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运用聚合酶链反应检测商业猪疫苗中的1型猪圆环病毒。

Detection of porcine circovirus type 1 in commercial pig vaccines using polymerase chain reaction.

作者信息

Quintana Josefina, Segalés Joaquim, Calsamiglia Maria, Domingo Mariano

机构信息

Centre de Recerca en Sanitat Animal (CReSA), Departament de Sanitat i d'Anatomia Animals, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.

出版信息

Vet J. 2006 May;171(3):570-3. doi: 10.1016/j.tvjl.2004.12.008. Epub 2005 Jan 19.

Abstract

The absence of extraneous viruses is a requirement in the quality control of vaccines for veterinary use in the European Pharmacopoeia. A polymerase chain reaction (PCR) assay for the detection of porcine circovirus type 1 (PCV1) and type 2 (PCV2) was evaluated in 18 commercial porcine vaccines. Since vaccine components may contain PCR enhancers or inhibitors, 13 of the studied vaccines (used as diluents) were subsequently spiked with different dilutions of PCV2 and tested by PCR. Although PCV2 DNA was not detected in any of the vaccines tested, PCV1 was detected in 2/18 vaccines (11%). Eleven out of 13 PCV2 spiked vaccines showed a positive PCR result. The lack of amplification observed in two spiked vaccines suggested that use of the PCR assay to detect PCV2 could depend on vaccine composition. The results of this exploratory study have demonstrated that PCR is a rapid and fairly sensitive method for the detection of porcine circoviruses as extraneous agents in vaccine products and can be used in the quality control of pig vaccines. The study has also indicated the need for optimising the sensitivity of PCR methods for PCV genome detection in vaccine products.

摘要

欧洲药典中规定兽用疫苗质量控制时不得含有外源病毒。对18种市售猪用疫苗进行了检测猪圆环病毒1型(PCV1)和2型(PCV2)的聚合酶链反应(PCR)分析。由于疫苗成分可能含有PCR增强剂或抑制剂,随后将13种受试疫苗(用作稀释剂)加入不同稀释度的PCV2并进行PCR检测。尽管在所检测的任何疫苗中均未检测到PCV2 DNA,但在18种疫苗中的2种(11%)检测到了PCV1。13种加入PCV2的疫苗中有11种PCR结果呈阳性。在两种加入PCV2的疫苗中未观察到扩增,这表明使用PCR分析检测PCV2可能取决于疫苗成分。这项探索性研究的结果表明,PCR是一种快速且相当灵敏的检测疫苗产品中外源因子猪圆环病毒的方法,可用于猪疫苗的质量控制。该研究还表明需要优化PCR方法检测疫苗产品中PCV基因组的灵敏度。

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