Rychlík I, van Kesteren L, Cardová L, Svestková A, Martínková R, Sisák F
Veterinary Research Institute, Hudcova, Brno, Czech Republic.
Lett Appl Microbiol. 1999 Oct;29(4):269-72. doi: 10.1046/j.1365-2672.1999.00622.x.
A simple and universal protocol for the rapid detection of Salmonella spp. in various samples using nested polymerase chain reaction (PCR) was developed. The protocol takes advantage of the rapid purification and concentration of Salmonella by centrifugation onto a layer of 60% sucrose solution. DNA was released by treatment with proteinase K and Triton X-100. Even without pre-enrichment, the detection limit for the nested PCR was 10(5) CFU g-1 of faeces. After pre-enrichment, it was possible to detect Salmonella in faeces where their original concentration was approximately 10(2) CFU g-1 of faeces and in meat samples, it was possible to detect Salmonella in samples where their original concentration was less than 10 cells g-1 of minced meat.
开发了一种使用巢式聚合酶链反应(PCR)快速检测各种样品中沙门氏菌属的简单通用方法。该方法利用将沙门氏菌通过离心富集到60%蔗糖溶液层上进行快速纯化和浓缩。用蛋白酶K和曲拉通X-100处理释放DNA。即使不进行预富集,巢式PCR的检测限为每克粪便10⁵CFU。预富集后,能够检测到原始浓度约为每克粪便10²CFU的粪便中的沙门氏菌,在肉类样品中,能够检测到原始浓度低于每克碎肉10个细胞的样品中的沙门氏菌。