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Recognition of extremophilic archaeal viruses by eukaryotic cells: a promising nanoplatform from the third domain of life

机译:真核细胞识别极端嗜性古细菌病毒:生命的第三领域的有前途的纳米平台

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摘要

Viruses from the third domain of life, Archaea, exhibit unusual features including extreme stability that allow their survival in harsh environments. In addition, these species have never been reported to integrate into human or any other eukaryotic genomes, and could thus serve for exploration of novel medical nanoplatforms. Here, we selected two archaeal viruses Sulfolobus monocaudavirus 1 (SMV1) and Sulfolobus spindle shaped virus 2 (SSV2) owing to their unique spindle shape, hyperthermostable and acid-resistant nature and studied their interaction with mammalian cells. Accordingly, we followed viral uptake, intracellular trafficking and cell viability in human endothelial cells of brain (hCMEC/D3 cells) and umbilical vein (HUVEC) origin. Whereas SMV1 is efficiently internalized into both types of human cells, SSV2 differentiates between HUVECs and hCMEC/D3 cells, thus opening a path for selective cell targeting. On internalization, both viruses localize to the lysosomal compartments. Neither SMV1, nor SSV2 induced any detrimental effect on cell morphology, plasma membrane and mitochondrial functionality. This is the first study demonstrating recognition of archaeal viruses by eukaryotic cells which provides good basis for future exploration of archaeal viruses in bioengineering and development of multifunctional vectors.
机译:来自第三生命领域的病毒古细菌具有异常的特征,包括极高的稳定性,可以在恶劣的环境中生存。此外,从未报道过这些物种可整合到人类或任何其他真核基因组中,因此可用于探索新型医学纳米平台。在这里,由于其独特的纺锤形,超耐热和耐酸的性质,我们选择了两种古细菌,即单硫磺化单孢子病毒1(SMV1)和硫磺形梭形病毒2(SSV2),并研究了它们与哺乳动物细胞的相互作用。因此,我们追踪了人脑内皮细胞(hCMEC / D3细胞)和脐静脉(HUVEC)来源的病毒摄取,细胞内运输和细胞活力。 SMV1可以有效地内化到两种类型的人类细胞中,而SSV2则可以在HUVEC和hCMEC / D3细胞之间进行区分,从而为选择性细胞靶向开辟了道路。在内部化过程中,两种病毒都位于溶酶体区室。 SMV1和SSV2均未对细胞形态,质膜和线粒体功能性产生任何有害影响。这是第一项证明真核细胞识别古细菌病毒的研究,为将来在生物工程和多功能载体开发中探索古细菌提供了良好的基础。

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