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庆大霉素保护试验以确定人TC7肠上皮细胞感染期间细胞内细菌的数量 。 (原文by后内容缺失)

Gentamicin Protection Assay to Determine the Number of Intracellular Bacteria during Infection of Human TC7 Intestinal Epithelial Cells by .

作者信息

Sharma Atin, Puhar Andrea

机构信息

The Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå, Sweden.

Umeå Centre for Microbial Research (UCMR), Umeå, Sweden.

出版信息

Bio Protoc. 2019 Jul 5;9(13):e3292. doi: 10.21769/BioProtoc.3292.

Abstract

is an intracellular bacterial pathogen that gains access to the gut epithelium using a specialized Type III Secretion System (T3SS). Various determinants mediating this invasive infection have been experimentally verified using the classical gentamicin protection assay presented here. In this assay epithelial cell lines are infected by bacteria and the extracellular bacteria are killed by gentamicin. The internalized bacteria, which are protected from the bactericidal action of gentamicin, are recovered by lysing the epithelial cells and enumerated by determining the colonies formed on solid medium. Various techniques based on light microscopy, such as immunofluorescence and bacteria expressing fluorescent proteins, are also used for studying intracellular bacteria. However, these techniques are not only labor intensive and require sophisticated equipment, but mostly are also not quantitative. Despite being an easy quantitative method to study invasiveness of bacteria, the gentamicin protection assay cannot distinguish between the survival and multiplication of the internalized bacteria over longer incubation periods. To alleviate the complications created by multiplication and dissemination of internalized bacteria, complementary assays like plaque formation assays are required. This protocol presents an easy and cost-effective method to determine the invasiveness and the capacity to establish an infection of under different conditions.

摘要

是一种细胞内细菌病原体,它利用专门的III型分泌系统(T3SS)进入肠道上皮。使用本文介绍的经典庆大霉素保护试验已通过实验验证了介导这种侵袭性感染的各种决定因素。在该试验中,上皮细胞系被细菌感染,细胞外细菌被庆大霉素杀死。免受庆大霉素杀菌作用的内化细菌通过裂解上皮细胞回收,并通过测定固体培养基上形成的菌落进行计数。基于光学显微镜的各种技术,如免疫荧光和表达荧光蛋白的细菌,也用于研究细胞内细菌。然而,这些技术不仅劳动强度大,需要精密设备,而且大多也不是定量的。尽管庆大霉素保护试验是一种研究细菌侵袭性的简单定量方法,但在较长的孵育期内,它无法区分内化细菌的存活和增殖。为了减轻内化细菌增殖和传播所带来的复杂性,需要像噬斑形成试验这样的补充试验。本方案提出了一种简单且经济高效的方法,用于确定在不同条件下的侵袭性和建立感染的能力。

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