Characterization of two Austrian porcine reproductive and respiratory syndrome virus (PRRSV) field isolates reveals relationship to East Asian strains
Tóm tắt
Từ khóa
Tài liệu tham khảo
Neumann EJ, Kliebenstein JB, Johnson CD, Mabry JW, Bush EJ, Seitzinger AH, Green AL, Zimmerman JJ (2005) Assessment of the economic impact of porcine reproductive and respiratory syndrome on swine production in the United States. J Am Vet Med Assoc 227:385–392
Nieuwenhuis N, Duinhof TF, van Nes A (2012) Economic analysis of outbreaks of porcine reproductive and respiratory syndrome virus in nine sow herds. Vet Rec 170:225
Wensvoort G, Terpstra C, Pol JM, ter Laak EA, Bloemraad M, de Kluyver EP, Kragten C, van Buiten L, den Besten A, Wagenaar F, Broekhuijsen JM, Moonen PL, Zetstra T, de Boer EA, Tibben HJ, de Jong MF, van’t Veld P, Groenland GJ, van Gennep JA, Voets MT, Verheijden JH, Braamskamp J (1991) Mystery swine disease in The Netherlands: the isolation of Lelystad virus. Vet Q 13:121–130
Nelsen CJ, Murtaugh MP, Faaberg KS (1999) Porcine reproductive and respiratory syndrome virus comparison: divergent evolution on two continents. J Virol 73:270–280
Murtaugh MP, Stadejek T, Abrahante JE, Lam TT, Leung FC (2010) The ever-expanding diversity of porcine reproductive and respiratory syndrome virus. Virus Res 154:18–30
Stadejek T, Oleksiewicz MB, Scherbakov AV, Timina AM, Krabbe JS, Chabros K, Potapchuk D (2008) Definition of subtypes in the European genotype of porcine reproductive and respiratory syndrome virus: nucleocapsid characteristics and geographical distribution in Europe. Arch Virol 153:1479–1488
Fields BN, Knipe DM, Howley PM (2013) Fields virology. Wolters Kluwer Health/Lippincott Williams & Wilkins, Philadelphia
Firth AE, Zevenhoven-Dobbe JC, Wills NM, Go YY, Balasuriya UB, Atkins JF, Snijder EJ, Posthuma CC (2011) Discovery of a small arterivirus gene that overlaps the GP5 coding sequence and is important for virus production. J Gen Virol 92:1097–1106
Johnson CR, Griggs TF, Gnanandarajah J, Murtaugh MP (2011) Novel structural protein in porcine reproductive and respiratory syndrome virus encoded by an alternative ORF5 present in all arteriviruses. J Gen Virol 92:1107–1116
Fang Y, Snijder EJ (2010) The PRRSV replicase: exploring the multifunctionality of an intriguing set of nonstructural proteins. Virus Res 154:61–76
Wissink EH, Kroese MV, van Wijk HA, Rijsewijk FA, Meulenberg JJ, Rottier PJ (2005) Envelope protein requirements for the assembly of infectious virions of porcine reproductive and respiratory syndrome virus. J Virol 79:12495–12506
Shi M, Lam TT, Hon CC, Hui RK, Faaberg KS, Wennblom T, Murtaugh MP, Stadejek T, Leung FC (2010) Molecular epidemiology of PRRSV: a phylogenetic perspective. Virus Res 154:7–17
Stadejek T, Stankevicius A, Murtaugh MP, Oleksiewicz MB (2013) Molecular evolution of PRRSV in Europe: current state of play. Vet Microbiol 165:21–28
Indik S, Schmoll F, Sipos W, Klein D (2005) Genetic variability of PRRS virus in Austria: consequences for molecular diagnostics and viral quantification. Vet Microbiol 107:171–178
Balka G, Hornyak A, Dan A, Ladinig A, Biksi I, Rusvai M (2010) PriProET based melting point analyses on PRRSV positive field samples. Mol Cell Probes 24:411–414
Jackova A, Vlasakova M, Mandelik R, Vilcek S (2013) Genetic typing of porcine reproductive and respiratory syndrome virus isolates from central European countries. Acta Virol 57:363–368
Kim HS, Kwang J, Yoon IJ, Joo HS, Frey ML (1993) Enhanced replication of porcine reproductive and respiratory syndrome (PRRS) virus in a homogeneous subpopulation of MA-104 cell line. Arch Virol 133:477–483
Zeman D, Neiger R, Yaeger M, Nelson E, Benfield D, Leslie-Steen P, Thomson J, Miskimins D, Daly R, Minehart M (1993) Laboratory investigation of PRRS virus infection in three swine herds. J Vet Diagn Invest 5:522–528
Weiland E, Wieczorek-Krohmer M, Kohl D, Conzelmann KK, Weiland F (1999) Monoclonal antibodies to the GP5 of porcine reproductive and respiratory syndrome virus are more effective in virus neutralization than monoclonal antibodies to the GP4. Vet Microbiol 66:171–186
Etherington GJ, Dicks J, Roberts IN (2005) Recombination analysis tool (RAT): a program for the high-throughput detection of recombination. Bioinformatics 21:278–281
Fetzer C, Pesch S, Ohlinger VF (2006) High risk of false positive results in a widely used diagnostic test for detection of the porcine reproductive and respiratory syndrome virus (PRRSV). Vet Microbiol 115:21–31
Martinez-Lobo FJ, Diez-Fuertes F, Simarro I, Castro JM, Prieto C (2011) Porcine reproductive and respiratory syndrome virus isolates differ in their susceptibility to neutralization. Vaccine 29:6928–6940
Nam E, Park CK, Kim SH, Joo YS, Yeo SG, Lee C (2009) Complete genomic characterization of a European type 1 porcine reproductive and respiratory syndrome virus isolate in Korea. Arch Virol 154:629–638
Novosel D, Stadejek T (2011) Genetic diversity of European genotype PRRSV in Central and Eastern Europe—an update. GenBank. http://ncbi.nlm.nih.gov/nuccore/JQ043208.1
Wernike K, Bonilauri P, Dauber M, Errington J, LeBlanc N, Revilla-Fernandez S, Hjulsager C, Isaksson M, Stadejek T, Beer M, Hoffmann B (2012) Porcine reproductive and respiratory syndrome virus: interlaboratory ring trial to evaluate real-time reverse transcription polymerase chain reaction detection methods. J Vet Diagn Invest 24:855–866
Balka G, Ladinig A, Ritzmann M, Saalmuller A, Gerner W, Kaser T, Jakab C, Rusvai M, Weissenbock H (2013) Immunohistochemical characterization of type II pneumocyte proliferation after challenge with type I porcine reproductive and respiratory syndrome virus. J Comp Pathol 149:322–330
OIE (2012) Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Office international des épizooties, Paris
van Vugt JJ, Storgaard T, Oleksiewicz MB, Botner A (2001) High frequency RNA recombination in porcine reproductive and respiratory syndrome virus occurs preferentially between parental sequences with high similarity. J Gen Virol 82:2615–2620
Brar MS, Shi M, Hui RK, Leung FC (2014) Genomic evolution of porcine reproductive and respiratory syndrome virus (PRRSV) isolates revealed by deep sequencing. PLoS One 9:e88807
Chen N, Cao Z, Yu X, Deng X, Zhao T, Wang L, Liu Q, Li X, Tian K (2011) Emergence of novel European genotype porcine reproductive and respiratory syndrome virus in mainland China. J Gen Virol 92:880–892
Li B, Gao S, Zhou T, Liu X, Lu H, Feng F (2014) Complete genome sequence of European genotype porcine reproductive and respiratory syndrome virus strain LNEU12 in Northern China. Genome Announc 2:e00957–01014
Zhou Z, Liu Q, Hu D, Yue X, Yu X, Zhang Q, Gu X, Ni J, Li X, Zhai X, Tian K (2013) Complete genome sequence of a European genotype porcine reproductive and respiratory syndrome virus in china. Genome Announc 1:e00175–00213
Oleksiewicz MB, Botner A, Toft P, Grubbe T, Nielsen J, Kamstrup S, Storgaard T (2000) Emergence of porcine reproductive and respiratory syndrome virus deletion mutants: correlation with the porcine antibody response to a hypervariable site in the ORF 3 structural glycoprotein. Virology 267:135–140
Meulenberg JJ, van Nieuwstadt AP, van Essen-Zandbergen A, Langeveld JP (1997) Posttranslational processing and identification of a neutralization domain of the GP4 protein encoded by ORF4 of Lelystad virus. J Virol 71:6061–6067
Vanhee M, Costers S, Van Breedam W, Geldhof MF, Van Doorsselaere J, Nauwynck HJ (2010) A variable region in GP4 of European-type porcine reproductive and respiratory syndrome virus induces neutralizing antibodies against homologous but not heterologous virus strains. Viral Immunol 23:403–413
Oleksiewicz MB, Botner A, Toft P, Normann P, Storgaard T (2001) Epitope mapping porcine reproductive and respiratory syndrome virus by phage display: the nsp2 fragment of the replicase polyprotein contains a cluster of B-cell epitopes. J Virol 75:3277–3290
Costers S, Vanhee M, Van Breedam W, Van Doorsselaere J, Geldhof M, Nauwynck HJ (2010) GP4-specific neutralizing antibodies might be a driving force in PRRSV evolution. Virus Res 154:104–113
Tian D, Wei Z, Zevenhoven-Dobbe JC, Liu R, Tong G, Snijder EJ, Yuan S (2012) Arterivirus minor envelope proteins are a major determinant of viral tropism in cell culture. J Virol 86:3701–3712
Li B, Fang L, Liu S, Zhao F, Jiang Y, He K, Chen H, Xiao S (2010) The genomic diversity of Chinese porcine reproductive and respiratory syndrome virus isolates from 1996 to 2009. Vet Microbiol 146:226–237
Verheije MH, Olsthoorn RC, Kroese MV, Rottier PJ, Meulenberg JJ (2002) Kissing interaction between 3′ noncoding and coding sequences is essential for porcine arterivirus RNA replication. J Virol 76:1521–1526
Frydas IS, Trus I, Kvisgaard LK, Bonckaert C, Reddy VR, Li Y, Larsen LE, Nauwynck HJ (2015) Different clinical, virological, serological and tissue tropism outcomes of two new and one old Belgian type 1 subtype 1 porcine reproductive and respiratory virus (PRRSV) isolates. Vet Res 46:37