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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Peptide nucleic acid-fluorescence in situ hybridization (PNA-FISH) assay for specific detection of Mycobacterium immunogenum and DNA-FISH assay for analysis of pseudomonads in metalworking fluids and sputum.
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Peptide nucleic acid-fluorescence in situ hybridization (PNA-FISH) assay for specific detection of Mycobacterium immunogenum and DNA-FISH assay for analysis of pseudomonads in metalworking fluids and sputum.

机译:用于分枝杆菌免疫原特异性检测的肽核酸荧光原位杂交(PNA-FISH)测定和用于金属加工液和痰液中假单核细胞分析的DNA-FISH测定。

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摘要

Specific and rapid detection and quantification of mycobacteria in contaminated metalworking fluid (MWF) are problematic due to complexity of the matrix and heavy background co-occurring microflora. Furthermore, cross-reactivity among neighboring species of Mycobacterium makes species differentiation difficult for this genus. Here, we report for the first time a species-specific peptide nucleic acid-fluorescence in situ hybridization (PNA-FISH) method for Mycobacterium immunogenum, a non-tuberculous Mycobacterium species prevalent in MWF and implicated in occupational lung disease hypersensitivity pneumonitis and pseudo-outbreaks. A novel species-specific 14-bp PNA probe was designed for M. immunogenum based on its 16S rRNA gene sequence and was validated for specificity, by testing against a panel of other phylogenetically closely related rapidly growing mycobacteria and representative species of gram-positive, gram-negative, and acid fast organisms. In addition, a DNA-FISH protocol was optimized for co-detection of Pseudomonas, the most predominantly co-occurring genus in contaminated MWF. Reliable quantification for both the test organisms was achieved at or above a cell density of 10(3)cellsml(-1), a recognized minimum limit for microscopic quantification. The mycobacterial PNA-FISH assay was successfully adapted to human sputum demonstrating its potential for clinical diagnostic applications in addition to industrial MWF monitoring, to assess MWF-associated exposures and pseudo-outbreaks.
机译:由于基质的复杂性和背景中同时存在的大量菌群,因此对污染的金属加工液(MWF)中的分枝杆菌进行特异性,快速的检测和定量分析存在问题。此外,分枝杆菌的邻近物种之间的交叉反应性使得该属难以进行物种分化。在这里,我们首次报道了一种针对分枝杆菌免疫原的种特异性肽核酸-荧光原位杂交(PNA-FISH)方法,一种非结核性分枝杆菌在MWF中盛行,并与职业性肺病超敏性肺炎和假性肺炎有关。爆发。一种新型的物种特异性14 bp PNA探针基于其16S rRNA基因序列设计用于免疫分枝杆菌,并通过针对一组其他系统发育密切相关的快速增长的分枝杆菌和代表性革兰氏阳性菌进行了验证,从而验证了特异性。革兰氏阴性和耐酸生物。此外,优化了DNA-FISH方案以共检测假单胞菌,这是被污染的MWF中最主要同时出现的属。在10(3)cellsml(-1)或更高的细胞密度(显微镜定量的公认最低限度)下,可以实现对两种测试生物的可靠定量。分枝杆菌PNA-FISH测定法成功地应用于人类痰液,证明了其在工业MWF监测之外的临床诊断应用潜力,以评估MWF相关的暴露和假性暴发。

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