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作 者:陶三菊[1] 何英[1] 陈伯权[1] 赵子江[1] 王焕琴[1] 杨冬荣[1] 刘琴芝[1]
机构地区:[1]中国预防医学科学院病毒学研究所
出 处:《中华实验和临床病毒学杂志》1997年第4期363-365,共3页Chinese Journal of Experimental and Clinical Virology
摘 要:1994年夏秋季从北京郊区采集的蚊子中分离到两株Colti病毒(北京95-70和北京95-75)。病毒在C6/36细胞引起明显的细胞病变,但在BHK-21和Vero细胞未见明显病变。对5’-碘脱氧尿苷和乙醚抵抗,表明为无包膜RNA病毒;对酸敏感,在pH3.0条件下病毒滴度降低3.5~4.5个对数以上。聚丙烯酰胺凝胶电泳显示病毒基因组为12节段RNA,两株病毒的电泳带型完全相同,与1991年分离的Colti病毒TRT2株带型基本一致,皆为6-6带型,但仔细比较至少有8条带的迁移率存在着细微差别。组织培养交叉中和试验表明,新分离株与TRT2株的抗原性未见明显差异,可能属同一血清型。病毒在C6/36细胞繁殖可能造成持续感染。Two strains (Beijing 95-70 and 95-75) of coltivirus were isolated from mosquitoes collected in Beijing during summerautumn in 1994. The viruses caused cytopathogenic effect on C6/36 cells but not on BHK-21 and Vero cells, and were not lethal for new born mice and three week old mice. The isolates were resistant to 5'-IdU and ether, but sensitive to acid pH3.0. There were 12 segments RNA shown by polyacrylamide gel electrophoresis (PAGE) and PAGE profile of the two isolates were similar (6-6). The PAGE profile was also similar to that of the TRT2 strain isolated in 1991, but there were at least 8 segments slightly different between the new isolates and TRT2 in band migration distance. Tissue culture crossneutralization test showed that the new isolates were antigenically related to TRT2 strain identified as coltivirus. Growth curve of the two isolates on C6/36 cells showed that virus titer began to rise at the first day after infection and continued to increase up to 7.0 Log TCID50 per 0.1ml and maintained a high level until the 21st day after infection. It seems that the virus may cause persistent infection on C6/36 cell.
关 键 词:COLTI病毒 呼肠病毒科/分离 蚊/病毒学 RNA.病毒
分 类 号:R373.3[医药卫生—病原生物学]
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