Inc/GFP chimera protein-based interactomics reveals host cellular interactions of Cps0558, a novel Chlamydia psittaci inclusion protein
Jean-Marc Gensch, Jana Scholz, Alyssa Ingmundson, Laura Rose, Joerg Doellinger, Sebastian Banhart, Dagmar Heuer

TL;DR
This study identifies a new Chlamydia psittaci inclusion protein and its host interaction partners using a novel chimera-based method.
Contribution
A novel Inc/GFP chimera protein-based interactomics approach is introduced for studying Chlamydia–host interactions.
Findings
Cps0558 is a novel C. psittaci Inc protein that interacts with ACAD11, a lipid metabolism-related host protein.
IncA interacts with host proteins involved in ubiquitylation, suggesting a role in modulating this system.
The chimera-based method confirms interactions in the native infection context, supporting physiological relevance.
Abstract
The obligate intracellular Gram-negative bacterium Chlamydia psittaci, a zoonotic pathogen transmissible between birds and humans, has played a pioneering role in research on its membrane-bound replicative niche termed the inclusion. Inclusion membrane proteins (Inc proteins) are crucial for Chlamydia–host interactions and were first identified in C. psittaci. This study investigates putative C. psittaci Inc proteins by a combination of in silico analyses, immunofluorescence and, strikingly, a new Inc/GFP chimera protein-based interactomics approach to identify host cellular interaction partners. Here, we report a novel C. psittaci Inc protein, Cps0558, along with respective host cellular interaction partners, in particular ACAD11, which is involved in lipid metabolism. We confirm their physical interaction in the native infection context, supporting the physiological relevance of our…
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Taxonomy
TopicsReproductive tract infections research · Gut microbiota and health · Bacterial Identification and Susceptibility Testing
