The ecdysteroid UDP-glucosyltransferase (egt) gene of a single enveloped nucleopolyhedrovirus was located using an Hz-SNPV gene-specific probe. This SNPV was found infecting a colony of Helicoverpa armigera (HaSNPV) in the Western Cape region of South Africa. The open reading frame of the HaSNPV-SA egt is 1.548 nucleotides long and encodes a predicted protein of 516 amino acids with a Mr of 58,897-kDa. The 5'-noncoding region contained an early transcription initiation motif (CAGT) and a baculovirus late transcription motif (ATAAG). A transcription enhancer sequence (GATA) was also identified. Two possible TATA boxes together with an AT rich region were also recognized. A putative signal peptide of 20 residues was present at the N-terminus of the predicted EGT sequence. A polyadenylation signal (AATAAA) was found downstream of the translation stop codon. Five Helicoverpa NPV EGT's that have an extremely high degree of nucleotide and amino acid sequence homology were used in this study. Single nucleotide polymorphisms (SNPs) within the gene were tabulated. The Helicoverpa NPV egts seem to be closely related to the egt genes of Mamestra configurata NPV (MacoNPV), Buzura suppressaria NPV (BusuSNPV) and Spodoptera exigua NPV (SeMNPV) with amino acid identities of approximately 50%. The Helicoverpa NPV EGTs show ten conserved motifs with other EGTs. A phylogenetic tree of 27 baculovirus EGTs and a human UDP-glucoronosyltransferase was constructed using Neighbour-joining within CLUSTAL X. That a secreted and active EGT is encoded by HaSNPV-SA was confirmed by assay of infected cell culture medium.
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http://dx.doi.org/10.1023/a:1025116301321 | DOI Listing |
J Gen Virol
December 2020
School of Molecular and Cell Biology, University of the Witwatersrand, Johannesburg, Private Bag 3, Wits 2050, South Africa.
Determination of the virulence of occlusion bodies (OBs), which are the horizontal transmission structures of nucleopolyhedroviruses (NPVs), is an important area of baculovirology. A method for inoculating an insect with an isolated OB was developed using Helicoverpa armigera nucleopolyhedrovirus (HearNPV) infection of second instar larvae as a model NPV-host pathosystem. In this novel method, laser capture microdissection (LCM) was used to directly catapult single OBs onto the surface of insect diet in bioassay containers.
View Article and Find Full Text PDFSaudi J Biol Sci
August 2020
Biology Department, Faculty of Science, Taibah University, Al-Sharm, Yanbu El-Bahr 46429, Saudi Arabia.
American bolloworm, Hubner (Noctuidae: Lepidoptera) is considered as a major pest of various crops all over the world. It is mainly controlled by indiscriminate use of synthetic insecticides in the world due to which this pest developed resistance to most of the available insecticides. Therefore, in the current study, the efficacy of virulent strain of HaNPV (0.
View Article and Find Full Text PDFSaudi J Biol Sci
June 2020
Institute of Plant Protection, MNS-University of Agriculture, Multan (60000), Pakistan.
Hübner (Lepidoptera: Noctuidae) is serious pests of cotton and several other crops. (HaNPV) can be important alternative to synthetic insecticides for the management of . However, the efficacy of HaNPV can vary in horizontal and vertical transmission.
View Article and Find Full Text PDFJ Econ Entomol
August 2020
Department of Biological Control, Iranian Research Institute of Plant Protection, Agricultural Research Education and Extension Organization, Tehran, Iran.
Cotton bollworm, Helicoverpa armigera Hubner, is a cosmopolitan polyphagous pest of many crops. Habrobracon hebetor Say and Helicoverpa armigera nucleopolyhedrovirus (HearNPV) are two important biocontrol agents used to manage this pest, sometimes in combination. We evaluated the sublethal effects of HearNPV on H.
View Article and Find Full Text PDFTurk J Biol
October 2019
Department of Biology, Faculty of Science, Karadeniz Technical University, Trabzon, Turkey.
This study reports a new Helicoverpa armigera nucleopolyhedrovirus (NPV) isolated from Heliothis peltigera (Denis & Schiffermuller), collected in the vicinity of Adana, Turkey. Infection was confirmed by tissue polymerase chain reaction and sequence analysis. Results showed that dead H.
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