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流感病毒温度敏感突变体的分离与初步鉴定

Isolation and preliminary characterization of temperature-sensitive mutants of influenza virus.

作者信息

Sugiura A, Tobita K, Kilbourne E D

出版信息

J Virol. 1972 Oct;10(4):639-47. doi: 10.1128/JVI.10.4.639-647.1972.

Abstract

Isolation of temperature-sensitive (ts) mutants was attempted from the WSN strain of influenza A virus which was grown and assayed in MDBK cells. After growth of wild-type virus in the presence of 5-fluorouracil, 15 ts mutants were selected for which the ratio of plaquing efficiency at 39.5 C to that at 33 C was 10(-3) or less. In pairwise crosses of ts mutants, recombination and complementation were either very efficient or undetectable. It is suggested, therefore, that the viral genome consists of physically discrete units and recombination occurs as an exchange of these units. All 15 mutants have been assigned with certainty into five recombination groups. Three mutants are suspected to be double mutants. Any two complementing mutants always recombined with each other, and noncomplementing mutants did not recombine. In physiological tests, mutants showed diverse patterns of functional defects at the nonpermissive temperature. However, it was not always possible to correlate these physiological defects with the results of genetic characterization.

摘要

尝试从在MDBK细胞中培养和检测的甲型流感病毒WSN株中分离温度敏感(ts)突变体。在野生型病毒于5-氟尿嘧啶存在下生长后,选择了15个ts突变体,其在39.5℃时的噬斑形成效率与在33℃时的噬斑形成效率之比为10(-3)或更低。在ts突变体的成对杂交中,重组和互补要么非常高效,要么无法检测到。因此,有人提出病毒基因组由物理上离散的单元组成,重组是这些单元的交换。所有15个突变体已被明确分为五个重组组。三个突变体被怀疑是双突变体。任何两个互补突变体总是相互重组,而非互补突变体不重组。在生理学测试中,突变体在非允许温度下表现出不同的功能缺陷模式。然而,并不总是能够将这些生理缺陷与遗传特征分析的结果相关联。

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本文引用的文献

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The Mechanism of Genetic Recombination in Phage.噬菌体中基因重组的机制
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