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Updated: May 27, 2026

Biomimetic Materials to Characterize Bacteria-host Interactions
Published on: November 16, 2015
Turnabout is fair play: use of the bacterial Multivalent Adhesion Molecule 7 as an antimicrobial agent
Anne Marie Krachler1, Hyeilin Ham, Kim Orth
1Department of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Abstract:
Pathogen attachment to host tissues is one of the initial and most crucial events during the establishment of bacterial infections and thus interference with this step could be an efficient strategy to fight bacterial colonization. Our recent work has identified one of the factors involved in initial binding of host cells by a wide range of Gram-negative pathogens, Multivalent Adhesion Molecule (MAM) 7. Interference with MAM7-mediated attachment, for example by pre-incubation of host cells with recombinant MAM7, significantly delays the onset of hallmarks of infection, such as pathogen-mediated cytotoxicity or the development of other adhesive structures such as actin pedestals. Thus, we are trying to develop tools based on MAM7 that can be used to prevent or diminish certain Gram-negative bacterial infections. Herein, we describe the use of bead-coupled MAM7 as an inhibitor of infection with the clinically relevant pathogen Pseudomonas aeruginosa.
Insights
Blocking pathogen attachment using Multivalent Adhesion Molecule (MAM) 7 can prevent bacterial infections. This study shows bead-coupled MAM7 inhibits Pseudomonas aeruginosa infection, offering a new strategy against Gram-negative pathogens.
Area of Science:
- Microbiology
- Infectious Diseases
- Biotechnology
Background:
- Pathogen attachment is a critical initial step in bacterial infections.
- Multivalent Adhesion Molecule (MAM) 7 is identified as a key factor in Gram-negative pathogen host cell binding.
- Interfering with pathogen adhesion presents a promising strategy to combat bacterial colonization.
Purpose of the Study:
- To develop novel tools based on MAM7 for preventing or reducing Gram-negative bacterial infections.
- To investigate the efficacy of bead-coupled MAM7 as an inhibitor of infection.
- To target the initial attachment phase of bacterial pathogenesis.
Main Methods:
- Utilizing recombinant MAM7 to interfere with pathogen-host cell attachment.
- Employing bead-coupled MAM7 as an infection inhibitor.
- Testing the inhibitory effect against the pathogen Pseudomonas aeruginosa.
Main Results:
- Pre-incubation with recombinant MAM7 significantly delays infection hallmarks like cytotoxicity.
- Bead-coupled MAM7 demonstrates inhibitory effects against Pseudomonas aeruginosa infection.
- Interference with MAM7-mediated attachment effectively reduces bacterial colonization.
Conclusions:
- MAM7 is a viable target for developing anti-infective strategies against Gram-negative bacteria.
- Bead-coupled MAM7 serves as an effective tool to inhibit bacterial infection.
- Targeting initial pathogen adhesion offers a novel approach to combat bacterial diseases.
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