State Key Laboratory of Veterinary Etiological Biology, National Professional Laboratory for Animal Echinococcosis, Key Laboratory of Veterinary Parasitology of Gansu Province, Key Laboratory of Zoonoses of Agriculture Ministry, Lanzhou Veterinary Research Institute, CAAS, Lanzhou, Gansu, P. R. China.
College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, P. R. China.
PLoS Negl Trop Dis. 2022 May 31;16(5):e0010435. doi: 10.1371/journal.pntd.0010435. eCollection 2022 May.
Almost all Echinococcus multilocularis (Em) infections occur in the liver of the intermediate host, causing a lethal zoonotic helminthic disease, alveolar echinococcosis (AE). However, the long non-coding RNAs (lncRNAs) expression profiles of the host and the potential regulatory function of lncRNA during Em infection are poorly understood. In this study, the profiles of lncRNAs and mRNAs in the liver of mice at different time points after Em infection were explored by microarray. Thirty-one differentially expressed mRNAs (DEMs) and 68 differentially expressed lncRNAs (DELs) were found continuously dysregulated. These DEMs were notably enriched in "antigen processing and presentation", "Th1 and Th2 cell differentiation" and "Th17 cell differentiation" pathways. The potential predicted function of DELs revealed that most DELs might influence Th17 cell differentiation and TGF-β/Smad pathway of host by trans-regulating SMAD3, STAT1, and early growth response (EGR) genes. At 30 days post-infection (dpi), up-regulated DEMs were enriched in Toll-like and RIG-I-like receptor signaling pathways, which were validated by qRT-PCR, Western blotting and downstream cytokines detection. Furthermore, flow cytometric analysis and serum levels of the corresponding cytokines confirmed the changes in cell-mediated immunity in host during Em infection that showed Th1 and Th17-type CD4+ T-cells were predominant at the early infection stage whereas Th2-type CD4+ T-cells were significantly higher at the middle/late stage. Collectively, our study revealed the potential regulatory functions of lncRNAs in modulating host Th cell subsets and provide novel clues in understanding the influence of Em infection on host innate and adaptive immune response.
几乎所有的细粒棘球蚴(Em)感染都发生在中间宿主的肝脏中,导致一种致命的人畜共患寄生虫病,泡型包虫病(AE)。然而,宿主的长非编码 RNA(lncRNA)表达谱及其在 Em 感染过程中的潜在调控功能尚不清楚。在这项研究中,通过微阵列探索了 Em 感染后不同时间点小鼠肝脏中 lncRNA 和 mRNA 的表达谱。发现 31 个差异表达的 mRNA(DEM)和 68 个差异表达的长非编码 RNA(DEL)连续失调。这些 DEM 显著富集于“抗原加工和呈递”、“Th1 和 Th2 细胞分化”和“Th17 细胞分化”途径。DEL 的潜在预测功能表明,大多数 DEL 可能通过反式调控 SMAD3、STAT1 和早期生长反应(EGR)基因,影响宿主 Th17 细胞分化和 TGF-β/Smad 通路。在感染后 30 天(dpi),上调的 DEM 富集于 Toll 样受体和 RIG-I 样受体信号通路,这通过 qRT-PCR、Western blot 和下游细胞因子检测得到验证。此外,流式细胞术分析和相应细胞因子的血清水平证实了宿主在 Em 感染期间细胞介导免疫的变化,表明在早期感染阶段 Th1 和 Th17 型 CD4+T 细胞占优势,而在中期/晚期 Th2 型 CD4+T 细胞显著升高。总之,我们的研究揭示了 lncRNA 调节宿主 Th 细胞亚群的潜在调控功能,并为理解 Em 感染对宿主固有和适应性免疫反应的影响提供了新的线索。