Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran.
Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran.
Vet Immunol Immunopathol. 2023 Oct;264:110658. doi: 10.1016/j.vetimm.2023.110658. Epub 2023 Sep 22.
The infectious bursal disease virus (IBDV) causes an acute and highly contagious immunosuppressive response in young chickens by targeting B lymphocytes in immune organs. Changes in regulatory T-cell ratio and apoptosis have been demonstrated during IBDV infection in these cells. The possible change in CD19 expression as the precursor of B cells after IBDV replication was detected in this study. Raji cells were infected with an IBDV isolate at MOIs of 1.0 and 3.0. The viral kinetics were determined using the characteristic virus-induced CPE, cell viability, and infectious titer. Induction of apoptosis and also changes in the CD19 expression within the virus infection were assessed by flow cytometry. The Raji cells were found to be susceptible to IBDV infection by producing marked CPEs dependent on MOI. The infectivity titers were determined in intra- and extracellular samples at the defined hours. The kinetics of early IBDV replication in Raji cells were nearly identical for both MOIs, but a significant difference in the infectivity titer was observed at 48 hpi. The quick apoptotic events were observed to be significantly higher in MOI 3.0, which was correlated with the lower virus titer. A significant CD19 expression change in the IBDV-infected Raji cells was revealed. The results suggested that Raji cells mimic the IBDV replication in lymphoid organs and the virus replication is related to CD19 expression frequencies in the lymphoid cells.
传染性法氏囊病病毒 (IBDV) 通过靶向免疫器官中的 B 淋巴细胞,在雏鸡中引起急性和高度传染性的免疫抑制反应。在这些细胞中感染 IBDV 时,已经证明调节性 T 细胞比例和细胞凋亡发生变化。本研究检测到 IBDV 复制后作为 B 细胞前体的 CD19 表达可能发生变化。用 MOI 为 1.0 和 3.0 的 IBDV 分离株感染 Raji 细胞。使用特征性病毒诱导的 CPE、细胞活力和感染滴度来确定病毒动力学。通过流式细胞术评估细胞凋亡的诱导以及病毒感染过程中 CD19 表达的变化。Raji 细胞易受 IBDV 感染,产生依赖 MOI 的明显 CPE。在规定的时间点,在细胞内和细胞外样本中测定感染性滴度。两种 MOI 的 Raji 细胞中早期 IBDV 复制的动力学几乎相同,但在 48 hpi 时观察到感染性滴度存在显著差异。在 MOI 3.0 下观察到的快速凋亡事件明显更高,这与较低的病毒滴度相关。在 IBDV 感染的 Raji 细胞中发现 CD19 表达发生显著变化。结果表明,Raji 细胞模拟了淋巴器官中的 IBDV 复制,病毒复制与淋巴细胞中 CD19 表达频率有关。