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Molecular identification of aflatoxigenic Aspergillus species in feedstuff samples
Nooshin Sohrabi1, Morteza Taghizadeh2
1Department of Biology, Payame Noor University, Tehran, Iran.
Background And Purpose:
Aflatoxins are naturally produced by some species of Aspergillus, such as A. flavus and A. parasiticus. Aflatoxins reportedly have carcinogenic effects on human, poultry, and livestock, and therefore could be linked to severe human illnesses. Aflatoxin biosynthesis pathway involves different clustered genes, including structural, regular, and unassigned genes. The present study was conducted to detect aflR, aflP, and aflD as three important genes contributing to aflatoxin B1 production cycle in Aspergillus species isolated from the feedstuffs of animal husbandry.
Materials And Methods:
This study was conducted on 25 isolates of A. flavus, A. parasiticus, A. nomius, and A. nidulans, isolated from animal feedstuff as a test group. The test group was compared with two standard strains (i.e., A. flavus and A. parasiticus) as aflatoxigenic reference organisms and negative controls (i.e., A. fumigatus, A. fusarium, and A. penicillium) in terms of the presence of aflR, aflP, and aflD genes using polymerase chain reaction (PCR). The determination of the toxigenicity and aflatoxin production of isolated Aspergillus species was accomplished using thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC).
Results:
The results obtained by the amplification of the selected genes by PCR method for the detection of aflatoxigenic Asprgillus species were significantly correlated with TLC and HPLC results. Accordingly, all samples, having positive results for aflatoxin B1 production in TLC and HPLC, were able to show the amplification of three target genes. However, 4 cases out of 6 (66%) non-aflatoxigenic isolates were positive for three or two genes.
Conclusion:
Based on the findings, the molecular detection of aflatoxin biosynthesis genes (i.e., aflP, aflD, and aflR) could be considered as a quick and reliable method for the detection of aflatoxigenic Aspergillus. Furthermore, this method could be useful in planning and implementing strategies targeted toward improving the safety of human or animal food.
Insights
Molecular detection of aflatoxin biosynthesis genes (aflR, aflP, aflD) in Aspergillus species provides a rapid and reliable method for identifying aflatoxin contamination in animal feedstuffs, enhancing food safety.
Area of Science:
- Mycology and Food Safety
- Molecular Biology and Toxicology
Background:
- Aflatoxins, produced by Aspergillus species, pose carcinogenic risks to humans and animals.
- Aflatoxin B1 biosynthesis involves key genes, including aflR, aflP, and aflD.
- Contamination of animal feedstuffs with aflatoxins is a significant food safety concern.
Purpose of the Study:
- To detect the presence of aflR, aflP, and aflD genes in Aspergillus species isolated from animal feed.
- To evaluate the utility of molecular detection for identifying aflatoxin B1 production.
Main Methods:
- Isolates of Aspergillus species (A. flavus, A. parasiticus, A. nomius, A. nidulans) were obtained from animal feed.
- Polymerase Chain Reaction (PCR) was used to detect the presence of aflR, aflP, and aflD genes.
- Toxigenicity and aflatoxin production were confirmed using Thin-Layer Chromatography (TLC) and High-Performance Liquid Chromatography (HPLC).
Main Results:
- PCR detection of the three target genes showed significant correlation with TLC and HPLC results for aflatoxin B1 production.
- All isolates positive for aflatoxin B1 production by TLC/HPLC exhibited amplification of the target genes.
- A proportion of non-aflatoxigenic isolates also showed positive results for two or three target genes.
Conclusions:
- Molecular detection of aflatoxin biosynthesis genes (aflP, aflD, aflR) is a rapid and reliable method for identifying aflatoxigenic Aspergillus.
- This molecular approach can aid in developing strategies to improve human and animal food safety.
- The study highlights the potential of molecular diagnostics in controlling aflatoxin contamination.
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