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Original Articles

An evolutionary divergent pestivirus lacking the Npro gene systemically infects a whale species

ORCID Icon, , , , , , , , & show all
Pages 1383-1392 | Received 23 Jun 2019, Accepted 30 Aug 2019, Published online: 17 Sep 2019

References

  • Becher P, Orlich M, Shannon AD, et al. Phylogenetic analysis of pestiviruses from domestic and wild ruminants. J Gen Virol. 1997;78:1357–1366. doi: 10.1099/0022-1317-78-6-1357
  • Becher P, Orlich M, Kosmidou A, et al. Genetic diversity of pestiviruses: identification of novel groups and implications for classification. Virology. 1999;262:64–71. doi: 10.1006/viro.1999.9872
  • Vilcek S, Ridpath JF, Van Campen H, et al. Characterization of a novel pestivirus originating from a pronghorn antelope. Virus Res. 2005;108:187–193. doi: 10.1016/j.virusres.2004.09.010
  • Blome S, Beer M, Wernike K. New leaves in the growing tree of pestiviruses. Adv Virus Res. 2017;99:139–160. doi: 10.1016/bs.aivir.2017.07.003
  • Wu Z, Ren X, Yang L, et al. Virome analysis for identification of novel Mammalian viruses in bat species from Chinese Provinces. J Virol. 2012;86:10999–11012. doi: 10.1128/JVI.01394-12
  • Firth C, Bhat M, Firth MA, et al. Detection of zoonotic pathogens and characterization of novel viruses carried by commensal Rattus norvegicus in New York City. MBio. 2014;5:e01933–14. doi: 10.1128/mBio.01933-14
  • Bekal S, Domier LL, Gonfa B, et al. A novel flavivirus in the soybean cyst nematode. J Gen Virol. 2014;95:1272–1280. doi: 10.1099/vir.0.060889-0
  • Peterhans E, Schweizer M. Pestiviruses: how to outmaneuver your hosts. Vet Microbiol. 2010;142:18–25. doi: 10.1016/j.vetmic.2009.09.038
  • Becher P, Tautz N. RNA recombination in pestiviruses: cellular RNA sequences in viral genomes highlight the role of host factors for viral persistence and lethal disease. RNA Biol. 2011;8:216–224. doi: 10.4161/rna.8.2.14514
  • Tautz N, Tews BA, Meyers G. The molecular biology of pestiviruses. Adv Vir Res. 2015;93:47–160. doi: 10.1016/bs.aivir.2015.03.002
  • Gottipati K, Holthauzen LMF, Ruggli N, et al. Pestivirus Npro directly interacts with interferon regulatory factor 3 monomer and dimer. Diamond MS, editor. J Virol. 2016;90:7740–7747. doi: 10.1128/JVI.00318-16
  • Fiebach AR, Guzylack-Piriou L, Python S, et al. Classical swine fever virus Npro limits type I interferon induction in plasmacytoid dendritic cells by interacting with interferon regulatory factor 7. J Virol. 2011;85:8002–8011. doi: 10.1128/JVI.00330-11
  • Kennedy S, Smyth JA, Cush PF, et al. Viral distemper now found in porpoises. Nature. 1988;336:21–21. doi: 10.1038/336021a0
  • de Graaf M, Bodewes R, van Elk CE, et al. Norovirus infection in harbor porpoises. Emerg Infect Dis. 2017;23:87–91. doi: 10.3201/eid2301.161081
  • van Elk C, van de Bildt M, van Run P, et al. Central nervous system disease and genital disease in harbor porpoises (Phocoena phocoena) are associated with different herpesviruses. Vet Res. 2016;47:28. doi: 10.1186/s13567-016-0310-8
  • van Beurden SJ, IJsseldijk LL, van de Bildt MWG, et al. A novel cetacean adenovirus in stranded harbour porpoises from the North Sea: detection and molecular characterization. Arch Virol. 2017;162:2035–2040. doi: 10.1007/s00705-017-3310-8
  • Endoh D, Mizutani T, Kirisawa R, et al. Species-independent detection of RNA virus by representational difference analysis using non-ribosomal hexanucleotides for reverse transcription. Nucleic Acids Res. 2005;33:e65. doi: 10.1093/nar/gni064
  • Allander T, Emerson SU, Engle RE, et al. A virus discovery method incorporating DNase treatment and its application to the identification of two bovine parvovirus species. Proc Natl Acad Sci. 2001;98:11609–11614. doi: 10.1073/pnas.211424698
  • Kruppa J, Jo WK, van der Vries E, et al. Virus detection in high-throughput sequencing data without a reference genome of the host. Infect Genet Evol. 2018;66:180–187. doi: 10.1016/j.meegid.2018.09.026
  • Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012;9:357–359. doi: 10.1038/nmeth.1923
  • Huson DH, Xie C. A poor man’s BLASTX - high-throughput metagenomic protein database search using PAUDA. Bioinformatics. 2014;30:38–39. doi: 10.1093/bioinformatics/btt254
  • Katoh K, Rozewicki J, Yamada KD. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. 2017.
  • Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33:1870–1874. doi: 10.1093/molbev/msw054
  • Liebler-Tenorio EM, Ridpath JF, Neill JD. Distribution of viral antigen and tissue lesions in persistent and acute infection with the homologous strain of noncytopathic bovine viral diarrhea virus. J Vet Diagnostic Investig. 2004;16:388–396. doi: 10.1177/104063870401600504
  • Cutlip RC, McClurkin AW, Coria MF. Lesions in clinically healthy cattle persistently infected with the virus of bovine viral diarrhea–glomerulonephritis and encephalitis. Am J Vet Res. 1980;41:1938–1941.
  • McClurkin AW, Littledike ET, Cutlip RC, et al. Production of cattle immunotolerant to bovine viral diarrhea virus. Can J Comp Med Rev Can Med Comp. 1984;48:156–161.
  • Brown C, Baker D, Barker I. The alimentary system. In: Maxie G, editor. Pathology of domestic animals. 5th ed. New York: Elsevier; 2007. p. 2340.
  • King BF. Comparative studies of structure and function in Mammalian placentas with special reference to maternal-fetal transfer of iron. Am Zool. 1992;32:331–342. doi: 10.1093/icb/32.2.331
  • Tratschin JD, Moser C, Ruggli N, et al. Classical swine fever virus leader proteinase Npro is not required for viral replication in cell culture. J Virol. 1998;72:7681–7684.
  • Gil LHVG, Ansari IH, Vassilev V, et al. The amino-terminal domain of bovine viral diarrhea virus Npro protein is necessary for alpha/beta interferon antagonism. J Virol. 2006;80:900–911. doi: 10.1128/JVI.80.2.900-911.2006
  • Mayer D, Hofmann MA, Tratschin J-D. Attenuation of classical swine fever virus by deletion of the viral Npro gene. Vaccine. 2004;22:317–328. doi: 10.1016/j.vaccine.2003.08.006
  • Lai VCH, Zhong W, Skelton A, et al. Generation and characterization of a hepatitis C virus NS3 protease-dependent bovine viral diarrhea virus. J Virol. 2000;74:6339–6347. doi: 10.1128/JVI.74.14.6339-6347.2000
  • Myers TM, Kolupaeva VG, Mendez E, et al. Efficient translation initiation is required for replication of bovine viral diarrhea virus subgenomic replicons. J Virol. 2001;75:4226–4238. doi: 10.1128/JVI.75.9.4226-4238.2001
  • Meyers G, Ege A, Fetzer C, et al. Bovine viral diarrhea virus: prevention of persistent fetal infection by a combination of two mutations affecting Erns RNase and Npro protease. J Virol. 2007;81:3327–3338. doi: 10.1128/JVI.02372-06
  • Braun BA, Marcovitz A, Camp JG, et al. Mx1 and Mx2 key antiviral proteins are surprisingly lost in toothed whales. Proc Natl Acad Sci. 2015;112:8036–8040. doi: 10.1073/pnas.1501844112
  • Verhelst J, Hulpiau P, Saelens X. Mx proteins: antiviral gatekeepers that restrain the uninvited. Microbiol Mol Biol Rev. 2013;77:551–566. doi: 10.1128/MMBR.00024-13