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Porcine circoviruses: a minuscule yet mammoth paradox

Published online by Cambridge University Press:  02 September 2008

Sheela Ramamoorthy
Affiliation:
Center for Molecular Medicine and Infectious Diseases, Department of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA
Xiang-Jin Meng*
Affiliation:
Center for Molecular Medicine and Infectious Diseases, Department of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA
*
*Corresponding author. E-mail: [email protected]

Abstract

Porcine circovirus type 2 (PCV2) is the primary causative agent for porcine circovirus-associated disease (PCVAD). PCVAD has been the cause of considerable economic losses to the pork industry worldwide. The disease is primarily characterized by wasting, enlarged lymph nodes, jaundice and weight loss in affected weanling pigs. Several other complex syndromes involving reproductive failure, enteritis, pneumonia and necrotizing dermatitis have also been associated with PCV2 infection. Lymphoid depletion, which is the hallmark lesion of PCVAD, predisposes the host to immunosuppression. Disease progression is further complicated by co-infections with other bacterial and viral pathogens. Despite the availability of effective vaccines for the last 2 years, newly emerging strains of the virus have been reported to cause more severe outbreaks in parts of the USA and Canada. While knowledge of the biology and pathogenesis of PCV2 has progressed considerably over the last 12 years since the disease was recognized, many questions still remain to be answered.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2008

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References

Albina, E, Truong, C, Hutet, E, Blanchard, P, Cariolet, R, L'Hospitalier, R, Mahe, D, Allee, C, Morvan, H, Amenna, N, Le Dimna, M, Madec, F and Jestin, A (2001). An experimental model for post-weaning multisystemic wasting syndrome (PMWS) in growing piglets. Journal of Comparative Pathology 125: 292303.CrossRefGoogle ScholarPubMed
Allan, GM, Mackie, DP, McNair, J, Adair, BM and McNulty, MS (1994a). Production, preliminary characterisation and applications of monoclonal antibodies to porcine circovirus. Veterinary Immunology and Immunopathology 43: 357371.CrossRefGoogle Scholar
Allan, GM, McNeilly, F, Foster, JC and Adair, BM (1994b). Infection of leucocyte cell cultures derived from different species with pig circovirus. Veterinary Microbiology 41: 267279.CrossRefGoogle ScholarPubMed
Allan, GM, Phenix, KV, Todd, D and McNulty, MS (1994c). Some biological and physico-chemical properties of porcine circovirus. Zentralblatt fur Veterinarmedizin B 41: 1726.Google ScholarPubMed
Allan, G, Meehan, B, Todd, D, Kennedy, S, McNeilly, F, Ellis, J, Clark, EG, Harding, J, Espuna, E, Botner, A and Charreyre, C (1998a). Novel porcine circoviruses from pigs with wasting disease syndromes. The Veterinary Record 142: 467468.Google ScholarPubMed
Allan, GM, McNeilly, F, Kennedy, S, McNeilly, F, Ellis, J, Clark, EG, Harding, J, Espuna, E, Botner, A and Charreyre, CE (1998b). Isolation of porcine circovirus-like viruses from pigs with a wasting disease in the USA and Europe. Journal of Veterinary Diagnostic Investigation 10: 310.CrossRefGoogle ScholarPubMed
Allan, GM, Mc Neilly, F, Meehan, BM, Kennedy, S, Mackie, DP, Ellis, JA, Clark, EG, Espuna, E, Saubi, N, Riera, P, Botner, A and Charreyre, CE (1999). Isolation and characterization of circoviruses from pigs with wasting syndromes in Spain, Denmark and Northern Ireland. Veterinary Microbiology 66: 115123.CrossRefGoogle ScholarPubMed
Allan, GM and Ellis, JA (2000). Porcine circoviruses: a review. Journal of Veterinary Diagnostic Investigation 12: 314.CrossRefGoogle ScholarPubMed
Allan, GM, McNeilly, F, Ellis, J, Krakowka, S, Meehan, B, McNair, I, Walker, I and Kennedy, S (2000a). Experimental infection of colostrum deprived piglets with porcine circovirus 2 (PCV2) and porcine reproductive and respiratory syndrome virus (PRRSV) potentiates PCV2 replication. Archives of Virology 145: 24212429.CrossRefGoogle ScholarPubMed
Allan, GM, McNeilly, F, Kennedy, S, Meehan, B, Ellis, J and Krakowka, S (2000b). Immunostimulation, PCV-2 and PMWS. The Veterinary Record 147: 170171.Google ScholarPubMed
Allan, GM, McNeilly, F, McNair, I, Curran, MD, Walker, I, Ellis, J, Konoby, C, Kennedy, S and Meehan, B (2000c). Absence of evidence for porcine circovirus type 2 in cattle and humans, and lack of seroconversion or lesions in experimentally infected sheep. Archives of Virology 145: 853857.CrossRefGoogle ScholarPubMed
Allan, GM, McNeilly, F, Ellis, J, Krakowka, S, Botner, A, McCullough, K, Nauwynck, H, Kennedy, S, Meehan, B and Charreyre, C (2004). PMWS: experimental model and co-infections. Veterinary Microbiology 98: 165168.CrossRefGoogle ScholarPubMed
Balasch, M, Segales, J, Rosell, C, Domingo, M, Mankertz, A, Urniza, A and Plana-Duran, J (1999). Experimental inoculation of conventional pigs with tissue homogenates from pigs with post-weaning multisystemic wasting syndrome. Journal of Comparative Pathology 121: 139148.CrossRefGoogle ScholarPubMed
Banks, M, Grierson, S, Tucker, D, Bailey, M, Donadeau, M, Sargent, C, King, D and Mellencamp, M (2006). Swine and circovirus. Developmental Biology (Basel) 126: 107113; discussion 325–106.Google ScholarPubMed
Bassaganya-Riera, J, Pogranichniy, RM, Jobgen, SC, Halbur, PG, Yoon, KJ, O'Shea, M, Mohede, I and Hontecillas, R (2003). Conjugated linoleic acid ameliorates viral infectivity in a pig model of virally induced immunosuppression. Journal of Nutrition 133: 32043214.CrossRefGoogle Scholar
Bassami, MR, Berryman, D, Wilcox, GE and Raidal, SR (1998). Psittacine beak and feather disease virus nucleotide sequence analysis and its relationship to porcine circovirus, plant circoviruses, and chicken anaemia virus. Virology 249: 453459.CrossRefGoogle ScholarPubMed
Blanchard, P, Mahe, D, Cariolet, R, Keranflec'h, A, Baudouard, M, Cordioli, P, Albina, E and Jestin, A (2003). Protection of swine against post-weaning multisystemic wasting syndrome (PMWS) by porcine circovirus type 2 (PCV2) proteins. Vaccine 21: 45654575.CrossRefGoogle ScholarPubMed
Bogdan, J, West, K, Clark, E, Konoby, C, Haines, D, Allan, G, McNeilly, F, Meehan, B, Krakowka, S and Ellis, JA (2001). Association of porcine circovirus 2 with reproductive failure in pigs: a retrospective study, 1995–1998. Canadian Veterinary Journal 42: 548550.Google ScholarPubMed
Bolin, SR, Stoffregen, WC, Nayar, GP and Hamel, AL (2001). Postweaning multisystemic wasting syndrome induced after experimental inoculation of cesarean-derived, colostrum-deprived piglets with type 2 porcine circovirus. Journal of Veterinary Diagnostic Investigation 13: 185194.CrossRefGoogle ScholarPubMed
Bratanich, A and Blanchetot, A (2006). A gene similar to the human hyaluronan-mediated motility receptor (RHAMM) gene is upregulated during Porcine Circovirus type 2 infection. Virus Genes 32: 145152.CrossRefGoogle Scholar
Castro, AM, Cortez, A, Ruiz, VL, Leomil, H, Moreno, AM, Doto, DS and Richtzenhain, LJ (2004). Detection and differentiation of porcine circoviruses in Brazilian pigs. The Veterinary Record 154: 728729.CrossRefGoogle ScholarPubMed
Chae, C (2004). Postweaning multisystemic wasting syndrome: a review of aetiology, diagnosis and pathology. The Veterinary Journal 168: 4149.CrossRefGoogle ScholarPubMed
Chang, HW, Jeng, CR, Lin, TL, Liu, JJ, Chia, MY, Tsai, YC, Chia, MY and Pang, VF (2006). Immunopathological effects of porcine circovirus type 2 (PCV2) on swine alveolar macrophages by in vitro inoculation. Veterinary Immunology and Immunopathology 110: 207219.CrossRefGoogle ScholarPubMed
Chang, HW, Jeng, CR, Lin, CM, Liu, JJ, Chang, CC, Tsai, YC, Chia, MY and Pang, VF (2007). The involvement of Fas/FasL interaction in porcine circovirus type 2 and porcine reproductive and respiratory syndrome virus co-inoculation-associated lymphocyte apoptosis in vitro. Veterinary Microbiology 122: 7282.CrossRefGoogle ScholarPubMed
Cheung, AK (2003a). Comparative analysis of the transcriptional patterns of pathogenic and nonpathogenic porcine circoviruses. Virology 310: 4149.CrossRefGoogle ScholarPubMed
Cheung, AK (2003b). The essential and nonessential transcription units for viral protein synthesis and DNA replication of porcine circovirus type 2. Virology 313: 452459.CrossRefGoogle ScholarPubMed
Cheung, AK (2003c). Transcriptional analysis of porcine circovirus type 2. Virology 305: 168180.CrossRefGoogle ScholarPubMed
Cheung, AK (2004a). Identification of an octanucleotide motif sequence essential for viral protein, DNA, and progeny virus biosynthesis at the origin of DNA replication of porcine circovirus type 2. Virology 324: 2836.CrossRefGoogle ScholarPubMed
Cheung, AK (2004b). Palindrome regeneration by template strand-switching mechanism at the origin of DNA replication of porcine circovirus via the rolling-circle melting-pot replication model. Journal of Virology 78: 90169029.CrossRefGoogle ScholarPubMed
Cheung, AK (2006). Regeneration of the replication-associated proteins tandem direct repeat recognition nucleotide sequence at the origin of DNA replication of porcine circovirus type 1. Virology 346: 3239.CrossRefGoogle ScholarPubMed
Cheung, AK, Lager, KM, Kohutyuk, OI, Vincent, AL, Henry, SC, Baker, RB, Rowland, RR and Dunham, AG (2007). Detection of two porcine circovirus type 2 genotypic groups in United States swine herds. Archives of Virology 152: 10351044.CrossRefGoogle ScholarPubMed
Choi, C, Chae, C and Clark, EG (2000). Porcine postweaning multisystemic wasting syndrome in Korean pig: detection of porcine circovirus 2 infection by immunohistochemistry and polymerase chain reaction. Journal of Veterinary Diagnostic Investigation 12: 151153CrossRefGoogle ScholarPubMed
Choi, C, Kim, J, Kang, IJ and Chae, C (2002a). Concurrent outbreak of PMWS and PDNS in a herd of pigs in Korea. The Veterinary Record 151: 484485.CrossRefGoogle Scholar
Choi, J, Stevenson, GW, Kiupel, M, Harrach, B, Anothayanontha, L, Kanitz, CL and Mittal, SK (2002b). Sequence analysis of old and new strains of porcine circovirus associated with congenital tremors in pigs and their comparison with strains involved with postweaning multisystemic wasting syndrome. Canadian Journal of Veterinary Research 66: 217224.Google ScholarPubMed
Clark, E (1996). Post-weaning multisystemic wasting syndrome. Proceedings of the Western Canadian Association of Swine Practitioners. pp. 1920, Saskatoon, Canada.Google Scholar
Csagola, A, Kecskemeti, S, Kardos, G, Kiss, I and Tuboly, T (2006). Genetic characterization of type 2 porcine circoviruses detected in Hungarian wild boars. Archives of Virology 151: 495507.CrossRefGoogle ScholarPubMed
D'Allaire, S, Moore, C and Cote, G (2007). A survey on finishing pig mortality associated with porcine circovirus diseases in Quebec. Canadian Veterinary Journal 48: 145146.Google ScholarPubMed
Darwich, L, Segales, J, Domingo, M and Mateu, E (2002). Changes in CD4(+), CD8(+), CD4(+)/CD8(+), and immunoglobulin M-positive peripheral blood mononuclear cells of postweaning multisystemic wasting syndrome-affected pigs and age-matched uninfected wasted and healthy pigs correlate with lesions and porcine circovirus type 2 load in lymphoid tissues. Clinical and Diagnostic Laboratory Immunology 9: 236242.Google ScholarPubMed
Darwich, L, Balasch, M, Plana-Duran, J, Segales, J, Domingo, M and Mateu, E (2003a). Cytokine profiles of peripheral blood mononuclear cells from pigs with postweaning multisystemic wasting syndrome in response to mitogen, superantigen or recall viral antigens. Journal of General Virology 84: 34533457.CrossRefGoogle ScholarPubMed
Darwich, L, Pie, S, Rovira, A, Segales, J, Domingo, M, Oswald, IP and Mateu, E (2003b). Cytokine mRNA expression profiles in lymphoid tissues of pigs naturally affected by postweaning multisystemic wasting syndrome. Journal of General Virology 84: 21172125.CrossRefGoogle ScholarPubMed
Darwich, L, Segales, J and Mateu, E (2004). Pathogenesis of postweaning multisystemic wasting syndrome caused by porcine circovirus 2: an immune riddle. Archives of Virology 149: 857874.CrossRefGoogle ScholarPubMed
Darwich, L, Segales, J, Resendes, A, Balasch, M, Plana-Duran, J and Mateu, E (2008). Transient correlation between viremia levels and IL-10 expression in pigs subclinically infected with porcine circovirus type 2 (PCV2). Research in Veterinary Science 84: 194198.CrossRefGoogle ScholarPubMed
Dorr, PM, Baker, RB, Almond, GW, Wayne, SR and Gebreyes, WA (2007). Epidemiologic assessment of porcine circovirus type 2 coinfection with other pathogens in swine. Journal of the American Veterinary Medical Association 230: 244250.CrossRefGoogle ScholarPubMed
Drolet, R, Larochelle, R, Morin, M, Delisle, B and Magar, R (2003). Detection rates of porcine reproductive and respiratory syndrome virus, porcine circovirus type 2, and swine influenza virus in porcine proliferative and necrotizing pneumonia. Veterinary Pathology 40: 143148.CrossRefGoogle ScholarPubMed
Dulac, GC and Afshar, A (1989). Porcine circovirus antigens in PK-15 cell line (ATCC CCL-33) and evidence of antibodies to circovirus in Canadian pigs. Canadian Journal of Veterinary Research 53: 431433.Google ScholarPubMed
Dupont, K, Nielsen, EO, Baekbo, P and Larsen, LE (2008). Genomic analysis of PCV2 isolates from Danish archives and a current PMWS case-control study supports a shift in genotypes with time. Veterinary Microbiology 128: 5664.CrossRefGoogle Scholar
Edwards, S and Sands, JJ (1994). Evidence of circovirus infection in British pigs. The Veterinary Record 134: 680681.CrossRefGoogle ScholarPubMed
Elbers, AR, Hunneman, WA, Vos, JH, Zeeuwen, AA, Peperkamp, MT and van Exsel, AC (2000). Increase in PDNS diagnoses in the Netherlands. The Veterinary Record 147: 311.Google ScholarPubMed
Ellis, J, Hassard, L, Clark, E, Harding, J, Allan, G, Willson, P, Strokappe, J, Martin, K, McNeilly, F, Meehan, B, Todd, D and Haines, D (1998). Isolation of circovirus from lesions of pigs with postweaning multisystemic wasting syndrome. Canadian Veterinary Journal 39: 4451.Google ScholarPubMed
Ellis, J, Krakowka, S, Lairmore, M, Haines, D, Bratanich, A, Clark, E, Allan, G, Konoby, C, Hassard, L, Meehan, B, Martin, K, Harding, J, Kennedy, S and McNeilly, F (1999). Reproduction of lesions of postweaning multisystemic wasting syndrome in gnotobiotic piglets. Journal of Veterinary Diagnostic Investigation 11: 314.CrossRefGoogle ScholarPubMed
Ellis, JA, Bratanich, A, Clark, EG, Allan, G, Meehan, B, Haines, DM, Harding, J, West, KH, Krakowka, S, Konoby, C, Hassard, L, Martin, K and McNeilly, F (2000). Coinfection by porcine circoviruses and porcine parvovirus in pigs with naturally acquired postweaning multisystemic wasting syndrome. Journal of Veterinary Diagnostic Investigation 12: 2127.CrossRefGoogle ScholarPubMed
Ellis, JA, Konoby, C, West, KH, Allan, GM, Krakowka, S, McNeilly, F, Meehan, B and Walker, I (2001). Lack of antibodies to porcine circovirus type 2 virus in beef and dairy cattle and horses in western Canada. The Canadian Veterinary Journal 42: 461464.Google ScholarPubMed
Ellis, J, Clark, E, Haines, D, West, K, Krakowka, S, Kennedy, S and Allan, GM (2004). Porcine circovirus-2 and concurrent infections in the field. Veterinary Microbiology 98: 159163.CrossRefGoogle ScholarPubMed
Fan, H, Ju, C, Tong, T, Huang, H, Lv, J and Chen, H (2007). Immunogenicity of empty capsids of porcine circovius type 2 produced in insect cells. Veterinary Research Communication 31: 487496.CrossRefGoogle ScholarPubMed
Fenaux, M, Halbur, PG, Gill, M, Toth, TE and Meng, XJ (2000). Genetic characterization of type 2 porcine circovirus (PCV-2) from pigs with postweaning multisystemic wasting syndrome in different geographic regions of North America and development of a differential PCR-restriction fragment length polymorphism assay to detect and differentiate between infections with PCV-1 and PCV-2. Journal of Clinical Microbiology 38: 24942503.CrossRefGoogle ScholarPubMed
Fenaux, M, Halbur, PG, Haqshenas, G, Royer, R, Thomas, P, Nawagitgul, P, Gill, M, Toth, TE and Meng, XJ (2002). Cloned genomic DNA of type 2 porcine circovirus is infectious when injected directly into the liver and lymph nodes of pigs: characterization of clinical disease, virus distribution, and pathologic lesions. Journal of Virology 76: 541551.CrossRefGoogle ScholarPubMed
Fenaux, M, Opriessnig, T, Halbur, PG and Meng, XJ (2003). Immunogenicity and pathogenicity of chimeric infectious DNA clones of pathogenic porcine circovirus type 2 (PCV2) and nonpathogenic PCV1 in weanling pigs. Journal of Virology 77: 1123211243.CrossRefGoogle ScholarPubMed
Fenaux, M, Opriessnig, T, Halbur, PG, Elvinger, F and Meng, XJ (2004a). A chimeric porcine circovirus (PCV) with the immunogenic capsid gene of the pathogenic PCV type 2 (PCV2) cloned into the genomic backbone of the nonpathogenic PCV1 induces protective immunity against PCV2 infection in pigs. Journal of Virology 78: 62976303.CrossRefGoogle ScholarPubMed
Fenaux, M, Opriessnig, T, Halbur, PG, Elvinger, F and Meng, XJ (2004b). Two amino acid mutations in the capsid protein of type 2 porcine circovirus (PCV2) enhanced PCV2 replication in vitro and attenuated the virus in vivo. Journal of Virology 78: 1344013446.CrossRefGoogle ScholarPubMed
Fenaux, M, Opriessnig, T, Halbur, PG, Xu, Y, Potts, B and Meng, XJ (2004c). Detection and in vitro and in vivo characterization of porcine circovirus DNA from a porcine-derived commercial pepsin product. Journal of General Virology 85: 33773382.CrossRefGoogle ScholarPubMed
Finlaison, D, Kirkland, P, Luong, R and Ross, A (2007). Survey of porcine circovirus 2 and postweaning multisystemic wasting syndrome in New South Wales piggeries. Australian Veterinary Journal 85: 304310.CrossRefGoogle ScholarPubMed
Fort, M, Olvera, A, Sibila, M, Segales, J and Mateu, E (2007). Detection of neutralizing antibodies in postweaning multisystemic wasting syndrome (PMWS)-affected and non-PMWS-affected pigs. Veterinary Microbiology 125: 244255.CrossRefGoogle ScholarPubMed
Gagnon, CA, Tremblay, D, Tijssen, P, Venne, MH, Houde, A and Elahi, SM (2007). The emergence of porcine circovirus 2b genotype (PCV-2b) in swine in Canada. Canadian Veterinary Journal 48: 811819.Google ScholarPubMed
Gibbs, MJ and Weiller, GF (1999). Evidence that a plant virus switched hosts to infect a vertebrate and then recombined with a vertebrate-infecting virus. Proceedings of the National Academy of Sciences of the United States of America 96: 80228027.CrossRefGoogle ScholarPubMed
Gilpin, DF, McCullough, K, Meehan, M, McNeilly, F, McNair, I, Stevenson, LS, Foster, JC, Ellis, JA, Krakowka, S, Adair, B and Allan, GM (2003). In vitro studies on the infection and replication of porcine circovirus type 2 in cells of the porcine immune system. Veterinary Immunology and Immunopathology 94: 149161.CrossRefGoogle ScholarPubMed
Grau-Roma, L and Segales, J (2007). Detection of porcine reproductive and respiratory syndrome virus, porcine circovirus type 2, swine influenza virus and Aujeszky's disease virus in cases of porcine proliferative and necrotizing pneumonia (PNP) in Spain. Veterinary Microbiology 119: 144151.CrossRefGoogle ScholarPubMed
Grau-Roma, L, Crisci, E, Sibila, M, Lopez-Soria, S, Nofrarias, M, Cortey, M, Fraile, L, Olvera, A and Segales, J (2008). A proposal on porcine circovirus type 2 (PCV2) genotype definition and their relation with postweaning multisystemic wasting syndrome (PMWS) occurrence. Veterinary Microbiology 128: 2335.CrossRefGoogle ScholarPubMed
Gresham, A, Jackson, G, Giles, N, Allan, G, McNeilly, F and Kennedy, S (2000). PMWS and porcine dermatitis nephropathy syndrome in Great Britain. The Veterinary Record 146: 143.Google ScholarPubMed
Grierson, SS, King, DP, Sandvik, T, Hicks, D, Spencer, Y, Drew, TW and Banks, M (2004). Detection and genetic typing of type 2 porcine circoviruses in archived pig tissues from the UK. Archives of Virology 149: 11711183.CrossRefGoogle ScholarPubMed
Grierson, SS, King, DP, Tucker, AW, Donadeu, M, Mellencamp, MA, Haverson, K, Banks, M and Bailey, M (2007). Ontogeny of systemic cellular immunity in the neonatal pig: correlation with the development of post-weaning multisystemic wasting syndrome. Veterinary Immunology and Immunopathology 119: 254268.CrossRefGoogle ScholarPubMed
Hamel, AL, Lin, LL and Nayar, GP (1998). Nucleotide sequence of porcine circovirus associated with postweaning multisystemic wasting syndrome in pigs. Journal of Virology 72: 52625267.CrossRefGoogle ScholarPubMed
Harding, JC (2004). The clinical expression and emergence of porcine circovirus 2. Veterinary Microbiology 98: 131135.CrossRefGoogle ScholarPubMed
Harding, JC (2007). Status of Porcine circovirus diseases in western Canada. Canadian Veterinary Journal 48: 267268.Google ScholarPubMed
Harding, J and Clark, EG (1997). Recognizing and diagnosing postweaning multisystemic wasting syndrome (PMWS). Swine Health and Production 5: 201203.Google Scholar
Harms, PA, Sorden, SD, Halbur, PG, Bolin, SR, Lager, KM, Morozov, I and Paul, PS (2001). Experimental reproduction of severe disease in CD/CD pigs concurrently infected with type 2 porcine circovirus and porcine reproductive and respiratory syndrome virus. Veterinary Pathology 38: 528539.CrossRefGoogle ScholarPubMed
Hasslung, FC, Berg, M, Allan, GM, Meehan, BM, McNeilly, F and Fossum, C (2003). Identification of a sequence from the genome of porcine circovirus type 2 with an inhibitory effect on IFN-alpha production by porcine PBMCs. Journal of General Virology 84: 29372945.CrossRefGoogle ScholarPubMed
Hesse, R, Kerrigan, M and Rowland, RR (2008). Evidence for recombination between PCV2a and PCV2b in the field. Virus Research 132: 201207.CrossRefGoogle ScholarPubMed
Ju, C, Fan, H, Tan, Y, Liu, Z, Xi, X, Cao, S, Wu, B and Chen, H (2005). Immunogenicity of a recombinant pseudorabies virus expressing ORF1-ORF2 fusion protein of porcine circovirus type 2. Veterinary Microbiology 109: 179190.CrossRefGoogle ScholarPubMed
Juhan, NM (2007). Molecular mechanisms of porcine circovirus 2 replication and pathogenesis. PhD Dissertation. Virginia Polytechnic and State University, Blacksburg, VA.Google Scholar
Kamstrup, S, Barfoed, AM, Frimann, TH, Ladekjaer-Mikkelsen, AS and Botner, A (2004). Immunisation against PCV2 structural protein by DNA vaccination of mice. Vaccine 22: 13581361.CrossRefGoogle ScholarPubMed
Kawashima, K, Katsuda, K and Tsunemitsu, H (2007). Epidemiological investigation of the prevalence and features of postweaning multisystemic wasting syndrome in Japan. Journal of Veterinary Diagnostic Investigation 19: 6068.CrossRefGoogle ScholarPubMed
Kekarainen, T, Montoya, M, Mateu, E and Segales, J (2008a). Porcine circovirus type 2-induced interleukin-10 modulated recall antigen responses. Journal of General Virology 89: 760765.CrossRefGoogle ScholarPubMed
Kekarainen, T, Montoya, M, Dominguez, J, Mateu, E and Segales, J (2008b). Porcine circovirus type 2 (PCV2) viral components immunomodulate recall antigen responses. Veterinary Immunology and Immunopathology 124: 4149.CrossRefGoogle ScholarPubMed
Kim, J and Chae, C (2004). Expression of monocyte chemoattractant protein-1 and macrophage inflammatory protein-1 in porcine circovirus 2-induced granulomatous inflammation. Journal of Comparative Pathology 131: 121126.CrossRefGoogle ScholarPubMed
Kim, JH and Lyoo, YS (2002). Genetic characterization of porcine circovirus-2 field isolates from PMWS pigs. Journal of Veterinary Science 3: 3139.CrossRefGoogle ScholarPubMed
Kim, J, Han, DU, Choi, C and Chae, C (2001). Differentiation of porcine circovirus (PCV)-1 and PCV-2 in boar semen using a multiplex nested polymerase chain reaction. Journal of Virology Methods 98: 2531.CrossRefGoogle ScholarPubMed
Kim, J, Chung, HK, Jung, T, Cho, WS, Choi, C and Chae, C (2002). Postweaning multisystemic wasting syndrome of pigs in Korea: prevalence, microscopic lesions and coexisting microorganisms. Journal of Veterinary Medical Sciences 64: 5762.CrossRefGoogle ScholarPubMed
Kim, J, Chung, HK and Chae, C (2003). Association of porcine circovirus 2 with porcine respiratory disease complex. Veterinary Journal 166: 251256.CrossRefGoogle ScholarPubMed
Kim, J, Ha, Y, Jung, K, Choi, C and Chae, C (2004). Enteritis associated with porcine circovirus 2 in pigs. Canadian Journal of Veterinary Research 68: 218221.Google ScholarPubMed
Kim, J, Ha, Y and Chae, C (2006). Potentiation of porcine circovirus 2-induced postweaning multisystemic wasting syndrome by porcine parvovirus is associated with excessive production of tumor necrosis factor-alpha. Veterinary Pathology 43: 718725.CrossRefGoogle ScholarPubMed
Kiss, I, Kecskemeti, S, Tuboly, T, Bajmocy, E and Tanyi, J (2000). New pig disease in Hungary: postweaning multisystemic wasting syndrome caused by circovirus (Short Communication). Acta Veterinaria Hungarica 48: 469475.CrossRefGoogle ScholarPubMed
Krakowka, S, Ellis, JA, McNeilly, F, Ringler, S, Rings, DM and Allan, G (2001). Activation of the immune system is the pivotal event in the production of wasting disease in pigs infected with porcine circovirus-2 (PCV-2). Veterinary Pathology 38: 3142.CrossRefGoogle ScholarPubMed
Krakowka, S, Ellis, J, McNeilly, F, Meehan, B, Oglesbee, M, Alldinger, S and Allan, G (2004). Features of cell degeneration and death in hepatic failure and systemic lymphoid depletion characteristic of porcine circovirus-2-associated postweaning multisystemic wasting disease. Veterinary Pathology 41: 471481.CrossRefGoogle ScholarPubMed
Krakowka, S, Ellis, J, McNeilly, F, Waldner, C and Allan, G (2005). Features of porcine circovirus-2 disease: correlations between lesions, amount and distribution of virus, and clinical outcome. Journal of Veterinary Diagnostic Investigation 17: 213222.CrossRefGoogle ScholarPubMed
Krakowka, S, Ellis, J, McNeilly, F, Waldner, C, Rings, DM and Allan, G (2007). Mycoplasma hyopneumoniae bacterins and porcine circovirus type 2 (PCV2) infection: induction of postweaning multisystemic wasting syndrome (PMWS) in the gnotobiotic swine model of PCV2-associated disease. Canadian Veterinary Journal 48: 716724.Google ScholarPubMed
Kyriakis, SC, Saoulidis, K, Lekkas, S, Miliotis Ch, C, Papoutsis, PA and Kennedy, S (2002). The effects of immuno-modulation on the clinical and pathological expression of postweaning multisystemic wasting syndrome. Journal of Comparative Pathology 126: 3846.CrossRefGoogle ScholarPubMed
Ladekjaer-Mikkelsen, AS, Nielsen, J, Storgaard, T, Botner, A, Allan, G and McNeilly, F (2001). Transplacental infection with PCV-2 associated with reproductive failure in a gilt. The Veterinary Record 148: 759760.Google Scholar
Ladekjaer-Mikkelsen, AS, Nielsen, J, Stadejek, T, Storgaard, T, Krakowka, S, Ellis, J, McNeilly, F, Allan, G and Botner, A (2002). Reproduction of postweaning multisystemic wasting syndrome (PMWS) in immunostimulated and non-immunostimulated 3-week-old piglets experimentally infected with porcine circovirus type 2 (PCV2). Veterinary Microbiology 89: 97114.CrossRefGoogle ScholarPubMed
Lager, KM, Gauger, PC, Vincent, AL, Opriessnig, T, Kehrli, ME Jr and Cheung, AK (2007). Mortality in pigs given porcine circovirus type 2 subgroup 1 and 2 viruses derived from DNA clones. The Veterinary Record 161: 428429.CrossRefGoogle ScholarPubMed
Larochelle, R, Bielanski, A, Muller, P and Magar, R (2000). PCR detection and evidence of shedding of porcine circovirus type 2 in boar semen. Journal of Clinical Microbiology 38: 46294632.CrossRefGoogle ScholarPubMed
Larochelle, R, Magar, R and D'Allaire, S (2002). Genetic characterization and phylogenetic analysis of porcine circovirus type 2 (PCV2) strains from cases presenting various clinical conditions. Virus Research 90: 101112.CrossRefGoogle ScholarPubMed
Larochelle, R, Magar, R and D'Allaire, S (2003). Comparative serologic and virologic study of commercial swine herds with and without postweaning multisystemic wasting syndrome. Canadian Journal of Veterinary Research 67: 114120.Google ScholarPubMed
LeCann, P, Albina, E, Madec, F, Cariolet, R and Jestin, A (1997). Piglet wasting disease. The Veterinary Record 141: 660.Google ScholarPubMed
Lefebvre, DJ, Costers, S, Van Doorsselaere, J, Misinzo, G, Delputte, PL and Nauwynck, HJ (2008). Antigenic differences among porcine circovirus type 2 strains, as demonstrated by the use of monoclonal antibodies. Journal of General Virology 89: 177187.CrossRefGoogle ScholarPubMed
Lekcharoensuk, P, Morozov, I, Paul, PS, Thangthumniyom, N, Wajjawalku, W and Meng, XJ (2004). Epitope mapping of the major capsid protein of type 2 porcine circovirus (PCV2) by using chimeric PCV1 and PCV2. Journal of Virology 78: 81358145.CrossRefGoogle ScholarPubMed
Liu, J, Chen, I and Kwang, J (2005). Characterization of a previously unidentified viral protein in porcine circovirus type 2-infected cells and its role in virus-induced apoptosis. Journal of Virology 79: 82628274.CrossRefGoogle ScholarPubMed
Liu, J, Chen, I, Du, Q, Chua, H and Kwang, J (2006). The ORF3 protein of porcine circovirus type 2 is involved in viral pathogenesis in vivo. Journal of Virology 80: 50655073.CrossRefGoogle ScholarPubMed
Liu, J, Zhu, Y, Chen, I, Lau, J, He, F, Lau, A, Wang, Z, Karuppannan, AK and Kwang, J (2007). The ORF3 protein of porcine circovirus type 2 interacts with porcine ubiquitin E3 ligase Pirh2 and facilitates p53 expression in viral infection. Journal of Virology 81: 95609567.CrossRefGoogle ScholarPubMed
Lopez-Soria, S, Segales, J, Nofrarias, M, Calsamiglia, M, Ramirez, H, Minguez, A, Serrano, IM, Marin, O and Callen, A (2004). Genetic influence on the expression of PCV disease. The Veterinary Record 155: 504.Google ScholarPubMed
Lyoo, KS, Park, YH and Park, BK (2001). Prevalence of porcine reproductive and respiratory syndrome virus, porcine circovirus type 2 and porcine parvovirus from aborted fetuses and pigs with respiratory problems in Korea. Journal of Veterinary Sciences 2: 201207.CrossRefGoogle ScholarPubMed
Madec, FRN, Eveno, E, Morvan, P, Larour, G, Jolly, JP, Le Diguerher, G, Cariolet, R, Blanchard, P and Jestin, A (2001). PMWS: on-farm observations and preliminary analytic epidemiology. Proceedings of the ssDNA Viruses Plants, Birds, Pigs and Primates (ESVV) Meeting. pp. 8687. Saint Malo, France.Google Scholar
Magar, R, Larochelle, R, Thibault, S and Lamontagne, L (2000a). Experimental transmission of porcine circovirus type 2 (PCV2) in weaned pigs: a sequential study. Journal of Comparative Pathology 123: 258269.CrossRefGoogle ScholarPubMed
Magar, R, Muller, P and Larochelle, R (2000b). Retrospective serological survey of antibodies to porcine circovirus type 1 and type 2. Canadian Journal of Veterinary Research 64: 184186.Google ScholarPubMed
Mahe, D, Blanchard, P, Truong, C, Arnauld, C, Le Cann, P, Cariolet, R, Madec, F, Albina, E and Jestin, A (2000). Differential recognition of ORF2 protein from type 1 and type 2 porcine circoviruses and identification of immunorelevant epitopes. Journal of General Virology 81: 18151824.Google ScholarPubMed
Maldonado, J, Segales, J, Martinez-Puig, D, Calsamiglia, M, Riera, P, Domingo, M and Artigas, C (2005). Identification of viral pathogens in aborted fetuses and stillborn piglets from cases of swine reproductive failure in Spain. Veterinary Journal 169: 454456.CrossRefGoogle ScholarPubMed
Mandrioli, L, Sarli, G, Panarese, S, Baldoni, S and Marcato, PS (2004). Apoptosis and proliferative activity in lymph node reaction in postweaning multisystemic wasting syndrome (PMWS). Veterinary Immunology and Immunopathology 97: 2537.CrossRefGoogle ScholarPubMed
Mankertz, A and Hillenbrand, B (2002). Analysis of transcription of porcine circovirus type 1. Journal of General Virology 83: 27432751.CrossRefGoogle ScholarPubMed
Mankertz, A, Persson, F, Mankertz, J, Blaess, G and Buhk, HJ (1997). Mapping and characterization of the origin of DNA replication of porcine circovirus. Journal of Virology 71: 25622566.CrossRefGoogle ScholarPubMed
Mankertz, A, Mankertz, J, Wolf, K and Buhk, HJ (1998a). Identification of a protein essential for replication of porcine circovirus. Journal of General Virology 79: 381384.CrossRefGoogle ScholarPubMed
Mankertz, J, Buhk, HJ, Blaess, G and Mankertz, A (1998b). Transcription analysis of porcine circovirus (PCV). Virus Genes 16: 267276.CrossRefGoogle ScholarPubMed
Mankertz, A, Mueller, B, Steinfeldt, T, Schmitt, C and Finsterbusch, T (2003). New reporter gene-based replication assay reveals exchangeability of replication factors of porcine circovirus types 1 and 2. Journal of Virology 77: 98859893.CrossRefGoogle Scholar
Mankertz, A, Caliskan, R, Hattermann, K, Hillenbrand, B, Kurzendoerfer, P, Mueller, B, Schmitt, C, Steinfeldt, T and Finsterbusch, T (2004). Molecular biology of porcine circovirus: analyses of gene expression and viral replication. Veterinary Microbiology 98: 8188.CrossRefGoogle ScholarPubMed
McIntosh, KA, Harding, JC, Ellis, JA and Appleyard, GD (2006a). Detection of porcine circovirus type 2 viremia and seroconversion in naturally infected pigs in a farrow-to-finish barn. Canadian Journal of Veterinary Research 70: 5861.Google Scholar
McIntosh, KA, Harding, JC, Parker, S, Ellis, JA and Appleyard, GD (2006b). Nested polymerase chain reaction detection and duration of porcine circovirus type 2 in semen with sperm morphological analysis from naturally infected boars. Journal of Veterinary Diagnostic Investigation 18: 380384.CrossRefGoogle ScholarPubMed
McKeown, NE, Opriessnig, T, Thomas, P, Guenette, DK, Elvinger, F, Fenaux, M, Halbur, PG and Meng, XJ (2005). Effects of porcine circovirus type 2 (PCV2) maternal antibodies on experimental infection of piglets with PCV2. Clinical and Diagnostic Laboratory Immunology 12: 13471351.Google ScholarPubMed
Meehan, BM, Creelan, JL, McNulty, MS and Todd, D (1997). Sequence of porcine circovirus DNA: affinities with plant circoviruses. Journal of General Virology 78: 221227.CrossRefGoogle ScholarPubMed
Meehan, BM, McNeilly, F, Todd, D, Kennedy, S, Jewhurst, VA, Ellis, JA, Hassard, LE, Clark, EG, Haines, DM and Allan, GM (1998). Characterization of novel circovirus DNAs associated with wasting syndromes in pigs. Journal of General Virology 79: 21712179.CrossRefGoogle ScholarPubMed
Meerts, P, Misinzo, G and Nauwynck, HJ (2005a). Enhancement of porcine circovirus 2 replication in porcine cell lines by IFN-gamma before and after treatment and by IFN-alpha after treatment. Journal of Interferon Cytokine Research 25: 684693.CrossRefGoogle ScholarPubMed
Meerts, P, Van Gucht, S, Cox, E, Vandebosch, A and Nauwynck, HJ (2005b). Correlation between type of adaptive immune response against porcine circovirus type 2 and level of virus replication. Viral Immunology 18: 333341.CrossRefGoogle ScholarPubMed
Meerts, P, Misinzo, G, Lefebvre, D, Nielsen, J, Botner, A, Kristensen, CS and Nauwynck, HJ (2006). Correlation between the presence of neutralizing antibodies against porcine circovirus 2 (PCV2) and protection against replication of the virus and development of PCV2-associated disease. BMC Veterinary Research 2: 6.CrossRefGoogle ScholarPubMed
Misinzo, G, Meerts, P, Bublot, M, Mast, J, Weingartl, HM and Nauwynck, HJ (2005). Binding and entry characteristics of porcine circovirus 2 in cells of the porcine monocytic line 3D4/31. Journal of General Virology 86: 20572068.CrossRefGoogle ScholarPubMed
Misinzo, G, Delputte, PL, Meerts, P, Lefebvre, DJ and Nauwynck, HJ (2006). Porcine circovirus 2 uses heparan sulfate and chondroitin sulfate B glycosaminoglycans as receptors for its attachment to host cells. Journal of Virology 80: 34873494.CrossRefGoogle ScholarPubMed
Misinzo, G, Delputte, PL, Lefebvre, DJ and Nauwynck, HJ (2008a). Increased yield of porcine circovirus-2 by a combined treatment of PK-15 cells with interferon-gamma and inhibitors of endosomal–lysosomal system acidification. Archives of Virology 153: 337342.CrossRefGoogle ScholarPubMed
Misinzo, G, Delputte, PL and Nauwynck, HJ (2008b). Inhibition of Endosomal–Lysosomal System Acidification Enhances Porcine Circovirus 2 Infection of Porcine Epithelial Cells. Journal of Virology 82: 11281135.CrossRefGoogle Scholar
Mori, M, Sato, K, Akachi, S, Asahi, S, Taniguchi, S and Narita, M (2000). Retrospective study of porcine circovirus 2 infection in Japan: seven cases in 1989. Veterinary Pathology 37: 667669.CrossRefGoogle ScholarPubMed
Morozov, I, Sirinarumitr, T, Sorden, SD, Halbur, PG, Morgan, MK, Yoon, KJ and Paul, PS (1998). Detection of a novel strain of porcine circovirus in pigs with postweaning multisystemic wasting syndrome. Journal of Clinical Microbiology 36: 25352541.CrossRefGoogle ScholarPubMed
Nayar, GP, Hamel, A and Lin, L (1997). Detection and characterization of porcine circovirus associated with postweaning multisystemic wasting syndrome in pigs. Canadian Veterinary Journal 38: 385386.Google ScholarPubMed
Nayar, GP, Hamel, AL, Lin, L, Sachvie, C, Grudeski, E and Spearman, G (1999). Evidence for circovirus in cattle with respiratory disease and from aborted bovine fetuses. Canadian Veterinary Journal 40: 277278.Google ScholarPubMed
Niagro, FD, Forsthoefel, AN, Lawther, RP, Kamalanathan, L, Ritchie, BW, Latimer, KS and Lukert, PD (1998). Beak and feather disease virus and porcine circovirus genomes: intermediates between the geminiviruses and plant circoviruses. Archives of Virology 143: 17231744.CrossRefGoogle ScholarPubMed
Nunez, A, McNeilly, F, Perea, A, Sanchez-Cordon, PJ, Huerta, B, Allan, G and Carrasco, L (2003). Coinfection by Cryptosporidium parvum and porcine circovirus type 2 in weaned pigs. Journal of Veterinary Medicine Series B. Infectious Diseases and Veterinary Public Health 50: 255258.CrossRefGoogle ScholarPubMed
O'Connor, B, Gauvreau, H, West, K, Bogdan, J, Ayroud, M, Clark, EG, Konoby, C, Allan, G and Ellis, JA (2001). Multiple porcine circovirus 2-associated abortions and reproductive failure in a multisite swine production unit. Canadian Veterinary Journal 42: 551553.Google Scholar
Okuda, Y, Ono, M, Yazawa, S and Shibata, I (2003). Experimental reproduction of postweaning multisystemic wasting syndrome in cesarean-derived, colostrum-deprived piglets inoculated with porcine circovirus type 2 (PCV2): investigation of quantitative PCV2 distribution and antibody responses. Journal of Veterinary Diagnostic Investigation 15: 107114.CrossRefGoogle ScholarPubMed
Olvera, A, Cortey, M and Segales, J (2007). Molecular evolution of porcine circovirus type 2 genomes: phylogeny and clonality. Virology 357: 175185.CrossRefGoogle ScholarPubMed
Opriessnig, T, Fenaux, M, Yu, S, Evans, RB, Cavanaugh, D, Gallup, JM, Pallares, FJ, Thacker, EL, Lager, KM, Meng, XJ and Halbur, PG (2004a). Effect of porcine parvovirus vaccination on the development of PMWS in segregated early weaned pigs coinfected with type 2 porcine circovirus and porcine parvovirus. Veterinary Microbiology 98: 209220.CrossRefGoogle ScholarPubMed
Opriessnig, T, Thacker, EL, Yu, S, Fenaux, M, Meng, XJ and Halbur, PG (2004b). Experimental reproduction of postweaning multisystemic wasting syndrome in pigs by dual infection with Mycoplasma hyopneumoniae and porcine circovirus type 2. Veterinary Pathology 41: 624640.CrossRefGoogle ScholarPubMed
Opriessnig, T, Fenaux, M, Thomas, P, Hoogland, MJ, Rothschild, MF, Meng, XJ and Halbur, PG (2006a). Evidence of breed-dependent differences in susceptibility to porcine circovirus type-2-associated disease and lesions. Veterinary Pathology 43: 281–29CrossRefGoogle ScholarPubMed
Opriessnig, T, Halbur, PG, Yu, S, Thacker, EL, Fenaux, M and Meng, XJ (2006b). Effects of the timing of the administration of Mycoplasma hyopneumoniae bacterin on the development of lesions associated with porcine circovirus type 2. The Veterinary Record 158: 149154.CrossRefGoogle ScholarPubMed
Opriessnig, T, McKeown, NE, Harmon, KL, Meng, XJ and Halbur, PG (2006c). Porcine circovirus type 2 infection decreases the efficacy of a modified live porcine reproductive and respiratory syndrome virus vaccine. Clinical and Vaccine Immunology 13: 923929CrossRefGoogle ScholarPubMed
Opriessnig, T, McKeown, NE, Zhou, EM, Meng, XJ and Halbur, PG (2006d). Genetic and experimental comparison of porcine circovirus type 2 (PCV2) isolates from cases with and without PCV2-associated lesions provides evidence for differences in virulence. Journal of General Virology 87: 29232932.CrossRefGoogle ScholarPubMed
Opriessnig, T, Ramamoorthy, S, Madson, DM, Patterson, AR, Pal, N, Meng, XJ and Halbur, PG (2007a). Experimental comparison of the virulence of PCV2a and PCV2b isolates in a conventional pigs model. Proceedings of the 88th Annual Meeting of the Conference of Research Workers in Animal Diseases. p. 145.Chicago, IL, USA.Google Scholar
Opriessnig, T, Meng, XJ and Halbur, PG (2007b). Porcine circovirus type 2 associated disease: update on current terminology, clinical manifestations, pathogenesis, diagnosis, and intervention strategies. Journal of Veterinary Diagnostic Investigation 19: 591615.CrossRefGoogle ScholarPubMed
Ostrowski, M, Galeota, JA, Jar, AM, Platt, KB, Osorio, FA and Lopez, OJ (2002). Identification of neutralizing and nonneutralizing epitopes in the porcine reproductive and respiratory syndrome virus GP5 ectodomain. Journal of Virology 76: 42414250.CrossRefGoogle ScholarPubMed
Pallares, FJ, Halbur, PG, Opriessnig, T, Sorden, SD, Villar, D, Janke, BH, Yaeger, MJ, Larson, DJ, Schwartz, KJ, Yoon, KJ and Hoffman, LJ (2002). Porcine circovirus type 2 (PCV-2) coinfections in US field cases of postweaning multisystemic wasting syndrome (PMWS). Journal of Veterinary Diagnostic Investigation 14: 515519.CrossRefGoogle ScholarPubMed
Park, JS, Kim, J, Ha, Y, Jung, K, Choi, C, Lim, JK, Kim, SH and Chae, C (2005). Birth abnormalities in pregnant sows infected intranasally with porcine circovirus 2. Journal of Comparative Pathology 132: 139144.CrossRefGoogle ScholarPubMed
Pensaert, MB, Sanchez, RE Jr, Ladekjaer-Mikkelsen, AS, Allan, GM and Nauwynck, HJ (2004). Viremia and effect of fetal infection with porcine viruses with special reference to porcine circovirus 2 infection. Veterinary Microbiology 98: 175183.CrossRefGoogle ScholarPubMed
Phaneuf, LR, Ceccarelli, A, Laing, JR, Moloo, B and Turner, PV (2007). Porcine dermatitis and nephropathy syndrome associated with porcine circovirus 2 infection in a Yorkshire pig. Journal of the American Association for Laboratory Animal Science 46: 6872.Google Scholar
Phenix, KV, Weston, JH, Ypelaar, I, Lavazza, A, Smyth, JA, Todd, D, Wilcox, GE and Raidal, SR (2001). Nucleotide sequence analysis of a novel circovirus of canaries and its relationship to other members of the genus Circovirus of the family Circoviridae. Journal of General Virology 82: 28052809.CrossRefGoogle ScholarPubMed
Pogranichnyy, RM, Yoon, KJ, Harms, PA, Swenson, SL, Zimmerman, JJ and Sorden, SD (2000). Characterization of immune response of young pigs to porcine circovirus type 2 infection. Viral Immunology 13: 143153.CrossRefGoogle ScholarPubMed
Pogranichniy, RM, Yoon, KJ, Harms, PA, Sorden, SD and Daniels, M (2002). Case-control study on the association of porcine circovirus type 2 and other swine viral pathogens with postweaning multisystemic wasting syndrome. Journal of Veterinary Diagnostic Investigation 14: 449456.CrossRefGoogle ScholarPubMed
Quintana, J, Segales, J, Rosell, C, Calsamiglia, M, Rodriguez-Arrioja, GM, Chianini, F, Folch, JM, Maldonado, J, Canal, M, Plana-Duran, J and Domingo, M (2001). Clinical and pathological observations on pigs with postweaning multisystemic wasting syndrome. The Veterinary Record 149: 357361.CrossRefGoogle ScholarPubMed
Ramirez-Mendoza, H, Martinez, C, Mercado, C, Castillo-Juarez, H, Hernandez, J and Segales, J (2007). Porcine circovirus type 2 antibody detection in backyard pigs from Mexico City. Research in Veterinary Sciences 83: 130132.CrossRefGoogle ScholarPubMed
Raye, W, Muhling, J, Warfe, L, Buddle, JRPalmer, C and Wilcox, GE (2005). The detection of porcine circovirus in the Australian pig herd. Australian Veterinary Journal 83: 300304.CrossRefGoogle ScholarPubMed
Resendes, AR, Majo, N, Segales, J, Mateu, E, Calsamiglia, M and Domingo, M (2004). Apoptosis in lymphoid organs of pigs naturally infected by porcine circovirus type 2. Journal of General Virology 85: 28372844.CrossRefGoogle ScholarPubMed
Rodriguez-Arrioja, GM, Segales, J, Calsamiglia, M, Resendes, A, Balasch, M, Plana-Duran, J, Casal, J and Domingo, M (2002). Dynamics of porcine circovirus type 2 infection in a herd of pigs with postweaning multisystemic wasting syndrome. American Journal of Veterinary Research 63: 354357.CrossRefGoogle Scholar
Rodriguez-Arrioja, GM, Segales, J, Domingo, M and Plana-Duran, J (2003a). Lack of PCV-2 infection in non-porcine species in Spain. The Veterinary Record 153: 371372.Google ScholarPubMed
Rodriguez-Arrioja, GM, Segales, J, Rosell, C, Rovira, A, Pujols, J, Plana-Duran, J and Domingo, M (2003b). Retrospective study on porcine circovirus type 2 infection in pigs from 1985 to 1997 in Spain. Journal of Veterinary Medicine Series B. Infectious Diseases and Veterinary Public Health 50: 99101.CrossRefGoogle ScholarPubMed
Rose, N, Larour, G, Le Diguerher, G, Eveno, E, Jolly, JP, Blanchard, P, Oger, A, Le Dimna, M, Jestin, A and Madec, F (2003). Risk factors for porcine post-weaning multisystemic wasting syndrome (PMWS) in 149 French farrow-to-finish herds. Preventive Veterinary Medicine 61: 209225.CrossRefGoogle ScholarPubMed
Rose, N, Blanchard, P, Cariolet, R, Grasland, B, Amenna, N, Oger, A, Durand, B, Balasch, M, Jestin, A and Madec, F (2007). Vaccination of porcine circovirus type 2 (PCV2)-infected sows against porcine Parvovirus (PPV) and Erysipelas: effect on post-weaning multisystemic wasting syndrome (PMWS) and on PCV2 genome load in the offspring. Journal of Comparative Pathology 136: 133144.CrossRefGoogle ScholarPubMed
Rosell, C, Segales, J, Plana-Duran, J, Balasch, M, Rodriguez-Arrioja, GM, Kennedy, S, Allan, GM, McNeilly, F, Latimer, KS and Domingo, M (1999). Pathological, immunohistochemical, and in-situ hybridization studies of natural cases of postweaning multisystemic wasting syndrome (PMWS) in pigs. Journal of Comparative Pathology 120: 5978.CrossRefGoogle ScholarPubMed
Rosell, C, Segales, J, Ramos-Vara, JA, Folch, JM, Rodriguez-Arrioja, GM, Duran, CO, Balasch, M, Plana-Duran, J and Domingo, M (2000a). Identification of porcine circovirus in tissues of pigs with porcine dermatitis and nephropathy syndrome. The Veterinary Record 146: 4043.CrossRefGoogle ScholarPubMed
Rosell, C, Segales, J, Rovira, A and Domingo, M (2000b). Porcine circovirosis in Spain. The Veterinary Record 146: 591592.Google ScholarPubMed
Sarli, G, Mandrioli, L, Laurenti, M, Sidoli, L, Cerati, C, Rolla, G and Marcato, PS (2001). Immunohistochemical characterisation of the lymph node reaction in pig post-weaning multisystemic wasting syndrome (PMWS). Veterinary Immunology and Immunopathology 83: 5367.CrossRefGoogle ScholarPubMed
Saxena, N, Nayar, D and Kapil, U (1997). Prevalence of underweight, stunting and wasting. Indian Pediatrics 34: 627631.Google ScholarPubMed
Schulze, C, Neumann, G, Grutze, I, Engelhardt, A, Mirle, C, Ehlert, F and Hlinak, A (2003). [Case report: Porcine circovirus type 2 infection in an European wild boar (Sus scrofa) in the state of Brandenburg, Germany]. Deutsche Tierarztliche Wochenschrift 110: 426428.Google Scholar
Seeliger, FA, Brugmann, ML, Kruger, L, Greiser-Wilke, I, Verspohl, J, Segales, J and Baumgartner, W (2007). Porcine circovirus type 2-associated cerebellar vasculitis in postweaning multisystemic wasting syndrome (PMWS)-affected pigs. Veterinary Pathology 44: 621634.CrossRefGoogle ScholarPubMed
Segales, J, Alonso, F, Rosell, C, Pastor, J, Chianini, F, Campos, E, Lopez-Fuertes, L, Quintana, J, Rodriguez-Arrioja, G, Calsamiglia, M, Pujols, J, Dominguez, J and Domingo, M (2001). Changes in peripheral blood leukocyte populations in pigs with natural postweaning multisystemic wasting syndrome (PMWS). Veterinary Immunology and Immunopathology 81: 3744.CrossRefGoogle ScholarPubMed
Segales, J, Allan, GM and Domingo, M (2005). Porcine circovirus diseases. Animal Health Research Reviews 6: 119142.CrossRefGoogle ScholarPubMed
Shi, K, Li, H, Guo, X, Ge, X, Jia, H, Zheng, S and Yang, H (2007). Changes in peripheral blood leukocyte subpopulations in piglets co-infected experimentally with porcine reproductive and respiratory syndrome virus and porcine circovirus type 2. Veterinary Microbiology 129: 367377.CrossRefGoogle ScholarPubMed
Shibahara, T, Sato, K, Ishikawa, Y and Kadota, K (2000). Porcine circovirus induces B lymphocyte depletion in pigs with wasting disease syndrome. Journal of Veterinary Medical Science 62: 11251131.CrossRefGoogle ScholarPubMed
Shibata, I, Okuda, Y, Yazawa, S, Ono, M, Sasaki, T, Itagaki, M, Nakajima, N, Okabe, Y and Hidejima, I (2003). PCR detection of porcine circovirus type 2 DNA in whole blood, serum, oropharyngeal swab, nasal swab, and feces from experimentally infected pigs and field cases. Journal of Veterinary Medical Science 65: 405408.CrossRefGoogle ScholarPubMed
Shibata, I, Okuda, Y, Kitajima, K and Asai, T (2006). Shedding of porcine circovirus into colostrum of sows. Journal of Veterinary Medicine Series B. Infectious Diseases and Veterinary Public Health 53: 278280.CrossRefGoogle ScholarPubMed
Shuai, J, Wei, W, Li, X, Chen, N, Zhang, Z, Chen, X and Fang, W (2007). Genetic characterization of porcine circovirus type 2 (PCV2) from pigs in high-seroprevalence areas in southeastern China. Virus Genes 35: 619627.CrossRefGoogle ScholarPubMed
Sibila, M, Calsamiglia, M, Segales, J, Blanchard, P, Badiella, L, Le Dimna, M, Jestin, A and Domingo, M (2004). Use of a polymerase chain reaction assay and an ELISA to monitor porcine circovirus type 2 infection in pigs from farms with and without postweaning multisystemic wasting syndrome. American Journal of Veterinary Reseach 65: 8892.CrossRefGoogle Scholar
Sipos, W, Duvigneau, JC, Willheim, M, Schilcher, F, Hartl, RT, Hofbauer, G, Exel, B, Pietschmann, P and Schmoll, F (2004). Systemic cytokine profile in feeder pigs suffering from natural postweaning multisystemic wasting syndrome (PMWS) as determined by semiquantitative RT-PCR and flow cytometric intracellular cytokine detection. Veterinary Immunology and Immunopathology 99: 6371.CrossRefGoogle ScholarPubMed
Sipos, W, Duvigneau, JC, Pietschmann, P, Schilcher, F, Hofbauer, G, Hartl, RT and Schmoll, F (2005). Porcine dermatitis and nephropathy syndrome (PDNS) is associated with a systemic cytokine expression profile indicative of proinflammation and a Th1 bias. Veterinary Immunology and Immunopathology 107: 303313.CrossRefGoogle Scholar
Song, Y, Jin, M, Zhang, S, Xu, X, Xiao, S, Cao, S and Chen, H (2007). Generation and immunogenicity of a recombinant pseudorabies virus expressing cap protein of porcine circovirus type 2. Veterinary Microbiology 119: 97104.CrossRefGoogle ScholarPubMed
Steinfeldt, T, Finsterbusch, T and Mankertz, A (2001). Rep and Rep′ protein of porcine circovirus type 1 bind to the origin of replication in vitro. Virology 291: 152160.CrossRefGoogle Scholar
Steinfeldt, T, Finsterbusch, T and Mankertz, A (2006). Demonstration of nicking/joining activity at the origin of DNA replication associated with the rep and rep′ proteins of porcine circovirus type 1. Journal of Virology 80: 62256234.CrossRefGoogle ScholarPubMed
Steinfeldt, T, Finsterbusch, T and Mankertz, A (2007). Functional analysis of cis- and trans-acting replication factors of porcine circovirus type 1. Journal of Virology 81: 56965704.CrossRefGoogle ScholarPubMed
Stevenson, GW, Kiupel, M, Mittal, SK, Choi, J, Latimer, KS and Kanitz, CL (2001). Tissue distribution and genetic typing of porcine circoviruses in pigs with naturally occurring congenital tremors. Journal of Veterinary Diagnostic Investigation 13: 5762.CrossRefGoogle ScholarPubMed
Stevenson, LS, McCullough, K, Vincent, I, Gilpin, DF, Summerfield, A, Nielsen, J, McNeilly, F, Adair, BM and Allan, GM (2006). Cytokine and C-reactive protein profiles induced by porcine circovirus type 2 experimental infection in 3-week-old piglets. Viral Immunology 19: 189195.CrossRefGoogle ScholarPubMed
Stevenson, LS, Gilpin, DF, Douglas, A, McNeilly, F, McNair, I, Adair, BM and Allan, GM (2007). T lymphocyte epitope mapping of porcine circovirus type 2. Viral Immunology 20: 389398.CrossRefGoogle ScholarPubMed
Studdert, MJ (1993). Circoviridae: new viruses of pigs, parrots and chickens. Australian Veterinary Journal 70: 121122.CrossRefGoogle ScholarPubMed
Thomson, J, Smith, B, Allan, G, McNeilly, F and McVicar, C (2000). PDNS, PMWS and porcine circovirus type 2 in Scotland. Porcine dermatitis and nephropathy syndrome. Post-weaning multisystemic wasting syndrome. The Veterinary Record 146: 651652.Google ScholarPubMed
Tischer, I, Rasch, R and Tochtermann, G (1974). Characterization of papovavirus- and picornavirus-like particles in permanent pig kidney cell lines. Zentralblatt Fuer Bakteriologie (Originale A) 226: 153167.Google ScholarPubMed
Tischer, I, Gelderblom, H, Vettermann, W and Koch, MA (1982). A very small porcine virus with circular single-stranded DNA. Nature 295: 6466.CrossRefGoogle ScholarPubMed
Tischer, I, Mields, W, Wolff, D, Vagt, M and Griem, W (1986). Studies on epidemiology and pathogenicity of porcine circovirus. Archives of Virology 91: 271276.CrossRefGoogle ScholarPubMed
Tischer, I, Peters, D, Rasch, R and Pociuli, S (1987). Replication of porcine circovirus: induction by glucosamine and cell cycle dependence. Archives of Virology 96: 3957.CrossRefGoogle ScholarPubMed
Truong, C, Mahe, D, Blanchard, P, Le Dimna, M, Madec, F, Jestin, A and Albina, E (2001). Identification of an immunorelevant ORF2 epitope from porcine circovirus type 2 as a serological marker for experimental and natural infection. Archives of Virology 146: 11971211.CrossRefGoogle ScholarPubMed
Vincent, IE, Carrasco, CP, Herrmann, B, Meehan, BM, Allan, GM, Summerfield, A and McCullough, KC (2003). Dendritic cells harbor infectious porcine circovirus type 2 in the absence of apparent cell modulation or replication of the virus. Journal of Virology 77: 1328813300.CrossRefGoogle ScholarPubMed
Vincent, IE, Carrasco, CP, Guzylack-Piriou, L, Carrasco, CP, Guzylack-Piriou, L, Herrmann, B, McNeilly, F, Allan, GM, Summerfield, A and McCullough, KC (2005). Subset-dependent modulation of dendritic cell activity by circovirus type 2. Immunology 115: 388398.CrossRefGoogle ScholarPubMed
Vincent, IE, Balmelli, C, Meehan, B, Allan, G, Summerfield, A and McCullough, KC (2007). Silencing of natural interferon producing cell activation by porcine circovirus type 2 DNA. Immunology 120: 4756.CrossRefGoogle ScholarPubMed
Vicente, J, Segales, J, Hofle, U, Balasch, M, Plana-Duran, J, Domingo, M and Gortazar, C (2004). Epidemiological study on porcine circovirus type 2 (PCV2) infection in the European wild boar (Sus scrofa). Veterinary Research 35: 243253.CrossRefGoogle ScholarPubMed
Wang, C, Huang, TS, Huang, CC, Tu, C, Jong, MH, Lin, SY and Lai, SS (2004). Characterization of porcine circovirus type 2 in Taiwan. Journal of Veterinary Medical Science 66: 469475.CrossRefGoogle ScholarPubMed
Wang, X, Jiang, W, Jiang, P, Li, Y, Feng, Z and Xu, J (2006). Construction and immunogenicity of recombinant adenovirus expressing the capsid protein of porcine circovirus 2 (PCV2) in mice. Vaccine 24: 33743380.CrossRefGoogle ScholarPubMed
Wellenberg, GJ, Stockhofe-Zurwieden, N, Boersma, WJ, De Jong, MF and Elbers, AR (2004a). The presence of co-infections in pigs with clinical signs of PMWS in The Netherlands: a case-control study. Research in Veterinary Science 77: 177184.CrossRefGoogle ScholarPubMed
Wellenberg, GJ, Stockhofe-Zurwieden, N, de Jong, MF, Boersma, WJ and Elbers, AR (2004b). Excessive porcine circovirus type 2 antibody titres may trigger the development of porcine dermatitis and nephropathy syndrome: a case-control study. Veterinary Microbiology 99: 203214.CrossRefGoogle ScholarPubMed
Wikstrom, FH, Meehan, BM, Berg, M, Timmusk, S, Elving, J, Fuxler, L, Magnusson, M, Allan, GM, McNeilly, F and Fossum, C (2007). Structure-dependent modulation of alpha interferon production by porcine circovirus 2 oligodeoxyribonucleotide and CpG DNAs in porcine peripheral blood mononuclear cells. Journal of Virology 81: 49194927.CrossRefGoogle ScholarPubMed
Woeste, K and Grosse Beilage, E (2007). [Transmission of agents of the porcine respiratory disease complex (PRDC) between swine herds: a review. Part 1 – Diagnosis, transmission by animal contact]. Deutsche Tierarztliche Wochenschrift 114: 324326, 328337.Google ScholarPubMed
Yang, JS, Song, DS, Kim, SY, Lyoo, KS and Park, BK (2003). Detection of porcine circovirus type 2 in feces of pigs with or without enteric disease by polymerase chain reaction. Journal of Veterinary Diagnostic Investigation 15: 369373.CrossRefGoogle ScholarPubMed
Yu, S, Opriessnig, T, Kitikoon, P, Nilubol, D, Halbur, PG and Thacker, E (2007a). Porcine circovirus type 2 (PCV2) distribution and replication in tissues and immune cells in early infected pigs. Veterinary Immunology and Immunopathology 115: 261272.CrossRefGoogle ScholarPubMed
Yu, S, Vincent, A, Opriessnig, T, Carpenter, S, Kitikoon Halbur, PG and Thacker, E (2007b). Quantification of PCV2 capsid transcript in peripheral blood mononuclear cells (PBMCs) in vitro. Veterinary Microbiology 123: 3442.CrossRefGoogle ScholarPubMed
Zhou, JY, Chen, QX, Ye, JX, Shen, HG, Chen, TF and Shang, SB (2006). Serological investigation and genomic characterization of PCV2 isolates from different geographic regions of Zhejiang province in China. Veterinary Research Communication 30: 205220.CrossRefGoogle ScholarPubMed