National Institute of Animal Science, Rural Development Administration, Wanju, Republic of Korea.
Laboratory of Veterinary Pathology and Biosafety Research Institute, College of Veterinary Medicine, Jeonbuk National University, Iksan, Republic of Korea.
Emerg Microbes Infect. 2024 Dec;13(1):2366406. doi: 10.1080/22221751.2024.2366406. Epub 2024 Jun 26.
African swine fever, caused by African swine fever virus (ASFV), is a highly contagious and fatal disease that poses a significant threat to the global pig industry. The limited information on ASFV pathogenesis and ASFV-host interactions has recently prompted numerous transcriptomic studies. However, most of these studies have focused on elucidating the transcriptome profiles of ASFV-infected porcine alveolar macrophages . Here, we analyzed dynamic transcriptional patterns in nine organ tissues (spleen, submandibular lymph node, mesenteric lymph node, inguinal lymph node, tonsils, lungs, liver, kidneys, and heart) obtained from pigs in the early stages of ASFV infection (1 and 3 d after viremia). We observed rapid spread of ASFV to the spleen after viremia, followed by broad transmission to the liver and lungs and subsequently, the submandibular and inguinal lymph nodes. Profound variations in gene expression patterns were observed across all organs and at all time-points, providing an understanding of the distinct defence strategies employed by each organ against ASFV infection. All ASFV-infected organs exhibited a collaborative response, activating immune-associated genes such as , thereby triggering a pro-inflammatory cytokine storm and interferon activation. Functional analysis suggested that ASFV exploits the PI3K-Akt signalling pathway to evade the host immune system. Overall, our findings provide leads into the mechanisms underlying pathogenesis and host immune responses in different organs during the early stages of infection, which can guide further explorations, aid the development of efficacious antiviral strategies against ASFV, and identify valuable candidate gene targets for vaccine development.
非洲猪瘟由非洲猪瘟病毒(ASFV)引起,是一种高度传染性和致命性疾病,对全球养猪业构成重大威胁。ASFV 发病机制和 ASFV-宿主相互作用的信息有限,最近促使了许多转录组研究。然而,大多数这些研究都集中在阐明 ASFV 感染猪肺泡巨噬细胞的转录组谱。在这里,我们分析了来自感染 ASFV 早期(病毒血症后 1 和 3 天)猪的九个器官组织(脾、颌下淋巴结、肠系膜淋巴结、腹股沟淋巴结、扁桃体、肺、肝、肾和心脏)的动态转录模式。我们观察到病毒血症后 ASFV 迅速传播到脾脏,随后广泛传播到肝脏和肺部,然后是颌下和腹股沟淋巴结。所有器官在所有时间点的基因表达模式都发生了深刻的变化,这为了解每个器官对 ASFV 感染的不同防御策略提供了依据。所有感染 ASFV 的器官都表现出协同反应,激活免疫相关基因,如,从而引发促炎细胞因子风暴和干扰素激活。功能分析表明,ASFV 利用 PI3K-Akt 信号通路来逃避宿主免疫系统。总之,我们的研究结果为感染早期不同器官的发病机制和宿主免疫反应提供了线索,有助于进一步探索,为开发有效的抗 ASFV 抗病毒策略提供支持,并确定疫苗开发的有价值的候选基因靶标。