Evaluation of ctxA gene expression of Vibrio cholerae strain 569B in the production of cholera vaccine

S. Vorobeva, A. V. Gaeva, O. S. Durakova, A. Kritsky, O. Gromova, O. A. Volokh
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Abstract

Cultivation of production strains of Vibrio cholerae is one of the most important stages in the production of cholera bivalent chemical vaccines. In the production of immunobiological preparations, it is necessary to use producer strains with stable properties that persist in a number of generations. The aim of this study was to evaluate the expression of the ctxA gene using molecular genetic methods of the V. cholerae 569B producing strain. By PCR with electrophoretic accounting of the results, the presence of this strain of the ctxA gene in the chromosome was established. The expression of this gene in all hourly samples of culture fluid was recorded by the method of PCR with reverse transcription, taking into account the results in real time and digital drip PCR. Immunochemical methods confirmed the presence of cholera toxin in the samples, with a maximum mark at the ninth hour, which corresponded to the maximum indicators of the “concentration of microbial cells”. Thus, molecular genetic methods have shown the stability of the production strain V. cholerae 569B in samples of 4 independent cultivations.
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霍乱弧菌569B株ctxA基因在霍乱疫苗生产中的表达评价
霍乱弧菌生产菌株的培养是霍乱二价化学疫苗生产的重要环节之一。在免疫生物学制剂的生产中,有必要使用具有稳定特性的生产菌株,并在几代内持续存在。本研究的目的是利用分子遗传学方法评价霍乱弧菌569B产生菌株ctxA基因的表达。通过PCR和电泳计算结果,确定该菌株在染色体上存在ctxA基因。用反转录PCR法记录每小时培养液样品中该基因的表达,同时考虑实时PCR和数字滴PCR的结果。免疫化学方法证实样品中存在霍乱毒素,在第9小时达到最大值,这与“微生物细胞浓度”的最高指标相对应。因此,分子遗传学方法在4个独立培养的样品中显示了生产菌株569B的稳定性。
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