Tang Qiyu, Li Weitian, Dai Na, Gao Yiming, Han Yu, Cheng Guofu, Gu Changqin
A Department of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei, China.
Avian Dis. 2017 Dec;61(4):491-502. doi: 10.1637/11732-073017-Reg.1.
Fowl cholera resulting from infection with Pasteurella multocida causes huge economic losses in the poultry industry. Necrotic hepatitis is reported to be a significant lesion associated with fowl cholera in chickens. Clarifying the underlying molecular mechanism of hepatic injury caused by P. multocida infection is needed to develop new strategies to control fowl cholera. Pasteurella multocida Q (the standard reference strain) and P. multocida 1G1 (a clinical strain) were used to infect healthy laying hens. Clinical signs were observed and gross lesions in livers were observed postmortem. Histologic lesions and the localization and expression of protein molecules associated with necroptosis, apoptosis, and inflammation in hepatic tissues were examined by hematoxylin and eosin staining and immunohistochemistry. Western blot analysis was used to determine the expression of liver injury-related genes. Necroptotic molecules such as RIPK1 (receptor interaction protein kinases 1), RIPK3 (receptor interaction protein kinases 3), and MLKL (mixed lineage kinase domain-like protein) were observed by immunostaining primarily in the cytoplasm of hepatocytes within or around necrotic foci, and inflammatory mediators HMGB1 (high-mobility group box 1) and IL-6 (interleukin-6) were found in the cytoplasm of heterophils, monocytes/macrophages, and hepatic sinusoids. In addition, MMP9 (matrix metalloproteinase 9) and TIMP1 (tissue inhibitor of metalloproteinase 1) were observed in hepatic parenchymal cells, inflammatory cells, and interstitial spaces, whereas the apoptotic effector molecule caspase-3 (cysteine-containing aspartic proteolytic enzymes 3) was mainly found in hepatocytes. The expression of RIPK1, RIPK3, and MLKL was significantly higher in the infected chickens than in the controls. HMGB1 and IL-6 protein levels were also increased in infected chickens relative to those in controls. Both MMP9 and TIMP1 were highly expressed in infected chickens. In addition, caspase-3 protein levels were significantly elevated in infected chickens. Necroptosis, apoptosis, and inflammation played a significant role in hepatic injury caused by P. multocida.
由多杀性巴氏杆菌感染引起的禽霍乱给家禽业造成了巨大的经济损失。据报道,坏死性肝炎是鸡禽霍乱的一种重要病变。为了制定控制禽霍乱的新策略,需要阐明多杀性巴氏杆菌感染导致肝损伤的潜在分子机制。使用多杀性巴氏杆菌Q(标准参考菌株)和多杀性巴氏杆菌1G1(临床菌株)感染健康的产蛋母鸡。观察临床症状,并在死后观察肝脏的大体病变。通过苏木精-伊红染色和免疫组织化学检查肝组织中的组织学病变以及与坏死性凋亡、凋亡和炎症相关的蛋白质分子的定位和表达。蛋白质印迹分析用于确定肝损伤相关基因的表达。通过免疫染色观察到坏死性凋亡分子,如RIPK1(受体相互作用蛋白激酶1)、RIPK3(受体相互作用蛋白激酶3)和MLKL(混合谱系激酶结构域样蛋白)主要存在于坏死灶内或周围肝细胞的细胞质中,在嗜异性粒细胞、单核细胞/巨噬细胞和肝血窦的细胞质中发现了炎症介质HMGB1(高迁移率族蛋白B1)和IL-6(白细胞介素-6)。此外,在肝实质细胞、炎性细胞和间质空间中观察到MMP9(基质金属蛋白酶9)和TIMP1(金属蛋白酶组织抑制剂1),而凋亡效应分子caspase-3(含半胱氨酸的天冬氨酸蛋白水解酶3)主要存在于肝细胞中。感染鸡中RIPK1、RIPK3和MLKL的表达明显高于对照组。与对照组相比,感染鸡中HMGB1和IL-6蛋白水平也有所升高。MMP9和TIMP1在感染鸡中均高表达。此外,感染鸡中caspase-3蛋白水平显著升高。坏死性凋亡、凋亡和炎症在多杀性巴氏杆菌引起的肝损伤中起重要作用。