UDC 619:636.2:578.833.3

doi: 10.15389/agrobiology.2015.4.399eng

ATYPICAL BOVINE PESTIVIRUSES (review)

A.G. Glotov, T.I. Glotova

Institute of Experimental Veterinary Science of Siberia and the Far East, Federal Agency of Scientific Organizations, pos. Krasnoobsk, Novosibirskii Region, Novosibirsk Province, 630501 Russia,
e-mail glotov_vet@mail.ru, t-glotova@mail.ru

Received January 27, 2015


Increasingly frequent outbreaks of atypical viral infections, detection of new viruses, modified isolates and quasitypes with a confirmed or potential emergence have become a worrying feature of the last decades characterized by extremely close international dealings. For the cattle industry, they pose real and serious threat because of a tendency to spread widely and quickly due to globalization and the use of standardized zootechnical and veterinary protocols. The Flaviviridae family comprises several genera of which the genus Pestivirus, including four viruses, i.e. the cattle viral diarrhea — mucosal disease (VD-MD) virus types 1 and 2, swine fever virus and sheep border disease virus, are important to farm animals (http://ictvonline.org/virusTaxonomy.asp). The characteristics of a new group of viruses genus Pestivirus of the Flaviviridae family, allocated in the period from 2000 to 2014 from the buffalo and cattle, as well as fetal calf serum used for cell cultures and vaccines production harvested in Australia, Canada, Mexico, Brazil and the United States and packaged in Europe (H. Schirrmeier et al., 2004; A. Cortez et al., 2006; E. Bianchi et al., 2011; B. Rodrigues et al., 2011; H. Xia et al., 2011; H. Xia et al., 2012; S. Peletto et al., 2012) are submitted in the review. The virus has been isolated in Thailand, Bangladesh and China (L. Liu et al., 2009; L. Mao et al., 2012; N. Haider et al., 2014). Messages on the isolation of the agent in other European countries, North America, Russia, India and Australia are absent (F.V. Bauermann et al., 2013). The widespread use of contaminated biological products can facilitate the penetration of the virus in different regions of continent causing their potential emergence for cattle. Strains of viruses presented cytopathic and noncytopathic biotypes not officially classified and have a variety titles in literature: a third type of viral diarrhea-mucosal disease in cattle (BVDV), an atypical pestivirus (HoBi-like), the fifth type of Pestivirus genus (N. Decaro et al., 2012). Based on phylogenetic analysis were identified two genetic groups: Brazilian and Thai, which differ from the prototype member of the genus - the BVD virus but having a great similarity in the manifestation of clinical signs, the ability to infect the foetus of cattle and buffalo (F.V. Bauermann et al., 2013). In cattle a spontaneous or experimental infection caused by HoBi-like virus is very similar to the cattle VD-MD and manifests as diarrhea, abortion, respiratory syndrome, persistent infection (F.V. Bauermann et al., 2013). The situation is aggravated by the fact that they like the BVDV are able to induce persistent infection and forms permanent epizootic foci (M.N. Weber et al., 2014). The discovery of this group of viruses requires a critical assessment of the diagnostic tools and vaccines against the BVDV. To date, the there are no tests for the detection of ruminants’ pestiviruses or their antibodies, particularly due to high variability of this virus group. That is why their laboratory diagnosis should not rely on the use of a single test. The best approach would be serological diagnosis of the herd followed by the identification of persistently infected animals, the virus isolation and molecular analysis (F.V. Bauermann et al., 2013). Given the lack of HoBi-like infection diagnostics, these viruses can remain unnoticed and, presumably, compromising the effectiveness of control or eradication programs of BVDV realized in certain European countries and the United States (K. Ståhl et al., 2004; J.F. Ridpath, 2010).

Keywords: pestiviruses, viral diarrhea-mucosal disease, atypical viruses, sequencing, genetic subgroups, fetal serum, buffalo, molecular diagnostics, control programs.

 

Full article (Rus)

Full text (Eng)

 

REFERENCES

  1. Harasawa R., Giangaspero M., Ibata G., Paton D.J. Giraffe strain of pestivirus: its taxonomic status based on the 50-untranslated region. Microbiol. Immunol., 2000, 44: 915-921 CrossRef
  2. Vilcek S., Ridpath J.F., Van Campen H., Cavender J.L., Warg J. Characterization of a novel pestivirus originating from a pronghorn antelope. Virus Res., 2005, 108: 187-193 CrossRef
  3. Kirkland P.D., Frost M.J., Finlaison D.S., King K.R., Ridpath J.F., Gu X. Identification of a novel virus in pigs — Bungowannah virus: a possible new species of pestivirus. Virus Res., 2007, 129: 26-34 CrossRef
  4. Giangaspero M., Apicellab S., Harasawa R. Numerical taxonomy of the genus Pestivirus: New software for genotyping based on the palindromic nucleotide substitutions method. J. Virol. Methods, 2013, 192: 59-67 CrossRef
  5. MacLachlan N.J., Dubovi E.J. Flaviviridae. In: Fenner’s veterinary virology. 4th edition /N.J. Mac-Lachlan, E.J. Dubovi (eds.). Academic Press, UK, 2011: 467-481.
  6. Rodrigues W.B., Otonel R.A., Fritzen J.T. Natural infection of calf with an atypical bovine pestivirus (BVDV-3). In: Proc. XXII National Meeting of Virology & VI Mercosur Meeting of Virology (Atibaia, Brazil). Virus Rev. Res., 2011, 16 (Suppl. 1): 74.
  7. Schirrmeier H., Strebelow G., Depner K., Hoffmann B., Beer M. Genetic and antigenic characterization of an atypical pestivirus isolate, a putative member of a novel pestivirus species. J. Gen. Virol., 2004, 85: 3647-3652 CrossRef
  8. Avalos-Ramirez R., Orlich M., Thiel H.-J., Becher P. Evidence for the presence of two novel Pestivirus species. Virology, 2001, 286: 456-465 CrossRef
  9. Bauermann F.V., Ridpath J.F., Weiblen R., Flores E.F. HoBi-like viruses: an emerging group of pestiviruses. J. Vet. Diagn. Invest., 2013, 25(1): 6-15 CrossRef
  10. Baker J.C. The clinical manifestations of bovine viral diarrhea virus infection. Vet. Clin. North Am. Food Anim. Pract., 1995, 11: 425-445.
  11. Kahn C.M. Bovine viral diarrhea and mucosal disease complex in intestinal diseases in ruminants. The Merck Vet., 2005, 9: 220.
  12. Ridpath J.F. Bovine viral diarrhea virus: global status. Vet. Clin. North Am. Food Anim. Pract., 2010, 26: 105-121 CrossRef
  13. Glotov A.G., Petrova O.G., Glotova T.I., Nefedchenko A.V., Tatar-
    chuk A.T., Koteneva S.V., Vetrov G.V., Sergeev A.N. Veterinariya, 2002, 3: 17-21.
  14. Glotov A.G., Kelling K.L. Rossiiskii veterinarnyi zhurnal, 2007, 12: 19-22.
  15. Gulyukin M.I., Yurov K.P., Glotov A.G., Donchenko N.A. Voprosy virusologii, 2013, 6: 13-18.
  16. Houe H. Epidemiological features and economical importance of bovine virus diarrhoea virus (BVDV) infections. Vet. Microbiol., 1999, 64: 89-107 CrossRef
  17. Giangaspero M., Harasawa R. Characterization of genotypes among bovine viral diarrhea virus type1 strains according to palindromic nucleotide substitutions in the genomic 5¢-untranslated region. J. Virol. Methods, 2014, 195: 34-53 CrossRef
  18. Tamura K., Peterson D., Peterson N., Stecher G., Nei M., Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol. Biol. Evol., 2011, 28: 2731-2739 CrossRef
  19. Thiel H.-J., Collett M.S., Gould E.A. Flaviviridae. In: Virus taxonomy — eighth report of the International Committee on the Taxonomy of Viruses /C.M. Fauquet, M.A. Mayo, J. Maniloff (eds.). San Diego, CA, 2005: 981-998.
  20. Liu L., Xia H., Wahlberg N., Belak S., Baule C. Phylogeny, classification and evolutionary insights into pestiviruses. Virology, 2009, 385: 351-357 CrossRef 
  21. Neill J.D., Bayles D.O., Ridpath J.F. Simultaneous rapid sequencing of multiple RNA virus genomes. J. Virol. Methods, 2014, 201: 68-72 CrossRef
  22. Cortez A., Heinemann M.B., Castro A.M., Soares R.M., Pinto A.M., Alfieri A.A., Flores E.F., Leite R.C., Richtzenhain L.J. Genetic characterization of Brazilian bovine viral diarrhea virus isolates by partial nucleotide sequencing of the 5¢-UTR region. Pesq. Vet. Bras., 2006, 26: 211-216.
  23. Mao L., Li W., Zhang W., Yang L., Jiang J. Genome sequence of a novel Hobi-like pestivirus in China. J.Virol., 2012, 86(22): 12444 CrossRef
  24. Ridpath J.F., Neill J.D., Vilcek S., Dubovi E.F., Carman S. Multiple outbreaks of severe acute BVDV in North America occurring between 1993 and 1995 linked to the same BVDV2 strain. Vet. Microbiol., 2006, 114: 196-204 CrossRef
  25. Yuzhakov A.G., Ustinova G.I., Glotov A.G., Glotova T.I., Nefedchen-ko A.V., Kungurtseva O.V., Zaberezhnyi A.D., Aliper T.I. Voprosy virusologii, 2009, 6: 43-47. 
  26. Yurov G.K., Alekseenkova S.V., Dias Khimenes K.A. Rossiiskii veterinarnyi zhurnal, 2013, 2: 24-28.
  27. Vilcek Š., Durkovi B., Kolesàrovà M., Greiser-Wilke I.. Paton D. Genetic diversity of international bovine viral diarrhea virus (BVDV) isolates: Identification of a new BVDV-1 genetic group. Vet. Res., 2004, 35: 609-615 CrossRef
  28. Liu L., Kampa J., Belák S., Baule C. Virus recovery and full-length sequence analysis of atypical bovine pestivirus Th/04_KhonKaen. Vet. Microbiol., 2009, 138: 62-68 CrossRef
  29. Decaro N., Lucente M.S., Mari V. Atypical pestivirus and severe respiratory disease in calves. Europe. Emerg. Infect. Dis., 2011, 17: 1549-1552 CrossRef 
  30. Decaro N., Mari V., Pinto P. «Hobi»-like pestivirus: Both biotypes isolated from diseased animal. J. Gen. Virol., 2012, 93: 1976-1983 CrossRef
  31. Weber M.N., Mosena A.C., Simoes S.V., Almeida L.L., Pessoa C.R., Budaszewski R.F., Silva T.R., Ridpath J.F., Riet-Correa F., Driemeier D., Cana C.W. Clinical presentation resembling mucosal disease associated with «HoBi»-like pestivirus in a field outbreak. Transbound. Emerg. Dis., 2014 CrossRef
  32. Xia H., Vijayaraghavan B., Belák S., Liu L. Detection and identification of the atypical bovine pestiviruses in commercial foetal bovine serum batches. PLoS ONE, 2011, 6(12): e28553 CrossRef
  33. Haider N., Rahman M.S., Khan S.U., Mikolon A., Gurley E.S., Osmani  M.G., Shanta I.S., Paul S.K., Macfarlane-Berry L., Islam A., Desmond J., Epstein J.H., Daszak P., Azim T., Luby S.P., Zeidner N., Rahman M.Z. Identification and epidemiology of a rare HoBi-like pestivirus strain in Bangladesh.Transbound. Emerg. Dis., 2014 CrossRef
  34. Bianchi E., Martins M., Weiblen R. Perfil genotípico e antigênico de amostras do vírus da diarréia viral bovina isoladas no Rio Grande do Sul (2000-2010) [Genotypic and antigenic profile of bovine viral diarrhea virus isolates from Rio Grande do Sul, Brazil (2000-2010)]. Pesq. Vet. Bras., 2011, 31: 649-655.
  35. Peletto S., Zuccon F., Pitti M., Gobbi E., Marco L.D., Caramelli M., Masoero L., Acutis P.L. Detection and phylogenetic analysis of an atypical pestivirus, strain IZSPLV_To. Res. Vet. Sci., 2012, 92(1): 147-150 CrossRef
  36. Jones K.E., Patel N.G., Levy M.A., Storeygard A., Balk D., Gittle-
    man J.L., Daszak P. Global trends in emerging infectious diseases. Nature, 1999, 451: 990-993 CrossRef
  37. Decaro N., Lucente M.S., Mari V. Hobi-like pestivirus in aborted bovine fetuses. J. Clin. Microbiol., 2012, 50: 509-512 CrossRef
  38. Decaro N., Sciarretta R., Lucente M.S. A nested PCR approach for unambiguous typing of pestiviruses infecting cattle. Mol. Cell. Probes, 2012, 26: 42-46 CrossRef
  39. Ståhl K., Kampa J., Alenius S., Persson W.A., Baule C., Aiumlamai S., Belák S. Natural infection of cattle with an atypical «HoBi»-like estivirus — implications for BVD control and for the safety of biological products. Vet. Res., 2004, 38: 517-523 CrossRef
  40. Decaro N., Mari V., Lucente M.S. Experimental infection of cattle, sheep and pigs with «Hobi»-like pestivirus. Vet. Microbiol., 2012, 155: 165-171 CrossRef
  41. Larska M., Polak M.P., Riitho V. Kinetics of single and dual infection of calves with an Asian atypical bovine pestivirus and a highly virulent strain of bovine viral diarrhoea virus 1. Comp. Immunol. Microbiol. Infect. Dis., 2012, 35: 381-390 CrossRef
  42. Kozas T., Aoki H., Nakajima N. Methods to select suitable fetal bovine serum for use in quality control assays for the detection of adventitious viruses from biological products. Biologicals, 2011, 39: 242-248 CrossRef
  43. Liu L., Xia H., Belák S., Baule C. A TaqMan real-time RT-PCR assay for selective detection of atypical bovine pestiviruses in clinical samples and biological products. J. Virol. Methods, 2008, 154: 82-85 CrossRef
  44. Xia H., Larska M., Giammarioli M., De Mia G.M., Cardeti G., Zhou W., Alenius S., Belák S., Liu L. Genetic detection and characterization of atypical bovine pestiviruses in foetal bovine sera claimed to be of Australian origin. Transbound. Emerg. Dis., 2013, 60(3): 284-288 CrossRef
  45. Sullivan D.G., Akkina R.K. A nested polymerase chain reaction assay to differentiate pestiviruses. Virus Res., 1995, 38: 231-239 CrossRef
  46. Kim S.G., Dubovi E.J. A novel simple one-step single-tube RT-duplex PCR method with an internal control for detection of bovine viral diarrhoea virus in bulk milk, blood, and follicular fluid samples. Biologicals, 2003, 31: 103-106 CrossRef
  47. Harasawa R., Giangaspero M. A novel method for pestivirus genotyping based on palindromic nucleotide substitutions in the 5¢-untranslated region. J. Virol. Methods, 1998, 70: 225-230.
  48. Lindberg A., Brownlie J., Gunn G.J. The control of bovine viral diarrhoea virus in Europe: today and in the future. Rev. Sci. Tech., 2006, 25: 961-979.
  49. Walz P.H., Grooms D.L., Passler T., Ridpath J.F., Tremblay R., Step D.L., Callan R.J., Givens M.D. Control of bovine viral diarrhea virus in ruminants. J. Vet. Intern. Med., 2010, 24: 476-486 CrossRef
  50. Helal M.A., Okamatsu H., Tajima M. Bovine viral diarrhea virus infection in a dairy herd with high prevalence of persistently infected calves. Jpn. J. Vet. Res., 2012, 60: 111-117.

back