Carmichael L E, Joubert J C, Pollock R V
Cornell Vet. 1981 Oct;71(4):408-27.
A canine parvovirus (CPV) strain (C-780916) was found attenuated for pups at 80, but not after 51 serial passages in dog kidney cell (DKC) cultures. A variant viral population ('large plaque') emerged after prolonged cultivation in DKC cultures that may be associated with reduced native virulence. Dogs vaccinated with modified CPV developed high hemagglutination-inhibiting (HI) antibody titers within 4 days of incoluation and antibody persisted. Vaccinated animals shed small amounts of virus in the feces that spread to contact dogs. After five back-passages in dogs the modified strain was not pathogenic for pups and the plaque characteristics of the virus isolated from the feces were typical of the attenuated strain. The modified live CPV did not cause infection of the fetus when inoculated parenterally into pregnant bitches at various stages of gestation. It was not pathogenic for neonatal pups. These results suggest that a safe and effective live homologous (CPV) vaccine has been developed which should aid substantially in controlling CPV infection.
一株犬细小病毒(CPV)毒株(C-780916)在80代时对幼犬表现出减毒效果,但在犬肾细胞(DKC)培养物中连续传代51次后则不然。在DKC培养物中长时间培养后出现了一种变异病毒群体(“大斑块”),这可能与天然毒力降低有关。用改良CPV疫苗接种的犬在接种后4天内产生了高血凝抑制(HI)抗体滴度,且抗体持续存在。接种疫苗的动物粪便中排出少量病毒,可传播给接触的犬只。在犬体内进行五次返传后,改良毒株对幼犬无致病性,从粪便中分离出的病毒斑块特征为典型的减毒株。当在妊娠不同阶段经非肠道途径接种给怀孕母犬时,改良活CPV不会导致胎儿感染。它对新生幼犬无致病性。这些结果表明,已开发出一种安全有效的活同源(CPV)疫苗,这应有助于在很大程度上控制CPV感染。