MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China.
Vet Microbiol. 2023 Mar;278:109663. doi: 10.1016/j.vetmic.2023.109663. Epub 2023 Jan 16.
Coinfection of Porcine circovirus type 2 (PCV2) and Glaesserella parasuis type 4 (GPS4) is widespread clinically, resulting in high morbidity and mortality, however, interactions between the two pathogens during coinfection and the coinfection pathogenesis are poorly understood. In this study, a piglet model coinfected with PCV2 and GPS4 was established; coinfection of the piglets' group showed more obvious symptoms, such as high fever and emaciation, and more severe histological lesions appeared in various organs. Importantly, piglets in the coinfection group produced lower levels of PCV2 and GPS4 antibodies, and showed high levels of inflammatory cytokines, TLR2, and TLR4, while the levels of CD4, CD8, MHC II, costimulatory molecules, and IL-12p40 were decreased. In addition, a model of macrophage 3D4/21 cells coinfection with PCV2 and GPS4 was established, coinfected cells exhibited increased expression of the cytokines IL-6, IL-8, TNF-α, IL-1β, and the receptors TLR2, TLR4, while decreased MHC II. We further demonstrate that cytokine production is associated with the activation of NF-κB and NLRP3 inflammasome signaling pathways, and TLR4 is also involved. Altogether, our findings suggest that coinfection with PCV2 and GPS4 exacerbates the inflammatory response, resulting in severe tissue damage, and probably impaired macrophage antigen presentation and T cell activation, resulting in immune dysregulation, aggravating host infection.
猪圆环病毒 2 型(PCV2)和副猪嗜血杆菌 4 型(GPS4)的混合感染在临床上广泛存在,导致高发病率和死亡率,但这两种病原体在混合感染时的相互作用和混合感染的发病机制尚不清楚。在本研究中,建立了 PCV2 和 GPS4 混合感染的仔猪模型;混合感染组的仔猪表现出更明显的症状,如高热和消瘦,并且在各种器官中出现更严重的组织病变。重要的是,混合感染组的仔猪产生的 PCV2 和 GPS4 抗体水平较低,并且表现出高水平的炎症细胞因子、TLR2 和 TLR4,而 CD4、CD8、MHC II、共刺激分子和 IL-12p40 的水平降低。此外,还建立了 PCV2 和 GPS4 混合感染巨噬细胞 3D4/21 细胞的模型,感染细胞中细胞因子 IL-6、IL-8、TNF-α、IL-1β 和受体 TLR2、TLR4 的表达增加,而 MHC II 的表达降低。我们进一步证明细胞因子的产生与 NF-κB 和 NLRP3 炎症小体信号通路的激活有关,并且 TLR4 也参与其中。总之,我们的研究结果表明,PCV2 和 GPS4 的混合感染加剧了炎症反应,导致严重的组织损伤,可能损害了巨噬细胞抗原呈递和 T 细胞激活,导致免疫失调,加重宿主感染。