Shi Fengyang, Xu Zhen, Gao Peng, Qu Yajin, Ge Xinna, Zhang Yongning, Han Jun, Guo Xin, Zhou Lei, Yang Hanchun
National Key Laboratory of Veterinary Public Health Safety, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Key Laboratory of Animal Epidemiology of Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing, China.
J Virol. 2025 Jul 22;99(7):e0069025. doi: 10.1128/jvi.00690-25. Epub 2025 Jun 12.
African swine fever virus (ASFV) is an economically devastating pathogen that can cause fatal infections in both domestic pigs and wild boar, with monocytes and macrophages as its target cells. For macrophages, phagocytosis is a fundamental and crucial process, which is usually suppressed by the virus, impeding pathogen clearance and antigen presentation. However, it was unexpectedly found that ASFV infection enhances the phagocytic ability of primary porcine alveolar macrophages (PAMs), as evaluated using an EGFP-labeled bacterial phagocytosis model. The phagocytic processes, including cell migration, bacterial adhesion, pseudopod extension, and pattern recognition receptor (PRR) expression, in ASFV-infected PAMs were systematically investigated. In addition, the upregulated PRRs were knocked down to analyze their role in enhanced phagocytosis. CD14, a receptor of LPS and phospholipid, was identified as being upregulated by ASFV, leading to enhanced bacterial uptake. Further exploration revealed that ASFV's genomic nucleic acid in infected PAMs activates the cGAS/STING/NF-κB pathway to increase CD14 expression. Meanwhile, the free ASFV nucleic acid released from infected PAMs can also activate CD14 expression in bystander PAMs via the TLR9 pathway, facilitating ASFV transmission via apoptotic bodies (ApoBDs). Moreover, the boosted bacterial phagocytosis in the early stages of ASFV infection potentially creates a more inflamed environment with more intense cytokine production. Here, it reveals a critical mechanism by which ASFV enhances CD14-dependent bacterial uptake in PAMs via the cGAS/STING/NF-κB and TLR9 pathways, promoting viral transmission through ApoBDs and amplifying inflammatory responses to bacterial co-infections, providing vital insights into ASFV pathogenesis and host immune manipulation.IMPORTANCEPorcine alveolar macrophages (PAMs) are the target cells of African swine fever virus (ASFV), but how ASFV impacts their phagocytic function is less known. Here, it was discovered that the nucleic acids of ASFV can enhance the expression of CD14, a receptor of LPS and phospholipid, in infected PAMs via the cGAS/STING/NF-κB pathway, or in bystander PAMs via the TLR9 pathway. Consequently, enhanced CD14 expression facilitates the uptake of bacteria and apoptotic bodies (ApoBDs), promoting the inflammatory response and ASFV cell-to-cell transmission. It provides new insights into the innate immunity response following ASFV infection and the transmission of ASFV.
非洲猪瘟病毒(ASFV)是一种具有经济破坏性的病原体,可导致家猪和野猪感染致死,其靶细胞为单核细胞和巨噬细胞。对于巨噬细胞而言,吞噬作用是一个基本且关键的过程,该过程通常会受到病毒抑制,从而阻碍病原体清除和抗原呈递。然而,令人意外的是,利用绿色荧光蛋白(EGFP)标记的细菌吞噬模型评估发现,ASFV感染可增强原代猪肺泡巨噬细胞(PAM)的吞噬能力。对ASFV感染的PAM中的吞噬过程,包括细胞迁移、细菌黏附、伪足延伸和模式识别受体(PRR)表达进行了系统研究。此外,对上调的PRR进行敲低以分析它们在增强吞噬作用中的作用。CD14是脂多糖和磷脂的受体,被确定为受ASFV上调,导致细菌摄取增加。进一步研究发现,感染的PAM中ASFV的基因组核酸激活cGAS/STING/NF-κB途径以增加CD14表达。同时,从感染的PAM释放的游离ASFV核酸也可通过TLR9途径激活旁观者PAM中的CD14表达,促进ASFV通过凋亡小体(ApoBD)传播。此外,ASFV感染早期增强的细菌吞噬作用可能会营造一个炎症更严重、细胞因子产生更强烈的环境。在此,揭示了一种关键机制,即ASFV通过cGAS/STING/NF-κB和TLR9途径增强PAM中CD14依赖性细菌摄取,促进病毒通过ApoBD传播并放大对细菌共感染的炎症反应,为ASFV发病机制和宿主免疫调控提供了重要见解。
猪肺泡巨噬细胞(PAM)是非洲猪瘟病毒(ASFV)的靶细胞,但ASFV如何影响其吞噬功能尚不清楚。在此发现,ASFV的核酸可通过cGAS/STING/NF-κB途径在感染的PAM中,或通过TLR9途径在旁观者PAM中增强脂多糖和磷脂受体CD14的表达。因此,CD14表达增强促进细菌和凋亡小体(ApoBD)的摄取,促进炎症反应和ASFV细胞间传播。它为ASFV感染后的固有免疫反应和ASFV传播提供了新见解。