Flow cytometry study of DNA transformation dynamics in ВНК-21/SUSP/ARRIAH cell culture during rabies virus reproduction

M. Guseva, M. Doronin, M. A. Shevchenko, D. V. Mikhalishin, A. V. Borisov, Yu. S. El’kina, T. V. Okovytaya, V. М. Zakharov, V. Mikhalishin
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Abstract

The study examines the DNA transformation dynamics of ВНК-21/SUSP/ARRIAH subline cells during rabies virus reproduction. Cells infected with the virus and control intact cells were cultivated under similar conditions. The identification of dependence of the virus infectivity on reproduction time revealed that the virus infectivity titre increased from (3.2 ± 0.2) lg CCID50/cm3 at the time of inoculation to (7.63 ± 0.3) lg CCID50/cm3 after 48 hours of reproduction, with the most intensive increase having been observed within the first 24 hours. The cell concentration changed from 0.5 to 1.9 million/cm3, i.e. increased by a factor of 3.8. After 24 hours, the cell growth rate slowed down. Findings from the examination of cell cycle phases during rabies virus reproduction in the host cell allowed for the estimation of duration and predominance of G1, S, G2 + M phases at different stages of cultivation. The dynamics of changes in the apoptotic cell population in the control and test samples was similar within 36 hours of cultivation. After the said period, the proportion of apoptotic infected cells was 28–42% higher than that of apoptotic control cells. After 9 hours, the proportion of cells undergoing G1 phase increased by 11.7% in the test samples, whereas it decreased by 16.6% in the control samples. Subsequently, the number of G1 phase cells in the control and test samples changed in the same way: a 40% decrease was observed after 15–18 hours, it was followed by a 45–46% growth jump, then again a 39–40% decrease and an increase were observed. After 33 hours of reproduction and till the end of cultivation, the proportion of infected cells undergoing G1 phase was significantly higher (by 12–21%) as compared with control cells. The percentage of S phase cells in the test and control samples was the same during the first day of the virus reproduction, with sharp jump-like 3.4- and 2.4-fold increases having been observed after 15 and 24 hours, respectively. After 24 hours, the infected and control cells began to demonstrate differences, which gradually increased from 8 to 137% by the end of reproduction. After 30 hours of reproduction, the proportion of test sample cells undergoing G2 + M phase began to decrease by 17–28% as compared with the control cells. The cell switch-over to the synthesis of complete rabies virus particles occurred after 24 hours of reproduction. This is indicated by changes in the host cell cycle phases, as well as by the slowing down of ВНК-21/SUSP/ARRIAH cell population growth.
对狂犬病毒繁殖过程中ВНК-21/SUSP/ARRIAH 细胞培养中 DNA 转化动态的流式细胞术研究
本研究考察了ВНК-21/SUSP/ARRIAH亚系细胞在狂犬病毒繁殖过程中的DNA转化动态。感染病毒的细胞和完整的对照细胞在相似的条件下进行培养。病毒感染性与繁殖时间的关系鉴定结果表明,病毒感染滴度从接种时的(3.2 ± 0.2)升CCID50/立方厘米增加到繁殖48小时后的(7.63 ± 0.3)升CCID50/立方厘米,在最初的24小时内病毒感染滴度增加最快。细胞浓度从 50 万个/立方厘米变为 190 万个/立方厘米,即增加了 3.8 倍。24 小时后,细胞生长速度减慢。对狂犬病毒在宿主细胞中繁殖过程中细胞周期各阶段的研究结果,可以估计出在不同培养阶段 G1、S、G2 + M 阶段的持续时间和主导地位。在培养的 36 小时内,对照样本和试验样本中凋亡细胞群的动态变化相似。36 小时后,凋亡感染细胞的比例比凋亡对照细胞高 28-42%。9 小时后,试验样本中进入 G1 期的细胞比例增加了 11.7%,而对照样本则减少了 16.6%。随后,对照样本和测试样本中 G1 期细胞的数量发生了同样的变化:15-18 小时后,观察到 G1 期细胞数量减少了 40%,随后增长了 45-46%,接着又减少了 39-40%,然后又增长了 39-40%。繁殖 33 小时后至培养结束,与对照细胞相比,处于 G1 期的感染细胞比例明显增加(12-21%)。在病毒繁殖的第一天,试验样本和对照样本中的 S 期细胞比例相同,但在 15 和 24 小时后分别出现了 3.4 倍和 2.4 倍的急剧跳跃式增长。24 小时后,感染细胞和对照细胞开始出现差异,到繁殖结束时,差异从 8%逐渐增加到 137%。繁殖 30 小时后,与对照细胞相比,处于 G2 + M 期的测试样本细胞比例开始下降 17-28%。繁殖 24 小时后,细胞开始转向合成完整的狂犬病毒颗粒。宿主细胞周期阶段的变化以及ВНК-21/SUSP/ARRIAH 细胞群增长速度的减缓都表明了这一点。
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