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Detection of Clostridium difficile toxin A by reversed passive latex agglutination.

机译:通过反向被动乳胶凝集检测艰难梭菌毒素A。

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摘要

A reversed passive latex agglutination (RPLA) assay for detecting Clostridium difficile toxin A is presented. Purified monoclonal antibody (mAb 37B5) was used for latex sensitization. The culture supernatants of 93 strains of C. difficile were tested by RPLA assay and the results compared with those of a commercially available latex agglutination test, PCR and cytotoxin assay with Vero cells. There was agreement between RPLA, cytotoxicity and PCR assays, but 29 strains were positive in the RPLA assay while 35 were positive in the cytotoxicity test and PCR using primer pair NK3-NK2 directed to the nonrepeating portion of the C. difficile toxin A gene. The 6 cytotoxic but RPLA-negative strains were demonstrated to be toxin A-negative/toxin B-positive strains in the PCR assay by using primer pair NK11-NK9 directed to the repeating portion of the C. difficile toxin A gene. There were no cross-reactions with culture supernatants of the other clostridial strains except for two strains of C. sordelli that produced hemorrhagic toxin (which is immunologically related to C. difficile toxin A).
机译:提出了一种反向被动乳胶凝集(RPLA)测定法,用于检测艰难梭菌毒素A。纯化的单克隆抗体(mAb 37B5)用于乳胶敏化。通过RPLA测定法测试了93个艰难梭菌菌株的培养物上清液,并将其结果与市售的乳胶凝集试验,PCR和Vero细胞的细胞毒素测定法进行了比较。 RPLA,细胞毒性和PCR分析之间存在一致性,但29株在RPLA分析中呈阳性,而35株在细胞毒性试验和PCR中呈阳性,使用针对艰难梭菌毒素A基因非重复部分的引物对NK3-NK2。通过使用针对艰难梭菌毒素A基因重复部分的引物对NK11-NK9,在PCR分析中证实这6种细胞毒性但RPLA阴性的菌株为毒素A阴性/毒素B阳性菌株。除了两个梭状芽胞杆菌产生出血性毒素(与艰难梭菌毒素A免疫相关)外,与其他梭菌菌株的培养上清液均无交叉反应。

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