Liu C, Air G M
Department of Microbiology, University of Alabama, Birmingham 35294.
Virology. 1993 May;194(1):403-7. doi: 10.1006/viro.1993.1276.
A neuraminidase (NA)-deficient mutant, designated NWS-Mvi, of the reassortant influenza virus A/NWS/33HA-A/tern/Australia/G70c/75NA (H1N9), was selected by passaging virus in MDCK cells in a medium containing neuraminidase from the bacterium Micromonospora viridifaciens and polyclonal antiserum against the influenza NA. Growth of the resulting mutant virus is dependent on the addition of neuraminidase to the medium. Western blot analysis showed that the neuraminidase protein was absent from the mutant virus particles, and Northern hybridization showed that RNA segment 6, which contains the coding information for the NA, had undergone massive deletion. Viral protein synthesis in cells infected with the mutant virus was not dependent on the addition of neuraminidase. In the absence of a functional NA, the NWS-Mvi mutant virus can infect MDCK cells with normal cytopathic effects. This neuraminidase-minus influenza virus serves as an excellent source of parent virus for reverse genetics experiments involving genes that encode a functional neuraminidase.
通过将重组流感病毒A/NWS/33HA-A/tern/Australia/G70c/75NA(H1N9)在含有来自绿色产色小单孢菌的神经氨酸酶和抗流感神经氨酸酶多克隆抗血清的培养基中的MDCK细胞中传代,筛选出了一种神经氨酸酶(NA)缺陷型突变体,命名为NWS-Mvi。所得突变病毒的生长依赖于向培养基中添加神经氨酸酶。蛋白质印迹分析表明,突变病毒颗粒中不存在神经氨酸酶蛋白,Northern杂交表明,包含NA编码信息的RNA片段6发生了大量缺失。感染突变病毒的细胞中的病毒蛋白合成不依赖于神经氨酸酶的添加。在没有功能性NA的情况下,NWS-Mvi突变病毒可以感染MDCK细胞并产生正常的细胞病变效应。这种不含神经氨酸酶的流感病毒是用于涉及编码功能性神经氨酸酶基因的反向遗传学实验的优良亲代病毒来源。