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作 者:于纪棉[1] 李如松[2] 倪健波[2] 魏姣姣 高峰[3] 王建峰[2] YU Ji - mian LI Ru - song NI Jian - bo WEI Jiao - jiao GAO Feng WANG Jian - feng(Ningbo College of Health Sciences, Ningbo, Zhejiang 315100, China)
机构地区:[1]宁波卫生职业技术学院,浙江宁波315100 [2]宁波出入境检验检疫局,浙江宁波315012 [3]盐城出入境检验检疫局,江苏盐城224002
出 处:《中国卫生检验杂志》2017年第9期1233-1236,1239,共5页Chinese Journal of Health Laboratory Technology
基 金:宁波市自然科学基金项目(2014A610273);宁波市科技创新团队(2015C110018);江苏检验检疫局科研项目(2014KJ03)
摘 要:目的建立嗜肺军团菌微滴式数字PCR(droplet digital PCR,ddPCR)检测方法,并与实时荧光定量PCR(realtime fluorescence quantitative PCR,qPCR)技术进行比较。方法针对嗜肺军团菌mip基因设计引物和探针,验证其特异性后,用于ddPCR和qPCR。优化ddPCR的退火温度、引物、探针浓度后,比较ddPCR和qPCR灵敏度和重复性,并对模拟样品进行检测。结果用5株非嗜肺军团菌测试特异性,结果表明具有良好的特异性。ddPCR与qPCR对DNA模板的检测限一致(42.6 fg),模拟样品检出限为300 cfu/ml,ddPCR的线性相关系数(0.999)略优于qPCR(0.982),ddPCR检测的RSD(0.78%~14.06%)均高于qPCR(0.30%~1.98%)。结论微滴式数字PCR方法灵敏度高、特异性强,可用于嗜肺军团菌检测,且可以对基因进行绝对定量。Objective To establish a droplet digital PCR(ddPCR) method for the detection of Legionella pneumophila and comparison with real - time fluorescence quantitative PCR ( qPCR). Methods The primers and probe were designed for ddPCR and qPCR according to mip gene after verifying its specificity. The annealing temperature, primer, probe concentration of ddPCR were optimized simultaneously. The sensitivity and repeatability of the 2 methods were compared, and the simulated samples were tested. Results The highly specificity of thisprimers and probe was evaluated using 5 non - targeted bacteria. The detection limits of ddPCR and qPCR for DNA were 42.6 fg and 300 cfu/ml for artificially samples. The ddPCR(0. 999) showed slightly higher degree of linearity than the qPCR (0. 982 ). The relative standard deviation (RSD) of ddPCR (0. 78 % - 14.06% ) was higher than that of qPCR(0.30% - 1. 98% ). Conclusion The ddPCR is of high sensitivity and specificity, and can be used for the detection of Legionella pneumophila. And it can perform full quantitativity to gene.
关 键 词:嗜肺军团菌 微滴式数字PCR 实时荧光定量PCR 检测
分 类 号:R378.99[医药卫生—病原生物学]
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