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与脊髓灰质炎病毒1型相比,25型回声病毒JV - 4参考株和野生型毒株在MRC5细胞中的复制情况。

Replication of echo virus type 25 JV-4 reference strain and wild type strains in MRC5 cells compared with that of poliovirus type 1.

作者信息

Bailly J L, Chambon M, Peigue-Lafeuille H, Charbonné F

机构信息

Service de Bactériologie-Virologie, Faculté de Médecine, Clermont-Ferrand, France.

出版信息

Arch Virol. 1994;137(3-4):327-40. doi: 10.1007/BF01309479.

Abstract

In echo virus type 25/JV-4 the shut off of host cell protein synthesis took significantly longer and the kinetics of the synthesis of viral proteins and viral RNA occurred much later than in the poliovirus. However, these characteristics impaired neither polyprotein processing nor virus production in the JV-4 strain. In contrast the two wild strains M.1262 and Th.222 had a lower virus yield than strain JV-4. The presence of a high Mr protein in the pattern of viral proteins of wild strains suggested that a defect in the polyprotein processing was responsible for the decreased virus yield. The infectious cycle of strain Th.222 differed from that of strains JV-4 and M.1262 in the rapid inhibition of host cell translation and the extent of viral protein synthesis. The sensitivity to actinomycin D was also investigated. Strain M.1262 was found to be insensitive. The virus yield of strains JV-4 and Th.222 was three- and fourfold lower respectively in the presence of actinomycin D. This sensitivity to the antibiotic was observed during viral RNA synthesis in strain JV-4 and during viral protein synthesis in strain Th.222. These results suggest that cellular factors are involved in the replication of echo virus type 25 strains in MRC5 cells.

摘要

在25型埃可病毒/JV - 4中,宿主细胞蛋白质合成的关闭时间明显更长,病毒蛋白质和病毒RNA合成的动力学过程比脊髓灰质炎病毒出现得晚得多。然而,这些特征既不影响JV - 4毒株中多聚蛋白的加工,也不影响病毒的产生。相比之下,两种野生毒株M.1262和Th.222的病毒产量低于JV - 4毒株。野生毒株病毒蛋白模式中存在高分子量蛋白表明,多聚蛋白加工缺陷是病毒产量下降的原因。Th.222毒株的感染周期在宿主细胞翻译的快速抑制和病毒蛋白合成程度方面与JV - 4和M.1262毒株不同。还研究了对放线菌素D的敏感性。发现M.1262毒株不敏感。在存在放线菌素D的情况下,JV - 4和Th.222毒株的病毒产量分别降低了三倍和四倍。在JV - 4毒株的病毒RNA合成过程以及Th.222毒株的病毒蛋白合成过程中观察到了这种对抗生素的敏感性。这些结果表明,细胞因子参与了25型埃可病毒在MRC5细胞中的复制。

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