Africanized honeybee venom (Apis mellifera) promotes human complement activation split products storm

Front Immunol. 2024 Nov 13:15:1463471. doi: 10.3389/fimmu.2024.1463471. eCollection 2024.

Abstract

Introduction: Complement activation split products are signatures of many immunopathological disorders. Among the laboratory findings observed in these diseases, a reduction in the level of circulating intact complement components can be mentioned, and this change has also been detected in envenomation by multiple Africanized honeybee (Apis mellifera) stings. Although envenomation by these animals elicits diverse life-threatening reactions, the capacity of bee venom (AmV) to activate the human complement system remains elusive.

Methods and findings: By coupling immunochemical and functional approaches, it was observed that AmV strongly consumes components of the alternative pathway (AP) of the complement system in normal human serum (NHS). Additionally, AmV interfered with classical (CP) and lectin pathways (LP) activities. In parallel, a high increase in Ba fragment levels was detected, suggesting that the changes in AP activity were due to its activation. Furthermore, an increase in the level of the C1s-C1INH complex and a decrease in the physiological level of MASP1-C1INH suggested that CP and LP were also activated in the presence of AmV. Strikingly, NHS exposed to increasing AmV concentrations varying from 5 to 1000 µg/mL presented a high generation of C3a, C4a and C5a anaphylatoxins, and sC5b-9 complexes assembly, thus reinforcing that AmV triggers complement activation.

Conclusion: These results show that AmV is a strong complement activator. This activation presents a mixed profile, with a predominance of AP activation. This suggests that complement split products can play important roles in the envenomation by Africanized honeybee, as they could induce diverse immunopathological events observed in patients and may also dictate patient clinical prognosis.

Keywords: Africanized honeybee; Apis mellifera venom; anaphylatoxins; complement pathways activation; immunopathology.

MeSH terms

  • Animals
  • Bee Venoms* / immunology
  • Bees / immunology
  • Complement Activation*
  • Complement Pathway, Alternative / immunology
  • Complement System Proteins / immunology
  • Complement System Proteins / metabolism
  • Humans
  • Insect Bites and Stings / immunology

Substances

  • Bee Venoms
  • Complement System Proteins

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by São Paulo Research Foundation (FAPESP) funding to the Center of Toxins, Immune Response and Cell Signaling (CeTICS) (grant 2013/07467-1). DT is a recipient of the CNPq Research Productivity Fellowship (Grant # 308390/2021-0). RO is a recipient of the CNPq Research Productivity Fellowship (Grant # 304720/2020-8). The funding agencies had no influence on study design, data interpretation, or formation of the manuscript.