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1000 Titel
  • Replication kinetics of pathogenic Eurasian orthohantaviruses in human mesangial cells
1000 Autor/in
  1. Boegelein, Lukas |
  2. Schreiber, Pamela |
  3. Philipp, Alexandra |
  4. Nusshag, Christian |
  5. Essbauer, Sandra |
  6. Zeier, Martin |
  7. Krautkrämer, Ellen |
1000 Verlag
  • BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-10-01
1000 Erschienen in
1000 Quellenangabe
  • 21(1):241
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12985-024-02517-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11446005/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Eurasian pathogenic orthohantaviruses cause hemorrhagic fever with renal syndrome (HFRS) characterized by acute kidney injury (AKI). The virulence of orthohantaviruses varies enormously and direct infection of different renal cell types contribute to pathogenesis. Glomerular mesangial cells play an essential role in the interplay between kidney cells and proper kidney function. Therefore, we analyzed the replication competence of different orthohantavirus species in primary mesangial cells and a mesangial cell line.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>We tested the suitability of the mesangial cell line CIHGM-1 (conditionally immortalized human glomerular mesangial cells) as cell culture model for orthohantavirus kidney infection by comparison with primary human renal mesangial cells (HRMCs). We analyzed infection with high pathogenic Hantaan virus (HTNV), moderate pathogenic Puumala virus (PUUV) and non-/low-pathogenic Tula virus (TULV).</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Effective viral spread was observed for PUUV only, whereas infection with HTNV and TULV was abortive. However, in contrast to TULV, HTNV exhibits an initially high infection rate and declines afterwards. This replication pattern was observed in HRMCs and CIHGM-1 cells. Viability or adhesion was neither impaired for PUUV-infected CIHGM-1 nor HRMCs. A loss of migration capacity was observed in PUUV-infected CIHGM-1 cells, but not in HRMCs.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>The identification of differences in the replication competence of pathogenic orthohantavirus strains in renal mesangial cells is of special interest and may provide useful insights in the virus-specific mechanisms of orthohantavirus induced AKI. The use of CIHGM-1 cells will facilitate the research in a relevant cell culture system.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Kinetics [MeSH]
lokal Puumala virus/pathogenicity [MeSH]
lokal Orthohantavirus/physiology [MeSH]
lokal Orthohantavirus/pathogenicity [MeSH]
lokal Cell line
lokal Humans [MeSH]
lokal Cell Line [MeSH]
lokal Animals [MeSH]
lokal Acute kidney injury
lokal Virus Replication [MeSH]
lokal HFRS
lokal Mesangial Cells/virology [MeSH]
lokal Mesangial cells
lokal Research
lokal Puumala virus/physiology [MeSH]
lokal Hantaan virus/pathogenicity [MeSH]
lokal Hantaan virus/physiology [MeSH]
lokal Hemorrhagic Fever with Renal Syndrome/virology [MeSH]
lokal Orthohantavirus
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Qm9lZ2VsZWluLCBMdWthcw==|https://frl.publisso.de/adhoc/uri/U2NocmVpYmVyLCBQYW1lbGE=|https://frl.publisso.de/adhoc/uri/UGhpbGlwcCwgQWxleGFuZHJh|https://frl.publisso.de/adhoc/uri/TnVzc2hhZywgQ2hyaXN0aWFu|https://frl.publisso.de/adhoc/uri/RXNzYmF1ZXIsIFNhbmRyYQ==|https://frl.publisso.de/adhoc/uri/WmVpZXIsIE1hcnRpbg==|https://frl.publisso.de/adhoc/uri/S3JhdXRrcsOkbWVyLCBFbGxlbg==
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1000 Label
1000 Förderer
  1. Medizinische Fakultät Heidelberg der Universität Heidelberg |
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1000 Dateien
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    1000 Förderer Medizinische Fakultät Heidelberg der Universität Heidelberg |
    1000 Förderprogramm -
    1000 Fördernummer -
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1000 Erstellt am 2025-07-07T03:23:10.457+0200
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1000 Objekt bearb. Tue Jul 29 23:24:06 CEST 2025
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