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@ARTICLE{Vzquez:484512,
      author       = {Vázquez, Cecilia Alejandra and Widerspick, Lina and
                      Thünauer, Roland and Schneider, Carola and Reimer, Rudolph
                      and Neira, Pedro and Olal, Catherine and Heung, Michelle and
                      Niemetz, Linda and Lawrence, Philip and Kucinskaite-Kodze,
                      Indre and Redecke, Lars and Escudero-Pérez, Beatriz},
      title        = {{N}ipah {V}irus {I}nfection {G}enerates {O}rdered
                      {S}tructures in {C}ellulo},
      journal      = {Viruses},
      volume       = {14},
      number       = {7},
      issn         = {1999-4915},
      address      = {Basel},
      publisher    = {MDPI},
      reportid     = {PUBDB-2022-06325},
      pages        = {1523},
      year         = {2022},
      abstract     = {Nipah virus (NiV) is a zoonotic paramyxovirus with a
                      fatality rate of up to $92\%$ in humans. While several
                      pathogenic mechanisms used by NiV to counteract host immune
                      defense responses have been described, all of the processes
                      that take place in cells during infection are not fully
                      characterized. Here, we describe the formation of ordered
                      intracellular structures during NiV infection. We observed
                      that these structures are formed specifically during NiV
                      infection, but not with other viruses from the same
                      Mononegavirales order (namely Ebola virus) or from other
                      orders such as Bunyavirales (Junín virus). We also
                      determined the kinetics of the appearance of these
                      structures and their cellular localization at the cellular
                      periphery. Finally, we confirmed the presence of these
                      NiV-specific ordered structures using structured
                      illumination microscopy (SIM), as well as their localization
                      by transmission electron microscopy (TEM), scanning electron
                      microscopy (SEM), and correlative light and electron
                      microscopy (CLEM). Herein, we describe a cytopathogenic
                      mechanism that provides a new insight into NiV biology.
                      These newly described ordered structures could provide a
                      target for novel antiviral approaches.},
      cin          = {DOOR ; HAS-User / U Lübeck / CSSB-CF-ALFM},
      ddc          = {050},
      cid          = {I:(DE-H253)HAS-User-20120731 /
                      $I:(DE-H253)U_L__beck-20211012$ /
                      I:(DE-H253)CSSB-CF-ALFM-20210629},
      pnm          = {633 - Life Sciences – Building Blocks of Life: Structure
                      and Function (POF4-633) / 6G3 - PETRA III (DESY) (POF4-6G3)},
      pid          = {G:(DE-HGF)POF4-633 / G:(DE-HGF)POF4-6G3},
      experiment   = {EXP:(DE-H253)P-P14-20150101},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:35891503},
      UT           = {WOS:000831704200001},
      doi          = {10.3390/v14071523},
      url          = {https://bib-pubdb1.desy.de/record/484512},
}