Host Killing Index

Host Killing Index is a quantitative measure of how effectively a biological agent eliminates its intended host, often a microbial cell, making it useful for comparing engineered constructs, treatments, or strains. The index is determined by comparing host survival or growth after exposure with an untreated control; reduced viability or population expansion indicates stronger killing, which may result from productive infection, toxin delivery, or another lethal interaction. In bioengineering, this metric supports evaluation of bacteriophages, antimicrobial systems, and genetically modified agents by linking design features to biological performance. It can guide candidate selection, optimize treatment conditions, and clarify host specificity and efficacy.

Host Killing Index - Related Videos

Research

JoVE EoE - Immunodiagnostics

Assessment of Opsonophagocytic Killing Activity against Bacterial Pathogens

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2025

The video shows an in vitro opsonophagocytic killing assay using a co-culture of human neutrophils with Streptococcus pneumoniae. Antibodies and complement proteins facilitate opsonization of the bacteria, enabling neutrophils to recognize and kill bacteria, showing successful neutrophil opsonophagocytic activity.

Detecting Bacterial Virulence Using Amoeba as a Host System

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2026

Source: Dubois, V., et al. Identification of Virulence Markers of Mycobacterium abscessus for Intracellular Replication in Phagocytes. J. Vis. Exp. (2018)This video demonstrates the procedure of co-culturing amoebae with mutant bacterial strains to evaluate their intracellular survival and identify virulence markers through differences in colony counts.

Isolation of Intracellular Pathogenic Bacteria from Infected Host Cells

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2026

Source: Sigal, N., et al. RNA Purification from Intracellularly Grown Listeria monocytogenes in Macrophage Cells. J. Vis. Exp. (2016).This video demonstrates the isolation of internalized pathogenic bacteria from infected bone marrow-derived macrophages (BMDMs). Bacteria are allowed to attach to host cells, and unattached bacteria are washed away. After internalization, an antibiotic is added to eliminate non-internalized bacteria. The host cells are lysed, centrifuged, and the supernatant is...

In Vitro Stimulation of Mouse Splenocytes with Heat-Killed Listeria monocytogenes

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2026

Source: Ahn, J. J., et al., Experimental Infection with Listeria monocytogenes as a Model for Studying Host Interferon-γ Responses. J. Vis. Exp. (2016)This video demonstrates the preparation of mouse splenocyte cultures from Listeria monocytogenes-infected mice for downstream cytokine analysis. It includes ex vivo bacteria-derived antigen stimulation and sample processing to study T cell responses.

In Vitro Evaluation of Bacterial Killing by Neonatal Mouse Splenic Phagocytes

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2026

Source: Seman, B. G., et.al. Neonatal Imaging Model of Gram-Negative Bacterial Sepsis. J. Vis. Exp. (2020)This video demonstrates the isolation of neutrophils and inflammatory monocytes from neonatal mouse spleens and their application in a luminescent bacterial killing assay. It covers mechanical dissociation, red blood cell lysis, magnetic bead–based cell enrichment, bacterial incubation, and antibiotic protection. Timed luminescence readings indicate initial bacterial internalization...

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