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Original Articles

PCV3-associated disease in the United States swine herd

, , , , , , , , , & show all
Pages 684-698 | Received 01 Feb 2019, Accepted 20 Apr 2019, Published online: 16 May 2019

References

  • Breitbart M, Delwart E, Rosario K, et al. ICTV Virus Taxonomy: Circoviridae. J Gen Virol. 2017;98:1997–1998.
  • Segalés J, Allan GM, Domingo M, et al. Diseases of swine. 10th edn. West Sussex: Wiley-Blackwell; 2012. Chapter 26.
  • Cheung AK. Comparative analysis of the transcriptional patterns of pathogenic and nonpathogenic porcine circoviruses. Virology. 2003;310:41–49. doi: 10.1016/S0042-6822(03)00096-5
  • Clark EG. Pathology of postweaning multisystemic wasting syndrome of pigs. Proc West Can Assoc Swine Prod. 1996: 22–25.
  • Harding JCS, Clark EG, Strokappe JH, et al. Postweaning multisystemic wasting syndrome: epidemiology and clinical presentation. Swine Health Prod. 1998;6:249–254.
  • Opriessnig T, Langohr I. Current state of knowledge on porcine circovirus type 2-associated lesions. Vet Pathol. 2013;50:23–38. doi: 10.1177/0300985812450726
  • Segalés J. Porcine circovirus type 2 (PCV2) infections: clinical signs, pathology and laboratory diagnosis. Virus Res. 2012;164:10–19. doi: 10.1016/j.virusres.2011.10.007
  • Ellis J. Porcine circovirus: a historical perspective. Vet Pathol. 2014;51:315–327. doi: 10.1177/0300985814521245
  • Allan GM, McNeilly F, Kennedy S, et al. Isolation of porcine circovirus-like viruses from pigs with a wasting disease in the USA and Europe. J Vet Diagn Invest. 1998;10:3–10. doi: 10.1177/104063879801000102
  • Allan G, McNeilly F, Walker IW, et al. Novel porcine circoviruses from pigs with wasting disease syndromes. Vet Rec. 1998;142:467–468. doi: 10.1136/vr.142.1.8
  • Sato K, Shibahara T, Ishikawa Y, et al. Evidence of porcine circovirus infection in pigs with wasting disease syndrome from 1985 to 1999 in Hokkaido, Japan. Journal of Veterinary Medical Science. 2000;62:627–633. doi: 10.1292/jvms.62.627
  • Ellis J, Hassard L, Clark E, et al. Isolation of circovirus from lesions of pigs with postweaning multisystemic wasting syndrome. Can Vet J. 1998;39:44–51.
  • Segalés J, Sitjar M, Domingo M, et al. First report of post-weaning multisystemic wasting syndrome in pigs in Spain. Vet Rec. 1997;141:600–601.
  • Choi C, Chae C, Clark EG. Porcine postweaning multisystemic wasting syndrome in Korean pig: detection of porcine circovirus 2 infection by immunohistochemistry and polymerase chain reaction. J Vet Diagn Invest. 2000;12:151–153. doi: 10.1177/104063870001200209
  • Allan GM, McNeilly F, Ellis J, et al. PMWS: experimental model and co-infections. Vet Microbiol. 2004;98:165–168. doi: 10.1016/j.vetmic.2003.10.009
  • Drolet R, Thibault S, D'Allaire S, et al. Porcine dermatitis and nephropathy syndrome (PDNS): an overview of the disease. Swine Health Prod. 1999;7:283–285.
  • West KH, Bystrom JM., Wojnarowicz Chris, et al. Myocarditis and abortion associated with intrauterine infection of sows with porcine circovirus 2. J Vet Diagn Invest. 1999;11:530–532. doi: 10.1177/104063879901100608
  • Brunborg IM, Jonassen CM., Moldal T, et al. Association of myocarditis with high viral load of porcine circovirus type 2 in several tissues in cases of fetal death and high mortality in piglets. A case study. J Vet Diagn Invest. 2007;19:368–375. doi: 10.1177/104063870701900405
  • Pittman JS. Reproductive failure associated with porcine circovirus type 2 in gilts. J Swine Health Prod. 2008;16:144–148.
  • Segalés J, Allan GM, Domingo M. Porcine circovirus diseases. Anim Health Res Rev. 2005;6:119–142. doi: 10.1079/AHR2005106
  • Hansen MS, Hjulsager CK., Bille-Hansen V, et al. Selection of method is crucial for the diagnosis of porcine circovirus type 2 associated reproductive failures. Vet Microbiol. 2010;144:203–209. doi: 10.1016/j.vetmic.2009.12.038
  • Palinski R, Piñeyro P, Shang P, et al. A novel porcine circovirus distantly related to known circoviruses is associated with porcine dermatitis and nephropathy syndrome and reproductive failure. J Virol. 2017;91:e01879–16. doi: 10.1128/JVI.01879-16
  • Phan TG, Giannitti F, Rossow S, et al. Detection of a novel circovirus PCV3 in pigs with cardiac and multi-systemic inflammation. Virol J. 2016;13:184. doi: 10.1186/s12985-016-0642-z
  • Fux R, Söckler C, Link EK, et al. Full genome characterization of porcine circovirus type 3 isolates reveals the existence of two distinct groups of virus strains. Virol J. 2018;15:25. doi: 10.1186/s12985-018-0929-3
  • Hayashi S, Ohshima Y, Furuya Y, et al. First detection of porcine circovirus type 3 in Japan. J Vet Med Sci. 2018;80:1468–1472. doi: 10.1292/jvms.18-0079
  • Kim SH, Park JY, Jung Jung, et al. Detection and genetic characterization of porcine circovirus 3 from aborted fetuses and pigs with respiratory disease in Korea. J Vet Sci. 2018;19:21–724. doi: 10.4142/jvs.2018.19.1.21
  • Yuzhakov AG, Raev SA., Alekseev KP, et al. First detection and full genome sequence of porcine circovirus type 3 in Russia. Virus Genes. 2018;54:608–611. doi: 10.1007/s11262-018-1582-z
  • Zhao D, Wang X, Gao Q, et al. 2018. Retrospective survey and phylogenetic analysis of porcine circovirus type 3 in Jiangsu province, China, 2008 to 2017. Arch Virol. 2018;163:2531–2538.
  • Kedkovid R, Woonwong Y, Arunorat J, et al. Porcine circovirus type 3 (PCV3) infection in grower pigs from a Thai farm suffering from porcine respiratory disease complex (PRDC). Veterinary Microbiology. 2018;215:71–76. doi: 10.1016/j.vetmic.2018.01.004
  • Faccini S, Barbieri I., Gilioli A., et al. Detection and genetic characterization of porcine circovirus type 3 in Italy. Transbound Emerg Dis. 2017;64:1661–1166. doi: 10.1111/tbed.12714
  • Franzo G, Legnardi M, Hjulsager CK, et al. Full-genome sequencing of porcine circovirus 3 field strains from Denmark, Italy and Spain demonstrates a high within-Europe genetic heterogeneity. Transbound Emerg Dis. 2018;65:602–606.
  • Kwon T, Yoo SJ, Park CK, et al. Prevalence of novel porcine circovirus 3 in Korean pig populations. Vet Microbiol. 2017;207:178–180. doi: 10.1016/j.vetmic.2017.06.013
  • Stadejek T, Wozniak A, Milek D, et al. First detection of porcine circovirus type 3 on commercial pig farms in Poland. Transbound Emerg Dis. 2017;64:1350–1353. doi: 10.1111/tbed.12672
  • Tochetto C, Lima DA, Varela APM, et al. Full-genome sequence of porcine circovirus type 3 recovered from serum of sows with stillbirths in Brazil. Transbound Emerg Dis. 2018;65:5–9. doi: 10.1111/tbed.12735
  • Ye X, Berg M, Fossum C, et al. Detection and genetic characterisation of porcine circovirus 3 from pigs in Sweden. Virol Sin. 2018;54:466–469.
  • Ku X, Chen F, Li P, et al. Identification and genetic characterization of porcine circovirus type 3 in China. Transbound Emerg Dis. 2017;64:703–708. doi: 10.1111/tbed.12638
  • Fu X, Fang B, Ma J, et al. Insights into the epidemic characteristics and evolutionary history of the novel porcine circovirus type 3 in southern China. Transbound Emerg Dis. 2018;65:296–303. doi: 10.1111/tbed.12752
  • Zhai SL, Zhou X, Zhang H, et al. Comparative epidemiology of porcine circovirus type 3 in pigs with different clinical presentations. Virol J. 2017;14:222. doi: 10.1186/s12985-017-0892-4
  • Shen H, Liu X, Zhang P, et al. Genome characterization of a porcine circovirus type 3 in South China. Transbound Emerg Dis. 2018;6:264–266. doi: 10.1111/tbed.12639
  • Opriessnig T, Yu S, Gallup JM, et al. Effect of vaccination with selective bacterins on conventional pigs infected with type 2 porcine circovirus. Vet Pathol. 2003;40:521–529. doi: 10.1354/vp.40-5-521
  • Chen HY, Li X-K, Cui B-A, et al. A TaqMan-based real-time polymerase chain reaction for the detection of porcine parvovirus. J Virol Methods. 2009;156:84–88. doi: 10.1016/j.jviromet.2008.10.029
  • Arruda BL, Arruda PH, Magstadt DR, et al. Identification of a divergent lineage porcine pestivirus in nursing piglets with congenital tremors and reproduction of disease following experimental inoculation. PLoS One. 2016;11:e0150104. doi: 10.1371/journal.pone.0150104
  • Kedkovid R, Woonwong Y, Arunorat J, et al. Porcine circovirus type 3 (PCV3) shedding in sow colostrum. Vet Microbiol. 2018;220:12–17. doi: 10.1016/j.vetmic.2018.04.032
  • Zheng S, Wu X, Zhang L, et al. The occurrence of porcine circovirus 3 without clinical infection signs in Shandong Province. Transbound Emerg Dis. 2017;64:1337–1341. doi: 10.1111/tbed.12667
  • de Groof A, Deijs M, Guelen L, et al. Atypical porcine pestivirus: a possible cause of congenital tremor type A-II in newborn piglets. Viruses. 2016;8:271. doi: 10.3390/v8100271
  • Mikami O, Nakajima H, Kawashima K, et al. Nonsuppurative myocarditis caused by porcine circovirus type 2 in a weak-born piglet. J Vet Med Sci. 2005;67:735–738. doi: 10.1292/jvms.67.735
  • Opriessnig T, Janke BH, Halbur PG. Cardiovascular lesions in pigs naturally or experimentally infected with porcine circovirus type 2. J Comp Pathol. 2006;134:105–110. doi: 10.1016/j.jcpa.2005.06.007
  • Li G, He W, Zhu H, et al. Origin, genetic diversity, and evolutionary dynamics of novel porcine circovirus 3. Adv Sci. 2018;5:1800275. doi: 10.1002/advs.201800275
  • Jacobsen B, Krueger L, Seeliger F, et al. Retrospective study of the occurrence of porcine circovirus 2 infection and associated entities in Northern Germany. Vet Microbiol. 2009;138:27–33. doi: 10.1016/j.vetmic.2009.02.005
  • Cazzini P, Watson VE, Brown HM. The many faces of Mott cells. Vet Clin Pathol. 2013;42:125–126. doi: 10.1111/vcp.12043
  • Hause BM, Collin EA, Anderson J, et al. Bovine rhinitis viruses are common in U. S. cattle with bovine respiratory disease. PLoS One. 2015;10:e0121998. doi: 10.1371/journal.pone.0121998
  • Neill JD, Bayles DO, Ridpath JF. Simultaneous rapid sequencing of multiple RNA virus genomes. Journal of Virological Methods. 2014;201:68–72. doi: 10.1016/j.jviromet.2014.02.016
  • Allander T, Tammi MT, Eriksson M, et al. Cloning of a human parvovirus by molecular screening of respiratory tract samples. Proc Natl Acad Sci USA. 2005;102:12891–12896. doi: 10.1073/pnas.0504666102