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用于研究嗜肺军团菌毒力分子机制的蜡螟感染模型

The Galleria mellonella Infection Model for Investigating the Molecular Mechanisms of Legionella Virulence.

作者信息

Frankel Gad, Schroeder Gunnar N

机构信息

MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.

Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.

出版信息

Methods Mol Biol. 2019;1921:333-346. doi: 10.1007/978-1-4939-9048-1_22.

Abstract

Legionella species evolved virulence factors to exploit protozoa as replicative niches in the environment. Cell culture infection models demonstrated that many of these factors also enable the bacteria to thrive in human macrophages; however, these models do not recapitulate the complex interactions between macrophages, lung epithelial, and additional immune cells, which are crucial to control bacterial infections. Thus, suitable infection models are required to understand which bacterial factors are important to trigger disease. Guinea pigs and, most frequently, mice have been successfully used as mammalian model hosts; however, ethical and economic considerations impede their use in high-throughput screening studies of Legionella isolates or small molecule inhibitors.Here, we describe the larvae of the lepidopteran Galleria mellonella as insect model of Legionella pathogenesis. Larvae can be obtained from commercial suppliers in large numbers, maintained without the need of specialized equipment, and infected by injection. Although lacking the complexity of a mammalian immune system, the larvae mount humoral and cellular immune responses to infection. L. pneumophila strain 130b and other prototype isolates withstand these responses and use the Defective in organelle trafficking/Intracellular multiplication (Dot/Icm) type IV secretion system (T4SS ) to inject effectors enabling survival and replication in hemocytes, insect phagocytes, ultimately leading to the death of the larvae. Differences in virulence between L. pneumophila isolates or gene deletion mutants can be analyzed using indicators of larval health and immune induction, such as pigmentation, mobility, histopathology, and survival. Bacterial replication can be measured by plating hemolymph or by immunofluorescence microscopy of isolated circulating hemocytes from infected larvae. Combined, these straightforward experimental readouts make G. mellonella larvae a versatile model host to rapidly assess the virulence of different Legionella isolates and investigate the role of specific virulence factors in overcoming innate host defense mechanisms.

摘要

嗜肺军团菌进化出毒力因子,以便在环境中利用原生动物作为复制场所。细胞培养感染模型表明,其中许多因子也能使细菌在人类巨噬细胞中大量繁殖;然而,这些模型无法重现巨噬细胞、肺上皮细胞和其他免疫细胞之间复杂的相互作用,而这些相互作用对于控制细菌感染至关重要。因此,需要合适的感染模型来了解哪些细菌因子对引发疾病很重要。豚鼠,最常用的是小鼠,已成功用作哺乳动物模型宿主;然而,伦理和经济方面的考虑阻碍了它们在嗜肺军团菌分离株或小分子抑制剂的高通量筛选研究中的应用。在此,我们描述鳞翅目昆虫大蜡螟的幼虫作为嗜肺军团菌致病机制的昆虫模型。幼虫可以从商业供应商处大量获得,无需专门设备即可饲养,并通过注射进行感染。尽管缺乏哺乳动物免疫系统的复杂性,但幼虫会对感染产生体液免疫和细胞免疫反应。嗜肺军团菌130b菌株和其他原型分离株能够抵御这些反应,并利用细胞器运输缺陷/细胞内增殖(Dot/Icm)IV型分泌系统(T4SS)注射效应蛋白,从而在血细胞(昆虫吞噬细胞)中存活和繁殖,最终导致幼虫死亡。可以使用幼虫健康和免疫诱导指标,如色素沉着、活动能力、组织病理学和存活率,来分析嗜肺军团菌分离株或基因缺失突变体之间的毒力差异。细菌复制可以通过接种血淋巴或对感染幼虫分离出的循环血细胞进行免疫荧光显微镜检查来测量。综合起来,这些简单直接的实验读数使大蜡螟幼虫成为一个通用的模型宿主,可快速评估不同嗜肺军团菌分离株的毒力,并研究特定毒力因子在克服宿主固有防御机制中的作用。

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