Martinez G, Harel J, Gottschalk M
Groupe de recherche sur les maladies infectieuses du porc, Faculté de médecine vétérinaire, Université de Montréal, St-Hyacinthe, Québec.
Can J Vet Res. 2001 Jan;65(1):68-72.
The aim of this study was to develop a simple and specific method for direct detection of Streptococcus agalactiae from cow's milk. The method was based on polymerase chain reaction (PCR) using species-specific and universal primers derived from the 16S rRNA gene. The amplification product was verified by restriction endonuclease digest and sequencing. Specific identification was proven on a collection of 147 S. agalactiae isolates of bovine and human origin. In addition, 17 strains belonging to different bacterial species that potentially can be found in milk samples also tested negative. The PCR developed was used for direct detection of S. agalactiae in milk, using for the first time with gram-positive bacteria the nucleic acid-binding properties of diatomaceous earth. The test, which has high specificity, high sensitivity (100 cfu/mL), and can be carried out in less than 24 h, represents an innovative diagnostic tool for the detection of S. agalactiae in milk.
本研究的目的是开发一种简单且特异的方法,用于直接从牛奶中检测无乳链球菌。该方法基于聚合酶链反应(PCR),使用源自16S rRNA基因的种特异性引物和通用引物。扩增产物通过限制性内切酶消化和测序进行验证。在147株牛源和人源无乳链球菌分离株上证实了特异性鉴定。此外,17株属于可能在牛奶样本中发现的不同细菌物种的菌株检测结果也为阴性。所开发的PCR用于直接检测牛奶中的无乳链球菌,首次将硅藻土的核酸结合特性用于革兰氏阳性菌。该检测具有高特异性、高灵敏度(100 cfu/mL),且可在不到24小时内完成,是检测牛奶中无乳链球菌的一种创新诊断工具。