Alphanudivirus oryrhinocerotis | |
---|---|
particle of Oryctes rhinoceros nudivirus showing the capsid surrounded by a thick envelope (scale bar = 50 nm) | |
Virus classification | |
(unranked): | Virus |
Class: | Naldaviricetes |
Order: | Lefavirales |
Family: | Nudiviridae |
Genus: | Alphanudivirus |
Species: | Alphanudivirus oryrhinocerotis |
Member virus | |
Oryctes rhinoceros nudivirus | |
Synonyms | |
|
The Oryctes rhinoceros nudivirus (OrNV) is a member of the species Alphanudivirus oryrhinocerotis in the family Nudiviridae . It causes lethal infections in larvae and adults of the coconut rhinoceros beetle ( Oryctes rhinoceros ), a serious pest of coconut and oil palms in tropical Asia and the Pacific. The virus was discovered by Alois Huger in 1963 while searching for diseases of O. rhinoceros in Malaysia. [1] It has been demonstrated to be an effective biological control agent against this beetle pest.
The Oryctes rhinoceros nudivirus develops in the nuclei of infected cells, where the rod-shaped capsids are assembled to a size of 180 x 65 nm. Like in other nudiviruses, the capsids have a characteristic thread-like tail. They acquire an envelope and the final virus particles have a size of 220 x 120 nm. [2]
The Oryctes rhinoceros nudivirus is a double-stranded DNA virus with a large circular DNA molecule. The example (representative) isolate Ma07 has 127,615 base pairs and 139 open reading frames. [3] [4] Among others, the genes are associated with DNA replication and virus structure. [2]
The virus is transmitted perorally in O. rhinoceros larvae and adults. In O. rhinoceros larvae, the virus multiplies mainly in the fat body. As a result, the fat body disintegrates and the infected larvae have a transparent appearance. In O. rhinoceros adult beetles, the virus infects mainly the cells of the midgut. Midgut cells killed by the virus are discharged into the gut lumen. The gut becomes filled with virus particles and the infected adult beetles excrete the virus, transmitting it efficiently within the O. rhinoceros population. [5] Transmission of the virus is important for maintaining it within the beetle population, since it does not persist for long outside its beetle host. [6]
Infected third instar larvae typically die after around 3 weeks, 1st and 2nd instars earlier. Virus infections are, however, not transmitted to the pupal stage and adult beetles emerging from the pupae are always uninfected. They acquire infections through contact with infected larvae or adult beetles in breeding sites, or during mating and feeding in coconut palms. Virus infections reduce the lifespan and fecundity of the adult beetles. Infected females stop laying eggs and there is no transmission through the egg stage. [6] [7] [8]
Alois Huger described the virus as being similar to viruses from the family Baculoviridae , but lacking the proteinaceous crystals which surround and protect baculovirus particles. [1] [5] He named it Rhabdionvirus oryctes, however it became subsequently mainly known as Oryctes rhinoceros virus (OrV). A genomic analysis in 2007 revealed similarities to another unassigned and non-occluded baculovirus, the Heliothis zea virus 1, but significant differences to other baculoviruses. Therefore, the new genus Nudivirus was proposed for both viruses within the Baculoviridae. [9]
Further studies on the Oryctes rhinoceros nudivirus and other non-occluded baculoviruses led to the conclusion that they are significantly different from other members of the family Baculoviridae. Therefore, in 2012/2013, the creation of a new family, the Nudiviridae , was proposed with several new genera replacing the genus Nudivirus. [10] [2] The Oryctes rhinoceros nudivirus was regarded as the type species (now called 'example') for the first genus, the genus Alphanudivirus, and for the new family. [2] Since the introduction of the binomial system in virus taxonomy, the species Alphanudivirus oryrhinocerotis is recognized with the Oryctes rhinoceros nudivirus belonging to this species. [4]
The Oryctes rhinoceros nudivirus has been found to be naturally present in Malaysia, Indonesia, the Philippines and India. It appears to be widely distributed in tropical parts of Asia, that is the native distribution range of its host, the coconut rhinoceros beetle. [5] [11] However, it was absent in the Pacific Islands invaded by O. rhinoceros and in the islands of the Maldives. [11] [12] [13] Releases of the virus into virus-free islands resulted in a significant reduction of the beetle population. [14] [11] [13]
The virus affects mainly the population of O. rhinoceros adults, spreading easily among adult beetles and reducing their lifespan and fecundity. In Samoa and the Maldives, where the virus was introduced, the infection rate among adult beetles was typically between 30 and 40% after its introduction, whereas the virus was only found in 10% or less of the larval breeding sites. [13] [15] In countries where the virus is naturally present (Philippines, Indonesia) the incidence of virus infections among adult beetles is also usually higher than the number of breeding sites containing the virus. [16] [17] [13]
Comparing O.rhinoceros populations before and after the introduction of the virus in the Maldives as well as populations in the Philippines and in Indonesia with different levels of virus prevalence showed that the average lifespan of adult beetles was reduced to less than one half in populations with a high level of virus infections. [13] This corresponds well to the reduced palm damage following the introduction of the virus. This reduction of palm damage was well documented in Samoa, American Samoa, Tonga and Fiji. [14] [11]
The palm damage depends on the density of palms, since the same number of O. rhinoceros adults per hectare will cause less damage in areas with a high palm density compared to areas with a low palm density. For accurate comparison of the effect of the virus on the O. rhinoceros population, it is therefore necessary to account for the density of the palms and convert the palm damage into an estimate of the number of feeding O. rhinoceros adults per hectare. [18] [13] In the Maldives, such a conversion showed that the introduction of the virus often reduced the number of O. rhinoceros adults attacking coconut palms to less than one quarter of the level before the release. [18]
There is evidence that some O. rhinoceros populations have developed resistance to the Oryctes rhinoceros nudivirus. This is reflected in a natural low level of virus infections in some populations (e.g. South Sulawesi and Java in Indonesia), combined with a high level of palm damage, [19] [13] as well as high resistance to artificial virus inoculations in the invasive O. rhinoceros population in Guam. In Guam, the resistant population was found to belong to a specific haplotype (haplotype G) of O. rhinoceros which is also present in Indonesia, the Philippines, Palau, Papua New Guinea and the Solomon Islands. [20]
At the same time it was shown in laboratory experiments that O. rhinoceros larvae and adults have different sensitivities to different strains of the virus. [21] [19] Virus releases with different strains in the Maldives supported these laboratory results. [18] Therefore, resistance to the virus seems to be a combination of a general insensitivity to virus inoculations and differences in the virulence of different virus strains.
This was also supported by virus releases in coconut plantations in Central Java, Indonesia. In Java, the O. rhinoceros population was initially thought to be virus free, [11] but was later found to have an extremely low level of natural virus infections, suggesting resistance to the virus. [19] In 1976 and 1977, O. rhinoceros adult beetles infected with a virus strain from Sumatra were released in 8 locations in Java, while keeping 4 nearby locations untreated for comparison. Three years after the release, the palm damage in the treated areas had declined from 67.5% to 20.8%, expressed in % of fronds damaged. In the untreated areas the damage had not changed significantly (69.4% before and 76.5% after the release). Resurveying the treated and untreated areas in 1987, 10 years after the virus release, still showed a low damage level in the treated areas (17.1%) and some reduction in the untreated areas (41.8%). [22]
Although the Oryctes rhinoceros nudivirus has been demonstrated to be able to suppress O. rhinoceros populations effectively, outbreaks by the beetle can still develop during replanting of coconut or oil palms, even in the presence of the virus. Under such conditions many breeding sites become available and transmission of the virus is often interrupted. Transmission of the virus occurs when infected adult beetles come in contact with healthy larvae and adults in breeding sites, apart from contact between adults in palm trees. [8]
During replanting, when many breeding places become available, the contact between adults and larvae is reduced, because many potential breeding places are not yet occupied. Under such conditions it is advisable to hide the decaying coconut or oil palm trunks by planting cover crops around them. Cover crops not only hide the decaying palm trunks from the beetle, they also have a repellent effect on O. rhinoceros. [23] In addition, the spread of the virus can be promoted by leaving a few dead standing coconut palms in the replanted area. Dead standing coconut palms are the most preferred breeding places, there is frequent contact between adult beetles and larvae in dead standing palms and they are hot spots for virus transmission. [16] [24] [13] As pointed out above, other factors like the density of palms or resistance to the virus can also influence the ecology of the virus.
Polydnaviriformidae ( PDV) is a family of insect viriforms; members are known as polydnaviruses. There are two genera in the family: Bracoform and Ichnoviriform. Polydnaviruses form a symbiotic relationship with parasitoid wasps. Ichnoviriforms (IV) occur in Ichneumonid wasps and Bracoviriforms (BV) in Braconid wasps. The larvae of wasps in both of those groups are themselves parasitic on Lepidoptera, and the polydnaviruses are important in circumventing the immune response of their parasitized hosts. Little or no sequence homology exists between BV and IV, suggesting that the two genera have been evolving independently for a long time.
Baculoviridae is a family of viruses. Arthropods, among the most studied being Lepidoptera, Hymenoptera and Diptera, serve as natural hosts. Currently, 85 species are placed in this family, assigned to four genera.
Dynastinae or rhinoceros beetles are a subfamily of the scarab beetle family (Scarabaeidae). Other common names – some for particular groups of rhinoceros beetles – include Hercules beetles, unicorn beetles or horn beetles. Over 1,500 species and 225 genera of rhinoceros beetles are known.
Cydia pomonella granulovirus (CpGV) is a granulovirus belonging to the family Baculoviridae. It has a double-stranded DNA genome that is approximately 123,500 base pairs in length with 143 ORFs. The virus forms small bodies called granules containing a single virion. CpGV is a virus of invertebrates – specifically Cydia pomonella, commonly known as the Codling moth. CpGV is highly pathogenic, it is known as a fast GV – that is, one that will kill its host in the same instar as infection; thus, it is frequently used as a biological pesticide.
Animal viruses are viruses that infect animals. Viruses infect all cellular life and although viruses infect every animal, plant, fungus and protist species, each has its own specific range of viruses that often infect only that species.
Mermithidae is a family of nematode worms that are endoparasites in arthropods. As early as 1877, Mermithidae was listed as one of nine subdivisions of the Nematoidea. Mermithidae are confused with the horsehair worms of the phylum Nematomorpha that have a similar life history and appearance.
Nudiviruses are animal viruses that constitute the family Nudiviridae. Insects and marine crustaceans serve as natural hosts. There are 11 species in this family, assigned to 4 genera. Diseases associated with this family include: death in larvae, chronic disease in adults.
Metarhizium majus is the name given to a group of fungal isolates that are known to be virulent against Scarabaeidae, a family of beetles. Previously, this species has had variety status in Metarhizium anisopliae and its name is derived from characteristically very large spores for the genus Metarhizium. There has been considerable interest in developing isolates of this species into mycoinsecticides: especially against the coconut and oil palm beetle pest Oryctes in SE Asia, the Pacific region and Africa.
Operophtera bruceata, the Bruce spanworm, hunter's moth, or native winter moth is a moth of the family Geometridae. The species was first described by George Duryea Hulst in 1886. It is found from coast to coast in southern Canada and the northern parts of the United States.
Oryctes rhinoceros, also known as coconut rhinoceros beetle, Asiatic rhinoceros beetle, and coconut palm rhinoceros beetle, is a large species of beetle, belonging to the rhinoceros beetles subfamily Dynastinae. Oryctes rhinoceros attacks coconut palms and other palms such as the economically important oil palm. It can cause serious damage to the developing fronds (leaves) up to death of the palm. The beetle breeds in decaying palm trunks or other organic matter like sawdust or compost heaps.
Cadang-cadang is a disease caused by Coconut cadang-cadang viroid (CCCVd), a lethal viroid of several palms including coconut, African oil palm, anahaw, and buri. The name cadang-cadang comes from the word gadang-gadang that means dying in Bicol. It was originally reported on San Miguel Island in the Philippines in 1927/1928. "By 1962, all but 100 of 250,000 palms on this island had died from the disease," indicating an epidemic. Every year one million coconut palms are killed by CCCVd and over 30 million coconut palms have been killed since Cadang-cadang was discovered. CCCVd directly affects the production of copra, a raw material for coconut oil and animal feed. Total losses of about 30 million palms and annual yield losses of about 22,000 metric tons of copra have been attributed to Cadang-cadang disease in the Philippines.
Hytrosaviridae is a family of double-stranded DNA viruses that infect insects. The name is derived from Hytrosa, sigla from the Greek Hypertrophia for 'hypertrophy' and 'sialoadenitis' for 'salivary gland inflammation.'
The South American palm weevil, Rhynchophorus palmarum, is a species of snout beetle. The adults are relatively large black beetles of approximately one and a half inch in length, and the larvae may grow to two inches in length.
Elaeis guineensis is a species of palm commonly just called oil palm but also sometimes African oil palm or macaw-fat. It is the principal source of palm oil. It is native to west and southwest Africa, specifically the area between Angola and The Gambia; the species name, guineensis, refers to the name for the area called Guinea, and not the modern country Guinea now bearing that name. The species is also now naturalised in Madagascar, Sri Lanka, Malaysia, Indonesia, Central America, Cambodia, the West Indies, and several islands in the Indian and Pacific Oceans. The closely related American oil palm E. oleifera and a more distantly related palm, Attalea maripa, are also used to produce palm oil.
Johannes A. Jehle is a German scientist for insect virology, and plant protection. The focus of his research is the use of microorganisms and viruses for biological control of insect pests and the development of sustainable methods for plant protection. He heads the Institute for Biological Plant Control of the Julius Kühn-Institut in Darmstadt and is an adjunct Professor at the Technical University Darmstadt. He was President of the Society of Invertebrate Pathology in 2016/2018.
Helicoverpa zea nudivirus 2 is an enveloped, rod-shaped, nonoccluded, double stranded DNA (dsDNA) sexually transmitted virus whose natural host is the corn earworm moth. At about 440 by 90 nm, it is the causative agent of the only sexually transmitted viral disease of any insect. It was originally identified in a colony of corn earworm moths established and maintained in Stoneville, Mississippi, U.S. and was found to be responsible for the sterility of those infected.
As with a number of other geographically isolated islands, Guam has problems with invasive species negatively affecting the natural biodiversity of the island.
Alois M. Huger was a German entomologist and a pioneer in insect pathology as well as in the use of insect pathogens for the biological control of pest insects. He worked mainly on the diagnosis of insect diseases in Darmstadt, Germany. Among others, he discovered a virus disease of the coconut palm rhinoceros beetle in Malaysia from a previously unknown group of viruses which provided long-term control of this pest when introduced into islands invaded by the beetle.
Hepatopancreatic parvoviruses (HPV) are viruses with single-stranded DNA genomes that are in the family Parvoviridae, and which infect shrimp, prawn and other crustaceans. HPV infects the epithelial cells of the host's hepatopancreas and midgut, leading to stunted growth at the early life stage. For shrimp farms, especially in Asian countries such as China, India and Indonesia, HPV can lead to economic losses in aquaculture due to the reduced production.