sense the JH signal through direct, specific binding, thus establishing a unique class of intracellular hormone receptors.

Topics: Animals; Base Sequence; Basic Helix-Loop-Helix Transcription Factors; Dimerization; Drosophila; Drosophila Proteins; Immunoprecipitation; Ligands; Methoprene; Models, Molecular; Molecular Sequence Data; Mutation; Pyridines; Real-Time Polymerase Chain Reaction; RNA Interference; Sequence Analysis, DNA; Sesquiterpenes; Signal Transduction; Transcription Factors

The ability of JHIII and three JHAs (hydroprene, pyriproxyfen and methoprene) to induce presoldier differentiation was tested in a highly derived termite, Nasutitermes takasagoensis (Isoptera: Nasutitermitinae), and induced presoldiers were examined morphologically and histologically. Hydroprene was the most effective hormone analog for the artificial induction of presoldier differentiation. Principal component analysis showed that hydroprene-induced presoldiers had similar external gross morphology to natural presoldiers found in the same colony. Induced presoldiers had a long, horn-like frontal projection, called a nasus, on the head. A well-developed reservoir and duct of the frontal gland were also observed inside the head. Scanning electron micrographs showed that the precursory structure forming the nasus (nasus disc) was developed under the cuticle of hydroprene-treated individuals just prior to the molt into presoldiers. Morphological changes in presoldier differentiation induced by hydroprene seemed to occur normally, compared with those in natural presoldiers. Thus, the present methods shown in this study will provide opportunities to conduct further molecular analyses on the molecular developmental bases of nasus formation during soldier differentiation in higher termites.

Topics: Animals; Fatty Acids, Unsaturated; Isoptera; Juvenile Hormones; Methoprene; Pyridines

In Australia, the brackish water mosquito Verrallina funerea (Theobald) (Diptera: Culicidae) is a serious pest and vector of Ross River and Barmah Forest viruses in coastal areas in the northeast of the continent. We report on the first extensive evaluation of the efficacy of various pesticides against this species, including laboratory dose-response assays and small plot field trials. In the laboratory, Ve. funerea was susceptible to temephos (Abate 100E) (lethal concentration, 95% endpoint [LC95] of 1.651 ppb), Bacillus thuringiensis subsp. israelensis de Barjac (Bti) (VectoBac 12AS) (LC95 of 0.033 ppm), s-methoprene (ProLink Liquid Larvicide [PLL]) (emergence inhibition, 95% endpoint [EI95] of 2.647 ppb), and technical grade pyriproxyfen (EI95 of 0.227 ppb). In contrast, Ve.funerea was highly refractory to Bacillus sphaericus Neide (VectoLex WG) (LC95 of >855.3 ppm). The survival of adults exposed as larvae to sublethal doses of s-methoprene was reduced for those doses greater than the EI50, although sex ratios were unaffected. Field trials demonstrated that Ve. funerea was susceptible to Bti (VectoBac G at 7 kg/ha) and s-methoprene (ProLink ProSand at 4 kg/ha), with these products giving >99 and >98% control, respectively. We also observed a significant increase in immature mortality in s-methoprene-treated pools, suggesting that s-methoprene field trials based solely on emergence inhibition of pupae may underestimate the efficacy of this insecticide.

Topics: Animals; Arboviruses; Bacillus; Culicidae; Female; Insect Vectors; Insecticides; Juvenile Hormones; Larva; Male; Methoprene; Mosquito Control; Pest Control, Biological; Pyridines; Queensland; Temefos

Analogues of insect juvenile hormones (juvenoids) have been tested for settling inhibition of cyprids from three species of barnacle, Balanus balanoides (L.), Balanus improvisus Darwin and Balanus amphitrite Darwin. Some 3-alkoxypyridine derivatives exhibited strong activity at mg litre(-1) concentrations; 3,7-dimethyloctyl 2-methyl-5-pyridyl ether (8) gave an EC(50) of 0.006 mg litre(-1) when tested on B. balanoides. When compound 8 and similar juvenoids were incorporated into paints, test panels kept in seawater for 8 months were free of barnacles.

Topics: Animals; Fatty Acids, Unsaturated; Juvenile Hormones; Methoprene; Paint; Phenylcarbamates; Pyridines; Thoracica

U.S. Environmental Protection Agency is charged with developing a screening and testing paradigm for detecting endocrine toxicity of chemicals that are subject to regulation under the Food Quality Protection and the Safe Drinking Water Acts. In this study, we developed and evaluated a screening assay that could be employed to detect juvenoid-related endocrine-modulating activity in an invertebrate species. Juvenoid activity, anti-juvenoid activity, and juvenoid potentiator activity of chemicals was assessed using the water flea Daphnia magna. Male sex determination is under the regulatory control of juvenoid hormone, presumably methyl farnesoate, and this endpoint was used to detect juvenoid modulating activity of chemicals. Eighteen chemicals were evaluated for juvenoid agonist activity. Positive responses were detected with the juvenoid hormones methyl farnesoate and juvenile hormone III along with the insect growth regulating insecticides pyriproxyfen, fenoxycarb, and methoprene. Weak juvenoid activity also was detected with the cyclodiene insecticide dieldrin. Assays performed repetitively with compounds that gave either strong positive, weak positive, or negative response were 100% consistent indicating that the assay is not prone to false positive or negative responses. Five candidate chemicals were evaluated for anti-juvenoid activity and none registered positive. Four chemicals (all trans-retinoic acid, methoprene, kinoprene, bisphenol A) also were evaluated for their ability to potentiate the activity of methyl farnesoate. All registered positive. Results demonstrate that an in vivo assay with a crustacean species customarily employed in toxicity testing can be used to effectively screen chemicals for juvenoid-modulating activity.

Topics: Animals; Benzhydryl Compounds; Daphnia; Ecdysteroids; Endocrine System; Endpoint Determination; Fatty Acids, Unsaturated; Female; Juvenile Hormones; Male; Methoprene; Pesticides; Phenols; Phytol; Pyridines; Reproducibility of Results; Sex Differentiation; Toxicity Tests; Tretinoin; United States; United States Environmental Protection Agency

Chironomid midge larvae are a valuable component of wastewater stabilisation pond (WSP) ecology. However, in high numbers, adult midge swarms can be a nuisance to near-by urban areas. Improving WSP treatment by incorporating aerobic or maturation ponds or by the addition of pre-treatment to reduce organic loading also increases the availability of aerobic sediment (midge larva habitat) in the pond system and the potential for midge nuisance problems. The efficacy of Maldison, an organophosphate traditionally used to control midge larvae in New Zealand WSPs, was compared to Bacillus thuringiensis var. israelensis (Bti), Methoprene, Pyriproxyfen and Diflubenzuron which are all more specific to insects and have fewer adverse environmental effects. Initial laboratory trials established the concentration of each compound required to achieve 95% control of the midge population. During 21-day small-scale trials within the WSP, Bti, Diflubenzuron and Maldison reduced live larvae numbers substantially (80-89%) compared to controls and adult midge emergence was markedly reduced by all compounds (72-96%). Large-scale trials with Bti (Vectobac WG) powder (1000 microg/L) only caused a slight reduction in midge larvae numbers compared to controls and had little effect on adult emergence, however, Methoprene (Prolink XRG granules) (50 microgAI/L) reduced midge adult emergence by approximately 80% over 25 days and has been used successfully to control several midge nuisance outbreaks.

Topics: Animals; Bacillus thuringiensis; Chironomidae; Diflubenzuron; Fishes; Insect Control; Insecticides; Larva; Methoprene; New Zealand; Pyridines; Waste Disposal, Fluid

Two juvenile hormone analogs (JHAs), pyriproxyfen and S-methoprene, were impregnated into dried tuna fish and fed to colonies of Monomorium pharaonis (L.) at very low concentrations (1.0, 2.0, 3.0, 4.0, and 5.0 microg/ml). Its effects on the production of sexuals and colonial growth were observed. Colonies treated with pyriproxyfen yielded sexuals with physical abnormalities. Both female and male sexuals developed bulbous wings, decreased melanization, and died shortly after emergence. Sexuals emerged from colonies treated with S-methoprene did not possess anomalous characteristics. Both pyriproxyfen and S-methoprene did not have significant effects on colonial growth because of the low concentrations of the baits. A commercial bait containing 0.3% S-methoprene (Bioprene-BM) also was evaluated for its efficacy on Pharaoh's ant colonies. Results showed that Pharaoh's ant colonies succumbed to the lethal effects of S-methoprene. Colony members were reduced significantly. Production of queens also decreased significantly in treated colonies and treated queens were unable to lay eggs. JHAs are slow acting and eliminate ant colonies at a relatively slow rate. At low concentrations, pyriproxyfen recorded baffling results, i.e., bulbous wings and demelanized exoskeleton, and it is vital that further studies are initiated to solidify these findings.

Topics: Animals; Ants; Dose-Response Relationship, Drug; Female; Insect Control; Insecticides; Male; Methoprene; Population Growth; Pyridines

Effectiveness and residual activity tests of granular formulations of 2 insect growth regulators (IGRs), s-methoprene and pyriproxyfen, against laboratory-reared larvae of 5 colonized mosquitoes, Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles quadrimaculatus, and Culex nigripalpus, were conducted in the laboratory and outdoors in plastic tubs. Culex quinquefasciatus was exposed to these two IGRs in the laboratory only. Each IGR formulation was applied at 0.02 and 0.05 ppm active ingredient (Al) against 5 of the 6 mosquito species both in the laboratory and the outdoor evaluations, whereas Cx. quinquefasciatus was exposed to 0.2 and 0.4 ppm AI of s-methoprene, and 0.1 and 0.2 ppm AI of pyriproxyfen in the laboratory. s-Methoprene at 0.02 and 0.05 ppm AI resulted in variable levels (<39-100%) of inhibition of adult emergence in the 5 species monitored for 6 weeks after treatment under both test conditions. Aedes taeniorhynchus was the most susceptible to s-methoprene in terms of initial and residual activity. Culex quinquefasciatus and Ae. albopictus were the most tolerant to s-methopene, with maximum emergence inhibitions amounting to 84% in Cx. quinquefasciatus at 0.4 ppm and 44.3% in Ae. albopictus at 0.05 ppm during the 1st week in the laboratory. Pyriproxyfen at comparable treatment rates to s-methoprene caused very high levels (>80-100% in most cases) of initial and residual emergence inhibitions of the tested species in the laboratory as well as outdoors. In several species, pyriproxyfen induced complete inhibition of adult emergence for several weeks after treatment, even at the lower rate of 0.02 ppm. The World Health Organization has recently recommended the use of pyriproxyfen for the control of some mosquito species at specified rates in certain habitats.

Topics: Aedes; Animals; Anopheles; Biological Assay; Culex; Culicidae; Florida; Insecticides; Larva; Methoprene; Pyridines

The efficacy of a photostable formulation of methoprene and two photostable juvenoids, fenoxycarb and pyriproxyfen, and their residual activity in inhibiting the emergence of adult cat fleas, Ctenocephalides felis (Bouché), was studied in topsoil. Nursery pots composed of clay, peat, and plastic, and wooden flats were used to hold soil samples. Treated soil samples were exposed to sunlight during the 63-d study period. Methoprene was as effective as fenoxycarb and pyriproxyfen against cat fleas for up to 42 d in clay, peat, and plastic pots at a concentration of 64.56 mg (AI)/m2 (6 mg [AI]/ft2), but its activity declined significantly thereafter. In contrast, fenoxycarb and pyriproxyfen showed strong residual activity for the entire 63 d. The activity of methoprene declined even more rapidly over time in wooden flats, while at the same concentrations the other two juvenoids showed significant residual activity for 63 d. Clay, peat, and plastic pots were therefore considered to be equally effective for evaluating the outdoor efficacy of juvenoids in comparison to the wooden flats. However, results obtained with wooden flats may be more realistic when testing residual activity of volatile chemicals such as methoprene. Fenoxycarb and pyriproxyfen showed strong efficacy and residual activity at concentrations of 8.07, 16.14, and 32.28 mg (AI)/m2, whereas methoprene did not cause a significant reduction of adult emergence at levels below 64.56 mg (AI)/m2. LC50 values for methoprene, fenoxycarb, and pyriproxyfen needed for preventing flea emergence when applied to topsoil were estimated to be 0.643, 0.031, and 0.028 ppm, respectively.

Topics: Animals; Cats; Juvenile Hormones; Methoprene; Pest Control, Biological; Pyridines; Siphonaptera; Soil; Time Factors

Laboratory toxicity studies were conducted in southeastern Queensland, Australia, to determine the acute lethal effects of a 1-h pulse exposure of selected insecticides to adult and juvenile (<72 h old) crimson-spotted rainbowfish, Melanotaenia duboulayi (Castlenau). In addition, to its ecological significance, this native fish is a predator of mosquitoes. Two organophosphate (OP) compounds (temephos and pirimiphos-methyl), an entomophathogenic bacterium (Bacillus thuringiensis variety israelensis [Bti]) and two insect growth regulators (IGRs) (s-methoprene and pyriproxyfen) were evaluated. Although none of the five insecticides were acutely toxic to adult M. duboulayi under the test conditions, temephos and pirimiphos-methyl were found to be toxic to juveniles, with 24 h pulse exposure LC50 values of 27 and 15 microg/liter (ppb), respectively. Of the two OPs, pirimiphos-methyl was the most toxic, with a lethal dose ratio (pulse exposure LC50 temephos/ pulse exposure LC50 pirimiphos-methyl) of 1.8 (95% CL 0.5-6.4). These pulse exposure LC50 values represented 40 and 4.5% of the estimated environmental concentrations (EEC) for a 15 cm deep water body, respectively. Bti and the two IGRs had no acute toxic effects at up to 10 and 12.5 times the EEC, respectively. Accordingly, in the interests of environmental conservation and integrated pest management (IPM), preference should be given to the latter three insecticides for control of mosquito larvae in juvenile M. duboulayi habitat.

Topics: Animals; Bacillus thuringiensis; Female; Fishes; Insecticides; Juvenile Hormones; Male; Methoprene; Organothiophosphorus Compounds; Pyridines; Queensland; Temefos

Five organophosphates (OPs) (chlorpyrifos, chlorpyrifos methyl, fenthion, malathion, and temephos), 3 pyrethroids (bifenthrin, cypermethrin, and permethrin), 1 phenyl pyrazole (fipronil), 2 microbial pesticides (Bacillus thuringiensis serovar. israelensis [B.t.i.] and Bacillus sphaericus), and 3 insect growth regulators (IGRs) (diflubenzuron, methoprene, and pyriproxyfen) were evaluated against field-collected Culex quinquefasciatus larvae from urban Dhaka, Bangladesh. The LC90 values of all OPs, except for temephos (LC90 = 0.0096 ppm), were high, ranging from 0.13 ppm (fenthion) to 2.882 ppm (chlorpyrifos methyl). Pyrethroid LC90 values were 0.021 ppm (bifenthrin), 0.00061 (cypermethrin), and 0.017 ppm (permethrin). Fipronil exhibited a superior activity with LC90 value of 0.000896 ppm. Technical powders of B.t.i. and B. sphaericus (VectoBac TP and VectoLex TP) were considered highly effective against the Cx. quinquefasciatus larvae. The IGRs also were effective with pyriproxyfen (LC90 = 0.0011 ppm), being 3 times and 47 times more active than diflubenzuron (LC90 = 0.0034 ppm) and methoprene (LC90 = 0.052 ppm), respectively. In general, toxicity ranking of chemicals and microbials tested was phenyl pyrazole > IGRs > pyrethroids > microbials > OPs.

Topics: Animals; Bangladesh; Culex; Diflubenzuron; Evaluation Studies as Topic; Insecticides; Juvenile Hormones; Larva; Methoprene; Pyridines

Cat flea, Ctenocephalides felis felis (Bouché), adults exposed to sprays of methoprene, pyriproxyfen, or fenoxycarb as cocooned pupae emerged approximately 1 d earlier than adults from water-treated control pupae. Mortality of adult fleas, after exposure to juvenile hormone mimics as pupae, was increased over that of controls. Females had higher mortality than males within the first 48 h of feeding. Fecundity of females exposed as pupae to juvenile hormone mimics was not different from that of controls. Early emergence of preemerged adults from treated cocoons is discussed along with reasons for higher female susceptibility to juvenile hormone mimics.

Topics: Animals; Carbamates; Cats; Female; Fertility; Juvenile Hormones; Male; Methoprene; Phenylcarbamates; Pupa; Pyridines; Sex Characteristics; Siphonaptera

Wandering larval, pharate pupal, pupal, and pharate adult stages of the cat flea, Ctenocephalides felis (Bouché), were identified by examination of cuticular cross sections via scanning electron microscopy. Visible morphological characteristics of each stage were identified and described. Various stages of the flea throughout metamorphosis were exposed to juvenile hormone mimics and insect developmental inhibitors. Wandering larvae treated with juvenile hormone mimics were unable to pupate, whereas treated pharate pupae ecdysed to the pupal stage but were unable to enclose. Pupae and pharate adults did not succumb to juvenile hormone mimic exposure, even at concentrations 3 orders of magnitude greater than those that killed 100% of the wandering larvae and the pharate pupae. Adult females were more susceptible to juvenile hormone mimics than males. Possible explanations for the variation in tolerance to juvenile hormone mimics of the differing stadia are discussed. None of the stages were susceptible to insect developmental inhibitor exposure. Analysis of catecholamines that are precursors of cuticle sclerotization and melanization were measured in the wandering larval through the pharate adult stages of the cat flea. N-acetyldopamine concentration was highest in the pupa stage when the flea had a hard, clear cuticle; N-beta-alanyldopamine concentration was highest during the production of the hard, dark cuticle of the pharate adult; and dopamine fluctuated throughout development but was highest in the pupal stage.

Topics: Animals; Benzamides; Cats; Insecticides; Juvenile Hormones; Larva; Methoprene; Microscopy, Electron, Scanning; Pupa; Pyridines; Siphonaptera

Sperm transfer into the epididymis was completed without a blood meal, when newly emerged male cat fleas. Ctenocephalides felis (Bouché), were exposed to filter papers treated with juvenile hormone III or the juvenile hormone mimics fenoxycarb, methoprene, or pyriproxyfen. As the concentration of juvenile hormone or the time of flea exposure to juvenile hormone or the juvenile hormone mimics increased, the percentage of fleas that transferred sperm also increased. The percentage of pyriproxyfen-treated males that transferred sperm reached 100% after 3 d: whereas, 7 d exposure to juvenile hormone, fenoxycarb and methoprene was required for 100% of the males to transfer sperm. Although sperm were present in the epididymis of treated fleas, insemination of females did not take place off the host either on juvenile hormone-treated filter paper or on juvenile hormone-treated dog hair.

Topics: Animals; Carbamates; Cats; Dogs; Eating; Epididymis; Female; Genitalia, Male; Insecticides; Insemination; Juvenile Hormones; Male; Methoprene; Molecular Mimicry; Phenylcarbamates; Pyridines; Sesquiterpenes; Siphonaptera; Spermatozoa; Testis

Residual effectiveness of the insect growth regulators pyriproxyfen and methoprene against cat flea, Ctenocephalides felis (Bouché), larvae were evaluated under simulated household conditions. Pyriproxyfen provided control of larvae for > 12 mo when applied at 1 mg and 0.2 mg/m2 and > or = 3 mo at the rate of 0.04 mg/m2. Methoprene applied at 1 mg/m2 provided control for > 12 mo and 6 mo at 0.2 mg/m2. No significant mortality was observed when methoprene was applied at 0.04 mg/m2.

Topics: Animals; Cats; Insect Control; Juvenile Hormones; Methoprene; Pyridines; Siphonaptera

The shrimp Leander tenuicornis is abundant in southeastern Queensland intertidal marsh pools and was chosen as an indicator species for toxicological studies with pesticides. Acute toxicity to this crustacean of temephos and 3 pesticide compounds under evaluation for registration in Australia (Bacillus thuringiensis var. israelensis, s-methoprene, and pyriproxyfen) was tested in 96-h laboratory trials. Temephos was the most toxic compound, with a median lethal concentration (LC50) of 0.01 ppm (0.33 times the estimated field concentration [EFC] for a 15-cm-deep pool). s-Methoprene was the least toxic compound, with an LC50 of 14.32 ppm (1,790 times the EFC). Bacillus thuringiensis var. israelensis and pyriproxyfen produced LC50 values of 60.9 x 10(6) ITU (176 times the EFC) and 0.098 ppm (12.25 times the EFC), respectively.

Topics: Animals; Bacillus thuringiensis; Female; Lethal Dose 50; Male; Methoprene; Palaemonidae; Pesticides; Pyridines; Temefos

Three insect growth regulators, fenoxycarb, methoprene, and pyriproxyfen, formulated as total release aerosols, were tested for their residual effectiveness on carpet in bioassays with cat flea, Ctenocephalides felis (Bouché), larvae. All treatments except methoprene produced significant mortality for the 7-mo duration of the test. In general, fenoxycarb and the higher rates of pyriproxyfen reduced adult flea emergence by > 80%.

Topics: Animals; Carbamates; Cats; Floors and Floorcoverings; Insect Control; Insecticides; Juvenile Hormones; Larva; Lethal Dose 50; Methoprene; Pesticide Residues; Phenylcarbamates; Pyridines; Siphonaptera

Adult cat fleas were exposed to residues of pyriproxyfen and methoprene in glass vials, then fed on a cat 24 h later to investigate the mode of action of juvenoid growth regulators on embryonic development in flea eggs. Eggs laid by pyriproxyfen-treated fleas within 70 h after exposure to this juvenoid were often devoid of yolk and frequently collapsed after oviposition. Minimal amounts of yolk were deposited in eggs laid after 70 h, and no blastoderm was formed. These results are significant because both modes of action were different than those observed earlier by investigators studying ovicidal effects in adult insects treated with juvenile hormone. In contrast to the pyriproxyfen results, eggs laid by methoprene-treated fleas showed no gross morphological effects, and these eggs remained turgid during embryogenesis. However, the eggs either did not hatch or the larvae died within hours after hatching. Histological examination of the eggs revealed that most of the eggs contained segmented embryos which had apparently died during blastokinesis. Although eggs of some insects exposed to juvenile hormone during oogenesis fail to undergo germ band formation, there was no evidence of this effect in methoprene-treated cat fleas.

Topics: Animals; Cats; Embryo, Nonmammalian; Embryonic Development; Female; Juvenile Hormones; Methoprene; Ovum; Pyridines; Siphonaptera

To determine if prolonged larval exposure to juvenile hormone (JH) could influence the decision to metamorphose, Drosophila melanogaster larvae were reared from hatching on medium containing either of the JH mimics, methoprene or 2-[1-methyl-2-(4-phenoxyphenoxy)-ethoxy]-pyridine (S31183). The latter was 23 times more active as a JH mimic in the white puparial assay (ED50 = 0.22 pmole). Larval development and pupariation were unaffected except at 1000 ppm methoprene and 10 ppm or higher S31183 where larval life was prolonged with increased mortality in the second instar. Adult eclosion was prevented by concentrations greater than 1 ppm methoprene and 0.1 ppm S31183. At low concentrations only adult abdominal development was affected, but at the higher concentrations an increasing percentage was blocked at the pupal stage. This latter effect was considerably diminished when the treatment was begun in the mid second instar. The methoprene-resistant mutations, Met1 and Met2, were 10 and 6 times more resistant to S31183 in the white puparial assay and about 20 times more resistant in the larval feeding experiments than the wild-type, indicating that the effects seen are typical of JH. These studies suggest that excess JH may affect adult development of imaginal structures if present at the onset of postembryonic cell proliferation of the imaginal discs or histoblasts. Thus, commitment for adult differentiation must occur early during this proliferative phase.

Topics: Abdomen; Animals; Drosophila melanogaster; Juvenile Hormones; Larva; Metamorphosis, Biological; Methoprene; Mutation; Pupa; Pyridines