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用于检测产毒白喉棒状杆菌的聚合酶链反应

Polymerase chain reaction for the detection of toxigenic Corynebacterium diphtheriae.

作者信息

Aravena-Román M, Bowman R, O'Neill G

机构信息

Department of Microbiology, University of Western Australia, Nedlands.

出版信息

Pathology. 1995 Jan;27(1):71-3. doi: 10.1080/00313029500169512.

Abstract

Several conventional methods have been described for the detection of Corynebacterium diphtheriae toxin, including Elek immunodiffusion, tissue culture using VERO cells and guinea pig inoculation. All these methods have the disadvantage of being either slow to complete or technically demanding, particularly when performed infrequently. We examined 64 strains of C. diphtheriae by PCR and Elek immunodiffusion, and strains showing a positive result in either assay were inoculated into guinea pigs. Seven isolates were positive in both Elek and PCR assays and subsequently positive in guinea pig inoculation assay. One isolate was negative in Elek testing but positive in PCR assay and guinea pig inoculation. All other isolates were negative in both Elek and PCR assays. The PCR assay is rapid with cycling and detection complete within 3-4 hrs of receipt of strains. PCR has now become the routine method for detection of C. diphtheriae toxin in our laboratory.

摘要

已经描述了几种用于检测白喉棒状杆菌毒素的传统方法,包括Elek免疫扩散法、使用VERO细胞的组织培养法和豚鼠接种法。所有这些方法都有完成速度慢或技术要求高的缺点,尤其是在不经常进行检测时。我们通过PCR和Elek免疫扩散法检测了64株白喉棒状杆菌,并将在任一检测中呈阳性结果的菌株接种到豚鼠体内。7株分离株在Elek和PCR检测中均呈阳性,随后在豚鼠接种试验中也呈阳性。1株分离株在Elek检测中呈阴性,但在PCR检测和豚鼠接种中呈阳性。所有其他分离株在Elek和PCR检测中均呈阴性。PCR检测速度快,在收到菌株后的3-4小时内即可完成循环和检测。PCR现已成为我们实验室检测白喉棒状杆菌毒素的常规方法。

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