Barlough J E, Stoddart C A, Sorresso G P, Jacobson R H, Scott F W
Lab Anim Sci. 1984 Dec;34(6):592-7.
Oronasal inoculation of minimal-disease cats with a virulent field isolate of canine coronavirus elicited a neutralizing antibody response that increased steadily over a two-month period, indicating in vivo amplification of the inoculated dose. A heterologous neutralizing antibody response to transmissible gastroenteritis virus could be detected three weeks after titers to canine coronavirus were first observed and was found to parallel the homologous response at a level approximately one log10 dilution lower. A modest anamnestic response detectable in both assays was observed after a second exposure to canine coronavirus. Cross-reacting antibodies to transmissible gastroenteritis virus were not detected by a kinetics-based enzyme-linked immunosorbent assay (KELA), however, until after cats had received multiple daily doses of canine coronavirus (third exposure). No clinical signs attributable to canine coronavirus were seen in inoculated cats, and virus could not be isolated from fecal or rectal swabs nor identified in fecal specimens by electron microscopy. Both virus-neutralizing and KELA titers were boosted by aerosol challenge with feline infectious peritonitis virus. Antibodies produced in response to canine coronavirus did not sensitize cats to subsequent feline infectious peritonitis virus challenge, but neither did they protect cats against the challenge dose.
用犬冠状病毒的强毒株对接种少量病毒的猫进行口鼻接种,引发了中和抗体反应,该反应在两个月内稳步增加,表明接种剂量在体内得到了扩增。在首次观察到针对犬冠状病毒的滴度三周后,可检测到对传染性胃肠炎病毒的异源中和抗体反应,并且发现该反应与同源反应平行,但水平低约一个对数10稀释度。在第二次接触犬冠状病毒后,在两种检测方法中均观察到适度的回忆反应。然而,基于动力学的酶联免疫吸附测定(KELA)直到猫每天多次接种犬冠状病毒(第三次接触)后才检测到针对传染性胃肠炎病毒的交叉反应抗体。接种的猫未出现可归因于犬冠状病毒的临床症状,并且无法从粪便或直肠拭子中分离出病毒,也无法通过电子显微镜在粪便标本中鉴定出病毒。用猫传染性腹膜炎病毒进行气溶胶攻击可提高病毒中和及KELA滴度。针对犬冠状病毒产生的抗体不会使猫对随后的猫传染性腹膜炎病毒攻击敏感,但也不能保护猫免受攻击剂量的影响。