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嗜吞噬细胞无形体改变蜱细胞 microRNA 表达,并通过靶向 R O U N D A B O U T 蛋白 2 通路上调 isc-mir-79,从而促进感染。

Anaplasma phagocytophilum modifies tick cell microRNA expression and upregulates isc-mir-79 to facilitate infection by targeting the Roundabout protein 2 pathway.

机构信息

SaBio. Instituto de Investigación en Recursos Cinegéticos IREC-CSIC-UCLM-JCCM, Ronda de Toledo s/n, 13005, Ciudad, Real, Spain.

UMR BIPAR, INRA, Ecole Nationale Vétérinaire d'Alfort, ANSES, Université Paris-Est, 94700, Maisons-Alfort, France.

出版信息

Sci Rep. 2019 Jun 24;9(1):9073. doi: 10.1038/s41598-019-45658-2.

DOI:10.1038/s41598-019-45658-2
PMID:31235752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6591238/
Abstract

The microRNAs (miRNAs) are a class of small noncoding RNAs that have important regulatory roles in multicellular organisms including innate and adaptive immune pathways to control bacterial, parasite and viral infections, and pathogens could modify host miRNA profile to facilitate infection and multiplication. Therefore, understanding the function of host miRNAs in response to pathogen infection is relevant to characterize host-pathogen molecular interactions and to provide new targets for effective new interventions for the control infectious diseases. The objective of this study was to characterize the dynamics and functional significance of the miRNA response of the tick vector Ixodes scapularis in response to Anaplasma phagocytophilum infection, the causative agent of human and animal granulocytic anaplasmosis. To address this objective, the composition of tick miRNAs, functional annotation, and expression profiling was characterized using high throughout RNA sequencing in uninfected and A. phagocytophilum-infected I. scapularis ISE6 tick cells, a model for tick hemocytes involved in pathogen infection. The results provided new evidences on the role of tick miRNA during pathogen infection, and showed that A. phagocytophilum modifies I. scapularis tick cell miRNA profile and upregulates isc-mir-79 to facilitate infection by targeting the Roundabout protein 2 (Robo2) pathway. Furthermore, these results suggested new targets for interventions to control pathogen infection in ticks.

摘要

微小 RNA(miRNAs)是一类小型非编码 RNA,在包括先天和适应性免疫途径在内的多细胞生物中具有重要的调节作用,以控制细菌、寄生虫和病毒感染,病原体可以修饰宿主 miRNA 谱,以促进感染和繁殖。因此,了解宿主 miRNA 对病原体感染的反应功能对于表征宿主-病原体分子相互作用以及为控制传染病的有效新干预措施提供新的靶点是相关的。本研究的目的是描述蜱虫载体 Ixodes scapularis 对嗜吞噬细胞无形体感染的 miRNA 反应的动态和功能意义,嗜吞噬细胞无形体是人类和动物粒细胞无形体病的病原体。为了实现这一目标,使用高通量 RNA 测序对未感染和感染嗜吞噬细胞无形体的 I. scapularis ISE6 蜱细胞(一种参与病原体感染的蜱血细胞模型)中的蜱 miRNA 的组成、功能注释和表达谱进行了表征。研究结果提供了有关蜱在病原体感染过程中 miRNA 作用的新证据,并表明嗜吞噬细胞无形体改变了蜱虫细胞 miRNA 谱,并上调了 isc-mir-79,通过靶向 Roundabout 蛋白 2(Robo2)途径促进感染。此外,这些结果为控制蜱虫中的病原体感染提供了新的干预靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/94aa8dd85928/41598_2019_45658_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/b7e0e1acb4f0/41598_2019_45658_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/1e477896d4f7/41598_2019_45658_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d62e10ac63b5/41598_2019_45658_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/a64d2d4d55b1/41598_2019_45658_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d5e60dad237a/41598_2019_45658_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d711d3d14c14/41598_2019_45658_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/68d3f0e1f550/41598_2019_45658_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/94aa8dd85928/41598_2019_45658_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/b7e0e1acb4f0/41598_2019_45658_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/1e477896d4f7/41598_2019_45658_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d62e10ac63b5/41598_2019_45658_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/a64d2d4d55b1/41598_2019_45658_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d5e60dad237a/41598_2019_45658_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/d711d3d14c14/41598_2019_45658_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/68d3f0e1f550/41598_2019_45658_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c37/6591238/94aa8dd85928/41598_2019_45658_Fig8_HTML.jpg

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