Vansnick Elke, De Rijk Pim, Vercammen Francis, Geysen Dirk, Rigouts Leen, Portaels Françoise
Veterinary Department, Institute of Tropical Medicine, Nationalestraat 155, 2000 Antwerp, Belgium.
Vet Microbiol. 2004 Jun 3;100(3-4):197-204. doi: 10.1016/j.vetmic.2004.02.006.
Recent publications reported the existence of IS900 like sequences in mycobacteria different from Mycobacterium avium subspecies paratuberculosis (Map). The primers used for IS900 detection of Map have amplified these sequences causing false positive results. In this study, we have developed two new PCR assays for the detection of Map. The first assay is based on the IS900 sequence using primers different from the ones previously reported, the second assay on the f57 sequence. The specificity of the tests was checked by analysis of 190 mycobacterial isolates (74 Map and 116 non-Map isolates). All Map strains were positive and all non-Map strains were negative. Serial dilutions of Map bacteria were used to assess the sensitivity of the assays. We achieved a sensitivity of 1CFU per PCR for both assays. In addition, a PCR-simulating computer programme was used to evaluate the specificity of the new IS900 primers. The combination of the two PCR assays has proven to be useful for the identification of Map but validation on a large range of clinical samples still needs to be done.
近期的出版物报道,在不同于副结核分枝杆菌鸟亚种(Map)的分枝杆菌中存在类IS900序列。用于检测Map的IS900引物扩增了这些序列,导致出现假阳性结果。在本研究中,我们开发了两种用于检测Map的新型PCR检测方法。第一种检测方法基于IS900序列,使用的引物与先前报道的不同,第二种检测方法基于f57序列。通过分析190株分枝杆菌分离株(74株Map和116株非Map分离株)来检查检测方法的特异性。所有Map菌株均为阳性,所有非Map菌株均为阴性。使用Map细菌的系列稀释液来评估检测方法的灵敏度。两种检测方法的灵敏度均达到每PCR 1CFU。此外,使用一个模拟PCR的计算机程序来评估新型IS900引物的特异性。这两种PCR检测方法的组合已被证明对Map的鉴定有用,但仍需要在大量临床样本上进行验证。