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1.
Curr Microbiol ; 81(6): 156, 2024 Apr 24.
Artigo em Inglês | MEDLINE | ID: mdl-38656548

RESUMO

Aspergillus fumigatus and Fusarium solani infections have become severe health threat; both pathogens are considered a priority due to the increasing emergence of antifungal-resistant strains and high mortality rates. Therefore, the discovery of new therapeutic strategies has become crucial. In this study, we evaluated the antifungal and antivirulence effects of vanillin and tannic acid against Aspergillus fumigatus and Fusarium solani. The minimum inhibitory concentrations of the compounds were determined by the microdilution method in RPMI broth in 96-well microplates according to CLSI. Conidial germination, protease production, biofilm formation, and in vivo therapeutic efficacy assays were performed. The results demonstrated that vanillin and tannic acid had antifungal activity against Aspergillus fumigatus, while tannic acid only exhibited antifungal activity against Fusarium solani. We found that vanillin and tannic acid inhibited conidial germination and secreted protease production and biofilm formation of the fungal pathogens using sub-inhibitory concentrations. Besides, vanillin and tannic acid altered the fungal membrane permeability, and both compounds showed therapeutic effect against aspergillosis and fusariosis in an infection model in Galleria mellonella larvae. Our results highlight the antivirulence effect of vanillin and tannic acid against priority pathogenic fungi as a possible therapeutic alternative for human fungal infections.


Assuntos
Antifúngicos , Aspergillus fumigatus , Benzaldeídos , Biofilmes , Fusarium , Testes de Sensibilidade Microbiana , Polifenóis , Taninos , Benzaldeídos/farmacologia , Fusarium/efeitos dos fármacos , Taninos/farmacologia , Antifúngicos/farmacologia , Biofilmes/efeitos dos fármacos , Aspergillus fumigatus/efeitos dos fármacos , Animais , Aspergilose/microbiologia , Aspergilose/tratamento farmacológico , Virulência/efeitos dos fármacos , Larva/microbiologia , Larva/efeitos dos fármacos , Fusariose/tratamento farmacológico , Fusariose/microbiologia , Esporos Fúngicos/efeitos dos fármacos , Mariposas/microbiologia , Mariposas/efeitos dos fármacos
2.
Neotrop Entomol ; 53(3): 669-681, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38478300

RESUMO

Over the last decade, essential oils (EOs) have become potential ingredients for insecticide formulations due to their widespread availability and perceived safety. Therefore, this study aimed to evaluate the toxicity and biochemical efficacy of basil (Ocimum basilicum) (Lamiaceae) against two destructive pests Noctuidae, Agrotis ipsilon (Hufnagel) and Spodoptera littoralis (Boisduval) (Lepidoptera: Noctuidae). In addition, a molecular docking study was performed to gain insight into the binding pattern between glutathione S-transferase (GST) and linalool, the main component of EO. GC-MS analysis of O. basilicum EO revealed that linalool is the most abundant compound (29.34%). However, the toxicity tests showed no significant difference between the values of LC50 of O. basilicum EO to A. ipsilon and S. littoralis. On the other hand, the sublethal experiments indicated that treating the second instar larvae with LC15 or LC50 values of O. basilicum EO significantly prolonged the larval duration in both insects, compared to the control. Regarding the biochemical effect of O. basilicum EO, the treatments significantly impacted the activity of detoxification enzymes. A notable elevation in glutathione S-transferase (GST) activity was recorded in A. ipsilon larvae compared with a reduction in S. littoralis larvae. The molecular docking analysis revealed that linalool bonded with the amino acid serine (SER 9) of GST, indicating its binding affinity with the enzyme. The obtained results could offer valuable insights into the mode of action of O. basilicum and can encourage the adoption of sustainable pest control practices that incorporate essential oils.


Assuntos
Inseticidas , Larva , Simulação de Acoplamento Molecular , Ocimum basilicum , Óleos Voláteis , Spodoptera , Animais , Ocimum basilicum/química , Spodoptera/efeitos dos fármacos , Larva/efeitos dos fármacos , Glutationa Transferase/metabolismo , Mariposas/efeitos dos fármacos , Monoterpenos Acíclicos , Cromatografia Gasosa-Espectrometria de Massas
3.
Molecules ; 27(3)2022 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-35163928

RESUMO

The aim of this study was to investigate and compare in detail both the antifungal activity in vitro (with planktonic and biofilm-forming cells) and the essential oil composition (EOs) of naturally growing (OMN) and cultivated (OMC) samples of Origanum majorana L. (marjoram). The essential oil composition was analyzed using GC-MS. The major constituent of both EOs was carvacrol: 75.3% and 84%, respectively. Both essential oils showed high antifungal activity against clinically relevant Candida spp. with IC50 and IC90 less than or equal to 0.5 µg mL-1 and inhibition of biofilm with a concentration of 3.5 µg mL-1 or less. Cultivated marjoram oil showed higher anti-biofilm activity against C. albicans. In addition, OMC showed greater inhibition of germ-tube formation (inhibition by 83% in Spider media), the major virulence factor of C. albicans at a concentration of 0.125 µg mL-1. Both EOs modulated cell surface hydrophobicity (CSH), but OMN proved to be more active with a CSH% up to 58.41%. The efficacy of O. majorana EOs was also investigated using Galleria mellonella larvae as a model. It was observed that while the larvae of the control group infected with C. albicans (6.0 × 108 cells) and not receiving treatment died in the controls carried out after 24 h, all larvae in the infected treatment group survived at the end of the 96th hour. When the treatment group and the infected group were evaluated in terms of vital activities, it was found that the difference was statistically significant (p < 0.001). The infection of larvae with C. albicans and the effects of O. majorana EOs on the hemocytes of the model organism and the blastospores of C. albicans were evaluated by light microscopy on slides stained with Giemsa. Cytological examination in the treatment group revealed that C. albicans blastospores were phagocytosed and morphological changes occurred in hemocytes. Our results indicated that the essential oil of both samples showed strong antifungal activities against planktonic and biofilm-forming C. albicans cells and also had an influence on putative virulence factors (germ-tube formation and its length and on CSH).


Assuntos
Antifúngicos/farmacologia , Candida albicans/efeitos dos fármacos , Larva/crescimento & desenvolvimento , Mariposas/crescimento & desenvolvimento , Óleos Voláteis/farmacologia , Origanum/química , Óleos de Plantas/farmacologia , Animais , Larva/efeitos dos fármacos , Mariposas/efeitos dos fármacos , Testes de Toxicidade
4.
Toxins (Basel) ; 13(12)2021 11 25.
Artigo em Inglês | MEDLINE | ID: mdl-34941680

RESUMO

Many plants show significant biological activity against pests due to their unique chemical constituents. It is important to identify effective constituents for their development and utilization as botanical pesticides. Our previous study showed that Artemisia lavandulaefolia essential oil had biological activity against Plutella xylostella. Here, we isolated and identified the constituents of essential oil from A. lavandulaefolia by silica gel column chromatography. The main constituents identified were eucalyptol and caryophyllene oxide, and they were confirmed by gas chromatography-mass spectrometry (GC-MS). Eucalyptol and caryophyllene oxide showed strong contact toxicity against P. xylostella larvae after 24 h of application (Median lethal dose, LD50 = 76.97 µL/mL and 20.71 mg/mL. Furthermore, the two active constituents against P. xylostella adults showed significant fumigant activity (Mmedian lethal concentration, LC50 = 3.25 µL/L and 1.06 mg/L, respectively. Finally, we measured the detoxification enzymes and acetylcholinesterase of the larvae treated with active constituents. The eucalyptol-treated larvae displayed enhanced carboxylesterase (CarE) and glutathione-S-transferase (GST) activities in an in vivo experiment, but it was lower for acetylcholinesterase (AchE) activity. The activities of the CarE and GST significantly decreased when exposed to caryophyllene oxide. In general, the two active constituents, eucalyptol and caryophyllene oxide, showed high insecticidal activity, which demonstrates their potential to be used as natural insecticides.


Assuntos
Artemisia/química , Inseticidas/farmacologia , Mariposas/efeitos dos fármacos , Óleos de Plantas/química , Animais , Bioensaio , Eucaliptol/química , Eucaliptol/farmacologia , Inseticidas/química , Larva/efeitos dos fármacos , Dose Letal Mediana , Óleos Voláteis/química , Sesquiterpenos Policíclicos/química , Sesquiterpenos Policíclicos/farmacologia
5.
PLoS One ; 16(12): e0259867, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34855796

RESUMO

Resistance management is very important for devising control strategies of polyphagous insect-pests like Helicoverpa armigera Hübner (Lepidoptera: Noctuidae). Considering the importance of resistance management, demographic features of selected and unselected populations of H. armigera were studied in 6 different treatments viz. emamectin benzoate, Helicoverpa armigera Nucleopolyhedrosis Virus (HaNPV), emamectin benzoate+HaNPV, spinetoram, spinetoram+HaNPV and control. Higher values for fecundity, intrinsic rate, the finite rate of increase (λ) were recorded in the control of selected as compared to the rest of treatment. Similarly, higher values for these population parameters viz. oviposition days, fecundity, intrinsic rate, the finite rate of increase were calculated in the unselected control. Similarly, net reproductive rate (R0) for selected and unselected control was higher as compared to the rest of the treatments. It may happen because these kinds of selection pressures can result in decreased fitness of the test insect thus decreased fitness of H. armigera in different treatments was observed as compared to the control. Additionally, quicker development of susceptible insects was observed because susceptible insects were growing without any stressor (xenobiotics) as compared to the rest which contributed to their faster development.


Assuntos
Inseticidas/farmacologia , Mariposas/efeitos dos fármacos , Mariposas/virologia , Nucleopoliedrovírus/patogenicidade , Animais , Agentes de Controle Biológico , Feminino , Fertilidade/efeitos dos fármacos , Ivermectina/análogos & derivados , Ivermectina/farmacologia , Larva/efeitos dos fármacos , Tábuas de Vida , Macrolídeos/farmacologia , Masculino , Mariposas/fisiologia , Oviposição/efeitos dos fármacos
6.
Artigo em Inglês | MEDLINE | ID: mdl-34343701

RESUMO

Cadmium (Cd) is a non-essential metal that is highly toxic to all living forms, characterized by an extremely high affinity for thiol (SH) groups. The aim of this work was to identify and experimentally verify metallothionein gene and to analyze the role of biological thiols in stress induced by short-term Cd exposure in Ostrinia nubilalis, one of the most important corn pests. The coding region of a metallothionein (MT) gene in O. nubilalis was identified, encoding protein, OnMT1, which contains 46 amino acids, including 12 cysteine residues, and has no aromatic amino acids. Phylogenetic analysis revealed that OnMT1 clustered together with metallothionein from Bombyx mori. Structural bioinformatics analysis strongly suggests that OnMT1 is a metallothionein with affinity for multiple transition metals. Further, in order to elucidate the role of biological thiols, O. nubilalis L5 larvae were exposed to increasing Cd concentrations in diet (6.85, 41.71, 77.35 mg kg-1) during a 48 h period, after which Cd concentration in larvae was measured (3.50, 12.02, 47.37 mg kg-1, respectively). Due to short-term Cd exposure, concentration of free protein SH groups and relative expression of OnMT1 and thioredoxin (Trx) genes was elevated, while the reduced glutathione content remained unchanged. The presented results provide evidence that OnMT1 plays a role in Cd detoxification and homeostasis, and confirm the importance of biological thiols, especially OnMT1 and Trx, in the early response of O. nubilalis to Cd poisoning, indicating interaction between Cd and thiol-linked redox reactions. Insects provide valuable insight into molecular adaptations to metals.


Assuntos
Cádmio/toxicidade , Mariposas/efeitos dos fármacos , Animais , Glutationa/metabolismo , Larva , Metalotioneína/genética , Metalotioneína/metabolismo , Mariposas/genética , Mariposas/metabolismo , Oxirredução , Filogenia , Estresse Fisiológico , Compostos de Sulfidrila/metabolismo , Tiorredoxinas/genética , Tiorredoxinas/metabolismo
7.
Artigo em Inglês | MEDLINE | ID: mdl-34461292

RESUMO

Cadmium (Cd) presence in terrestrial ecosystems is a serious threat that requires continuous development of biomonitoring tools. Ideally, a suitable biomarker of exposure should respond to the toxicant consistently in different populations regardless of previous exposure to pollution. Here we considered the activities and isoform patterns of certain proteases and acid phosphatases (ACP) in the midgut of Lymantria dispar larvae as well as the integrated biomarker response (IBR) for application in Cd biomonitoring. We compared the responses of caterpillars originating from unpolluted and polluted localities after they had been chronically subjected to dietary Cd (50 and 100 µg Cd/g dry food). The population inhabiting the unpolluted forest was far more sensitive to Cd exposure as the activities of total proteases, trypsin (TRY) and leucine aminopeptidase (LAP) were mostly reduced while the activities of total and non-lysosomal ACP were increased. Non-lysosomal ACP activity was elevated in larvae from the contaminated site in response to the higher Cd concentration. Exposure to the metal resulted in numerous alterations in the pattern of enzyme isoforms, but the responses of the two populations were similar except that larvae from the polluted locality were more tolerant to the lower Cd concentration. Non-lysosomal ACP activity and the appearance of ACP isoforms 4 and 5 together with the IBR index are the most promising indicators of Cd presence, potentially applicable even in populations with a history of exposure to pollution. TRY and total ACP activities could be used to monitor populations at uncontaminated localities.


Assuntos
Cádmio/toxicidade , Mariposas/efeitos dos fármacos , Fosfatase Ácida/genética , Fosfatase Ácida/metabolismo , Animais , Sistema Digestório/efeitos dos fármacos , Sistema Digestório/enzimologia , Poluentes Ambientais/toxicidade , Larva , Leucil Aminopeptidase/genética , Leucil Aminopeptidase/metabolismo , Mariposas/embriologia , Tripsina/genética , Tripsina/metabolismo
8.
Nat Prod Res ; 35(9): 1566-1571, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-31507220

RESUMO

Coumarin (2H-1-benzopyran-2-one) is a phenolic compound derived from the shikimate pathway and synthesized by various medicinal and aromatic plants as parent molecule of a large group of secondary metabolites, namely coumarins. Its main utilization is as fixative in perfumes and flavour enhancer. Given its role as phytoalexin and phagodepression activity, herein we evaluated for the first time its efficacy against several insect species: the green peach aphid, Myzus persicae, the moth Spodoptera littoralis, the housefly, Musca domestica and the filariasis vector Culex quinquefasciatus. Two non-target species were also included in our toxicity evaluation experiments: the ladybug Harmonia axyridis and the earthworm Eisenia fetida. Results highlighted remarkable selectivity of coumarin, being highly toxic to M. persicae aphids (LC50(90) values of 1.3(1.9) mg L-1) and friendly to natural enemies of aphids as well as soil invertebrates.


Assuntos
Afídeos/efeitos dos fármacos , Cumarínicos/toxicidade , Animais , Culex/efeitos dos fármacos , Moscas Domésticas/efeitos dos fármacos , Concentração Inibidora 50 , Inseticidas/toxicidade , Larva/efeitos dos fármacos , Mariposas/efeitos dos fármacos , Extratos Vegetais/química , Sementes/química , Spodoptera/efeitos dos fármacos , Testes de Toxicidade
9.
Toxins (Basel) ; 13(1)2020 Dec 24.
Artigo em Inglês | MEDLINE | ID: mdl-33374143

RESUMO

Insecticidal proteins from Bacillus thuringiensis (Bt) are used widely in sprays and transgenic crops to control insect pests. However, evolution of resistance by pests can reduce the efficacy of Bt toxins. Here we analyzed resistance to Bt toxins Cry1Ac and Cry1Fa in the diamondback moth (Plutella xylostella), one of the world's most destructive pests of vegetable crops. We used CRISPR/Cas9 gene editing to create strains with knockouts of the ATP-binding cassette (ABC) transporter genes PxABCC2, PxABCC3, or both. Bioassay results show that knocking out either gene alone caused at most 2.9-fold resistance but knocking out both caused >10,320-fold resistance to Cry1Ac and 380-fold resistance to Cry1Fa. Cry1Ac resistance in the double knockout strain was recessive and genetically linked with the PxABCC2/PxABCC3 loci. The results provide insight into the mechanism of cross-resistance to Cry1Fa in diamondback moth. They also confirm previous work with this pest showing that mutations disrupting both genes cause higher resistance to Cry1Ac than mutations affecting either PxABCC2 or PxABCC3 alone. Together with previous work, the results here highlight the value of using single and multiple gene knockouts to better understand the independent and synergistic effects of putative Bt toxin receptors on resistance to Bt toxins.


Assuntos
Transportadores de Cassetes de Ligação de ATP/genética , Toxinas de Bacillus thuringiensis/química , Toxinas de Bacillus thuringiensis/farmacologia , Endotoxinas/química , Endotoxinas/farmacologia , Proteínas Hemolisinas/química , Proteínas Hemolisinas/farmacologia , Resistência a Inseticidas/genética , Mariposas/efeitos dos fármacos , Mariposas/genética , Animais , Bacillus thuringiensis , Sistemas CRISPR-Cas , Edição de Genes , Larva , Proteína 2 Associada à Farmacorresistência Múltipla , Proteínas de Neoplasias
10.
J Food Sci ; 85(10): 3363-3371, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32885433

RESUMO

The objectives of this study were to develop insect-resistant adhesives and apply them to a cardboard packaging system for preventing Plodia interpunctella (Hübner) (Lepidoptera: Pyralidae) larvae infestation. Cinnamon essential oil (CO), an insecticide, was encapsulated with maltodextrin (CS/MD/CO), ß-cyclodextrin (CS/ß-CD/CO), and polyvinyl alcohol (CS/PVA/CO) in corn starch (CS) paste. This resulted in a sustained and gradual release of CO from the starch-based insect-proof adhesives. Penetration pathways of insects into corrugated cardboard boxes were investigated through the use of a screening test for infestation profiling. Microscopic images of encapsulated CO in an oil in water (O/W) emulsion were observed to confirm the morphology of the adhesives. Adhesion forces of CS, CS/CO, CS/MD/CO, CS/ß-CD/CO, and CS/PVA/CO were determined to be 6.2 N, 4.0 N, 3.1 N, 6.0 N, and 5.8 N, respectively. Consequently, significant decreases of adhesion force in the CS/CO and CS/MD/CO were found to be due to the presence of the surfactant (Span® 80) and the low adhesive properties of MD. The duration of the insecticidal activities of the developed adhesives was evaluated by measuring their release rates for 14 days and repellent profiles up to 24 hr and 40 days. As a result, CS/ß-CD/CO and CS/PVA/CO were found to have an inhibited rapid release and sustained repellent profiles. In conclusion, CS/ß-CD/CO and CS/PVA/CO were determined to be suitable for encapsulation models and could be applied to industrial cardboard containers to prevent cases of insect invasion. PRACTICAL APPLICATION: Corn starch-based natural adhesives with an insect-proof property were applied to food containers consisted of corrugated cardboard boxes. Cornflake cereal packaging using insect-proof corrugated cardboard successfully prohibited pest invasion in commercial food distribution simulation model. Developed insecticidal adhesives are able to control insect penetration in distribution and storage steps.


Assuntos
Cinnamomum zeylanicum/química , Repelentes de Insetos/farmacologia , Mariposas/efeitos dos fármacos , Óleos Voláteis/farmacologia , Óleos de Plantas/farmacologia , Adesivos , Animais , Embalagem de Alimentos/métodos , Repelentes de Insetos/química , Insetos/efeitos dos fármacos , Larva/efeitos dos fármacos , Óleos Voláteis/química , Óleos de Plantas/química , Álcool de Polivinil , Amido
11.
J Agric Food Chem ; 68(40): 11282-11289, 2020 Oct 07.
Artigo em Inglês | MEDLINE | ID: mdl-32926621

RESUMO

Fluorinated organic compounds represent a growing and important family of commercial chemicals. Introduction of fluorine into active ingredients has become an effective way to develop modern crop protection products. Given the particular properties of fluorine and high efficiency and selectivity of diamide insecticides, we designed and synthesized 27 anthranilic diamides analogues containing fluoro-sustituted phenylpyrazole. A preliminary bioassay indicated that most target compounds exhibited good biological activity against Mythimna separata and Plutella xylostella. Compound IIIf containing a 2,4,6-trifluoro-substituted benzene ring showed 43% insecticidal activity against M. separata at 0.1 mg L-1, while the control chlorantraniliprole was 36%. The activity of IIIe against P. xylostella at 10-5 mg L-1 was 94%, compared with that of the control being 70%. Thus, introduction of fluorine into diamide insecticides was useful for increasing activity. Insect electrophysiology studies showed that the calcium concentration in the nerve cells of third M. separata larvae was elevated by IIIf, which further confirmed that ryanodine receptor (RyR) was its potential target.


Assuntos
Benzeno/química , Inseticidas/síntese química , Inseticidas/farmacologia , Pirazóis/química , Animais , Benzeno/farmacologia , Bloqueadores dos Canais de Cálcio/química , Bloqueadores dos Canais de Cálcio/farmacologia , Proteínas de Insetos/antagonistas & inibidores , Proteínas de Insetos/química , Proteínas de Insetos/metabolismo , Inseticidas/química , Larva/efeitos dos fármacos , Larva/crescimento & desenvolvimento , Larva/metabolismo , Estrutura Molecular , Mariposas/efeitos dos fármacos , Mariposas/crescimento & desenvolvimento , Mariposas/metabolismo , Pirazóis/farmacologia , Canal de Liberação de Cálcio do Receptor de Rianodina/química , Canal de Liberação de Cálcio do Receptor de Rianodina/metabolismo , Relação Estrutura-Atividade
12.
J Agric Food Chem ; 68(39): 10618-10625, 2020 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-32866373

RESUMO

On the basis of the scaffolds widely used in drug design, a series of novel spirooxindole derivatives containing hydantoin, thiohydantoin, urea, and thiourea moieties have been designed, synthesized, characterized, and first evaluated for their biological activities. The diastereoselectivity mechanism is proposed, and the systematic conformational analysis is performed. The bioassay results show that the target compounds possess moderate to good antiviral activities against tobacco mosaic virus (TMV), among which compound 22 shows the highest antiviral activity in vitro as well as inactivation, curative, and protection activities in vivo (45 ± 1, 47 ± 3, 50 ± 1, and 51 ± 1%, 500 mg/L, respectively), higher than ribavirin (38 ± 1, 36 ± 1, 38 ± 1, and 36 ± 1%, 500 mg/L, respectively). Thus, compound 22 is a promising candidate for anti-TMV development. Most of these compounds show broad-spectrum fungicidal activities against 14 kinds of phytopathogenic fungi and selective fungicidal activities against Physalospora piricola, Sclerotinia sclerotiorum, and Rhizoctonia cerealis. Additionally, some of these compounds exhibit insecticidal activity against Culex pipiens pallens, Mythimna separata, Helicoverpa armigera, and Pyrausta nubilalis. Compound 17 exhibits the highest larvicidal activity (LC50 was 0.32 mg/L) against C. pipiens pallens.


Assuntos
Antivirais/síntese química , Antivirais/farmacologia , Fungicidas Industriais/síntese química , Fungicidas Industriais/farmacologia , Inseticidas/síntese química , Inseticidas/farmacologia , Animais , Antivirais/química , Culex/efeitos dos fármacos , Desenho de Fármacos , Fungos/efeitos dos fármacos , Fungicidas Industriais/química , Hidantoínas/química , Inseticidas/química , Estrutura Molecular , Mariposas/efeitos dos fármacos , Relação Estrutura-Atividade , Tioidantoínas/química , Tioureia/química , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Ureia/química
13.
Ecotoxicol Environ Saf ; 201: 110828, 2020 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-32531576

RESUMO

Toosendanin (TSN), which is extracted from the root bark of Melia toosendan Siebold and Zuccarini, has multiple modes of action against insects. Especially, this compound has a potent stomach poisoning activity against several lepidoptera pests. In this paper, the signs of toxicity, digestive enzymes activity, the histopathological changes and immuno-electron microscopic localization of TSN in the midgut epithelium of Mythimna separate Walker larvae were investigated for better understanding its action mechanism against insects. The bioassay results indicated that TSN has strong stomach poisoning against the fifth-instar larvae of M. separata (LC50 = 252.23 µg/mL). The typical poisoned symptom were regurgitation and paralysis. Activities of digestive enzymes had no obvious changes after treatment with LC80 dose of TSN. The midgut epithelial cells of insect were damaged by TSN, showing the degeneration of microvilli, hyperplasia of smooth endoplasmic reticulum and condensation of chromatin. Immunohistochemical analysis revealed that the gold particles existed on the microvilli of columnar cells and goblet cells, and gradually accumulated with the exacerbation of poisoning symptoms, showing that TSN targets on the microvilli of the midgutcells. Therefore, TSN acts on digestive system and locates in the microvilli of midgutcells of M. separata.


Assuntos
Sistema Digestório/efeitos dos fármacos , Medicamentos de Ervas Chinesas/farmacologia , Células Epiteliais/efeitos dos fármacos , Inseticidas/farmacologia , Larva/efeitos dos fármacos , Microvilosidades/efeitos dos fármacos , Mariposas/efeitos dos fármacos , Animais , Sistema Digestório/ultraestrutura , Células Epiteliais/ultraestrutura , Microscopia Eletrônica de Transmissão , Microvilosidades/ultraestrutura , Mariposas/crescimento & desenvolvimento
14.
Chemosphere ; 256: 127103, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32447114

RESUMO

The effects of Ajwain essential oil and its major constituents were investigated against newly fourth instar larvae of Tuta absoluta, a major pest of tomato cropping in Iran and other parts of the world. The study included individual efficacy of each compound and determination of their synergistic or antagonistic efficacy. We also determined the activities of detoxifying enzymes in treated insects. According to the results, the Ajwain essential oil and thymol showed the highest toxicity against T. absoluta larvae (LC50 = 6.14 and 7.72 µL/mL, respectively, and LC30 = 3.05 and 3.57 µL/mL, respectively). The ɤ-terpinene and p-cymene had lesser toxicity compared to other compounds. The larvicidal potency increased by binary mixtures of active constituents, such as thymol + p-cymene and thymol + É¤-terpinene. On the other hand, ɤ-terpinene + p-cymene mixture demonstrated antagonistic effect on the larvae. The esterases and glutathione S-transferases were significantly increased in all treatments. Finally, our results revealed a significant inhibition of AChE activity in the treated larvae by all treatments except for ɤ-terpinene + p-cymene. In vitro experiments representing AChE inhibition with IC50 values were recorded 0.370, 0.457, 0.528, 1.094 and 1.323 µL/mL for thymol + p-cymene, thymol + É¤-terpinene, thymol, ɤ-terpinene and p-cymene, respectively. Thymol demonstrated significant potential as a controlling agent of T. absoluta larvae, both larvicidal, compatible with other compounds with strong AChE inhibition properties. These finding could pave the way for development of new botanicals based on EO constituents which should be completed with preparation of an efficient formulation and field trials.


Assuntos
Apiaceae , Lepidópteros/efeitos dos fármacos , Óleos Voláteis/toxicidade , Animais , Carum , Cimenos , Irã (Geográfico) , Larva/efeitos dos fármacos , Solanum lycopersicum , Mariposas/efeitos dos fármacos , Timol/toxicidade
15.
J Agric Food Chem ; 68(22): 6092-6103, 2020 Jun 03.
Artigo em Inglês | MEDLINE | ID: mdl-32392414

RESUMO

Athetis lepigone is a polyphagous pest found around the world that feeds on maize, wheat, and various other important crops. Although it exhibits a degree of resistance to various chemical insecticides, an effective pest-control method has not yet been developed. The sex pheromone communication system plays an essential role in the mating and reproduction of moths, in which pheromone-binding proteins (PBPs) are crucial genes. In this study, we cloned and purified the protein AlepPBP1 using an E. coli expression system and found it had a higher binding affinity to two sex pheromones of A. lepigone, namely, Z7-12:Ac and Z9-14:Ac (with Ki 0.77 ± 0.10 and 1.10 ± 0.20 µM, respectively), than to other plant volatiles. The binding-mode analysis of protein conformation with equilibrium stabilization was obtained using molecular dynamics (MD) simulation and indicated that hydrophobic interactions involving several nonpolar residues were the main driving force for the binding affinity of AlepPBP1 with sex pheromones. Computational alanine scanning (CAS) was performed to further identify key amino acid residues and validate their binding contributions. Each key residue, including Phe36, Trp37, Val52, and Phe118, was subsequently mutated into alanine using site-directed mutagenesis. Binding assays showed that the efficient binding abilities to Z7-12:Ac (F36A, W37A, and F118A) and Z9-14:Ac (F36A, W37A, V52A, and F118A) were almost lost in the mutated proteins. Our results demonstrated that these key amino acid residues are crucial for determining the binding ability of AlepPBP1 to sex pheromones. These findings provide a basis for the use of AlepPBP1 in the studies as a specific target for the development of novel behavioral antagonists with marked inhibition or mating-disruption abilities using computer-aided drug design (CADD).


Assuntos
Proteínas de Transporte/metabolismo , Proteínas de Insetos/metabolismo , Mariposas/metabolismo , Atrativos Sexuais/metabolismo , Motivos de Aminoácidos , Animais , Proteínas de Transporte/química , Proteínas de Transporte/genética , Feminino , Proteínas de Insetos/química , Proteínas de Insetos/genética , Cinética , Masculino , Simulação de Acoplamento Molecular , Mariposas/química , Mariposas/efeitos dos fármacos , Mariposas/genética , Ligação Proteica , Atrativos Sexuais/química , Atrativos Sexuais/farmacologia
16.
Arch Insect Biochem Physiol ; 104(3): e21676, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32323892

RESUMO

The gut microbiota plays an important role in pheromone production, pesticide degradation, vitamin synthesis, and pathogen prevention in the host animal. Therefore, similar to gut morphology and digestive enzyme activity, the gut microbiota may also get altered under plant defensive compound-induced stress. To test this hypothesis, Dendrolimus superans larvae were fed either aconitine- or nicotine-treated fresh leaves of Larix gmelinii, and Lymantria dispar larvae were fed either aconitine- or nicotine-treated fresh leaves of Salix matsudana. Subsequently, the larvae were sampled 72hr after diet administration and DNA extracted from larval enteric canals were employed for gut microbial 16S ribosomal RNA gene sequencing (338 F and 806 R primers). The sequence analysis revealed that dietary nicotine and aconitine influenced the dominant bacteria in the larval gut and determined their abundance. Moreover, the effect of either aconitine or nicotine on D. superans and L. dispar larvae had a greater dependence on insect species than on secondary plant metabolites. These findings further our understanding of the interaction between herbivores and host plants and the coevolution of plants and insects.


Assuntos
Aconitina/farmacologia , Microbioma Gastrointestinal/efeitos dos fármacos , Mariposas/microbiologia , Nicotina/farmacologia , Animais , Bactérias/classificação , Bactérias/genética , Larix , Larva/efeitos dos fármacos , Larva/microbiologia , Mariposas/efeitos dos fármacos , Mariposas/crescimento & desenvolvimento , Folhas de Planta , RNA Ribossômico 16S , Salix
17.
Biomolecules ; 10(4)2020 03 27.
Artigo em Inglês | MEDLINE | ID: mdl-32230960

RESUMO

Amphibian skin is a multifunctional organ that plays key roles in defense, breathing, and water balance. In this study, skin secretion samples of the fire salamander (Salamandra salamandra) were separated using RP-HPLC and de novo sequenced using MALDI-TOF MS/MS. Next, we used an in silico platform to screen antioxidant molecules in the framework of density functional theory. One of the identified peptides, salamandrin-I, [M + H]+ = 1406.6 Da, was selected for solid-phase synthesis; it showed free radical scavenging activity against DPPH and ABTS radicals. Salamandrin-I did not show antimicrobial activity against Gram-positive and -negative bacteria. In vitro assays using human microglia and red blood cells showed that salamandrin-I has no cytotoxicity up to the concentration of 100 µM. In addition, in vivo toxicity tests on Galleria mellonella larvae resulted in no mortality at 20 and 40 mg/kg. Antioxidant peptides derived from natural sources are increasingly attracting interest. Among several applications, these peptides, such as salamandrin-I, can be used as templates in the design of novel antioxidant molecules that may contribute to devising strategies for more effective control of neurological disease.


Assuntos
Proteínas de Anfíbios/química , Proteínas de Anfíbios/farmacologia , Antioxidantes/farmacologia , Salamandra , Pele/química , Proteínas de Anfíbios/isolamento & purificação , Animais , Antibacterianos/química , Antibacterianos/farmacologia , Antioxidantes/química , Dicroísmo Circular , Avaliação Pré-Clínica de Medicamentos , Humanos , Testes de Sensibilidade Microbiana , Mariposas/efeitos dos fármacos , Peptídeos/química , Peptídeos/farmacologia , Testes de Toxicidade
18.
J Chem Ecol ; 46(3): 308-316, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32016775

RESUMO

Polyphenol oxidases (PPOs) as inducible defense proteins, contribute to tea (Camellia sinensis) resistance against tea geometrid larvae (Ectropis grisescens), and this resistance has been associated with the jasmonic acid (JA) signaling by testing geometrid performance in our previous work. However, the regulation of PPO-based defense by JA and other hormone signaling underlying these defense responses is poorly understood. Here, we investigated the role of phytohormones in regulating the PPO response to tea geometrids. We profiled levels of defense hormones, PPO activity and CsPPO genes in leaves infested with tea geometrids. Then, hormone levels were manipulated by exogenous application of methyl jasmonate (MeJA), gibberellin acid (GA3), abscisic acid (ABA), JA biosynthesis inhibitors (sodium diethyldithiocarbamate trihydrate, DIECA and salicylhydroxamic acid, SHAM) and GA inhibitor (uniconazole, UNI). Upon geometrid attack, JA levels significantly increased, whereas GA levels notably decreased and ABA level was slightly decreased. And the PPO activity significantly increased in line with the transcript levels of CsPPO2 and CsPPO4 but not CsPPO1. There were an obvious antagonistic cross-talk between JA and GA signals and an association among JA signals, PPO response and herbivore resistance in tea plants. Pretreatment with MeJA increased PPO activity by activating the transcripts of CsPPO2 and CsPPO4, whereas application of JA inhibitor DIECA suppressed PPO activity. GA3 strongly enhanced PPO activity, but ABA did not alter PPO activity. These findings strongly suggest that JA is a central player in PPO-mediated tea resistance against tea geometrids in a manner that prioritizes defense over growth.


Assuntos
Antibiose , Camellia sinensis/metabolismo , Catecol Oxidase/metabolismo , Ciclopentanos/metabolismo , Mariposas/fisiologia , Oxilipinas/metabolismo , Reguladores de Crescimento de Plantas/farmacologia , Proteínas de Plantas/metabolismo , Ácido Abscísico/metabolismo , Acetatos/metabolismo , Animais , Antibiose/efeitos dos fármacos , Camellia sinensis/efeitos dos fármacos , Ciclopentanos/antagonistas & inibidores , Giberelinas/antagonistas & inibidores , Giberelinas/metabolismo , Herbivoria/efeitos dos fármacos , Larva/efeitos dos fármacos , Larva/fisiologia , Mariposas/efeitos dos fármacos , Oxilipinas/antagonistas & inibidores , Transdução de Sinais
19.
Food Chem Toxicol ; 138: 111184, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32061727

RESUMO

Marsh rosemary (Ledum palustre, Ericaceae) has been widely used in the traditional medicine of various regions worldwide, and as insect repellent. Little is known on its essential oil insecticidal potential. This study explored the insecticidal effects of the essential oil obtained from L. palustre growing in Poland on selected insect pests and vectors. GC-MS analysis evidenced an uncommon chemotype characterized by ascaridole (35.3% as sum of cis-ascaridole and isoascaridole) and p-cymene (25.5%). The essential oil was effective against Culex quinquefasciatus, Spodoptera littoralis and Musca domestica, showing LC50/LD50 of 66.6 mg L-1, 117.2 µg larva-1 and 61.4 µg adult-1, respectively. It was not toxic to non-target Eisenia fetida earthworms and moderately toxic to Daphnia magna microcrustaceans, over the positive control α-cypermethrin. The essential oil cytotoxicity on human keratinocytes and fibroblasts showed high IC50 values (71.3 and 84.4 µg mL-1, respectively). Comet assay data highlighted no DNA damages. Based on our findings, this essential oil, characterized by the ascaridole/p-cymene chemotype, could be a candidate for the formulation of botanical insecticides; large-scale production of green insecticides by this rare species may be assured by ex situ cultivation and biotechnological techniques.


Assuntos
Monoterpenos Cicloexânicos/farmacologia , Inseticidas/farmacologia , Óleos Voláteis/farmacologia , Peróxidos/farmacologia , Rosmarinus/química , Animais , Linhagem Celular , Ensaio Cometa , Culex/efeitos dos fármacos , Culicidae/efeitos dos fármacos , Monoterpenos Cicloexânicos/análise , Cimenos/análise , Cimenos/farmacologia , Daphnia/efeitos dos fármacos , Moscas Domésticas/efeitos dos fármacos , Humanos , Repelentes de Insetos/análise , Repelentes de Insetos/farmacologia , Inseticidas/análise , Queratinócitos/citologia , Queratinócitos/efeitos dos fármacos , Larva/efeitos dos fármacos , Mosquitos Vetores/efeitos dos fármacos , Mariposas/efeitos dos fármacos , Óleos Voláteis/análise , Oligoquetos/efeitos dos fármacos , Peróxidos/análise , Polônia , Piretrinas/análise , Piretrinas/farmacologia , Spodoptera/efeitos dos fármacos
20.
J Insect Sci ; 20(1)2020 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-32061083

RESUMO

Plant tannins, polyphenolic plant secondary metabolites are involved in important chemical defense processes in plants. In this study, tannic acid was used as the standard of plant tannins to determine the effects on nutritional indices and activities of glutathione S-transferases (GSTs), cytochrome P450 monooxygenase (CYP450), carboxylesterase (CarE), and acetylcholinesterase (AChE) in fourth-instar larvae of Hyphantria cunea (Drury) by feeding on an artificial diet containing tannic acid under different treatments. We found that tannic acid significantly affected the digestive capacity and food utilization rate of H. cunea larvae. A tannic acid concentration of less than 2.0% promoted feeding and the utilization of undesirable food by H. cunea larvae, while inhibitory effects were observed at high concentrations (>2.5%). Tannic acid had a significant effect on the activity of detoxification enzymes and AChE in H. cunea larvae in concentration-dependent and time-dependent manners (P < 0.05). These results provide new insights into the potential mechanisms underlying detoxification in H. cunea larvae against tannic acid in host plants.


Assuntos
Mariposas/efeitos dos fármacos , Taninos/farmacologia , Acetilcolinesterase/metabolismo , Fenômenos Fisiológicos da Nutrição Animal , Animais , Carboxilesterase/metabolismo , Sistema Enzimático do Citocromo P-450/metabolismo , Glutationa Transferase/metabolismo , Inativação Metabólica , Larva/efeitos dos fármacos , Larva/enzimologia , Mariposas/enzimologia , Mariposas/crescimento & desenvolvimento
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