Van Hamme Evelien, Dewerchin Hannah L, Cornelissen Els, Verhasselt Bruno, Nauwynck Hans J
Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.
Department of Clinical Chemistry, Microbiology and Immunology, Faculty of Medicine and Health Science, Ghent University, 9000 Gent, Belgium.
J Gen Virol. 2008 Sep;89(Pt 9):2147-2156. doi: 10.1099/vir.0.2008/001602-0.
Feline infectious peritonitis virus (FIPV), a coronavirus that causes a lethal chronic disease in cats, enters feline monocytes via endocytosis. In this study, the pathway of internalization is characterized by evaluating the effect of chemical inhibitors and/or expression of dominant-negative (DN) proteins on the percentage of internalized virions per cell and infection. Further, co-localization studies were performed to determine the involvement of certain cellular internalization proteins. FIPV is not internalized through a clathrin-mediated pathway, as chlorpromazine, amantadine and DN eps15 did not influence virus uptake and FIPV did not co-localize with clathrin. The caveolae-mediated pathway could be excluded based on the inability of genistein and DN caveolin-1 to inhibit virus uptake and lack of co-localization between FIPV and caveolin-1. Dynamin inhibitory peptide and DN dynamin effectively inhibited virus internalization. The inhibitor strongly reduced uptake to 20.3+/-1.1% of uptake in untreated cells. In the presence of DN dynamin, uptake was 58.7+/-3.9% relative to uptake in untransduced cells. Internalization of FIPV was slightly reduced to 85.0+/-1.4 and 87.4+/-6.1% of internalization in control cells by the sterol-binding drugs nystatin and methyl-beta-cyclodextrin, respectively. Rho GTPases were inhibited by Clostridium difficile toxin B, but no effect was observed. These results were confirmed with infection studies showing that infection was not influenced by chlorpromazine, amantadine and genistein, but was significantly reduced by dynamin inhibition and nystatin. In conclusion, these results indicate that FIPV enters monocytes through a clathrin- and caveolae-independent pathway that strongly depends on dynamin and is slightly sensitive to cholesterol depletion.
猫传染性腹膜炎病毒(FIPV)是一种可在猫身上引发致命慢性疾病的冠状病毒,它通过内吞作用进入猫单核细胞。在本研究中,内化途径通过评估化学抑制剂和/或显性负性(DN)蛋白对每个细胞内化病毒粒子百分比及感染的影响来进行表征。此外,还进行了共定位研究以确定某些细胞内化蛋白的参与情况。FIPV并非通过网格蛋白介导的途径内化,因为氯丙嗪、金刚烷胺和DN eps1五未影响病毒摄取,且FIPV与网格蛋白未共定位。基于染料木黄酮和DN小窝蛋白-1无法抑制病毒摄取以及FIPV与小窝蛋白-1之间缺乏共定位,小窝介导的途径也可被排除。动力蛋白抑制肽和DN动力蛋白有效抑制了病毒内化。该抑制剂将摄取量大幅降低至未处理细胞摄取量的20.3±1.1%。在存在DN动力蛋白的情况下,摄取量相对于未转导细胞的摄取量为58.7±3.9%。制霉菌素和甲基-β-环糊精这两种固醇结合药物分别将FIPV的内化略微降低至对照细胞内化量的85.0±1.4%和87.4±6.1%。艰难梭菌毒素B抑制了Rho GTP酶,但未观察到效果。感染研究证实了这些结果,表明感染不受氯丙嗪、金刚烷胺和染料木黄酮的影响,但动力蛋白抑制和制霉菌素使其显著降低。总之,这些结果表明FIPV通过一种不依赖网格蛋白和小窝的途径进入单核细胞,该途径强烈依赖动力蛋白且对胆固醇耗竭略有敏感。