C3 complement inhibition by Sicpin, a salivary protein from Simulium nigrimanum 2328025

P Paola Valenzuela Leon (National Institute of Allergy and Infectious Diseases, National Institutes of Health) M Molly Ring (NIH) B Brian Bonilla (NIH) A Andrezza Chagas (NIH/WRAIR) E Eric Calvo

Abstract

Abstract Introduction Complement inhibition is a key strategy used by many blood-feeding arthropods to ensure successful feeding. Mosquitoes, ticks, sand flies, and other hematophagous species secrete salivary proteins that block different steps of the complement cascade. These inhibitors prevent complement-mediated lysis and inflammation at the feeding site, allowing the arthropod to feed efficiently while also creating a more permissive environment for pathogen transmission Methods Here, we characterize the anti-complement activity of Sicpin, a salivary protein from the blackfly Simulium nigrimanum. Sicpin was found to inhibit all three pathways of complement activation. Surface plasmon resonance analysis revealed a strong and specific interaction with C3, with no detectable binding to other complement components common to the pathways. Results The binding induces a conformational change in C3 that blocks the interaction with the C3 convertase, consequently inhibiting the deposition of downstream complement proteins. Additionally, in both acute lung injury and sepsis models, Sicpin enhances survival and exhibits anti-inflammatory activity. Conclusion These findings support that Sicpin modulates the complement system, with potential implications for pathogen transmission, blood feeding, and therapeutic development Funding Source NIH Topic Categories Innate Immune Responses and Host Defense: Molecular Mechanisms (INM)

Article Details

Volume / Issue Vol. 215, Issue Supplement_1
Published August 01, 2026
ISSN 0022-1767
Publisher American Association of Immunologists

Authors (5)

P

Paola Valenzuela Leon

National Institute of Allergy and Infectious Diseases, National Institutes of Health

M

Molly Ring

NIH

B

Brian Bonilla

NIH

A

Andrezza Chagas

NIH/WRAIR

E

Eric Calvo