Microbial Containment Complex, National Institute of Virology, Indian Council of Medical Research, Sus Road Pashan, Pune 411021, India.
In Vitro Cell Dev Biol Anim. 2009 Oct;45(9):491-5. doi: 10.1007/s11626-009-9218-1. Epub 2009 Jun 16.
A new cell line from the neonate larvae of Aedes aegypti (L) mosquito was established and characterized. The cell line at the 50th passage (P) level consisted of three prominent cell types, i.e., epithelial-like cells (92%), fibroblast-like cells (7%), and giant cells ( approximately 1%). Karyological analysis showed diploid (2n = 6) number of chromosomes in >75% cells at P-50. The growth kinetics studied at 52nd passage level showed approximately tenfold increase in cell number over a 10-d study period. The species specificity studies using DNA amplification fingerprinting profile analysis using RAPD primers demonstrated 100% homology with the host profile showing the integrity of the cell line. Electron microscopy revealed the absence of mycoplasma or other adventitious agents. The cell line supported the multiplication of seven arboviruses, i.e., Chikungunya (CHIK), Japanese encephalitis, West Nile, dengue 2 (DEN-2), Chandipura, vesicular stomatitis, and Chittoor viruses. The cell line did not replicate Ganjam and Kaisodi viruses. CHIK virus yield in the new cell line was approximately 3log and 0.5log 50% tissue culture infective dose (TCID(50))/mL higher than Vero E6 and C6/36 cell lines, respectively. In the case of DEN-2 virus, it yielded 1log TCID(50)/mL higher than Vero E6, but lesser than C6/36 cell line. Due to its high susceptibility to a broad spectrum of viruses, the new cell line may find application in virus isolation during epidemics and in antigen production.
从埃及伊蚊(L)幼蚊中建立并鉴定了一种新的细胞系。第 50 代(P)水平的细胞系由三种明显的细胞类型组成,即上皮样细胞(92%)、成纤维样细胞(7%)和巨细胞(约 1%)。核型分析显示,超过 75%的细胞具有二倍体(2n=6)染色体数。在第 52 代水平进行的生长动力学研究表明,在 10 天的研究期间,细胞数量增加了约 10 倍。使用 RAPD 引物进行 DNA 扩增指纹图谱分析的物种特异性研究显示,与宿主图谱的同源性为 100%,表明细胞系的完整性。电子显微镜显示没有支原体或其他外来物质。该细胞系支持七种虫媒病毒的增殖,即基孔肯雅热(CHIK)、日本脑炎、西尼罗河、登革热 2 型(DEN-2)、钱迪普拉、水疱性口炎和奇托病毒。该细胞系不能复制甘贾姆和凯索迪病毒。CHIK 病毒在新细胞系中的产量比 Vero E6 和 C6/36 细胞系分别高约 3log 和 0.5log 50%组织培养感染剂量(TCID50)/mL。在 DEN-2 病毒的情况下,它的产量比 Vero E6 高 1log TCID50/mL,但比 C6/36 细胞系低。由于其对广泛谱病毒的高敏感性,新细胞系可能在流行期间的病毒分离和抗原生产中得到应用。