The Effect of Feed Contamination with Mycotoxins on Animals and Ways for Prevention and Degradation of Mycotoxins

Authors

  • Oana Ciobotaru University of Agronomic Sciences and Veterinary Medicine – Bucharest, Faculty of Biotechnologies, 59 Mărăşti Blvd, 011464 Bucharest, Romania
  • Iulian Grosu University of Agronomic Sciences and Veterinary Medicine – Bucharest, Faculty of Biotechnologies, 59 Mărăşti Blvd, 011464 Bucharest, Romania
  • Calina Petruta Cornea University of Agronomic Sciences and Veterinary Medicine – Bucharest, Faculty of Biotechnologies, 59 Mărăşti Blvd, 011464 Bucharest, Romania

Keywords:

animal illness, Aspergillus flavus, mycotoxins

Abstract

Mycotoxins are secondary metabolites produced by fungi that are capable of causing illness and sometimes death to animals and not only animals even humans. In 1960 it was established that some fungal metabolites, now called mycotoxins, that have a destructive effect on animal health, since then people were interested on the effect and the way to stop it. Among them, aflatoxins, B1, B2, G1 & G2 synthesized mainly by Aspergillus flavus/ Aspergillus parasiticus are known to induce severe effects on animal: can cause liver damage, decreased milk production, reduced reproductively and suppressed immunity in animals consuming low dietary concentrations, decreased feed intake and efficiency, weight loss, jaundice, drop in milk production, nervous signs, bleeding and death. The aim of this work was the isolation of aflatoxin producing fungi in order to investigate new ways that can determinate, inhibit or degradation of aflatoxin, ochratoxin, using lactic bacteria and yeast. A number of 14 Aspergillus spp. isolates were selected from wheat, barley, triticale, oats, and sunflower seeds and identified, based on macroscopic and microscopic features as A.flavus/A.parasiticus. The ability of aflatoxin biosynthesis was detected on PDA medium with β cyclodextrine and sodium deoxycholate were evaluated by TLC and RIDA Screen R-biopharm. At this stage of experiments 3 fungal isolates, designated as GE2, G32, T11 were selected as aflatoxin B1, B2, G1 and used for further analysis (molecular identification, interactions with LAB and yeasts).

References

Huwig A1, Freimund S, Käppeli O, Dutler H., Mycotoxin detoxication of animal feed by different adsorbents., Toxicol Lett. 2001 Jun 20; 122(2):179-88.

Mehdi Razzaghi-Abyaneh, Aflatoxins - Recent Advances and Future Prospects, Janeza Trdine 9, 51000 Rijeka, Croatia, January, 2013

Fente, C. A., J. Jaimez Ordaz, B. I. Vazquez, C. M. Franco, and A. Cepeda. April 1999. Patent P9900776.

Ana Carolina RITTER, Michele HOELTZ, Isa Beatriz NOLL, Toxigenic potential of Aspergillus flavus tested in different culture conditions, Ciência e Tecnologia de Alimentos, ISSN 0101-2061, 2011

Davis N D, Iyer S K, Diener U L. Improved method of screening for aflatoxin with a coconut agar medium. Appl Environ Microbiol. 1987; 53:1593–1595

Ordaz, J.J. et. al. Development of method for direct visual determination of aflatoxin production by colonies of the Aspergillus flavus group. International Journal of Food Microbiology, v. 83, p. 219-225, 2003.

Yazdani, D., Tan, Y.H., Zainal Abidin, M.A., & Jaganath E.B. (2010).Screening of phytochemical from ethnomedicinal plants in Malaysia for use against toxigenic Aspergillus flavus. Journal of medicinal plant research 6(42), 5464-5468.

Vázquez B I, Fente C A, Franco C M, Cepeda A, Mahuzier G, Prognon P. Preliminary study on fluorimetry detection of aflatoxins Q1, P1 and B1 using heptakis-di-o-methyl-β-cyclodextrin as post-column HPLC reagent. Anal Commun. 1999; 36:5–7

Franco C M, Fente C A, Vázquez B I, Cepeda A, Mahuzier G, Prognon P. Interaction between cyclodextrins and aflatoxins Q1, M1 and P1: fluorescence and chromatographic studies. J Chromatogr A. 1998; 815:21–29. .

Hara S, Fennell D L, Hesseltine C W. Aflatoxin producing strains of Aspergillus flavus detected by fluorescence of agar medium under ultraviolet light. Appl Microbiol. 1974; 27:1118–1123

Nesheim S, United States. Food and Drug Administration, Silica Gel for Thin Layer Chromatography of Aflatoxins. Office of Legislative and Governmental Services, U.S. Food and Drug Administration, 1968.

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Published

2023-09-05