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麻疹病毒蚀斑后代诱导干扰素能力的变异

Variation in ability of measles virus plaque progeny to induce interferon.

作者信息

McKimm J, Rapp F

出版信息

Proc Natl Acad Sci U S A. 1977 Jul;74(7):3056-9. doi: 10.1073/pnas.74.7.3056.

Abstract

Plaque progeny of three interferon (IF)-inducing strains of measles virus (Edmonston, Schwarz, and CC) were examined for ability to induce IF in BSC-1 cells. Only after passage in Vero cells did any of the Edmonston progeny induce IF. The vast majority of plaque progeny selected from the Schwarz strain induced IF, even though this virus was originally derived from the Edmonston strain. This property was retained even after serial plaque purification of the progeny. However, the Schwarz-derived CC strain consisted of a population generally unable to induce IF. Stocks grown from both Edmonston and CC plaques demonstrating the IF+ phenotype maintained this characteristic as a whole, but it was not a property that was inherited by all progeny in the stocks. Levels of IF induced were approximately the same for all strains, even though the proportion of inducing progeny varied markedly among them. These noninducing variants appeared to be normal, fully infectious measles virions. The results suggest that induction of IF by measles virus is at least partially under the genetic control of the virus.

摘要

检测了三种诱导干扰素(IF)的麻疹病毒株(埃德蒙斯顿株、施瓦茨株和CC株)的蚀斑后代在BSC - 1细胞中诱导IF的能力。只有埃德蒙斯顿株的后代在传代至非洲绿猴肾细胞(Vero细胞)后才诱导IF。从施瓦茨株中挑选出的绝大多数蚀斑后代都能诱导IF,尽管该病毒最初源自埃德蒙斯顿株。即使对子代进行连续蚀斑纯化后,这一特性仍得以保留。然而,源自施瓦茨株的CC株群体通常无法诱导IF。从表现出IF+表型的埃德蒙斯顿株和CC株蚀斑中培养的病毒株整体上保持了这一特性,但这并非该病毒株中所有子代都具有的遗传特性。尽管各株诱导子代的比例差异显著,但所有毒株诱导IF的水平大致相同。这些非诱导性变异体似乎是正常的、具有完全感染性的麻疹病毒粒子。结果表明,麻疹病毒诱导IF至少部分受病毒的遗传控制。

相似文献

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Interferon induction by measles virus.麻疹病毒诱导干扰素
Intervirology. 1981;16(4):250-9. doi: 10.1159/000149274.

本文引用的文献

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Preliminary tests of a highly attenuated measles vaccine.一种高度减毒麻疹疫苗的初步试验。
Am J Dis Child. 1962 Mar;103:386-9. doi: 10.1001/archpedi.1962.02080020398042.
10
Current concepts of interferon and interferon induction.干扰素与干扰素诱导的当前概念
Annu Rev Med. 1970;21:17-46. doi: 10.1146/annurev.me.21.020170.000313.

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