- -

Viral haemorrhagic disease: RHDV type 2 ten years later

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Viral haemorrhagic disease: RHDV type 2 ten years later

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Capucci, Lorenzo es_ES
dc.contributor.author Cavadini, Patrizia es_ES
dc.contributor.author Lavazza, Antonio es_ES
dc.date.accessioned 2022-05-18T12:10:53Z
dc.date.available 2022-05-18T12:10:53Z
dc.date.issued 2022-03-31
dc.identifier.issn 1257-5011
dc.identifier.uri http://hdl.handle.net/10251/182688
dc.description.abstract [EN] Until the early 1980s, it was totally unknown that lagomorphs were the hosts of several caliciviruses, which were included in the genus Lagovirus by the International Committee on Taxonomy of Viruses (ICTV) in 2000. In those years, two new diseases appeared, with very similar clinical and pathological profiles and associated high mortality rates: rabbit haemorrhagic disease (RHD) in rabbits and European Brown Hare Syndrome (EBHS) in European brown hares. It took a few years to ascertain that both diseases, actually acute and fatal forms of hepatitis, were caused by two genetically related caliciviruses, but they were finally classified by ICTV into two distinct viral species on the basis of their molecular characterisation and epidemiological data: RHDV in rabbit and EBHSV in brown hare. RHD has had a devastating effect on rabbit farms, causing great economic damage, especially in China, where RHD was first noticed around 1982, and in Europe. RHD has also severely affected wild rabbit populations, whose drastic decline has caused serious ecological imbalances in territories such as Spain, where rabbits are a central link in the wildlife food chain. Since the early 1990s, with the increased availability on the market of RHDV vaccines effective in protecting rabbits from RHD, the impact of the disease on rabbit farms has been significantly reduced. In the following years, also considering that RHDV is an endemic virus that cannot be eradicated, farmers learned how to manage the continuous use of RHDV vaccine in relation to the epidemiological situation, the type of breeding farm and the costs of vaccination prophylaxis. Although precarious, management of the RHD risk for rabbit farmers reached an acceptable equilibrium, which was, however, completely upset starting from 2010 by the emergence of another lagovirus also causing RHD. The genome of the newly emerged virus shows limited differences from that of RHDV, but the phenotypic traits of the two viruses are distinctive in at least three main respects: 1) The antigenic profile of the virus (the face of the virus recognised by the antibodies) is largely different from that of RHDV. 2) Newborn rabbits only a couple of weeks old die of RHD when infected with the new virus, while RHDV infections run asymptomatic until 7-8 wk of age. 3) The new virus, which started in Europe, has spread over the years to several continents, affecting wild and/or domestic rabbit populations. During this worldwide distribution, the new virus infected several lagomorph species and was shown to cause RHD in most of them. Considering these marked differences and the fact that the new virus is not a variant of RHDV, we proposed the name RHDV type 2 (RHDV2). All these main distinctive traits that differentiate RHDV from RHDV2 have the following consequences in practice: 1) The antigenic difference between RHDV and RHDV2 (their faces ) is so great that we need new specific vaccines to control RHDV2 (i.e. RHDV2 is a new serotype). 2) In the event of an RHDV2 infection in suckling rabbits, the presence of maternal antibodies to RHDV2 in the blood is the only way to prevent RHD. In contrast, newborns are naturally resistant to RHD if infected with RHDV and therefore, in terms of protection, the presence of maternal antibodies is useless. 3) When RHD outbreaks occur in territories where rabbits live in sympatry with populations of other lagomorphs, viral contamination in the environment reaches sufficiently high levels to facilitate the transmission of RHDV2 to other lagomorphs, including those with a lower susceptibility to infection than the rabbit. Taken together, these phenotypic traits characteristic of RHDV2 are the reason for its rapid spread across the territory and the concomitant disappearance of RHDV. Probably the most striking example of the epidemiological consequences related to the peculiar features of RHDV2 is its rapid spread in the USA and Mexico, where it is now practically endemic. There, despite repeated isolated outbreaks of RHD caused by RHDV from 2000 onwards in small rabbit farms, RHDV has never been able to become endemic. es_ES
dc.language Inglés es_ES
dc.publisher Universitat Politècnica de València es_ES
dc.relation.ispartof World Rabbit Science es_ES
dc.rights Reconocimiento - No comercial - Compartir igual (by-nc-sa) es_ES
dc.subject Rabbit hemorrhagic disease es_ES
dc.subject Virology es_ES
dc.subject Serotype es_ES
dc.subject Serology es_ES
dc.subject Diagnosis es_ES
dc.subject Prophylaxis es_ES
dc.title Viral haemorrhagic disease: RHDV type 2 ten years later es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.4995/wrs.2022.16505
dc.rights.accessRights Abierto es_ES
dc.description.bibliographicCitation Capucci, L.; Cavadini, P.; Lavazza, A. (2022). Viral haemorrhagic disease: RHDV type 2 ten years later. World Rabbit Science. 30(1):1-11. https://doi.org/10.4995/wrs.2022.16505 es_ES
dc.description.accrualMethod OJS es_ES
dc.relation.publisherversion https://doi.org/10.4995/wrs.2022.16505 es_ES
dc.description.upvformatpinicio 1 es_ES
dc.description.upvformatpfin 11 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 30 es_ES
dc.description.issue 1 es_ES
dc.identifier.eissn 1989-8886
dc.relation.pasarela OJS\16505 es_ES
dc.description.references Anthony S.J., Epstein J.H., Murray K.A., Navarrete-Macías I., Zambrana-Torrelio C.M., Solovyov A., Ojeda-Flores R., Arrigo N.C., Islam A., Ali Khan S., Hosseini P., Bogich T.L., Olival K.J., Sánchez-León M.D., Karesh W.B., Goldstein T., Luby S.P., Morse S.S., Mazet J.A.K., Daszak P., Lipkin W.I. 2013. A strategy to estimate unknown viral diversity in mammals. mBio, 4: e00598-13. https://doi.org/10.1128/mBio.00598-13 es_ES
dc.description.references Baratelli M., Molist-Badiola J., Puigredon-Fontanet A., Pascual M., Boix O., Mora-Igual F.X., Woodward M., Lavazza A., Capucci L. 2020. Characterization of the maternally derived antibody immunity against RHDV-2 after administration in breeding does of an inactivated vaccine. Vaccines, 8: 484. https://doi.org/10.3390/vaccines8030484 es_ES
dc.description.references Camarda A., Pugliese N., Cavadini P. Circella E., Capucci L., Caroli A., Legretto M., Mallia E. Lavazza A. 2014. Detection of the new emerging rabbit hemorrhagic disease type 2 virus (RHDV2) in Sicily from rabbit (Oryctolagus cuniculus) and Italian hare (Lepus corsicanus). Res. Vet. Sci., 97: 642-645 https://doi.org/10.1016/j.rvsc.2014.10.008 es_ES
dc.description.references Capucci L., Frigoli G., Ronsholt L., Lavazza A., Brocchi E., Rossi C. 1995. Antigenicity of the Rabbit Hemorrhagic Disease Virus studied by its reactivity with monoclonal antibodies. Virus Res., 37: 221-238. https://doi.org/10.1016/0168-1702(95)00033-M es_ES
dc.description.references Capucci L., Cavadini P., Schiavitto M., Lombardi G., Lavazza A. 2017. Increased pathogenicity in rabbit haemorrhagic disease virus type 2 (RHDV2). Vet. Rec., 180: 246. https://doi.org/10.1136/vr.104132 es_ES
dc.description.references Capucci L., Fallacara F., Grazioli S., Lavazza A Pacciarini Ml, Brocchi E. 1998. A further step in the evolution of rabbit haemorrhagic disease virus: the appearance of the first consistent antigenic variant. Virus Res., 58, 115-126. es_ES
dc.description.references https://doi.org/10.1016/S0168-1702(98)00106-3 es_ES
dc.description.references Capucci L., Fusi P., Lavazza A., Pacciarini M.L., Rossi C. 1996. Detection and preliminary characterization of a new rabbit calicivirus related to Rabbit Hemorrhagic Disease Virus but nonpathogenic. J. Virol, 70: 8614-8623. https://doi.org/10.1128/jvi.70.12.8614-8623.1996 es_ES
dc.description.references Capucci L., Scicluna M.T., Lavazza A. 1991. Diagnosis of viral haemorrhagic disease of rabbits and the European brown hare syndrome. Rev. Sci. Tech. Off. Int. Epiz., 10: 347-370. es_ES
dc.description.references Cavadini, P., Molinari, S., Pezzoni, G., Chiari, M., Brocchi, E., Lavazza, A., Capucci, L. 2015. Identification of a new nonpathogenic lagovirus in Lepus europeaus. In Proc.: 10th International Congress for Veterinary Virology, 9th Annual Epizone Meeting: “Changing Viruses in a Changing World”, August 31st–September 3rd, Montpellier, France. pp. 76-77. es_ES
dc.description.references Cavadini P., Molinari S., Merzoni F., Vismarra A., Posautz A., Alzaga Gil V., Chiari M., Giannini F., Capucci L., Lavazza A. 2021. Occurrence of the non-pathogenic hare calicivirus (HaCV Lagovirus GII.2) in captive reared and free-living wild hares in Europe. Transbound. Emerg. Dis., 68: 509-518. https://doi.org/10.1111/tbed.13706 es_ES
dc.description.references Droillard C., Lemaitre E., Chatel M., Guitton J. S., Marchandeau S., Eterradossi N., Le Gall-Reculé G. 2018. First complete genome sequence of a hare calicivirus strain isolated from Lepus europaeus. Microbiol. Res. Announ., 7. https://doi.org/10.1128/MRA.01224-18 es_ES
dc.description.references Elsworth P., Cooke B.D., Kovaliski J., Sinclair R., Holmes E.C., Strive T. 2014. Increased virulence of rabbit haemorrhagic disease virus associated with genetic resistance in wild Australian rabbits (Oryctolagus cuniculus). Virology, 464-465: 415-423. https://doi.org/10.1016/j.virol.2014.06.037. es_ES
dc.description.references ICTV Virus Taxonomy 2019. 2019 Release, EC 51, Berlin, Germany, July 2019. es_ES
dc.description.references Kerr P.J., Ghedin E., DePasse J.V., Fitch A., Cattadori I.M., Hudson P.J., Tscharke D.C., Read A.F., Holmes E.C. 2012. Evolutionary History and Attenuation of Myxoma Virus on Two Continents. PLoS Pathog., 8: e1002950. https://doi.org/10.1371/journal.ppat.1002950 es_ES
dc.description.references Lavazza, A., Scicluna, M. T., Capucci, L. 1996. Susceptibility of hares and rabbits to the European Brown Hare Syndrome Virus (EBHSV) and Rabbit Hemorrhagic Disease Virus (RHDV) under experimental conditions. J. Vet. Med. B, 43: 401-410. https://doi.org/10.1111/j.1439-0450.1996.tb00332.x es_ES
dc.description.references Lavazza A., Cavadini P., Barbieri I., Tizzani P., Pinheiro A., Abrantes J., Esteves P.J., Grilli G., Gioia E., Zanoni M., Meneguz P.G., Guitton J-S., Marchandeau S., Chiari M., Capucci L. 2015. Field and experimental data indicate that the eastern cottontail (Sylvilagus floridanus) is susceptible to infection with European brown hare syndrome (EBHS) virus and not with rabbit haemorrhagic disease (RHD) virus. Vet. Res., 46: 13 https://doi.org/10.1186/s13567-015-0149-4 es_ES
dc.description.references Le Gall-Reculé G., Lavazza,A., Bertagnoli S., Zwingelstein F., Cavadini P., Martinelli N., Lombardi G., Guérin J-L., Lemaitre E., Decors A., Marchandeau S., Capucci L. 2013. Emergence of a new lagovirus related to Rabbit Haemorrhagic Disease virus. Vet. Res., 44: 81. https://doi.org/10.1186/1297-9716-44-81 es_ES
dc.description.references Le Gall-Reculé G., Zwingelstein, F., Boucher, S., Le Normand, B., Plassiart, G., Portejoie, Y., Decors, S. Bertagnoli, J-L. Guérin, Marchandeau, S. 2011a. Detection of a new variant of rabbit haemorrhagic disease virus in France. Vet. Rec., 168: 137-138. https://doi.org/10.1136/vr.d697 es_ES
dc.description.references Le Gall-Reculé G., Zwingelstein F., Fages M.-P., Bertagnoli S., Gelfi J., Aubineau J., Roobrouck A., Botti G., Lavazza A., Marchandeau S. 2011b. Characterisation of a non-pathogenic and nonprotective infectious rabbit lagovirus related to RHDV. Virology, 410: 395-402. https://doi.org/10.1016/j.virol.2010.12.001 es_ES
dc.description.references Mahar J.E., Hall R.N., Shi M., Mourant R., Huang N., Strive T., Holmes E.C. 2019. The discovery of three new hare lagoviruses reveals unexplored viral diversity in this genus. Virus Evolution, 9. https://doi.org/10.1101/466557 es_ES
dc.description.references Marchandeau S., Le Gall-Recule G., Bertagnoli S., Aubineau J., Botti G., Lavazza A. 2005. Serological evidence for a non-protective RHDV-like virus. Vet. Res., 36: 53-62. https://doi.org/10.1051/vetres:2004049 es_ES
dc.description.references Neimanis A.S., Ahola H., Pettersson U.L., Lopes A.M., Abrantes J., Zohari S., Esteves P.J., Gavier-Widén D. 2018. Overcoming species barriers: an outbreak of Lagovirus europaeus GI.2/RHDV2 in an isolated population of mountain hares (Lepus timidus) BMC Vet. Res. 14: 367. https://doi.org/10.1186/s12917-018-1694-7 es_ES
dc.description.references OIE. 2021. OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals – 3.7.2.RHD chapter. Retrieved from https://www.oie.int/fileadmin/Home/eng/Health_standards/tahm/3.07.02_RHD.pdf Accessed October 2021 es_ES
dc.description.references Ohlinger R.F., Haas B., Meyers G., Weiland F., Thiel H.J. 1990. Identification and characterization of the virus causing rabbit haemorrhagic disease. J. Virol., 64: 3331-3336. https://doi.org/10.1128/jvi.64.7.3331-3336.1990 es_ES
dc.description.references Puggioni G., Cavadini P., Maestrale C., Scivoli R., Botti G., Ligios C., Le Gall-Reculé G., Lavazza A., Capucci L. 2013. The new French 2010 variant of the rabbit hemorrhagic disease virus causes an RHD-like disease in the Sardinian Cape hare (Lepus capensis mediterraneus). Vet. Res., 44: 95. https://doi.org/10.1186/1297-9716-44-96 es_ES
dc.description.references Racaniello V. 2013. How many viruses on Earth? Virology Blog. 6/9/2013. es_ES
dc.description.references https://www.virology.ws/2013/09/06/how-manyviruses-on-earth/ Accessed October 2021. es_ES
dc.description.references Rodák L., Šmíd B., Valíček L., Veselý T., Štěpánek J., Hampl J., Jurák E. 1990. Enzyme-linked Immunosorbent Assay of Antibodies to Rabbit Haemorrhagic Disease Virus and Determination of its Major Structural Proteins. J. General Virol., 71: 1075-1080. https://doi.org/10.1099/0022-1317-71-5-1075 es_ES
dc.description.references Strive T., Wright J.D., Robinson A.J. 2009. Identification and partial characterisation of a new Lagovirus in Australian wild rabbits. Virology, 384: 97-105. https://doi.org/10.1016/j.virol.2008.11.004 es_ES
dc.description.references Taggart P.L., Hall RN., Cox T.E., Kovaliski J., McLeod S.R., Strive T. 2021. Changes in virus transmission dynamics following the emergence of RHDV2 shed light on its competitive advantage over previously circulating variants. Transbound. Emerg. Dis., 16 March 2021. https://doi.org/10.1111/tbed.14071 es_ES
dc.description.references Velarde R., Cavadini P., Neimanis A., Cabezón O., Chiari M., Gaffuri A., Lavín S., Grilli G., Gavier-Widén D., Lavazza A., Capucci L. 2017. Spillover events of infection of brown hares (Lepus europaeus) with rabbit haemorrhagic disease type 2 virus (RHDV2) caused sporadic cases of an European Brown hare syndrome like-disease in Italy and Spain. Transbound.Emerg. Dis., 64: 1750-1761. https://doi.org/10.1111/tbed.12562 es_ES
dc.description.references Wirblich C., Meyers G., Ohlinger V.F., Capucci L., Eskens U., Haas B., Thiel H.J. 1994. European brown hare syndrome virus – relationship to rabbit hemorrhagic disease virus and other caliciviruses. J. Virol., 68: 5164-5173. https://doi.org/10.1128/JVI.68.8.5164-5173.1994 es_ES


Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem