Hegyi A, Kolb A F
Institute of Virology and Immunology, University of Würzburg, Germany.
J Gen Virol. 1998 Jun;79 ( Pt 6):1387-91. doi: 10.1099/0022-1317-79-6-1387.
Feline aminopeptidase N (fAPN) is a major cell surface receptor for feline infectious peritonitis virus (FIPV), transmissible gastroenteritis virus (TGEV), human coronavirus 229E (HCV 229E) and canine coronavirus (CCV). By using chimeric molecules assembled from porcine, human and feline APN we have analysed the determinants involved in the coronavirus receptor function of fAPN. Our results show that amino acids 670-840 of fAPN are critically involved in its FIPV and TGEV receptor function whereas amino acids 135-297 are essential for the HCV 229E receptor function. We also demonstrate that a chimeric molecule assembled from human and porcine APN is able to act as a receptor for FIPV. This is surprising as neither human nor porcine APN by themselves mediate FIPV infection. These results suggest that different determinants in the APN protein are involved in mediating the coronavirus receptor function.
猫氨基肽酶N(fAPN)是猫传染性腹膜炎病毒(FIPV)、传染性胃肠炎病毒(TGEV)、人冠状病毒229E(HCV 229E)和犬冠状病毒(CCV)的主要细胞表面受体。通过使用由猪、人和猫APN组装而成的嵌合分子,我们分析了参与fAPN冠状病毒受体功能的决定因素。我们的结果表明,fAPN的氨基酸670 - 840对其FIPV和TGEV受体功能至关重要,而氨基酸135 - 297对HCV 229E受体功能必不可少。我们还证明,由人和猪APN组装而成的嵌合分子能够作为FIPV的受体。这很令人惊讶,因为单独的人或猪APN都不能介导FIPV感染。这些结果表明,APN蛋白中的不同决定因素参与介导冠状病毒受体功能。