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Addressing Current Challenges in Poultry Meat Safety: Development of a Cultivation and Colony Hybridization Approach to Recover Enterotoxigenic Clostridium perfringens from Broiler Chicken Carcasses.
Kakese Mukosa, Rosette; Thibodeau, Alexandre; Morris Fairbrother, John; Thériault, William; Gaucher, Marie-Lou.
Afiliación
  • Kakese Mukosa R; Research Chair in Meat Safety, Department of Pathology and Microbiology, Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
  • Thibodeau A; Research Group on Infectious Diseases in Animal Production, Department of Pathology and Microbiology, Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
  • Morris Fairbrother J; Research Chair in Meat Safety, Department of Pathology and Microbiology, Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
  • Thériault W; Research Group on Infectious Diseases in Animal Production, Department of Pathology and Microbiology, Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
  • Gaucher ML; Swine and Poultry Infectious Diseases Research Centre (CRIPA-FRQNT), Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
Pathogens ; 13(1)2023 Dec 28.
Article en En | MEDLINE | ID: mdl-38251337
ABSTRACT
Enterotoxigenic Clostridium perfringens is one of the main causes of foodborne illness in Canada. The use of a conventional bacterial culture approach to isolate enterotoxigenic C. perfringens from poultry meat is common. This approach is based on the phenotype attributable to a double hemolysis phenomenon, whereas few enterotoxigenic strains of C. perfringens produce it, which further complicates the study of the reservoirs of this important pathogen. The objectives of the current study were to validate the ability of a digoxigenin-labeled probe to detect the C. perfringens cpe gene and to validate the use of either a filtration or a direct plating approach, combined with colony hybridization to detect enterotoxigenic C. perfringens. Pure DNA and pure colonies of enterotoxigenic C. perfringens and broiler chicken carcass rinsate samples were subjected to colony hybridization. The results showed that the synthesized DNA probe can detect the cpe gene from both DNA and pure colonies of enterotoxigenic C. perfringens, and from colonies grown from carcass rinsates artificially contaminated with enterotoxigenic C. perfringens. Our study suggests that this isolation method is a promising tool for a better understanding of the epidemiology of this zoonotic pathogen.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pathogens Año: 2023 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pathogens Año: 2023 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Suiza