Ranavirus

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Ranavirus
CSIRO ScienceImage 2010 Ranavirus Pathogen.jpg
Transmission electron micrograph of ranaviruses (dark hexagons) gathering at the cell border and leaving the cell via a process called "budding".
Virus classification OOjs UI icon edit-ltr.svg
(unranked): Virus
Realm: Varidnaviria
Kingdom: Bamfordvirae
Phylum: Nucleocytoviricota
Class: Megaviricetes
Order: Pimascovirales
Family: Iridoviridae
Subfamily: Alphairidovirinae
Genus:Ranavirus
Transmission electron micrograph of a cell infected with ranaviruses, which gather in the cytoplasm and in the assembly bodies next to the contorted nucleus. CSIRO ScienceImage 2315 Ranaviruses.jpg
Transmission electron micrograph of a cell infected with ranaviruses, which gather in the cytoplasm and in the assembly bodies next to the contorted nucleus.

Ranavirus is a genus of viruses in the family Iridoviridae . [1] There are six other genera of viruses within the family Iridoviridae , but Ranavirus is the only one that includes viruses that are infectious to amphibians and reptiles. Additionally, it is one of the three genera within this family which infect teleost fishes, along with Lymphocystivirus and Megalocytivirus . [2]

Contents

Ecological impact

The Ranaviruses, like the Megalocytiviruses, are an emerging group of closely related dsDNA viruses which cause systemic infections in a wide variety of wild and cultured fresh and saltwater fishes. As with Megalocytiviruses, Ranavirus outbreaks are therefore of considerable economic importance in aquaculture, as epizootics can result in moderate fish loss or mass mortality events of cultured fishes. Unlike Megalocytiviruses, however, Ranavirus infections in amphibians have been implicated as a contributing factor in the global decline of amphibian populations. [3] [4] The impact of Ranaviruses on amphibian populations has been compared to the chytrid fungus Batrachochytrium dendrobatidis , the causative agent of chytridiomycosis. [5] [6] [7] In the UK, the severity of disease outbreaks is thought to have increased due to climate change. [8]

Etymology

Rana is derived from the Latin for "frog", [9] reflecting the first isolation of a Ranavirus in 1960s from the Northern leopard frog ( Lithobates pipiens ). [10] [11] [12]

Evolution

VOA report about Ranavirus

The ranaviruses appear to have evolved from a fish virus which subsequently infected amphibians and reptiles. [13]

Hosts

Anuran hosts

Urodelan hosts

Reptilian hosts

Taxonomy

The genus contains the following species: [24]

The family Iridoviridae is divided into seven genera which include Chloriridovirus , Iridovirus , Lymphocystivirus , Megalocytivirus , and Ranavirus. [1] The genus Ranavirus contains three viruses known to infect amphibians (Ambystoma tigrinum virus (ATV), Bohle iridovirus (BIV), and frog virus 3). [25]

Structure

Ranaviruses are large icosahedral DNA viruses measuring approximately 150 nm in diameter with a large single linear dsDNA genome of roughly 105 kbp [26] which codes for around 100 gene products. [27] The main structural component of the protein capsid is the major capsid protein (MCP).

GenusStructureSymmetryCapsidGenomic arrangementGenomic segmentation
RanavirusPolyhedralT=133 or 147LinearMonopartite

Replication

Ranaviral replication is well studied using Frog virus 3 (FV3). [25] [26] Replication of FV3 occurs between 12 and 32 degrees Celsius. [27] Ranaviruses enter the host cell by receptor-mediated endocytosis. [28] Viral particles are uncoated and subsequently move into the cell nucleus, where viral DNA replication begins via a virally encoded DNA polymerase. [29] Viral DNA then abandons the cell nucleus and begins the second stage of DNA replication in the cytoplasm, ultimately forming DNA concatemers. [29] The viral DNA is then packaged via a headful mechanism into infectious virions. [25] The ranavirus genome, like other iridoviral genomes is circularly permuted and exhibits terminally redundant DNA. [29] There is evidence that ranavirus infections target macrophages as a mechanism for gaining entry to cells. [30]

GenusHost detailsTissue tropismEntry detailsRelease detailsReplication siteAssembly siteTransmission
RanavirusFrogs; snakesNoneCell receptor endocytosisLysis; buddingNucleusCytoplasmContact

Transmission

Transmission of ranaviruses is thought to occur by multiple routes, including contaminated soil, direct contact, waterborne exposure, and ingestion of infected tissues during predation, necrophagy or cannibalism. [11] [31] Ranaviruses are relatively stable in aquatic environments, persisting several weeks or longer outside a host organism. [11]

Epizoology

Amphibian mass mortality events due to Ranavirus have been reported in Asia, Europe, North America, and South America. [11] Ranaviruses have been isolated from wild populations of amphibians in Australia, but have not been associated with mass mortality on that continent. [11] [32] [33]

Pathogenesis

Synthesis of viral proteins begins within hours of viral entry [27] with necrosis or apoptosis occurring as early as a few hours post infection. [26] [34]

Seasonal disease dynamics

There are several hypotheses for seasonal outbreak patterns observed for Ranavirosis mortality events. [35] Ranaviruses grow in vitro between 8-30 °C, however for most isolates, warmer temperature result in faster viral replication. [35] A combination of this optimal growth temperature along with shifts in larval amphibian susceptibility result in seasonal outbreak events most often observed during warm summer months. [36] Amphibian mortality events are often observed as larval amphibians reach late Gosner stages approaching metamorphosis. [37] As larval amphibians reach metamorphic stages of development, their immune system is reorganized prior to the development of adult tissues. [38] During this time period, amphibians are stressed, and their immune systems are down regulated. This decrease in immune function and warmer environmental temperatures allows for greater viral replication and cellular damage to occur. Across 64 mortality events in the United States 54% were found to occur between June-August. [36]

Environmental persistence

The environmental persistence of Ranaviruses is not understood well, however in realistic environmental conditions the T90 value of an FV3-like virus is 1 day. [39] The duration of persistence is likely affected by temperature and microbial conditions. It is unlikely that ranaviruses persist in the environment outside of host species between outbreak events. Researchers have explored several pathogen reservoirs for the virus which might explain how the virus can persist within an amphibian community. In some amphibian populations, sub-clinically infected individuals may serve as reservoirs for the pathogen. [6] These sub-clinically infected individuals are responsible for reintroduction of the virus to the larval population. With ranaviruses being capable of infected multiple taxa, and with there being differences in susceptibility between taxa, it is likely that sympatric fish and reptile species may serve as reservoirs for virus as well. Interclass transmission has been proven through the use of mesocosm studies. [40]

Gross pathology

Gross lesions associated with Ranavirus infection include erythema, generalized swelling, hemorrhage, limb swelling, and swollen and friable livers. [11]

See also

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References

  1. 1 2 "Iridoviridae". ICTV Online (10th) Report.
  2. ↑ Whittington, RJ; Becker, JA; Dennis, MM (2010). "Iridovirus infections in finfish – critical review with emphasis on ranaviruses". Journal of Fish Diseases. 33 (2): 95–122. doi:10.1111/j.1365-2761.2009.01110.x. PMID   20050967.
  3. ↑ Teacher, A. G. F.; Cunningham, A. A.; Garner, T. W. J. (10 June 2010). "Assessing the long-term impact of Ranavirus infection in wild common frog populations: Impact of Ranavirus on wild frog populations". Animal Conservation. 13 (5): 514–522. doi:10.1111/j.1469-1795.2010.00373.x. S2CID   85889833.
  4. ↑ Price, Stephen J.; Garner, Trenton W.J.; Nichols, Richard A.; Balloux, François; Ayres, César; Mora-Cabello de Alba, Amparo; Bosch, Jaime (November 2014). "Collapse of Amphibian Communities Due to an Introduced Ranavirus". Current Biology. 24 (21): 2586–2591. doi: 10.1016/j.cub.2014.09.028 . PMID   25438946.
  5. ↑ Jancovich, James K; Mao, Jinghe; Chinchar, V.Gregory; Wyatt, Christopher; Case, Steven T; Kumar, Sudhir; Valente, Graziela; Subramanian, Sankar; Davidson, Elizabeth W; Collins, James P; Jacobs, Bertram L (2003). "Genomic sequence of a ranavirus (family Iridoviridae) associated with salamander mortalities in North America". Virology. 316 (1): 90–103. doi: 10.1016/j.virol.2003.08.001 . PMID   14599794.
  6. 1 2 Brunner, Jesse L.; Schock, Danna M.; Davidson, Elizabeth W.; Collins, James P. (2004). "Intraspecific Reservoirs: Complex Life History and the Persistence of a Lethal Ranavirus". Ecology. 85 (2): 560. doi:10.1890/02-0374.
  7. ↑ Pearman, Peter B.; Garner, Trenton W. J. (2005). "Susceptibility of Italian agile frog populations to an emerging strain of Ranavirus parallels population genetic diversity". Ecology Letters. 8 (4): 401. doi:10.1111/j.1461-0248.2005.00735.x.
  8. ↑ Price, Stephen J.; Leung, William T. M.; Owen, Christopher J.; Puschendorf, Robert; Sergeant, Chris; Cunningham, Andrew A.; Balloux, Francois; Garner, Trenton W. J.; Nichols, Richard A. (9 May 2019). "Effects of historic and projected climate change on the range and impacts of an emerging wildlife disease". Global Change Biology. 25 (8): 2648–2660. Bibcode:2019GCBio..25.2648P. doi:10.1111/gcb.14651. hdl: 10026.1/13802 . ISSN   1354-1013. PMID   31074105. S2CID   149444899.
  9. ↑ Harper, Douglas. "frog". Online Etymology Dictionary .
  10. ↑ Granoff, A; Came, PE; Rafferty, KA (1965). "The isolation and properties of viruses from Rana pipiens: their possible relationship to the renal adenocarcinoma of the leopard frog". Annals of the New York Academy of Sciences. 126 (1): 237–255. Bibcode:1965NYASA.126..237G. doi:10.1111/j.1749-6632.1965.tb14278.x. PMID   5220161. S2CID   1534726.
  11. 1 2 3 4 5 6 Gray, MJ; Miller, DL; Hoverman, JT (2009). "Ecology and pathology of amphibian ranaviruses". Diseases of Aquatic Organisms. 87 (3): 243–266. doi: 10.3354/dao02138 . PMID   20099417.
  12. ↑ Rafferty, KA (1965). "The cultivation of inclusion-associated viruses from Lucke tumor frogs". Annals of the New York Academy of Sciences. 126 (1): 3–21. Bibcode:1965NYASA.126....3R. doi:10.1111/j.1749-6632.1965.tb14266.x. PMID   5220167. S2CID   38763155.
  13. ↑ Jancovich, JK; Bremont, M; Touchman, JW; Jacobs, BL (2010). "Evidence for multiple recent host species shifts among the Ranaviruses (family Iridoviridae)". J Virol. 84 (6): 2636–2647. doi:10.1128/JVI.01991-09. PMC   2826071 . PMID   20042506.
  14. ↑ First identification of a ranavirus from green pythons (Chondropython viridis); Williamson; Coupar; Middleton; Hengstberger; Gould; Selleck; Wise; Kattenbelt; Cunningham; Lee (2002). "First identification of a ranavirus from green pythons (Chondropython viridis)". Journal of Wildlife Diseases. 38 (2): 239–52. doi:10.7589/0090-3558-38.2.239. PMID   12038121. S2CID   17427050.
  15. ↑ Benetka V. (2007). "First report of an iridovirus (genus Ranavirus) infection in a leopard tortoise (Geochelone pardalis pardalis)" (PDF). Vet Med Austria. 94: 243–248.
  16. ↑ De Matos, A. P.; Caeiro, M. F.; Papp, T; Matos, B. A.; Correia, A. C.; Marschang, R. E. (2011). "New viruses from Lacerta monticola (Serra da Estrela, Portugal): Further evidence for a new group of nucleo-cytoplasmic large deoxyriboviruses (NCLDVs)". Microscopy and Microanalysis. 17 (1): 101–8. Bibcode:2011MiMic..17..101A. doi:10.1017/S143192761009433X. PMID   21138619. S2CID   21932480.
  17. ↑ Mao, J; Hedrick, RP; Chinchar, VG (1997). "Molecular characterization, sequence analysis, and taxonomic position of newly isolated fish iridoviruses". Virology. 229 (1): 212–220. doi: 10.1006/viro.1996.8435 . PMID   9123863.
  18. 1 2 Johnson, A. J.; Pessier, A. P.; Jacobson, E. R. (2007). "Experimental transmission and induction of ranaviral disease in Western Ornate box turtles (Terrapene ornata ornata) and red-eared sliders (Trachemys scripta elegans)". Veterinary Pathology. 44 (3): 285–97. doi: 10.1354/vp.44-3-285 . PMID   17491069.
  19. ↑ Blahak S., Uhlenbrok C. "Ranavirus infections in European terrestrial tortoises in Germany". Proceedings of the 1st International Conference on Reptile and Amphibian Medicine; Munich, Germany. 4–7 March 2010; pp. 17–23
  20. ↑ McKenzie, C. M.; Piczak, M.L.; Snyman, H. N.; Joseph, T.; Theijin, C.; Chow-Fraser, P.; Jardine, C. M. (2019). "First report of ranavirus mortality in a common snapping turtle Chelydra serpentina" (PDF). Diseases of Aquatic Organisms. 132 (3): 221–227. doi:10.3354/dao03324. PMID   31188138. S2CID   92405818.
  21. ↑ Chen, Z. X.; Zheng, J. C.; Jiang, Y. L. (1999). "A new iridovirus isolated from soft-shelled turtle". Virus Research. 63 (1–2): 147–51. doi:10.1016/S0168-1702(99)00069-6. PMID   10509727.
  22. ↑ Marschang, R. E.; Braun, S; Becher, P (2005). "Isolation of a ranavirus from a gecko (Uroplatus fimbriatus)". Journal of Zoo and Wildlife Medicine. 36 (2): 295–300. doi:10.1638/04-008.1. JSTOR   20096453. PMID   17323572. S2CID   20616080.
  23. ↑ Goodman, R.; Hargadon, K; Carter, E. (2018). "Detection of Ranavirus in Eastern Fence Lizards and Eastern Box Turtles in Central Virginia". Northeastern Naturalist. 25 (3): 391–398. doi:10.1656/045.025.0306. S2CID   91510246.
  24. ↑ "Virus Taxonomy: 2020 Release". International Committee on Taxonomy of Viruses (ICTV). March 2021. Retrieved 22 May 2021.
  25. 1 2 3 Chinchar VG, Essbauer S, He JG, Hyatt A, Miyazaki T, Seligy V, Williams T (2005). "Family Iridoviridae" pp. 145–162 in Fauquet CM, Mayo MA, Maniloff J, Desselburger U, Ball LA (eds). Virus Taxonomy, Eighth report of the International Committee on Taxonomy of Viruses. Academic Press, San Diego, USA.
  26. 1 2 3 Williams T, Barbosa-Solomieu V, Chinchar GD (2005). "A decade of advances in iridovirus research" 173-148. In Maramorosch K, Shatkin A (eds). Advances in virus research, Vol. 65 Academic Press, New York, USA.
  27. 1 2 3 Chinchar, VG (2002). "Ranaviruses (family Iridoviridae) emerging cold-blooded killers". Archives of Virology. 147 (3): 447–470. doi: 10.1007/s007050200000 . PMID   11958449. S2CID   24928231.
  28. ↑ Eaton, Heather E.; Ring, Brooke A.; Brunetti, Craig R. (2010). "The genomic diversity and phylogenetic relationship in the family Iridoviridae". Viruses. 2 (7): 1458–75. doi: 10.3390/v2071458 . PMC   3185713 . PMID   21994690.
  29. 1 2 3 Goorha, R (1982). "Frog virus 3 DNA replication occurs in two stages". Journal of Virology. 43 (2): 519–28. doi:10.1128/JVI.43.2.519-528.1982. PMC   256155 . PMID   7109033.
  30. ↑ Girdhar, Khyati; Powis, Amaya; Raisingani, Amol; Chrudinová, Martina; Huang, Ruixu; Tran, Tu; Sevgi, Kaan; Dogus Dogru, Yusuf; Altindis, Emrah (29 September 2021). "Viruses and Metabolism: The Effects of Viral Infections and Viral Insulins on Host Metabolism". Annual Review of Virology. 8 (1): 373–391. doi: 10.1146/annurev-virology-091919-102416 . ISSN   2327-056X. PMC   9175272 . PMID   34586876.
  31. ↑ Brenes, Roberto; Gray, Matthew J.; Waltzek, Thomas B.; Wilkes, Rebecca P.; Miller, Debra L. (25 March 2014). "Transmission of Ranavirus between Ectothermic Vertebrate Hosts". PLOS ONE. 9 (3): e92476. Bibcode:2014PLoSO...992476B. doi: 10.1371/journal.pone.0092476 . ISSN   1932-6203. PMC   3965414 . PMID   24667325.
  32. ↑ Speare, R; Smith, JR (1992). "An iridovirus-like agent isolated from the ornate burrowing frog Limnodynastes ornatus in northern Australia". Diseases of Aquatic Organisms. 14: 51–57. doi: 10.3354/dao014051 .
  33. ↑ Cullen, BR; Owens, L (2002). "Experimental challenge and clinical cases of Bohle iridovirus (BIV) in native Australian anurans". Diseases of Aquatic Organisms. 49 (2): 83–92. doi: 10.3354/dao049083 . PMID   12078986.
  34. ↑ Chinchar, VG; Bryan, L; Wang, J; Long, S; Chinchar, GD (2003). "Induction of apoptosis in frog virus 3-infected cells". Virology. 306 (2): 303–312. doi: 10.1016/S0042-6822(02)00039-9 . PMID   12642103.
  35. 1 2 Brunner, Jesse L; Storfer, Andrew; Gray, Matthew J; Hoverman, Jason T (2015). Ranaviruses: Lethal Pathogens of Ectothermic Vertebrates. New York: Springer. p. 71-104. doi:10.1007/978-3-319-13755-1_4. ISBN   978-3-319-13755-1.
  36. 1 2 Green, D E; Converse, K A; Schrader, A K (2002). "Epizootiology of sixty-four amphibian morbidity and mortality events in the USA, 1996-2001". Domestic Animal/Wildlife Interface: Issues for Disease Control, Conservation, Sustainable Food Production, and Emerging Diseases. 969 (1): 323–339. Bibcode:2002NYASA.969..323G. doi:10.1111/j.1749-6632.2002.tb04400.x. PMID   12381613. S2CID   33944909.
  37. ↑ Green, D E; Converse, K A (2005). "Diseases of frogs and toads". Wildlife Diseases: Landscape Epidemiology, Spatial Distribution, and Utilization of Remote Sensing Technology.: 89-117.
  38. ↑ Rollins-Smith, L A (1998). "Metamorphosis and the amphibian immune system". Immunological Reviews. 166: 221–230. doi:10.1111/j.1600-065X.1998.tb01265.x. PMID   9914915. S2CID   27561247.
  39. ↑ Johnson, A F; Brunner, J L (2014). "Persistence of an amphibian ranavirus in aquatic communities". Diseases of Aquatic Organisms. 111 (2): 129–138. doi: 10.3354/dao02774 . PMID   25266900.
  40. ↑ Brenes, Roberto; Gray, MJ; Waltzek, TB; Wilkes, RP; Miller, DL (2014). "Transmission of Ranavirus between Ectothermic Vertebrate Hosts". PLOS ONE. 9 (3): e92476. Bibcode:2014PLoSO...992476B. doi: 10.1371/journal.pone.0092476 . PMC   3965414 . PMID   24667325.

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