Delmée M
Microbiology Unit, Université Catholique de Louvain, Brussels, Belgium.
Clin Microbiol Infect. 2001 Aug;7(8):411-6. doi: 10.1046/j.1198-743x.2001.00294.x.
The laboratory diagnosis of Clostridium difficile-associated disease (CDAD) is based on culture and toxin detection in fecal specimens. Culture is performed on a commercially available selective media. C. difficile colony morphology is typical when viewed under a dissecting microscope. Definitive identification is best obtained by gas liquid chromatography. Culture is very sensitive but, when used alone without toxin testing, it leads to low specificity and misdiagnosis of CDAD when high rates of asymptomatic carriage exist. Toxin detection by a tissue culture cytotoxin assay followed by neutralisation with specific antiserum is often considered the standard. However, this approach lacks sensitivity and has not detected up to 30% of patients with confirmed CDAD. Multiple enzyme immunoassays (EIAs) have been introduced by various manufacturers for the detection of toxin A alone or for both toxins A and B. Some of these are designed to give results in less than 1 h. Comparative studies of EIA kits reported that the sensitivity and specificity are slightly lower than cytotoxin assays. Toxigenic culture tests C. difficile isolates for toxin production: colonies isolated on selective media are tested for in-vitro toxin production either by a cytotoxicity assay or by direct EIA. It has higher sensitivity than the cytotoxicity assay and equivalent specificity. In the routine laboratory, culture and toxin detection should be performed on every specimen and, in culture-positive and fecal toxin-negative cases, toxigenic cultures should be performed on isolated colonies.
艰难梭菌相关性疾病(CDAD)的实验室诊断基于粪便标本中的培养和毒素检测。培养在市售的选择性培养基上进行。在解剖显微镜下观察时,艰难梭菌的菌落形态是典型的。通过气相色谱法可最佳地进行确诊。培养非常敏感,但单独使用而不进行毒素检测时,在无症状携带率高的情况下会导致CDAD的低特异性和误诊。通过组织培养细胞毒素测定法检测毒素,然后用特异性抗血清进行中和,通常被认为是标准方法。然而,这种方法缺乏敏感性,未检测出高达30%的确诊CDAD患者。多家制造商推出了多种酶免疫测定法(EIA)用于单独检测毒素A或同时检测毒素A和B。其中一些设计为在不到1小时内得出结果。EIA试剂盒的比较研究报告称,其敏感性和特异性略低于细胞毒素测定法。产毒培养试验检测艰难梭菌分离株的毒素产生:在选择性培养基上分离的菌落通过细胞毒性测定法或直接EIA检测体外毒素产生。它比细胞毒性测定法具有更高的敏感性和相当的特异性。在常规实验室中,应对每个标本进行培养和毒素检测,在培养阳性且粪便毒素阴性的病例中,应对分离的菌落进行产毒培养。