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金黄色葡萄球菌感染的小鼠模型。

Murine Models for Staphylococcal Infection.

机构信息

Division of Infectious Disease, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.

出版信息

Curr Protoc. 2021 Mar;1(3):e52. doi: 10.1002/cpz1.52.

Abstract

Staphylococcus aureus is a Gram-positive bacterium that colonizes almost every organ in humans and mice and is a leading cause of diseases worldwide. S. aureus infections can be challenging to treat due to widespread antibiotic resistance and their ability to cause tissue damage. The primary modes of transmission of S. aureus are via direct contact with a colonized or infected individual or invasive spread from a colonization niche in the same individual. S. aureus can cause a myriad of diseases, including skin and soft tissue infections (SSTIs), osteomyelitis, pneumonia, endocarditis, and sepsis. S. aureus infection is characterized by the formation of purulent lesions known as abscesses, which are rich in live and dead neutrophils, macrophages, and surrounded by a capsule containing fibrin and collagen. Different strains of S. aureus produce varying amounts of toxins that evade and/or elicit immune responses. Therefore, animal models of S. aureus infection provide a unique opportunity to understand the dynamics of organ-specific immune responses and modifications in the pathogen that could favor the establishment of the pathogen. With advances in in vivo imaging of fluorescent transgenic mice, combined with fluorescent/bioluminescent bacteria, we can use mouse models to better understand the immune response to these types of infections. By understanding the host and bacterial dynamics within various organ systems, we can develop therapeutics to eliminate these pathogens. This module describes in vivo mouse models of both local and systemic S. aureus infection. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Murine model of Staphylococcus aureus subcutaneous infection Alternate Protocol: Murine tape stripping skin infection model Basic Protocol 2: Sample collection to determine skin structure, production of inflammatory mediators, and bacterial load Basic Protocol 3: Murine model of post-traumatic Staphylococcus aureus osteomyelitis Basic Protocol 4: Intravenous infection of the retro-orbital sinus Support Protocol: Preparation of the bacterial inoculum.

摘要

金黄色葡萄球菌是一种革兰氏阳性细菌,它定植于人类和小鼠的几乎每个器官,是全球疾病的主要原因。由于广泛的抗生素耐药性和引起组织损伤的能力,金黄色葡萄球菌感染的治疗具有挑战性。金黄色葡萄球菌的主要传播途径是直接接触定植或感染个体,或在同一个体的定植部位进行侵袭性传播。金黄色葡萄球菌可引起多种疾病,包括皮肤和软组织感染(SSTIs)、骨髓炎、肺炎、心内膜炎和败血症。金黄色葡萄球菌感染的特征是形成称为脓肿的化脓性病变,脓肿富含活的和死的中性粒细胞、巨噬细胞,并被含有纤维蛋白和胶原蛋白的胶囊包围。不同的金黄色葡萄球菌株产生不同数量的毒素,这些毒素可以逃避和/或引发免疫反应。因此,金黄色葡萄球菌感染的动物模型提供了一个独特的机会,可以了解特定器官免疫反应的动态变化,以及病原体的改变,这些改变可能有利于病原体的建立。随着体内荧光转基因小鼠成像技术的进步,结合荧光/生物发光细菌,我们可以使用小鼠模型来更好地理解这些类型感染的免疫反应。通过了解不同器官系统中的宿主和细菌动态,我们可以开发消除这些病原体的疗法。本模块描述了金黄色葡萄球菌局部和全身感染的体内小鼠模型。 © 2021 威立出版社。 基本方案 1:金黄色葡萄球菌皮下感染的小鼠模型 可选方案 1:小鼠胶带剥离皮肤感染模型 基本方案 2:收集样本以确定皮肤结构、炎症介质的产生和细菌负荷 基本方案 3:创伤后金黄色葡萄球菌骨髓炎的小鼠模型 基本方案 4:经眶后窦静脉感染 支持方案:细菌接种物的制备。

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