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感染犬弓首蛔虫引起内脏和脑幼虫移行症的BALB/c小鼠血浆循环微小RNA的变化

Alterations of plasma circulating microRNAs in BALB/c mice with Toxocara canis visceral and cerebral larva migrans.

作者信息

Yang Yifan, Chen Yi, Zheng Zhiwan, Lin Lijun, Chen Xueqiu, Yang Chenyu, Zhong Die, Wu Haiyan, Xiong Zhiwei, Liu Sishi, Wang Tao, Yang Yi, Du Aifang, Ma Guangxu

机构信息

College of Animal Sciences, Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Zhejiang University, Hangzhou, China.

Department of Pathogenic Biology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, China.

出版信息

Parasit Vectors. 2024 Jun 12;17(1):256. doi: 10.1186/s13071-024-06327-0.

Abstract

BACKGROUND

Human toxocariasis is a neglected parasitic disease characterised by the syndromes visceral, cerebral, and ocular larva migrans. This disease is caused by the migrating larvae of Toxocara roundworms from dogs and cats, affecting 1.4 billion people globally. Via extracellular vesicles (EVs), microRNAs have been demonstrated to play roles in host-parasite interactions and proposed as circulating biomarkers for the diagnosis and follow-up of parasitic diseases.

METHODS

Small RNA-seq was conducted to identify miRNAs in the infective larvae of T. canis and plasma EV-containing preparations of infected BALB/c mice. Differential expression analysis and target prediction were performed to indicate miRNAs involved in host-parasite interactions and miRNAs associated with visceral and/or cerebral larva migrans in the infected mice. Quantitative real-time polymerase chain reaction (PCR) was used to amplify circulating miRNAs from the infected mice.

RESULTS

This study reports host and parasite miRNAs in the plasma of BALB/c mice with visceral and cerebral larva migrans and demonstrates the alterations of these miRNAs during the migration of larvae from the livers through the lungs and to the brains of infected mice. After filtering unspecific changes in an irrelevant control, T. canis-derived miRNAs and T. canis infection-induced differential miRNAs are predicted to modulate genes consistently involved in mitogen-activated protein kinase (MAPK) signalling and pathways regulating axon guidance and pluripotency of stem in the infected mice with visceral and cerebral larva migrans. For these plasma circulating miRNAs predicted to be involved in host-parasite crosstalk, two murine miRNAs (miR-26b-5p and miR-122-5p) are experimentally verified to be responsive to larva migrans and represent circulating biomarker candidates for visceral and cerebral toxocariasis in BALB/c mice.

CONCLUSIONS

Our findings provide novel insights into the crosstalk of T. canis and the mammalian host via plasma circulating miRNAs, and prime agents and indicators for visceral and cerebral larva migrans. A deep understanding of these aspects will underpin the diagnosis and control of toxocariasis in humans and animals.

摘要

背景

人体弓蛔虫病是一种被忽视的寄生虫病,其特征为内脏幼虫移行症、脑幼虫移行症和眼幼虫移行症综合征。这种疾病由犬弓蛔虫和猫弓蛔虫的移行幼虫引起,全球有14亿人受其影响。通过细胞外囊泡(EVs),已证明微小RNA在宿主-寄生虫相互作用中发挥作用,并被提议作为寄生虫病诊断和随访的循环生物标志物。

方法

进行小RNA测序以鉴定犬弓蛔虫感染性幼虫和感染BALB/c小鼠的含血浆EV制剂中的微小RNA。进行差异表达分析和靶标预测,以表明参与宿主-寄生虫相互作用的微小RNA以及与感染小鼠内脏和/或脑幼虫移行症相关的微小RNA。使用定量实时聚合酶链反应(PCR)扩增感染小鼠的循环微小RNA。

结果

本研究报告了患有内脏和脑幼虫移行症的BALB/c小鼠血浆中的宿主和寄生虫微小RNA,并证明了这些微小RNA在幼虫从感染小鼠的肝脏经肺向脑移行过程中的变化。在过滤无关对照中的非特异性变化后,预测犬弓蛔虫来源的微小RNA和犬弓蛔虫感染诱导的差异微小RNA可调节感染内脏和脑幼虫移行症小鼠中始终参与丝裂原活化蛋白激酶(MAPK)信号传导以及调节轴突导向和干细胞多能性的途径的基因。对于这些预测参与宿主-寄生虫相互作用的血浆循环微小RNA,实验验证了两种小鼠微小RNA(miR-26b-5p和miR-122-5p)对幼虫移行有反应,并代表BALB/c小鼠内脏和脑弓蛔虫病的循环生物标志物候选物。

结论

我们的研究结果为犬弓蛔虫与哺乳动物宿主通过血浆循环微小RNA的相互作用以及内脏和脑幼虫移行症的主要因素和指标提供了新的见解。对这些方面的深入理解将为人类和动物弓蛔虫病的诊断和控制提供支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d07/11167859/2a5f7d10d5ad/13071_2024_6327_Fig1_HTML.jpg

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