首页> 外文期刊>Annals of laboratory medicine. >Evaluation of Dual-Color Fluorescence In Situ Hybridization With Peptide Nucleic Acid Probes for the Detection of Mycobacterium tuberculosis and Non-Tuberculous Mycobacteria in Clinical Specimens
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Evaluation of Dual-Color Fluorescence In Situ Hybridization With Peptide Nucleic Acid Probes for the Detection of Mycobacterium tuberculosis and Non-Tuberculous Mycobacteria in Clinical Specimens

机译:肽核酸探针双色荧光原位杂交在临床标本中检测结核分枝杆菌和非结核分枝杆菌的评估

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Background: Peptide nucleic acid (PNA) probes are artificial DNA analogues with a hydrophobic nature that can penetrate the mycobacterial cell wall. We evaluated a FISH method for simultaneous detection and identification of Mycobacterium tuberculosis (MTB) and non-tuberculous mycobacteria (NTM) in clinical respiratory specimens using differentially labeled PNA probes. Methods: PNA probes targeting the mycobacterial 16S ribosomal RNA were synthesized. The cross-reactivity of MTB- and NTM-specific probes was examined with reference strains and 10 other frequently isolated bacterial species. A total of 140 sputum specimens were analyzed, comprising 100 MTB-positive specimens, 21 NTM-positive specimens, and 19 MTB/NTM-negative specimens; all of them were previously confirmed by PCR and culture. The PNA FISH test results were graded by using the United States Centers for Disease Control and Prevention-recommended scale and compared with the results from the fluorochrome acid-fast bacterial stain. Results: The MTB- and NTM-specific PNA probes showed no cross-reactivity with other tested bacterial species. The test results demonstrated 82.9% agreement with the culture results with diagnostic sensitivity of 80.2% and diagnostic specificity of 100.0% (kappa=0.52, 95% confidence interval: 0.370-0.676). Conclusions: Dual-color PNA FISH showed high specificity for detecting and identifying mycobacteria in clinical specimens. However, because of its relatively low sensitivity, this method could be more applicable to culture confirmation. In application to direct specimens , the possibility of false-negative results needs to be considered.
机译:背景:肽核酸(PNA)探针是具有疏水性质的人造DNA类似物,可穿透分枝杆菌细胞壁。我们使用差异标记的PNA探针评估了FISH方法,用于同时检测和鉴定临床呼吸道标本中的结核分枝杆菌(MTB)和非结核分枝杆菌(NTM)。方法:合成针对分枝杆菌16S核糖体RNA的PNA探针。 MTB和NTM特异性探针的交叉反应性与参考菌株和其他10种经常分离的细菌种类进行了检查。共分析了140个痰标本,包括100个MTB阳性标本,21个NTM阳性标本和19个MTB / NTM阴性标本。所有这些都先前已通过PCR和培养得到证实。通过使用美国疾病控制和预防中心推荐的量表对PNA FISH测试结果进行分级,并与耐荧光染料酸性染料染色的结果进行比较。结果:特定于MTB和NTM的PNA探针与其他受测细菌没有交叉反应。测试结果显示与培养结果一致82.9%,诊断灵敏度为80.2%,诊断特异性为100.0%(kappa = 0.52,95%置信区间:0.370-0.676)。结论:双色PNA FISH对临床标本中分枝杆菌的检测和鉴定具有很高的特异性。但是,由于其灵敏度较低,因此该方法可能更适用于培养确认。在直接样品中,需要考虑假阴性结果的可能性。

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