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Development and evaluation of the kit for detection of SARS-associated Coronavirus RNA.

机译:检测SARS相关冠状病毒RNA的试剂盒的开发和评价。

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AIM: To develop a diagnostic kit for detection of SARS (severe acute respiratory syndrome)-related coronavirus RNA based on reverse transcription and polymerase chain reaction and to estimate its specificity and sensitivity. MATERIAL AND METHODS: 68 virus and bacterial cultures, 240 clinical samples from people without SARS symptoms and also 22 RNA samples from patients with SARS symptoms received during the epidemic in Beijing were used. RESULTS: The specificity of the kit was determined using animal coronaviruses and other bacterial and viral strains, causing acute respiratory and intestinal infections, and was shown to be 100%. The sensitivity of the kit in different clinical samples was 2.2 x 10(3) genome equivalents of recombinant SARS RNA in 1 ml of the specimen. The kit was evaluated in the Institute of Microbiology and Epidemiology of Beijing (China) using SARS-cov viral suspension and clinical samples from patients with suspected SARS. It was shown that kit was able to detect 10 TCID/50 ml of SARS-Cov virus. Testing of clinical samples from patients with suspected SARS showed that diagnostic sensitivity of the kit was 95%. Detection of the SARS-Cov RNA was more effective in feces compared to sputum 990 and 40%, respectively). CONCLUSION: The kit "AmpliSens SARS" for qualitative detection of SARS-related coronavirus RNA by reverse transcription and polymerase chain reaction (PCR) in nasopharyngeal wash/aspirates, naso/oropharyngeal swabs, plasma, and extract from feces has been developed in the Central Research Institute for Epidemiology of the RF Ministry of Health. The kit contains reagents for RNA isolation and purification, cDNA synthesis by reverse transcription of RNA, for PCR and for electrophoretic analysis of amplified products. The kit also contains recombinant positive and internal control samples allowing to control efficiency of analysis and showed good analytical and diagnostic characteristics.
机译:目的:基于逆转录和聚合酶链反应,开发用于检测SARS(严重急性呼吸道综合征)的冠状病毒RNA的诊断试剂盒,并估计其特异性和敏感性。材料和方法:68例病毒和细菌培养物,使用来自人群的240名临床样本,没有SARS症状,也使用了在北京流行病中收到的SARS症状患者的22个RNA样本。结果:使用动物冠状病毒和其他细菌和病毒菌株测定试剂盒的特异性,导致急性呼吸和肠道感染,并显示为100%。在不同临床样品中的试剂盒的敏感性为2.2×10(3)个基因组当量的重组SAR RNA,在1mL样品中。该试剂盒在北京(中国)的微生物学和流行病学研究所评估,使用SARS-COV病毒悬浮液和受疑SARS患者的临床样本。结果表明,试剂盒能够检测10个TCID / 50ml SARS-COV病毒。疑似SARS患者的临床样本测试表明,试剂盒的诊断敏感性为95%。与痰990和40%分别相比,SARS-COV RNA的检测在粪便中更有效)。结论:在中央开发了通过逆转录/吸气,鼻咽癌和聚合酶链反应(PCR)对SARS相关冠状病毒RNA进行定性检测的试剂盒“SARS”,中央卫生院射频流行病学研究所。该试剂盒含有用于RNA分离和纯化的试剂,通过RNA的逆转录,用于PCR的CDNA合成,并用于扩增产物的电泳分析。该试剂盒还含有重组阳性和内部对照样品,可控制分析效率并显示出良好的分析和诊断特性。

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