The response to oxidative stress of Fusobacterium nucleatum grown in continuous culture

FEMS Microbiology Letters

Volumn 187, Issue 1, 2000, Pages 31-34

  Diaz, Patricia I ^a   Zilm, Peter S ^a   Rogers, Anthony H ^a  

^a UNIVERSITY OF ADELAIDE   (Australia)

Author keywords

Continuous culture; Fusobacterium nucleatum; NADH oxidase; Oxidative stress; Redox potential; Superoxide dismutase

Indexed keywords

CATALASE; PEROXIDASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

ANAEROBIC GROWTH; ARTICLE; ATMOSPHERE; BIOMASS; CONTINUOUS CULTURE; ENZYME ACTIVITY; FUSOBACTERIUM NUCLEATUM; OXIDATION REDUCTION POTENTIAL; OXIDATIVE STRESS; PRIORITY JOURNAL;

ACETATES; AEROBIOSIS; BUTYRATES; CATALASE; CULTURE MEDIA; FUSOBACTERIUM NUCLEATUM; MULTIENZYME COMPLEXES; NADH, NADPH OXIDOREDUCTASES; NITROGEN; OXIDATION-REDUCTION; OXYGEN; PEROXIDASE; SUPEROXIDE DISMUTASE;

FUSOBACTERIUM NUCLEATUM;

EID: 0034212240     PISSN: 03781097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1097(00)00174-9     Document Type: Article

References (22)

1. Tanner A., Bouldin H. The microbiota of early periodontitis lesions in adults. J. Clin. Periodontol. 86:1989;467-471.
2. Dzink J.L., Haffajee A.D., Socransky S.S. The predominant cultivable microbiota of active and inactive periodontal lesions. J. Clin. Periodontol. 15:1988;316-323.
3. Bartold P.M., Gully N.J., Zilm P.S., Rogers A.H. Identification of components in Fusobacterium nucleatum chemostat-culture supernatants that are potent inhibitors of human gingival fibroblast proliferation. J. Periodontal Res. 26:1991;314-322.
4. Bradshaw D.J., Marsh P.D., Watson G.K., Allison C. Role of Fusobacterium nucleatum and coaggregation in anaerobe survival in planktonic and biofilm oral microbial communities during aeration. Infect. Immun. 66:1998;4729-4732.
5. Marquis R.E. Oxygen metabolism, oxidative stress and acid-base physiology of dental plaque biofilms. J. Ind. Microbiol. 15:1995;198-207.
6. Shah H.N., Williams R.A.D., Bowden G.H., Hardie J.M. Comparison of the biochemical properties of Bacteroides melaninogenicus from human dental plaque and other sites. J. Appl. Bacteriol. 41:1976;473-492.
7. Amano A., Tamagawa H., Takagaki M., Murakami Y., Shizukuishi S., Tsunemitsu A. Relationship between enzyme activities involved in oxygen metabolism and oxygen tolerance in black-pigmented Bacteroides. J. Dent. Res. 67:1988;1196-1199.
8. Higuchi M. The effect of oxygen on the growth and mannitol fermentation of Streptococcus mutans. J. Gen. Microbiol. 130:1984;1819-1826.
9. McCord J.M., Fridovich I. Superoxide dismutase. An enzymic function for Erythrocuprein (Hemocuprein). J. Biol. Chem. 244:1969;6049-6055.
10. Maehly, A.C. and Chance, B. (1957) The assay of catalase and peroxidase. In: Methods of Biochemical Analysis, 3rd Edn. (Bergmeyer, H.U., Ed.), vol. 1, pp. 357-381. Interscience, New York.
11. Hosoya T., Kondo Y. The enzyme substrate compounds and mechanism of action of the hydroperoxidases. J. Biochem. 52:1962;180-184.
12. Guerrant G.O., Lambert M.A., Moss C.W. Analysis of short-chain fatty acids from anaerobic bacteria by high performance liquid chromatography. J. Clin. Microbiol. 16:1982;355-360.
13. Leke N., Grenier D., Goldner M., Mayrand D. Effects of hydrogen peroxide on growth and selective properties of Porphyromonas gingivalis. FEMS Microbiol. Lett. 174:1999;347-353.
14. Ter Steeg P.F., van der Hoeven J.S., de Jong M.H., van Munster P.J.J., Jansen M.J.H. Enrichment of subgingival microflora on human serum leading to accumulation of Bacteroides species, Peptostreptococci and Fusobacteria. Antonie Van Leeuwenhoek Int. J. Gen. Mol. Microbiol. 53:1987;261-271.
15. Rogers A.H., Zilm P.S., Gully N.J., Pfennig A.L., Marsh P.D. Aspects of the growth and metabolism of Fusobacterium nucleatum ATCC 10953 in continuous culture. Oral Microbiol. Immunol. 6:1991;250-255.
16. Gottschalk, G. (1986) Bacterial Fermentation. In: Bacterial Metabolism, 2nd Edn., pp. 208-282. Springer-Verlag, New York.
17. Riondet C., Cachon C., Waché Y., Alcaraz G., Diviès C. Extracellular oxidoreduction potential modifies carbon and energy electron flow in Escherichia coli. J. Bacteriol. 182:2000;620-626.
18. Lynch M.C., Kuramitsu H.K. Role of superoxide dismutase activity in the physiology of Porphyromonas gingivalis. Infect Immun. 67:1999;3367-3375.
19. Amano A., Ishimoto T., Tamagawa H., Shizukuishi S. Role of superoxide dismutase in resistance of Porphyromonas gingivalis to killing by polymorphonuclear leukocytes. Infect. Immun. 60:1992;712-714.
20. Caldwell C.E., Marquis R.E. Oxygen metabolism by Treponema denticola. Oral Microbiol. Immunol. 14:1999;66-72.
21. Higuchi M. Reduced nicotinamide adenine dinucleotide oxidase involvement in defence against oxygen toxicity of Streptococcus mutans. Oral Microbiol. Immunol. 7:1992;309-314.
22. Avzat I., Chapuy-Regaud S., Le Bras G., Dos Santos D., Ogunniyi A.D., Le Thomas I., Gavel J.-R., Paton J.C., Trombe M.-C. The NADH oxidase of Streptococcus pneumoniae: its involvement in competence and virulence. Mol. Microbiol. 34:1999;1018-1028.