Itoh M, Isegawa Y, Hotta H, Homma M
Department of Microbiology, Kobe University School of Medicine, Japan.
J Gen Virol. 1997 Dec;78 ( Pt 12):3207-15. doi: 10.1099/0022-1317-78-12-3207.
A field strain of Sendai virus (SeV) Ohita-M1 (M1) was isolated from an epidemic in an animal laboratory by passaging in mice. A mutant strain, Ohita-MVC11 (MVC11), was then obtained by passaging M1 in rhesus monkey (LLC-MK2) cells. MVC11 was adapted to LLC-MK2 cells and produced 20 times higher levels of infectious virus than M1. This increased production of infectious virus in LLC-MK2 cells was associated with enhanced viral gene expression. However, MVC11 could not replicate efficiently in mouse lung and was not lethal to mice even when inoculated at a titre of 8 x 10(5) cell-infecting units (CIU) per mouse. On the other hand, with an inoculum of only 4 x 10(1) CIU per mouse, corresponding to 1 LD50, M1 replicated well in mouse lung and was highly virulent to mice. Nucleotide and deduced amino acid sequence analyses of the entire genomes of M1 and MVC11 revealed that adaptation to LLC-MK2 cells and the attenuation of mouse pathogenicity of MVC11 were associated with only two amino acid substitutions; one on the C protein (Phe substituted by Ser at position 170) and the other on the RNA polymerase, the L protein (Glu substituted by Ala at position 2050).
从动物实验室的一次疫情中通过在小鼠体内传代分离出仙台病毒(SeV)大分-M1(M1)的一株野毒株。然后通过在恒河猴(LLC-MK2)细胞中传代M1获得了一株突变株,大分-MVC11(MVC11)。MVC11适应了LLC-MK2细胞,产生的感染性病毒水平比M1高20倍。LLC-MK2细胞中感染性病毒产量的增加与病毒基因表达增强有关。然而,MVC11在小鼠肺中不能有效复制,即使以每只小鼠接种8×10⁵细胞感染单位(CIU)的滴度接种也不会对小鼠致死。另一方面,每只小鼠仅接种4×10¹ CIU的接种物,相当于1个半数致死量(LD50),M1在小鼠肺中能很好地复制,并且对小鼠具有高致病性。对M1和MVC11的全基因组进行核苷酸和推导氨基酸序列分析表明,对LLC-MK2细胞的适应以及MVC11对小鼠致病性的减弱仅与两个氨基酸替换有关;一个在C蛋白上(第170位的苯丙氨酸被丝氨酸取代),另一个在RNA聚合酶L蛋白上(第2050位的谷氨酸被丙氨酸取代)。