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Molecular and HPLC-based approaches for detection of aflatoxin B and ochratoxin A released from toxigenic Aspergillus species in processed meat. | LitMetric

AI Article Synopsis

  • The study investigated the presence of harmful Aspergillus species in processed meat products from Egypt, focusing on the levels of mycotoxins aflatoxin B and ochratoxin A.
  • The findings revealed the highest mold counts in sausage samples, with A. flavus and A. ochraceus found in varying prevalence across basterma, sausage, and minced meat.
  • This research highlights a significant public health risk from mycotoxin contamination in processed meats, especially with aflatoxin B linked to basterma, marking the first use of advanced detection methods in this context within Egypt.

Article Abstract

Background: Meat-products are considered an enriched media for mycotoxins. This study aimed to investigate the prevalence of toxigenic Aspergillus species in processed meat samples, HPLC-quantitative measurement of aflatoxin B and ochratoxin A residues, and molecular sequencing of aflR1 and pks genes. One hundred and twenty processed beef meat specimens (basterma, sausage, and minced meat; n = 40 for each) were collected from Ismailia Province, Egypt. Samples were prepared for total mold count, isolation, and identification of Aspergillus species. All samples were analyzed for the production of both Aflatoxin B and Ochratoxin A mycotoxins by HPLC. Molecular identification of Aspergillus flavus and Aspergillus ochraceus was performed using PCR amplification of the internal transcribed spacer (ITS) region; furthermore, the aflR1 and pks genes were sequenced.

Results: The total mold count obtained from sausage samples was the highest one, followed by minced meat samples. The prevalence of A. flavus was (15%), (7.5%), and (10%), while the prevalence of A. ochraceus was (2.5%), (10%), and (0%) in the examined basterma, sausage, and minced meat samples, respectively. Using PCR, the ITS region was successfully amplified in all the tested A. flavus and A. ochraceus strains. Aflatoxin B was detected in six basterma samples (15%). Moreover, the ochratoxin A was detected only in four sausage samples (10%). The aflR1 and pks genes were amplified and sequenced successfully and deposited in the GenBank with accession numbers MF694264 and MF694264, respectively.

Conclusions: To the best of our knowledge, this is the first report concerning the HPLC-Molecular-based approaches for the detection of aflatoxin B and ochratoxin A in processed beef meat in Egypt. The production of aflatoxin B and ochratoxin A in processed meat constitutes a public health threat. Aflatoxin B is commonly associated with basterma samples. Moreover, ochratoxin A was detected frequently in sausage samples. The routine inspection of mycotoxins in processed meat products is essential to protect human consumers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956122PMC
http://dx.doi.org/10.1186/s12866-021-02144-yDOI Listing

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