首页> 美国卫生研究院文献>The Journal of General Virology >A short treatment of cells with the lanthanide ions La3+ Ce3+ Pr3+ or Nd3+ changes the cellular chemistry into a state in which RNA replication of flaviviruses is specifically blocked without interference with host-cell multiplication
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A short treatment of cells with the lanthanide ions La3+ Ce3+ Pr3+ or Nd3+ changes the cellular chemistry into a state in which RNA replication of flaviviruses is specifically blocked without interference with host-cell multiplication

机译:用镧系离子La3 +Ce3 +Pr3 +或Nd3 +短时间处理细胞会改变细胞化学状态其中黄病毒的RNA复制被特异性阻断而不会干扰宿主细胞的繁殖

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摘要

Alpha- and flaviviruses contain class II fusion proteins, which form ion-permeable pores in the target membrane during virus entry. The pores generated during entry of the alphavirus Semliki Forest virus have been shown previously to be blocked by lanthanide ions. Here, analyses of the influence of rare earth ions on the entry of the flaviviruses West Nile virus and Uganda S virus revealed an unexpected effect of lanthanide ions. The results showed that a 30 s treatment of cells with an appropriate lanthanide ion changed the cellular chemistry into a state in which the cells no longer supported the multiplication of flaviviruses. This change occurred in cells treated before, during or after infection, did not inhibit multiplication of Semliki Forest virus and did not interfere with host-cell multiplication. The change was generated in vertebrate and insect cells, and was elicited in the presence of actinomycin D. In vertebrate cells, the change was elicited specifically by La3+, Ce3+, Pr3+ and Nd3+. In insect cells, additional lanthanide ions had this activity. Further analyses showed that lanthanide ion treatment blocked the ability of the host cell to support the replication of flavivirus RNA. These results open two areas of research: the study of molecular alterations induced by lanthanide ion treatment in uninfected cells and the analysis of the resulting modifications of the flavivirus RNA replicase complex. The findings possibly open the way for the development of a general chemotherapy against flavivirus diseases such as Dengue fever, Japanese encephalitis, West Nile fever and yellow fever.
机译:α和黄病毒包含II类融合蛋白,它们在病毒进入过程中在靶膜上形成离子可渗透的孔。先前已证明在阿尔法病毒塞姆利基森林病毒进入过程中产生的孔被镧系元素离子堵塞。在这里,分析稀土离子对黄病毒西尼罗河病毒和乌干达S病毒进入的影响揭示了镧系元素离子的出乎意料的作用。结果表明,用适当的镧系元素离子对细胞进行30 s的处理后,细胞化学状态变为细胞不再支持黄病毒繁殖的状态。这种变化发生在感染前,感染中或感染后的细胞中,没有抑制Semliki Forest病毒的繁殖,也没有干扰宿主细胞的繁殖。这种变化是在脊椎动物和昆虫细胞中产生的,并且是在放线菌素D的存在下引起的。在脊椎动物细胞中,该变化是由La 3 + ,Ce 3 + ,Pr 3 + 和Nd 3 + 。在昆虫细胞中,其他镧系元素离子具有这种活性。进一步的分析表明,镧系元素离子处理阻断了宿主细胞支持黄病毒RNA复制的能力。这些结果打开了两个研究领域:研究镧系元素离子处理在未感染细胞中引起的分子变化,以及对黄病毒RNA复制酶复合物的修饰修饰的分析。该发现可能为开发针对黄病毒疾病(如登革热,日本脑炎,西尼罗河热和黄热病)的一般化学疗法开辟了道路。

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