Saravanan P, Sen A, Balamurugan V, Bandyopadhyay S K, Singh R K
National Morbillivirus Referral Laboratory, Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus, Distt. Nainital, Uttaranchal 263138, India.
Biologicals. 2008 Jan;36(1):1-6. doi: 10.1016/j.biologicals.2007.03.005. Epub 2007 Jul 19.
Peste des petits ruminants (PPR) is a highly contagious and economically important viral disease of goats and sheep. A homologous Vero cell-based attenuated PPR vaccine developed in our laboratory and used extensively throughout the country, is available for control of PPR. The presently used quality control test, titration in Vero cells for PPR virus titre in vaccine batches, takes at least 6-8days to determine the quality and dose of vaccine. In this study, 74 freeze-dried PPR vaccine batches were tested simultaneously by both virus titration and PPR sandwich ELISA (S-ELISA) to correlate the titre of the vaccine virus with reactivity in S-ELISA. It was found that the vaccine batches with titre more than 10(3)TCID(50)/ml gave positive results in S-ELISA and correlated well with the virus titre of the freeze-dried vaccines. The correlation coefficient between the virus titration and S-ELISA reactivity was estimated as 0.96, indicating a high correlation between the two parameters based on 74 batches of freeze-dried PPR vaccine. The vaccine batches with titres of 3.0, 4.3, 4.5, 5.0, 6.5 and 7.0 had shown a positive reaction when tested in two-fold dilutions in S-ELISA at 1, 5, 6, 7, 8 and 9log2 titres, respectively. The test vaccine batches were found to be negative in S-ELISA when the titre of the vaccine was less than 10(3)TCID50/ml, suggesting that the vaccine could not be passed for field use. It is concluded that S-ELISA could be a preliminary tool useful for the quality control of PPR vaccine as it is rapid and easy to perform when compared to virus titration.
小反刍兽疫(PPR)是山羊和绵羊的一种高度传染性且具有重要经济意义的病毒性疾病。我们实验室研发的一种基于同源Vero细胞的减毒PPR疫苗在全国广泛使用,可用于控制PPR。目前使用的质量控制测试,即通过在Vero细胞中滴定来测定疫苗批次中PPR病毒滴度,至少需要6 - 8天才能确定疫苗的质量和剂量。在本研究中,同时采用病毒滴定和PPR夹心ELISA(S - ELISA)对74批冻干PPR疫苗进行检测,以关联疫苗病毒滴度与S - ELISA中的反应性。结果发现,病毒滴度超过10(3)TCID(50)/ml的疫苗批次在S - ELISA中呈阳性结果,且与冻干疫苗的病毒滴度相关性良好。病毒滴定与S - ELISA反应性之间的相关系数估计为0.96,表明基于74批冻干PPR疫苗,这两个参数之间具有高度相关性。病毒滴度分别为3.0、4.3、4.5、5.0、6.5和7.0的疫苗批次,在S - ELISA中以1、5、6、7、8和9log2滴度进行两倍稀释检测时,均显示阳性反应。当疫苗滴度低于10(3)TCID50/ml时,测试的疫苗批次在S - ELISA中呈阴性,这表明该疫苗不能通过现场使用的检测。结论是,与病毒滴定相比,S - ELISA快速且易于操作,可作为PPR疫苗质量控制的一种初步有用工具。