Chiang Yu-Cheng, Fan Chih-Ming, Liao Wan-Wen, Lin Chien-Ku, Tsen Hau-Yang
Institute of Industrial Biotechnology, Hung Kuang University, 34 Chung-Chi Road, Shalu, Taichung County, 433 Taiwan, Republic of China.
J Food Prot. 2007 Dec;70(12):2855-9. doi: 10.4315/0362-028x-70.12.2855.
Staphylococcus aureus may cause foodborne disease outbreaks and staphylococcal infections and is one of the major causes of mastitis. Rapid and reliable methods for detection of this microorganism in milk and other foods are needed. In this study, we designed a primer set from the sequence of the heat shock protein gene htrA, a gene coding for high-temperature-requirement A (HtrA) protein, and used it for real-time PCR detection of S. aureus isolates: 16 reference strains and 40 strains isolated from food-poisoning cases. All strains tested generated positive results. Bacterial strains other than S. aureus, including strains of other Staphylococcus species, did not produce positive results. When this primer set was used for the real-time PCR detection of S. aureus in milk and meat samples without the preenrichment step, samples with target cell numbers greater than 10(3) CFU/ml or CFU/g could be detected, indicating the potential quantitative ability of this real-time PCR assay. With a 10-h preenrichment step, however, a detection limit of 1 CFU/ml or CFU/g could be obtained.
金黄色葡萄球菌可能导致食源性疾病暴发和葡萄球菌感染,并且是乳腺炎的主要病因之一。因此需要快速可靠的方法来检测牛奶和其他食品中的这种微生物。在本研究中,我们根据热休克蛋白基因htrA(一种编码高温需求A(HtrA)蛋白的基因)的序列设计了一组引物,并将其用于金黄色葡萄球菌分离株的实时PCR检测:16株参考菌株和40株从食物中毒病例中分离出的菌株。所有测试菌株均产生阳性结果。除金黄色葡萄球菌外的其他细菌菌株,包括其他葡萄球菌属的菌株,均未产生阳性结果。当该引物组用于牛奶和肉类样品中金黄色葡萄球菌的实时PCR检测而无需预富集步骤时,目标细胞数大于10³CFU/ml或CFU/g的样品可以被检测到,这表明该实时PCR检测方法具有潜在的定量能力。然而,经过10小时的预富集步骤后,检测限可达到1 CFU/ml或CFU/g。