Dumonceaux M, Fauville Dufaux M, Ooms J, De Wit L, Sonck P, Content J
Department of Virology, Institut Pasteur, 642 rue Engeland, Brussels, B-1180, Belgium.
Mol Cell Probes. 1997 Aug;11(4):251-8. doi: 10.1006/mcpr.1997.0110.
The complete nucleotide sequence of 85A antigen of Mycobacterium gordonae was determined. This gene encodes 339 amino acids, including 43 amino acids for the signal peptide, followed by a mature protein of 296 amino acids. A polymerase chain reaction (PCR) assay for the rapid detection of M. gordonae DNA using two pairs of oligonucleotide primers, derived from our sequence, is described. This one-step PCR has been used successfully to amplify 38 strains of M. gordonae. Conversely, the primers did not amplify DNA from any of the 25 mycobacterial species tested. The results suggest that this PCR assay could be a good alternative to existing commercial assays for the specific identification of M. gordonae on early culture on solid medium or on early BACTEC broth culture.
测定了戈登分枝杆菌85A抗原的完整核苷酸序列。该基因编码339个氨基酸,其中包括43个氨基酸的信号肽,随后是一个由296个氨基酸组成的成熟蛋白。描述了一种使用从我们的序列中衍生的两对寡核苷酸引物快速检测戈登分枝杆菌DNA的聚合酶链反应(PCR)检测方法。这种一步法PCR已成功用于扩增38株戈登分枝杆菌。相反,这些引物未扩增出所检测的25种分枝杆菌中的任何一种的DNA。结果表明,这种PCR检测方法可能是现有商业检测方法的一个很好的替代方法,可用于在固体培养基上早期培养或在早期BACTEC肉汤培养中对戈登分枝杆菌进行特异性鉴定。