Stoddart M E, Gaskell R M, Harbour D A, Gaskell C J
Department of Veterinary Medicine, Langford House, Bristol, Gt. Britain.
Vet Microbiol. 1988 Feb;16(2):145-58. doi: 10.1016/0378-1135(88)90039-9.
Eight specific pathogen-free cats were inoculated orally or parenterally with a cell culture-adapted strain of feline infectious peritonitis virus (FIPV). Faeces and oropharyngeal swabs were monitored daily for infectious virus by inoculation of feline embryo lung cells. Virus was recovered from both sites for approximately 2 weeks after inoculation, before clinical signs of disease developed. Peripheral blood lymphocytes collected from these cats were tested in an in-vitro blastogenic assay using concanavalin A (con A) and FIPV antigen. All cats showed a profound suppression of the response to con A which only recovered to pre-inoculation levels in 2 cats, one of which survived. These 2 cats also responded to FIPV antigen on the 21st day after infection, the greater response being in the survivor. The other cats, surviving 16-18 days, developed no response to FIPV antigen. Antibody titres, measured by immunofluorescence and by virus neutralization, rose rapidly to very high levels in all cats, regardless of the route of inoculation.
八只特定病原体-free猫通过口服或肠胃外途径接种了适应细胞培养的猫传染性腹膜炎病毒(FIPV)毒株。通过接种猫胚胎肺细胞,每天监测粪便和口咽拭子中的传染性病毒。接种后约2周内,在疾病临床症状出现之前,从这两个部位都能检测到病毒。从这些猫身上采集的外周血淋巴细胞,使用刀豆球蛋白A(Con A)和FIPV抗原进行体外增殖试验检测。所有猫对Con A的反应都受到严重抑制,只有两只猫恢复到接种前水平,其中一只存活。这两只猫在感染后第21天也对FIPV抗原产生反应,存活的猫反应更强。其他存活16 - 18天的猫对FIPV抗原没有反应。通过免疫荧光和病毒中和法测量的抗体滴度,在所有猫中都迅速上升到非常高的水平,无论接种途径如何。