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Participation of complement in host defense against capsule-deficient Haemophilus influenzae
Insights
Complement protein C3 is crucial for fighting capsule-deficient Haemophilus influenzae infections. Depleting C3 in rats significantly increased their susceptibility to infection, highlighting complement
Area of Science:
- Immunology
- Microbiology
- Bacterial Pathogenesis
Background:
- Capsule-deficient Haemophilus influenzae poses a significant infection risk.
- The role of complement in immunity against such strains is not fully understood.
Purpose of the Study:
- To investigate the role of complement C3 in host defense against capsule-deficient H. influenzae.
- To determine if residual capsular antigen influences virulence in these strains.
Main Methods:
- Rats were depleted of C3 using cobra venom factor.
- Animals were challenged with different strains of capsule-deficient H. influenzae.
- Bacteremia and mortality rates were assessed in C3-depleted and control rats.
Main Results:
- C3 depletion significantly enhanced bacterial survival and susceptibility to infection.
- C3-depleted rats developed bacteremia and increased mortality compared to controls.
- Virulence differences among capsule-deficient variants were not linked to residual capsular antigen.
Conclusions:
- Complement C3 plays a vital role in host defense against capsule-deficient H. influenzae.
- Residual capsular antigen does not account for interstrain virulence differences in these bacteria.
Abstract:
To investigate the role of complement in immunity to capsule-deficient Haemophilus influenzae, rats were depleted of C3 with cobra venom factor and challenged with three different strains of capsule-deficient H. influenzae. Two of them (Rd and U1) did not elaborate type b capsular antigen, whereas the other (S2) elaborated 0.16% of the amount made by its type b parent strain. Depletion of C3 significantly enhanced early intravascular bacterial survival after intravenous inoculation and strikingly increased the susceptibility of rats to infection with capsule-deficient H. influenzae. After intraperitoneal inoculation with strain Rd or U1, C3-depleted rats developed bacteremia, whereas control rats did not; challenge with strain S2 resulted in transient bacteremia in normal rats and in death in C3-depleted animals. To determine whether the greater virulence of strain S2, as compared with strain Rd or U1, was accounted for by the small amounts of capsular antigen it elaborated, we also compared its relative virulence to that of three genetically closely related capsule-deficient variants elaborating either small amounts of type b capsule or producing no detectable b antigen. No difference in virulence was observed among these four variants; all C3-depleted rats inoculated developed bacteremia of similar magnitude followed by similar mortality rates. These studies demonstrate a significant role for complement in host defense mechanisms against capsule-deficient H. influenzae and suggest that interstrain differences of virulence are not attributable to residual elaboration of small amounts of type b capsule.
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