Schulz Stephan, Cabras Antonello Domenico, Kremer Marcus, Weirich Gregor, Miethke Thomas, Bösmüller Hans-Christian, Höfler Heinz, Werner Martin, Fend Falko
Institute of Pathology, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Mod Pathol. 2005 Feb;18(2):274-82. doi: 10.1038/modpathol.3800289.
Diagnosis of infections caused by mycobacteria, especially nontuberculous mycobacteria still represents a difficult task both in microbiology and pathology. The aim of this study was to determine the frequency of mycobacterial DNA detectable by PCR in formalin-fixed paraffin-embedded tissues showing suspicious granulomatous lesions. A total of 190 archival specimens were analyzed, using a nested PCR protocol, which amplifies a fragment of the mycobacterial 65-kDa heat-shock protein gene. Restriction fragment-length polymorphisms and sequencing were utilized to further analyze the obtained PCR products. Corresponding microbiological culture results were available for 41 cases. We detected mycobacterial DNA in 119 cases (63%), of which 71 (60%) were positive for Mycobacterium tuberculosis complex DNA and 41 (34%) for DNA of nontuberculous mycobacteria. Seven cases (6%) could not be subtyped for technical reasons. The largest group of nontuberculous mycobacteria comprised 29 cases (25% of the 119 positive cases), which were assigned to Mycobacterium fortuitum complex. Mycobacterium avium-intracellulare complex was detected in eight (7%) cases, Mycobacterium gordonae in three (2.5%) and Mycobacterium rhodesiae in a single case (0.8%). All cases of Mycobacterium tuberculosis were unequivocally identified by restriction fragment-length polymorphism analysis. In contrast, sequencing provided a gain of information over restriction fragment-length polymorphism analysis in 37% of the nontuberculous mycobacteria cases (15 of 41). Alignment studies on DNA of nontuberculous mycobacteria showed frequent sequence variations, supporting the existence of sequevars. Comparison of molecular data to available results of microbiological culture assays showed a good concordance of 83%. In conclusion, amplification and sequencing of the mycobacterial 65-kDa heat-shock protein gene is an excellent tool for species identification of mycobacteria, especially nontuberculous mycobacteria, in formalin-fixed paraffin-embedded tissues.
分枝杆菌感染的诊断,尤其是非结核分枝杆菌感染的诊断,在微生物学和病理学领域仍然是一项艰巨的任务。本研究的目的是确定在福尔马林固定石蜡包埋组织中显示可疑肉芽肿病变的情况下,通过聚合酶链反应(PCR)检测到分枝杆菌DNA的频率。共分析了190份存档标本,采用巢式PCR方案,该方案扩增分枝杆菌65 kDa热休克蛋白基因的一个片段。利用限制性片段长度多态性和测序进一步分析获得的PCR产物。41例病例有相应的微生物培养结果。我们在119例(63%)中检测到分枝杆菌DNA,其中71例(60%)结核分枝杆菌复合群DNA呈阳性,41例(34%)非结核分枝杆菌DNA呈阳性。7例(6%)因技术原因无法进行亚型分类。最大的非结核分枝杆菌组包括29例(占119例阳性病例的25%),被归类为偶然分枝杆菌复合群。在8例(7%)中检测到鸟分枝杆菌-胞内分枝杆菌复合群,3例(2.5%)中检测到戈登分枝杆菌,1例(0.8%)中检测到罗得西亚分枝杆菌。所有结核分枝杆菌病例均通过限制性片段长度多态性分析明确鉴定。相比之下,在37%的非结核分枝杆菌病例(41例中的15例)中,测序比限制性片段长度多态性分析提供了更多信息。对非结核分枝杆菌DNA的比对研究显示序列变异频繁,支持序列变种的存在。分子数据与微生物培养试验的现有结果比较显示,一致性良好,为83%。总之,分枝杆菌65 kDa热休克蛋白基因的扩增和测序是福尔马林固定石蜡包埋组织中分枝杆菌,尤其是非结核分枝杆菌菌种鉴定的优秀工具。