Titlebook: Salmonella; Methods and Protocol Heide Schatten Book 2021Latest edition Springer Science+Business Media, LLC, part of Springer Nature 2021

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CRISPR Typing of , Isolates from Different Resources, can not only reveal the phylogenic difference among isolates belonging to the identical serotype, but also show good correspondence with . serotypes. Here we describe the protocol of CRISPR typing method used in ., and the approaches to analyze the genetic relationship among different strains.

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Immunomagnetic Separation of , with Tailored Magnetic Micro- and Nanocarriers,el developments that are needed involve solid-phase preconcentration procedures which can be easily integrated with emerging technologies. Here, we describe the immunomagnetic separation (IMS) of . using magnetic carriers. Nano (300 nm) and micro (2.8 μm) sized magnetic particles are modified with a

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Self-Labeling Enzyme Tags for Translocation Analyses of , Effector Proteins,dependent on the translocation of effector proteins by two distinct type III secretion systems (T3SS) into the host cell. To unravel host-pathogen interactions, dedicated imaging techniques visualizing . effector proteins during the infection are essential. Here we describe a new approach utilizing

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Correlative Light and Scanning Electron Microscopy to Study Interactions of , with Polarized Epithepolarized epithelial cells by . sv. Typhimurium. Scanning electron microscopy provides highest resolution of surface structures of infected cells, providing ultrastructure of the apical side of host cells and infecting .. Combining both methods toward correlative light and scanning electron microsco

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Production of Murine Macrophages from Hoxb8-Immortalized Myeloblasts: Utility and Use in the Contexthe ability of . to survive/replicate in macrophages, particularly in the liver and spleen, is crucial for virulence. Transformed macrophage cell lines and primary macrophages prepared from mouse bone marrow are commonly used models for the study of . infection. However, these models raise technical

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Generation of Random , Transcriptional Fusions in the Genome of ,random transcriptional fusions of the . operon to genes of the . genome, (2) screen for specific fusions with constitutive expression, . pathogenicity island 1-related expression, or . pathogenicity island 2-related expression, and (3) determine the site of . integration.

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Detection and Characterization of , Serotypes by Simple PCR Technologies,ing how we understand disease landscape. This technology has been found amenable to application on various strategies for management and control of infectious diseases. The main advantage with PCR technologies, when applied optimally, is the high sensitivity and short-turn-around time for results, t