<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Klausmann S</dc:creator>
  <dc:creator>Sydler T</dc:creator>
  <dc:creator>Summerfield A</dc:creator>
  <dc:creator>Lewis FI</dc:creator>
  <dc:creator>Weilenmann R</dc:creator>
  <dc:creator>Sidler X</dc:creator>
  <dc:creator>Brugnera E</dc:creator>
  <dc:date>2015</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Although porcine circovirus type 2 (PCV2)-associated diseases have been evaluated for known immune evasion strategies, the pathogenicity of these viruses remained concealed for decades. Surprisingly, the same viruses that cause panzootics in livestock are widespread in young, unaffected animals. Recently, evidence has emerged that circovirus-like viruses are also linked to complex diseases in humans, including children. We detected PCV2 genome-carrying cells in fetal pig thymi. To elucidate virus pathogenicity, we developed a new pig infection model by in vivo transfection of recombinant PCV2 and the immunosuppressant cofactor cyclosporine A. Using flow cytometry, immunofluorescence and fluorescence in situ hybridization, we found evidence that PCV2 dictates positive and negative selection of maturing T cells in the thymus. We show for the first time that PCV2-infected cells reside at the corticomedullary junction of the thymus. In diseased animals, we found polyclonal deletion of single positive cells (SPs) that may result from a loss of major histocompatibility complex class-II expression at the corticomedullary junction. The percentage of PCV2 antigen-presenting cells correlated with the degree of viremia and, in turn, the severity of the defect in thymocyte maturation. Moreover, the reversed T-cell receptor/CD4-coreceptor expression dichotomy on thymocytes at the CD4(+)CD8(interm) and CD4SP cell stage is viremia-dependent, resulting in a specific hypo-responsiveness of T-helper cells. We compare our results with the only other better-studied member of Circoviridae, chicken anemia virus. Our data show that PCV2 infection leads to thymocyte selection dysregulation, adding a valuable dimension to our understanding of virus pathogenicity.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/245127</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/emi.2015.15</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/26038767</dc:relation>
  <dc:source>Emerging microbes &amp; infections. - 2015</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">CD4+ thymocyte maturation diversion</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Circoviridae porcine circovirus type 2 pathogenicity</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">T-helper cell hypo-responsiveness</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">adaptive immune response failure</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">dendritic cell feedback</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">in vivo anergy</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">polyclonal negative selection</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">thymic kinetic signaling model</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">CD4 Antigens</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Circoviridae Infections</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Circovirus</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Cyclosporine</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Disease Models, Animal</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Goats</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Immune Evasion</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Immunosuppressive Agents</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns20="xml" ns20:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns21="xml" ns21:lang="en">Random Allocation</dc:subject>
  <dc:subject xmlns:ns22="xml" ns22:lang="en">Rats</dc:subject>
  <dc:subject xmlns:ns23="xml" ns23:lang="en">Receptors, Antigen, T-Cell</dc:subject>
  <dc:subject xmlns:ns24="xml" ns24:lang="en">Signal Transduction</dc:subject>
  <dc:subject xmlns:ns25="xml" ns25:lang="en">Swine</dc:subject>
  <dc:subject xmlns:ns26="xml" ns26:lang="en">Swine Diseases</dc:subject>
  <dc:subject xmlns:ns27="xml" ns27:lang="en">T-Lymphocytes</dc:subject>
  <dc:subject xmlns:ns28="xml" ns28:lang="en">Thymus Gland</dc:subject>
  <dc:subject xmlns:ns29="xml" ns29:lang="en">Transfection</dc:subject>
  <dc:title xmlns:ns30="xml" ns30:lang="en">T-cell reprogramming through targeted CD4-coreceptor and T-cell receptor expression on maturing thymocytes by latent Circoviridae family member porcine circovirus type 2 cell infections in the thymus.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
