Free access
Vet. Res.
Volume 41, Number 1, January-February 2010
Number of page(s) 16
Published online 14 October 2009
How to cite this article Vet. Res. (2010) 41:12
References of  Vet. Res. (2010) 41:12
  1. Alcaraz M.J., Fernández P., Guillén M.I., Antiinflammatory actions of the heme oxygenase-1 pathway, Curr. Pharm. Des. (2003) 9:2541–2551 [CrossRef] [PubMed].
  2. Benjamini Y., Hochberg Y., Controlling the false discovery rate: a practical and powerful approach to multiple testing, J. R. Stat. Soc. Ser. B (1995) 57:289–300.
  3. Chianini F., Majó N., Segalés J., Domínguez J., Domingo M., Immunohistochemical characterisation of PCV2 associate lesions in lymphoid and nonlymphoid tissues of pigs with natural postweaning multisystemic wasting syndrome (PMWS), Vet. Immunol. Immunopathol. (2003) 94:63–75 [CrossRef] [PubMed].
  4. Faure-André G., Vargas P., Yuseff M.I., Heuzé M., Diaz J., Lankar D., et al., Regulation of dendritic cell migration by CD74, the MHC class II-associated invariant chain, Science (2008) 322:1705–1710 [CrossRef] [PubMed].
  5. Fernandes L.T., Mateu E., Sibila M., Fort M., Andaluz A., McNeilly F., et al., Lack of in vitro and in vivo effects of lipopolysaccharide (LPS) on porcine circovirus type 2 infection, Viral Immunol. (2007) 20:541–552 [CrossRef] [PubMed].
  6. Fernandes L.T., Tomás A., Bensaid A., Pérez-Enciso M., Sibila M., Sánchez A., Segalés J., Exploratory study on the transcriptional profile of pigs subclinically infected with porcine circovirus type 2, Anim. Biotechnol. (2009) 20:96–109 [CrossRef] [PubMed].
  7. Flori L., Rogel-Gaillard C., Cochet M., Lemonnier G., Hugot K., Chardon P., et al., Transcriptomic analysis of the dialogue between Pseudorabies virus and porcine epithelial cells during infection, BMC Genomics (2008) 9:123 [CrossRef] [PubMed].
  8. Flori L., Rogel-Gaillard C., Mariani V., Lemonnier G., Cochet M., Hugot K., et al., A combined transcriptomic approach to analyse the dialogue between pseudorabies virus and porcine cells, Dev. Biol. (2008) 132:99–104.
  9. Fok P.T., Huang K.C., Holland P.C., Nalbantoglu J., The Coxsackie and adenovirus receptor binds microtubules and plays a role in cell migration, J. Biol. Chem. (2007) 282:7512–7521 [CrossRef] [PubMed].
  10. Fort M., Olvera A., Sibila M., Segalés J., Mateu E., Detection of neutralizing antibodies in postweaning multisystemic wasting syndrome (PMWS)-affected and non-PMWS-affected pigs, Vet. Microbiol. (2007) 125:244–255 [CrossRef] [PubMed].
  11. Fort M., Sibila M., Allepuz A., Mateu E., Roerink F., Segalés J., Porcine circovirus type 2 (PCV2) vaccination of conventional pigs prevents viremia against PCV2 isolates of different genotypes and geographic origins, Vaccine (2008) 26: 1063–1071.
  12. Fort M., Fernandes L.T., Nofrarias M., Díaz I., Sibila M., Pujols J., et al., Development of cellmediated immunity to porcine circovirus type 2 10 (PCV2) in caesarean-derived, colostrum-deprived piglets, Vet. Immunol. Immunopathol. (2009) 129:101–107 [CrossRef] [PubMed].
  13. Gao G., Luo H., The ubiquitin-proteasome pathway in viral infections, Can. J. Physiol. Pharmacol. (2006) 84:5–14 [CrossRef] [PubMed].
  14. Genini S., Delputte P.L., Malinverni R., Cecere M., Stella A., Nauwynck H.J., Giuffra E., Genomewide transcriptional response of primary alveolar macrophages following infection with porcine reproductive and respiratory syndrome virus, J. Gen. Virol. (2008) 89:2550–2564 [CrossRef] [PubMed].
  15. Gentleman R.C., Carey V.J., Bates D.M., Bolstad B., Dettling M., Dudoit S., et al., Bioconductor: open software development for computational biology and bioinformatics, Genome Biol. (2004) 5:80 [CrossRef].
  16. Harding J.C.S., Clark E.G., Recognizing and diagnosing postweaning multisystemic wasting syndrome (PMWS), J. Swine Health Prod. (1997) 5:201–203.
  17. Hedegaard J., Skovgaard K., Mortensen S., Sørensen P., Jensen T.K., Hornshøj H., et al., Molecular characterisation of the early response in pigs to experimental infection with Actinobacillus pleuropneumoniae using cDNA microarrays, Acta Vet. Scand. (2007) 49:11 [CrossRef] [PubMed].
  18. Herrmann J., Lerman L.O., Lerman A., Ubiquitin and ubiquitin-like proteins in protein regulation, Circ. Res. (2007) 100:1276–1291 [CrossRef] [PubMed].
  19. Irizarry R.A., Hobbs B., Collin F., Beazer-Barclay Y.D., Antonellis K.J., Scherf U., Speed T.P., Exploration, normalization, and summaries of high density oligonucleotide array probe level data, Biostatistics (2003) 4:249–264 [CrossRef] [PubMed].
  20. Ladekjaer-Mikkelsen A.S., Nielsen J., Stadejek T., Storgaard T., Krakowka S., Ellis J., et al., Reproduction of postweaning multisystemic wasting syndrome (PMWS) in immunostimulated and nonimmunostimulated 3-week-old piglets experimentally infected with porcine circovirus type 2 (PCV2), Vet. Microbiol. (2002) 89:97–114 [CrossRef] [PubMed].
  21. Lee C., Bachand A., Murtaugh M.P., Yoo D., Differential host cell gene expression regulated by the porcine reproductive and respiratory syndrome virus GP4 and GP5 glycoproteins, Vet. Immunol. Immunopathol. (2004) 102:189–198 [CrossRef] [PubMed].
  22. Lewis C.R., Ait-Ali T., Clapperton M., Archibald A.L., Bishop S., Genetic perspectives on host responses to porcine reproductive and respiratory syndrome (PRRS), Viral Immunol. (2007) 20:343–358 [CrossRef] [PubMed].
  23. Liu J., Zhu Y., Chen I., Lau J., He F., Lau A., et al., The ORF3 protein of porcine circovirus type 2 interacts with porcine ubiquitin E3 ligase Pirh2 and facilitates p53 expression in viral infection, J. Virol. (2007) 81:9560–9567 [CrossRef] [PubMed].
  24. Livak K.J., Schmittgen T.D., Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method, Methods (2001) 25:402–408 [CrossRef] [PubMed].
  25. López-Soria S., Segalés J., Rose N., Vinãs M.J., Blanchard P., Madec F., et al., An exploratory study on risk factors for postweaning multisystemic wasting syndrome (PMWS) in Spain, Prev. Vet. Med. (2005) 69:97–107 [CrossRef] [PubMed].
  26. Madec F., Eveno E., Morvan P., Hamon L., Blanchard P., Cariolet R., et al., Post-weaning multisystemic wasting syndrome (PMWS) in pigs in France: clinical observations from follow-up studies on affected farms, Livest. Prod. Sci. (2000) 63:223–233 [CrossRef].
  27. Meerts P., Van Gucht S., Cox E., Vandebosch A., Nauwynck H.J., Correlation between type of adaptive immune response against porcine circovirus type 2 and level of virus replication, Viral Immunol. (2005) 18:333–341 [CrossRef] [PubMed].
  28. Meerts P., Misinzo G., Lefebvre D., Nielsen J., Bøtner A., Kristensen C.S., Nauwynck H.J., 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 Vet. Res. (2006) 2:6 [CrossRef] [PubMed].
  29. Misinzo G., Meerts P., Bublot M., Mast J., Weingartl H.M., Nauwynck H.J., Binding and entry characteristics of porcine circovirus 2 in cells of the porcine monocytic line 3D4/31, J. Gen. Virol. (2005) 86:2057–2068 [CrossRef] [PubMed].
  30. Misinzo G., Delputte P.L., Lefebvre D.J., Nauwynck H.J., Porcine circovirus 2 infection of epithelial cells is clathrin-, caveolae- and dynaminindependent, actin and Rho-GTPase-mediated, and enhanced by cholesterol depletion, Virus Res. (2009) 139:1–9 [CrossRef] [PubMed].
  31. Ochieng J., Furtak V., Lukyanov P., Extracellular functions of galectin-3, Glycoconj. J. (2004) 19:527–535 [CrossRef] [PubMed].
  32. Opriessnig T., Fenaux M., Thomas P., Hoogland M.J., Rothschild M.F., Meng X.J., Halbur P.G., Evidence of breed-dependent differences in susceptibility to porcine circovirus type-2-associated disease and lesions, Vet. Pathol. (2006) 43:281–293 [CrossRef] [PubMed].
  33. Opriessnig T., Patterson A.R., Madson D.M., Pal N., Rothschild M., Kuhar D., et al., Difference in severity of porcine circovirus type 2 (PCV2)-induced pathological lesions between Landrace and Pietrain pigs, J. Anim. Sci. (2009) 87:1582–1590 [CrossRef] [PubMed].
  34. Petroski M.D., The ubiquitin system, disease, and drug discovery, BMC Biochem. (2008) 9:S7 [CrossRef] [PubMed].
  35. Provençal M., Michaud M., Beaulieu E., Ratel D., Rivard G.E., Gingras D., Béliveau R., Tissue factor pathway inhibitor (TFPI) interferes with endothelial cell migration by inhibition of both the Erk pathway and focal adhesion proteins, Thromb. Haemost. (2008) 99:576–585 [PubMed].
  36. Rose N., Abhervé-Guéguen A., Le Diguerher G., Eveno E., Jolly J.P., Blanchard P., et al., Effet de la génétique Piétrain sur l'expression clinique de la maladie de l'amaigrissement du porcelet (MAP), étude dans 4 élevages naisseurs-engraisseurs, Journées Recherche Porcine (2004) 36:339–344.
  37. Sadler A.J., Williams B.R., Interferon-inducible antiviral effectors, Nat. Rev. Immunol. (2008) 8:559–568 [CrossRef] [PubMed].
  38. Sallusto F., Cella M., Danieli C., Lanzavecchia A., Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products, J. Exp. Med. (1995) 182:389–400 [CrossRef] [PubMed].
  39. Sanchez R.E. Jr, Meerts P., Nauwynck H.J., Pensaert M.B., Change of porcine circovirus 2 target cells in pigs during development from fetal to early postnatal life, Vet. Microbiol. (2003) 95:15–25 [CrossRef] [PubMed].
  40. Smyth G.K., Linear models and empirical bayes methods for assessing differential expression in microarray experiments, Stat. Appl. Genet. Mol. Biol. (2004) 3:3 [MathSciNet].
  41. Sorden S.D., Update on porcine circovirus and postweaning multisystemic wasting syndrome, J. Swine Health Prod. (2000) 8:133–136.
  42. Stevenson L.S., McCullough K., Vincent I., Gilpin D.F., Summerfield A., Nielsen J., et al., Cytokine and C-reactive protein profiles induced by porcine circovirus type 2 experimental infection in 3-week-old piglets,Viral Immunol. (2006) 19:189–195.
  43. Timpl R., Sasaki T., Kostka G., Chu M.L., Fibulins: a versatile family of extracellular matrix proteins, Nat. Rev. Mol. Cell Biol. (2003) 4:479–489 [CrossRef] [PubMed].
  44. Tomás A., Fernandes L.T., Valero O., Segalés J., A meta-analysis on experimental infections with porcine circovirus type 2 (PCV2), Vet. Microbiol. (2008) 132:260–273 [CrossRef] [PubMed].
  45. Tsai S., Mir B., Martin A.C., Estrada J.L., Bischoff S.R., Hsieh W.P., et al., Detection of transcriptional difference of porcine imprinted genes using different microarray platforms, BMC Genomics (2006) 7:328 [CrossRef] [PubMed].
  46. Vincent I.E., Balmelli C., Meehan B., Allan G., Summerfield A., McCullough K.C., Silencing of natural interferon producing cell activation by porcine circovirus type 2 DNA, Immunology (2007) 120:47–56 [PubMed].
  47. Wang Y., Couture O.P., Qu L., Uthe J.J., Bearson S.M., Kuhar D., et al., Analysis of porcine transcriptional response to Salmonella enterica serovar choleraesuis suggests novel targets of NFkappaB are activated in the mesenteric lymph node, BMC Genomics (2008) 9:437 [CrossRef] [PubMed].
  48. West M.A., Wallin R.P., Matthews S.P., Svensson H.G., Zaru R., Ljunggren H.G., et al., Enhanced dendritic cell antigen capture via toll-like receptor-induced actin remodelling, Science (2004) 305:1153–1157 [CrossRef] [PubMed].
  49. Wilson C.L., Miller C.J., Simpleaffy: a BioConductor package for Affymetrix Quality Control and data analysis, Bioinformatics (2005) 21:3683–3685 [CrossRef] [PubMed].
  50. Zhao S.H., Kuhar D., Lunney J.K., Dawson H., Guidry C., Uthe J.J., et al., Gene expression profiling in Salmonella choleraesuis-infected porcine lung using a long oligonucleotide microarray, Mamm. Genome (2006) 17:777–789 [CrossRef] [PubMed].