Your browser doesn't support javascript.
loading
Bacteriological evaluation and advanced SYBR-green multiplex real-time PCR assay for detection of minced meat adulteration.
El-Sheikh, Soad H; Whab, Reham M Abdel; ElDaly, Rania A; Raslan, Mona T; Fahmy, Hanan A; El-Demerdash, Azza S.
Afiliação
  • El-Sheikh SH; Department of Food Hygiene, Agriculture Research Centre (ARC), Animal Health Research Institute (AHRI), Zagazig, Egypt.
  • Whab RMA; Department of Food Hygiene, Agriculture Research Centre (ARC), Animal Health Research Institute (AHRI), Zagazig, Egypt.
  • ElDaly RA; Department of Botany and Microbiology, Faculty of Science, Arish University, Al-Arish, Egypt.
  • Raslan MT; Department of Food Hygiene, Agriculture Research Centre (ARC), Animal Health Research Institute (AHRI), Giza, Egypt.
  • Fahmy HA; Department of Biotechnology, Agricultural Research Centre, Animal Health Research Institute, Giza, Egypt.
  • El-Demerdash AS; Laboratory of Biotechnology, Department of Microbiology, Agriculture Research Centre (ARC), Animal Health Research Institute (AHRI), Zagazig, Egypt.
Open Vet J ; 14(1): 389-397, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38633161
ABSTRACT

Background:

Minced meat is a valuable source of nutrients, but it is vulnerable to contamination by microorganisms commonly present in the environment. In addition, there is a risk of adulteration with cheaper meat sources, which can be harmful to consumers.

Aim:

It is crucial to identify meat adulteration with distinct microbiological analysis for legal, economic, religious, and public health purposes.

Methods:

A total of 100 minced meat samples were collected from several markets in Sharkia Governorate, Egypt. These samples were then subjected to bacteriological testing and an advanced multiplex PCR method. This method enables the detection of bovine, equine, porcine, and dog species in meat samples with just one step.

Results:

The adulterated samples had a higher total bacterial count and pH values compared to pure bovine meat. These differences in bacterial count and pH values were statistically significant, with p-values of 0.843 (log10) and 0.233, respectively. The frequency of Escherichia coli occurrence was 13%, and the O111 serotype was predominant in the adulterated samples. Listeria monocytogenes and Staphylococcus aureus were isolated with prevalence rates of 3% and 29%, respectively. Besides, the SYBR-green multiplex real-time PCR assay used in this study detected adulteration with dog, equine, and porcine meats in the examined samples at rates of 9%, 5%, and 4%, respectively.

Conclusion:

This method provides a sensitive and specific approach to detect issues related to well-being and safety.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Contaminação de Alimentos / Diaminas / Benzotiazóis / Carne Limite: Animals Idioma: En Revista: Open Vet J Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Contaminação de Alimentos / Diaminas / Benzotiazóis / Carne Limite: Animals Idioma: En Revista: Open Vet J Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito
...