Abstract

Nontypeable Haemophilus influenzae (NTHi) is a Gram-negative human pathogen that causes infections mainly in the upper and lower respiratory tract. The bacterium is associated with bronchitis and exacerbations in patients suffering from chronic obstructive pulmonary disease and frequently causes acute otitis media in preschool children. We have previously demonstrated that the binding of C4b binding protein (C4BP) is important for NTHi complement evasion. In this study, we identified outer membrane protein 5 (P5) of NTHi as a novel ligand of C4BP. Importantly, we observed significantly lower C4BP binding and decreased serum resistance in P5-deficient NTHi mutants. Surface expression of recombinant P5 on Escherichia coli conferred C4BP binding and consequently increased serum resistance. Moreover, P5 expression was positively correlated with C4BP binding in a series of clinical isolates. We revealed higher levels of P5 surface expression and consequently more C4BP binding in isolates from the lower respiratory tract of chronic obstructive pulmonary disease patients and tonsil specimens compared with isolates from the upper respiratory tract and the bloodstream (invasive strains). Our results highlight P5 as an important protein for protecting NTHi against complement-mediated killing.

Highlights

  • ObjectivesBecause microbial interactions with host proteins can be mediated by multiple synchronous mechanisms, we aimed to determine the contribution of protein 5 (P5) to the interaction with human C4b binding protein (C4BP)

  • In this study we identified protein 5 (P5) to be important for the ability of Nontypeable Haemophilus influenzae (NTHi) to recruit the human complement inhibitor C4b binding protein (C4BP) to the bacterial surface

  • Serum resistance assays revealed that the addition of C4BP increased survival in wild-type but not P5 mutant strains

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Summary

Objectives

Because microbial interactions with host proteins can be mediated by multiple synchronous mechanisms, we aimed to determine the contribution of P5 to the interaction with human C4BP

Methods
Results
Conclusion
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