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Updated: Mar 31, 2026

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
Published on: January 3, 2012
MARTX toxins as effector delivery platforms
Hannah E Gavin1, Karla J F Satchell2
1Department of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Abstract:
Bacteria frequently manipulate their host environment via delivery of microbial 'effector' proteins to the cytosol of eukaryotic cells. In the case of the multifunctional autoprocessing repeats-in-toxins (MARTX) toxin, this phenomenon is accomplished by a single, >3500 amino acid polypeptide that carries information for secretion, translocation, autoprocessing and effector activity. MARTX toxins are secreted from bacteria by dedicated Type I secretion systems. The released MARTX toxins form pores in target eukaryotic cell membranes for the delivery of up to five cytopathic effectors, each of which disrupts a key cellular process. Targeted cellular processes include modulation or modification of small GTPases, manipulation of host cell signaling and disruption of cytoskeletal integrity. More recently, MARTX toxins have been shown to be capable of heterologous protein translocation. Found across multiple bacterial species and genera--frequently in pathogens lacking Type 3 or Type 4 secretion systems--MARTX toxins in multiple cases function as virulence factors. Innovative research at the intersection of toxin biology and bacterial genetics continues to elucidate the intricacies of the toxin as well as the cytotoxic mechanisms of its diverse effector collection.
Insights
Bacteria use multifunctional autoprocessing repeats-in-toxins (MARTX) toxins to inject effector proteins into host cells. These toxins disrupt cellular processes and function as virulence factors in many bacterial pathogens.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Pathogenesis
Background:
- Bacteria deliver effector proteins into eukaryotic cells to manipulate host environments.
- Multifunctional autoprocessing repeats-in-toxins (MARTX) are large toxins mediating this delivery.
Purpose of the Study:
- To elucidate the mechanisms of MARTX toxin secretion, translocation, and effector activity.
- To understand the role of MARTX toxins in bacterial virulence.
Main Methods:
- Investigating Type I secretion systems for MARTX toxin export.
- Analyzing pore formation in eukaryotic cell membranes.
- Characterizing the function of individual effector proteins delivered by MARTX.
Main Results:
- MARTX toxins are secreted via Type I secretion systems and form pores for effector delivery.
- Effectors target GTPases, signaling pathways, and the cytoskeleton.
- MARTX toxins can translocate heterologous proteins and act as virulence factors.
Conclusions:
- MARTX toxins are versatile virulence factors employed by diverse bacterial pathogens.
- Understanding MARTX toxin function provides insights into bacterial manipulation of host cells.
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