Kakese Mukosa Rosette, Thibodeau Alexandre, Morris Fairbrother John, Thériault William, Gaucher Marie-Lou
Research Chair in Meat Safety, Department of Pathology and Microbiology, Faculty of Veterinary Medicine, University of Montreal, Montreal, QC J2S 2M2, Canada.
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.
Pathogens. 2023 Dec 28;13(1):30. doi: 10.3390/pathogens13010030.
Enterotoxigenic is one of the main causes of foodborne illness in Canada. The use of a conventional bacterial culture approach to isolate enterotoxigenic from poultry meat is common. This approach is based on the phenotype attributable to a double hemolysis phenomenon, whereas few enterotoxigenic strains of 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 gene and to validate the use of either a filtration or a direct plating approach, combined with colony hybridization to detect enterotoxigenic . Pure DNA and pure colonies of enterotoxigenic and broiler chicken carcass rinsate samples were subjected to colony hybridization. The results showed that the synthesized DNA probe can detect the gene from both DNA and pure colonies of enterotoxigenic , and from colonies grown from carcass rinsates artificially contaminated with enterotoxigenic . Our study suggests that this isolation method is a promising tool for a better understanding of the epidemiology of this zoonotic pathogen.
产肠毒素菌是加拿大食源性疾病的主要病因之一。采用传统细菌培养方法从禽肉中分离产肠毒素菌很常见。这种方法基于归因于双重溶血现象的表型,然而很少有产肠毒素菌菌株会产生这种现象,这使得对这种重要病原体储存库的研究更加复杂。本研究的目的是验证地高辛标记探针检测该基因的能力,并验证过滤或直接平板接种方法与菌落杂交相结合用于检测产肠毒素菌的适用性。将产肠毒素菌的纯DNA、纯菌落以及肉鸡胴体冲洗液样本进行菌落杂交。结果表明,合成的DNA探针能够从产肠毒素菌的DNA和纯菌落中,以及从人工污染了产肠毒素菌的胴体冲洗液中生长的菌落中检测到该基因。我们的研究表明,这种分离方法是更好地了解这种人畜共患病原体流行病学的一种有前景的工具。