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L* Protein of Theiler's Murine Encephalomyelitis Virus Is Required for Virus Growth in a Murine Macrophage-Like Cell Line

机译:泰勒氏鼠脑脊髓炎病毒的L *蛋白是小鼠巨噬细胞样细胞系中病毒生长所必需的

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摘要

We sought to confirm the importance of L* protein for growth of Theiler's murine encephalomyelitis virus (TMEV) in a macrophage-like cell line, J774-1. The protein is out of frame with the polyprotein and synthesized in DA but not GDVII subgroup strains of TMEV. A recombinant virus, DANCL*/GD, which substitutes the DA 5′ noncoding and L* coding regions for the corresponding regions of GDVII and synthesizes L* protein, grew with little restriction in J774-1 cells. In contrast, another recombinant virus, DANCL*-1/GD, which has an ACG rather than an AUG as the starting codon of L* protein at nucleotide 1079, resulting in no synthesis of L* protein, did not grow well. No significant difference between the rates of adsorption to J774-1 cells of these viruses was observed. RNase protection assay demonstrated that DANCL*/GD viral RNA significantly increased, whereas only a minimal increase was observed for DANCL*-1/GD. The present study suggests that L* protein is required for virus growth in macrophages.
机译:我们试图确认L *蛋白对于巨噬细胞样细胞系J774-1中泰勒氏鼠脑脊髓炎病毒(TMEV)生长的重要性。该蛋白与多蛋白不符,并在TMEV的DA而不是GDVII亚组中合成。重组病毒DANCL * / GD将DA 5'非编码区和L *编码区替换为GDVII的相应区域并合成L *蛋白,在J774-1细胞中几乎没有限制地生长。相反,另一种重组病毒DANCL * -1 / GD不能很好地生长,该病毒在核苷酸1079处具有ACG而不是AUG作为L *蛋白的起始密码子,导致没有合成L *蛋白。在这些病毒对J774-1细胞的吸附速率之间没有观察到显着差异。 RNase保护测定表明DANCL * / GD病毒RNA显着增加,而DANCL * -1 / GD仅观察到最小的增加。本研究表明,L *蛋白是巨噬细胞中病毒生长所必需的。

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