RESUMO
Spray-dried animal plasma (SDP) in feed for several animal species provides health benefits, but research about use of SDP in shrimp feed is very limited. The objectives of the present study were to investigate the effects of dietary SDP on growth performance, feed utilization, immune responses, and prevention of Vibrio parahaemolyticus infection in Pacific white shrimp (Litopenaeus vannamei). In Experiment 1, the post-larvae were divided into five groups (four tank/group and 80 shrimp/tank) and fed four times daily diets with porcine SDP at 0, 1.5, 3, 4.5, and 6% of the diet for 45 days. In Experiment 2, the surviving shrimp from Experiment 1 were redistributed into six groups: four SDP groups as in Experiment 1 plus the positive and negative controls (four tank/group and 30 shrimp/tank). They were then challenged with V. parahaemolyticus by immersion at 105 colony-forming units (CFU)/mL and were fed with the same diets for another 4 days. In Experiment 1, shrimp fed 4.5% or 6% SDP diets had significantly higher body weight, survival rate, and improved feed conversion ratio. The immune parameters (total hemocyte count and phagocytic, phenoloxidase, and superoxide dismutase activities) of the shrimp fed 3-6% SDP diets also showed significant enhancement compared to the control. In Experiment 2, the survival rates of the 3-6% SDP groups were significantly higher than the positive control at day 4 after the immersion challenge. Likewise, the histopathological study revealed milder signs of bacterial infection in the hepatopancreas of the 3-6% SDP groups compared to the challenged positive control and 1.5% SDP groups. In conclusion, shrimp fed diets with SDP, especially at 4.5-6% of the diet, showed significant improvement in overall health conditions and better resistance to V. parahaemolyticus infection.
Assuntos
Suplementos Nutricionais/análise , Resistência à Doença , Penaeidae/crescimento & desenvolvimento , Plasma/química , Vibrio parahaemolyticus/imunologia , Ração Animal/análise , Animais , Peso Corporal , Hemócitos/metabolismo , Imunidade Inata , Larva/crescimento & desenvolvimento , Larva/imunologia , Larva/virologia , Penaeidae/imunologia , Penaeidae/virologia , Fagócitos/metabolismo , Secagem por Atomização , SuínosRESUMO
ETHNOPHARMACOLOGICAL RELEVANCE: Traditional Indian medicine has utilized Aeglemarmelos (L.) Corr. commonly called as bael in several indigenous systems against various diseases. Bioactive components isolated from various plant parts of A. marmelos were used in ethno-medicine. More precisely they are known for its antiviral property against various human and animal viruses. AIM OF THE STUDY: The study was conducted to investigate the antiviral activity of A.marmelos against Bombyx mori nucleopolyhedrovirus (BmNPV). MATERIALS AND METHODS: Among the various crude extracts tested, hexane extracts of leaves of A. marmelos with promising anti-BmNPV activity was subjected to bioactivity guided fractionation based on column chromatography. Out of 40 fractions obtained from the fractionation, fractions showing similar TLC profiles were pooled into 14 fractions. A fraction with potential activity was used to purify a molecule with anti-BmNPV activity. This molecule was characterized through structural and functional analyses. RESULTS: The functionally and structurally characterized molecule in the fraction with prospective anti-BmNPV activity revealed a single crystal compound 'seselin' (8, 8-dimethyl pyrido oxazine-2-one). CONCLUSION: It is therefore understood that this seselin compound could be used as a natural medicine for the management of NPV infection in the silkworm larvae under commercial conditions after suitable field evaluations.
Assuntos
Aegle , Antivirais/uso terapêutico , Bombyx/efeitos dos fármacos , Cumarínicos/uso terapêutico , Larva/efeitos dos fármacos , Animais , Antivirais/farmacologia , Bombyx/virologia , Cumarínicos/farmacologia , Trato Gastrointestinal/efeitos dos fármacos , Trato Gastrointestinal/patologia , Hemócitos/efeitos dos fármacos , Proteínas de Insetos/metabolismo , Larva/virologia , Simulação de Acoplamento Molecular , Nucleopoliedrovírus , Extratos Vegetais/farmacologia , Extratos Vegetais/uso terapêutico , Folhas de PlantaRESUMO
The viral cathepsin from Bombyx mori Nuclear Polyhedrosis Virus (BmNPV-Cath) is a broad-spectrum protease that participates in the horizontal transmission of this virus in silkworm by facilitating solubilization of the integument of infected caterpillars. When a B. mori farm is attacked by BmNPV, there are significant sericultural losses because no drugs or therapies are available. In this work, the structure of viral cathepsin BmNPV-Cath was used as a target for virtual screening simulations, aiming to identify potential molecules that could be used to treat the infection. Virtual screening of the Natural Products library from the Zinc Database selected four molecules. Theoretical calculations of ΔGbinding by the molecular mechanics Poisson-Boltzmann surface analysis (MM-PBSA) method indicated that the molecule Zinc12888007 (Bm5) would have high affinity for the enzyme. The in vivo infection models of B. mori caterpillars with BmNPV showed that treatment with a dose of 100 µg Bm5 dissolved in Pluronic-F127 0.02% was able to reduce the mortality of caterpillars in 22.6%, however, it did not impede the liquefaction of dead bodies. Our results suggest a role of BmNPV-Cath in generating a pool of amino acids necessary for viral replication and indicate a mechanism to be exploited in the search for treatments for grasserie disease of the silkworm.
Assuntos
Bombyx/virologia , Catepsinas/química , Simulação de Acoplamento Molecular , Simulação de Dinâmica Molecular , Nucleopoliedrovírus/enzimologia , Proteínas Virais/química , Animais , Avaliação Pré-Clínica de Medicamentos , Larva/virologia , Ligantes , Estrutura Terciária de Proteína , Pupa/virologia , Análise de SobrevidaRESUMO
Nucleopolyhedrovirus is an effective biocontrol agent but for its biggest disadvantage of short persistence under sunlight conditions. In this study, 10 plant extracts were evaluated as ultraviolet (UV) protectants to improve the persistence of Spodoptera littoralis multiple-embedded nucleopolyhedrovirus (SpliMNPV) against cotton leafworm (Spodoptera littoralis Boisduval). In the primary lab screening test, 5 out of 10 additives (cloves, henna, green tea, pomegranate, and grape extracts) presented a high rate of virus protection with original activity remaining (OAR) percentage of 100%, 97%, 91%, 90.6%, and 77%, respectively, when used at a concentration of 1% and exposed to UVB for a period of 1 h. A secondary screening was then performed with these best five extracts at a concentration of 0.5% and for an exposure timing of 5 h to UVB. Among these, clove and henna that showed highest protection with OAR values of 96.6% and 76.5%, respectively, were selected for the field trials. When applied on cabbage in the field during sunny summer conditions, clove and henna extracts enhanced the persistence of SpliMNPV by twofold. These findings are encouraging to be applied in the field studies.
Assuntos
Nucleopoliedrovírus/fisiologia , Controle Biológico de Vetores/métodos , Spodoptera/virologia , Animais , Larva/crescimento & desenvolvimento , Larva/virologia , Nucleopoliedrovírus/efeitos da radiação , Arábia Saudita , Spodoptera/crescimento & desenvolvimento , Luz SolarRESUMO
The smaller tea tortrix, Adoxophyes honmai (Lepidoptera: Tortricidae), is an economically important pest of tea in Japan. Previous work showed that a fast-killing nucleopolyhedrovirus (NPV) isolated from A. orana (AdorNPV) and a slow-killing NPV isolated from A. honmai (AdhoNPV) are both infectious to A. honmai larvae. Field application of these different NPVs was conducted against an A. honmai larval population in tea plants, and the control efficacy and transmission rate of the two NPVs were compared. The slow-killing AdhoNPV showed lower field efficacy, in terms of preventing damage caused by A. honmai larvae against the tea plants, than the fast-killing AdorNPV. However, AdhoNPV had a significantly higher horizontal transmission rate than AdorNPV. These results show that AdorNPV is suitable as an inundative agent, while AdhoNPV is an appropriate inoculative agent.
Assuntos
Lepidópteros/fisiologia , Lepidópteros/virologia , Nucleopoliedrovírus/crescimento & desenvolvimento , Nucleopoliedrovírus/isolamento & purificação , Animais , Japão , Larva/fisiologia , Larva/virologia , Controle Biológico de Vetores/métodos , Análise de Sobrevida , Chá/parasitologiaRESUMO
BACKGROUND & OBJECTIVES: Mosquito control is facing a threat due to the emergence of resistance to synthetic insecticides. Insecticides of botanical origin could serve as potential alternatives in future. Larvicidal efficacies of different parts of mangrove plants belonging to Rhizophoraceae family were tested against the late IV instar larvae of dengue vector, Aedes aegypti. METHODS: Different plant parts (leaf, bark, root, stilt root, hypocotyl and flower) of Rhizophoraceae family mangrove plants (Bruguiera cylindrica, Ceriops decandra, Rhizophora mucronata and R. apiculata) were collected from Karangadu southeast coast of India. The larval mortality was observed after 24 h exposure. Repellency bioassays were carried out in a 10 Χ 10 Χ 3 m room at 27- 35°C and 60- 80% RH. The bark (A3 and E1) and stilt root (A3 and E4) fractions of R. mucronata with different concentrations (0.25, 0.50, 0.75, 1, 2 and 4 mg/cm) were applied on one arm. RESULTS: The stilt root crude extract of R. mucronata showed maximum larvicidal activity (LC50 value 0.0275 ± 0.0066 µg/ml and LC90 = 0.0695 ± 0.156 µg/ml) followed by the bark extract (LC50 value of 0.03 ± 0.0076 µg/ml and LC90 = 0.0915 ± 0.156 µg/ml). Column chromatographic fractions of R. mucronata bark extracts (E1) showed maximum larvicidal activity (LC50 = 0.0496 ± 0.0085 µg/ml and LC90 = 0.1264 ± 0.052 µg/ml) followed by the acetone extract (LC50 = 0.0564 ± 0.0069 µg/ml and LC90 = 0.1187 ± 0.05 µg/ml). Ethanolic fraction (E4) of R. mucronata stilt root extracts showed maximum larvicidal activity (LC50 = 0.0484 ± 0.0078 µg/ml and LC90 = 0.1191 ± 0.025 µg/ml) followed by acetone fraction (A3) (LC50 = 0.0419 ± 0.0059 µg/ml and LC90 = 0.0955 ± 0.069 µg/ml). Repellent activity of R. mucronata stilt root and bark extracts (A3) showed maximum percentage of protection (97.5%) with 9.1 h protection time at 4 mg concentration of the stilt root extract. Moreover, ethanolic fraction of the stilt root (E4) extract showed maximum percentage of protection (100%) with 10 h protection time at 4 mg concentration. GC-MS analysis revealed that R. mucronata possesses variety of biopesticidal compounds. INTERPRETATION & CONCLUSION: The results as well as the significance of this preliminary investigation highlight the importance of R. mucronata as a novel source for natural insecticidal products.
Assuntos
Aedes/efeitos dos fármacos , Dengue/prevenção & controle , Insetos Vetores/efeitos dos fármacos , Inseticidas/farmacologia , Controle de Mosquitos/métodos , Extratos Vegetais/farmacologia , Rhizophoraceae/química , Aedes/virologia , Animais , Bioensaio/métodos , Vírus da Dengue , Índia , Insetos Vetores/virologia , Inseticidas/análise , Inseticidas/isolamento & purificação , Larva/efeitos dos fármacos , Larva/virologia , Dose Letal Mediana , Casca de Planta/química , Extratos Vegetais/análise , Extratos Vegetais/isolamento & purificação , Raízes de Plantas/químicaRESUMO
Antimicrobial peptides (AMPs), both synthetic and from natural sources, have raised interest recently as potential alternatives to antibiotics. Cyto-insectotoxin (Cit1a) is a 69-amino-acid antimicrobial peptide isolated from the venom of the central Asian spider Lachesana tarabaevi. The synthetic gene Cit1a fused with the enhanced green fluorescent protein (EGFP) gene was expressed as the EGFP-Cit1a fusion protein using a cysteine protease-deleted Bombyx mori nucleopolyhedrovirus (BmNPV-CP(-)) bacmid in silkworm larva and pupa. The antimicrobial effect of the purified protein was assayed using disk diffusion and broth microdilution methods. The minimum inhibitory concentration of EGFP-Cit1a was also measured against several bacterial strains and showed similar antimicrobial activity to that of the synthetic Cit1a reported earlier. The EGFP-Cit1a fusion protein showed antibiotic activity toward gram-positive and gram-negative bacteria at the micromolar concentration level. These results show that active Cit1a can be produced and purified in silkworm, although this peptide is insecticidal. This study demonstrates the potential of active Cit1a purified from silkworms to use as an antimicrobial agent.
Assuntos
Peptídeos Catiônicos Antimicrobianos/isolamento & purificação , Peptídeos Catiônicos Antimicrobianos/metabolismo , Aracnídeos/enzimologia , Bactérias/efeitos dos fármacos , Venenos de Aranha/química , Animais , Peptídeos Catiônicos Antimicrobianos/genética , Aracnídeos/genética , Baculoviridae/genética , Bombyx/virologia , Clonagem Molecular , Expressão Gênica , Vetores Genéticos , Larva/virologia , Testes de Sensibilidade Microbiana , Pupa/virologia , Proteínas Recombinantes/genética , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/metabolismoRESUMO
Thrips-transmitted Iris yellow spot virus (IYSV) (Family Bunyaviridae, Genus Tospovirus) affects onion production in the United States and worldwide. The presence of IYSV in Georgia was confirmed in 2003. Two important thrips species that transmit tospoviruses, the onion thrips (Thrips tabaci (Lindeman)) and the tobacco thrips (Frankliniella fusca (Hinds)) are known to infest onion in Georgia. However, T. tabaci is the only confirmed vector of IYSV. Experiments were conducted to test the vector status of F. fusca in comparison with T. tabaci. F. fusca and T. tabaci larvae and adults reared on IYSV-infected hosts were tested with antiserum specific to the nonstructural protein of IYSV through an antigen coated plate ELISA. The detection rates for F. fusca larvae and adults were 4.5 and 5.1%, respectively, and for T. tabaci larvae and adults they were 20.0 and 24.0%, respectively, indicating that both F. fusca and T. tabaci can transmit IYSV. Further, transmission efficiencies of F. fusca and T. tabaci were evaluated by using an indicator host, lisianthus (Eustoma russellianum (Salisbury)). Both F. fusca and T. tabaci transmitted IYSV at 18.3 and 76.6%, respectively. Results confirmed that F. fusca also can transmit IYSV but at a lower efficiency than T. tabaci. To attest if low vector competency of our laboratory-reared F. fusca population affected its IYSV transmission capability, a Tomato spotted wilt virus (Family Bunyaviridae, Genus Tospovirus) transmission experiment was conducted. F. fusca transmitted Tomato spotted wilt virus at a competent rate (90%) suggesting that the transmission efficiency of a competent thrips vector can widely vary between two closely related viruses.
Assuntos
Ensaio de Imunoadsorção Enzimática/métodos , Insetos Vetores/virologia , Cebolas/virologia , Doenças das Plantas/virologia , Tisanópteros/virologia , Tospovirus/fisiologia , Agricultura , Animais , Gentianaceae/virologia , Georgia , Insetos Vetores/crescimento & desenvolvimento , Larva/crescimento & desenvolvimento , Larva/virologia , Dados de Sequência Molecular , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Análise de Sequência de RNA , Especificidade da Espécie , Tisanópteros/crescimento & desenvolvimento , Tospovirus/genéticaRESUMO
Screening and evaluating anti- hepatitis C virus (HCV) drugs in vivo is difficult worldwide, mainly because of the lack of suitable small animal models. We investigate whether zebrafish could be a model organism for HCV replication. To achieve NS5B-dependent replication an HCV sub-replicon was designed and created with two vectors, one with HCV ns5b and fluorescent rfp genes, and the other containing HCV's 5'UTR, core, 3'UTR and fluorescent gfp genes. The vectors containing sub-replicons were co-injected into zebrafish zygotes. The sub-replicon amplified in liver showing a significant expression of HCV core RNA and protein. The sub-replicon amplification caused no abnormality in development and growth of zebrafish larvae, but induced gene expression change similar to that in human hepatocytes. As the amplified core fluorescence in live zebrafish was detectable microscopically, it rendered us an advantage to select those with replicating sub-replicon for drug experiments. Ribavirin and oxymatrine, two known anti-HCV drugs, inhibited sub-replicon amplification in this model showing reduced levels of HCV core RNA and protein. Technically, this method had a good reproducibility and is easy to operate. Thus, zebrafish might be a model organism to host HCV, and this zebrafish/HCV (sub-replicon) system could be an animal model for anti-HCV drug screening and evaluation.
Assuntos
Antivirais/farmacologia , Avaliação Pré-Clínica de Medicamentos/métodos , Hepacivirus/efeitos dos fármacos , Peixe-Zebra/virologia , Alcaloides/farmacologia , Animais , Western Blotting , Modelos Animais de Doenças , Doenças dos Peixes/prevenção & controle , Doenças dos Peixes/virologia , Amplificação de Genes/efeitos dos fármacos , Regulação Viral da Expressão Gênica/efeitos dos fármacos , Vetores Genéticos/administração & dosagem , Vetores Genéticos/genética , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Hepacivirus/genética , Hepacivirus/metabolismo , Hepatite C/genética , Hepatite C/metabolismo , Hepatite C/prevenção & controle , Hepatócitos/efeitos dos fármacos , Hepatócitos/metabolismo , Hepatócitos/virologia , Humanos , Hibridização In Situ , Larva/genética , Larva/metabolismo , Larva/virologia , Microinjeções , Microscopia de Fluorescência , Quinolizinas/farmacologia , Replicon/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Ribavirina/farmacologia , Regiões não Traduzidas/genética , Proteínas não Estruturais Virais/genética , Proteínas não Estruturais Virais/metabolismo , Peixe-Zebra/genética , Peixe-Zebra/metabolismoRESUMO
Larvae of the potato tubermoth (PTM), Phthorimaea operculella, feed on potato plants and tubers and are a major pest in the tropics and subtropics worldwide, causing up to 100% damage. The PTM granulovirus (PhopGV) provides significant potato protection, but little is known about its effect on larval development or its histopathology. Here we show that only 10% of larvae exited from PhopGV-treated tubers (1.4×10(8) granule/ml), lagging significantly behind controls, and most of these died by 72 h after emergence. Histopathology studies showed the fat body and epidermis were the principal tissues infected. PhopGV morphogenesis was similar to other GVs, the exception being small vesicles between mature granules.
Assuntos
Granulovirus/fisiologia , Mariposas/virologia , Solanum tuberosum , Animais , Granulovirus/ultraestrutura , Larva/crescimento & desenvolvimento , Larva/ultraestrutura , Larva/virologia , Mariposas/crescimento & desenvolvimento , Mariposas/ultraestrutura , Controle Biológico de VetoresRESUMO
BACKGROUND: Nucleopolyhedrovirus (SeNPV) and Microplitis pallidipes are important biological control agents of Spodoptera exigua populations. The interactions between these agents and their combined effect on pest control were investigated in the laboratory and in commercial greenhouses. RESULTS: Microplitis pallidipes searched for and deposited eggs in more healthy larvae than virus-infected larvae 3 days after viral infection. Each female parasitoid that developed in a virus-infected host oviposited in a virus-infected host, or emerged from a cocoon carrying virus transmitted to 4.0, 7.6 or 2.4 healthy larvae respectively. Each female parasitoid exposed to a mixture of virus and 10% honey water solution transmitted the virus to 2.2 healthy larvae. In an experiment with cabbage growing in commercial greenhouses, the pest population reduction was greater by M. pallidipes carrying SeNPV (82.3-89.7% reduction) than by parasitoids without virus (59.5-62.4% reduction). CONCLUSIONS: Control of S. exigua was greater with M. pallidipes plus SeNPV than with M. pallidipes alone. Microplitis pallidipes preferred healthy hosts to infected hosts. Parasitoids were able to complete their development in virus-infected hosts before the hosts died from the virus infection. The parasitoid ovipositors contaminated with the virus could carry and transmit SeNPV.
Assuntos
Himenópteros/crescimento & desenvolvimento , Himenópteros/virologia , Nucleopoliedrovírus/patogenicidade , Controle Biológico de Vetores/métodos , Spodoptera/parasitologia , Spodoptera/virologia , Animais , Beta vulgaris/parasitologia , Feminino , Himenópteros/fisiologia , Larva/parasitologia , Larva/virologia , Nucleopoliedrovírus/crescimento & desenvolvimento , Oviposição , Doenças das Plantas/parasitologia , Spodoptera/crescimento & desenvolvimento , Fatores de TempoRESUMO
Anticarsia gemmatalis nucleopolyhedrovirus (AgMNPV) is being used in Brazil as a biological insecticide. Host plant resistance of soybean to insects is been searched for and some authors have mentioned the interference of plant chemistry in virus efficiency. Interactions among soybean extracts of genotypes used as a source of resistance (PI 274454 and PI 227687) with different AgMNPV concentrations in populations of A. geatalis susceptible (S) and resistant (R) to the virus were studied at laboratory condition. Higher mortality was observed when larvae fed on diets with extracts of the soybean genotypes compared with those fed on a plain diet (control). The mean lethal concentration (LC50) was reduced about 10 ties in the S-population fed on diets containing PI 274454 extracts and different concentrations of AgMNPV, compared to control diet. Additive effect was predominantly observed when larvae fed on diets with extracts of soybean genotypes (PI 274454 and PI 227687) and AgMNPV for both larval populations. The pupal weight was negatively influenced by the extracts incorporated to the diets compared to control, for both larval populations, notably for R-population. The results suggest that, in general, leaf extracts of soybean resistant genotype did not cause any harmful effect on virus efficiency.
O nucleopoliedrovirus de Anticarsia gemmatalis (AgMNPV) tem sido utilizado como um inseticida biológico no Brasil. A resistência de plantas de soja a insetos tem sido pesquisada e alguns autores têm mencionado a interferência de substâncias químicas de plantas sobre a eficiência de vírus. As interações entre extratos de genótipos de soja utilizados como fontes de resistência (PI 274454 e PI 227687) com diferentes concentrações do AgMNPV em populações de A. gemmatalis suscetível (S) e resistente (R) ao vírus foram estudadas em condições de laboratório. Mortalidades elevadas foram observadas quando as larvas foram alimentadas com dietas contendo extratos dos genótipos de soja, em relação às larvas alimentadas com dieta artificial sem a presença de extratos (testemunha). A concentração letal média (CL50) foi reduzida em aproximadamente 10 vezes, na população s alimentada com dieta contendo extratos da PI 274454 e diferentes concentrações do AgMNPV, comparada à dieta testemunha. Um efeito aditivo foi predominantemente observado quando as larvas se alimentaram em dietas com extratos dos genótipos de soja (PI 274454 e PI 227687) e o AgMNPV, para ambas as populações (S e R). O peso de pupa foi negativamente influenciado pela dieta contendo os extratos em relação à dieta testemunha, para ambas as populações, com destaque para a população R. Os resultados indicam que, no geral, os extratos de folhas de genótipos de soja resistentes não causam efeitos negativos na eficiência do vírus.
Assuntos
Animais , Mariposas/virologia , Nucleopoliedrovírus/fisiologia , Controle Biológico de Vetores/métodos , Extratos Vegetais/farmacologia , Glycine max/química , Genótipo , Interações Hospedeiro-Parasita , Larva/virologia , Glycine max/genética , Glycine max/parasitologiaRESUMO
Anticarsia gemmatalis nucleopolyhedrovirus (AgMNPV) is being used in Brazil as a biological insecticide. Host plant resistance of soybean to insects is been searched for and some authors have mentioned the interference of plant chemistry in virus efficiency. Interactions among soybean extracts of genotypes used as a source of resistance (PI 274454 and PI 227687) with different AgMNPV concentrations in populations of A. geatalis susceptible (S) and resistant (R) to the virus were studied at laboratory condition. Higher mortality was observed when larvae fed on diets with extracts of the soybean genotypes compared with those fed on a plain diet (control). The mean lethal concentration (LC50) was reduced about 10 ties in the S-population fed on diets containing PI 274454 extracts and different concentrations of AgMNPV, compared to control diet. Additive effect was predominantly observed when larvae fed on diets with extracts of soybean genotypes (PI 274454 and PI 227687) and AgMNPV for both larval populations. The pupal weight was negatively influenced by the extracts incorporated to the diets compared to control, for both larval populations, notably for R-population. The results suggest that, in general, leaf extracts of soybean resistant genotype did not cause any harmful effect on virus efficiency.
Assuntos
Glycine max/química , Mariposas/virologia , Nucleopoliedrovírus/fisiologia , Controle Biológico de Vetores/métodos , Extratos Vegetais/farmacologia , Animais , Genótipo , Interações Hospedeiro-Parasita , Larva/virologia , Dose Letal Mediana , Glycine max/genética , Glycine max/parasitologiaRESUMO
The tea slug moth Iragoidae fasciata (Lepidoptera, Eucleidae) is one of the main insect pests that attack tea bushes. A new nucleopolyhedrovirus (NPV) called Iragoidae fasciata NPV (IrfaNPV) was recently isolated from diseased larvae. An 11,626 bp fragment of the viral genomic DNA containing the polyhedrin gene and other 12 genes was cloned and sequenced. Gene comparison and phylogenetic analysis showed that IrfaNPV is a member of the Group I NPVs. However, the genomic organization of IrfaNPV is highly distinct. In addition, electron microscopy analysis showed that IrfaNPV is a single nucleocapsid NPV (SNPV). An inoculation assay showed that IrfaNPV is semi-permissive in the Trichoplusia ni cell line Tn-5Bl-4. Bioassays on lethal concentration (LC(50)) and lethal time (LT(50)) were conducted to test the susceptibility of I. fasciata larvae to the virus.
Assuntos
Mariposas/virologia , Nucleopoliedrovírus/isolamento & purificação , Animais , Camellia sinensis/parasitologia , Linhagem Celular , Larva/virologia , Dados de Sequência Molecular , Nucleocapsídeo/genética , Nucleocapsídeo/ultraestrutura , Nucleopoliedrovírus/classificação , Nucleopoliedrovírus/genética , Nucleopoliedrovírus/ultraestrutura , FilogeniaRESUMO
A granulosis virus (GV) was isolated from the diseased caterpillars of Arctornis submarginata (Walker) (Lymantriidae), a defoliating pest of tea from Darjeeling foothill region. The phase contrast and transmission electron microscopic studies identified the virus as granulosis virus. SDS-PAGE analysis of major protein of the occlusion bodies was found to be 31 kDa, characteristic for granulin. The total genomic DNA was isolated. The major band found was of molecular weight 16 kDa. Bioassay conducted with the occlusion bodies (OBs) of the virus showed LC(50) value of 4.46 x 10(4) OBs/ml for the second instar caterpillars. Median lethal time (LT(50)) were 6.6 days for 1 x 10(4)OBs/ml, 5.09 days for 1 x 10(5) OBs/ml, 4.45 days for 1 x 10(6) OBs/ml and 3.87 days for 1 x 10(7) OBs/ml concentrations. The results indicated the potential of the virus for its future application as microbial pesticide against A. submarginata in future.
Assuntos
Camellia sinensis , Granulovirus/patogenicidade , Mariposas/virologia , Animais , Eletroforese em Gel de Poliacrilamida , Corpo Adiposo/virologia , Genoma Viral , Granulovirus/genética , Granulovirus/isolamento & purificação , Índia , Larva/crescimento & desenvolvimento , Larva/virologia , Mariposas/crescimento & desenvolvimento , Controle Biológico de Vetores , Chá , Cultura de VírusRESUMO
Liquid suspensions and dry formulations of a granulovirus (family Baculoviridae, genus Granulovirus, PoGV) derived from infected larvae and the bacterium Bacillus thuringiensis subsp. kurstaki (Berliner) (Btk) were evaluated for control of the potato tuberworm, Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), in stored tubers. Laboratory bioassays at 25 degrees C showed that both PoGV and a wettable powder (WP) formulation of Btk incorporated with carriers (water, talc, sand, diatomaceous earth, and kaolin clay), were effective against neonate larvae. Depending on the technique, 100% larval mortality was achieved at concentrations as low as 0.025 larval equivalents (LE) PoGV per kg tuber and 150 mg Btk WP per kg tuber. However, 100% mortality was never achieved with tests on preinfested tubers, ostensibly due to the higher dosage required to kill older instars inside tubers. The most effective PoGV formulations were dipping (water) and talc, with dipping most effective for postinfestation treatments, causing up to 91.6% mortality at 0.4 LE per kg. There was no significant effect of formulation in the Btk treatments. The protective effects of residues were also evaluated under longer-term storage conditions. Batches of tubers treated with PoGV or Btk via dipping (up to 0.1 LE and 150 mg WP per kg tuber) were stored in cages containing an initial potato tuberworm infestation (10% of tubers). Although potato tuberworm populations were reduced by up to 98.4% after 2 mo at 25 degrees C, no treatments prevented the development and reproduction of the F1 generation. The sprouting of stored tubers seemed to be a limiting factor for sustained control. No significant treatment effects were detected in similar cages held at 12 degrees C for 4.5 mo. Improved strategies for the application of PoGV and Btk for long-term potato tuberworm control in tuber stores, including the use of chemical sprout suppressants, are discussed.
Assuntos
Bacillus thuringiensis/fisiologia , Granulovirus/fisiologia , Mariposas/microbiologia , Controle Biológico de Vetores/métodos , Solanum tuberosum/parasitologia , Animais , Larva/crescimento & desenvolvimento , Larva/microbiologia , Larva/virologia , Mariposas/crescimento & desenvolvimento , Mariposas/virologia , Tubérculos/parasitologia , TemperaturaRESUMO
We reported that dietary selenium (Se) impacted the growth and development of Trichoplusia ni reared for many generations on diet containing extremely low levels of Se. Larvae had an elevated resistance to per os infection with a baculovirus. In this study, we examine how dietary Se (in the form of selenite) affects the growth, development, and Se content of Heliothis virescens that have been laboratory reared for less than two years. Larvae fed a commercial tobacco budworm diet supplemented with greater than 20 ppm Se grew at a slower rate than insects fed lower levels of Se and had an increase in the amount of Se sequestered in pupae. Larvae fed diets containing from 10-60 ppm Se exhibited elevated plasma concentrations of the micronutrient and increased plasma virucidal activity against Helicoverpa zea single nucleopolyhedrovirus (HzSNPV). Larvae reared on diet supplemented with 10 or 60 ppm Se until the onset of the penultimate instar were then infected per os or by injection with increasing concentrations of the baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV). Larvae fed dietary Se and infected with occluded virus per os displayed a significantly lower mortality compared with infected larvae not fed Se. Our results suggest that dietary Se levels are directly correlated with plasma Se levels, and that plasma Se levels are in turn correlated with baculovirus resistance.
Assuntos
Baculoviridae/fisiologia , Mariposas/virologia , Selênio/sangue , Animais , Dieta , Larva/virologiaRESUMO
The complete nucleotide sequence of a new insect picorna-like virus, Ectropis obliqua picorna-like virus (EoPV), which causes a fatal infection of Ectropis obliqua larvae, has been determined. The genomic RNA of EoPV is 9394 nt in length and contains a single, large open reading frame (nt 391-9351) encoding a polyprotein of 2987 aa. Sequence comparisons with other viral polyproteins revealed that the consensus sequences for picornavirus RNA helicase, protease and RNA-dependent RNA polymerase proteins are found on the genome in order in the 5'-->3' direction. All structural genes were located at the 5' terminus. In terms of sequence similarity, identity and genome organization, EoPV resembles mammalian picornaviruses and three other insect picorna-like viruses: Infectious flacherie virus of silkworm, Sacbrood virus of honeybee and Perina nuda picorna-like virus (PnPV). Phylogenetic analysis showed that EoPV is most closely related to PnPV and suggests that these four insect picorna-like viruses might constitute a new group of insect-infectious RNA viruses.