...
首页> 外文期刊>BMC Genomics >Simultaneous transcriptional profiling of Leishmania major and its murine macrophage host cell reveals insights into host-pathogen interactions
【24h】

Simultaneous transcriptional profiling of Leishmania major and its murine macrophage host cell reveals insights into host-pathogen interactions

机译:利什曼原虫及其鼠巨噬细胞宿主细胞的同时转录分析揭示了宿主-病原体相互作用的见解

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Parasites of the genus Leishmania are the causative agents of leishmaniasis, a group of diseases that range in manifestations from skin lesions to fatal visceral disease. The life cycle of Leishmania parasites is split between its insect vector and its mammalian host, where it resides primarily inside of macrophages. Once intracellular, Leishmania parasites must evade or deactivate the host's innate and adaptive immune responses in order to survive and replicate. We performed transcriptome profiling using RNA-seq to simultaneously identify global changes in murine macrophage and L. major gene expression as the parasite entered and persisted within murine macrophages during the first 72?h of an infection. Differential gene expression, pathway, and gene ontology analyses enabled us to identify modulations in host and parasite responses during an infection. The most substantial and dynamic gene expression responses by both macrophage and parasite were observed during early infection. Murine genes related to both pro- and anti-inflammatory immune responses and glycolysis were substantially upregulated and genes related to lipid metabolism, biogenesis, and Fc gamma receptor-mediated phagocytosis were downregulated. Upregulated parasite genes included those aimed at mitigating the effects of an oxidative response by the host immune system while downregulated genes were related to translation, cell signaling, fatty acid biosynthesis, and flagellum structure. The gene expression patterns identified in this work yield signatures that characterize multiple developmental stages of L. major parasites and the coordinated response of Leishmania-infected macrophages in the real-time setting of a dual biological system. This comprehensive dataset offers a clearer and more sensitive picture of the interplay between host and parasite during intracellular infection, providing additional insights into how pathogens are able to evade host defenses and modulate the biological functions of the cell in order to survive in the mammalian environment.
机译:利什曼原虫属的寄生虫是利什曼原虫病的病原体,利什曼原虫病是一系列疾病,其表现形式从皮肤损害到致命内脏疾病。利什曼原虫寄生虫的生命周期在其昆虫媒介和哺乳动物宿主之间分配,后者主要生活在巨噬细胞内部。一旦进入细胞内,利什曼原虫寄生虫必须逃避或失活宿主的先天性和适应性免疫反应才能生存和复制。我们使用RNA-seq进行了转录组分析,以同时确定在感染的前72小时内寄生虫进入并在鼠巨噬细胞内持续存在时,鼠巨噬细胞和L.主要基因表达的总体变化。差异基因表达,途径和基因本体分析使我们能够确定感染期间宿主和寄生虫反应中的调节。在早期感染中观察到了巨噬细胞和寄生虫的最实质和最动态的基因表达反应。与促炎和抗炎免疫反应以及糖酵解相关的鼠基因被上调,而与脂质代谢,生物发生和Fcγ受体介导的吞噬作用相关的基因被下调。上调的寄生虫基因包括那些旨在减轻宿主免疫系统氧化反应影响的基因,而下调的基因则与翻译,细胞信号传导,脂肪酸的生物合成和鞭毛结构有关。在这项工作中确定的基因表达模式产生了特征性特征,这些特征性特征描述了利什曼原虫感染的巨噬细胞在双重生物系统的实时环境中的主要寄生虫的多个发育阶段和协同反应。这个全面的数据集提供了细胞内感染过程中宿主与寄生虫之间相互作用的更清晰,更敏感的图景,为病原体如何逃避宿主防御并调节细胞的生物学功能以在哺乳动物环境中生存提供了更多见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号