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[基于colA基因的PCR检测系统用于临床样本中钩端螺旋体检测的开发]

[Development of PCR test system based on colA gene for detection of leptospirae in clinical material].

作者信息

Vaganova A N, Stoianova N A, Tokarevich N K

出版信息

Zh Mikrobiol Epidemiol Immunobiol. 2011 Sep-Oct(5):67-71.

Abstract

AIM

Development of primers for the detection of leptospirae in clinical material including urine.

MATERIALS AND METHODS

Study of specificity and sensitivity of primers complementary to colA gene in standard PCR by using DNA preparation of cultures of pathogenic and saprophytic leptospirae, biological materials from healthy humans and dogs, including contaminated with pathogenic leptospirae culture.

RESULTS

Specific interaction of these primers with DNA of pathogenic leptospirae of 14 serogroups was established. Sensitivity of the technique was 50 cells in 1 ml of sample.

CONCLUSION

The primers described fulfill the requirements for the sensitivity and specificity and can be recommended for the detection of leptospirae in both serum and urine.

摘要

目的

开发用于检测包括尿液在内的临床材料中钩端螺旋体的引物。

材料与方法

通过使用致病性和腐生性钩端螺旋体培养物的DNA制剂、来自健康人和狗的生物材料(包括被致病性钩端螺旋体培养物污染的材料),研究标准PCR中与colA基因互补的引物的特异性和敏感性。

结果

确定了这些引物与14个血清群的致病性钩端螺旋体DNA的特异性相互作用。该技术的敏感性为每1毫升样品中50个细胞。

结论

所述引物满足敏感性和特异性要求,可推荐用于血清和尿液中钩端螺旋体的检测。

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