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一种用于检测新型口服脊髓灰质炎病毒2型中Sabin 2病毒污染的定量一步法逆转录聚合酶链反应方法的开发。

Development of a Quantitative One-Step RT-PCR Method for the Detection of Sabin 2 Virus Contamination in a Novel Oral Poliovirus Vaccine Type 2.

作者信息

Manukyan Hasmik, Tritama Erman, Wahid Rahnuma, Ansari Azeem, Konz John, Chumakov Konstantin, Laassri Majid

机构信息

Division of Viral Products, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD 20993, USA.

Research and Development Division, PT. Bio Farma, Bandung 40161, Indonesia.

出版信息

Vaccines (Basel). 2021 Jun 23;9(7):688. doi: 10.3390/vaccines9070688.

Abstract

To control circulating vaccine-derived type 2 poliovirus outbreaks, a more genetically stable novel Oral Poliovirus Vaccine type 2 (nOPV2) was developed by targeted modifications of Sabin 2 genome. Since the use of OPV2 made of Sabin 2 strain has been stopped, it is important to exclude the possibility that batches of nOPV2 are contaminated with Sabin 2 virus. Here, we report the development of a simple quantitative one-step reverse-transcription polymerase chain reaction assay for the detection and quantitation of Sabin 2 virus in the presence of overwhelming amounts of nOPV2 strain. The method is specific and linear within 8 log range even in the presence of relevant amounts of nOPV2 virus. It is sensitive, with a lower limit of detection of 0.2 CCID/mL (an equivalent of 198 genome copies per mL), and generates reproducible results. This assay can be used for quality control and lot release of the nOPV2.

摘要

为控制循环疫苗衍生2型脊髓灰质炎病毒疫情,通过对Sabin 2基因组进行靶向修饰,研发出了一种基因更稳定的新型2型口服脊髓灰质炎疫苗(nOPV2)。由于已停止使用由Sabin 2毒株制成的OPV2,排除nOPV2批次被Sabin 2病毒污染的可能性很重要。在此,我们报告了一种简单的定量一步法逆转录聚合酶链反应检测方法的开发,用于在存在大量nOPV2毒株的情况下检测和定量Sabin 2病毒。该方法具有特异性,即使在存在相关量的nOPV2病毒时,在8个对数范围内也呈线性。它很灵敏,检测下限为0.2 CCID/mL(相当于每毫升198个基因组拷贝),并能产生可重复的结果。该检测方法可用于nOPV2的质量控制和批放行。

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