Walzer Katelyn A, Chi Jen-Tsan
a Department of Molecular Genetics and Microbiology , Duke University School of Medicine , Durham , North Carolina , USA.
b Center for Genomic and Computational Biology , Duke University School of Medicine , Durham , North Carolina , USA.
RNA Biol. 2017 Apr 3;14(4):442-449. doi: 10.1080/15476286.2017.1294307. Epub 2017 Feb 17.
This review focuses on the role of trans-kingdom movement of small RNA (sRNA) molecules between parasites, particularly Plasmodium falciparum, and their respective host cells. While the intercellular transfer of sRNAs within organisms is well recognized, recent studies illustrate many examples of trans-kingdom sRNA exchange within the context of host-parasite interactions. These interactions are predominantly found in the transfer of host sRNAs between erythrocytes and the invading P. falciparum, as well as other host cell types. In addition, parasite-encoded sRNAs can also be transferred to host cells to evade the immune system. The transport of these parasite sRNAs in the body fluids of the host may also offer means to detect and monitor the parasite infection. These isolated examples may only represent the tip of the iceberg in which the transfer of sRNA between host and parasites is a critical aspect of host-pathogen interactions. In addition, the levels of these sRNAs and their speed of transfer may vary dramatically under different contexts to push the biologic equilibrium toward the benefit of hosts vs. parasites. Therefore, these sRNA transfers may offer potential strategies to detect, prevent or treat parasite infections. Here, we review a brief history of the discovery of host erythrocyte sRNAs, their transfers and interactions in the context of P. falciparum infection. We also provide examples and discuss the functional significance of the reciprocal transfer of parasite-encoded sRNAs into hosts. These understandings of sRNA exchanges are put in the context of their implications for parasite pathogenesis, host defenses and the evolution of host polymorphisms driven by host interactions with these parasites.
本综述聚焦于小RNA(sRNA)分子在寄生虫(尤其是恶性疟原虫)与其各自宿主细胞之间的跨界转移作用。虽然生物体内部sRNA的细胞间转移已得到充分认识,但最近的研究揭示了宿主 - 寄生虫相互作用背景下许多跨界sRNA交换的例子。这些相互作用主要存在于红细胞与入侵的恶性疟原虫以及其他宿主细胞类型之间宿主sRNA的转移中。此外,寄生虫编码的sRNA也可以转移到宿主细胞以逃避免疫系统。这些寄生虫sRNA在宿主体液中的运输也可能提供检测和监测寄生虫感染的手段。这些孤立的例子可能只是冰山一角,其中宿主与寄生虫之间sRNA的转移是宿主 - 病原体相互作用的一个关键方面。此外,这些sRNA的水平及其转移速度在不同情况下可能会有显著差异,从而推动生物平衡朝着有利于宿主或寄生虫的方向发展。因此,这些sRNA转移可能提供检测、预防或治疗寄生虫感染的潜在策略。在这里,我们回顾了宿主红细胞sRNA发现的简要历史,以及它们在恶性疟原虫感染背景下的转移和相互作用。我们还提供了例子并讨论了寄生虫编码的sRNA向宿主反向转移的功能意义。对sRNA交换的这些理解是基于它们对寄生虫发病机制、宿主防御以及由宿主与这些寄生虫相互作用驱动的宿主多态性进化的影响。