SENSITIVITY OF ACTINOBACILLUS-ACTINOMYCETEMCOMITANS AND HAEMOPHILUS-APHROPHILUS TO OXIDATIVE KILLING

被引:13
作者
DONGARI, AI [1 ]
MIYASAKI, KT [1 ]
机构
[1] UNIV CALIF LOS ANGELES,CTR HLTH SCI,SCH DENT,ORAL BIOL SECT,CHS 63-050,LOS ANGELES,CA 90024
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 1991年 / 6卷 / 06期
关键词
BACTERICIDAL; XANTHINE XANTHINE OXIDASE; HYDROGEN PEROXIDE; SUPEROXIDE ANION; OXIDATIVE KILLING; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS; HAEMOPHILUS-APHROPHILUS;
D O I
10.1111/j.1399-302X.1991.tb00508.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
We examined the killing of Actinobacillus actinomycetemcomitans and Haemophilus aphrophilus by oxygen metabolites generated by the xanthine-xanthine oxidase (X-XO) system. This system generates a mixture of oxidants, including superoxide radical, hydrogen peroxide, hydroxyl radical, and possibly singlet oxygen. Differential sensitivity to the X-XO system was observed among strains of A. actinomycetemcomitans; notably, 2 catalase-deficient strains and 2 strains representative of serotypes b and c were the most susceptible. H. aphrophilus was not sensitive. The amount of oxidants produced by the X-XO system more closely correlated with killing than the ratio of oxidant production. Cytochrome c, superoxide dismutase, catalase, dimethyl sulfoxide, and desferrioxamine were used to determine the role of superoxide radical, hydrogen peroxide and hydroxyl radical in the bactericidal process. Hydrogen peroxide was the major bactericidal agent against A. actinomycetemcomitans. Superoxide anion participated in killing of A. actinomycetemcomitans to varying but lesser degrees. The intracellular generation of hydroxyl radical was implicated in the killing of several strains. We conclude that (i) strains of A. actinomycetemcomitans are differentially sensitive to the bactericidal effects of the X-XO system and (ii) of the oxidants produced by the X-XO system, hydrogen peroxide is the most bactericidal against A. actinomycetemcomitans.
引用
收藏
页码:363 / 372
页数:10
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共 43 条
  • [1] Ambruso DR, Johnston RB, Lactoferrin enhances hydroxyl radical production by human neutrophils, neutrophil particulate fractions, and an enzymatic generating system, J Clin Invest, 67, pp. 352-360, (1981)
  • [2] Ananthaswamy HN, Eisenstark KA, Re‐pair of H<sub>2</sub>‐O<sub>2</sub> induced single‐strand breaks in Escherichia coli deoxyribonucleic acid, J Bacteriol, 130, pp. 187-191, (1976)
  • [3] Beauchamp C, Fridovich I, Mechanism for the production of ethylene from methional. Generation of the hydroxyl radical by xanthine oxidase, J Biol Chem, 245, pp. 4641-4646, (1970)
  • [4] Curnutte JT, Kuver R, Scott PJ, Activation of neutrophil NAD(P)H oxidase in a cell free system, J Biol Chem, 262, pp. 5563-5569, (1987)
  • [5] DeChatelet LK, Initiation of the respiratory burst in human PMNs: a critical review, J Reticuloendothel Soc, 24, pp. 73-91, (1978)
  • [6] Elsbach P, Weiss J, A reevaluation of the roles of oxygen dependent and oxygen independent microbicidal systems of phagocytes, Rev Infect Dis, 5, pp. 843-853, (1983)
  • [7] Frederiksen W, Kilian M, Haemophilus‐Pasteurella‐Actinobacillus: their significance in human medicine, Haemophilus Pasteurella Actinobacillus, pp. 39-55, (1981)
  • [8] Fridovich I, Quantitative aspects of the production of superoxide anion radical by milk xanthine oxidase, J Biol Chem, 245, pp. 4053-4057, (1970)
  • [9] Fridovich I, Biological effects on the superoxide radical, Arch Biochem Bio-phys, 247, pp. 1-11, (1986)
  • [10] Gabig TG, Babior BM, The oxygen forming oxidase responsible for the respiratory burst in human neutrophils. Properties of the solubilized enzyme, J Biol Chem, 254, pp. 9070-9074, (1979)