Evidence map›Paper›PMID 25674771›Full record

ArticleViruses2015

Evaluation of virus inactivation by formaldehyde to enhance biosafety of diagnostic electron microscopy.

Lars Möller, Livia Schünadel, Andreas Nitsche, Ingeborg Schwebke, Manuela Hanisch, Michael Laue

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

41 citing papers in PubMed, 75 citations in OpenAlex.

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  13. Functional 20S Proteasomes in Retroviruses: Evidence in Favor.International journal of molecular sciences · 2024
    Article
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  18. Development of a sensitive, high-throughput extraction protocol for qPCR detection of African swine fever virus in formalin-fixed, paraffin-embedded tissues.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2023
    Article
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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

6 authors at 1 institution in 1 country.

Lars MöllerAdvanced Light and Electron Microscopy (ZBS 4), Robert Koch Institute, Berlin D-13353, Germany. MoellerL@rki.de.
Livia SchünadelHighly Pathogenic Viruses (ZBS 1), Robert Koch Institute, Berlin D-13353, Germany. SchuenadelL@rki.de.
Andreas NitscheHighly Pathogenic Viruses (ZBS 1), Robert Koch Institute, Berlin D-13353, Germany. NitscheA@rki.de.
Ingeborg SchwebkeHospital Hygiene, Infection Prevention and Control (FG 14), Robert Koch Institute, Berlin D-13353, Germany. SchwebkeI@rki.de.
Manuela HanischHospital Hygiene, Infection Prevention and Control (FG 14), Robert Koch Institute, Berlin D-13353, Germany. HanischM@rki.de.
Michael LaueAdvanced Light and Electron Microscopy (ZBS 4), Robert Koch Institute, Berlin D-13353, Germany. LaueM@rki.de.
Robert Koch Institute · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formaldehyde (FA) fixation of infectious samples is a well-established protocol in diagnostic electron microscopy of viruses. However, published experimental data that demonstrate virus inactivation by these fixation procedures are lacking. Usually, fixation is performed immediately before the sample preparation for microscopy. The fixation procedure should transform viruses in a non-infectious but nonetheless structurally intact form in order to allow a proper diagnosis based on morphology. FA provides an essential advantage in comparison to other disinfectants, because it preserves the ultrastructure of biological material without interfering significantly with the preparation (i.e., the negative staining) and the detection of viruses. To examine the efficiency of FA inactivation, we used Vaccinia virus, Human adenovirus and Murine norovirus as models and treated them with FA under various conditions. Critical parameters for the inactivation efficiency were the temperature, the duration of the FA treatment, and the resistance of the virus in question. Our results show that FA inactivation at low temperature (4 °C) bears a high risk of incomplete inactivation. Higher temperatures (25 °C) are more efficient, although they still require rather long incubation times to fully inactivate a complex and highly robust virus like Vaccinia. A protocol, which applied 2% buffered FA for 60 min and a temperature-shift from 25 to 37 °C after 30 min was efficient for the complete inactivation of all test viruses, and therefore has the potential to improve both biosafety and speed of diagnostic electron microscopy.

Indexed as

Equipment SafetyMicroscopy, ElectronAnimalsDisinfectantsDisinfectionFormaldehydeHumansVirusesVirus InactivationDisinfectantsFormaldehyde

Identifiers

PMID25674771
PMCPMC4353909
OpenAlexW2132431566

What OpenQuestion holds

Textmetadata
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.