Pathogen Elution

Pathogen elution is a laboratory method for recovering microorganisms or their components from a surface, filter, tissue, or other sample matrix into a liquid suspension for analysis. The process uses an elution buffer and controlled washing, agitation, or incubation to disrupt interactions between the pathogen and the material, allowing particles or cells to transfer into the fluid phase. Researchers can then concentrate the eluate or analyze it using culture, microscopy, immunoassays, or molecular detection methods. In immunology and infection research, pathogen elution supports recovery assessment, environmental and clinical sampling, transmission studies, and evaluation of pathogen detection or removal procedures.

Pathogen Elution - Related Videos

Education

JoVE Core - Analytical Chemistry

High-Performance Liquid Chromatography: Elution Process

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2024

In High-Performance Liquid Chromatography (HPLC), the elution process is critical to the separation of analytes and the quality of chromatographic results. Elution describes how compounds move through the column and separate based on their interactions with the mobile and stationary phases. This process determines the resolution, peak shape, and retention times in the chromatogram, which are essential for identifying and quantifying components in complex mixtures. Understanding the elution...

Research

JoVE Journal - Immunology and Infection
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Single Cell Measurements of Vacuolar Rupture Caused by Intracellular Pathogens

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Cited by 22 •

2013

We describe a method for tracking the endomembrane rupture elicited by the intracellular bacteria Shigella flexneri and Mycobacterium tuberculosis upon host cell invasion. Our assay makes use of CCF4, a host cytoplasmic FRET probe in live or fixed cells. This reporter is degraded by an enzyme activity present on the bacterial surface.

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials

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Cited by 5 •

2023

Here, we present a protocol to evaluate the antibacterial efficacy of an antibiotic-eluting polymer to simulate prophylactic clinical application by using a commercially available real-time ATP-based luminescent microbial viability assay. This method enables the monitoring of the longitudinal activity of drug-eluting materials and can be widely adapted to test anti-microbial drug delivery platforms.

CN-GELFrEE - Clear Native Gel-eluted Liquid Fraction Entrapment Electrophoresis

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Cited by 11 •

2016

This protocol describes how to prepare and perform clear native gel-eluted liquid fraction entrapment electrophoresis (CN-GELFrEE), a native separation technique for non-covalent biomolecular assemblies and proteins from heterogeneous samples that is compatible with various downstream protein analysis techniques.

Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens

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Cited by 84 •

2011

The Virochip is a pan-viral microarray designed to simultaneously detect all known viruses as well as novel viruses on the basis of conserved sequence homology. Here we demonstrate how to run a Virochip assay to analyze clinical samples for the presence of both known and unknown viruses.

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