Dezengrini Renata, Weiblen Rudi, Flores Eduardo Furtado
Setor de Virologia, Departamento de Medicina Veterinária Preventiva, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.
J Virol Methods. 2006 Oct;137(1):51-7. doi: 10.1016/j.jviromet.2006.05.032. Epub 2006 Jul 18.
Contamination of cell cultures with adventitious viruses may pose serious risks for virology diagnosis, research and vaccine production. This article reports the selection and characterization of three cell lines resistant to bovine viral diarrhea virus (BVDV), a major contaminant of cell cultures. The resistant cells were obtained from canine (MDCK), swine (PK-15) and rabbit (RK-13) parental cell lines by expanding and cloning cells that survived lytic infection with BVDV. All three selected cell lines were resistant to three standard BVDV strains and to 10 field isolates as demonstrated by immunofluorescence for viral antigens and by co-cultivation with susceptible cells. Inoculation of selected cells with BVDV (10 TCID50/cell) resulted in frequencies of infection of <10(-5) (MDCK-R, PK-15R) and 3.3 x 10(-4) (RK-13R). Comparing to the parental cell lines, these cells were >10,000-, >20,000- and 600-fold less susceptible to BVDV, respectively. Inoculation of resistant cells with BVDV in the presence of polyethylene-glycol increased the frequency of infection in the order of >437-, >346- and 87-fold, respectively, indicating that resistance is probably due to a block in viral entry. Nevertheless, each resistant cell line retained the susceptibility to three other viruses that replicate in the parental cells. Thus, these cells may be useful for many virology purposes, with a very low risk of BVDV contamination.
细胞培养物被外源病毒污染可能会给病毒学诊断、研究及疫苗生产带来严重风险。本文报道了三种对细胞培养物的主要污染物——牛病毒性腹泻病毒(BVDV)具有抗性的细胞系的筛选及特性鉴定。抗性细胞是通过对经BVDV裂解感染后存活的细胞进行传代培养和克隆,从犬源(MDCK)、猪源(PK - 15)和兔源(RK - 13)亲本细胞系中获得的。通过病毒抗原免疫荧光检测以及与易感细胞共培养表明,所有三种筛选出的细胞系对三种标准BVDV毒株和10株野外分离株均具有抗性。用BVDV(10 TCID50/细胞)接种所选细胞,感染频率分别为<10^(-5)(MDCK - R、PK - 15R)和3.3×10^(-4)(RK - 13R)。与亲本细胞系相比,这些细胞对BVDV的敏感性分别降低了>10000倍、>20000倍和600倍。在聚乙二醇存在的情况下用BVDV接种抗性细胞,感染频率分别增加了>437倍、>346倍和87倍,这表明抗性可能是由于病毒进入受阻。然而,每个抗性细胞系对在亲本细胞中复制的其他三种病毒仍保持敏感性。因此,这些细胞可用于多种病毒学研究目的,且BVDV污染风险极低。