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Updated: Mar 3, 2026

Analysis of Yersinia enterocolitica Effector Translocation into Host Cells Using Beta-lactamase Effector Fusions
Published on: October 13, 2015
Extra! Extracellular Effector Delivery into Host Cells via the Type 3 Secretion System.
1Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA melissakendall@virginia.edu.
Pathogenic bacteria use the type three secretion system (T3SS) to inject toxins. A new study shows bacterial toxins can be delivered to host cells by first binding to the T3SS outside the bacterial cell.
Area of Science:
- Microbiology
- Molecular Biology
- Pathogenesis
Background:
- The type three secretion system (T3SS) is a crucial virulence factor in many bacterial pathogens.
- T3SS facilitates the delivery of effector proteins into host cells, enabling pathogen manipulation of host functions.
- The conventional model involves effector translocation directly from within the T3SS into the host cell.
Purpose of the Study:
- To investigate an alternative mechanism of effector protein translocation mediated by the T3SS.
- To characterize the translocation pathway of the EspC effector from enteropathogenic Escherichia coli.
Main Methods:
- Utilized molecular genetics and cell biology techniques to study effector translocation.
- Investigated the interaction of EspC with the T3SS and its subsequent entry into host cells.
Main Results:
- Demonstrated that the EspC effector binds to the exterior of the T3SS.
- Showed that EspC gains access to the host cell cytoplasm via the T3SS pore.
- Identified a novel extracellular-initiated translocation mechanism for T3SS effectors.
Conclusions:
- The study reveals a previously unrecognized mechanism for bacterial effector delivery.
- This alternative translocation pathway, involving extracellular T3SS binding, is likely employed by other T3SS-utilizing pathogens.
- Findings expand our understanding of bacterial virulence strategies and T3SS function.
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