Zeng Ling-Bing, Xu Jin, Li Yan-Qiu, Wang Yao, Xiao Yi, Fan Yu-Ding, Zhou Yong
Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Jingzhou 434000, China.
Bing Du Xue Bao. 2009 Nov;25(6):460-6.
By using cell culture and virus infection methods, a new reovirus had been isolated from channel catfish (Ictalurus punctatus) suffered with severe hemorrhage and had been identified as channel catfish reovirus (CCRV) after artificial infection in fish, electron microscopy observation, physical-chemical tests, genomic SDS-PAGE analysis and sequencing. In artificial infection test, the typical symptoms of channel catfish hemorrhage as naturally occurred could be reproduced. The isolated virus could cause typical cytopathic effect in CCO and CCK cell lines. Electron microscopy observation of ultra-thin section samples of CCRV infected CCO and CCK cells revealed that the virus replicated in cytoplasm, arrayed in crystalline, and had a non-enveloped double capsid with a diameter of 60-70 nm. Frozen-thawed, 56 degrees C 1 h, chloroform and ether had no significant effects on CCRV titer, 65 degrees C 1 h could significantly inactivated the viral infectivity. The CCRV genome SDS-PAGE analysis and nuclease sensitivity test showed that the virus genome was the same as that of viruses in Aquareovirudae and consisted of 11 segments of dsRNA assigned into three classes L1, L2, L3; M1, M2, M3 and S1, S2, S3, S4, S5 with a range of size from 0.9 to 4.4 kb. The Cloning and sequencing of the CCRV S4 segment indicated the nucleic acid number of CCRV S4 was 909 bp in length, which was exactly the same as that of GCRV S4 (AF403396) and GSRV S4 (AF403407) segments. The BLAST of CCRV S4 sequence in NCBI GenBank showed that it had a 99% and 90% similarity in sequence to the GCRV S4 and GSRV S4 segments, respectively.
通过细胞培养和病毒感染方法,从患有严重出血病的斑点叉尾鮰(Ictalurus punctatus)中分离出一种新型呼肠孤病毒,经鱼类人工感染、电子显微镜观察、理化检测、基因组SDS-PAGE分析和测序后,被鉴定为斑点叉尾鮰呼肠孤病毒(CCRV)。在人工感染试验中,可重现斑点叉尾鮰自然发生的典型出血症状。分离出的病毒可在CCO和CCK细胞系中引起典型的细胞病变效应。对CCRV感染的CCO和CCK细胞超薄切片样本进行电子显微镜观察发现,该病毒在细胞质中复制,呈晶体排列,具有直径为60-70nm的无包膜双衣壳。冻融、56℃ 1小时、氯仿和乙醚对CCRV滴度无显著影响,65℃ 1小时可显著灭活病毒感染力。CCRV基因组SDS-PAGE分析和核酸酶敏感性试验表明,该病毒基因组与水生呼肠孤病毒科病毒的基因组相同,由11条dsRNA片段组成,分为L1、L2、L3;M1、M2、M3和S1、S2、S3、S4、S5三类,大小范围为0.9至4.4kb。CCRV S4片段的克隆和测序表明,CCRV S4的核酸长度为909bp,与草鱼呼肠孤病毒S4(AF403396)和鳜鱼呼肠孤病毒S4(AF403407)片段完全相同。在NCBI GenBank中对CCRV S4序列进行BLAST分析表明,它与草鱼呼肠孤病毒S4和鳜鱼呼肠孤病毒S4片段的序列相似性分别为99%和90%。