Geissler K, Schneider K, Platzer G, Truyen B, Kaaden O R, Truyen U
Institute for Medical Microbiology, Infectious and Epidemic Diseases, Ludwig Maximilians University, Munich, Germany.
Virus Res. 1997 May;48(2):193-206. doi: 10.1016/s0168-1702(97)01440-8.
The capsid protein genes of five feline calicivirus (FCV) isolates associated with different disease manifestations were cloned and sequenced. The viruses represented two recent isolates from cats with chronic stomatitis, one recent isolate from a cat with acute stomatitis, one recent isolate each from a cat with acute respiratory symptoms and the classical limping syndrome strain FCV-2280. The amino acid sequences were compared with eight other published sequences and analyzed for their relationships. Phylogenetic analysis of the complete capsid protein sequences or of known antigenic regions of that protein (hypervariable regions A and E) did not group the isolates of different disease manifestations in distinct subclusters. Monoclonal antibodies (MAbs) generated against either a chronic stomatitis isolate or a recent isolate associated with respiratory symptoms were tested against a panel of 11 recent isolates and four "classical' FCV strains, covering all known disease associations. With those MAbs no obvious clustering with respect to disease manifestation could be seen. Four specific sera prepared in rabbits against our prototype isolates also failed to cluster those isolates according to the disease manifestations when examined in neutralization tests. From these antigenic and genetic analyses of the capsid protein the hypothesis of the existence of biotypes of FCV responsible for distinct disease manifestations could not be confirmed.
对五株与不同疾病表现相关的猫杯状病毒(FCV)分离株的衣壳蛋白基因进行了克隆和测序。这些病毒代表了两株来自患有慢性口炎的猫的近期分离株、一株来自患有急性口炎的猫的近期分离株、一株来自患有急性呼吸道症状的猫的近期分离株以及经典的跛行综合征毒株FCV - 2280。将氨基酸序列与其他八个已发表的序列进行比较,并分析它们之间的关系。对完整的衣壳蛋白序列或该蛋白的已知抗原区域(高变区A和E)进行系统发育分析,并没有将具有不同疾病表现的分离株归为不同的亚群。针对一株慢性口炎分离株或一株与呼吸道症状相关的近期分离株产生的单克隆抗体(MAb),对一组11株近期分离株和4株“经典”FCV毒株进行了检测,这些毒株涵盖了所有已知的疾病关联情况。使用这些单克隆抗体,未发现与疾病表现有明显的聚类现象。在中和试验中,用兔制备的针对我们原型分离株的四种特异性血清也未能根据疾病表现对这些分离株进行聚类。从衣壳蛋白的这些抗原和遗传分析中,无法证实存在负责不同疾病表现的FCV生物型这一假设。