Zhang Zhenjie, Liu Shaoqiong, Ma Chengtai, Zhao Peng, Cui Zhizhong
Collaborative Innovation Center for the Origin and Control of Emerging Infectious Diseases, Taishan Medical College, Taian 271000, China.
College of Veterinary Medicine, Shandong Agricultural University, Taian 271018, China.
Poult Sci. 2015 Jun;94(6):1150-7. doi: 10.3382/ps/pev063. Epub 2015 Mar 31.
Chickens infected with Marek's disease virus (MDV) carry the virus consistently for a long time, which increases the incidence and rate of virus-induced multi-organ tumors and increases its potential for horizontal transmission. There is a positive correlation between very virulent (vv) MDV quantity and the pathology. The purpose of this study was to determine the vvMDV loads dynamics in different phases, and the correlation between the viral quantity and tumor development. We used a SYBR Green duplex real-time quantitative PCR (q-PCR) assay to detect and quantify MDV loads and distributions in different tissues, targeting the Eco-Q protein gene (meq) of the virus and the house-keeping ovotransferrin (ovo) gene of chickens. The q-PCR was performed using different tissue DNA preparations derived from chickens which were infected with 1,000 pfu of the SDWJ1302 strain and tissue samples were collected from control and MDV-infected birds on 7, 10, 15, 21, 28, 40, 60, and 90 d post-infection (DPI). The data indicated that the MDV genome was almost quantifiable in immune organs of infected chickens as early as 7 DPI, and the number of MDV genome copies in the blood and different organs peaked by 28 DPI, but then gradually decreased by 40 DPI. The levels of viral quantity in the lymphocytes, liver, and spleen were all higher than those in other organs, and that in the feather follicles was the highest among different phases of MDV infection. The vvMDV could still be detected in peripheral blood and tissues by 90 DPI, and the vast existence of virus will stimulate tissue destruction. The data provided further evidence of viral infection involving multi-organ distribution and mainly involving immune organ proliferation, resulting in immunosuppression.
感染马立克氏病病毒(MDV)的鸡会长期持续携带该病毒,这增加了病毒诱导的多器官肿瘤的发生率和比例,并提高了其水平传播的可能性。超强毒(vv)MDV的数量与病理学之间存在正相关。本研究的目的是确定不同阶段vvMDV载量的动态变化,以及病毒数量与肿瘤发展之间的相关性。我们使用SYBR Green双重实时定量PCR(q-PCR)检测方法,以病毒的Eco-Q蛋白基因(meq)和鸡的看家卵转铁蛋白(ovo)基因为靶点,检测并定量不同组织中的MDV载量和分布。使用感染了1000 pfu SDWJ1302株的鸡的不同组织DNA制剂进行q-PCR,并在感染后7、10、15、21、28、40、60和90天(DPI)从对照鸡和MDV感染鸡中采集组织样本。数据表明,早在感染后7天,感染鸡的免疫器官中MDV基因组几乎就可被定量,血液和不同器官中MDV基因组拷贝数在感染后28天达到峰值,但随后在感染后40天逐渐下降。淋巴细胞、肝脏和脾脏中的病毒数量水平均高于其他器官,且在MDV感染的不同阶段,毛囊中的病毒数量水平最高。到感染后90天,仍可在外周血和组织中检测到vvMDV,病毒的大量存在会刺激组织破坏。这些数据进一步证明了病毒感染涉及多器官分布,主要涉及免疫器官增殖,从而导致免疫抑制。