Fu Yan, Feng Yan, Dong Hong-Jun
Ningbo Municipal Centre for Disease Control and Prevention, Ningbo 315010, Zhejiang, China.
Zhongguo Yi Miao He Mian Yi. 2010 Feb;16(1):20-4.
To investigate the change on infection capacity of measles epidemic strain after continuous passage from Vero cell line, and to analyze the possible reasons in genetic level that caused change on cell-recognition site.
Measles virus epidemic strain Ningbo 05-2 was continuous passaged from Vero cells and Cytopathic Effect (CPE) was observed and recorded. After confirmation by real-time Reverse Transcription-Polymerase Chain Reaction (RT-PCR), hemagglutinating activity of Ningbo 05-2/P18 was detected using hemagglutination (HA) test and the completed sequences within Hemagglutinin (H) and Necleoprotein (N) gene were amplified by RT-PCR.
Measles epidemic strain Ningbo 05-2 has been continuous cultured for 17 times (P18) on Vero cells, but CPE began to be observed from the 13th passage. Although the passaged strains were confirmed as measles virus by real-time RT-PCR, the hemagglutinating activity of Ningbo 05-2/P18 was still negative. Compared with the Ningbo 05-2, there were three amino acid mutations within H protein of Ningbo 05-2/P18 (312aa, 314aa, 546aa), which changed the beta-sheet on the 311aa and the beta-turn during 312aa to 316aa to the alpha-helix. Phylogenetic tree based on H gene indicated the Ningbo 05-2/P18 still belonged to sub-genotype H(1b), locating at the same branch with the original strain. However, sequences of the original and passaged strains were identical within N protein.
Only a few amino acid mutations within H protein could results in cell-recognition site alternative of measles epidemic strain after continuous culture in Vero cell line, and consequently affecting the infection of measles virus.
研究麻疹流行株在Vero细胞系上连续传代后感染能力的变化,并从基因水平分析导致细胞识别位点变化的可能原因。
将麻疹病毒流行株宁波05-2在Vero细胞上连续传代,观察并记录细胞病变效应(CPE)。经实时逆转录-聚合酶链反应(RT-PCR)确认后,采用血凝试验检测宁波05-2/P18的血凝活性,并通过RT-PCR扩增血凝素(H)基因和核蛋白(N)基因的完整序列。
麻疹流行株宁波05-2在Vero细胞上连续传代17次(P18),但从第13代开始出现CPE。虽然传代毒株经实时RT-PCR确认为麻疹病毒,但宁波05-2/P18的血凝活性仍为阴性。与宁波05-2相比,宁波05-2/P18的H蛋白有3个氨基酸突变(312aa、314aa、546aa),使311aa处的β-折叠和312aa至316aa处的β-转角变为α-螺旋。基于H基因的系统发育树表明,宁波05-2/P18仍属于H(1b)亚基因型,与原始毒株位于同一分支。然而,原始毒株和传代毒株的N蛋白序列相同。
麻疹流行株在Vero细胞系中连续培养后,H蛋白仅发生少数氨基酸突变即可导致细胞识别位点改变,进而影响麻疹病毒的感染。