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在未处理或经γ干扰素处理的小鼠L929细胞中生长的普氏立克次体对DNA、rRNA和蛋白质的合成。

Synthesis of DNA, rRNA, and protein by Rickettsia prowazekii growing in untreated or gamma interferon-treated mouse L929 cells.

作者信息

Gao Q, Turco J, Winkler H H

机构信息

Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile 36688.

出版信息

Infect Immun. 1993 Jun;61(6):2383-9. doi: 10.1128/iai.61.6.2383-2389.1993.

Abstract

The syntheses of DNA, rRNA, and protein by Rickettsia prowazekii growing in mouse fibroblastic L929 cells were measured at various times after the addition of gamma interferon (IFN-gamma) to correlate the inhibition of a site of macromolecular synthesis with the established IFN-gamma-induced inhibition of rickettsial growth. A method was developed to measure the syntheses of DNA, rRNA, and protein by R. prowazekii during a 2-h pulse-labeling period while the rickettsiae were growing within cultured host cells that had intact macromolecular synthesis. This method involved incubation of the rickettsia-infected cells with a radioactive precursor (H3 32PO4 or Tran35S-label), purification of the rickettsiae, purification of rickettsial nucleic acids, and analysis of rickettsial nucleic acids and proteins by electrophoresis and autoradiography. A key feature of the method involved the use of calculated specific activities from a densitometric analysis of gels and autoradiograms, a procedure that made the data independent of rickettsial recovery. Rickettsial DNA and rRNA syntheses were both inhibited 12 h after the addition of IFN-gamma to infected cultures, whereas the synthesis of rickettsial proteins was not inhibited at this time. In contrast, at 20 h after the addition of IFN-gamma, rickettsial DNA, rRNA, and protein syntheses were all inhibited.

摘要

在向感染鼠成纤维细胞L929的普氏立克次体培养物中添加γ干扰素(IFN-γ)后的不同时间,测定了其DNA、rRNA和蛋白质的合成,以将大分子合成位点的抑制与已确定的IFN-γ诱导的立克次体生长抑制相关联。开发了一种方法,用于在2小时脉冲标记期间测定普氏立克次体的DNA、rRNA和蛋白质合成,而立克次体在具有完整大分子合成的培养宿主细胞内生长。该方法包括用放射性前体(H3 32PO4或Tran35S标记)孵育感染立克次体的细胞、纯化立克次体、纯化立克次体核酸,以及通过电泳和放射自显影分析立克次体核酸和蛋白质。该方法的一个关键特征是使用通过凝胶和放射自显影片的光密度分析计算的比活性,这一程序使数据独立于立克次体的回收率。向感染培养物中添加IFN-γ后12小时,立克次体DNA和rRNA合成均受到抑制,而此时立克次体蛋白质合成未受抑制。相比之下,添加IFN-γ后20小时,立克次体DNA、rRNA和蛋白质合成均受到抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf7d/280859/f7ad8eddfa57/iai00018-0128-a.jpg

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