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运用网络理论推断钩端螺旋体属和智人种之间的病原体-宿主相互作用。

Inferring pathogen-host interactions between Leptospira interrogans and Homo sapiens using network theory.

机构信息

Gujarat Biotechnology Research Centre, Department of Science & Technology, Government of Gujarat, Gandhinagar, 382011, India.

出版信息

Sci Rep. 2019 Feb 5;9(1):1434. doi: 10.1038/s41598-018-38329-1.

Abstract

Leptospirosis is the most emerging zoonotic disease of epidemic potential caused by pathogenic species of Leptospira. The bacterium invades the host system and causes the disease by interacting with the host proteins. Analyzing these pathogen-host protein interactions (PHPIs) may provide deeper insight into the disease pathogenesis. For this analysis, inter-species as well as intra-species protein interactions networks of Leptospira interrogans and human were constructed and investigated. The topological analyses of these networks showed lesser connectivity in inter-species network than intra-species, indicating the perturbed nature of the inter-species network. Hence, it can be one of the reasons behind the disease development. A total of 35 out of 586 PHPIs were identified as key interactions based on their sub-cellular localization. Two outer membrane proteins (GpsA and MetXA) and two periplasmic proteins (Flab and GlyA) participating in PHPIs were found conserved in all pathogenic, intermediate and saprophytic spp. of Leptospira. Furthermore, the bacterial membrane proteins involved in PHPIs were found playing major roles in disruption of the immune systems and metabolic processes within host and thereby causing infectious disease. Thus, the present results signify that the membrane proteins participating in such interactions hold potential to serve as effective immunotherapeutic candidates for vaccine development.

摘要

钩端螺旋体病是一种最具流行潜力的新兴人畜共患传染病,由致病性钩端螺旋体引起。细菌通过与宿主蛋白相互作用入侵宿主系统并引发疾病。分析这些病原体-宿主蛋白相互作用(PHPIs)可能会深入了解疾病的发病机制。为此,构建并研究了钩端螺旋体 interrogans 和人类的种间和种内蛋白相互作用网络。这些网络的拓扑分析表明,种间网络的连接性小于种内网络,表明种间网络的性质受到干扰。因此,这可能是疾病发展的原因之一。根据亚细胞定位,从 586 个 PHPIs 中确定了 35 个为关键相互作用。参与 PHPIs 的两种外膜蛋白(GpsA 和 MetXA)和两种周质蛋白(Flab 和 GlyA)在所有致病性、中间型和腐生型钩端螺旋体中均保守。此外,参与 PHPIs 的细菌膜蛋白被发现主要作用于破坏宿主的免疫系统和代谢过程,从而导致传染病。因此,目前的结果表明,参与这些相互作用的膜蛋白有可能成为疫苗开发的有效免疫治疗候选物。

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