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1.
J Invertebr Pathol ; 192: 107770, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-35597278

RESUMEN

The olive leaf moth (jasmine moth), Palpita vitrealis (Lepidoptera: Crambidae), is an important insect pest of olives in several Mediterranean countries. A new alphabaculovirus was isolated from diseased larvae of P. vitrealis in Egypt, first in Giza in spring 2005 and again in Marsa Matrouh in 2019.The larvae exhibited typical symptoms of a baculovirus infection. Light and scanning electron microscopy studies revealed polyhedral occlusion bodies. Transmission electron microscopy of ultrathin sections of purified OBs revealed virions with multiple embedded nucleocapsids. The identity of the two virus isolates was confirmed by sequencing the partial polyhedrin and lef-8 genes, and sequence comparison suggested a relationship to group I alphabaculoviruses. Therefore, this virus was termed Palpita vitrealis nucleopolyhedrovirus (PaviNPV). Whole genome sequencing of the PaviNPV isolate from Giza (Gz05) revealed a genome of 117,533 bp, 131 open reading frames (ORFs) and four homologous repeat (hr) regions. Phylogenetic reconstruction and genetic distance analyses using 38 core genes indicated that PaviNPV should be considered to belong to a novel species within the genus Alphabaculovirus. In bioassays, PaviNPV was highly virulent against second-instar larvae of P. vitrealis. The study reports a novel baculovirus that might have potential as a biological control agent of the olive leaf moth.


Asunto(s)
Mariposas Nocturnas , Nucleopoliedrovirus , Olea , Animales , Egipto , Genoma Viral , Larva , Olea/genética , Filogenia , Hojas de la Planta
2.
J Econ Entomol ; 110(3): 924-930, 2017 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-28460121

RESUMEN

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.


Asunto(s)
Nucleopoliedrovirus/fisiología , Control Biológico de Vectores/métodos , Spodoptera/virología , Animales , Larva/crecimiento & desarrollo , Larva/virología , Nucleopoliedrovirus/efectos de la radiación , Arabia Saudita , Spodoptera/crecimiento & desarrollo , Luz Solar
3.
Virology ; 410(2): 360-7, 2011 Feb 20.
Artículo en Inglés | MEDLINE | ID: mdl-21190707

RESUMEN

An up to 10,000-fold resistance against the biocontrol agent Cydia pomonella granulovirus (CpGV) was observed in field populations of codling moth, C. pomonella, in Europe. Following different experimental approaches, a modified peritrophic membrane, a modified midgut receptor, or a change of the innate immune response could be excluded as possible resistance mechanisms. When CpGV replication was traced by quantitative PCR in different tissues of susceptible and resistant insects after oral and intra-hemocoelic infection, no virus replication could be detected in any of the tissues of resistant insects, suggesting a systemic block prior to viral DNA replication. This conclusion was corroborated by fluorescence microscopy using a modified CpGV (bacCpGV(hsp-eGFP)) carrying enhanced green fluorescent gene (eGFP), which showed that infection in resistant insects did not spread. In conclusion, the different lines of evidence indicate that CpGV can enter but not replicate in the cells of resistant codling moth larvae.


Asunto(s)
Granulovirus/patogenicidad , Lepidópteros/virología , Replicación Viral , Animales , ADN Viral/biosíntesis , Europa (Continente) , Genes Reporteros , Proteínas Fluorescentes Verdes/metabolismo , Microscopía Fluorescente , Reacción en Cadena de la Polimerasa/métodos , Coloración y Etiquetado/métodos
4.
J Invertebr Pathol ; 84(2): 75-82, 2003 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-14615215

RESUMEN

The common cutworm (Agrotis segetum) and the black cutworm (Agrotis ipsilon) are serious soil pests of many vegetable and field crops all over the world. We have demonstrated the cross-infectivity of two baculoviruses, A. segetum nucleopolyhedrovirus (AgseNPV) and A. ipsilon nucleopolyhedrovirus (AgipNPV) for these two insect pests. The susceptibility of A. segetum to AgipNPV was confirmed by DNA restriction endonuclease analyses of DNA isolated from virus harvested from infected A. segetum larvae. For an initial comparison of both viruses, partial polyhedrin sequences were amplified by PCR, cloned, and sequenced. Both viruses shared a very similar polyhedrin gene sequence resulting in only three amino acid substitutions. Phylogenetic analyses clearly demonstrated that both viruses belong to NPV group II and are most closely related to a clade consisting of Spodoptera exigua NPV, Spodoptera frugiperda NPV, and Spodoptera littoralis NPV. Since AgipNPV shows high virulence for both cutworm species, it appears to be a suitable candidate as a single biological control agent of A. segetum and A. ipsilon.


Asunto(s)
ADN Viral/análisis , Lepidópteros/virología , Nucleopoliedrovirus/genética , Nucleopoliedrovirus/patogenicidad , Filogenia , Animales , Secuencia de Bases , Enzimas de Restricción del ADN , Datos de Secuencia Molecular , Proteínas de la Matriz de Cuerpos de Oclusión , Control Biológico de Vectores , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN , Proteínas Virales/genética , Proteínas Estructurales Virales
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