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鉴定和分析非洲猪瘟病毒的 285L 和 K145R 蛋白。

Identification and characterization of the 285L and K145R proteins of African swine fever virus.

机构信息

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald-Insel Riems, Germany.

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald-Insel Riems, Germany.

出版信息

J Gen Virol. 2019 Sep;100(9):1303-1314. doi: 10.1099/jgv.0.001306. Epub 2019 Jul 30.

Abstract

African swine fever (ASF) is a lethal disease of domestic pigs and wild boar, against which no vaccines are available to date. The large dsDNA genome of African swine fever virus (ASFV) contains up to 167 ORFs predicted to encode proteins. The functions and antigenic properties of many of these proteins are still unknown, which impedes vaccine development. Based on the results of mass spectrometry-based proteome analyses of ASFV-infected cells, two highly abundant but previously uncharacterized viral proteins, p285L and pK145R, were investigated in detail. To this end, monospecific rabbit antisera and corresponding gene deletion mutants of ASFV were prepared. RNA and immunoblot analyses revealed that p285L is an early gene product expressed prior to viral DNA replication, whereas pK145R is a true late protein. The predicted membrane protein p285L could be localized in purified ASFV particles. In contrast, pK145R was not detectable in virions, but accumulated diffusely in the cytoplasm of infected cells. Deletion of 285L or K145R from the genome of a virulent ASFV strain from Armenia did not significantly affect spread and productive growth in a permissive wild boar lung cell line, nor in primary macrophage cultures. Future studies must elucidate, whether p285L and pK145R, although non-essential for propagation of ASFV, are relevant for replication or virulence in swine. Furthermore, it remains to be investigated whether deletion of the abundant ASFV proteins p285L or pK145R might support serological differentiation from wild-type-infected animals.

摘要

非洲猪瘟(ASF)是一种致命的家猪和野猪疾病,目前尚无可用的疫苗。非洲猪瘟病毒(ASFV)的大型 dsDNA 基因组包含多达 167 个开放阅读框,预计这些阅读框编码蛋白质。这些蛋白质中的许多功能和抗原特性仍然未知,这阻碍了疫苗的开发。基于基于质谱的 ASFV 感染细胞的蛋白质组分析结果,详细研究了两种高度丰富但以前未表征的病毒蛋白 p285L 和 pK145R。为此,制备了单特异性兔抗血清和相应的 ASFV 基因缺失突变体。RNA 和免疫印迹分析表明,p285L 是一种在病毒 DNA 复制之前表达的早期基因产物,而 pK145R 是一种真正的晚期蛋白。预测的膜蛋白 p285L 可在纯化的 ASFV 颗粒中定位。相比之下,pK145R 在病毒粒子中不可检测,但在感染细胞的细胞质中弥散积累。从亚美尼亚的一种强毒 ASFV 株的基因组中缺失 285L 或 K145R 不会显著影响在允许的野猪肺细胞系或原代巨噬细胞培养物中的传播和有效生长。未来的研究必须阐明,尽管 p285L 和 pK145R 对于 ASFV 的传播不是必需的,但它们是否与猪的复制或毒力相关。此外,仍需研究是否删除丰富的 ASFV 蛋白 p285L 或 pK145R 可能支持与野生型感染动物的血清学分化。

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