Related Experiment Video
Updated: Jun 4, 2026

Humanized Mouse Model to Study Bacterial Infections Targeting the Microvasculature
Published on: April 1, 2014
Molecular recognition mechanisms of meningococci : identifying receptor-ligand pairs involved in microbe-host
1Department of Pathology & Microbiology, School of Medical Sciences, University of Bristol, UK.
Abstract:
Neisseria meningitidis is a human specific pathogen and resides primarily in the nasopharynx of its host. The molecular-recognition mechanisms that operate at the host-microbe interface to impart such precise host/tissue specificity are not fully defined. Given the host muco-cilliary clearance mechanisms, an obvious prerequisite for colonization is the ability of bacteria to make firm and rapid contact with the nasopharyngeal mucosa. The specificity for the niche indicates that one or more meningococcal adhesins have evolved an exquisite level of affinity for particular target molecules. They also exhibit considerable structural and phase modulations that aid in immune evasion. These properties have been exploited to derive distinct phenotypes for investigations on the mechanisms of adhesion. The in vitro investigations that use cell cultures of human origin or "humanized" cells (created by transfection of animal cells with human DNA) have identified a number of receptors targeted by meningococci. Detailed examination of the molecular mechanisms of bacterial ligation with the receptors will clarify the basis of tissue specificity and tropism and provide information that may lead to novel strategies to control the disease. We will describe some of the methods we have implemented over the years for such investigations.
Insights
Neisseria meningitidis colonizes the human nasopharynx using specific adhesins for host cell attachment. Understanding these molecular interactions is key to developing new strategies against this pathogen.
Area of Science:
- Microbiology
- Immunology
- Molecular Biology
Background:
- Neisseria meningitidis is a human-specific pathogen colonizing the nasopharynx.
- Host-microbe interactions, specifically bacterial adhesion, are crucial for colonization but not fully understood.
- Bacterial adhesins and host receptors mediate tissue specificity and immune evasion.
Purpose of the Study:
- To investigate the molecular mechanisms of Neisseria meningitidis adhesion to the human nasopharyngeal mucosa.
- To identify specific bacterial adhesins and host cell receptors involved in host-microbe recognition.
- To explore how these interactions contribute to tissue tropism and immune evasion.
Main Methods:
- Utilizing in vitro cell culture models of human origin.
- Employing "humanized" cells engineered with human DNA for experimental systems.
- Analyzing distinct bacterial phenotypes to study adhesion mechanisms.
Main Results:
- Identification of multiple host cell receptors targeted by Neisseria meningitidis.
- Characterization of molecular mechanisms underlying bacterial-host cell ligation.
- Insights into the role of adhesins in determining tissue specificity.
Conclusions:
- Detailed examination of bacterial-receptor interactions clarifies Neisseria meningitidis tissue specificity.
- Understanding adhesion mechanisms provides a basis for novel disease control strategies.
- The study highlights the importance of host-microbe molecular recognition in pathogenesis.
More Related Videos
12:58Visualisation and Quantification of Intracellular Interactions of Neisseria meningitidis and Human α-actinin by Confocal Imaging
Published on: October 24, 2010
07:42Fluorescence Assays for the Study of Mycobacterium tuberculosis Interaction with the Immune Receptor SLAMF1
Published on: February 28, 2025
Related Concept Videos
Bacterial Meningitis II: Pathophysiology
Modern Molecular Taxonomy
Antigens Involved in Adaptive Immunity
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
Bacterial Meningitis
Receptor-mediated Endocytosis
Receptor-mediated Endocytosis
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...