分子信标
肽核酸
假阳性率
荧光
化学
假阳性悖论
色谱法
分子生物学
生物
核酸
生物化学
寡核苷酸
DNA
光学
统计
物理
机器学习
计算机科学
数学
作者
Shan Wu,Xiaofeng Zhang,Jiangbing Shuai,Ke Li,Huizhen Yu,Chenchen Jin
出处
期刊:PubMed
日期:2016-07-04
卷期号:56 (7): 1105-12
被引量:2
摘要
To simplify the PNA-FISH (Peptide nucleic acid-fluorescence in situ hybridization) test, molecular beacon based PNA probe combined with fluorescence scanning detection technology was applied to replace the original microscope observation to detect Listeria monocytogenesThe 5′ end and 3′ end of the L. monocytogenes specific PNA probes were labeled with the fluorescent group and the quenching group respectively, to form a molecular beacon based PNA probe.When PNA probe used for fluorescence scanning and N1 treatment as the control, the false positive rate was 11.4%, and the false negative rate was 0; when N2 treatment as the control, the false positive rate decreased to 4.3%, but the false negative rate rose to 18.6%. When beacon based PNA probe used for fluorescence scanning, taken N1 treatment as blank control, the false positive rate was 8.6%, and the false negative rate was 1.4%; taken N2 treatment as blank control, the false positive rate was 5.7%, and the false negative rate was 1.4%. Compared with PNA probe, molecular beacon based PNA probe can effectively reduce false positives and false negatives. The success rates of hybridization of the two PNA probes were 83.3% and 95.2% respectively; and the rates of the two beacon based PNA probes were 91.7% and 90.5% respectively, which indicated that labeling the both ends of the PNA probe dose not decrease the hybridization rate with the target bacteria.The combination of liquid phase PNA-FISH and fluorescence scanning method, can significantly improve the detection efficiency.
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