References: Nudiviridae

References: Nudiviridae

Allain, T. W., G. D. Stentiford, D. Bass, D. C. Behringer and J. Bojko (2020). A novel nudivirus infecting the invasive demon shrimp Dikerogammarus haemobaphes (Amphipoda). Sci Rep 10: 14816. [PubMed]

Bateman, K. S., R. Kerr, G. D. Stentiford, T. P. Bean, C. Hooper, B. Van Eynde, D. Delbare, J. Bojko, O. Christiaens, C. N. T. Taning, G. Smagghe, M. M. van Oers and R. van Aerle (2021). Identification and full characterisation of two novel crustacean infecting members of the family Nudiviridae provides support for two subfamilies. Viruses 13: 1694. [PubMed]

Bergoin, M. and B. Guelpa (1977). Dissolution des inclusions du virus de la polyédrose nucléaire du diptère Tipula paludosa MEIG. Etude ultrastructurale du virion. [Dissolution of polyhedra of the nuclear polyhedrosis virus of the leatherjacket Tipula paludosa MEIG. Ultrastructural study of the virion" target="ictvref">PubMed]. Arch Virol 53: 243-54. [PubMed]

Bézier, A., G. Harichaux, K. Musset, V. Labas and E. A. Herniou (2017). Qualitative proteomic analysis of Tipula oleracea nudivirus occlusion bodies. J Gen Virol 98: 284-95. [PubMed]

Bézier, A., J. Thézé, F. Gavory, J. Gaillard, J. Poulain, J. M. Drezen and E. A. Herniou (2015). The genome of the nucleopolyhedrosis-causing virus from Tipula oleracea sheds new light on the Nudiviridae family. J Virol 89: 3008-25. [PubMed]

Bojko, J., P. D. Stebbing, A. M. Dunn, K. S. Bateman, F. Clark, R. C. Kerr, S. Stewart-Clark, Á. Johannesen and G. D. Stentiford (2018). Green crab Carcinus maenas symbiont profiles along a North Atlantic invasion route. Dis Aquat Organ 128: 147-68. [PubMed]

Burand, J. P., W. Kim, C. L. Afonso, E. R. Tulman, G. F. Kutish, Z. Lu and D. L. Rock (2012). Analysis of the genome of the sexually transmitted insect virus Helicoverpa zea nudivirus 2. Viruses 4: 28-61. [PubMed]

Burand, J. P. and H. Lu (1997). Replication of a gonad-specific insect virus in TN-368 cells in culture. J Invertebr Pathol 70: 88-95. [PubMed]

Burand, J. P., C. P. Rallis and W. Tan (2004). Horizontal transmission of Hz-2V by virus infected Helicoverpa zea moths. J Invertebr Pathol 85: 128-31. [PubMed]

Burand, J. P., B. Stiles and H. A. Wood (1983). Structural and intracellular proteins of the nonoccluded baculovirus HZ-1. J Virol 46: 137-42. [PubMed]

Chaivisuthangkura, P., C. Tawilert, T. Tejangkura, S. Rukpratanporn, S. Longyant, W. Sithigorngul and P. Sithigorngul (2008). Molecular isolation and characterization of a novel occlusion body protein gene from Penaeus monodon nucleopolyhedrovirus. Virology 381: 261-7. [PubMed]

Chao, Y. C., H. A. Wood, C. Y. Chang, H. J. Lee, W. C. Shen and H. T. Lee (1992). Differential expression of Hz-1 baculovirus genes during productive and persistent viral infections. J Virol 66: 1442-8. [PubMed]

Cheng, C. H., S. M. Liu, T. Y. Chow, Y. Y. Hsiao, D. P. Wang, J. J. Huang and H. H. Chen (2002). Analysis of the complete genome sequence of the Hz-1 virus suggests that it is related to members of the Baculoviridae. J Virol 76: 9024-34. [PubMed]

Cheng, R. L., Y. Xi, Y. H. Lou, Z. Wang, J. Y. Xu, H. J. Xu and C. X. Zhang (2014). Brown planthopper nudivirus DNA integrated in its host genome. J Virol 88: 5310-8. [PubMed]

Crawford, A. M. (1982). A coleopteran cell line derived from Heteronychus arator (Coleoptera: Scarabaeidae). In Vitro-Plant 18: 813-6.

Crawford, A. M. and C. Sheehan (1985). Replication of Oryctes baculovirus in cell culture: viral morphogenesis, infectivity and protein synthesis. J Gen Virol 66: 529-39.

Granados, R. R., T. Nguyen and B. Cato (1978). An insect cell line persistently infected with a baculovirus-like particle. Intervirology 10: 309-17. [PubMed]

Hamm, J. J., J. E. Carpenter and E. L. Styer (1996). Oviposition day effect on incidence of agonadal progeny of Helicoverpa zea (Lepidoptera: Noctuidae) infected with a virus. Ann Entomol Soc Am 89: 266-75.

Herniou, E. A., E. Huguet, J. Thézé, A. Bézier, G. Periquet and J. M. Drezen (2013). When parasitic wasps hijacked viruses: genomic and functional evolution of polydnaviruses. Philos Trans R Soc Lond B Biol Sci 368: 20130051. [PubMed]

Hill, T. and R. L. Unckless (2018). The dynamic evolution of Drosophila innubila Nudivirus. Infect Genet Evol 57: 151-7. [PubMed]

Holt, C. C., M. Stone, D. Bass, K. S. Bateman, R. van Aerle, C. L. Daniels, M. van der Giezen, S. H. Ross, C. Hooper and G. D. Stentiford (2019). The first clawed lobster virus Homarus gammarus nudivirus (HgNV n. sp.) expands the diversity of the Nudiviridae. Sci Rep 9: 10086. [PubMed]

Huang, Y. S., M. Hedberg and C. Y. Kawanishi (1982). Characterization of the DNA of a nonoccluded baculovirus, Hz-1V. J Virol 43: 174-81. [PubMed]

Huger, A. M. (1966). A virus disease of the Indian rhinoceros beetle, Oryctes rhinoceros(Linnaeus), caused by a new type of insect virus, Rhabdionvirus oryctes gen. n., sp. n. J Invertebr Pathol 8: 38-51. [PubMed]

Huger, A. M. (1985). A new virus disease of crickets (Orthoptera: Gryllidae) causing macronucleosis of fatbody. J Invert Pathol 45: 108-11.

Huger, A. M. (1991). Baculoviridae. Nonoccluded baculoviruses. In Altas of Invertebrate Viruses, pp. 287-319. Edited by J. R. Adams & J. R. Bonami. Boca Raton, Florida: CRC Press, Inc.

Huger, A. M. (2005). The Oryctes virus: its detection, identification, and implementation in biological control of the coconut palm rhinoceros beetle, Oryctes rhinoceros (Coleoptera: Scarabaeidae). J Invertebr Pathol 89: 78-84. [PubMed]

Kelly, D. C., T. Lescott, M. D. Ayres, D. Carey, A. Coutts and K. A. Harrap (1981). Induction of a nonoccluded baculovirus persistently infecting Heliothis zea cells by Heliothis armigera and Trichoplusia ni nuclear polyhedrosis viruses. Virology 112: 174-89. [PubMed]

Lightner, D. V., R. Redman and T. Bell (1983). Observations on the geographic distribution, pathogenesis and morphology of the baculovirus from Penaeus monodon Fabricius. Aquaculture 32: 209-33.

Lightner, D. V. and R. M. Redman (1981a). A baculovirus-caused disease of the penaeid shrimp, Penaeus monodon. J Invertebr Pathol 38: 299-302.

Lightner, D. V. and R. M. Redman (1981b). A baculovirus-caused disease of the penaeid shrimp, Penaeus monodon. J Invert Pathol 38: 299-302.

Liu, S., T. W. Sappington, B. S. Coates and B. C. Bonning (2021). Nudivirus sequences identified from the Southern and Western corn rootworms (Coleoptera: Chrysomelidae). Viruses 13: 269. [PubMed]

Lupiani, B., A. K. Raina and C. Huber (1999). Development and use of a PCR assay for detection of the reproductive virus in wild populations of Helicoverpa zea (Lepidoptera: Noctuidae). J Invertebr Pathol 73: 107-12. [PubMed]

McIntosh, A. H., J. J. Grasela and C. M. Ignoffo (2007). In vitro host range of the Hz-1 nonoccluded virus in insect cell lines. In Vitro Cell Dev Biol Anim 43: 196-201. [PubMed]

Meynardier, G., G. Ricou and M. Bergoin (1964). Virose à corps d'inclusion chez Tipula paludosa (Diptera) en France. Re Pathol Vég Entomol Agric Fr 43: 113-8.

Palmer, W. H., N. C. Medd, P. M. Beard and D. J. Obbard (2018). Isolation of a natural DNA virus of Drosophila melanogaster, and characterisation of host resistance and immune responses. PLoS Pathog 14: e1007050. [PubMed]

Payne, C. C. (1974). The isolation and characterization of a virus from Oryctes rhinoceros. J Gen Virol 25: 105-16. [PubMed]

Payne, C. C., D. Compson and S. M. de Looze (1977). Properties of the nucleocapsids of a virus isolated from Oryctes rhinoceros. Virology 77: 269-80. [PubMed]

Petersen, J. M., A. Bézier, J. M. Drezen and M. M. van Oers (2022). The naked truth: An updated review on nudiviruses and their relationship to bracoviruses and baculoviruses. J Invertebr Pathol 189: 107718. [PubMed]

Raina, A. K. and J. R. Adams (1995). Gonad-specific virus of corn earworm. Nature 374: 770.

Raina, A. K., J. R. Adams, B. Lupiani, D. E. Lynn, W. Kim, J. P. Burand and E. M. Dougherty (2000). Further characterization of the gonad-specific virus of corn earworm, Helicoverpa zea. J Invertebr Pathol 76: 6-12. [PubMed]

Raina, A. K. and B. Lupiani (2006). Acquisition, persistence, and species susceptibility of the Hz-2V virus. J Invertebr Pathol 93: 71-4. [PubMed]

Rallis, C. P. and J. P. Burand (2002a). Pathology and ultrastructure of Hz-2V infection in the agonadal female corn earworm, Helicoverpa zea. J Invertebr Pathol 81: 33-44. [PubMed]

Rallis, C. P. and J. P. Burand (2002b). Pathology and ultrastructure of the insect virus, Hz-2V, infecting agonadal male corn earworms, Helicoverpa zea. J Invertebr Pathol 80: 81-9. [PubMed]

Ralston, A. L., Y. S. Huang and C. Y. Kawanishi (1981). Cell culture studies with the IMC-Hz-1 nonoccluded virus. Virology 115: 33-44. [PubMed]

Ramle, M., M. B. Wahid, K. Norman, T. R. Glare and T. A. Jackson (2005). The incidence and use of Oryctes virus for control of rhinoceros beetle in oil palm plantations in Malaysia. J Invertebr Pathol 89: 85-90. [PubMed]

Rennie, J. (1923). Polyhedral disease in Tipula paludosa MEIG. Proc R Phy Soc Edinb 20: 265-8.

Schoonvaere, K., G. Smagghe, F. Francis and D. C. de Graaf (2018). Study of the metatranscriptome of eight social and solitary wild bee species reveals novel viruses and bee parasites. Front Microbiol 9: 177. [PubMed]

Smith, K. M. (1956). The structure of insect virus particles. J Biophys Biochem Cyt 2: 301-6. [PubMed]

Smith, K. M. and N. Xeros (1954). An unusual virus disease of a dipterous larva. Nature 173: 866-7. [PubMed]

Stentiford, G. D., K. Bateman and S. W. Feist (2004). Pathology and ultrastructure of an intranuclear bacilliform virus (IBV) infecting brown shrimp Crangon crangon (Decapoda: Crangonidae). Dis Aquat Organ 58: 89-97. [PubMed]

Tanaka, S., R. L. Harrison, H. Arai, Y. Katayama, T. Mizutani, M. N. Inoue, J. Miles, S. D. G. Marshall, C. Kitalong and M. Nakai (2021). Confirmation of Oryctes rhinoceros nudivirus infections in G-haplotype coconut rhinoceros beetles (Oryctes rhinoceros) from Palauan PCR-positive populations. Sci Rep 11: 18820. [PubMed]

Thézé, J., A. Bézier, G. Periquet, J. M. Drezen and E. A. Herniou (2011). Paleozoic origin of insect large dsDNA viruses. Proc Natl Acad Sci U S A 108: 15931-5. [PubMed]

Unckless, R. L. (2011). A DNA virus of Drosophila. PLoS One 6: e26564. [PubMed]

Van Eynde, B., O. Christiaens, D. Delbare, K. Cooreman, K. S. Bateman, G. D. Stentiford, A. M. Dullemans, M. M. van Oers and G. Smagghe (2018). Development and application of a duplex PCR assay for detection of Crangon crangon bacilliform virus in populations of European brown shrimp (Crangon crangon). J Invertebr Pathol 153: 195-202. [PubMed]

Velamoor, S., A. Mitchell, B. M. Humbel, W. Kim, C. Pushparajan, G. Visnovsky, L. N. Burga and M. Bostina (2020). Visualizing nudivirus assembly and egress. MBio 11: e01333-20. [PubMed]

Wallace, M. A., K. A. Coffman, C. Gilbert, S. Ravindran, G. F. Albery, J. Abbott, E. Argyridou, P. Bellosta, A. J. Betancourt, H. Colinet, K. Eric, A. Glaser-Schmitt, S. Grath, M. Jelic, M. Kankare, I. Kozeretska, V. Loeschcke, C. Montchamp-Moreau, L. Ometto, B. S. Onder, D. J. Orengo, J. Parsch, M. Pascual, A. Patenkovic, E. Puerma, M. G. Ritchie, O. Rota-Stabelli, M. F. Schou, S. V. Serga, M. Stamenkovic-Radak, M. Tanaskovic, M. S. Veselinovic, J. Vieira, C. P. Vieira, M. Kapun, T. Flatt, J. González, F. Staubach and D. J. Obbard (2021). The discovery, distribution, and diversity of DNA viruses associated with Drosophila melanogaster in Europe. Virus Evol 7: veab031. [PubMed]

Wang, Y.-J., J. P. Burand and J. A. Jehle (2007a). Nudivirus genomics: diversity and classification. Virol Sin 22: 128-36.

Wang, Y., O. R. Bininda-Emonds, M. M. van Oers, J. M. Vlak and J. A. Jehle (2011). The genome of Oryctes rhinoceros nudivirus provides novel insight into the evolution of nuclear arthropod-specific large circular double-stranded DNA viruses. Virus Genes 42: 444-56. [PubMed]

Wang, Y., R. G. Kleespies, A. M. Huger and J. A. Jehle (2007b). The genome of Gryllus bimaculatus nudivirus indicates an ancient diversification of baculovirus-related nonoccluded nudiviruses of insects. J Virol 81: 5395-406. [PubMed]

Wang, Y., M. M. van Oers, A. M. Crawford, J. M. Vlak and J. A. Jehle (2007c). Genomic analysis of Oryctes rhinoceros virus reveals genetic relatedness to Heliothis zea virus 1. Arch Virol 152: 519-31. [PubMed]

Webster, C. L., F. M. Waldron, S. Robertson, D. Crowson, G. Ferrari, J. F. Quintana, J. M. Brouqui, E. H. Bayne, B. Longdon, A. H. Buck, B. P. Lazzaro, J. Akorli, P. R. Haddrill and D. J. Obbard (2015). The discovery, distribution, and evolution of viruses associated with Drosophila melanogaster. PLoS Biol 13: e1002210. [PubMed]

Wu, Y. L., C. P. Wu, S. T. Lee, H. Tang, C. H. Chang, H. H. Chen and Y. C. Chao (2010). The early gene hhi1 reactivates Heliothis zea nudivirus 1 in latently infected cells. J Virol 84: 1057-65. [PubMed]

Wu, Y. L., C. P. Wu, C. Y. Liu, P. W. Hsu, E. C. Wu and Y. C. Chao (2011). A non-coding RNA of insect HzNV-1 virus establishes latent viral infection through microRNA. Sci Rep 1: 60. [PubMed]

Yang, Y. T., D. Y. Lee, Y. Wang, J. M. Hu, W. H. Li, J. H. Leu, G. D. Chang, H. M. Ke, S. T. Kang, S. S. Lin, G. H. Kou and C. F. Lo (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: 628. [PubMed]

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