Miyazawa T, Ikeda Y, Nakamura K, Naito R, Mochizuki M, Tohya Y, Vu D, Mikami T, Takahashi E
Department of Veterinary Microbiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Japan.
Microbiol Immunol. 1999;43(6):609-12. doi: 10.1111/j.1348-0421.1999.tb02447.x.
Feline parvovirus (FPV) was isolated rather frequently from the peripheral blood mononuclear cells (PBMCs) of cats in northern Vietnam by coculturing with MYA-1 cells (an interleukin-2-dependent feline T lymphoblastoid cell line) or Crandell feline kidney (CRFK) cells (a feline renal cell line). Efficiency of virus isolation was higher in MYA-1 cells than in CRFK cells. Interestingly, among the 17 cats from which FPV was isolated, 9 cats were positive for virus neutralizing (VN) antibody against FPV, indicating that FPV infected PBMCs and was not eliminated from PBMCs even in the presence of VN antibodies in the cats.
通过与MYA-1细胞(一种依赖白细胞介素-2的猫T淋巴母细胞系)或克兰德尔猫肾(CRFK)细胞(一种猫肾细胞系)共培养,在越南北部的猫外周血单个核细胞(PBMC)中相当频繁地分离出猫细小病毒(FPV)。病毒在MYA-1细胞中的分离效率高于CRFK细胞。有趣的是,在分离出FPV的17只猫中,有9只猫针对FPV的病毒中和(VN)抗体呈阳性,这表明FPV感染了PBMC,即使猫体内存在VN抗体,也未从PBMC中清除。