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Rat cytomegalovirus efficiently replicates in dendritic cells and induces changes in their transcriptional profile.
Madela-Mönchinger, Julia Cecilia; Wolf, Silver Anthony; Wyler, Emanuel; Bauer, Agnieszka; Mischke, Marius; Möller, Lars; Juranic Lisnic, Vanda; Landthaler, Markus; Malyshkina, Anna; Voigt, Sebastian.
Afiliação
  • Madela-Mönchinger JC; Department of Infectious Diseases, Robert Koch Institute, Berlin, Germany.
  • Wolf SA; Genome Competence Center, Department of MFI, Robert Koch Institute, Berlin, Germany.
  • Wyler E; Laboratory for RNA Biology, Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Bauer A; Department of Infectious Diseases, Robert Koch Institute, Berlin, Germany.
  • Mischke M; Institute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Möller L; Advanced Light and Electron Microscopy, Robert Koch Institute, Berlin, Germany.
  • Juranic Lisnic V; Center for Proteomics, University of Rijeka, Faculty of Medicine, Rijeka, Croatia.
  • Landthaler M; Laboratory for RNA Biology, Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Malyshkina A; Institute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Voigt S; Institute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Front Immunol ; 14: 1192057, 2023.
Article em En | MEDLINE | ID: mdl-38077365
ABSTRACT
Dendritic cells (DC) play a crucial role in generating and maintaining antiviral immunity. While DC are implicated in the antiviral defense by inducing T cell responses, they can also become infected by Cytomegalovirus (CMV). CMV is not only highly species-specific but also specialized in evading immune protection, and this specialization is in part due to characteristic genes encoded by a given virus. Here, we investigated whether rat CMV can infect XCR1+ DC and if infection of DC alters expression of cell surface markers and migration behavior. We demonstrate that wild-type RCMV and a mutant virus lacking the γ-chemokine ligand xcl1 (Δvxcl1 RCMV) infect splenic rat DC ex vivo and identify viral assembly compartments. Replication-competent RCMV reduced XCR1 and MHCII surface expression. Further, gene expression of infected DC was analyzed by bulk RNA-sequencing (RNA-Seq). RCMV infection reverted a state of DC activation that was induced by DC cultivation. On the functional level, we observed impaired chemotactic activity of infected XCR1+ DC compared to mock-treated cells. We therefore speculate that as a result of RCMV infection, DC exhibit diminished XCR1 expression and are thereby blocked from the lymphocyte crosstalk.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Muromegalovirus / Infecções por Citomegalovirus Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Muromegalovirus / Infecções por Citomegalovirus Idioma: En Ano de publicação: 2023 Tipo de documento: Article