Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agricultural and Forestry Sciences, Beijing 100097, China.
College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Viruses. 2022 Dec 20;15(1):6. doi: 10.3390/v15010006.
Marek's disease virus (MDV) infection results in Marek's disease (MD) in chickens, a lymphoproliferative and oncogenic deadly disease, leading to severe economic losses. The spleen and bursa are the most important lymphoid and major target organs for MDV replication. The immune response elicited by MDV replication in the spleen and bursa is critical for the formation of latent MDV infection and reactivation. However, the mechanism of the host immune response induced by MDV in these key lymphoid organs during the latent and reactivation infection phases is not well understood. In the study, we focused on the replication dynamics of a vaccine MDV strain MDV/CVI988 and a very virulent MDV strain MDV/RB1B in the spleen and bursa in the latent and reactivation infection phases (7-28 days post-inoculation [dpi]), as well as the expression of some previously characterized immune-related molecules. The results showed that the replication ability of MDV/RB1B was significantly stronger than that of MDV/CVI988 within 28 days post-infection, and the replication levels of both MDV strains in the spleen were significantly higher than those in the bursa. During the latent and reactivation phase of MDV infection (7-28 dpi), the transcriptional upregulation of chicken IL-1β, IL6, IL-8L1 IFN-γ and PML in the spleen and bursa induced by MDV/RB1B infection was overall stronger than that of MDV/CVI988. However, compared to MDV/RB1Binfection, MDV/CVI988 infection resulted in a more effective transcriptional activation of CCL4 in the latent infection phase (7-14 dpi), which may be a characteristic distinguishing MDV vaccine strain from the very virulent strain.
马立克氏病病毒(MDV)感染导致鸡马立克氏病(MD),这是一种淋巴增生性和致癌性的致命疾病,导致严重的经济损失。脾脏和法氏囊是 MDV 复制的最重要的淋巴器官和主要靶器官。MDV 复制在脾脏和法氏囊中引起的免疫反应对于潜伏 MDV 感染和再激活的形成至关重要。然而,宿主对 MDV 在这些关键淋巴器官中的复制所引起的免疫反应的机制在潜伏和再激活感染阶段尚不清楚。在这项研究中,我们专注于疫苗 MDV 株 MDV/CVI988 和非常强毒力 MDV 株 MDV/RB1B 在潜伏和再激活感染阶段(感染后 7-28 天)在脾脏和法氏囊中的复制动态,以及一些先前表征的免疫相关分子的表达。结果表明,在感染后 28 天内,MDV/RB1B 的复制能力明显强于 MDV/CVI988,并且两种 MDV 株在脾脏中的复制水平明显高于法氏囊。在 MDV 感染的潜伏和再激活阶段(7-28 dpi),由 MDV/RB1B 感染引起的脾脏和法氏囊中鸡 IL-1β、IL6、IL-8L1 IFN-γ 和 PML 的转录上调总体上强于 MDV/CVI988。然而,与 MDV/RB1B 感染相比,MDV/CVI988 感染导致潜伏感染阶段(7-14 dpi)中 CCL4 的转录激活更有效,这可能是区分 MDV 疫苗株和非常强毒力株的特征。