Salmonella Typhimurium Infection of Human Monocyte-Derived Macrophages

Stephanie K. Lathrop, Kendal G. Cooper, Kelsey A. Binder, Tregei Starr, Veena Mampilli, Corrella S. Detweiler, Olivia Steele-Mortimer
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引用次数: 12

Abstract

The successful infection of macrophages by non-typhoidal serovars of Salmonella enterica is likely essential to the establishment of the systemic disease they sometimes cause in susceptible human populations. However, the interactions between Salmonella and human macrophages are not widely studied, with mouse macrophages being a much more common model system. Fundamental differences between mouse and human macrophages make this less than ideal. Additionally, the inability of human macrophage-like cell lines to replicate some properties of primary macrophages makes the use of primary cells desirable. Here we present protocols to study the infection of human monocyte-derived macrophages with Salmonella Typhimurium. These include a method for differentiating monocyte-derived macrophages in vitro and protocols for infecting them with Salmonella Typhimurium, as well as assays to measure the extent of infection, replication, and death. These protocols are useful for the investigation of both bacterial and host factors that determine the outcome of infection. © 2018 by John Wiley & Sons, Inc.

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鼠伤寒沙门菌感染人单核细胞源性巨噬细胞
肠道沙门氏菌非伤寒血清型成功感染巨噬细胞可能是建立它们有时在易感人群中引起的全身性疾病所必需的。然而,沙门氏菌与人类巨噬细胞之间的相互作用尚未得到广泛研究,小鼠巨噬细胞是一种更常见的模型系统。小鼠和人类巨噬细胞之间的根本差异使得这种方法不太理想。此外,人巨噬细胞样细胞系无法复制原代巨噬细胞的某些特性,因此需要使用原代细胞。在这里,我们提出了研究人类单核细胞来源的巨噬细胞感染鼠伤寒沙门菌的方案。这些包括在体外分化单核细胞来源的巨噬细胞的方法和鼠伤寒沙门氏菌感染它们的方案,以及测量感染程度、复制和死亡的试验。这些方案对于调查决定感染结果的细菌和宿主因素都是有用的。©2018 by John Wiley &儿子,Inc。
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来源期刊
Current Protocols in Microbiology
Current Protocols in Microbiology Immunology and Microbiology-Parasitology
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期刊介绍: Current Protocols in Microbiology provides detailed, step-by-step instructions for analyzing bacteria, animal and plant viruses, fungi, protozoans and other microbes. It offers updated coverage of emerging technologies and concepts, such as biofilms, quorum sensing and quantitative PCR, as well as proteomic and genomic methods. It is the first comprehensive source of high-quality microbiology protocols that reflects and incorporates the new mandates and capabilities of this robust and rapidly evolving discipline.
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