International Livestock Research Institute, P.O. Box 30709-00100, Nairobi, Kenya.
Vet Parasitol. 2011 Jun 30;179(1-3):62-8. doi: 10.1016/j.vetpar.2011.01.057. Epub 2011 Mar 1.
The current Infection and Treatment Method of vaccination against East Coast fever comprises an inoculation of live Theileria parva sporozoites and simultaneous administration of oxytetracycline. Immunization with a combination of parasite types has been shown to provide broader protection than inoculation of individual strains. In this study, we used a high-throughput capillary electrophoresis system to determine the genotypic composition of the Muguga Cocktail, a widely used vaccine stabilate derived from three seed stabilates-Muguga, Serengeti-transformed and Kiambu 5. Five satellite markers were used to genotype the vaccine and reference stabilates from two commercial-scale preparations of the vaccine. In addition, 224 cloned cell lines established by infection of bovine lymphocytes with T. parva parasites from the component stabilates were genotyped. The results indicate that, for the recently prepared batch, there are at least eight genotypes in each of the Muguga and the Serengeti-transformed stabilates, while parasites from the Kiambu 5 stabilate showed no diversity at the five loci. The Serengeti-transformed stabilate contained parasites of the Kiambu 5 genotype and of two genotypes present in the Muguga stabilate, whereas there were no genotypes common to the Muguga and Kiambu 5 stabilates. When stabilates from the two vaccine batches were compared, no allelic variations were identified between the Muguga and Kiambu 5 parasites, while lack of sufficient clones prevented a full comparison of the Serengeti-transformed stabilates. The findings will facilitate examination of the extent to which the vaccine strains become resident in areas under vaccination, the identification of 'breakthrough' strains and the establishment of the quality assurance protocols to detect variations in the production of the vaccine. The cloned cell lines will be useful for further understanding the antigenic diversity of parasites in the vaccine.
东非牛瘟的现行感染与治疗方法包括接种活泰勒虫孢子和同时使用土霉素。用寄生虫混合类型进行免疫已被证明比单独接种株能提供更广泛的保护。在这项研究中,我们使用高通量毛细管电泳系统来确定 Muguga 鸡尾酒(一种广泛使用的疫苗稳定剂)的基因型组成,该稳定剂由三种种子稳定剂(Muguga、Serengeti 转化和 Kiambu 5)衍生而来。使用五个卫星标记对两种商业规模制备的疫苗和参考稳定剂进行基因分型。此外,还对来自成分稳定剂的 T. parva 寄生虫感染牛淋巴细胞建立的 224 个克隆细胞系进行了基因分型。结果表明,对于最近制备的批次,Muguga 和 Serengeti 转化稳定剂中每个都至少有 8 种基因型,而 Kiambu 5 稳定剂中的寄生虫在五个基因座上没有多样性。Serengeti 转化稳定剂含有 Kiambu 5 基因型的寄生虫和 Muguga 稳定剂中存在的两种基因型的寄生虫,而 Muguga 和 Kiambu 5 稳定剂中没有共同的基因型。当比较两种疫苗批次的稳定剂时,Muguga 和 Kiambu 5 寄生虫之间没有发现等位基因变异,而缺乏足够的克隆阻止了对 Serengeti 转化稳定剂的充分比较。这些发现将有助于检查疫苗株在接种区域内定居的程度,鉴定“突破”株,并建立质量保证协议来检测疫苗生产中的变异。克隆细胞系将有助于进一步了解疫苗中寄生虫的抗原多样性。