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感染细粒棘球蚴病绵羊肝脏中的基因表达谱

Gene Expression Profile in the Liver of Sheep Infected with Cystic Echinococcosis.

作者信息

Hui Wenqiao, Jiang Song, Liu Xianxia, Ban Qian, Chen Sheng, Jia Bin

机构信息

Institute of Animal Husbandary and Veterinary Medicine, Anhui Academy of Agriculture Sciences, Road Nongkenan, Hefei, 230031, Anhui, People's Republic of China.

College of Animal Science and Technology, Shihezi University, Road Beisi, Shihezi, 832003, Xinjiang, People's Republic of China.

出版信息

PLoS One. 2016 Jul 28;11(7):e0160000. doi: 10.1371/journal.pone.0160000. eCollection 2016.

Abstract

BACKGROUND

Cystic Echinococcosis (CE), caused by infection with the Echinococcus granulosus (E. granulosus), represents considerable health problems in both humans and livestock. Nevertheless, the genetic program that regulates the host response to E. granulosus infection is largely unknown. Previously, using microarray analysis, we found that the innate immunity played a vital role in the E. granulosus defense of the intestine tissue where E. granulosus first invaded. Subsequently, we turned our attention to investigating the molecular immune mechanism in its organ target, the liver, which is where the E. granulosus metacestodes are established and live for very long periods. In this work, the microarray-based methodology was used to study gene expression profiles in the liver of sheep infected with E. granulosus at 8 weeks post infection, corresponding to the early cystic established phase.

METHODS

A total of 6 female-1-year-old healthy Kazakh sheep were used for the experiments. Three Kazakh sheep were orally infected with E. granulosus eggs, and the others remained untreated and served as controls. Sheep were humanely euthanized and necropsized at 8 weeks post-infection (the early stage of cyst established). The microarray was used to detect differential hepatic gene expression between CE infection sheep and healthy controls at this time point. Real-time PCR was used to validate the microarray data.

RESULTS

We found that E. granulosus infection induces 153 differentially expressed genes in the livers of infected sheep compared with healthy controls. Among them, 87 genes were up-regulated, and 66 genes were notably down-regulated. Functional analysis showed that these genes were associated with three major functional categories: (a) metabolism, (b) the immune system and (c) signaling and transport. Deeper analysis indicated that complement together with other genes associated with metabolism, played important roles in the defense of E. granulosus infection.

CONCLUSION

The present study identified genes profiling in the liver tissue of E. granulosus infection in sheep. The expression pattern obtained here could be helpful for understanding the molecular immunity mechanisms of host responses to E. granulosus infection. However, it is necessary to carry out further studies to evalute the role of these genes.

摘要

背景

由细粒棘球绦虫(E. granulosus)感染引起的囊型包虫病(CE)给人类和家畜带来了相当严重的健康问题。然而,调节宿主对细粒棘球绦虫感染反应的遗传程序在很大程度上尚不清楚。此前,通过微阵列分析,我们发现先天免疫在细粒棘球绦虫首次侵入的肠道组织防御中起着至关重要的作用。随后,我们将注意力转向研究其器官靶点肝脏中的分子免疫机制,细粒棘球绦虫的囊尾蚴在肝脏中形成并长期存活。在这项工作中,基于微阵列的方法被用于研究感染细粒棘球绦虫8周后的绵羊肝脏中的基因表达谱,这一时期对应于早期囊型形成阶段。

方法

总共6只1岁的健康哈萨克雌性绵羊用于实验。3只哈萨克绵羊经口感染细粒棘球绦虫卵,其余绵羊不进行处理作为对照。在感染后8周(囊型形成的早期阶段)对绵羊进行人道安乐死并剖检。使用微阵列检测此时CE感染绵羊和健康对照之间肝脏基因表达的差异。实时PCR用于验证微阵列数据。

结果

我们发现与健康对照相比,细粒棘球绦虫感染诱导感染绵羊肝脏中有153个差异表达基因。其中,87个基因上调,66个基因显著下调。功能分析表明这些基因与三个主要功能类别相关:(a)代谢,(b)免疫系统,以及(c)信号传导和转运。进一步分析表明,补体以及其他与代谢相关的基因在防御细粒棘球绦虫感染中发挥重要作用。

结论

本研究确定了绵羊细粒棘球绦虫感染肝脏组织中的基因谱。这里获得的表达模式可能有助于理解宿主对细粒棘球绦虫感染反应的分子免疫机制。然而,有必要进行进一步研究以评估这些基因的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a2f/4965101/f017ff72eab1/pone.0160000.g001.jpg

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