RESUMEN
The implementation of Integrated Pest Management in current agricultural practice is a convenient and very effective strategy to keep pest populations under control. The use of biological control agents, such as Phytoseiulus persimilis, is key for the success of such an approach. This predatory mite is widely used as it is very effective for controlling Tetranychus urticae, one of the most devastating crop pests. Here, we identify several mutations located in the voltage-gated sodium channel (VGSC) of commercially sourced P. persimilis that correlate with a reduced susceptibility to the pyrethroid deltamethrin. We found that the mites sourced from two different biocontrol product companies have intrinsic genotypic differences that correlate with their phenotype when tested with different concentrations of deltamethrin. Mites from Syngenta Bioline, carrying the mutations M918L and A1536T, were able to survive deltamethrin concentrations of up to 10 ppm, while the mites from Koppert Biological Systems, with the combination M918L, L925V and S1539T, survived treatment with 40 ppm. All of the point mutations identified in the predatory mite samples are located in a particular region of the VGSC, previously proposed as the binding site for this family of pesticides and identified as a 'hot spot' for resistance.
Asunto(s)
Proteínas de Artrópodos/genética , Resistencia a Medicamentos/genética , Mutación , Nitrilos/farmacología , Piretrinas/farmacología , Tetranychidae/genética , Canales de Sodio Activados por Voltaje/genética , Acaricidas/farmacología , Secuencia de Aminoácidos , Animales , Proteínas de Artrópodos/metabolismo , Secuencia de Bases , Mutación Puntual , Alineación de Secuencia , Tetranychidae/metabolismo , Canales de Sodio Activados por Voltaje/metabolismoRESUMEN
The notion that small changes can have large consequences in the climate or ecosystems has become popular as the concept of tipping points. Typically, tipping points are thought to arise from a loss of stability of an equilibrium when external conditions are slowly varied. However, this appealingly simple view puts us on the wrong foot for understanding a range of abrupt transitions in the climate or ecosystems because complex environmental systems are never in equilibrium. In particular, they are forced by diurnal variations, the seasons, Milankovitch cycles and internal climate oscillations. Here we show how abrupt and sometimes even irreversible change may be evoked by even small shifts in the amplitude or time scale of such environmental oscillations. By using model simulations and reconciling evidence from previous studies we illustrate how these phenomena can be relevant for ecosystems and elements of the climate system including terrestrial ecosystems, Arctic sea ice and monsoons. Although the systems we address are very different and span a broad range of time scales, the phenomena can be understood in a common framework that can help clarify and unify the interpretation of abrupt shifts in the Earth system.
RESUMEN
The peach potato aphid, Myzus persicae, is one of the most important agricultural pests of temperate climates. It is mainly controlled through the judicious application of insecticides; however, over time, aphids have developed resistance to many insecticidal classes. The recent introduction of synthetic diamide insecticides, with a novel mode of action, potentially offers new tools to control aphid populations. These diamides act on the ryanodine receptor (RyR), a large endoplasmic calcium release channel. In this study we have cloned cDNAs encoding the complete open reading frame of the RyR from M. persicae. The open reading frame is 15,306 base pairs long and encodes a protein of 5101 amino acids. The aphid RyR shares many of the features of other insect and vertebrate RyRs, including a highly conserved transmembrane region. However, unlike the other RyRs characterised to date, the M. persicae channel does not display alternative splicing at any stage of its developmental cycle, so it cannot generate functional variants of the channel.
Asunto(s)
Áfidos/metabolismo , Proteínas de Insectos/genética , Canal Liberador de Calcio Receptor de Rianodina/genética , Empalme Alternativo , Animales , Áfidos/clasificación , Clonación Molecular , Regulación del Desarrollo de la Expresión Génica , Genoma de los Insectos , Proteínas de Insectos/metabolismo , ARN Mensajero/genética , Canal Liberador de Calcio Receptor de Rianodina/metabolismoRESUMEN
The monitoring of the susceptibility offleas to insecticides has typically been conducted by exposing adults on treated surfaces. Other methods such as topical applications of insecticides to adults and larval bioassays on treated rearing media have been developed. Unfortunately, baseline responses of susceptible strains of cat flea, Ctenocephalides felis (Bouchè), except for imidacloprid, have not been determined for all on-animal therapies and new classes of chemistry now being used. However, the relationship between adult and larval bioassays of fleas has not been previously investigated. The adult and larval bioassays of fipronil and imidacloprid were compared for both field-collected isolates and laboratory strains. Adult topical bioassays of fipronil and imidacloprid to laboratory strains and field-collected isolates demonstrated that LD50s of fipronil and imidacloprid ranged from 0.11 to 0.40 nanograms per flea and 0.02 to 0.18 nanograms per flea, respectively. Resistance ratios for fipronil and imidacloprid ranged from 0.11 to 2.21. Based on the larval bioassay published for imidacloprid, a larval bioassay was established for fipronil and reported in this article. The ranges of the LC50s of fipronil and imidacloprid in the larval rearing media were 0.07-0.16 and 0.11-0.21 ppm, respectively. Resistance ratios for adult and larval bioassays ranged from 0.11 to 2.2 and 0.58 to 1.75, respectively. Both adult and larval bioassays provided similar patterns for fipronil and imidacloprid. Although the adult bioassays permitted a more precise dosage applied, the larval bioassays allowed for testing isolates without the need to maintain on synthetic or natural hosts.
Asunto(s)
Ctenocephalides/efectos de los fármacos , Imidazoles/farmacología , Resistencia a los Insecticidas , Insecticidas/farmacología , Nitrocompuestos/farmacología , Pirazoles/farmacología , Animales , Ctenocephalides/genética , Ctenocephalides/crecimiento & desarrollo , Ctenocephalides/fisiología , Femenino , Larva/efectos de los fármacos , Larva/genética , Larva/fisiología , Dosificación Letal Mediana , Masculino , NeonicotinoidesRESUMEN
Spiromesifen is a novel insecticide and is classed as a tetronic acid derivative. It targets the insects' acetyl-coenzyme A carboxylase (ACCase) enzyme, causing a reduction in lipid biosynthesis. At the time of this publication, there are no reports of resistance to this class of insecticides in insects although resistance has been observed in several mite species. The greenhouse whitefly Trialeurodes vaporariorum (Westwood) is a serious pest of protected vegetable and ornamental crops in temperate regions of the world and spiromesifen is widely used in its control. Mortality rates of UK and European populations of T. vaporariorum to spiromesifen were calculated and up to 26-fold resistance was found. We therefore sought to examine the molecular mechanism underlying spiromesifen resistance in this important pest. Pre-treatment with piperonyl butoxide did not synergize spiromesifen, suggesting a target-site resistance mechanism. The full length ACCase gene was sequenced for a range of T. vaporariorum strains and a strong association was found between spiromesifen resistance and a glutamic acid substitution with lysine in position 645 (E645K) of this gene. A TaqMan allelic discrimination assay confirmed these findings. Although this resistance is not considered sufficient to compromise the field performance of spiromesifen, this association of E645K with resistance is the first report of a potential target site mechanism affecting an ACCase inhibitor in an arthropod species.
Asunto(s)
Acetil-CoA Carboxilasa/genética , Sustitución de Aminoácidos/genética , Hemípteros/enzimología , Hemípteros/genética , Resistencia a los Insecticidas/genética , Insecticidas/toxicidad , Compuestos de Espiro/toxicidad , Acetil-CoA Carboxilasa/química , Acetil-CoA Carboxilasa/metabolismo , Alelos , Secuencia de Aminoácidos , Animales , Secuencia Conservada/genética , Femenino , Hemípteros/efectos de los fármacos , Resistencia a los Insecticidas/efectos de los fármacos , Larva/enzimología , Masculino , Datos de Secuencia Molecular , Butóxido de Piperonilo/toxicidad , Mutación Puntual/genética , Estructura Terciaria de Proteína , Alineación de Secuencia , Análisis de Secuencia de Proteína , Análisis de SupervivenciaRESUMEN
A global resurgence of bed bugs (Hemiptera: Cimicidae) has led to renewed scientific interest in these insects. The current bed bug upsurge appears to have started almost synchronously in the late 1990 s in Europe, the U.S.A. and Australia. Several factors have led to this situation, with resistance to applied insecticides making a significant contribution. With a growing number of insecticides (DDT, carbamates, organophosphates etc.) being no longer available as a result of regulatory restrictions, the mainstay chemistry used for bed bug control over the past few decades has been the pyrethroid insecticides. With reports of increasing tolerance to pyrethroids leading to control failures on the rise, containing and eradicating bed bugs is proving to be a difficult task. Consequently, several recent studies have focused on determining the mode of action of pyrethroid resistance in bed bug populations sourced from different locations. Correct identification of the factor(s) responsible for the increasing resistance is critical to the development of effective management strategies, which need to be based, wherever possible, on firm scientific evidence. Here we review the literature on this topic, highlighting the mechanisms thought to be involved and the problems currently faced by pest control professionals in dealing with a developing pandemic.
Asunto(s)
Chinches/efectos de los fármacos , Chinches/fisiología , Resistencia a los Insecticidas , Insecticidas , Piretrinas , Animales , Infestaciones Ectoparasitarias/prevención & control , Aptitud Genética , Control de Insectos/normas , Ninfa/efectos de los fármacos , Ninfa/fisiología , Dinámica PoblacionalRESUMEN
The brown planthopper, Nilaparvata lugens, is an economically significant pest of rice throughout Asia and has evolved resistance to many insecticides including the neonicotinoid imidacloprid. The resistance of field populations of N. lugens to imidacloprid has been attributed to enhanced detoxification by cytochrome P450 monooxygenases (P450s), although, to date, the causative P450(s) has (have) not been identified. In the present study, biochemical assays using the model substrate 7-ethoxycoumarin showed enhanced P450 activity in several resistant N. lugens field strains when compared with a susceptible reference strain. Thirty three cDNA sequences encoding tentative unique P450s were identified from two recent sequencing projects and by degenerate PCR. The mRNA expression level of 32 of these was examined in susceptible, moderately resistant and highly resistant N. lugens strains using quantitative real-time PCR. A single P450 gene (CYP6ER1) was highly overexpressed in all resistant strains (up to 40-fold) and the level of expression observed in the different N. lugens strains was significantly correlated with the resistance phenotype. These results provide strong evidence for a role of CYP6ER1 in the resistance of N. lugens to imidacloprid.
Asunto(s)
Sistema Enzimático del Citocromo P-450/metabolismo , Hemípteros/enzimología , Imidazoles , Proteínas de Insectos/metabolismo , Insecticidas , Nitrocompuestos , Secuencia de Aminoácidos , Animales , Sistema Enzimático del Citocromo P-450/genética , ADN Complementario/química , Femenino , Dosificación de Gen , Hemípteros/genética , Proteínas de Insectos/genética , Resistencia a los Insecticidas/genética , Datos de Secuencia Molecular , Neonicotinoides , Reacción en Cadena de la PolimerasaRESUMEN
Aphids are major pests of crops, causing hundreds of millions of dollars worth of damage annually. Ion channel proteins are often the targets of modern insecticides and mutations in ion channel genes can lead to resistance to many leading classes of insecticides. The sequencing of the pea aphid, Acyrthosiphon pisum, genome has now allowed detailed in silico analysis of the aphid ion channels. The study has revealed significant differences in the composition of the ion channel families between the aphid and other insects. For example A. pisum does not appear to contain a homologue of the nACh receptor alpha 5 gene whilst the calcium channel beta subunit has been duplicated. These variations could result in differences in function or sensitivity to insecticides. The genome sequence will allow the study of aphid ion channels to be accelerated, leading to a better understanding of the function of these economically important channels. The potential for identifying novel insecticide targets within the aphid is now a step closer.
Asunto(s)
Áfidos/genética , Genes de Insecto , Proteínas de Insectos/genética , Canales Iónicos/genética , Secuencia de Aminoácidos , Animales , Áfidos/metabolismo , Evolución Molecular , Duplicación de Gen , Genoma de los Insectos , Proteínas de Insectos/química , Proteínas de Insectos/metabolismo , Insecticidas/farmacología , Canales Iónicos/química , Canales Iónicos/metabolismo , Datos de Secuencia Molecular , Familia de Multigenes , Pisum sativum/parasitología , Filogenia , Homología de Secuencia de AminoácidoRESUMEN
We investigated pyrethroid resistance mechanisms in Tetranychus urticae strains from Greece. Combined bioassay, biochemical and synergistic data indicated that although P450 mono-oxygenase activities were associated with the trait, target site insensitivity was the major resistance component. A 3.3 kb cDNA fragment of the T. urticae para sodium channel gene encompassing segment 4 of domain II to segment 6 of domain IV was obtained by a degenerate PCR strategy. The T. urticae sequence showed highest identity (56%) to the scabies mite, Sarcoptes scabiei, and was phylogenetically classified within the divergent group of Arachnida. Comparison of resistant and susceptible strains identified the point mutation F1538I in segment 6 of domain III, which is known to confer strong resistance to pyrethroids, along with a second mutation (A1215D) in the intracellular linker connecting domains II and III with an unknown role. Three transcripts were identified corresponding to the k and l alternative exons. The mode of inheritance of resistance was confirmed as incompletely recessive, which is consistent with a target site mechanism for pyrethroids.
Asunto(s)
Resistencia a los Insecticidas/efectos de los fármacos , Resistencia a los Insecticidas/genética , Mutación/genética , Piretrinas/toxicidad , Canales de Sodio/genética , Tetranychidae/efectos de los fármacos , Tetranychidae/genética , Empalme Alternativo/efectos de los fármacos , Secuencia de Aminoácidos , Animales , Clonación Molecular , Cruzamientos Genéticos , Femenino , Genes de Insecto , Patrón de Herencia/efectos de los fármacos , Patrón de Herencia/genética , Masculino , Datos de Secuencia Molecular , Organotiofosfatos/toxicidad , Filogenia , Butóxido de Piperonilo/toxicidad , ARN Mensajero/genética , ARN Mensajero/metabolismo , Alineación de Secuencia , Canales de Sodio/química , Análisis de SupervivenciaRESUMEN
Recent advances in the characterisation of insect sodium channel gene sequences have identified a small number of point mutations within the channel protein that are implicated in conferring target-site resistance to pyrethroid insecticides (so-called knockdown resistance or kdr). The L1014F (leucine-to-phenylalanine) mutation located in the centre of segment 6 of the domain II region (IIS6) of the sodium channel (the so-called kdr trait) has been detected in the peach-potato aphid, Myzus persicae (Sulzer), and is considered to be the primary cause of pyrethroid resistance in this species. Here we report on the characterisation of a second mutation, M918T (methione-to-threonine), within the nearby IIS4-S5 intracellular linker (the so-called super-kdr trait) in a field clone also possessing L1014F, with both mutations present in heterozygous form. The resistance phenotype of M. persicae clones possessing various combinations of L1014F and M918T to a wide range of pyrethroids (both Type I and II) was assessed in leaf-dip bioassays and to lambda-cyhalothrin applied at up to ten times the recommended field rate as foliar sprays to aphids feeding on whole plants. Bioassay results demonstrated that presence of both mutations was associated with extreme resistance to all the pyrethroids tested relative to aphids lacking the mutations. Furthermore, this resistance well exceeded that shown by aphids that were homozygous for L1014F but lacking M918T. However, pre-treatment with piperonyl butoxide in the leaf-dip bioassays failed to suppress pyrethroid resistance in aphids carrying one or both of the mutations. The relevance of these findings for monitoring and managing pyrethroid resistance in M. persicae populations in the field is discussed.
Asunto(s)
Áfidos/genética , Resistencia a los Insecticidas/genética , Mutación Missense/genética , Piretrinas/toxicidad , Canales de Sodio/genética , Secuencia de Aminoácidos , Animales , Áfidos/efectos de los fármacos , Secuencia de Bases , Bioensayo , Brassica , Genotipo , Datos de Secuencia Molecular , Análisis de Secuencia de ADNRESUMEN
Mutations in the DIIS4-S5 linker and DIIS5 have identified hotspots of pyrethroid and DDT interaction with the Drosophila para sodium channel. Wild-type and mutant channels were expressed in Xenopus oocytes and subjected to voltage-clamp analysis. Substitutions L914I, M918T, L925I, T929I and C933A decreased deltamethrin potency, M918T, L925I and T929I decreased permethrin potency and T929I, L925I and I936V decreased fenfluthrin potency. DDT potency was unaffected by M918T, but abolished by T929I and reduced by L925I, L932F and I936V, suggesting that DIIS5 contains at least part of the DDT binding domain. The data support a computer model of pyrethroid and DDT binding.
Asunto(s)
DDT/farmacología , Drosophila melanogaster/efectos de los fármacos , Drosophila melanogaster/metabolismo , Piretrinas/farmacología , Canales de Sodio/metabolismo , Animales , DDT/química , Drosophila melanogaster/genética , Electrofisiología , Modelos Moleculares , Datos de Secuencia Molecular , Estructura Molecular , Mutación/genética , Técnicas de Placa-Clamp , Unión Proteica , Piretrinas/química , Alineación de Secuencia , Canales de Sodio/química , Canales de Sodio/genética , Xenopus laevisRESUMEN
The long term use of many insecticides is continually threatened by the ability of insects to evolve resistance mechanisms that render the chemicals ineffective. Such resistance poses a serious threat to insect pest control both in the UK and worldwide. Resistance may result from either an increase in the ability of the insect to detoxify the insecticide or by changes in the target protein with which the insecticide interacts. DDT, the pyrethrins and the synthetic pyrethroids (the latter currently accounting for around 17% of the world insecticide market), act on the voltage-gated sodium channel proteins found in insect nerve cell membranes. The correct functioning of these channels is essential for normal transmission of nerve impulses and this process is disrupted by binding of the insecticides, leading to paralysis and eventual death. Some insect pest populations have evolved modifications of the sodium channel protein which prevent the binding of the insecticide and result in the insect developing resistance. Here we review some of the work (done at Rothamsted Research and elsewhere) that has led to the identification of specific residues on the sodium channel that may constitute the DDT and pyrethroid binding sites.
Asunto(s)
DDT/metabolismo , Proteínas de Insectos/metabolismo , Insecticidas/metabolismo , Piretrinas/metabolismo , Canales de Sodio/metabolismo , Regulación Alostérica , Animales , Sitios de Unión , DDT/química , Proteínas de Insectos/química , Proteínas de Insectos/genética , Resistencia a los Insecticidas , Insecticidas/química , Modelos Moleculares , Estructura Molecular , Piretrinas/química , Canales de Sodio/química , Canales de Sodio/genética , Relación Estructura-ActividadRESUMEN
We report the complete cDNA sequence of the Anopheles gambiae voltage-gated sodium channel (VGSC) alpha-subunit isolated from mature adult mosquitoes. The genomic DNA contains 35 deduced exons with a predicted translation of Asunto(s)
Anopheles/genética
, Componentes Genómicos/genética
, Resistencia a los Insecticidas/genética
, Filogenia
, Piretrinas/toxicidad
, ARN Mensajero/genética
, Canales de Sodio/genética
, Secuencia de Aminoácidos
, Animales
, Secuencia de Bases
, Análisis por Conglomerados
, Cartilla de ADN/genética
, ADN Complementario/genética
, Componentes del Gen
, Datos de Secuencia Molecular
, Polimorfismo de Nucleótido Simple/genética
, Estructura Terciaria de Proteína
, Análisis de Secuencia de ADN
, Especificidad de la Especie
RESUMEN
DDT inhibits Na channel inactivation and deactivation, promotes Na channel activation and reduces the resting potential of Xenopus oocytes expressing the Drosophila para Na channel. These changes are only marginally influenced by the single mutation M918T (super-kdr) but are reduced approximately 10-fold by either the single mutation L1014F (kdr) or the double mutation L1014F+M918T, both of which confer resistance to the pyrethroids permethrin and deltamethrin. We conclude that DDT binds either to or in the region of L1014 on IIS6 but only weakly to M918 on the IIS4-S5 linker, which is part of a high-affinity binding site for permethrin and deltamethrin.
Asunto(s)
DDT , Proteínas de Drosophila/efectos de los fármacos , Proteínas de Drosophila/genética , Insecticidas , Canales de Sodio/efectos de los fármacos , Canales de Sodio/genética , Animales , Drosophila melanogaster/genética , Inhibidores Enzimáticos/farmacología , Resistencia a los Insecticidas/genética , Activación del Canal Iónico/efectos de los fármacos , Activación del Canal Iónico/genética , Isoleucina/genética , Potenciales de la Membrana/efectos de los fármacos , Nitrilos , Permetrina , Mutación Puntual , Piretrinas , Xenopus laevisRESUMEN
OBJECTIVE: To compare the effectiveness of the Bug Buster kit with a single treatment of over the counter pediculicides for eliminating head lice. DESIGN: Single blind, multicentre, randomised, comparative clinical study. SETTING: Four counties in England and one county in Scotland. PARTICIPANTS: 133 young people aged 2-15 years with head louse infestation: 56 were allocated to the Bug Buster kit and 70 to pediculicide treatment. INTERVENTIONS: Home use of proprietary pediculicides (organophosphate or pyrethroid) or the Bug Buster kit. MAIN OUTCOME MEASURE: Presence of head lice 2-4 days after end of treatment: day 5 for the pediculicides and day 15 for the Bug Buster kit. RESULTS: The cure rate using the Bug Buster kit was significantly greater than that for the pediculicides (57% v 13%; relative risk 4.4, 95% confidence interval 2.3 to 8.5). Number needed to treat for the Bug Buster kit compared with the pediculicides was 2.26. CONCLUSION: The Bug Buster kit was the most effective over the counter treatment for head louse infestation in the community when compared with pediculicides.
Asunto(s)
Insecticidas , Infestaciones por Piojos/prevención & control , Malatión , Pediculus , Permetrina , Dermatosis del Cuero Cabelludo/prevención & control , Adolescente , Animales , Niño , Preescolar , Preparaciones para el Cabello , Humanos , Higiene , Lactante , Medicamentos sin Prescripción , Factores de Riesgo , Método Simple Ciego , Resultado del TratamientoAsunto(s)
Acetilcolinesterasa/genética , Áfidos/efectos de los fármacos , Áfidos/enzimología , Resistencia a los Insecticidas/genética , Insecticidas/farmacología , Acetilcolinesterasa/metabolismo , Animales , Áfidos/genética , Clonación Molecular , Regulación Enzimológica de la Expresión Génica/genética , Mutación/genéticaRESUMEN
We have identified two mutations in the ace1 gene of Aphis gossypii that are associated with insensitivity of acetylcholinesterase (AChE) to carbamate and organophosphate insecticides. The first of these, S431F (equivalent to F331 in Torpedo californica), is associated with insensitivity to the carbamate insecticide pirimicarb in a range of A. gossypii clones. The S431F mutation is also found in the peach-potato aphid, Myzus persicae (Sulzer), and a rapid RFLP diagnostic allows the identification of individuals of both aphid species with a resistant genotype. This diagnostic further revealed the presence of S431 in several other pirimicarb-susceptible aphid species. The serine at this position in the wild-type enzyme has only been reported for aphids and provides a molecular explanation of why pirimicarb has a specific aphicidal action. A less specific insensitivity to a wide range of carbamates and organophosphates is associated with a second mutation, A302S (A201 in T. californica).
Asunto(s)
Acetilcolinesterasa/genética , Áfidos/genética , Carbamatos , Mutación/genética , Organofosfatos , Acetilcolinesterasa/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Análisis por Conglomerados , Cartilla de ADN , Resistencia a los Insecticidas/genética , Modelos Moleculares , Datos de Secuencia Molecular , Filogenia , Polimorfismo de Longitud del Fragmento de Restricción , Conformación Proteica , Alineación de Secuencia , Análisis de Secuencia de ADN , Especificidad de la EspecieRESUMEN
The effects of two pyrethroids on recombinant wild-type and mutant (pyrethroid-resistant) Na+ channels of Drosophila melanogaster have been studied. Three mutations that confer resistance (kdr/superkdr) to pyrethroids were inserted, either individually or in combination, into the para Na+ channel of D. melanogaster: L1014F in domain IIS6, M918T in the IIS4-S5 linker, and T929I in domain IIS5. Channels were expressed in Xenopus laevis oocytes and the effects of the pyrethroids permethrin (type I) and deltamethrin (type II) on Na+ currents were investigated using voltage clamp. The Na+ channels deactivated slowly after deltamethrin treatment, the resultant "tail" currents being used to quantify the effects of this pyrethroid. The Hill slope of 2 for deltamethrin action on the wild-type channel and the mutant L1014F channel is indicative of cooperative binding at two or more sites on these channels. In contrast, binding to the mutants M918T and T929I is noncooperative. Tail currents for the wild-type channel and L1014F channel decayed biphasically, whereas those for M918T and T929I mutants decayed monophasically. The L1014F mutant was approximately 20-fold less sensitive than the wild-type to deltamethrin. Surprisingly, the sensitivity of the double mutant M918T+L1014F to deltamethrin was similar to that of M918T alone, whereas the sensitivity of T929I+L1014F was >30,000-fold lower than that of T929I. Permethrin was less potent than deltamethrin, and its binding to all channel types was noncooperative. The decays of permethrin-induced tail currents were exclusively monophasic. These findings are discussed in terms of the properties and possible locations of pyrethroid binding sites on the D. melanogaster Na+ channel.
Asunto(s)
Drosophila melanogaster/efectos de los fármacos , Insecticidas/toxicidad , Permetrina/toxicidad , Piretrinas/toxicidad , Canales de Sodio/metabolismo , Sustitución de Aminoácidos , Animales , Relación Dosis-Respuesta a Droga , Isoleucina/genética , Metionina/genética , Mutación , Nitrilos , Canales de Sodio/efectos de los fármacos , Canales de Sodio/genética , Tirosina/genéticaRESUMEN
We show that single-point mutations conferring target-site resistance (kdr) to pyrethroids and DDT in aphids and houseflies, and gene amplification conferring metabolic resistance (carboxylesterase) to organophosphates and carbamates in aphids, can have deleterious pleiotropic effects on fitness. Behavioural studies on peach-potato aphids showed that a reduced response to alarm pheromone was associated with both gene amplification and the kdr target-site mutation. In this species, gene amplification was also associated with a decreased propensity to move from senescing leaves to fresh leaves at low temperature. Housefly genotypes possessing the identical kdr mutation were also shown to exhibit behavioural differences in comparison with susceptible insects. In this species, resistant individuals showed no positional preference along a temperature gradient while susceptible genotypes exhibited a strong preference for warmer temperatures.
Asunto(s)
Áfidos/genética , Moscas Domésticas/genética , Resistencia a los Insecticidas/genética , Animales , DDT/farmacología , Esterasas/biosíntesis , Esterasas/genética , Amplificación de Genes , Genotipo , Proteínas de Insectos/genética , Mutación Puntual , Prunus/parasitología , Piretrinas/farmacología , Sesquiterpenos/farmacología , Canales de Sodio/genética , Solanum tuberosum/parasitología , TemperaturaRESUMEN
Gene sequences encoding putative acetylcholinesterases have been reported for four hemipteran insect species. Although acetylcholinesterase insensitivity occurs in insecticide-resistant populations of each of these species, no mutations were detected in the gene sequences from the resistant insects. This, coupled with a series of experiments using novel reversible inhibitors to compare the biochemical characteristics of acetylcholinesterase from a range of insect species, showed that the cloned cDNA fragments are unlikely to encode the hemipteran synaptic acetylcholinesterases, and there is likely to be a second ace locus.