Deng Feng, Ye Gang, Liu Qianqian, Navid Muhammad Tariq, Zhong Xiaoli, Li Youwen, Wan Chunyun, Xiao Shaobo, He Qigai, Fu Zhen F, Peng Guiqing
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Viruses. 2016 Feb 23;8(3):55. doi: 10.3390/v8030055.
Porcine epidemic diarrhea virus (PEDV), a member of Alphacoronavirus, has caused huge economic losses for the global pork industry recently. The spike (S) protein mediates PEDV entry into host cells. Herein, we investigated the interactions between the S protein and its receptor porcine aminopeptidase N (pAPN) or co-receptor sugars. The C-terminal domain (CTD) of the S1 domain is bound to pAPN. The prototype strain demonstrated similar receptor-binding activity compared with the variant field isolate. Three loops at the tips of the β-barrel domains did not play crucial roles in the PEDV S-pAPN association, indicating that PEDV conforms to a different receptor recognition model compared with transmissible gastroenteritis virus (TGEV), porcine respiratory CoV (PRCV), and human coronavirus NL63 (HCoV-NL63). The N-terminal domain (NTD) of the PEDV S1 domain could bind sugar, a possible co-receptor for PEDV. The prototype strain exhibited weaker sugar-binding activity compared with the variant field isolate. Strategies targeting the receptor binding domain (RBD) may be helpful for developing vaccines or antiviral drugs for PEDV. Understanding the differences in receptor binding between the prototype and the variant strains may provide insight into PEDV pathogenesis.
猪流行性腹泻病毒(PEDV)是甲型冠状病毒的一种,最近给全球猪肉产业造成了巨大经济损失。刺突(S)蛋白介导PEDV进入宿主细胞。在此,我们研究了S蛋白与其受体猪氨肽酶N(pAPN)或共受体糖类之间的相互作用。S1结构域的C末端结构域(CTD)与pAPN结合。与变异的田间分离株相比,原型毒株表现出相似的受体结合活性。β桶状结构域顶端的三个环在PEDV S-pAPN结合中不起关键作用,这表明与传染性胃肠炎病毒(TGEV)、猪呼吸道冠状病毒(PRCV)和人冠状病毒NL63(HCoV-NL63)相比,PEDV符合不同的受体识别模式。PEDV S1结构域的N末端结构域(NTD)可以结合糖类,这是PEDV可能的共受体。与变异的田间分离株相比,原型毒株表现出较弱的糖类结合活性。针对受体结合域(RBD)的策略可能有助于开发针对PEDV的疫苗或抗病毒药物。了解原型毒株和变异毒株之间受体结合的差异可能有助于深入了解PEDV的发病机制。