Ear necrosis reduction in pigs after vaccination against PCV2

Research in Veterinary Science

Volumn 91, Issue 1, 2011, Pages 125-128

  Pejsak, Z ^a   Markowska Daniel, I ^a   Pomorska Mol M ^a   Porowski, M ^b   Kolacz R ^c  

^a NATIONAL VETERINARY RESEARCH INSTITUTE   (Poland)

^b Vet Com   (Poland)

^c WROC AW UNIVERSITY OF ENVIRONMENTAL AND LIFE SCIENCES   (Poland)

Author keywords

Ear necrosis syndrome; PCV2; Pigs; Vaccination

Indexed keywords

CIRCOVAC; PORCINE CIRCOVIRUS TYPE 2 VACCINE; UNCLASSIFIED DRUG; VIRUS VACCINE;

ANIMAL EXPERIMENT; ARTICLE; CHI SQUARE TEST; CIRCOVIRUS; CONTROLLED STUDY; DISEASE SEVERITY; DRUG EFFICACY; EAR DISEASE; EAR NECROSIS SYNDROME; FEMALE; KRUSKAL WALLIS TEST; NONHUMAN; PIGLET; PORCINE CIRCOVIRUS TYPE 2; POSTWEANING MULTISYSTEMIC WASTING SYNDROME; PREVALENCE; VACCINATION;

ANIMALS; CIRCOVIRIDAE INFECTIONS; CIRCOVIRUS; EAR; FEMALE; NECROSIS; SWINE; SWINE DISEASES; VACCINATION; VIRAL VACCINES; WASTING SYNDROME;

SUIDAE;

EID: 79959841548     PISSN: 00345288     EISSN: 15322661     Source Type: Journal    
DOI: 10.1016/j.rvsc.2010.08.015     Document Type: Article

References (32)

1. Allan G.M., Ellis J.A. Porcine circovirus: a review. J. Vet. Diagn. Invest. 2000, 12:3-14.
2. Allan G., Andréoni C., Joisel F., Beattie V., Charreyre C. Porcine cirkovirosis-eradication of the disease in the herd with acute and persistent infection. Magazyn Wet. 2009, 6:580-583.
3. Angen O., Oliveira S., Ahrens P., Svensmark B., Leser T.D. Development of an improved species specific PCR test for detection of Haemophilus parasuis. Vet. Microbiol. 2007, 119:266-276.
4. Artiushin S., Stipkovits L., Minion F.C. Development of polymerase chain reaction primers to detect Mycoplasma hyopneumoniae. Mol. Cell. Probes 1993, 7:381-385.
5. Calsamiglia M., Fraile L., Espinal A., Cuxart A., Seminati S., Martin M. Sow porcine circovirus type 2 (PCV2) status effect on litter mortality in postweaning multisystemic wasting syndrome (PMWS). Res. Vet. Sci. 2007, 82:299-304.
6. Cameron R. Diseases of Swine 2006, Ames, Iowa, USA Blackwell Publishing, pp. 179-198. ninth ed.
7. Coignoul F.L., Bertram T.A., Martineau G.P. Pathology of an ulcerative dermatitis in Belgian Landrace sows. Vet. Pathol. 1985, 22:306-310.
8. Darwich L., Balasch M., Plana-Duran J., Segales J., Domingo M., Mateu E. Cytokine profiles of peripheral blood mononuclear cells from pigs with postweaning multisystemic wasting syndrome in response to mitogen, superantigen or recall viral antigens. J. Gen. Virol. 2003, 84:3453-3457.
9. Fort M., Sibila M., Pérez-Martín E., Nofrarías M., Mateu E., Segalés J. One dose of a porcine circovirus 2 (PCV2) sub-unit vaccine administered to 3-week-old conventional piglets elicits cell-mediated immunity and significantly reduces PCV2 viremia in an experimental model. Vaccine 2009, 27:4031-4037.
10. Joisel F., Charreyre C., Coulombe L., Noël J.C., Longo S. Vaccination of sows and gilts against PCV2 diseases: field experiences in Europe. Adv. Pork Prod. 2008, 19:183-195.
11. Kołodziejczyk P., Szczotka A., Pejsak Z. Application of PCR technique for diagnosing Mycoplasma hyopneumoniae infection in swine. Medycyna Wet. 2004, 60:591-596.
12. Krakowka S., Ellis J.A., McNeilly F., Gilpin D., Meehan B., McCullough K., Allan G.A. Immunologic features of porcine circovirus type 2 infection. Virol. Immunol. 2002, 15:567-582.
13. Markowska-Daniel I., Kowalczyk A. Identifying Streptococcus suis using PCR. Medycyna Wet. 2005, 61:522-525.
14. Markowska-Daniel I., Jabłoński A., Nowak A., Stepniewska K., Pejsak Z. Elaboration of a PCR test for the detection of Pasteurella multocida dermonecrotoxigenic strains in nasal swabs of pigs. Medycyna Wet. 2009, 65:542-545.
15. Markowska-Daniel I., Stepniewska K., Pejsak Z. Detection of Pasteurella multocida and Bordetella bronchiseptica, etiological agents of atrophic rhinitis, by means of PCR tests. Medycyna Wet. 2010, 66:45-50.
16. Mirt D. Lesions of so-called flank biting and necrotic ear syndrome in pigs. Vet. Rec. 1999, 144:92-96.
17. Misinzo G., Delputte P.L., Lefebvre D.J., Nauwynck H.J. Porcine circovirus 2 infection of epithelial cells is clathrin-, caveolae- and dynamin-independent, actin and Rho-GTPase-mediated, and enhanced by cholesterol depletion. Virus Res. 2009, 139:1-9.
18. Molnár T., Glávits R., Szeredi L., Dán Á. Occurrence of porcine dermatitis and nephropathy syndrome in Hungary. Acta Vet. Hung. 2002, 50:5-16.
19. Oliveira S. Improving rate of success in isolating Haemophilus parasuis from clinical samples. J. Swine Health Prod. 2004, 12:308-309.
20. Oliveira S. Haemophilus parasuis diagnostics. J. Swine Health Prod. 2007, 15:99-103.
21. Olson L.D. Gross and microscopic lesions of middle and inner ear infections in swine. Am. J. Vet. Res. 1981, 42:1433-1440.
22. Opriessnig T., Madson D.M., Prickett J.R., Kuhar D., Lunney J.K., Elsener J., Halbur P.G. Effect of porcine circovirus type 2 (PCV2) vaccination on porcine reproductive and respiratory syndrome virus (PRRSV) and PCV2 coinfection. Vet. Microbiol. 2008, 18:103-1014.
23. Petersen H.H., Nielsen E.O., Hassing A.G., Ersbøll A.K., Nielsen J.P. Prevalence of clinical signs of disease in Danish finisher pigs. Vet. Rec. 2008, 162:377-382.
24. Richardson J.A., Morter R.L., Rebar A.H., Olander H.J. Lesions of porcine necrotic ear syndrome. Vet. Pathol. 1984, 21:152-157.
25. Sipos W., Duvigneau J.C., Willheim M., Schilcher F., Hartl R.T., Hofbauer G., Exel B., Pietschmann P., Schmoll F. 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. Vet. Immunol. Immunopathol. 2004, 99:63-71.
26. Stadejek T., Podgórska K., Kołodziejczyk P., Bogusz R., Kozaczyński W., Pejsak Z. First report of postweaning multisystemic wasting syndrome in pigs in Poland. Medycyna Wet. 2006, 3:297-301.
27. Szczotka A., Markowska-Daniel I. Biochemical features of Polish isolates of Streptococcus suis. Medycyna Wet. 2006, 62:566-569.
28. Tanabe T., Hisaaki S., Hideki S., Watanabe K., Hirano M., Hirose K., Kurosawa S., Nakano K., Saito H., Maehara N. Correlation between occurrence of exudative epidermitis and exfoliative toxin-producing ability of Staphyulococcus hyicus. Vet. Microbiol. 1996, 48:9-17.
29. Tomas A., Fernandes L.T., Valero O., Segales J. A meta-analysis on experimental infections with porcine circovirus type 2 (PCV2). Vet. Microbiol. 2008, 132:260-273.
30. Truszczyński M., Pejsak Z. Mycoplasma suis and porcine eperythrozoonosis, including achievements of the last years. Medycyna Wet. 2009, 65:223-227.
31. Vincent I.E., Carrasco C.P., Herrmann B., Meehan B.M., Allan G.M., Summerfield A., McCullough K.C. Dendritic cells harbor infectious porcine circovirus type 2 in the absence of apparent cell modulation or replication of the virus. J. Virol. 2003, 77:13288-13300.
32. Vincent I.E., Carrasco C.P., Guzylack-Piriou L., Herrmann B., McNeilly F., Allan G.M., Summerfield A., McCullough K.C. Subset-dependent modulation of dendritic cell activity by circovirus type 2. Immunology 2005, 115:388-398.