Larvae Of Strain Research Articles

Etude De L’efficacité Du Cashew Nut Shell Liquid (CNSL) De Anacardium Occidentale L. Extrait À Froid Sur Le Contrôle De Anopheles Gambiae S.L Résistant Aux Pyréthrinoïdes

In order to combat the vectors of malaria, it is necessary to know their behavior with regard to the insecticide products envisaged. The present study is aimed at the CNSL efficiency test extracted from the seed hull of Anacardium occidentale L. for the control of pyrethroid-resistant Anopheles gambiae s.l. Sensitivity tests were carried out on the larvae of stages 2, 3 and 4 of An. gambiae of the wild and Kis-kdr strains carrying the Kdr gene. The "Kisumu" strain devoid of resistance gene served as a control. The mortalities were read after 24 hours of exposure. LD50 and DL90 were determined using the log-probit method of dose determination corresponding to a proportion. The high LD50 determined is 0.0042 mg / ml and corresponds to the LD50 of the larvae of stage 2 of the wild strain. The low LD50 is determined on stage 2 larvae "Kisumu". The high DL90 is determined on stage 4 larvae of the wild strain. The low LD90 determined corresponds to stage 2 larvae "Kisumu". The comparison of the LD between the different strains shows a low sensitivity to CNSL of the larvae of resistant strains compared to the control strain, indicating the influence of the resistance factor kdr on the CNSL efficiency. However, the low-dose CNSL larvicidal activity on the larvae of the kdr-carrying strains provides an alternative advantage in the management of vector resistance to pyrethroids

Etude De L’efficacité De L’huile De Thevetia Neriifolia Pour Le Contrôle De Anopheles Gambiae S.L Résistant Aux Pyréthrinoïdes

Effective control of pyrethroid-resistant malaria vectors requires new alternative measures. The purpose of this study is to test the effectiveness of Thevetia oil extracted from seed kernels to control malaria transmission by An. gambiae s.l. Sensitivity tests were carried out on larvae of Stages 3 and 4 of An. gambiae s.s of wild-type and pyrethroid-resistant Kis-kdr. The susceptible reference strain "Kisumu" served as a control. Mortality was read 24 hours and 48 hours after exposure. LD50 and 90 for 24 hours and 48 hours were determined using the log-probit method of determining the dose corresponding to a proportion. The high LD50s determined in 24 hours and 48 hours correspond to doses that kill 50% of Stage 3 larvae in wild populations in 24 hours and 48 hours. Low LD50s refer to stage 4 "Kisumu" larvae. The strong DL90 in 24 hours and 48 hours correspond respectively to stage 3 larvae of the Kis-kdr and wild-type strains. The comparison of the LD between the different strains shows the influence of the resistance on the sensitivity of the larvae of the strains resistant to the oil tested. However, the larvicidal effect of Thevetia oil on the larvae of resistant strains may elicit formulations for alternative measures in vector resistance management to pyrethroids.

Four Complete Paenibacillus larvae Genome Sequences.

ABSTRACTFour complete genome sequences of genetically distinct Paenibacillus larvae strains have been determined. Pacific BioSciences single-molecule real-time (SMRT) sequencing technology was used as the sole method of sequence determination and assembly. The chromosomes exhibited a G+C content of 44.1 to 44.2% and a molecular size range of 4.29 to 4.67 Mbp.

Suitability of two agglomerated commercial microdiets for rearing larvae of different strains of Coregonus lavaretus under cold-water conditions

The suitability of two agglomerated commercial microdiets (“Gemma micro®” and “O.range®” from now on called diet A and diet B) as a starter feed was tested on larvae of European whitefish (Coregonus lavaretus). Two strains (Baltic and Alpine) were tested in a 60-day experiment under ambient cold-water conditions (average 7.6 ± 1.9°C). The experiment was carried out in 400-L PVC tanks with a stocking density of 5,000 larvae per tank. Samples were removed weekly to determine growth, survival and feed acceptance, in addition to water quality. Striking differences between the feeds and different strains were observed. For one diet, growth and survival were distinctively higher in strain 1 compared to strain 2, where it was invariably low with both diets. For the second diet, growth and survival in strain 1 were also low and similar to strain 2. Feed acceptance in strain 1 was found higher compared to strain 2. Final weights were significantly different with strain 1 being heavier; however, in terms of relative growth rate, no differences between strains were found. Strong differences in the performance in terms of growth, survival and feed acceptance of different strains of European whitefish became apparent. Furthermore, the rearing of larvae exclusively on standard agglomerated commercial microdiets under cold-water conditions is possible, but not every microdiet is suitable.

Multilocus sequence typing, biochemical and antibiotic resistance characterizations reveal diversity of North American strains of the honey bee pathogen Paenibacillus larvae.

Paenibacillus larvae is a Gram positive bacterium and the causative agent of the most widespread fatal brood disease of honey bees, American foulbrood (AFB). A total of thirty-three independent Paenibacillus larvae isolates from various geographical origins in North America and five reference strains were investigated for genetic diversity using multilocus sequence typing (MLST). This technique is regarded to be a powerful tool for epidemiological studies of pathogenic bacteria and is widely used in genotyping assays. For MLST, seven housekeeping gene loci, ilvD (dihydroxy-acid dyhydrogenase), tri (triosephosphate isomerase), purH (phospharibosyl-aminoimidazolecarboxamide), recF (DNA replication and repair protein), pyrE (orotate phosphoribosyltransferase), sucC (succinyl coenzyme A synthetase β subunit) and glpF (glycerol uptake facilitator protein) were studied and applied for primer designs. Previously, ERIC type DNA fingerprinting was applied to these same isolates and the data showed that almost all represented the ERIC I type, whereas using BOX-PCR gave an indication of more diversity. All isolates were screened for resistance to four antibiotics used by U.S. beekeepers, showing extensive resistance to tetracycline and the first records of resistance to tylosin and lincomycin. Our data highlight the intraspecies relationships of P. larvae and the potential application of MLST methods in enhancing our understanding of epidemiological relationships among bacterial isolates of different origins.

Susceptibility of Trogoderma granarium Everts and Trogoderma inclusum LeConte (Coleoptera: Dermestidae) to residual contact insecticides

Commercial formulations of the pyrethroid insecticides β-cyfluthrin and deltamethrin were evaluated for delayed mortality of Trogoderma granarium (Everts), the khapra beetle, and T. inclusum (LeConte), the larger cabinet beetle. Ten 3-4 week-old larvae of either species were exposed on treated concrete arenas for 1, 2, 3, and 7 d then transferred into 175 ml diet cups containing 5 g of untreated rearing media for 30 d to evaluate delayed mortality. In a subsequent study, residual efficacy of β-cyfluthrin, deltamethrin, and chlorfenapyr was evaluated at 0–12 wks post-treatment against adults and larvae of a laboratory and a field strain of T. granarium. Ten adults or larvae of either strain were exposed on treated arenas at selected wks post-treatment and mortality was assessed after 4 and 30 d of exposure for adults and larvae, respectively. In the first study, delayed morality of T. granarium and T. inclusum larvae was <26% when exposed on arenas treated with the two pyrethroids, and T. inclusum larvae were less susceptible than T. granarium. Adult mortality was 90–100% for both strains of T. granarium across post-treatment assays regardless of insecticide treatment and there was no difference between strains. All three insecticides produced 100% mortality for the laboratory strain of T. granarium larvae in initial post-treatment assays, but then efficacy declined. Field strain larvae were more tolerant to the insecticides than laboratory strain larvae, and larvae of both T. granarium strains were more tolerant than adults. Longer exposure times were required to produce complete mortality of larvae compared to adults. All three insecticides provided residual efficacy of adults for up to three months.

Status resistensi terhadap fosfin pada Tribolium castaneum Herbst (Coleoptera: Tenebrionidae) dari gudang penyimpanan biji kakao di Makassar Sulawesi Selatan

Control of postharvest pest on cocoa beans during storage is generally conducted by fumigation with phosphine. Long-term exposure to phosphine and improper fumigation practices could stimulate the development of resistant strains against phosphine. The aims of this research were to know the resistance status of red flour beetle Tribolium castaneum Herbst (Coleoptera: Tenebrionidae) against phosphine from cocoa bean storages in Makassar, South Sulawesi and to conduct the field efficacy test of phosphine against insects resistant strain to confirm their resistance status. The study was conducted by collecting T. castaneum from five different cocoa beans storages in Makassar. Resistance status was tested in the laboratory using the standard method recommended by FAO and by conducting field efficacy test on adult strains resistant to phosphine. The results showed the presence of insect resistance to phosphine. Adult, pupae, and larvae of T. castaneum were found to be resistant to phosphine with the resistance factors of 1.15–8.08, 1.58–13.63, 1.53–3.25, respectively. The results of field efficacy tests showed that dosage 2 tablets/m 3 was effective in controlling resistant strain of adult, pupae, and larvae of T. castaneum .

Cytotoxic and genotoxic actions of Casiopeina III-Ea (Cas III-Ea) in somatic and germ cells of Drosophila melanogaster

ABSTRACTCasiopeinas® are a group of newly synthesized drugs designed to treat cancer. These copper (Cu) complexes exhibit cytostatic, cytotoxic, genotoxic, and antineoplastic activities through different mechanisms of action. To evaluate the influence of these compounds, some in vivo studies were performed using predominantly somatic cells. The aim of the present study was to examine the cytotoxic and genotoxic actions of Casiopeina III-Ea (Cas III-Ea) in somatic as well as germ cells of Drosophila melanogaster. For cytotoxicity, the productivity and some morphometric parameters were measured and genotoxicity was assessed by means of the somatic mutation and recombination test assay in the wing. For this purpose, second-instar larvae of the Canton-S strain were treated with different concentrations of Cas III-Ea. The emerged adults were weighed, the area of the wings determined, and the number of trichomes of the region Cʹ counted. The productivity of treated males was measured by a brood method to monitor the influence of Cas III-Ea on spermatozoa, meiotic stage cells, and spermatogonia. For genotoxicity, mwh + /+ flr3 larvae 48 hr age were chronically treated within the same concentration range. Results indicated that Cas III-Ea at all concentrations tested significantly increased the productivity per couple in Brood III (spermatids) while at 1 mM a marked elevation was noted in the three broods tested. In contrast, the weight and size of individuals as well as the size and number of cells in the wing were decreased significantly. Data suggest that Cas III-Ea is a weak genotoxic but selective mutagen. Failure to obtain a dose-related genotoxic response suggests that one of the preferred mechanisms of action of Cas III-Ea is to induce apoptosis.

Larvas de linhagens de tilápia do Nilo submetidas à frequências alimentares sob baixa temperatura

RESUMO O manejo alimentar adequado associado a animais com maior rendimento e resistência a ambientes específicos, como águas com temperaturas abaixo da adequada à espécie, são determinantes para uma maior produtividade. Portanto, objetivou-se com o presente estudo comparar o desempenho da larvicultura de duas linhagens de tilápia do Nilo (Oreochromis niloticus) submetidas a diferentes frequências alimentares com temperatura abaixo da faixa ótima para crescimento. Larvas das linhagens tailandesa (720 indivíduos com peso de 24,3 mg e comprimento total de 12,4 mm) e GIFT (720 exemplares com 22,5 mg e 12,0 mm), foram distribuídas em 24 aquários de 4L, na densidade de 15 larvas. L−1, 60 larvas aquário−1, sob aeração constante, fotoperíodo natural e temperatura a 23 °C, em sistema com recirculação com termostato. Elas foram submetidas a três frequências alimentares: 2, 5 e 8 vezes.dia−1, em delineamento inteiramente casualizado, em esquema fatorial 2 linhagens x 3 frequências, com quatro repetições cada. Exceto a temperatura, os demais parâmetros de qualidade da água, amônia, nitrito, nitrato, turbidez, condutividade e pH, mantiveram-se adequados para a espécie. A linhagem tailandesa apresentou maiores comprimentos total e padrão, peso, fator de condição de Fulton, sobrevivência e biomassa, do que a GIFT. A frequência alimentar 5 vezes.dia−1 gerou maiores valores para as larvas em peso, comprimento total e padrão, do que as submetidas à frequência de 2 vezes.dia−1, e valores iguais, quando comparadas as submetidas à frequência de 8 vezes.dia−1. Na temperatura de 23 °C devese empregar as tilápias da linhagem tailandesa alimentadas 5 vezes.dia−1.

Midgut-based resistance to oral infection by a nucleopolyhedrovirus in the laboratory-selected strain of the smaller tea tortrix, Adoxophyes honmai (Lepidoptera: Tortricidae).

A strain of Adoxophyes honmai resistant to Adoxophyes honmai nucleopolyhedrovirus (AdhoNPV) was established from a field-collected colony by repeated selection. Fifth-instar larvae of this resistant strain (R-strain) had over 66 666-fold greater resistance in terms of 50 % lethal concentration values to oral infection of AdhoNPV than non-selected strain larvae (susceptible for AdhoNPV; S2-strain). In this study, the mechanism of resistance to AdhoNPV was determined in R-strain larvae. An assessment of viral genome replication in AdhoNPV-infected S2- and R-strain larvae by quantitative PCR showed no viral genome replication occurring in R-strain larvae. Transcription of AdhoNPV ie-1, vp39 and polyhedrin genes was also not detected in R-strain midgut cells. Besides, a fluorescent brightener had no effect on AdhoNPV infection in either S2- or R-strain. However, binding and fusion of occlusion-derived virus with R-strain were significantly lower than those of S2-strain. These findings suggest that R-strain Adoxophyeshonmai larvae possess a midgut-based resistance to oral infection by AdhoNPV in which midgut epithelial cells are infected less efficiently.

Characterization and expression profiling of ATP-binding cassette transporter genes in the diamondback moth, Plutella xylostella (L.).

BackgroundATP-binding cassette (ABC) transporters are one of the major transmembrane protein families found in all organisms and play important roles in transporting a variety of compounds across intra and extra cellular membranes. In some species, ABC transporters may be involved in the detoxification of substances such as insecticides. The diamondback moth, Plutella xylostella (L.), a destructive pest of cruciferous crops worldwide, is an important species to study as it is resistant to many types of insecticides as well as biological control Bacillus thuringiensis toxins.ResultsA total of 82 ABC genes were identified from our published P. xylostella genome, and grouped into eight subfamilies (ABCA-H) based on phylogenetic analysis. Genes of subfamilies ABCA, ABCC and ABCH were found to be expanded in P. xylostella compared with those in Bombyx mori, Manduca sexta, Heliconius melpomene, Danaus plexippus, Drosophila melanogaster, Tetranychus urticae and Homo sapiens. Phylogenetic analysis indicated that many of the ABC transporters in P. xylostella are orthologous to the well-studied ABC transporter genes in the seven other species. Transcriptome- and qRT-PCR-based analysis elucidated physiological effects of ABC gene expressions of P. xylostella which were developmental stage- and tissue-specific as well as being affected by whether or not the insects were from an insecticide-resistant strain. Two ABCC and one ABCA genes were preferentially expressed in midgut of the 4th-instar larvae of a susceptible strain (Fuzhou-S) suggesting their potential roles in metabolizing plant defensive chemicals. Most of the highly expressed genes in insecticide-resistant strains were also predominantly expressed in the tissues of Malpighian tubules and midgut.ConclusionsThis is the most comprehensive study on identification, characterization and expression profiling of ABC transporter genes in P. xylostella to date. The diversified features and expression patterns of this gene family may be associated with the evolutionary capacity of this species to develop resistance to a wide range of insecticides and biological toxins. Our findings provide a solid foundation for future functional studies on specific ABC transporter genes in P. xylostella, and for further understanding of their physiological roles and regulatory pathways in insecticide resistance.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3096-1) contains supplementary material, which is available to authorized users.

Virulence Differences among Melissococcus plutonius Strains with Different Genetic Backgrounds in Apis mellifera Larvae under an Improved Experimental Condition

European foulbrood (EFB) caused by Melissococcus plutonius is an important bacterial disease of honeybee larvae. M. plutonius strains can be grouped into three genetically distinct groups (CC3, CC12 and CC13). Because EFB could not be reproduced in artificially reared honeybee larvae by fastidious strains of CC3 and CC13 previously, we investigated a method to improve experimental conditions using a CC3 strain and found that infection with a potassium-rich diet enhanced proliferation of the fastidious strain in larvae at the early stage of infection, leading to the appearance of clear clinical symptoms. Further comparison of M. plutonius virulence under the conditions revealed that the representative strain of CC12 was extremely virulent and killed all tested bees before pupation, whereas the CC3 strain was less virulent than the CC12 strain, and a part of the infected larvae pupated. In contrast, the tested CC13 strain was avirulent, and as with the non-infected control group, most of the infected brood became adult bees, suggesting differences in the insect-level virulence among M. plutonius strains with different genetic backgrounds. These strains and the improved experimental infection method to evaluate their virulence will be useful tools for further elucidation of the pathogenic mechanisms of EFB.

Synthesis and Biological Evaluation of 3,5-Dimethoxystilbene Analogs.

In our continuing effort to discover natural product-based pest management agents, derivatives of 3,5-dimethoxystilbene were synthesized yielding 27 new and six known compounds. Compounds 11 and 12 showed strong Aedes aegypti larvicidal activity (LC50 45.31 and 49.93 μm, respectively). Furthermore, 11 and 12 exhibited high effectiveness against larvae of pesticide-susceptible and pyrethroid-resistant strains of Ae. aegypti; activity against the adult mosquitoes was low. Compounds 6f, 6g, and 6i at either 83.3 or 166.7 μg/ml reduced the mobility of second-stage juveniles (J2) of the root-knot nematode (Meloidogyne incognita) that hatched from eggs immersed in the test compounds for 7 days. However, there was little or no effect on J2 placed directly into these compounds, and none of the analogs suppressed M. incognita egg hatch. The compounds were tested for inhibition of some agriculturally important fungi; 6a, 7a, and 7e demonstrated strong inhibition of Colletotrichum species. Activity of the stilbenes against some human pathogens was also explored; 11, 12, and 16 showed moderate inhibitory activity against Cryptococcus neoformans, Staphylococcus aureus, methicillin-resistant S. aureus, and Mycobacterium intracellulare. Except for 11 and 12, which were active against mosquito larvae and some human pathogens, no single analog demonstrated activity in all the tests, indicating specific activities. Synthesis of the analogs and structure-activity relationships are discussed.

First detection of Paenibacillus larvae the causative agent of American Foulbrood in a Ugandan honeybee colony.

Paenibacillus larvae is a highly contagious and often lethal widely distributed pathogen of honeybees, Apis mellifera but has not been reported in eastern Africa to date. We investigated the presence of P. larvae in the eastern and western highland agro-ecological zones of Uganda by collecting brood and honey samples from 67 honeybee colonies in two sampling occasions and cultivated them for P. larvae. Also, 8 honeys imported and locally retailed in Uganda were sampled and cultivated for P. larvae. Our aim was to establish the presence and distribution of P. larvae in honeybee populations in the two highland agro-ecological zones of Uganda and to determine if honeys that were locally retailed contained this lethal pathogen. One honeybee colony without clinical symptoms for P. larvae in an apiary located in a protected area of the western highlands of Uganda was found positive for P. larvae. The strain of this P. larvae was genotyped and found to be ERIC I. In order to compare its virulence with P. larvae reference strains, in vitro infection experiments were conducted with carniolan honeybee larvae from the research laboratory at Ghent University, Belgium. The results show that the virulence of the P. larvae strain found in Uganda was at least equally high. The epidemiological implication of the presence of P. larvae in a protected area is discussed.

Protection of honeybee Apis mellifera by its endogenous and exogenous lactic flora against bacterial infections

Abstract Lactic acid bacteria (LAB) symbionts of honeybees are certainly playing key roles in their host's colony functioning. The defense against bacterial pathogen invasion by endogenous LAB has been considered as promising and usable phenomenon. This study addresses bacteriocinogeny as one of antibacterial action mode displayed by bacteria. The honeybee endogenous LAB isolated from worker honeybee intestines (61 strains), queen honeybee intestines (16 strains) and beebread (25 strains) were tested for bacteriocin production ability. We checked also well characterized bacteriocin producing LAB strains against bacteria causing American foulbrood (AFB) – Paenibacillus larvae aiming possible use of exogenous LAB for control AFB in honeybees and in the same time to observe the vulnerability of endogenous bacteria exposed to bacteriocin producers. We demonstrated that none of 102 studied LAB strains, isolated from worker honeybee intestines, from queen honeybee intestines and from beebread, produced bacteriocins detectable by the well diffusion method (WDM). All of them failed to inhibit two strains of P. larvae . Three exogenous bacteriocin-producing LAB strains were tested against the same pathogens and against 25 endogenous bacterial isolates representing 11 different LAB species. The screening showed that all the tested exogenous bacteriocin-producing strains inhibited the tested P. larvae strains. The endogenous LAB strains exhibited varied sensitivity profiles when treated with bacteriocin-producing strains. This raises similar challenges to those observed in antibiotic applications leading to dysbacteriosis, even though the efficacy of these bacteriocins against P. larvae in an in vitro system is evident.

Multiple Locus Variable number of tandem repeat Analysis: A molecular genotyping tool for Paenibacillus larvae.

SummaryAmerican Foulbrood, caused by Paenibacillus larvae, is the most severe bacterial disease of honey bees (Apis mellifera). To perform genotyping of P. larvae in an epidemiological context, there is a need of a fast and cheap method with a high resolution. Here, we propose Multiple Locus Variable number of tandem repeat Analysis (MLVA). MLVA has been used for typing a collection of 209 P. larvae strains from which 23 different MLVA types could be identified. Moreover, the developed methodology not only permits the identification of the four Enterobacterial Repetitive Intergenic Consensus (ERIC) genotypes, but allows also a discriminatory subdivision of the most dominant ERIC type I and ERIC type II genotypes. A biogeographical study has been conducted showing a significant correlation between MLVA genotype and the geographical region where it was isolated.

Experimental bacteriophage treatment of honeybees (Apis mellifera) infected with Paenibacillus larvae, the causative agent of American Foulbrood Disease.

ABSTRACTAmerican Foulbrood Disease (AFB) is an infection of honeybees caused by the bacterium Paenibacillus larvae. One potential remedy involves using biocontrol, such as bacteriophages (phages) to lyse P. larvae. Therefore, bacteriophages specific for P. larvae were isolated to determine their efficacy in lysing P. larvae cells. Samples from soil, beehive materials, cosmetics, and lysogenized P. larvae strains were screened; of 157 total samples, 28 were positive for at least one P. larvae bacteriophage, with a total of 30. Newly isolated bacteriophages were tested for the ability to lyse each of 11 P. larvae strains. Electron microscopy demonstrated that the phage isolates were from the family Siphoviridae. Seven phages with the broadest host ranges were combined into a cocktail for use in experimental treatments of infected bee larvae; both prophylactic and post-infection treatments were conducted. Results indicated that although both pre- and post-treatments were effective, prophylactic administration of the phages increased the survival of larvae more than post-treatment experiments. These preliminary experiments demonstrate the likelihood that phage therapy could be an effective method to control AFB.

Field-Evolved Mode 1 Resistance of the Fall Armyworm to Transgenic Cry1Fa-Expressing Corn Associated with Reduced Cry1Fa Toxin Binding and Midgut Alkaline Phosphatase Expression.

Insecticidal protein genes from the bacterium Bacillus thuringiensis (Bt) are expressed by transgenic Bt crops (Bt crops) for effective and environmentally safe pest control. The development of resistance to these insecticidal proteins is considered the most serious threat to the sustainability of Bt crops. Resistance in fall armyworm (Spodoptera frugiperda) populations from Puerto Rico to transgenic corn producing the Cry1Fa insecticidal protein resulted, for the first time in the United States, in practical resistance, and Bt corn was withdrawn from the local market. In this study, we used a field-collected Cry1Fa corn-resistant strain (456) of S. frugiperda to identify the mechanism responsible for field-evolved resistance. Binding assays detected reduced Cry1Fa, Cry1Ab, and Cry1Ac but not Cry1Ca toxin binding to midgut brush border membrane vesicles (BBMV) from the larvae of strain 456 compared to that from the larvae of a susceptible (Ben) strain. This binding phenotype is descriptive of the mode 1 type of resistance to Bt toxins. A comparison of the transcript levels for putative Cry1 toxin receptor genes identified a significant downregulation (>90%) of a membrane-bound alkaline phosphatase (ALP), which translated to reduced ALP protein levels and a 75% reduction in ALP activity in BBMV from 456 compared to that of Ben larvae. We cloned and heterologously expressed this ALP from susceptible S. frugiperda larvae and demonstrated that it specifically binds with Cry1Fa toxin. This study provides a thorough mechanistic description of field-evolved resistance to a transgenic Bt crop and supports an association between resistance and reduced Cry1Fa toxin binding and levels of a putative Cry1Fa toxin receptor, ALP, in the midguts of S. frugiperda larvae.

Daily rhythm of insecticide susceptibility in the silkworm Bombyx mori

This study investigated daily changes in susceptibility to insecticides in the silkworm Bombyx mori (Lepidoptera: Bombycidae). The daily rhythm of permethrin susceptibility in fifth instar larvae of the p63-silkworm strain was significant, with the lowest mortality rate during the late photophase under a 12-h light–12-h dark cycle. The rhythms were similar whether permethrin was intraperitoneally injected into hemolymph or topically applied to the dorsal abdomen. Drug intake through the cuticle probably did not significantly contribute to the organization of this susceptibility rhythm. We also found that the daily susceptibility profiles depended on insecticide type and silkworm strain. Temporal susceptibility variations might be attributable to the drug metabolic system. To our knowledge, this is the first description of an insecticide susceptibility rhythm in the larval stage of lepidopteran insects. Specifically timed delivery of insecticides might enable more efficient control of pest caterpillars that cause serious crop damage.

Sublethal effects of Bt toxin and chlorpyrifos on various Spodoptera exigua populations

AbstractBt cotton (Cry1Ac) has been commercially grown in China since 1997, saving China's cotton production from attack by Bt‐target pests and also tremendously reducing pesticide usage. In recent years, however, Bt cotton, with 4.2 million ha of cultivation, has suffered from a secondary target pest, Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae). In China, growers have even had to re‐adopt conventional pesticides to control the pest, and this practice has already caused serious pesticide residue. In order to clarify the sublethal effects of chemical pesticide, the responses of a Bt‐susceptible and a Bt‐tolerant (Bt10) S. exigua strain to three treatment combinations were examined, including Bt toxin, sublethal chlorpyrifos, and Bt + sublethal chlorpyrifos. The susceptible and the Bt10 strain responded differently to dual pressure. Bt toxin + sublethal chlorpyrifos treatment lowered larval mortality and stimulated population increase of the susceptible S. exigua, whereas it delayed growth and development of the Bt10 strain. Under dual pressure, although larvae of the Bt10 strain developed faster than larvae of the susceptible strain, the Bt10 population experienced higher larval mortality, prolonged pupal duration, decreased pupal weight, decreased emergence rate, and shortened adult longevity. Compared with the susceptible strain, the Bt10 strain was deleteriously affected by sublethal chlorpyrifos. The Bt‐tolerant/resistant S. exigua population was more vulnerable to chemical pesticides like chlorpyrifos regardless of whether it was exposed to Bt toxin or not. Our study provides a reference for increasing the efficacy of control of S. exigua in Bt‐cotton planting areas.