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Published on: March 17, 2014
Gram-positive bacteria-induced granulocytopenia and pulmonary leukostasis in rabbits
Abstract:
Pneumococci have been shown to induce granulocytopenia and pulmonary leukostasis which might contribute to morbidity and mortality in pneumococcal sepsis. We studied whether other gram-positive species (groups A and B streptococci, Staphylococcus aureus, Bacillus cereus, and Clostridium perfringens) could also induce these phenomena. Rabbits were challenged with nonviable preparations of each species, and all five species induced profound granulocytopenia (mean decrease of 90%) and pulmonary leukostasis. In vitro studies of serum incubated with these species of bacteria showed a mean consumption of total hemolytic complement of 90%, a mean increase of chemotactic activity for granulocytes of 204%, and a mean augmentation of granulocyte adherence of 45% (compared with 18% for the control). Infusion of sonicate-exposed sera induced granulocytopenia in recipient rabbits. Thus, several nonviable gram-positive species can interact with serum to activate the complement system, generate C5a bioactivity, augment granulocyte adherence, and generate a neutropenia-inducing factor. These alterations may contribute to granulocytopenia or pulmonary leukostasis, which may play a role in the morbidity and mortality associated with gram-positive bacterial infections.
Insights
Several gram-positive bacteria, including streptococci and staphylococci, trigger granulocytopenia and pulmonary leukostasis by activating the complement system. These effects may contribute to severe illness in bacterial infections.
Area of Science:
- Immunology
- Microbiology
- Pathophysiology
Background:
- Pneumococci are known to cause granulocytopenia and pulmonary leukostasis, contributing to pneumococcal sepsis severity.
- The role of other gram-positive bacteria in inducing these phenomena remains less understood.
Purpose of the Study:
- To investigate whether other common gram-positive bacterial species can induce granulocytopenia and pulmonary leukostasis.
- To explore the mechanisms by which these bacteria interact with the host immune system.
Main Methods:
- Rabbits were challenged with nonviable preparations of Group A and B streptococci, Staphylococcus aureus, Bacillus cereus, and Clostridium perfringens.
- In vitro studies assessed complement consumption, granulocyte chemotaxis, and granulocyte adherence in rabbit serum incubated with these bacteria.
- The effects of infusing sonicate-exposed sera into recipient rabbits were evaluated.
Main Results:
- All five tested gram-positive species induced profound granulocytopenia (90% decrease) and pulmonary leukostasis in rabbits.
- Incubation of serum with these bacteria led to significant complement consumption (90%), increased granulocyte chemotaxis (204%), and augmented granulocyte adherence (45%).
- Infusion of sera exposed to bacterial sonicates induced granulocytopenia in recipient rabbits, indicating the presence of a neutropenia-inducing factor.
Conclusions:
- Several nonviable gram-positive species can activate the complement system, leading to C5a generation, enhanced granulocyte adherence, and a neutropenia-inducing factor.
- These complement-mediated alterations may contribute to granulocytopenia and pulmonary leukostasis.
- These phenomena likely play a significant role in the morbidity and mortality associated with gram-positive bacterial infections.
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