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刚地弓形虫感染诱导牛单核细胞来源的巨噬细胞中一种与分离株毒力相关的促炎基因表达谱。

Neospora caninum infection induces an isolate virulence-dependent pro-inflammatory gene expression profile in bovine monocyte-derived macrophages.

机构信息

Saluvet, Animal Health Department, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, 28040, Madrid, Spain.

Saluvet-Innova, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, 28040, Madrid, Spain.

出版信息

Parasit Vectors. 2020 Jul 25;13(1):374. doi: 10.1186/s13071-020-04239-3.

Abstract

BACKGROUND

Neospora caninum is an obligate intracellular parasite, and its ability to survive inside host immune cells may be a key mechanism for the establishment of infection in cattle. In vitro studies carried out by our group have shown that N. caninum is able to replicate in bovine macrophages (MØs), alter their microbicidal mechanisms and exploit their motility. Furthermore, host-cell control seems to be isolate virulence-dependent.

METHODS

To investigate the molecular basis underlying the innate responses in MØs against N. caninum and the mechanisms of parasite manipulation of the host cell environment, the transcriptome profile of bovine monocyte-derived MØs infected with high-virulence (Nc-Spain7) or low-virulence (Nc-Spain1H) N. caninum isolates was studied.

RESULTS

Functional enrichment revealed upregulation of genes involved in chemokine signalling, inflammation, cell survival, and inhibition of genes related with metabolism and phagolysosome formation. MØs activation was characterized by the induction of a predominantly M1 phenotype with expression of TLR2, TLR3 and TLR9 and activation of the NF-ƙB signalling pathway. Heat-killed N. caninum tachyzoites failed to activate NF-ƙB, and to inhibit lysosomal activity and apoptosis, which indicates active modulation by the parasite. The FoxO signalling pathway, Th1-Th2 differentiation, glycosaminoglycan degradation and apoptosis were pathways enriched only for low virulent Nc-Spain1H infection. In addition, Nc-Spain1H infection upregulated the IL12A and IL8 pro-inflammatory cytokines, whereas IL23 was downregulated by high virulent Nc-Spain7.

CONCLUSIONS

This study revealed mechanisms implicated in the recognition of N. caninum by bovine MØs and in the development of the subsequent immune response. NF-ƙB seems to be the main signalling pathway implicated in the pro-inflammatory bovine MØs response against this pathogen. Apoptosis and phagolysosome maturation are processes repressed by N. caninum infection, which may guarantee its intracellular survival. The results also indicate that Nc-Spain7 may be able to partially circumvent the pro-inflammatory response whereas Nc-Spain1H induces a protective response to infection, which may explain the more efficient transmission of the high-virulence Nc-Spain7 isolate observed in vivo.

摘要

背景

刚地弓形虫是一种必需的细胞内寄生虫,其在宿主免疫细胞内生存的能力可能是其在牛体内建立感染的关键机制。我们小组进行的体外研究表明,刚地弓形虫能够在牛巨噬细胞(MØ)中复制,改变其杀菌机制并利用其运动能力。此外,宿主细胞的控制似乎与分离的毒力依赖性有关。

方法

为了研究 MØ 对刚地弓形虫固有反应的分子基础以及寄生虫对宿主细胞环境的操纵机制,研究了高毒力(Nc-Spain7)和低毒力(Nc-Spain1H)刚地弓形虫分离株感染的牛单核细胞衍生 MØ 的转录组谱。

结果

功能富集显示,参与趋化因子信号转导、炎症、细胞存活的基因上调,而与代谢和吞噬体形成相关的基因下调。MØ 的激活表现为诱导主要的 M1 表型,表达 TLR2、TLR3 和 TLR9,并激活 NF-ƙB 信号通路。热灭活的刚地弓形虫速殖子未能激活 NF-ƙB,并抑制溶酶体活性和细胞凋亡,这表明寄生虫的活性调节。FoxO 信号通路、Th1-Th2 分化、糖胺聚糖降解和细胞凋亡仅在低毒力 Nc-Spain1H 感染时富集。此外,Nc-Spain1H 感染上调了促炎细胞因子 IL12A 和 IL8,而高毒力 Nc-Spain7 下调了 IL23。

结论

本研究揭示了牛 MØ 识别刚地弓形虫和随后免疫反应发展所涉及的机制。NF-ƙB 似乎是参与针对这种病原体的促炎牛 MØ 反应的主要信号通路。凋亡和吞噬体成熟是被刚地弓形虫感染抑制的过程,这可能保证其细胞内生存。研究结果还表明,Nc-Spain7 可能能够部分规避促炎反应,而 Nc-Spain1H 则诱导对感染的保护性反应,这可能解释了在体内观察到的高毒力 Nc-Spain7 分离株更有效的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f611/7382829/23071b9e834e/13071_2020_4239_Fig1_HTML.jpg

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