Literature DB >> 28216416

In silico analysis sheds light on the structural basis underlying the ribotoxicity of trichothecenes-A tool for supporting the hazard identification process.

Luca Dellafiora1, Gianni Galaverna2, Chiara Dall'Asta3.   

Abstract

Deoxynivalenol is a food borne mycotoxin belonging to the trichothecenes family that may cause severe injuries in human and animals. The inhibition of protein synthesis via the interaction with the ribosome has been identified as a crucial mechanism underlying toxic action. However, it is not still fully understood how and to what extent compounds belonging to trichothecenes family affect human and animal health. In turn, this scenario causes delay in managing the related health risk. Aimed at supporting the hazard identification process, the in silico analysis may be a straightforward tool to investigate the structure-activity relationship of trichothecenes, finding out molecules of possible concern to carry forth in the risk assessment process. In this framework, this work investigated through a molecular modeling approach the structural basis underlying the interaction with the ribosome under a structure-activity relationship perspective. To identify further forms possibly involved in the total trichothecenes-dependent ribotoxic load, the model was challenged with a set of 16 trichothecene modified forms found in plants, fungi and animals, including also compounds never tested before for the capability to bind and inhibit the ribosome. Among them, only the regiospecific glycosylation in the position 3 of the sesquiterpenoid scaffold (i.e. T-2 toxin-3-glucuronide, α and β isomers of T-2 toxin-3-glucoside and deoxynivalenol-3-glucuronide) was found impairing the interaction with the ribosome, while the other compounds tested (i.e. neosolaniol, nivalenol, fusarenon-X, diacetoxyscirpenol, NT-1 toxin, HT-2 toxin, 19- and 20-hydroxy-T-2 toxin, T-2 toxin triol and tetraol, and 15-deacetyl-T-2 toxin), were found potentially able to inhibit the ribosome. Accordingly, they should be included with high priority in further risk assessment studies in order to better characterize the trichothecenes-related hazard.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Deoxynivalenol; Modified mycotoxins; Ribotoxicity; Toxicity; Toxicodynamic; Trichothecenes; in silico toxicology

Mesh:

Substances:

Year:  2017        PMID: 28216416     DOI: 10.1016/j.toxlet.2017.02.015

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  11 in total

1.  Combinatory Exposure to Urolithin A, Alternariol, and Deoxynivalenol Affects Colon Cancer Metabolism and Epithelial Barrier Integrity in vitro.

Authors:  Julia Groestlinger; Carina Seidl; Elisabeth Varga; Giorgia Del Favero; Doris Marko
Journal:  Front Nutr       Date:  2022-06-24

2.  Exploring the dermotoxicity of the mycotoxin deoxynivalenol: combined morphologic and proteomic profiling of human epidermal cells reveals alteration of lipid biosynthesis machinery and membrane structural integrity relevant for skin barrier function.

Authors:  Giorgia Del Favero; Lukas Janker; Benjamin Neuditschko; Julia Hohenbichler; Endre Kiss; Lydia Woelflingseder; Christopher Gerner; Doris Marko
Journal:  Arch Toxicol       Date:  2021-04-23       Impact factor: 5.153

Review 3.  Toxicodynamics of Mycotoxins in the Framework of Food Risk Assessment-An In Silico Perspective.

Authors:  Luca Dellafiora; Chiara Dall'Asta; Gianni Galaverna
Journal:  Toxins (Basel)       Date:  2018-01-23       Impact factor: 4.546

4.  Alternaria toxins as casein kinase 2 inhibitors and possible consequences for estrogenicity: a hybrid in silico/in vitro study.

Authors:  Georg Aichinger; Luca Dellafiora; Foteini Pantazi; Giorgia Del Favero; Gianni Galaverna; Chiara Dall'Asta; Doris Marko
Journal:  Arch Toxicol       Date:  2020-04-23       Impact factor: 5.153

5.  On the Mechanism of Action of Anti-Inflammatory Activity of Hypericin: An In Silico Study Pointing to the Relevance of Janus Kinases Inhibition.

Authors:  Luca Dellafiora; Gianni Galaverna; Gabriele Cruciani; Chiara Dall'Asta; Renato Bruni
Journal:  Molecules       Date:  2018-11-22       Impact factor: 4.411

6.  Structure Elucidation and Toxicity Analysis of the Degradation Products of Deoxynivalenol by Gaseous Ozone.

Authors:  Mengmeng Li; Erqi Guan; Ke Bian
Journal:  Toxins (Basel)       Date:  2019-08-15       Impact factor: 4.546

Review 7.  Co-Occurrence and Combinatory Effects of Alternaria Mycotoxins and other Xenobiotics of Food Origin: Current Scenario and Future Perspectives.

Authors:  Francesco Crudo; Elisabeth Varga; Georg Aichinger; Gianni Galaverna; Doris Marko; Chiara Dall'Asta; Luca Dellafiora
Journal:  Toxins (Basel)       Date:  2019-11-03       Impact factor: 4.546

8.  The Ribosome-Binding Mode of Trichothecene Mycotoxins Rationalizes Their Structure-Activity Relationships.

Authors:  Weijun Wang; Yan Zhu; Nadine Abraham; Xiu-Zhen Li; Matthew Kimber; Ting Zhou
Journal:  Int J Mol Sci       Date:  2021-02-05       Impact factor: 5.923

Review 9.  Updated Review of the Toxicity of Selected Fusarium Toxins and Their Modified Forms.

Authors:  Adam Pierzgalski; Marcin Bryła; Joanna Kanabus; Marta Modrzewska; Grażyna Podolska
Journal:  Toxins (Basel)       Date:  2021-10-29       Impact factor: 4.546

10.  Primary and Immortalized Human Respiratory Cells Display Different Patterns of Cytotoxicity and Cytokine Release upon Exposure to Deoxynivalenol, Nivalenol and Fusarenon-X.

Authors:  Silvia Ferreira Lopes; Gaëlle Vacher; Eleonora Ciarlo; Dessislava Savova-Bianchi; Thierry Roger; Hélène Niculita-Hirzel
Journal:  Toxins (Basel)       Date:  2017-10-25       Impact factor: 4.546

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