Recruitment of C4b-binding protein is not a complement evasion strategy employed by Staphylococcus aureus

Shuxian Li, Serena Bettoni, Frida Mohlin, Joan A. Geoghegan, Anna M Blom, Maisem Laabei

Research output: Contribution to journalArticlepeer-review

Abstract

Complement offers a first line of defence against infection through the opsonization of microbial pathogens, recruitment of professional phagocytes to the infection site and the coordination of inflammatory responses required for the resolution of infection. Staphylococcus aureus is a successful pathogen that has developed multiple mechanisms to thwart host immune responses. Understanding the precise strategies employed by S. aureus to bypass host immunity will be paramount for the development of vaccines and or immunotherapies designed to prevent or limit infection. To gain a better insight into the specific immune evasion mechanisms used by S. aureus we examined the pathogen’s interaction with the soluble complement inhibitor, C4b-binding protein (C4BP). Previous studies indicated that S. aureus recruits C4BP using a specific cell-wall-anchored surface protein and that bound C4BP limits complement deposition on the staphylococcal surface. Using flow-cytometric-based bacterial-protein binding assays we observed no interaction between S. aureus and C4BP. Moreover, we offer a precautionary warning that C4BP isolated from plasma can be co-purified with minute quantities of human IgG, which can distort binding analysis between S. aureus and human-derived proteins. Combined our data indicates that recruitment of C4BP is not a complement evasion strategy employed by S. aureus
Original languageEnglish
Number of pages10
JournalMicrobiology
Volume169
Issue number9
Early online date5 Sept 2023
DOIs
Publication statusPublished - 30 Sept 2023

Bibliographical note

Funding information

This work was supported by an Academy of Medical Sciences Springboard Grant (ML; SBF006\1023), ESCMID research grant (ML) and a Swedish Research Council (AB).

Keywords

  • C4b-binding protein
  • Staphylococcus aureus
  • complement
  • immune evasion

ASJC Scopus subject areas

  • Microbiology

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