Zur Bruegge Jennifer, Backes Christina, Gölz Greta, Hemmrich-Stanisak Georg, Scharek-Tedin Lydia, Franke Andre, Alter Thomas, Einspanier Ralf, Keller Andreas, Sharbati Soroush
Institute of Veterinary Biochemistry, Department of Veterinary Medicine, Freie Universität Berlin, Germany.
Chair for Clinical Bioinformatics, Saarland University , Germany.
Eur J Microbiol Immunol (Bp). 2016 Jun 24;6(2):99-108. doi: 10.1556/1886.2016.00015.
The role of microRNAs (miRNAs) in infectious diseases is becoming more and more apparent, and the use of miRNAs as a diagnostic tool and their therapeutic application has become the major focus of investigation. The aim of this study was to identify miRNAs involved in the immune signaling of macrophages in response to Arcobacter (A.) butzleri infection, an emerging foodborne pathogen causing gastroenteritis. Therefore, primary human macrophages were isolated and infected, and miRNA expression was studied by means of RNAseq. Analysis of the data revealed the expression of several miRNAs, which were previously associated with bacterial infections such as miR-155, miR-125, and miR-212. They were shown to play a key role in Toll-like receptor signaling where they act as fine-tuners to establish a balanced immune response. In addition, miRNAs which have yet not been identified during bacterial infections such as miR-3613, miR-2116, miR-671, miR-30d, and miR-629 were differentially regulated in A. butzleri-infected cells. Targets of these miRNAs accumulated in pathways such as apoptosis and endocytosis - processes that might be involved in A. butzleri pathogenesis. Our study contributes new findings about the interaction of A. butzleri with human innate immune cells helping to understand underlying regulatory mechanisms in macrophages during infection.
微小RNA(miRNA)在传染病中的作用日益明显,将miRNA用作诊断工具及其治疗应用已成为研究的主要焦点。本研究的目的是鉴定参与巨噬细胞免疫信号传导以响应布氏嗜冷杆菌感染的miRNA,布氏嗜冷杆菌是一种新兴的食源性病原体,可引起肠胃炎。因此,分离并感染了原代人巨噬细胞,并通过RNA测序研究了miRNA的表达。数据分析揭示了几种miRNA的表达,这些miRNA先前与细菌感染有关,如miR-155、miR-125和miR-212。它们在Toll样受体信号传导中起关键作用,在其中作为微调器来建立平衡的免疫反应。此外,在细菌感染期间尚未鉴定出的miRNA,如miR-3613、miR-2116、miR-671、miR-30d和miR-629,在布氏嗜冷杆菌感染的细胞中受到差异调节。这些miRNA的靶标在凋亡和内吞作用等途径中积累,这些过程可能与布氏嗜冷杆菌的发病机制有关。我们的研究为布氏嗜冷杆菌与人类先天免疫细胞的相互作用提供了新的发现,有助于理解感染期间巨噬细胞中的潜在调节机制。