Lin Xian, Huang Canhui, Shi Jian, Wang Ruifang, Sun Xin, Liu Xiaokun, Zhao Lianzhong, Jin Meilin
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, P.R. China.
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, P.R. China; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei, P.R. China.
PLoS One. 2015 Apr 23;10(4):e0124086. doi: 10.1371/journal.pone.0124086. eCollection 2015.
Swine influenza virus and Streptococcus suis are two important contributors to the porcine respiratory disease complex, and both have significant economic impacts. Clinically, influenza virus and Streptococcus suis co-infections in pigs are very common, which often contribute to severe pneumonia and can increase the mortality. However, the co-infection pathogenesis in pigs is unclear. In the present study, co-infection experiments were performed using swine H1N1 influenza virus and Streptococcus suis serotype 2 (SS2). The H1N1-SS2 co-infected pigs exhibited more severe clinical symptoms, serious pathological changes, and robust apoptosis of lungs at 6 days post-infection compared with separate H1N1 and SS2 infections. A comprehensive gene expression profiling using a microarray approach was performed to investigate the global host responses of swine lungs against the swine H1N1 infection, SS2 infection, co-infection, and phosphate-buffered saline control. Results showed 457, 411, and 844 differentially expressed genes in the H1N1, SS2, and H1N1-SS2 groups, respectively, compared with the control. Noticeably, genes associated with the immune, inflammatory, and apoptosis responses were highly overexpressed in the co-infected group. Pathway analysis indicated that the cytokine-cytokine receptor interactions, MAPK, toll-like receptor, complement and coagulation cascades, antigen processing and presentation, and apoptosis pathway were significantly regulated in the co-infected group. However, the genes related to these were less regulated in the separate H1N1 and SS2 infection groups. This observation suggested that a certain level of synergy was induced by H1N1 and SS2 co-infection with significantly stronger inflammatory and apoptosis responses, which may lead to more serious respiratory disease syndrome and pulmonary pathological lesion.
猪流感病毒和猪链球菌是猪呼吸道疾病综合征的两个重要致病因素,二者均具有重大经济影响。临床上,猪流感病毒与猪链球菌的共感染十分常见,常引发严重肺炎并可增加死亡率。然而,猪的共感染发病机制尚不清楚。在本研究中,使用猪H1N1流感病毒和2型猪链球菌(SS2)进行了共感染实验。与单独感染H1N1和SS2相比,H1N1-SS2共感染的猪在感染后6天表现出更严重的临床症状、更严重的病理变化以及肺部更强的细胞凋亡。采用微阵列方法进行了全面的基因表达谱分析,以研究猪肺对猪H1N1感染、SS2感染、共感染以及磷酸盐缓冲盐水对照的整体宿主反应。结果显示,与对照组相比,H1N1、SS2和H1N1-SS2组中分别有457、411和844个差异表达基因。值得注意的是,与免疫、炎症和凋亡反应相关的基因在共感染组中高度过表达。通路分析表明,细胞因子-细胞因子受体相互作用、丝裂原活化蛋白激酶、Toll样受体、补体和凝血级联反应、抗原加工和呈递以及凋亡通路在共感染组中受到显著调节。然而,在单独的H1N1和SS2感染组中,与这些相关的基因调节较少。这一观察结果表明,H1N1和SS2共感染诱导了一定程度的协同作用,炎症和凋亡反应明显更强,这可能导致更严重的呼吸道疾病综合征和肺部病理损伤。