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Published on: October 13, 2015
A Co-infection Model System and the Use of Chimeric Proteins to Study Chlamydia Inclusion Proteins Interaction
1Department of Molecular Biophysics and Biochemistry, Yale University New Haven, CT, USA.
Insights
Chlamydia trachomatis inclusion membrane proteins (Inc) interact with each other. Researchers used a co-infection model to show IncD self-interacts, revealing mechanisms of bacterial-host interactions.
Area of Science:
- Microbiology
- Cell Biology
- Bacterial Pathogenesis
Background:
- Chlamydia trachomatis is an obligate intracellular bacterium causing trachoma and STDs.
- Chlamydia resides in a host-derived inclusion vacuole during infection.
- Inclusion membrane proteins (Inc) are crucial for bacterial replication but their functions and interactions are poorly understood.
Purpose of the Study:
- To investigate Inc protein self-interaction using IncD as a model.
- To understand the molecular mechanisms of Inc protein function and host interaction.
Main Methods:
- Developed a co-infection model system to express tagged Inc proteins on the same inclusion.
- Designed chimeric Inc proteins to identify interaction domains.
- Utilized IncD as a model to study Inc/Inc interactions.
Main Results:
- Demonstrated that IncD can self-interact.
- Showed that the full-length IncD protein is necessary for dimerization and/or oligomerization.
- Established a generalized approach to study Inc protein interactions.
Conclusions:
- Inc proteins can self-interact, suggesting complex functional roles.
- Understanding Inc protein interactions is key to deciphering Chlamydia pathogenesis.
- This study provides a framework for characterizing Inc protein interactions with themselves and host factors.
Abstract:
Chlamydia trachomatis is an obligate intracellular bacterium associated with trachoma and sexually transmitted diseases. During its intracellular developmental cycle, Chlamydia resides in a membrane bound compartment called the inclusion. A subset of Type III secreted effectors, the inclusion membrane proteins (Inc), are inserted into the inclusion membrane. Inc proteins are strategically positioned to promote inclusion interaction with host factors and organelles, a process required for bacterial replication, but little is known about Inc proteins function or host interacting partners. Moreover, it is unclear whether each Inc protein has a distinct function or if a subset of Inc proteins interacts with one another to perform their function. Here, we used IncD as a model to investigate Inc/Inc interaction in the context of Inc protein expression in C. trachomatis. We developed a co-infection model system to display different tagged Inc proteins on the surface of the same inclusion. We also designed chimeric Inc proteins to delineate domains important for interaction. We showed that IncD can self-interact and that the full-length protein is required for dimerization and/or oligomerization. Altogether our approach can be generalized to any Inc protein and will help to characterize the molecular mechanisms by which Chlamydia Inc proteins interact with themselves and/or host factors, eventually leading to a better understanding of C. trachomatis interaction with the mammalian host.

