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Baculoviruses
The family Baculoviridae includes the nuclear polyhedrosis viruses (NPV) and
granulosis viruses (GV). These are double-stranded DNA viruses (dsDNA) with rod-shaped
nucleocapsids. The infectious virus particles or virions are occluded in protein bodies called polyhedra (NPV) or granules (GV). NPV polyhedra are larger than the virions (usually 1-15 µm) and may contain many virions. Infection with baculoviruses occurs when a susceptible host eats the polyhedra or granules, which are dissolved in the basic digestive gut juices. The virions are released when the protein matrices dissolve. The virions enter the nuclei of midgut cells and eventually infect many of the tissues and organs in the insect, primarily the fat body, epidermis, and blood cells. Nonoccluded baculoviruses (NOB), or nudiviruses, are not occluded in polyhedra and have recently been removed from the Baculoviridae. They are currently sedis incertae.
Infection with baculovirus was historically called "wilting
disease" because the tissues of the host liquefy and infection of the epidermis causes the host to appear to melt, releasing virus particles into the environment.
Baculoviruses are considered to be the most beneficial of the insect viruses to man, because of their utility in insect control, their specificity to the arthropods, and their more recent use in fundamental biological studies using molecular techniques. Nevertheless, they also cause diseases in beneficial insects and, therefore, use in the environment as biological control agents requires an understanding of host range and the mechanisms that control host specificity (Miller,
L.K., 1997). An excellent text for detailed information about baculoviruses is "The
Baculoviruses" (1997) edited by Lois Miller. Nuclear Polyhedrosis VirusesNPVs are largely restricted to insects and most species are relatively host specific. They are known to infect over 500 species of insects, and are best known from the Lepidoptera. They have also been recovered from Hymenoptera, Diptera, Thysanura, Trichoptera and Crustacea (shrimp) (Federici, 1997). The NPV from Autographica californica (AcMNPV) is the one of the most intensively studied species. The infectious virus particles or virions of NPVs can be enveloped singly (SNPV type) or multiply (MNPV type- in photo) (Federici, 1997) and are occluded in protein bodies called polyhedra. NPV polyhedra may contain few to many virions. After ingestion by the host and reproduction in the midgut cells, other tissues and organs in the insect become infected, primarily the fat body, epidermis, and blood cells. Insect larvae infected with NPV usually die from 5 to 12 days after infection depending on viral dose, temperature, and the larval instar at the time of infection. Just before dying, larvae often crawl to the tops of plants or any other available structure where they die and decompose. Millions of polyhedra are contained in the fluid mass of the disintegrating larvae and fall into feeding zones (leaves, leaf litter) where they can be ingested by other conspecific larvae. NPV epizootics are very impressive and, although they are important as naturally occurring mortality factors for many insect species, they often occur after the pest insect has exceeded the economic injury level. This is especially true when the crop that is being damaged by this insect has a relatively low economic threshold. Biological Control: NPVs must replicate in the nuclei of living host cells. They cannot be produced in culture media without living cells. This means that the production of NPV isolates as microbial insecticides requires a colony of insects or an acceptable insect tissue culture. This is more expensive than producing organisms such as the bacterium Bacillus thuringiensis in an artificial medium. Used as a microbial insecticide, NPVs can provide relatively fast kill and many are very host specific. All are specific to arthropods, most to a narrow range of Lepidoptera. Research on the production of NPVs as microbial insecticides has been primarily aimed at developing more efficient methods of production in insect tissue culture, as well as developing more virulent NPV strains. Most of the research on virulence involves inserting genes that produce toxic substances into the polyhedral gene. For example, genes for insect specific toxins, inserted into the polyhedral gene locus are expressed at the time that the polyhedral gene would have been expressed. The toxins kill the insect at an earlier stage than occurs in a normal infection (Black et al., 1997). One NPV that has been formulated for insect control is the MNPV of the gypsy moth, Lymantria dispar, or LdMNPV as Gypcheck. Granulosis VirusesGranulosis viruses (GV) are closely related to NPVs and are similar in structure and pathogenesis. The major difference between these two groups is that the virions are singly occluded into small occlusion bodies called granules. Like the NPVs, reproduction begins in the nuclei of host cells. Tissues infected and gross pathology are also very similar to NPVs. GVs have only been recorded from Lepidoptera. There are three major genetic types of GV. Type 1 GV described from the cabbage looper, Trichoplusia ni, only infects the midgut cells and subsequently the fat body cells. Because it does not infect the tracheal matrix or epidermis, larvae may live longer than NPV-infected insects. Type 2 GVs, first isolated from the codling moth, Cydia pomonella, parallels NPV infections. Type 3, known only from the western grapeleaf skeletonizer, Harrisina brillians, infects only the midgut tissues (Federici, 1997). Biological Control: Several GVs have been formulated as microbial insecticides, for example, GV from the codling moth, Cydia pomonella. Like NPV, these viruses are produced in vivo because of difficulties producing them in cell culture. In vivo production costs and narrow host spectrum limits their attractiveness to industry. |
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Questions? Please send feedback to lsolter@uiuc.edu Copyright © Midwest Institute for Biological Control, 2004 This page was last updated June 2, 2004 |
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