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斑马鱼幼体全蛋白质组分析揭示的宿主-病原体相互作用

Host-Pathogen Interaction as Revealed by Global Proteomic Profiling of Zebrafish Larvae.

作者信息

Díaz-Pascual Francisco, Ortíz-Severín Javiera, Varas Macarena A, Allende Miguel L, Chávez Francisco P

机构信息

Laboratorio de Microbiología de Sistemas, Departamento de Biología, Facultad de Ciencias, Universidad de ChileSantiago, Chile.

Centro FONDAP de Regulación del Genoma, Universidad de ChileSantiago, Chile.

出版信息

Front Cell Infect Microbiol. 2017 Jul 25;7:334. doi: 10.3389/fcimb.2017.00334. eCollection 2017.

Abstract

The outcome of a host-pathogen interaction is determined by the conditions of the host, the pathogen, and the environment. Although numerous proteomic studies of -grown microbial pathogens have been performed, proteomic approaches are still rare. In addition, increasing evidence supports that studies inadequately reflect conditions. Choosing the proper host is essential to detect the expression of proteins from the pathogen . Numerous studies have demonstrated the suitability of zebrafish () embryos as a model to studies of infection. In most zebrafish-pathogen studies, infection is achieved by microinjection of bacteria into the larvae. However, few reports using static immersion of bacterial pathogens have been published. In this study we infected 3 days post-fertilization (DPF) zebrafish larvae with PAO1 by immersion and injection and tracked the immune response by the zebrafish. Additionally, by using non-isotopic (Q-exactive) metaproteomics we simultaneously evaluated the proteomic response of the pathogen ( PAO1) and the host (zebrafish). We found some zebrafish metabolic pathways, such as hypoxia response via HIF activation pathway, were exclusively enriched in the larvae exposed by static immersion. In contrast, we found that inflammation mediated by chemokine and cytokine signaling pathways was exclusively enriched in the larvae exposed by injection, while the integrin signaling pathway and angiogenesis were solely enriched in the larvae exposed by immersion. We also found important virulence factors from that were enriched only after exposure by injection, such as the Type-III secretion system and flagella-associated proteins. On the other hand, proteins involved in processes like biofilm formation, and cellular responses to antibiotic and starvation were enriched exclusively after exposure by immersion. We demonstrated the suitability of zebrafish embryos as a model for host-pathogen based proteomic studies in . Our global proteomic profiling identifies novel molecular signatures that give systematic insight into zebrafish- interaction.

摘要

宿主与病原体相互作用的结果由宿主、病原体和环境的条件决定。尽管已经对培养的微生物病原体进行了大量蛋白质组学研究,但蛋白质组学方法仍然很少见。此外,越来越多的证据表明,这些研究不足以反映实际情况。选择合适的宿主对于检测病原体的蛋白质表达至关重要。许多研究已经证明斑马鱼胚胎作为感染研究模型的适用性。在大多数斑马鱼与病原体的研究中,感染是通过将细菌显微注射到幼虫体内实现的。然而,使用细菌病原体静态浸泡的报道很少。在本研究中,我们通过浸泡和注射用铜绿假单胞菌PAO1感染受精后3天(DPF)的斑马鱼幼虫,并追踪斑马鱼的免疫反应。此外,通过使用非同位素(Q-Exactive)宏蛋白质组学,我们同时评估了病原体(PAO1)和宿主(斑马鱼)的蛋白质组学反应。我们发现一些斑马鱼代谢途径,如通过HIF激活途径的缺氧反应,仅在静态浸泡暴露的幼虫中富集。相反,我们发现由趋化因子和细胞因子信号通路介导的炎症仅在注射暴露的幼虫中富集,而整合素信号通路和血管生成仅在浸泡暴露的幼虫中富集。我们还发现来自铜绿假单胞菌的重要毒力因子仅在注射暴露后富集,如III型分泌系统和鞭毛相关蛋白。另一方面,参与生物膜形成以及细胞对抗生素和饥饿反应等过程的蛋白质仅在浸泡暴露后富集。我们证明了斑马鱼胚胎作为基于宿主-病原体蛋白质组学研究模型的适用性。我们的全球蛋白质组学分析确定了新的分子特征,为斑马鱼与铜绿假单胞菌的相互作用提供了系统的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04b4/5524664/7662e5843c8d/fcimb-07-00334-g0001.jpg

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