Nudivirus

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Nudiviridae
Nudivirus virion.jpg
Schematic drawing
Virus classification OOjs UI icon edit-ltr.svg
(unranked): Virus
Class: Naldaviricetes
Order: Lefavirales
Family:Nudiviridae
Genera

Nudiviruses are a genus of anthropod viruses that constitute the family Nudiviridae. [1] Insects and marine crustaceans serve as natural hosts to this family of viruses. Nudiviruses are double-stranded DNA viruses, with their genome notably ranging from 130-140 kilobases in length. There are 20 species in this family, assigned to 4 genera. [2] [3] Diseases associated with this family include: death in larvae, and chronic disease in adults. [2] [4] [5]

Contents

Taxonomy

The family Nudiviridae contains the following genera: [5]

Classification History

During their first discovery, nudiviruses were classified as a subgroup in the Baculoviridae family. Originally it was assumed that nudiviruses were nooccluded baculoviruses. In 2007, the genus Nudivirus was proposed to include viruses similar to the Oryctes rhinoceros virus. [6] In 2013, Nudiviruses were classified as the family Nudiviridae. [7] Today, nudiviruses are assigned to the class Naldaviricetes that is composed of three other large dsDNA virus families: Baculoviridae, Hytrosaviridae and Nimaviridae.

Species

Nudiviruses infect only insects and marine crustaceans. [4]

Virus Transmission

Transmission of nudiviruses occurs horizontally by feeding [9] , mating and vertically from mother to offspring [9] [24] . Infections can be lethal for the larvae [25] and can possibly reduce the fitness of the host by reducing offspring production and survival among adults. [26] [27]

Structure and life cycle

Nudiviridae replication cycle E01333-20-F4.large.jpg
Nudiviridae replication cycle
Virion structures of the betanudivirus HzNV-1. Virion structures of the betanudivirus HzNV-1.jpg
Virion structures of the betanudivirus HzNV-1.

Nudiviruses are double stranded DNA viruses, characterized by their rod shape. Their virions are made of a single nucleocapsid surrounded by an envelope and range from 30nm to 120nm in length [28] . They replicate in the nucleus of infected host cells and in some parasitoid wasp species, a nudivirus genome, in proviral form, is integrated into the wasp genome and produces virus like particles called polydnaviruses that are injected into lepidopteran larvae and are thought to facilitate parasitization of the larvae [29] .

Nudiviruses have localized infection and are associated with specific cell pathogenesis and varies among species. Vesicles containing virions have been observed for HzNV-2 [30] [31] and OrNV [32] and aid in infecting subsequent cells. Virions sexually transmitted during mating, like Hznv-2, target reproductive tissues, cause the malformation of reproductive tissues in infected adult Helicoverpa Zea [31] [33] . In cells, enveloped and non enveloped particles were observed in the nucleus and have been found to successfully replicate in infect ovarian moth cell lines, but did not replicate in fat body cells. [34] [35] In OrNV, replication occurs in the nucleus in midgut and fat body cells. [36] In TpNV, replication occurs in the nucleus of the salvalary glands [37] . The specific cell localization is a distinctive characteristic that differentiates nudivruses from baculoviruses.

Three species form Occlusion bodies (OBs), ToNV [38] , PmNV [15] and OrNV. In PmNV OBs are transmitted orally and are sensitive to acid conditions. Host proteins may be involved in the formation of nudiviral OBs. [37]

Currently, there is not a general life cycle established for nudiviruses.

Genome

Genome map of Oryctes rhinoceros nudivirus (click on image to enlarge it) OrNV genome ICTV.jpg
Genome map of Oryctes rhinoceros nudivirus (click on image to enlarge it)

Gene content comparison and phylogenetic analyses show that nudiviruses share 20 core genes with baculoviruses and form a monophyletic sister group with them. Fossil calibration estimate this association arose 100 million years ago(Mya), while the last common ancestor of nudiviruses and baculoviruses existed approximately 312 Mya. Baculoviruses and nudiviruses differ in gene content, genome organization, cytopathology, infection of adults and most likely in host range. [39] The 20 core genes common in both baculoviruses and nudiviruses are involved in RNA transcription, DNA replication, virion structural components and many other functions. [40] Gene content and sequence similarity suggest that the nudiviruses GbNV, HzNV-1, and OrNV form a monophyletic group of nonoccluded double-stranded DNA viruses, which separated from the baculovirus lineage before this radiated into dipteran-, hymenopteran-, and lepidopteran-specific clades of occluded nucleopolyhedroviruses and granuloviruses. [39] The coding sequences vary among the nudivirus species and encode between 87 to 154 proteins depending on the species.

The order of the genes in the genomes of the viruses found in nudiviridae are poorly conserved. [41]

There are 32 core genes conserved among nudiviruses that are involved in various viral functions. [42] [43] [44]

The conservation of the 8 pif proteins, suggest the mode of infection for nudiviruses is conserved.

Tandem Direct Repeat Regions

Tandem direct repeats (Drs) are a common feature found in nudiviruses. These regions are characterized by their imperfect palindromic core. [10] The number direct repeat regions vary among nudivirus species and hypothesized to function like baculovirus Homologous regions. These regions can play a role in replication and can act as enhancers [45] [46] [47] . The drs identified in various nudivirus genomes have no homology to each other and are present in both coding and noncoding regions.

OrNV: 14 repeat regions 30-84 bp in length with varying AT% [48]

GbNV: 14 repeat regions 11 to 42 bp in length up to 96% AT rich. [10]

ToNv: 5 repeat regions 160-262 bp in length. [49]

HzNV-1: 6 repeat regions 24- 81 bp in length. [11]

HgNV: 7 repeat regions 58.8 to188 bp in length. [12]

PmNV: 10 repeat regions [12] .

Genome integration

Some nudiviruses have the ability to integrate into their host genome, like FaENV [50] , NiENV, VcENV that are permently integrated into their host and HzNV-1 that integrates as part of an latent infection. A latent HzNV-1 infection can be reactivated generate a lytic viral infection [51] The ability of these viruses to maintain their replication after integration distinguishes them their baculovirus ancestor. [52] [53]

Defense mechanisms

In many organisms, apoptosis can be regarded as an early defense mechanism against viral infection. Some viral genes allow the cell to survive for longer while producing more virions; Heliothis zea Nudivirus 1 (HzNV-1 or Hz-1 virus), a nudivirus with a broad host range, has been shown to block an induced-apoptosis gene (hhi1). A functional anti-apoptosis gene, (Hz-iap2), has been found to suppress the hhi1 gene which can cause the cell to die. A second inhibitor gene (Ac-iap2) to the hhi1 gene has been also discovered, but its function is still uncertain. [54]

Nudivirus encoded microRNAs

Micro RNAs (miRNAs) are small non-coding RNA molecules that play important roles in the regulation of genes in eukaryotic organisms. Virus encoded miRNAs are commonly reported in DNA viruses [55] and several nudiviruses have been reported to encode miRNAs. The first reported nudivirus encoded miRNA was from Heliothis zea nudivirus-1 which was shown to regulate virus latency. [56] Two other viruses Drosophila innubila nudivirus and Oryctes rhinoceros nudivirus have also been reported to encode miRNA molecules from transcriptomic studies, [57] [58] however the role of these miRNAs and their role in virus-host interactions is yet to be experimentally determined.

Utilization for Pest Control

In the southwest Pacific islands, OrNV has been shown to be an effective biocontrol agent against the palm pest, the coconut rhinoceros beetle [59] .

Etymology

The word "nudivirus" comes from the Latin nudus, which means naked and virus, poison. Naked refers to the fact that most do not have the dense protein bodies which surround baculoviruses. [60] However occluded nudiviruses, with such protein bodies, such as those of Tipula oleracea and Penaeus monodon have been characterized. [61]

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References

  1. Harrison, RL; Herniou, EA; Bézier, A; Jehle, JA; Burand, JP; Theilmann, DA; Krell, PJ; van Oers, MM; Nakai, M; ICTV Report Consortium (January 2020). "ICTV Virus Taxonomy Profile: Nudiviridae". The Journal of General Virology. 101 (1): 3–4. doi: 10.1099/jgv.0.001381 . PMC   7414434 . PMID   31935180.
  2. 1 2 "ICTV Report Nudiviridae" . Retrieved 3 February 2021.
  3. Petersen, Jirka M.; Bézier, Annie; Drezen, Jean-Michel; van Oers, Monique M. (1 March 2022). "The naked truth: An updated review on nudiviruses and their relationship to bracoviruses and baculoviruses". Journal of Invertebrate Pathology. 189: 107718. doi:10.1016/j.jip.2022.107718. ISSN   0022-2011. PMID   35077776.
  4. 1 2 "Viral Zone". ExPASy. Retrieved 13 August 2015.
  5. 1 2 "Virus Taxonomy: 2020 Release". International Committee on Taxonomy of Viruses (ICTV). March 2021. Retrieved 12 May 2021.
  6. Wang, Y.; van Oers, M.M.; Crawford, A.M.; Vlak, J.M. & Jehle, J.A. (2007). "Genomic analysis of Oryctes rhinoceros virus reveals genetic relatedness to Heliothis zea virus 1". Archives of Virology. 152 (3): 519–531. doi:10.1007/s00705-006-0872-2. PMID   17106621. S2CID   10264332.
  7. ICTV proposals 2013.003a-KI et al., J. E. Jehle et al. Retrieved 21 November 2015.
  8. Hill, Tom; Unckless, Robert L. (January 2018). "The dynamic evolution of Drosophila innubila Nudivirus". Infection, Genetics and Evolution. 57: 151–157. doi:10.1016/j.meegid.2017.11.013. PMC   5725240 . PMID   29155284.
  9. 1 2 3 Unckless, Robert L. (28 October 2011). DeSalle, Robert (ed.). "A DNA Virus of Drosophila". PLOS ONE. 6 (10): e26564. doi: 10.1371/journal.pone.0026564 . ISSN   1932-6203. PMID   22053195.
  10. 1 2 3 Wang, Yongjie; Kleespies, Regina G.; Huger, Alois M.; Jehle, Johannes A. (15 May 2007). "The Genome of Gryllus bimaculatus Nudivirus Indicates an Ancient Diversification of Baculovirus-Related Nonoccluded Nudiviruses of Insects". Journal of Virology. 81 (10): 5395–5406. doi:10.1128/JVI.02781-06. ISSN   0022-538X. PMC   1900193 . PMID   17360757.
  11. 1 2 Burand, John P.; Kim, Woojin; Afonso, Claudio L.; Tulman, Edan R.; Kutish, Gerald F.; Lu, Zhiqiang; Rock, Daniel L. (6 January 2012). "Analysis of the Genome of the Sexually Transmitted Insect Virus Helicoverpa zea Nudivirus 2". Viruses. 4 (1): 28–61. doi: 10.3390/v4010028 . ISSN   1999-4915. PMC   3280521 . PMID   22355451.
  12. 1 2 3 Holt, Corey C.; Stone, Michelle; Bass, David; Bateman, Kelly S.; van Aerle, Ronny; Daniels, Carly L.; van der Giezen, Mark; Ross, Stuart H.; Hooper, Chantelle; Stentiford, Grant D. (12 July 2019). "The first clawed lobster virus Homarus gammarus nudivirus (HgNV n. sp.) expands the diversity of the Nudiviridae". Scientific Reports. 9 (1): 10086. doi:10.1038/s41598-019-46008-y. ISSN   2045-2322. PMC   6626001 . PMID   31300678.
  13. Etebari, Kayvan; Filipović, Igor; Rašić, Gordana; Devine, Gregor J.; Tsatsia, Helen; Furlong, Michael J. (March 2020). "Complete genome sequence of Oryctes rhinoceros nudivirus isolated from the coconut rhinoceros beetle in Solomon Islands". Virus Research. 278: 197864. doi:10.1016/j.virusres.2020.197864. PMID   31945420.
  14. Lee, S.; Park, K.-H.; Nam, S.-H.; Kwak, K.-W.; Choi, J.-Y. (12 March 2015). "First Report of Oryctes rhinoceros nudivirus (Coleoptera: Scarabaeidae) Causing Severe Disease in Allomyrina dichotoma in Korea". Journal of Insect Science. 15 (1): 26. doi:10.1093/jisesa/iev002. ISSN   1536-2442. PMC   4535134 . PMID   25765317.
  15. 1 2 Yang, Yi-Ting; Lee, Der-Yen; Wang, Yongjie; Hu, Jer-Ming; Li, Wen-Hsiung; Leu, Jiann-Horng; Chang, Geen-Dong; Ke, Huei-Mien; Kang, Shin-Ting; Lin, Shih-Shun; Kou, Guang-Hsiung; Lo, Chu-Fang (December 2014). "The genome and occlusion bodies of marine Penaeus monodon nudivirus (PmNV, also known as MBV and PemoNPV) suggest that it should be assigned to a new nudivirus genus that is distinct from the terrestrial nudiviruses". BMC Genomics. 15 (1). doi: 10.1186/1471-2164-15-628 . ISSN   1471-2164.
  16. Allain, Thomas W.; Stentiford, Grant D.; Bass, David; Behringer, Donald C.; Bojko, Jamie (9 September 2020). "A novel nudivirus infecting the invasive demon shrimp Dikerogammarus haemobaphes (Amphipoda)". Scientific Reports. 10 (1): 14816. doi:10.1038/s41598-020-71776-3. ISSN   2045-2322. PMC   7481228 . PMID   32908207.
  17. Bojko, Jamie; Duermit-Moreau, Elizabeth; Gandy, Ryan; Behringer, Donald C. (1 November 2023). "A new member of the Nudiviridae from the Florida stone crab (Menippe mercenaria)". Virology. 588: 109910. doi:10.1016/j.virol.2023.109910. ISSN   0042-6822. PMID   37844408.
  18. Bojko, Jamie; Walters, Erin; Burgess, Amy; Behringer, Donald C. (1 October 2022). "Rediscovering "Baculovirus-A" (Johnson, 1976): The complete genome of 'Callinectes sapidus nudivirus'". Journal of Invertebrate Pathology. 194: 107822. doi:10.1016/j.jip.2022.107822. ISSN   0022-2011. PMID   36030880.
  19. Liu, Sijun; Sappington, Thomas W.; Coates, Brad S.; Bonning, Bryony C. (9 February 2021). "Nudivirus Sequences Identified from the Southern and Western Corn Rootworms (Coleoptera: Chrysomelidae)". Viruses. 13 (2): 269. doi: 10.3390/v13020269 . ISSN   1999-4915. PMC   7916170 . PMID   33572446.
  20. Schoonvaere, Karel; Smagghe, Guy; Francis, Frédéric; de Graaf, Dirk C. (14 February 2018). "Study of the Metatranscriptome of Eight Social and Solitary Wild Bee Species Reveals Novel Viruses and Bee Parasites". Frontiers in Microbiology. 9. doi: 10.3389/fmicb.2018.00177 . ISSN   1664-302X. PMID   29491849.
  21. 1 2 Bateman, Kelly S.; Kerr, Rose; Stentiford, Grant D.; Bean, Tim P.; Hooper, Chantelle; Van Eynde, Benigna; Delbare, Daan; Bojko, Jamie; Christiaens, Olivier; Taning, Clauvis N. T.; Smagghe, Guy; van Oers, Monique M.; van Aerle, Ronny (26 August 2021). "Identification and Full Characterisation of Two Novel Crustacean Infecting Members of the Family Nudiviridae Provides Support for Two Subfamilies". Viruses. 13 (9): 1694. doi: 10.3390/v13091694 . ISSN   1999-4915. PMC   8472649 . PMID   34578276.
  22. Bézier, Annie; Thézé, Julien; Gavory, Frederick; Gaillard, Julien; Poulain, Julie; Drezen, Jean-Michel; Herniou, Elisabeth A. (15 March 2015). McFadden, G. (ed.). "The Genome of the Nucleopolyhedrosis-Causing Virus from Tipula oleracea Sheds New Light on the Nudiviridae Family". Journal of Virology. 89 (6): 3008–3025. doi:10.1128/JVI.02884-14. ISSN   0022-538X. PMC   4337555 . PMID   25540386.
  23. 1 2 3 Stratton, Cheyenne E.; Reisinger, Lindsey S.; Behringer, Donald C.; Gray, Shannon N.; Larson, Eric R.; Bojko, Jamie (1 October 2024). "North American crayfish harbour diverse members of the Nudiviridae". Virology. 598: 110183. doi:10.1016/j.virol.2024.110183. ISSN   0042-6822. PMID   39029331.
  24. Hamm, John J.; Carpenter, James E.; Styer, Eloise L. (1 March 1996). "Oviposition Day Effect on Incidence of Agonadal Progeny of Helicoverpa zea (Lepidoptera: Noctuidae) Infected with a Virus". Annals of the Entomological Society of America. 89 (2): 266–275. doi:10.1093/aesa/89.2.266. ISSN   1938-2901.
  25. Lee, S.; Park, K.-H.; Nam, S.-H.; Kwak, K.-W.; Choi, J.-Y. (12 March 2015). "First Report of Oryctes rhinoceros nudivirus (Coleoptera: Scarabaeidae) Causing Severe Disease in Allomyrina dichotoma in Korea". Journal of Insect Science. 15 (1): 26. doi:10.1093/jisesa/iev002. ISSN   1536-2442. PMC   4535134 . PMID   25765317.
  26. Unckless RL. (2011) A DNA Virus of Drosophila. Published online 2011 October 28
  27. Bézier, Annie; Thézé, Julien; Gavory, Frederick; Gaillard, Julien; Poulain, Julie; Drezen, Jean-Michel; Herniou, Elisabeth A. (15 March 2015). McFadden, G. (ed.). "The Genome of the Nucleopolyhedrosis-Causing Virus from Tipula oleracea Sheds New Light on the Nudiviridae Family". Journal of Virology. 89 (6): 3008–3025. doi:10.1128/JVI.02884-14. ISSN   0022-538X. PMC   4337555 . PMID   25540386.
  28. "Genus: Alphanudivirus | ICTV". ictv.global. Retrieved 15 November 2024.
  29. Stoltz, Donald B.; Vinson, S. Bradleigh (1 January 1979), Lauffer, Max A.; Bang, Frederik B.; Maramorosch, Karl; Smith, Kenneth M. (eds.), "Viruses and Parasitism in Insects", Advances in Virus Research, 24, Academic Press: 125–171, doi:10.1016/S0065-3527(08)60393-0, ISBN   978-0-12-039824-9, PMID   389003 , retrieved 15 November 2024
  30. Rallis, Christopher P; Burand, John P (1 June 2002). "Pathology and ultrastructure of the insect virus, Hz-2V, infecting agonadal male corn earworms, Helicoverpa zea". Journal of Invertebrate Pathology. 80 (2): 81–89. doi:10.1016/S0022-2011(02)00102-7. ISSN   0022-2011. PMID   12383433.
  31. 1 2 Raina, Ashok K; Adams, Jean R; Lupiani, Blanca; Lynn, Dwight E; Kim, Woojin; Burand, John P; Dougherty, Edward M (1 July 2000). "Further Characterization of the Gonad-Specific Virus of Corn Earworm, Helicoverpa zea". Journal of Invertebrate Pathology. 76 (1): 6–12. doi:10.1006/jipa.2000.4942. ISSN   0022-2011. PMID   10963397.
  32. Velamoor, Sailakshmi; Mitchell, Allan; Humbel, Bruno M.; Kim, WonMo; Pushparajan, Charlotte; Visnovsky, Gabriel; Burga, Laura N.; Bostina, Mihnea (25 August 2020). Moscona, Anne (ed.). "Visualizing Nudivirus Assembly and Egress". mBio. 11 (4). doi:10.1128/mBio.01333-20. ISSN   2161-2129. PMC   7439470 . PMID   32788378.
  33. Burand, John P. (October 2009). "The sexually transmitted insect virus, Hz-2V". Virologica Sinica. 24 (5): 428–435. doi:10.1007/s12250-009-3046-z. ISSN   1674-0769.
  34. Lu, Hua; Burand, John P (January 2001). "Replication of the Gonad-Specific Virus Hz-2V in Ld652Y Cells Mimics Replication in Vivo". Journal of Invertebrate Pathology. 77 (1): 44–50. doi:10.1006/jipa.2000.4990. PMID   11161993.
  35. Burand, John P.; Lu, Hua (September 1997). "Replication of a Gonad-Specific Insect Virus in TN-368 Cells in Culture". Journal of Invertebrate Pathology. 70 (2): 88–95. doi:10.1006/jipa.1997.4676. PMID   9281395.
  36. Payne, C. C. (1 October 1974). "The Isolation and Characterization of a Virus from Oryctes rhinoceros". Journal of General Virology. 25 (1): 105–116. doi:10.1099/0022-1317-25-1-105. ISSN   0022-1317. PMID   4430894.
  37. 1 2 Bézier, Annie; Harichaux, Grégoire; Musset, Karine; Labas, Valérie; Herniou, Elisabeth A (1 February 2017). "Qualitative proteomic analysis of Tipula oleracea nudivirus occlusion bodies". Journal of General Virology. 98 (2): 284–295. doi:10.1099/jgv.0.000661. ISSN   0022-1317. PMID   28284235.
  38. Keown, Jeremy R.; Crawshaw, Adam D.; Trincao, Jose; Carrique, Loïc; Gildea, Richard J.; Horrell, Sam; Warren, Anna J.; Axford, Danny; Owen, Robin; Evans, Gwyndaf; Bézier, Annie; Metcalf, Peter; Grimes, Jonathan M. (13 July 2023). "Atomic structure of a nudivirus occlusion body protein determined from a 70-year-old crystal sample". Nature Communications. 14 (1): 4160. doi:10.1038/s41467-023-39819-1. ISSN   2041-1723. PMC   10345106 . PMID   37443157.
  39. 1 2 Mayo, M.A. (1995). Murphy, F.A.; Fauquet, C.M.; Bishop, D.H.L.; et al. (eds.). Unassigned Viruses. In: Virus Taxonomy: The Sixth Report of the International Committee on Taxonomy of Viruses. Springer-Verlag, Wien. pp. 504–507.
  40. Wang, Yongjie & Jehle, Johannes A. (2009). "Nudiviruses and other large, double-stranded circular DNA viruses of invertebrates: New insights on an old topic". Journal of Invertebrate Pathology. 101 (3): 187–193. doi:10.1016/j.jip.2009.03.013. PMID   19460388.
  41. Petersen, Jirka Manuel; Burgess, Amy L.; van Oers, Monique M.; Herniou, Elisabeth A.; Bojko, Jamie (August 2024). "Nudiviruses in free-living and parasitic arthropods: evolutionary taxonomy". Trends in Parasitology. 40 (8): 744–762. doi:10.1016/j.pt.2024.06.009. PMID   39019701.
  42. Cheng, Ruo-Lin; Li, Xiao-Feng; Zhang, Chuan-Xi (13 April 2020). "Nudivirus Remnants in the Genomes of Arthropods". Genome Biology and Evolution. 12 (5): 578–588. doi:10.1093/gbe/evaa074. ISSN   1759-6653. PMC   7250505 . PMID   32282886.
  43. Zhang, Yu; Wang, Jianhua; Han, Guan-Zhu (March 2020). "Chalcid wasp paleoviruses bridge the evolutionary gap between bracoviruses and nudiviruses". Virology. 542: 34–39. doi:10.1016/j.virol.2020.01.007. PMID   32056666.
  44. Burke, Gaelen R (April 2014). "Common themes in three independently derived endogenous nudivirus elements in parasitoid wasps". Current Opinion in Insect Science. 32: 28–35. doi:10.1016/j.cois.2018.10.005. ISSN   2214-5745. PMID   31113628.
  45. Cochran, Mark A.; Faulkner, Peter (March 1983). "Location of Homologous DNA Sequences Interspersed at Five Regions in the Baculovirus AcMNPV Genome". Journal of Virology. 45 (3): 961–970. doi:10.1128/jvi.45.3.961-970.1983. ISSN   0022-538X. PMID   16789237.
  46. Hilton, Sally; Winstanley, Doreen (1 May 2007). "Identification and functional analysis of the origins of DNA replication in the Cydia pomonella granulovirus genome". Journal of General Virology. 88 (5): 1496–1504. doi:10.1099/vir.0.82760-0. ISSN   0022-1317. PMID   17412979.
  47. Guarino, Linda A.; Summers, Max D. (October 1986). "Nuclear Polyhedrosis Virus Enhances Delayed-Early Gene Expression". Journal of Virology. 60 (1): 215–223. doi:10.1128/jvi.60.1.215-223.1986. ISSN   0022-538X. PMID   16789258.
  48. Wang, Yongjie; Kleespies, Regina G.; Huger, Alois M.; Jehle, Johannes A. (15 May 2007). "The Genome of Gryllus bimaculatus Nudivirus Indicates an Ancient Diversification of Baculovirus-Related Nonoccluded Nudiviruses of Insects". Journal of Virology. 81 (10): 5395–5406. doi:10.1128/JVI.02781-06. ISSN   0022-538X. PMC   1900193 . PMID   17360757.
  49. Bézier, Annie; Thézé, Julien; Gavory, Frederick; Gaillard, Julien; Poulain, Julie; Drezen, Jean-Michel; Herniou, Elisabeth A. (15 March 2015). McFadden, G. (ed.). "The Genome of the Nucleopolyhedrosis-Causing Virus from Tipula oleracea Sheds New Light on the Nudiviridae Family". Journal of Virology. 89 (6): 3008–3025. doi:10.1128/JVI.02884-14. ISSN   0022-538X. PMC   4337555 . PMID   25540386.
  50. Burke, Gaelen R; Simmonds, Tyler J; Sharanowski, Barbara J; Geib, Scott M (1 October 2018). Larracuente, Amanda (ed.). "Rapid Viral Symbiogenesis via Changes in Parasitoid Wasp Genome Architecture". Molecular Biology and Evolution. 35 (10): 2463–2474. doi:10.1093/molbev/msy148. ISSN   0737-4038. PMID   30053110.
  51. Lin, Chi-Long; Lee, Jin-Ching; Chen, Shih-Shun; Alan Wood, H.; Li, Ming-Liang; Li, Chih-Fen; Chao, Yu-Chan (January 1999). "Persistent Hz-1 Virus Infection in Insect Cells: Evidence for Insertion of Viral DNA into Host Chromosomes and Viral Infection in a Latent Status". Journal of Virology. 73 (1): 128–139. doi:10.1128/jvi.73.1.128-139.1999. ISSN   0022-538X. PMC   103816 . PMID   9847315.
  52. Petersen, Jirka M.; Bézier, Annie; Drezen, Jean-Michel; van Oers, Monique M. (1 March 2022). "The naked truth: An updated review on nudiviruses and their relationship to bracoviruses and baculoviruses". Journal of Invertebrate Pathology. 189: 107718. doi:10.1016/j.jip.2022.107718. ISSN   0022-2011. PMID   35077776.
  53. Cheng, Ruo-Lin; Li, Xiao-Feng; Zhang, Chuan-Xi (1 May 2020). Schaack, Sarah (ed.). "Nudivirus Remnants in the Genomes of Arthropods". Genome Biology and Evolution. 12 (5): 578–588. doi:10.1093/gbe/evaa074. ISSN   1759-6653. PMC   7250505 . PMID   32282886.
  54. Wu, Yueh-Lung; Wu, Carol P.; Liu, Catherine Y. Y.; Lee, Song-Tay; Lee, Hsiao-Ping; Chao, Yu-Chan (2011). "Heliothis zea Nudivirus 1 Gene hhi1 Induces Apoptosis Which Is Blocked by the Hz-iap2 Gene and a Noncoding Gene, pag1". Journal of Virology . 85 (14): 6856–6866. doi:10.1128/JVI.01843-10. PMC   3126586 . PMID   21543471.
  55. Kincaid RP, Sullivan CS (2012). "Virus-encoded microRNAs: an overview and a look to the future". PLOS Pathog. 8 (12): e1003018. doi: 10.1371/journal.ppat.1003018 . PMC   3534370 . PMID   23308061.
  56. Wu YL, Wu CP, Liu CY, Hsu PW, Wu EC, Chao YC (2011). "A non-coding RNA of insect HzNV-1 virus establishes latent viral infection through microRNA". Sci Rep. 1: 60. Bibcode:2011NatSR...1...60W. doi:10.1038/srep00060. PMC   3216547 . PMID   22355579.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  57. Webster CL, Waldron FM, Robertson S, Crowson D, Ferrari G, Quintana JF; et al. (2015). "The Discovery, Distribution, and Evolution of Viruses Associated with Drosophila melanogaster". PLOS Biol. 13 (7): e1002210. doi: 10.1371/journal.pbio.1002210 . PMC   4501690 . PMID   26172158.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  58. Etebari K, Parry R, Beltran MJB, Furlong MJ (2020). "Transcription Profile and Genomic Variations of Oryctes Rhinoceros Nudivirus in Coconut Rhinoceros Beetles". J Virol. 94 (22). doi:10.1128/JVI.01097-20. PMC   7592217 . PMID   32878889.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  59. Etebari, Kayvan; Parry, Rhys; Beltran, Marie Joy B.; Furlong, Michael J. (27 October 2020). Parrish, Colin R. (ed.). "Transcription Profile and Genomic Variations of Oryctes Rhinoceros Nudivirus in Coconut Rhinoceros Beetles". Journal of Virology. 94 (22). doi:10.1128/JVI.01097-20. ISSN   0022-538X. PMC   7592217 . PMID   32878889.
  60. Moscardi, Flávio (1999). "Assessment of the Application of Baculoviruses for Control of Lepidoptera". Annual Review of Entomology . 44 (1). Annual Reviews: 257–289. doi:10.1146/annurev.ento.44.1.257. ISSN   0066-4170. PMID   15012374. p. 260, "This strategy has been successful with the non-occluded virus of the rhinoceros beetle, Oryctes rhinoceros, in coconut palms (183)."
  61. Bézier A, Thézé J, Gavory F, Gaillard J, Poulain J, Drezen JM, Herniou EA (March 2015). "The genome of the nucleopolyhedrosis-causing virus from Tipula oleracea sheds new light on the Nudiviridae family". J. Virol. 89 (6): 3008–25. doi:10.1128/JVI.02884-14. PMC   4337555 . PMID   25540386.