<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>Lannes, Nils</dc:creator>
  <dc:creator>Garcia-Nicolàs, Obdullio</dc:creator>
  <dc:creator>Démoulins, Thomas</dc:creator>
  <dc:creator>Summerfield, Artur</dc:creator>
  <dc:creator>Filgueira, Luis</dc:creator>
  <dc:date>2019-03-18</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The neurotropic Japanese encephalitis virus (JEV) is responsible for Japanese  encephalitis, an uncontrolled inflammatory disease of the central nervous system.  Microglia cells are the unique innate immune cell type populating the brain that cross- communicate with neurons via the CX3CR1-CX3CL1 axis. However, microglia may  serve as a viral reservoir for JEV. Human microglia are able to transmit JEV infectivity  to neighbouring cells in a cell-to-cell contact-dependent manner. Using JEV-treated  human blood monocyte-derived microglia, the present study investigates molecular  mechanisms behind cell-to-cell virus transmission by human microglia. For that  purpose, JEV-associated microglia were co-cultured with JEV susceptible baby  hamster kidney cells under various conditions. Here, we show that microglia hosting  JEV for up to 10 days were able to transmit the virus to susceptible cells. Interestingly,  neutralizing anti-JEV antibodies did not completely abrogate cell-to-cell virus  transmission. Hence, intracellular viral RNA could be a contributing source of  infectious virus material upon intercellular interactions. Importantly, the CX3CL1- CX3CR1 axis was a key regulator of cell-to-cell virus transmission from JEV-hosting  human microglia. Our findings suggest that human microglia may be a source of  infection for neuronal populations and sustain JEV brain pathogenesis in long-term  infection. Moreover, the present work emphasizes on the critical role of the CX3CR1- CX3CL1 axis in JEV pathogenesis mediating transmission of infectious genomic JEV  RNA.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307679</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307679/files/fil_cdc.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-019-41302-1</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Scientific Reports. - 2019, vol. 9, no. 1, p. 4833</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">CX 3 CR1-CX 3 CL1-dependent cell-to-cell Japanese encephalitis virus transmission by human microglial cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
