Marlinda Lobo de Souza

Baculovirus Pesticides: Present State and Future Perspectives

Baculoviruses pesticides are ideal tools in integrated pest management programs as they are usually highly specific to their host insects; thus, they do not affect other arthropods including pest predators and parasitoids. They are also safe to vertebrates and plants and to the biosphere. Over 50 baculovirus products have been used against different insect pests worldwide, and all have been produced in vivo, mostly on insects reared on artificial diets. However, there are cases of significant viral production in the field by applying a baculovirus against natural populations of the insect host and collecting dead or moribund larvae for further processing into a formulated product. Despite the considerable number of programs worldwide utilizing baculoviruses as biopesticides, their use is still low compared to another biological insecticide based on the bacterium Bacillus thuringiensis Berliner. As of the present, there are no programs using in vitro commercial production of baculovirus due to several technical limitations, and further developments in this area are much needed. Use of the baculovirus of the velvetbean caterpillar in Brazil has experienced a setback over the past 7 years due to modifications in cultural practices by soybean growers. Slow speed of kill by viral pesticides is a limitation that has led to considerable research effort toward developing faster killing agents through genetic modifications by either deleting or inserting toxin genes from scorpions and spiders into their genomes. However, these GMOs have not been used in practice due to significant resistance by the public to modified baculovirus genomes. Effective public extension services and farmer education toward application of biopesticides are much needed to expand the use of these products worldwide.

Characterization of the Ecdysteroid UDP-Glucosyltransferase (egt) Gene of Anticarsia gemmatalis Nucleopolyhedrovirus

The Anticarsia gemmatalis nucelopolyhedrovirus (AgMNPV) egt gene was cloned, sequenced and its expression characterized by RT-PCR and western blot analysis. Sequence analysis of the gene indicated the presence of an open reading frame (ORF) of 1482 nucleotides, which codes for a polypeptide of 494 amino acids. A TATA box and a conserved regulatory sequence (CATT) found in other baculovirus early genes were present in the promoter region of the egt gene. A poly-A consensus sequence was present in the 3′ untranslated region (3′-UTR) of the gene. Homology comparisons showed that the EGT protein of AgMNPV is most closely related (95.9% amino acid sequence identity) to the EGT from the Choristoneura fumiferana DEF nucleopolyhedrovirus (CfDEF). Transcriptional analysis of the AgMNPV egt gene showed that egt-specific transcripts can be detected both early and late in infection. The EGT protein was detected, by western blot analysis, in the intra- (from 12 to 48 h post-infection) and extra-cellular (from 12 to 96 h post-infection) fractions of infected insect cells. The AgMNPV Bgl II-F fragment, which has homology to the AcMNPV ie-1 gene, was cloned and used to cotransfect SF21 cells with the cloned AgMNPV egt gene. EGT activity was observed, suggesting that AgMNPV ie-1 can transactivate egt expression.

Physical maps and virulence of Anticarsia gemmatalis nucleopolyhedrovirus genomic variants.

Summary. Seventeen plaque purified isolates of two viral preparations of Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV), were analyzed in terms of the genomic changes after digestion of their DNAs with HindIII and PstI restriction enzymes. The 1979 AgMNPV wild type preparation (AgMNPV-’79) resulted in six different variants and the 1985 viral commercial preparation (AgMNPV-’85), in eleven. The genomic variation of all the isolates was mapped showing that those from 1985 presented more heterogeneity with changes mapped in additional sites in comparison to the AgMNPV-’79 variants. Their virulence was compared by infecting two Lepidopteran cell lines, Spodoptera frugiperda (IPLB-SF-21AE) and Anticarsia gemmatalis (UFL-AG-286). The results indicated that there was some difference in virulence within the AgMNPV-’85 variants. This commercial preparation had been applied in soybean fields in Brazil over several years to control the velvetbean caterpillar defoliation.

Accumulation of few-polyhedra mutants upon serial passage of Anticarsia gemmatalis multiple nucleopolyhedrovirus in cell culture.

Anticarsia gemmatalis nucleopolyhedrovirus (AgMNPV) has been widely used to control the velvetbean caterpillar, Anticarsia gemmatalis, in Brazil. To date, AgMNPV has been produced by larval infection and, due to in vivo production limitations and the continuing high demand for the biopesticide, attempts should be made to develop in vitro production of this virus. In order to investigate the effects caused by serial passage of AgMNPV in cell culture, we carried out a total of ten passages and analyzed the morphological and the genomic changes of the virus. After six passages, the many-polyhedra (MP) phenotype started to switch to the few-polyhedra (FP) phenotype which rapidly accumulated in the virus population. Ultrastructural analysis showed typical signs of FP mutant formation such as decrease in the number of polyhedra per cell, polyhedra aberrant morphology and low numbers of virions occluded in the protein matrix. Also enhanced BV production was observed from the fifth passage indicating that FP mutants were becoming predominant in comparison to the wild type virus. Restriction endonuclease analysis of the viral DNA revealed that lower and higher passages had similar profiles indicating that there were no large insertions or deletions or rearrangements in their genomes and indicating the generation of FP mutants instead of defective interfering viruses.

Biologia molecular de baculovírus e seu uso no controle biológico de pragas no Brasil

Baculoviruses are insect viruses found mainly in Lepidoptera. The family Baculoviridae is taxonomically divided in two genera, Nucleopolyhedrovirus and Granulovirus, which differ by occlusion body morphology. NPVs (Nucleopolyhedroviruses) have polyhedrical inclusion bodies (PIBs) containing multiple viral particles, while GVs (Granuloviruses) appear to be generally single particles occluded in oval shaped occlusion bodies. During the life cycle, two different viral progenies are produced: BV (Budded Virus) and PDV (Polyhedra Derived Virus), which are essential for the infectious process and virus propagation in host cells. Baculoviruses are being used for pest control and they are especially safe due to their specificity and invertebrate-restricted host range. Baculoviruses have been used as vectors for high level protein expression ofheterologous genes from prokaryotic and eukaryotic organisms. Also, recombinant DNA techniques have allowed the production of genetically modified viral insecticides. This study is a review on the taxonomy, structure, replication and molecular biology of baculoviruses, as well as their use as bioinsecticides in Brazil.

Detection and identification of baculovirus pesticides by multitemperature single-strand conformational polymorphism

The method of single-strand conformational polymorphism (SSCP) was modified in our laboratories for the characterization of baculoviruses, insect viruses with great potential for use as bioinsecticides in biological protection programs. A series of primers were synthesized after the comparison of the polyhedrin gene sequences of over 20 baculoviruses. Polyhedrin is a highly conserved protein which is responsible for the persistence of the virus in the environment. Universal primers were designed which could be used in polymerase chain reactions (PCR) containing genomic DNA from an array of nucleopolyhedrosis viruses (NPVs) including these which are used as biopesticides against important pests of forests and crops, such as Anticarsia gemmatalis, Spodoptera frugiperda, Lymantria dispar, Lymantria monacha and many others. PCR products were denatured and subjected to single-strand DNA electrophoresis at variable temperatures (MSSCP) where, after silver staining, they gave ssDNA band patterns characteristic for each baculovirus species. This technique can be potentially applied to detect baculoviruses in insects collected in the field, as well as to plant tissues and the excrements or bodies of predators without need for sequencing the PCR products. Sometimes MSSCP can be used not only for species determination but also as an indication of genomic variability which can be related to infectivity.

Identification of a new nucleopolyhedrovirus from naturally-infected Condylorrhiza vestigialis (Guenée) (Lepidoptera: Crambidae) larvae on poplar plantations in South Brazil

A baculovirus was isolated from larvae of Condylorrhiza vestigialis (Guenée) (Lepidoptera: Crambidae), a pest of a forest species known as Poplar (family Salicaceae, genus: Populus) with high economic value. Electron microscopy analysis of the occlusion body obtained from diseased larvae showed polyhedra containing multiple nucleocapsids per envelope. This baculovirus was thus named Condylorrhiza vestigialis multiple nucleopolyhedrovirus (CoveMNPV) and characterized by its DNA restriction endonuclease pattern, polyhedral protein, viral protein synthesis, and infectivity in insect cell lines. Restriction endonuclease profiles of viral DNA digested with five restriction enzymes were obtained and the CoveMNPV genome size was estimated to be 81+/-2.5 kbp. The isolation of the polyhedra (OBs) was done from the crude extract of infected larvae by ultracentrifugation through sucrose gradients. These viral particles were analyzed by denaturing polyacrylamide gel electrophoresis (SDS-PAGE), which showed a strong band with approximately 33 kDa, corresponding to the main protein of the occlusion bodies (polyhedrin). Also, a similar band was observed for CoveMNPV infected Spodoptera frugiperda cells (SF-21 AE) pulse-labeled with [(35)S] methionine and fractionated by SDS-PAGE. Of the four insect cell lines tested for susceptibility to CoveMNPV infection, the SF-21 AE was the most susceptible with occlusion bodies produced in most of the inoculated cells. This is the first record of an NPV from C. vestigialis.

Host-specific transcription of nucleopolyhedrovirus gene homologues in productive and abortive Anticarsia gemmatalis MNPV infections

SummaryIn a previous report, we showed that Anticarsia gemmatalis nucleo- polyhedrovirus (AgMNPV) infections of Choristoneura fumiferana IPRI-CF-124T and Bombyx mori BM-5 cell lines are abortive, whereas A. gemmatalis UFL-AG-286 cells efficiently produce infectious virus and polyhedral inclusion bodies (PIBs). In the present study, we explored transcription patterns in these infections using representative temporal classes of Autographa californica MNPV (AcMNPV) genes. Northern analyses were carried out using internal fragments of AcMNPV genes that hybridized strongly with AgMNPV genomic DNA. The results showed that ie-1(immediate-early) homologue, but not dnapol (delayed-early) homologue of AgMNPV was transcribed efficiently in the abortive infections. Transcription of gp67 (late) and polh (very late) homologues was minimal in C. fumiferana cells and undetectable in B. mori cells. Transcription patterns in AgMNPV-infected A. gemmatalis cells were similar to those reported for productive AcMNPV infections. These data are consistent with our previous observation that early cytopathic effect, but not infectious virus or PIBs are detected in abortive infections with AgMNPV. Our results suggest that C. fumiferana and B. mori cells restrict AgMNPV infections at the transcriptional level and that this block likely occurs between immediate-early and delayed-early phases of the NPV cycle. Our data do not preclude the possibility of additional restrictions at other stages.

High genetic stability of peroral infection factors from Anticarsia gemmatalis MNPV over 20years of sampling.

The Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV) has been used as a biopesticide since the early 1980s in Brazil to control the major pest of soybean crops, the velvetbean caterpillar, Anticarsia gemmatalis. To monitor the genetic diversity over space and time we sequenced four pif genes (pif1, pif2, pif3 and pif4) from AgMNPV isolates collected from different regions of South America, as well as of seasonal isolates, sampled during a two-decade field experiment. Although all genes presented low levels of polymorphism, the pif-2 carries a slightly higher number of polymorphic sites. Overall, this study reveals that pif genes have remained stable after 20 years of repeated field application.

Identificação e caracterização de isolado brasileiro do vírus de poliedrose nuclear da lagarta do cartucho-do-milho

A nuclear polyhedrosis virus (NPV) from Spodoptera frugiperda (Smith) caterpillars (Lepidoptera: Noctuidae), collected from diseased insects in Sete Lagoas, MG, was confirmed and identified. The pathology of infected caterpillars is characteristic of NPV. The virus showed tropism by ectoderm cells, fat cells, and tracheocytes. Viral particles (polyhedra and alkali released virions - ARVs) were purified through diferential centrifugations in sucrose gradient, and the polyhedral band was located in the inferior third part of the tube. Increasing time of polyhedral digestion with alkaline solution resulted in higher dissolution of occluded bodies (polyhedra) consequently releasing virions. Five bands were formed for the alkali released virions. The electrophoretic pattern of S. frugiperda NPV was compared to the one of Anticarsia gemmatalis (Hubner) NPV for polyhedra as well as ARVs. A peptide of 32,000 dalton was characterized as the polyhedrin of S. frugiperda NPV.