Evidence map›Paper›PMID 34209992›Full record

ArticleToxics2021

Direct Comparison of the Lowest Effect Concentrations of Mutagenic Reference Substances in Two Ames Test Formats.

Bernhard Rainer, Elisabeth Pinter, Lukas Prielinger, Chiara Coppola, Maricel Marin-Kuan, Benoit Schilter, Silvia Apprich, Manfred Tacker

Open access · goldAbstract read
In one paragraph

Article in Toxics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Bernhard RainerDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.
Elisabeth PinterDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.ORCID 0000-0002-5027-5147
Lukas PrielingerDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.ORCID 0000-0002-1605-6565
Chiara CoppolaDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.
Maricel Marin-KuanNestle Research-Chemical Food Safety, 1000 Lausanne, Switzerland.
Benoit SchilterNestle Research-Chemical Food Safety, 1000 Lausanne, Switzerland.
Silvia ApprichDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.ORCID 0000-0002-3514-7227
Manfred TackerDepartment of Applied Life Sciences, University of Applied Sciences, FH Campus Wien, 1030 Vienna, Austria.
Hochschule Campus Wien · ATNestlé (Switzerland) · CH

Funding

Österreichische Forschungsförderungsgesellschaft 866854
6 · The paper itself

Abstract

The Ames assay is the standard assay for identifying DNA-reactive genotoxic substances. Multiple formats are available and the correct choice of an assay protocol is essential for achieving optimal performance, including fit for purpose detection limits and required screening capacity. In the present study, a comparison of those parameters between two commonly used formats, the standard pre-incubation Ames test and the liquid-based Ames MPF™, was performed. For that purpose, twenty-one substances with various modes of action were chosen and tested for their lowest effect concentrations (LEC) with both tests. In addition, two sources of rat liver homogenate S9 fraction, Aroclor 1254-induced and phenobarbital/β-naphthoflavone induced, were compared in the Ames MPF™. Overall, the standard pre-incubation Ames and the Ames MPF™ assay showed high concordance (>90%) for mutagenic vs. non-mutagenic compound classification. The LEC values of the Ames MPF™ format were lower for 17 of the 21 of the selected test substances. The S9 source had no impact on the test results. This leads to the conclusion that the liquid-based Ames MPF™ assay format provides screening advantages when low concentrations are relevant, such as in the testing of complex mixtures.

Indexed as

Ames assaybacterial reverse mutationcomplex mixturesfood contact materialsgenotoxicitylowest effective concentration (LEC)mutagenicityS9 comparison

Identifiers

PMID34209992
PMCPMC8309791
OpenAlexW3175134624

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.