Open AccessThe role of neutrophils and monocytic cells in controlling the initiation of Clostridium perfringens gas gangrene
Author(s) -
O'Brien David K.,
Therit Blair H.,
Woodman Michael E.,
Melville Stephen B.
Publication year - 2007
Publication title -
fems immunology & medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1574-695X
pISSN - 0928-8244
DOI - 10.1111/j.1574-695x.2007.00235.x
Subject(s) - gas gangrene , clostridium perfringens , microbiology and biotechnology , phagocyte , biology , infiltration (hvac) , monocyte , immunology , gangrene , phagocytosis , bacteria , pathology , medicine , genetics , physics , thermodynamics
Clostridium perfringens is a common cause of the fatal disease gas gangrene (myonecrosis). Established gas gangrene is notable for a profound absence of neutrophils and monocytic cells (phagocytes), and it has been suggested that the bactericidal activities of these cells play an insignificant role in controlling the progression of the infection. However, large inocula of bacteria are needed to establish an infection in experimental animals, suggesting phagocytes may play a role in inhibiting the initiation of gangrene. Examination of tissue sections of mice infected with a lethal (1 × 10 9 ) or sublethal (1 × 10 6 ) inoculum of C. perfringens revealed that phagocyte infiltration in the first 3 h postinfection was inhibited with a lethal dose but not with a sublethal dose, indicating that exclusion of phagocytes begins very early in the infection cycle. Experiments in which mice were depleted of either circulating monocytes or neutrophils before infection with C. perfringens showed that monocytes play a role in inhibiting the onset of gas gangrene at intermediate inocula but, although neutrophils can slow the onset of the infection, they are not protective. These results suggest that treatments designed to increase monocyte infiltration and activate macrophages may lead to increased resistance to the initiation of gas gangrene.