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Susceptibility of CCB cell line to different fish viruses

机译:CCB细胞系对不同鱼类病毒的敏感性

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In spite of the establishment of modern techniques like PCR for virus detection, virus isolations in susceptible fish cell lines are still the basis for international certification of most notifiable viral fish diseases mentioned by the OIE and the European Union (OIE, 2000; European Commission, 1996). Cell cultures may change in susceptibility (Lorenzen et al., 1999, unpublished own findings,). If no regular susceptibility checks are done in the laboratory, using an alternative sensitive cell culture might therefore increase the chance of isolating a certain virus. The CCB (common carp brain) cell line, developed by and cultured according to Neukirch et al., 1999, was originally developed for the diagnosis of koi herpesvirus (KHV). Moreover, we isolated other viruses from diseased koi in CCB cells. Besides KHV, myxoviruses, birna- and/or reoviruses (not all isolates were identified) and rhabdoviruses (spring viraemia of carp virus, SVCV) were obtained (Neukirch Kunz, 2001). The susceptibility of CCB cells was also investigated for viruses isolated from golden ide, European eel and salmonids. CCB cells and the standard cell lines used in our laboratory: Epithelioma papulosum cyprinid, EPC (Tomasec and Fijan, 1971), Chinook Salmon Embryo, CHSE (Fryer et al., 1965) and Eel kidney, EK-1 (Chen et al., 1982) for the different viruses were inoculated with the following viruses: infectious pancreatic necrosis virus (IPNV, strains Sp, Ab and Ni), viral haemorrhagic septicaemia virus (VHSV, serotype I, II and III), infectious haematopoietic necrosis virus (IHNV), golden ide reovirus (GiRV), chum salmon reovirus (CSV), herpesvirus anguillae (HVA), and another eel virus designated A sub(1)B virus. Non-infected cell lines were incubated as negative controls. Two passages were carried out in the cell lines before quantification of virus infectivity by titration of supernatants in 10-fold dilution steps (Mayr et al., 1977). Table 1 summarizes the inoculated viruses used, and results concerning titration of virus infectivity obtained in both the routine cell lines and the CCB cell line.
机译:尽管建立了用于病毒检测的PCR等现代技术,但易感性鱼类细胞系中的病毒分离仍然是国际兽疫局和欧盟提到的最应报告的病毒性鱼类疾病国际认证的基础(OIE,2000;欧洲委员会, 1996)。细胞培养物的药敏性可能会发生变化(Lorenzen等,1999,未发表的发现)。如果在实验室中没有进行定期的药敏检查,那么使用其他敏感的细胞培养物可能会增加分离出某种病毒的机会。由Neukirch等人(1999年)开发并根据其培养的CCB(鲤鱼脑)细胞系最初被开发用于诊断锦鲤疱疹病毒(KHV)。此外,我们还从CCB细胞中患病的锦鲤中分离出其他病毒。除KHV外,还获得了粘液病毒,双歧杆菌和/或呼肠孤病毒(未鉴定出所有分离株)和弹状病毒(鲤鱼病毒春季病毒血症,SVCV)(Neukirch Kunz,2001年)。还研究了CCB细胞对从金丝,欧洲鳗鱼和鲑鱼中分离出的病毒的敏感性。 CCB细胞和我们实验室中使用的标准细胞系:塞浦路斯上皮瘤,EPC(Tomasec和Fijan,1971),Chinook鲑鱼胚胎,CHSE(Fryer等,1965)和鳗鱼肾,EK-1(Chen等。 (1982年),将以下病毒接种到不同的病毒中:传染性胰腺坏死病毒(IPNV,菌株Sp,Ab和Ni),病毒性出血败血病病毒(VHSV,I,II和III型血清型),传染性造血性坏死病毒(IHNV) ),金伊德呼肠孤病毒(GiRV),Chum鲑呼肠孤病毒(CSV),疱疹病毒安圭拉虫(HVA)和另一种鳗鱼病毒,称为A sub(1)B病毒。将未感染的细胞系孵育作为阴性对照。在细胞系中进行两次传代,然后通过以10倍稀释步骤滴定上清液来定量病毒感染力(Mayr等,1977)。表1总结了所使用的接种病毒,以及关于在常规细胞系和CCB细胞系中获得的病毒感染力滴定的结果。

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