Shanghai Veterinary Research Institute, Key Laboratory of Animal Parasitology of Ministry of Agriculture and Rural Affairs, Chinese Academy of Agricultural Sciences, Shanghai, China.
Shanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Tongji University School of Medicine, Shanghai, China.
Front Cell Infect Microbiol. 2022 Feb 28;12:803242. doi: 10.3389/fcimb.2022.803242. eCollection 2022.
is a genus of parasitic trematodes that undergoes complex migration in final hosts, finally developing into adult worms, which are responsible for egg production and disease dissemination. Recent studies documented the importance of extracellular vesicles (EVs) in the regulation of host-parasite interactions. Herein, we investigated the microRNA (miRNA) profiles of EVs isolated from host plasma at different stages of infection (lung stage: 3 days post-infection (dpi), and liver stages: 14 and 21 dpi) to identify miRNA cargo potentially involved in the pathogenesis and immune regulation of schistosomiasis. Characterization of the isolated plasma EVs revealed their diameter to be approximately 100 nm, containing typical EV markers such as Hsp70 and Tsg101. Deep sequencing analysis indicated the presence of 811 known and 15 novel miRNAs with an increasing number of differential miRNAs from the lung stage (27 miRNAs) to the liver stages (58 and 96 miRNAs at 14 and 21 dpi, respectively) in the plasma EVs of infected mice compared to EVs isolated from the uninfected control. In total, 324 plasma EV miRNAs were shown to be co-detected among different stages of infection and the validation of selected miRNAs showed trends of abundance similar to deep sequencing analysis. For example, and showed higher abundance, whereas and showed lower abundance in the plasma EVs of infected mice at 3, 14, and 21 dpi as compared to those of uninfected mice. In addition, bioinformatic analysis combined with PCR validation of the miRNA targets, particularly those associated with the immune system and parasitic infectious disease, indicated a significant increase in the expression of and in contrast to the decreased expression of , and . Our results suggested that the abundance of miRNA cargo of the host plasma EVs was related to the stages of infection. Further studies on the roles of these miRNAs may reveal the regulatory mechanism of the host-parasite interaction. Moreover, the differentially abundant miRNA cargo in host EVs associated with infection may also provide valuable clues for identifying novel biomarkers for schistosomiasis diagnosis.
是寄生性吸虫的一个属,在终末宿主中经历复杂的迁移,最终发育为成虫,成虫负责产卵和疾病传播。最近的研究证明了细胞外囊泡(EVs)在调节宿主-寄生虫相互作用中的重要性。在此,我们研究了从宿主血浆中分离的 EV 在 感染的不同阶段(肺期:感染后 3 天(dpi),肝期:14 和 21 dpi)的 miRNA 谱,以鉴定可能参与血吸虫病发病机制和免疫调节的 miRNA 货物。分离的血浆 EV 的特征表明其直径约为 100nm,包含 HSP70 和 Tsg101 等典型的 EV 标志物。深度测序分析表明,与未感染对照相比,感染小鼠血浆 EV 中存在 811 种已知和 15 种新的 miRNA,从肺期(27 种 miRNA)到肝期(14 和 21dpi 分别为 58 和 96 种 miRNA)的差异 miRNA 数量不断增加。总共检测到 324 种在不同感染阶段共同存在的血浆 EV miRNA,对选定 miRNA 的验证表明其丰度趋势与深度测序分析相似。例如,在感染小鼠的血浆 EV 中,和 表现出更高的丰度,而 和 则表现出更低的丰度,与未感染小鼠相比,在感染小鼠的血浆 EV 中,3、14 和 21dpi 时的丰度更高。此外,结合 miRNA 靶标生物信息学分析和 PCR 验证,特别是与免疫系统和寄生虫感染性疾病相关的靶标,表明和 的表达显著增加,而 、 和 的表达显著降低。我们的研究结果表明,宿主血浆 EV 的 miRNA 货物丰度与 感染的阶段有关。对这些 miRNA 作用的进一步研究可能揭示宿主-寄生虫相互作用的调节机制。此外,与 感染相关的宿主 EV 中差异丰富的 miRNA 货物也可能为鉴定血吸虫病诊断的新型生物标志物提供有价值的线索。