Evidence map›Paper›PMID 33847775›Full record

ArticleArchives of toxicology2021

In vitro interactions of Alternaria mycotoxins, an emerging class of food contaminants, with the gut microbiota: a bidirectional relationship.

Francesco Crudo, Georg Aichinger, Jovana Mihajlovic, Elisabeth Varga, Luca Dellafiora, Benedikt Warth, Chiara Dall'Asta, David Berry, Doris Marko

Abstract read
In one paragraph

Article in Archives of toxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Natural Dibenzo-α-Pyrones: Friends or Foes?International journal of molecular sciences · 2021
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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

9 authors.

Francesco CrudoDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria.
Georg AichingerDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria.
Jovana MihajlovicDepartment of Microbiology and Ecosystem Science, Centre for Microbiology and Environmental Systems Science, University of Vienna, Althanstr. 14, 1090, Vienna, Austria.
Elisabeth VargaDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria.
Luca DellafioraDepartment of Food and Drug, University of Parma, Parco Area delle Scienze 27/A, 43124, Parma, Italy.
Benedikt WarthDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria.
Chiara Dall'AstaDepartment of Food and Drug, University of Parma, Parco Area delle Scienze 27/A, 43124, Parma, Italy.
David BerryDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria.
Doris MarkoDepartment of Food Chemistry and Toxicology, University of Vienna, Währinger Str. 38, 1090, Wien, Austria. doris.marko@univie.ac.at.ORCID http://orcid.org/0000-0001-6568-2944

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human gut microbiota plays an important role in the maintenance of human health. Factors able to modify its composition might predispose the host to the development of pathologies. Among the various xenobiotics introduced through the diet, Alternaria mycotoxins are speculated to represent a threat for human health. However, limited data are currently available about the bidirectional relation between gut microbiota and Alternaria mycotoxins. In the present work, we investigated the in vitro effects of different concentrations of a complex extract of Alternaria mycotoxins (CE; containing eleven mycotoxins; e.g. 0.153 µM alternariol and 2.3 µM altersetin, at the maximum CE concentration tested) on human gut bacterial strains, as well as the ability of the latter to metabolize or adsorb these compounds. Results from the minimum inhibitory concentration assay showed the scarce ability of CE to inhibit the growth of the tested strains. However, the growth kinetics of most of the strains were negatively affected by exposure to the various CE concentrations, mainly at the highest dose (50 µg/mL). The CE was also found to antagonize the formation of biofilms, already at concentrations of 0.5 µg/mL. LC-MS/MS data analysis of the mycotoxin concentrations found in bacterial pellets and supernatants after 24 h incubation showed the ability of bacterial strains to adsorb some Alternaria mycotoxins, especially the key toxins alternariol, alternariol monomethyl ether, and altersetin. The tendency of these mycotoxins to accumulate within bacterial pellets, especially in those of Gram-negative strains, was found to be directly related to their lipophilicity.

Indexed as

Gastrointestinal MicrobiomeMycotoxinsAlternariaChromatography, LiquidFood ContaminationHumansLactonesTandem Mass SpectrometryLactonesMycotoxinsAdsorptionBiofilmChemical mixtureLipophilicityMicrobiome

Identifiers

PMID33847775
PMCPMC8241668

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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.