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In Vitro Killing of Oral Capnocytophaga by Granule Fractions of Human Neutrophils is Associated with Cathepsin G Activity

Overview
Journal J Clin Invest
Specialty General Medicine
Date 1991 May 1
PMID 2022730
Citations 9
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Abstract

The Capnocytophaga are inhabitants of the hypoxic human gingival crevice that are normally prevented by neutrophils from causing periodontal and systemic infection. To identify potential nonoxidative bactericidal mechanisms against Capnocytophaga within human neutrophils, gel filtration chromatography was used to fractionate neutrophil granule extracts. Seven granule fractions, designated A through G, were obtained. The Capnocytophaga were most sensitive to killing by fraction D. Fraction D exhibited substantial bactericidal activity under aerobic and anaerobic conditions. The bactericidal activity associated with ion-exchange subfractions D8-D11, which contained primarily cathepsin G as assessed by enzymatic activity, amino acid composition, and NH2-terminal sequence. Heat-inactivation, diisopropylfluorophosphate, PMSF, and N-benzyloxycarbonylglycylleucylphenylalanyl-chloromethyl ketone inhibited bactericidal activity against Capnocytophaga sputigena but not Escherichia coli. We conclude that (a) human neutrophil cathepsin G is an important antimicrobial system against the Capnocytophaga, (b) the bactericidal activity of cathepsin G against Capnocytophaga is oxygen independent, and (c) an intact enzyme active site is involved in the killing of C. sputigena but not E. coli. We suggest that human neutrophil cathepsin G is an important antimicrobial system against certain oral bacteria and that cathepsin G kills bacteria by two distinct mechanisms.

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References
1.
Hovde C, Gray B . Characterization of a protein from normal human polymorphonuclear leukocytes with bactericidal activity against Pseudomonas aeruginosa. Infect Immun. 1986; 54(1):142-8. PMC: 260128. DOI: 10.1128/iai.54.1.142-148.1986. View

2.
Miyasaki K, Wilson M, Brunetti A, Genco R . Oxidative and nonoxidative killing of Actinobacillus actinomycetemcomitans by human neutrophils. Infect Immun. 1986; 53(1):154-60. PMC: 260090. DOI: 10.1128/iai.53.1.154-160.1986. View

3.
Wilson M, Bronson P, Dudas K, Apicella M, Genco R . Capnocytophaga species: increased resistance of clinical isolates to serum bactericidal action. J Infect Dis. 1987; 156(1):99-106. DOI: 10.1093/infdis/156.1.99. View

4.
Van Dyke T, Offenbacher S, Henson P . Association of an abnormality of neutrophil chemotaxis in human periodontal disease with a cell surface protein. Infect Immun. 1987; 55(9):2262-7. PMC: 260688. DOI: 10.1128/iai.55.9.2262-2267.1987. View

5.
Shafer W, Morse S . Cleavage of the protein III and major iron-regulated protein of Neisseria gonorrhoeae by lysosomal cathepsin G. J Gen Microbiol. 1987; 133(1):155-62. DOI: 10.1099/00221287-133-1-155. View