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麻疹病毒准种对上皮细胞和淋巴细胞的周期性适应:To V,还是 not to V。

Cyclical adaptation of measles virus quasispecies to epithelial and lymphocytic cells: To V, or not to V.

机构信息

Department of Molecular Medicine, Mayo Clinic, Rochester, MN, United States of America.

Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, MN, United States of America.

出版信息

PLoS Pathog. 2019 Feb 15;15(2):e1007605. doi: 10.1371/journal.ppat.1007605. eCollection 2019 Feb.

Abstract

Measles virus (MeV) is dual-tropic: it replicates first in lymphatic tissues and then in epithelial cells. This switch in tropism raises the question of whether, and how, intra-host evolution occurs. Towards addressing this question, we adapted MeV either to lymphocytic (Granta-519) or epithelial (H358) cells. We also passaged it consecutively in both human cell lines. Since passaged MeV had different replication kinetics, we sought to investigate the underlying genetic mechanisms of growth differences by performing deep-sequencing analyses. Lymphocytic adaptation reproducibly resulted in accumulation of variants mapping within an 11-nucleotide sequence located in the middle of the phosphoprotein (P) gene. This sequence mediates polymerase slippage and addition of a pseudo-templated guanosine to the P mRNA. This form of co-transcriptional RNA editing results in expression of an interferon antagonist, named V, in place of a polymerase co-factor, named P. We show that lymphocytic-adapted MeV indeed produce minimal amounts of edited transcripts and V protein. In contrast, parental and epithelial-adapted MeV produce similar levels of edited and non-edited transcripts, and of V and P proteins. Raji, another lymphocytic cell line, also positively selects V-deficient MeV genomes. On the other hand, in epithelial cells V-competent MeV genomes rapidly out-compete the V-deficient variants. To characterize the mechanisms of genome re-equilibration we rescued four recombinant MeV carrying individual editing site-proximal mutations. Three mutations interfered with RNA editing, resulting in almost exclusive P protein expression. The fourth preserved RNA editing and a standard P-to-V protein expression ratio. However, it altered a histidine involved in Zn2+ binding, inactivating V function. Thus, the lymphocytic environment favors replication of V-deficient MeV, while the epithelial environment has the opposite effect, resulting in rapid and thorough cyclical quasispecies re-equilibration. Analogous processes may occur in natural infections with other dual-tropic RNA viruses.

摘要

麻疹病毒(MeV)是双嗜性的:它首先在淋巴组织中复制,然后在上皮细胞中复制。这种嗜性的转变提出了一个问题,即在宿主内是否以及如何发生进化。为了解决这个问题,我们使 MeV 适应淋巴细胞(Granta-519)或上皮细胞(H358)。我们还连续在这两种人类细胞系中传代。由于传代的 MeV 具有不同的复制动力学,我们试图通过进行深度测序分析来研究生长差异的潜在遗传机制。淋巴细胞适应性复制可重复性地导致在位于磷蛋白(P)基因中部的 11 个核苷酸序列内积累变体。该序列介导聚合酶滑变,并在 P mRNA 上添加一个伪模板鸟苷。这种形式的共转录 RNA 编辑导致干扰素拮抗剂 V 的表达,而不是聚合酶共因子 P。我们表明,淋巴细胞适应性 MeV 确实产生少量编辑的转录物和 V 蛋白。相比之下,亲本和上皮适应性 MeV 产生相似水平的编辑和未编辑的转录物,以及 V 和 P 蛋白。另一种淋巴细胞系 Raji 也对缺乏 V 的 MeV 基因组进行了积极选择。另一方面,在上皮细胞中,V 有效的 MeV 基因组迅速取代缺乏 V 的变体。为了表征基因组再平衡的机制,我们拯救了携带单个编辑位点近端突变的四个重组 MeV。三个突变干扰了 RNA 编辑,导致几乎只表达 P 蛋白。第四个突变保留了 RNA 编辑和标准的 P 到 V 蛋白表达比例,但改变了一个参与 Zn2+结合的组氨酸,从而使 V 功能失活。因此,淋巴细胞环境有利于缺乏 V 的 MeV 的复制,而上皮环境则产生相反的效果,导致快速和彻底的循环准种再平衡。类似的过程可能发生在其他双嗜性 RNA 病毒的自然感染中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b3f/6395005/d8d08680b5d7/ppat.1007605.g006.jpg

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