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Moraxella catarrhalis Evades Host Innate Immunity via Targeting Cartilage Oligomeric Matrix Protein
Guanghui Liu1, Henrik Gradstedt1, David Ermert1
1Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, SE-205 02 Malmö, Sweden;
Abstract:
Moraxella catarrhalis is a respiratory tract pathogen commonly causing otitis media in children and acute exacerbations in patients suffering from chronic obstructive pulmonary disease. Cartilage oligomeric matrix protein (COMP) functions as a structural component in cartilage, as well as a regulator of complement activity. Importantly, COMP is detected in resident macrophages and monocytes, alveolar fluid, and the endothelium of blood vessels in lung tissue. We show that the majority of clinical isolates of M. catarrhalis (n = 49), but not other tested bacterial pathogens, bind large amounts of COMP. COMP interacts directly with the ubiquitous surface protein A2 of M. catarrhalis. Binding of COMP correlates with survival of M. catarrhalis in human serum by inhibiting bactericidal activity of the complement membrane attack complex. Moreover, COMP inhibits phagocytic killing of M. catarrhalis by human neutrophils. We further observed that COMP reduces bacterial adhesion and uptake by human lung epithelial cells, thus protecting M. catarrhalis from intracellular killing by epithelial cells. Taken together, our findings uncover a novel mechanism that M. catarrhalis uses to evade host innate immunity.
Insights
Moraxella catarrhalis evades immune responses by binding cartilage oligomeric matrix protein (COMP). This interaction protects the bacteria from complement, neutrophils, and epithelial cells, aiding survival in the host.
Area of Science:
- Microbiology
- Immunology
- Bacterial Pathogenesis
Background:
- Moraxella catarrhalis is a significant respiratory pathogen.
- Cartilage oligomeric matrix protein (COMP) is found in lung tissue and modulates immune responses.
Purpose of the Study:
- To investigate the interaction between Moraxella catarrhalis and COMP.
- To determine the role of COMP in M. catarrhalis immune evasion.
Main Methods:
- Testing binding of COMP to clinical isolates of M. catarrhalis.
- Investigating the interaction between COMP and M. catarrhalis surface protein A2.
- Assessing the effect of COMP on bacterial survival in human serum, neutrophil phagocytosis, and epithelial cell uptake.
Main Results:
- Most M. catarrhalis isolates bind significant amounts of COMP, unlike other bacteria.
- COMP directly interacts with M. catarrhalis surface protein A2.
- COMP binding inhibits complement-mediated killing, neutrophil phagocytosis, and epithelial cell clearance of M. catarrhalis.
Conclusions:
- Moraxella catarrhalis utilizes COMP binding as a novel immune evasion strategy.
- COMP protects M. catarrhalis from key components of the innate immune system.
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