Evidence map›Paper›PMID 34073735›Full record

ArticleViruses2021

Validation of Inactivation Methods for Arenaviruses.

Silke Olschewski, Anke Thielebein, Chris Hoffmann, Olivia Blake, Jonas Müller, Sabrina Bockholt, Elisa Pallasch, Julia Hinzmann, Stephanie Wurr, Neele Neddersen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 32% of its field
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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Hantavirus stability and inactivation.PLoS neglected tropical diseases · 2026
    Article
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  6. Review
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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

13 authors at 2 institutions in 1 country.

Silke OlschewskiDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Anke ThielebeinDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Chris HoffmannDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Olivia BlakeDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Jonas MüllerDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Sabrina BockholtDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Elisa PallaschDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Julia HinzmannDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Stephanie WurrDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Neele NeddersenDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Toni RiegerDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Stephan GüntherDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Lisa OestereichDepartment of Virology, Bernhard-Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.ORCID 0000-0003-0098-7485
Bernhard Nocht Institute for Tropical Medicine · DEGerman Center for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several of the human-pathogenic arenaviruses cause hemorrhagic fever and have to be handled under biosafety level 4 conditions, including Lassa virus. Rapid and safe inactivation of specimens containing these viruses is fundamental to enable downstream processing for diagnostics or research under lower biosafety conditions. We established a protocol to test the efficacy of inactivation methods using the low-pathogenic Morogoro arenavirus as surrogate for the related highly pathogenic viruses. As the validation of chemical inactivation methods in cell culture systems is difficult due to cell toxicity of commonly used chemicals, we employed filter devices to remove the chemical and concentrate the virus after inactivation and before inoculation into cell culture. Viral replication in the cells was monitored over 4 weeks by using indirect immunofluorescence and immunofocus assay. The performance of the protocol was verified using published inactivation methods including chemicals and heat. Ten additional methods to inactivate virus in infected cells or cell culture supernatant were validated and shown to reduce virus titers to undetectable levels. In summary, we provide a robust protocol for the validation of chemical and physical inactivation of arenaviruses in cell culture, which can be readily adapted to different inactivation methods and specimen matrices.

Indexed as

Virus InactivationAnimalsArenavirusCell Culture TechniquesCell LineCells, CulturedChlorocebus aethiopsDisinfectionHumansReproducibility of ResultsSpecimen HandlingVero Cellsarenaviruseshigh-risk pathogensinactivation

Identifiers

PMID34073735
PMCPMC8225210
OpenAlexW3164821150

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.