Ramishvili L G, Maglakelidze D A, Labadze T N
Georgian National Center of Veterinarian Diagnosis and Expert Evaluations, Tbilisi.
Mol Gen Mikrobiol Virusol. 2001(2):30-3.
Canine rotavirus was isolated in MA104 roller culture of rhesus macaque cells. Two passages in gnotobiotic puppies and two in colostrum-free puppies resulted in isolation of strain P of canine rotavirus. After 20 passages in MA104 culture the virus was adapted to MDCK culture. Optimal conditions for accumulation of canine rotavirus and its antigen (9.01 g TCD50/ml) in MDCK culture are trypsin pretreatment of the virus inoculate in the final concentration of 50 mcg/ml for 30 min at 37 degrees C, presence of trypsin (10 mcg/ml) in the maintenance medium, multiplicity of infection 0.1 TCD50/ml, and incubation in roller culture at 37 degrees C during 24-30 h. After 60 passages in cell culture, canine rotavirus completely lost its virulence for colostrum-free puppies but retained antigenic activity and induced manifest seroconversion in infected.
犬轮状病毒是在恒河猴细胞的MA104滚瓶培养物中分离出来的。在无菌幼犬中传代两次,在无初乳幼犬中传代两次后,分离出犬轮状病毒P株。在MA104培养物中传代20次后,该病毒适应了MDCK培养。在MDCK培养中积累犬轮状病毒及其抗原(9.01 g TCD50/ml)的最佳条件是:将接种病毒用胰蛋白酶预处理,终浓度为50 mcg/ml,在37℃下处理30分钟;维持培养基中存在胰蛋白酶(10 mcg/ml);感染复数为0.1 TCD50/ml;在37℃下滚瓶培养24 - 30小时。在细胞培养中传代60次后,犬轮状病毒对无初乳幼犬完全丧失毒力,但保留了抗原活性,并在感染动物中诱导明显的血清转化。