Evidence map›Paper›PMID 37632012›Full record

ArticleViruses2023

Differences in the Susceptibility of Human Tubular Epithelial Cells for Infection with Orthohantaviruses.

Pamela Schreiber, Ann-Kathrin Friedrich, Gefion Gruber, Christian Nusshag, Lukas Boegelein, Sandra Essbauer, Josephine Uhrig, Martin Zeier, Ellen Krautkrämer

Abstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Pamela SchreiberDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Ann-Kathrin FriedrichDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Gefion GruberDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Christian NusshagDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.ORCID 0000-0001-7776-3784
Lukas BoegeleinDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Sandra EssbauerBundeswehr Institute of Microbiology, Department Virology and Intracellular Agents, German Centre for Infection Research, Munich Partner Site, D-80937 Munich, Germany.
Josephine UhrigDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Martin ZeierDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.
Ellen KrautkrämerDepartment of Nephrology, University of Heidelberg, D-69120 Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diseases induced by infection with pathogenic orthohantaviruses are characterized by a pronounced organ-specific manifestation. Pathogenic Eurasian orthohantaviruses cause hemorrhagic fever with renal syndrome (HFRS) with often massive proteinuria. Therefore, the use of a relevant kidney cell culture would be favorable to analyze the underlying cellular mechanisms of orthohantavirus-induced acute kidney injury (AKI). We tested different human tubular epithelial cell lines for their suitability as an in vitro infection model. Permissiveness and replication kinetics of highly pathogenic Hantaan virus (HTNV) and non-/low-pathogenic Tula virus (TULV) were analyzed in tubular epithelial cell lines and compared to human primary tubular epithelial cells. Ana-lysis of the cell line HK-2 revealed the same results for viral replication, morphological and functional effects as observed for HTNV in primary cells. In contrast, the cell lines RPTEC/TERT1 and TH1 demonstrated only poor infection rates after inoculation with HTNV and are unusable as an infection model. While pathogenic HNTV infects primary tubular and HK-2 cells, non-/low-pathogenic TULV infects neither primary tubular cells nor the cell line HK-2. Our results show that permissiveness of renal cells varies between orthohantaviruses with differences in pathogenicity and that HK-2 cells demonstrate a suitable in vitro model to study viral tropism and pathogenesis of orthohantavirus-induced AKI.

Indexed as

Acute Kidney InjuryHantaan virusOrthohantavirusRNA VirusesEpithelial CellsHumansKidneyacute kidney injurycell-to-cell contactsHantaan viruskidneyorthohantaviruspathogenesisreceptortubular epitheliumTula virus

Identifiers

PMID37632012
PMCPMC10459294

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.