Toxic Effects Induced by Exposure to Mycotoxins

A special issue of Journal of Fungi (ISSN 2309-608X).

Deadline for manuscript submissions: closed (15 August 2023) | Viewed by 3481

Special Issue Editors


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Guest Editor
1. Graduate Program in Pharmacology, Federal University of Santa Maria, Santa Maria, Brazil
2. Graduate Program in Food Science and Technology, Federal University of Santa Maria, Santa Maria, Brazil
Interests: mycotoxins; aflatoxinB1; fumonisin B1; animal models of toxicity induced by mycotoxins; oxidative stress markers; behavioral analyses; antioxidants and natural compounds in models of toxicity

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Guest Editor
Graduate Program in Pharmacology, Federal University of Santa Maria, Santa Maria, Brazil
Interests: animal models; oxidative stress markers; behavioral analyses; antioxidants and natural compounds in models of toxicity

Special Issue Information

Dear Colleagues,

The contamination of food by mycotoxins is a public health challenge worldwide. Accordingly, the consumption of mycotoxin-contaminated food brings a myriad of problems, from health impairments to economic losses. The toxic effects of mycotoxins occur either acutely or chronically, and vary upon species, age, sex, dose, exposure time and mycotoxin or mycotoxin mixture present. Moreover, mycotoxins present variable degrees of carcinogenicity according to the International Agency for Research on Cancer (IARC), and thus exposure to these contaminants should be avoided. Therefore, understanding the mechanisms underlying the toxic actions of mycotoxins, as well as the screening of strategies with potential to reduce the damage caused by these toxins are necessary. In this context, manuscripts dealing with the toxic effects induced by mycotoxins using behavioral, biochemical, and molecular markers are encouraged, as well as those studies investigating protocols and compounds to mitigate the toxic effects caused by mycotoxins.

Dr. Ana Flávia Furian
Dr. Mauro Schneider Oliveira
Guest Editors

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Keywords

  • mycotoxins
  • toxicity
  • biochemical marker
  • molecular marker
  • oxidative stress
  • bioactive

Published Papers (2 papers)

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Research

13 pages, 2502 KiB  
Article
Pitaya Juice Consumption Protects against Oxidative Damage Induced by Aflatoxin B1
by Luiggi Müller Madalosso, Franciéle Romero Machado Balok, Vandreza Cardoso Bortolotto, Mustafa Munir Mustafa Dahleh, Lucas Gabriel Backes, Elizabeth Sabryna Sarquis Escalante, Fernanda Vilhalba Benites, Francisco Andrey da Silva e Silva, Hecson Jesser Segat and Silvana Peterini Boeira
J. Fungi 2023, 9(9), 874; https://doi.org/10.3390/jof9090874 - 24 Aug 2023
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Abstract
Mycotoxins are toxic fungal metabolites and are responsible for contaminating several foods. The intake of foods contaminated by these substances is related to hepatotoxicity and carcinogenic effects, possibly due to increasing oxidative stress. The current study evaluated Pitaya fruit juice’s antioxidant effects on [...] Read more.
Mycotoxins are toxic fungal metabolites and are responsible for contaminating several foods. The intake of foods contaminated by these substances is related to hepatotoxicity and carcinogenic effects, possibly due to increasing oxidative stress. The current study evaluated Pitaya fruit juice’s antioxidant effects on oxidative damage aflatoxin B1 (AFB1)-induced. Rats received 1.5 mL of Pitaya juice via gavage (for 30 days), and on the 31st day, they received AFB1 (250 µg/kg, via gavage). Forty-eight hours after the AFB1 dose, rats were euthanized for dosages of alanine transaminase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP); dosage of oxidative markers (thiobarbituric acid reactive species (TBARS), reactive species (RS)) and antioxidant defenses (catalase (CAT), superoxide dismutase (SOD), Glutathione S-transferase (GST) activities and Glutathione (GSH)) levels in the liver; and detection of Heat shock protein 70 (Hsp-70) and nuclear factor- erythroid 2-related factor 2 (Nrf2) immunocontent in the liver. Our results indicated that the Pitaya juice reduced ALP activity. Further, rats exposed to AFB1 experienced liver damage due to the increase in TBARS, RS, and Hsp-70 and the reduction in CAT, GSH, and Nrf2. Pitaya juice could, however, protect against these damages. Finally, these results indicated that pre-treatment with Pitaya juice was effective against the oxidative damage induced. However, other aspects may be elucidated in the future to discover more targets of its action against mycotoxicosis. Full article
(This article belongs to the Special Issue Toxic Effects Induced by Exposure to Mycotoxins)
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20 pages, 7982 KiB  
Article
Mycotoxins from Tomato Pathogenic Alternaria alternata and Their Combined Cytotoxic Effects on Human Cell Lines and Male Albino Rats
by Ahmed Mahmoud Ismail, Eman Said Elshewy, Sherif Mohamed El-Ganainy, Donato Magistà, Ahlam Farouk Hamouda, Khalid A. Alhudaib, Weaam Ebrahim and Mustafa I. Almaghasla
J. Fungi 2023, 9(3), 282; https://doi.org/10.3390/jof9030282 - 21 Feb 2023
Cited by 3 | Viewed by 1975
Abstract
The Alternaria species are considered to produce a plethora of several mycotoxins constituting a risk factor for both human and animal health. This work aimed mainly to explore the cytotoxicity of a combined mixture of altenuene (ALT), alternariol (AOH), tenuazonic acid (TeA), and [...] Read more.
The Alternaria species are considered to produce a plethora of several mycotoxins constituting a risk factor for both human and animal health. This work aimed mainly to explore the cytotoxicity of a combined mixture of altenuene (ALT), alternariol (AOH), tenuazonic acid (TeA), and altenuisol (AS) toxins produced by pathogenic A. alternata toward human oral epithelial cells (PCS-200-014), lung fibroblast cells (WI-38), and male albino rats. The sequencing of the multi-locus, RNA polymerase second largest subunit (rpb2), glyceraldehyde-3-phosphate dehydrogenase (gapdh), and Alternaria major allergen gene (Alt a 1) was performed to infer relationships among isolated Alternaria species. The phylogenetic analysis of gapdh, rpb2, and Alt-a 1 sequence data indicated that all isolates resided in A. alternata. The pathogenic potentiality of A. alternata was investigated on tomato plants cv. super strain B under greenhouse conditions, and all isolates were pathogenic to tomato plants, with significant (p < 0.05) variations. The ability of A. alternata isolates to produce mycotoxins was also explored using high-performance liquid chromatography (HPLC). All tested isolates were able to produce at least one of the assessed mycotoxins—ALT, AOH, TeA, and AS—and ALT was reported as the dominant mycotoxin, produced by 80% of A. alternata isolates. The cytotoxic properties of the combined mixture of ALT, AOH, TeA, and AS at concentrations of 31.25, 62.50, 125, 250, and 500 µg/mL were assessed via the MTT assay method after exposure for 24 h versus the control. The treatment of both cell lines with combined mixtures of ALT, AOH, TeA, and AS showed a dose-dependent decrease in cell viability. The highest concentrations tested at 62.50, 125, 250, and 500 µg/mL significantly decreased cell viability and caused cell damage compared to the lowest concentration of 31.25 µg/mL and the control. The cytotoxicity and genotoxicity of the combined mixtures of ALT, AOH, TeA, and AS on male albino rats were also investigated via the gene expression of (TNF-α) and using hematological (CBC), chemical (alanine aminotransferase (ALT), aspartate aminotransferase (AST) and urea and creatinine), and histopathological analyses. A marked increase was observed in the levels of ALT, AST, urea and creatinine, TNF-α gene expression, red blood cells (RBCs), white blood cells (WBCs), hemoglobin (Hb), and packed cell volume % (PCV) after 28 days of exposure relative to the untreated control. Pathological alterations were also observed in the liver and kidney tissues of rats. Conclusively, this work provides a new understanding on the cytotoxicity and genotoxicity of mycotoxins of pathogenic A. alternata from tomatoes. Full article
(This article belongs to the Special Issue Toxic Effects Induced by Exposure to Mycotoxins)
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