Introduction
Bacteria of the genus Veillonella Prévot are anaerobic, Gram-negative cocci (Rogosa, 1984). The type species was originally described by Veillon and Zuber (Veillon and Zuber, 1898) as Staphylococcus parvulus and renamed by Prévot (Prévot, 1933) as Veillonella parvula. Although all strains of Veillonella are phenotypically very similar, seven species are recognized by DNA homology analysis (Mays et al., 1982). The seven species can be identified by restriction fragment length polymorphism (RFLP) analysis of restriction enzyme digests of their 16S ribosomal DNA (Sato et al., 1997a). Veillonellae are found in the alimentary canal of warm-blooded animals and can constitute a major fraction of the bacteria on the epithelial surfaces of the human oral cavity.
Veillonellae are characterized by their unusual metabolism. They generally are unable to ferment carbohydrates including glucose but grow well anaerobically on lactate, pyruvate, malate or fumarate. They possess methyl...
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Literature Cited
Arai, T., A. Kusakabe, and S. Komatsu. 1984 A survey of plasmids in Veillonella strains isolated from human oral cavity Kitasato Arch. Exp. Med. 57 233–237
Asanuma, N., M. Iwamoto, and T. Hino. 1999 Effect of the addition of fumarate on methane production by ruminal microorganisms in vitro J. Dairy Sci. 82 780–787
Babaahmady, K. G., P. D. Marsh, S. J. Challacombe, and H. N. Newman. 1997 Variations in the predominant cultivable microflora of dental plaque at defined subsites on approximal tooth surfaces in children Arch. Oral Biol. 42 101–111
Barnhart, R. A., M. R. Weitekamp, and R. C. Aber. 1983 Osteomyelitis caused by Veillonella Am. J. Med. 74 902–904
Bartlett, J. G., and S. M. Finegold. 1972 Anaerobic pleuropulmonary infections Medicine 51 413–450
Bartlett, J. G., S. L. Gorbach, and S. M. Finegold. 1974 The bacteriology of aspiration pneumonia Am. J. Med. 56 202–207
Basson, N. J., and C. W. van Wyk. 1996 The establishment of a community of oral bacteria that controls the growth of Candida albicans in a chemostat Oral Microbiol. Immunol. 11 199–202
Beatrix, B., K. Bendrat, S. Rospert, and W. Buckel. 1990 The biotin-dependent sodium ion pump glutaconyl-CoA decarboxylase from Fusobacterium nucleatum (subsp. nucleatum) Arch. Microbiol. 154 362–369
Beumont, M. G., J. Duncan, S. D. Mitchell, J. L. Esterhai Jr., and P. H. Edelstein. 1995 Veillonella myositis in an immunocompromised patient Clin. Infect. Dis. 21 678–679
Bladen, H. A., and S. E. Mergenhagen. 1964 Ultrastructure of Veillonella and morphological correlation of an outer membrane with particles associated with endotoxic activity J. Bacteriol. 88 1482–1492
Bladen, H. A., H. Gewurz, and S. E. Mergenhagen. 1967 Interactions of the complement system with the surface and endotoxic lipopolysaccharide of Veillonella alcalescens J. Exp. Med. 125 767–786
Bladen, H., G. Hageage, F. Pollock, and R. Harr. 1970 Plaque formation in vitro on wires by gram-negative oral microorganisms (Veillonella) Arch. Oral Biol. 15 127–133
Borchardt, K. A., M. Baker, and R. Gelber. 1977 Veillonella parvula septicemia and osteomyelitis (letter) Ann. Internat. Med. 86 63–64
Bouhnik, Y., S. Alain, A. Attar, B. Flourié, L. Raskine, M. J. Sanson-Le Pors, and J. C. Rambaud. 1999 Bacterial populations contaminating the upper gut in patients with small intestinal bacterial overgrowth syndrome Am. J. Gastroenterol. 94 1327–1331
Boyar, R. M., and G. H. Bowden. 1985 The microflora associated with the progression of incipient carious lesions of children living in a water-fluoridated area Caries Res. 19 298–306
Bradshaw, D. J., and P. D. Marsh. 1998 Analysis of pH-driven disruption of oral microbial communities in vitro Caries Res. 32 456–462
Brazier, J. S., and T. V. Riley. 1988 UV red fluorescence of Veillonella spp J. Clin. Microbiol. 26 383–384
Brook, I. 1996 Veillonella infections in children J. Clin. Microbiol. 34 1283–1285
Buckel, W., and R. Semmler. 1982 A biotin dependent sodium pump glutaconyl coenzyme A decarboxylase from Acidaminococcus fermentans FEBS Lett. 148 35–38
Burnett, G. W., and G. S. Schuster. 1978 Infections of the tooth pulp and periapical tissues Oral microbiology and infectious diseases (special edition) Williams and Wilkins Baltimore MD 244–253
Campos, M. S., L. D. Q. Campos e Silva, J. R. Rehder, M. B. Lee, T. O’Brien, and P. J. McDonnell. 1994 Anaerobic flora of the conjunctival sac in patients with AIDS and with anophthalmia compared with normal eyes Acta Ophthalmol. 72 241–245
Cavallaro, J. J., L. S. Wiggs, and J. M. Miller. 1997 Evaluation of the BBL Crystal Anaerobe identification system J. Clin. Microbiol. 35 3186–3191
Chow, A. W., J. R. Marshall, and L. B. Guze. 1975 Anaerobic infections of the female genital tract: Prospects and perspectives Obstetrical Gynecological Survey 30
Chow, A. W., V. Patten, and L. B. Guze. 1975 Rapid screening of Veillonella by ultraviolet fluorescence J. Clin. Microbiol. 2 546–548
Clark, W. B., L. L. Bammann, and R. J. Gibbons. 1978 Comparative estimates of bacterial affinities and adsorption sites on hydroxyapatite surfaces Infect. Immun. 19 846–853
Clark, W. B., E. L. Webb, T. T. Wheeler, W. Fischlschweiger, D. C. Birdsell, and B. J. Mansheim. 1981 Role of surface fimbriae (fibrils) in the adsorption of Actinomyces species to saliva-treated hydroxyapatite surfaces Infect. Immun. 33 908–917
Dahlén, G., and I. Ericsson. 1983 Differentiation between Gram-negative anaerobic bacteria by pyrolysis gas chromatography of lipopolysaccharides J. Gen. Microbiol. 129 557–563
Delwiche, E. A., J. J. Pestka, and M. L. Tortorello. 1985 The veillonellae: gram-negative cocci with a unique physiology Ann. Rev. Microbiol. 39 175–183
Denger, K., and B. Schink. 1992 Energy conservation by succinate decarboxylation in Veillonella parvula J. Gen. Microbiol. 138 967–971
De Vries, W., C. Donkers, M. Boellaard, and A. H. Stouthamer. 1978 Oxygen metabolism by the anaerobic bacterium Veillonella alcalescens Arch. Microbiol. 119 167–174
Dimroth, P. 1981 Characterization of a membrane-bound biotin-containing enzyme: Oxaloacetate decarboxylase from Klebsiella aerogenes Eur. J. Biochem. 115 353–358
Dimroth, P. 1985 Biotin-dependent decarboxylases as energy transducing systems Ann. NY Acad. Sci. 447 72–85
Dimroth, P. 1994 Bacterial sodium ion-coupled energetics Ant. v. Leeuwenhoek 65 381–395
Distler, W., and A. Kroncke. 1980 Acid formation by mixed cultures of cariogenic strains of Streptococcus mutans and Veillonella alcalescens Arch. Oral Biol. 25 655–658
Distler, W., and A. Kroncke. 1981 Acid formation by mixed cultures of dental plaque bacteria Actinomyces and Veillonella Arch. Oral Biol. 26 123–126
Doré, P., R. Robert, G. Grollier, J. Rouffineau, H. Lanquetot, J. M. Charrière, and J. L. & Fauchère. 1996 Incidence of anaerobes in ventilator-associated pneumonia with use of a protected specimen brush Am. J. Respir. Crit. Care Med. 153 1292–1298
Durant, J. A., D. J. Nisbet, and S. C. Ricke. 1997 Comparison of batch culture growth and fermentation of a poultry Veillonella isolate and selected Veillonella species grown in a defined medium Anaerobe 3 391–397
Dzink, J. L., A. C. R. Tanner, A. D. Haffajee, and S. S. Socransky. 1985 Gram-negative species associated with active destructive periodontal lesions J. Clin. Periodontol. 12 648–659
Dzink, J. L., S. S. Socransky, and A. D. Haffajee. 1988 The predominant cultivable microbiota of active and inactive lesions of destructive periodontal diseases J. Clin. Periodontol. 15 316–323
Ellen, R. P., D. W. Banting, and E. D. Fillery. 1985 Longitudinal microbiological investigation of a hospitalized population of older adults with a high root surface caries risk J. Dent. Res. 64 1377–1381
Fisher, R. G., and M. R. Denison. 1996 Veillonella parvula bacteremia without an underlying source J. Clin. Microbiol. 34 3235–3236
Foca, A., G. Matera, M. C. Liberto, M. D. Berlinghieri, and S. K. Ng. 1990 Veillonella lipopolysaccharides reduce microbicidal activity of human neutrophils, but do not affect monocyte function J. Immunol. Immunopharmacol. 10 1990–1990
Forsythe, S. J., and J. A. Cole. 1987 Nitrite accumulation during anaerobic nitrate reduction by binary suspensions of bacteria isolated from the achlorhydric stomach J. Gen. Microbiol. 133 1845–1849
Frederick, J., and A. I. Braude. 1974 Anaerobic infection of the paranasal sinuses N. Engl. J. Med. 290 135–137
Gerritse, J., F. Schut, and J. C. Gottschal. 1992 Modelling of mixed chemostat cultures of an aerobic bacterium, Comamonas testosteroni, and an anaerobic bacterium, Veillonella alcalescens: Comparison with experimental data Appl. Environ. Microbiol. 58 1466–1476
Gibbons, R. J., S. S. Socransky, and B. Kapsimalis. 1964 Establishment of human indigenous bacteria in germ-free mice J. Bacteriol. 88 1316–1323
Gibbons, R. J., and M. Nygaard. 1970 Interbacterial aggregation of plaque bacteria Arch. Oral Biol. 15 1397–1400
Gibbons, R. J., and J. van Houte. 1971 Selective bacterial adherence to oral epithelial surfaces and its role as an ecological determinant Infect. Immun. 3 567–573
Goldstein, E. J., D. M. Citron, and S. M. Finegold. 1984 Role of anaerobic bacteria in bite-wound infections Rev. Infect. Dis. 6 Suppl. 1 S177–S183
Greaves, W. L., and A. B. Kaiser. 1984 Endocarditis due to Veillonella alcalescens South Med. J. 77 1211–1212
Gremer, L., and O. Meyer. 1996 Characterization of xanthine dehydrogenase from the anaerobic bacterium Veillonella atypica and identification of a molybdopterin-cytosine-dinucleotide-containing molybdenum cofactor Eur. J. Biochem. 238 862–866
Handley, P. S., D. W. Harty, J. E. Wyatt, C. R. Brown, J. P. Doran, and A. C. Gibbs. 1987 A comparison of the adhesion, coaggregation and cell-surface hydrophobicity properties of fibrillar and fimbriate strains of Streptococcus salivarius J. Gen. Microbiol. 133 3207–3217
Hardie, J. M., and G. H. Bowden. 1974 The normal microbial flora of the mouth Soc. Appl. Bacteriol. Symp. Ser. 3 47–83
Harty, D. W., and P. S. Handley. 1988 Fermentation products, amino acid utilization, maintenance energies and growth yields for the fibrillar Streptococcus salivarius HB and a non-fibrillar mutant HB-B grown in continuous culture under glucose limitation J. Appl. Bacteriol. 65 143–152
Heineman, H. S., and A. I. Braude. 1963 Anaerobic infection of the brain Am. J. Med. 35 682–697
Hewett, M. J., K. W. Knox, and D. G. Bishop. 1971 Biochemical studies on lipopolysaccharides of Veillonella Eur. J. Biochem. 19 169–175
Hilpert, W., and P. Dimroth. 1983 Purification and characterization of a new sodium-transport decarboxylase. Methylmalonyl-CoA decarboxylase from Veillonella alcalescens Eur. J. Biochem. 132 579–587
Hinton Jr., A., and M. E. Hume. 1995 Synergism of lactate and succinate as metabolites utilized by Veillonella to inhibit the growth of Salmonella typhimurium and Salmonella enteritidis in vitro Avian Dis. 39 309–316
Hinton Jr., A., and M. E. Hume. 1997 Inhibition of Listeria monocytogenes growth by Veillonella cultured on tartrate medium Clin. Infect. Dis. 25 Suppl. 2 S120–S120
Hofstad, T., and T. Kristoffersen. 1970 Chemical composition of endotoxin from oral Veillonella Acta Pathol. Microbiol. Scand. (B) Microbiol. Immunol. 78 760–764
Holdeman, L. V., E. P. Cato, and W. E. C. Moore. 1977 Anaerobe Laboratory Manual, 4th edn Anaerobe Laboratory, Virginia Polytechnic Institute and State University Blacksburg VA
Hoshino, E. 1987 L-serine enhances the anaerobic lactate metabolism of Veillonella dispar ATCC 17745 J. Dent. Res. 66 1162–1165
Houston, S., D. Taylor, and R. Rennie. 1997 Prosthetic valve endocarditis due to Veillonella dispar: Successful medical treatment following penicillin desensitization Clin. Infect. Dis. 24 1013–1014
Huder, J. B., and P. Dimroth. 1993 Sequence of the sodium ion pump methylmalonyl-CoA decarboxylase from Veillonella parvula J. Biol. Chem. 268 24564–24571
Huder, J. B., and P. Dimroth. 1995 Expression of the sodium ion pump methylmalonyl-coenzyme A-decarboxylase from Veillonella parvula and of mutated enzyme specimens in Escherichia coli J. Bacteriol. 177 3623–3630
Hughes, C. V., P. E. Kolenbrander, R. N. Andersen, and L. V. H. Moore. 1988 Coaggregation properties of human oral Veillonella spp.: Relationship to colonization site and oral ecology Appl. Environ. Microbiol. 54 1957–1963
Hughes, C. V., C. A. Roseberry, and P. E. Kolenbrander. 1990 Isolation and characterization of coaggregation-defective mutants of Veillonella atypica Arch. Oral Biol. 35 123S–125S
Hughes, C. V., R. N. Andersen, and P. E. Kolenbrander. 1992 Characterization of Veillonella atypica PK1910 adhesin-mediated coaggregation with oral Streptococcus spp Infect. Immun. 60 1178–1186
Inderlied, C. B., and E. A. Delwiche. 1973 Nitrate reduction and the growth of Veillonella alcalescens J. Bacteriol. 114 1206–1212
Isogai, E., H. Isogai, H. Sawada, H. Kaneko, and N. Ito. 1985 Microbial ecology of plaque in rats with naturally occurring gingivitis Infect. Immun. 48 520–527
Janssen, P. H. 1992 Growth yield increase and ATP formation linked to succinate decarboxylation in Veillonella parvula Arch. Microbiol. 157 442–445
Johnson, J. L., and B. Harich. 1983 Ribosomal ribonucleic acid homology among species of the genus Veillonella Prévot Int. J. Syst. Bacteriol. 33 760–764
Jones, D. C., R. Bainton, and H. M. Dunn. 1989 A cervicofacial infection due to Veillonella parvula in a patient with myxoedema Br. Dent. J. 166 339–340
Jones, S. J. 1972 A special relationship between spherical and filamentous microorganisms in mature human dental plaque Arch. Oral Biol. 17 613–616
Kafkewitz, D., and E. A. Delwiche. 1972 Ribose utilization by Veillonella alcalescens J. Bacteriol. 109 1144–1148
Kamio, Y. 1987 Structural specificity of diamines covalently linked to peptidoglycan for cell growth of Veillonella alcalescens and Selenomonas ruminantium J. Bacteriol. 169 4837–4840
Kamio, Y., and K. Nakamura. 1987 Putrescine and cadaverine are constituents of peptidoglycan in Veillonella alcalescens and Veillonella parvula J. Bacteriol. 169 2881–2884
Kilian, M., A. Thylstrup, and O. Fejerskov. 1979 Predominant plaque flora of Tanzanian children exposed to high and low water fluoride concentrations Caries Res. 13 330–343
Kolenbrander, P. E., and R. A. Celesk. 1983 Coaggregation of human oral Cytophaga species and Actinomyces israelii Infect. Immun. 40 1178–1185
Kolenbrander, P. E., and R. N. Andersen. 1986 Multigeneric aggregations among oral bacteria: A network of independent cell-to-cell interactions J. Bacteriol. 168 851–859
Kolenbrander, P. E. 1988 Intergeneric coaggregation among human oral bacteria and ecology of dental plaque Ann. Rev. Microbiol. 42 627–656
Kolenbrander, P. E., and R. N. Andersen. 1988 Intergeneric rosettes: sequestered surface recognition among human periodontal bacteria Appl. Environ. Microbiol. 54 1046–1050
Kolenbrander, P. E., R. N. Andersen, and L. V. H. Moore. 1989 Coaggregation of Fusobacterium nucleatum, Selenomonas flueggei, Selenomonas infelix, Selenomonas noxia, and Selenomonas sputigena with strains from 11 genera of oral bacteria Infect. Immun. 57 3194–3203
Könönen, E., S. Asikainen, and H. Jousimies-Somer. 1992 The early colonization of gram-negative anaerobic bacteria in edentulous infants Oral Microbiol. Immunol. 7 28–31
Könönen, E., S. Asikainen, M. Saarela, J. Karjalainen, and H. Jousimies-Somer. 1994 The oral Gram-negative anaerobic microflora in young children: Longitudinal changes from edentulous to dentate mouth Oral Microbiol. Immunol. 9 136–141
Kwon, Y. M., J. R. Salinas, J. A. Durant, D. J. Nisbet, and S. C. Ricke. 1997 Volatile fatty acid sensitivity of Veillonella CF3 from a continuous-flow probiotic culture J. Food Safety 17 59–67
Lambe Jr., D. W., D. H. Vroon, and C. W. Rietz. 1974 Infections due to anaerobic cocci In: A. Galows, R. M. DeHaan, V. R. Dowell Jr., and L. B. Guze (Eds.) Anaerobic Bacteria: Role in Disease Charles C. Thomas Springfield IL
Lee, K. H., M. F. J. Maiden, A. C. R. Tanner, and H. P. Weber. 1999 Microbiota of successful osseointegrated dental implants J. Periodontol. 70 131–138
Liaw, Y. S., P. C. Yang, Z. G. Wu, C. J. Yu, D. B. Chang, L. N. Lee, S. H. Kuo, and K. T. Luh. 1994 The bacteriology of obstructive pneumonitis. A prospective study using ultrasound-guided transthoracic needle aspiration Am. J. Respir.Crit. Care Med. 149 1648–1653
Liljemark, W. F., and R. J. Gibbons. 1971 Ability of Veillonella and Neisseria species to attach to oral surfaces and their proportions present indigenously Infect. Immun. 4 264–268
Listgarten, M. A. 1976 Structure of the microbial flora associated with periodontal health and disease in man J. Periodontol. 47 1–18
Liu, J. W., J. J. Wu, L. R. Wang, L. J. Teng, and T. C. Huang. 1998 Two fatal cases of Veillonella bacteremia Eur. J. Clin. Microbiol. Infect. Dis. 17 62–64
Loesche, W. J., and S. A. Syed. 1978 Bacteriology of human experimental gingivitis: effect of plaque and gingivitis score Infect. Immun. 21 830–839
Loesche, W. J., S. Eklund, R. Earnest, and B. Burt. 1984 Longitudinal investigation of bacteriology of human fissure decay: Epidemiological studies in molars shortly after eruption Infect. Immun. 46 765–772
Loewe, L., P. Rosenblatt, and E. Alture-Werber. 1946 A refractory case of subacute bacterial endocarditis due to Veillonella gazogenes clinically arrested by a combination of penicillin, sodium para-aminohippurate and heparin Am. Heart J. 32 327–338
London, J., and J. Allen. 1990 Purification and characterization of a Bacteroides loeschei adhesin that interacts with procaryotic and eucaryotic cells J. Bacteriol. 172 2527–2534
Loughrey, A. C., and E. W. Chew. 1990 Endocarditis caused by Veillonella dispar (letter) J. Infect. 21 319–321
MacFarlane, T. W. 1984 The oral ecology of patients with severe Sjogren’s syndrome Microbios 41 99–106
Marik, P. E., and P. Careau. 1999 The role of anaerobes in patients with ventilator-associated pneumonia and aspiration pneumonia: A prospective study Chest 115 178–183
Marounek, M., and S. Bartos. 1987 Interactions between rumen amylolytic and lactate-utilizing bacteria in growth on starch J. Appl. Bacteriol. 63 233–238
Martin, W. J., M. Gardner, and J. A. I. Washington. 1972 In vitro antimicrobial susceptibility of anaerobic bacteria isolated from clinical specimens Antimicrob. Ag. Chemother. 1 148–158
Martin, W. J. 1974 Isolation and indentification of anaerobic bacteria in the clinical laboratory: A 2-year experience Mayo Clin. Proc. 49 300–308
Mashimo, P. A., Y. Murayama, H. Reynolds, C. Mouton, S. A. Ellison, and R. J. Genco. 1981 Eubacterium saburreum and Veillonella parvula: a symbiotic association or oral strains J. Periodontol. 52 374–379
Mays, T. D., L. V. Holdeman, W. E. C. Moore, M. Rogosa, and J. L. Johnson. 1982 Taxonomy of the genus Veillonella Prévot Int. J. Syst. Bacteriol. 32 28–36
McBride, B. C., and J. S. van der Hoeven. 1981 Role of interbacterial adherence in colonization of the oral cavities of gnotobiotic rats infected with Streptococcus mutans and Veillonella alcalescens Infect. Immun. 33 467–472
McCabe, R. M., and J. A. Donkersloot. 1977 Adherence of Veillonella species mediated by extracellular glucosyltransferase from Streptococcus salivarius Infect. Immun. 18 726–734
McCarthy, C., M. L. Snyder, and R. B. Parker. 1965 The indigenous oral flora of man. I: The newborn to the 1-year-old infant Arch. Oral Biol. 10 61–70
McDermid, A. S., A. S. McKee, D. C. Ellwood, and P. D. Marsh. 1986 The effect of lowering the pH on the composition and metabolism of a community of nine oral bacteria grown in a chemostat J. Gen. Microbiol. 132 1205–1214
Melville, S. B., T. A. Michel, and J. M. Macy. 1988 Pathway and sites for energy conservation in the metabolism of glucose by Selenomonas ruminantium J. Bacteriol. 170 5298–5304
Mergenhagen, S. E., E. G. Hampp, and H. W. Scherp. 1961 Preparation and biological activities of endotoxins from oral bacteria J. Infect. Dis. 108 304–310
Mikx, F. H., J. S. van der Hoeven, K. G. Konig, A. J, Plasschaert, and B. Guggenheim. 1972 Establishment of defined microbial ecosystems in germ-free rats. I: The effect of the interactions of Streptococcus mutans or Streptococcus sanguis with Veillonella alcalescens on plaque formation and caries activity Caries Res. 6 211–23
Mikx, F. H., and J. S. van der Hoeven. 1975 Symbiosis of Streptococcus mutans and Veillonella alcalescens in mixed continuous cultures Arch. Oral Biol. 20 407–410
Milnes, A. R., and G. H. Bowden. 1985 The microflora associated with developing lesions of nursing caries Caries Res. 19 289–297
Milnes, A. R., G. H. Bowden, E. Gates, and R. Tate. 1993 Predominant cultivable microorganisms on the tongue of preschool children Microb. Ecol. Health Dis. 6 229–235
Minah, G. E., G. B. Lovekin, and J. P. Finney. 1981 Sucrose-induced ecological response of experimental dental plaques from caries-free and caries-susceptible Human volunteers Infect. Immun. 34 662–675
Moore, L. V. H., J. L. Johnson, and W. E. C. Moore. 1987 Selenomonas noxia spp. nov., Selenomonas flueggei spp. nov., Selenomonas infelix spp. nov., Selenomonas dianae spp. nov., and Selenomonas artemidis spp. nov., from the human gingival crevice Int. J. Syst. Bacteriol. 37 271–280
Moore, L. V. H., W. E. C. Moore, E. P. Cato, R. M. Smibert, J. A. Burmeister, A. M. Best, and R. R. Ranney. 1987 Bacteriology of human gingivitis J. Dent. Res. 66 989–995
Moore, W. E. C., E. P. Cato, and L. V. Holdeman. 1969 Anaerobic bacteria of the gastrointestinal flora and their occurrence in clinical infections J. Infect. Dis. 119 641–649
Moore, W. E. C., L. V. Holdeman, R. M. Smibert, I. J. Good, J. A. Burmeister, K. G. Palcanis, and R. R. Ranney. 1982 Bacteriology of experimental gingivitis in young adult humans Infect. Immun. 38 651–667
Moore, W. E. C., L. V. Holdeman, R. M. Smibert, D. E. Hash, J. A. Burmeister, and R. R. Ranney. 1982 Bacteriology of severe periodontitis in young adult humans Infect. Immun. 38 1137–1148
Moore, W. E. C., L. V. Holdeman, E. P. Cato, R. M. Smibert, J. A. Burmeister, and R. R. Ranney. 1983 Bacteriology of moderate (chronic) periodontitis in mature human adults Infect. Immun. 42 510–515
Moore, W. E. C., L. V. Holdeman, E. P. Cato, R. M. Smibert, J. A. Burmeister, K. G. Palcanis, and R. R. Ranney. 1985 Comparative bacteriology of juvenile periodontitis Infect. Immun. 48 507–519
Moore, W. E. C. 1987 Microbiology of periodontal disease J. Periodont. Res. 22 335–341
Moore, W. E. C., J. A. Burmeister, C. N. Brooks, R. R. Ranney, K. H. Hinkelmann, R. M. Schieken, and L. V. H. Moore. 1993 Investigation of the influences of puberty, genetics, and environment on the composition of subgingival periodontal floras Infect. Immun. 61 2891–2898
Mori, T., T. Ebe, M. Takahashi, H. Isonuma, H. Ikemoto, and T. Oguri. 1993 Lung abscess: Analysis of 66 cases from 1979 to 1991 Intern. Med. 32 278–284
Nagy, K. N., I. Sonkodi, I. Szöke, E. Nagy, and H. N. Newman. 1998 The microflora associated with human oral carcinomas Oral Oncol. 34 304–308
Newman, M. G., V. Grinenco, M. Weiner, I. Angel, H. Karge, and R. Nisengard. 1978 Predominant microbiota associated with periodontal health in the aged J. Periodontol. 49 553–559
Ng, S. K., and I. R. Hamilton. 1974 Gluconeogenesis by Veillonella parvula M4: Evidence for the indirect conversion of pyruvate to P-enolpyruvate Can. J. Microbiol. 20 19–28
Olsen, I. 1997 Salient structural features in the chemical composition of oral anaerobes, with particular emphasis on plasmalogens and sphingolipids Rev. Med. Microbiol. 8 Suppl. 1 S3–S6
Pacheco-Delahaye, E., B. Bouchet, C. Andrieux, P. Raibaud, O. Szylit, and D. J. Gallant. 1994 Breakdown of amylomaize starch granules in gnotobiotic rats associated with four bacterial strains isolated from conventional rat microflora J. Sci. Food Agric. 65 487–495
Pang, Y., T. Bosch, and M. C. Roberts. 1994 Single polymerase chain reaction for the detection of tetracycline-resistant determinants Tet K and Tet L Mol. Cell Probes 8 417–422
Pestka, J. J., and E. A. Delwiche. 1983 An alternative pathway for 3-phosphoglycerate generation in Veillonella Can. J. Microbiol. 29 218–224
Pouchot, J., P. Vinceneux, C. Michon, A. Mathieu, and Y. Boussougant. 1992 Pyogenic sacroiliitis due to Veillonella parvula (letter; comment) Clin. Infect. Dis. 15 175–175
Prévot, A. R. 1933 Études de systématique bactérienne. I: Lois générales. II: Cocci anaérobies Ann. Sci. Nat. Bot. 15 23–260
Ramotar, K., J. M. Conly, H. Chubb, and T. J. Louie. 1984 Production of menaquinones by intestinal anaerobes J. Infect. Dis. 150 213–218
Richardson, R. L., and M. Jones. 1958 A bacteriologic census of human saliva J. Dent. Res. 37 697–709
Ritz, H. L. 1967 Microbial population shifts in developing human dental plaque Arch. Oral Biol. 12 1561–1568
Roberts, M. C., and B. J. Moncla. 1988 Tetracycline resistance and TetM in oral anaerobic bacteria and Neisseria perflava-N. sicca Antimicrob. Agents Chemother. 32 1271–1273
Robrish, S. A., W. Reid, and M. I. Krichevsky. 1972 Distribution of enzymes forming polysaccharides from sucrose and the composition of extracellular polysaccharide synthesized by Streptococcus mutans Appl. Microbiol. 24 184–190
Rogosa, M. 1956 A selective medium for the isolation and enumeration of the veillonella from the oral cavity J. Bacteriol. 72 533–536
Rogosa, M., R. J. Fitzgerald, M. E. MacKintosh, and A. J. Beaman. 1958 Improved medium for selective isolation of Veillonella J. Bacteriol. 76 455–456
Rogosa, M. 1964 The genus Veillonella. I: General cultural ecological, and biochemical considerations J. Bacteriol. 87 162–170
Rogosa, M., and F. S. Bishop. 1964 The genus Veillonella. II: Nutritional studies J. Bacteriol. 87 574–580
Rogosa, M., and F. S. Bishop. 1964 The genus Veillonella. III: Hydrogen sulfide production by growing cultures J. Bacteriol. 88 37–41
Rogosa, M. 1965 The genus Veillonella. IV: Serological groupings and genus and species emendations J. Bacteriol. 90 704–709
Rogosa, M., M. I. Krichevsky, and F. S. Bishop. 1965 Truncated glycolytic system in Veillonella J. Bacteriol. 90 164–171
Rogosa, M. 1971 Transfer of Veillonella Prévot and Acidaminococcus Rogosa from Neiseriaceae to Veillonellaceae fam. nov., and the inclusion of Megasphaera Rogosa in Veillonellaceae Int. J. Syst. Bacteriol. 21 231–233
Rogosa, M. 1984 Anaerobic Gram-negative cocci. Family 1: Veillonellaceae rogosa 1971 In: N. R. Krieg, and J. G. Holt (Eds.) [{http://www.cme.msu.edu/bergeys/} {Bergey’s Manual of Systematic Bacteriology}] Williams and Wilkins Baltimore, MD 1 680–685
Ruoff, K. L., and E. A. Delwiche. 1977 Nitrate-reductase electron-transport cofactors in Veillonella alcalescens Can. J. Microbiol. 23 1562–1567
Samuelov, N. S., R. Datta, M. K. Jain, and J. G. Zeikus. 1990 Microbial decarboxylation of succinate to propionate Ann. NY Acad. Sci. 589 697–704
Sato, M., E. Hoshino, S. Nomura, and K. Ishioka. 1993 Salivary microflora of geriatric edentulous persons wearing dentures Microb. Ecol. Health Dis. 6 293–399
Sato, T., J. Matsuyama, M. Sato, and E. Hoshino. 1997 Differentiation of Veillonella atypica, Veillonella dispar and Veillonella parvula using restricted fragment-length polymorphism analysis of 16S rDNA amplified by polymerase chain reaction Oral Microbiol. Immunol. 12 350–353
Sato, T., M. Sato, J. Matsuyama, and E. Hoshino. 1997 PCR-restriction fragment length polymorphism analysis of genes coding for 16S rRNA in Veillonella spp Int. J. Syst. Bacteriol. 47 1268–1270
Shimizu, Y. 1968 Experimental studies on the bacteriophages of the Veillonella strains isolated from the oral cavity Odontology (Tokyo) 55 533–541
Singer, R. E., and B. A. Buckner. 1981 Butyrate and propionate: Important components of toxic dental plaque extracts Infect. Immun. 32 458–463
Singh, N., and V. L. Yu. 1992 Osteomyelitis due to Veillonella parvula: case report and review Clin. Infect. Dis. 14 361–363
Slack, G. L., and G. H. Bowden. 1965 Preliminary studies of experimental dental plaque in vivo Fluorine Res. Dent. Caries Prev. 3 193–215
Slobodkin, A., and W. Verstraete. 1993 Isolation and characterization of Veillonella spp. from methanogenic granular sludge Appl. Microbiol. Biotechnol. 39 649–653
Slots, J. 1977 Microflora in the healthy gingival sulcus in man Scand. J. Dent. Res. 85 247–254
Slots, J., D. Moenbo, J. Langebaek, and A. Frandsen. 1978 Microbiota of gingivitis in man Scand. J. Dent. Res. 86 174–181
Socransky, S. S., A. D. Manganiello, D. Propas, V. Oram, and J. van Houte. 1977 Bacteriological studies of developing supragingival dental plaque J. Periodontal Res. 12 90–106
Stackebrandt, E., H. Pohla, R. Kroppenstedt, H. Hippe, and C. R. Woese. 1985 16S rRNA analysis of Sporomusa, Selenomonas, and Megasphaera on the phylogenetic origin of gram-positive eubacteria Arch. Microbiol. 143 270–276
Summanen, P. H., D. A. Talan, C. Strong, M. McTeague, R. Bennion, J. E. Thompson Jr., M. L. Väisänen, G. Moran, M. Winer, and S. M. Finegold. 1995 Bacteriology of skin and soft-tissue infections: comparison of infections in intravenous drug users and individuals with no history of intravenous drug use Clin. Infect. Dis. 20 S279–S289
Sutter, V. L. 1984 Anaerobes as normal oral flora Rev. Infect. Dis. 6 Suppl. 1 S62–S66
Syed, S. A., and W. J. Loesche. 1978 Bacteriology of human experimental gingivitis: Effect of plaque age Infect. Immun. 21 821–829
Tanner, A., C.-H. Lai, and M. Maiden. 1992 Characteristics of oral Gram-negative species In: J. Slots, and M. A. Taubman (Eds.) Contemporary oral microbiology and immunology Mosby-Year Book St. Louis, MO 299–341
Tanner, A., M. F. J. Maiden, B. J. Paster, and F. E. Dewhirst. 1994 The impact of 16S ribosomal RNA-based phylogeny on the taxonomy of oral bacteria Periodontol. 2000, 5 26–51
Theilade, E., J. Theilade, L. Mikkelsen. 1982 Microbiological studies on early dento-gingival plaque on teeth and Mylar strips in humans J. Periodontal Res. 17 12–25
Tortorello, M. L., and E. A. Delwiche. 1983 Utilization of fructose and ribose in lipopolysaccharide synthesis by Veillonella parvula Infect. Immun. 41 423–425
Tortosa, M., M. I. Cho, T. J. Wilkens, V. J. Iacono, and J. J. Pollock. 1981 Bacteriolysis of Veillonella alcalescens by lysozyme and inorganic anions present in saliva Infect. Immun. 32 1261–1273
Totsuka, M. 1976 Studies on veillonellophages isolated from washings of human oral cavity Bull. Tokyo Med. Dent. Univ. 23 261–273
Totsuka, M. 1988 Phage-receptor on the cell wall of Veillonella rodentium Ant. v. Leeuwenhoek 54 229–233
Totsuka, M., and T. Ono. 1989 Purification and characterization of bacteriophage receptor on Veillonella rodentium cells: Phage-receptor on Veillonella Ant. v. Leeuwenhoek 56 263–271
Ungkanont, K., R. F. Yellon, J. L. Weissman, M. L. Casselbrant, H. González-Valdepeña, and C. D. Bluestone. 1995 Head and neck space infections in infants and children Otolaryngol. Head Neck Surg. 112 375–382
van der Hoeven, J. S., A. I. Toorop, and R. H. Mikx. 1978 Symbiotic relationship of Veillonella alcalescens and Streptococcus mutans in dental plaque in gnotobiotic rats Caries Res. 12 142–147
van der Hoeven, J. S., M. H. de Jong, and P. E. Kolenbrander. 1985 In vivo studies of microbial adherence in dental plaque In: S. E. Mergenhagen, and B. Rosan (Eds.) Molecular Basis of Oral Microbial Adhesion American Society for Microbiology Washington, DC 220–227
Veillon, A., and M. M. Zuber. 1898 Researches sur quelques microbes strictement anaérobies et leur rôle en pathologie Arch. Med. Exp. 10 517–545
Wallace, R. J., N. McKain, G. A. Broderick, L. M. Rode, N. D. Walker, C. J. Newbold, and J. Kopecny. 1997 Peptidases of the rumen bacterium, Prevotella ruminicola Anaerobe 3 35–42
Weerkamp, A. H., and B. C. McBride. 1980 Characterization of the adherence properties of Streptococcus salivarius Infect. Immun. 29 459–468
Weiss, E. I., J. London, P. E. Kolenbrander, A. R. Hand, and R. Siraganian. 1988 Localization and enumeration of fimbria-associated adhesins of Bacteroides loescheii J. Bacteriol. 170 1123–1128
Wexler, H. M., E. Molitoris, D. Molitoris, and S. M. Finegold. 1998 In vitro activity of levofloxacin against a selected group of anaerobic bacteria isolated from skin and soft tissue infections Antimicrob. Agents Chemother. 42 984–986
Whiteley, H. R., and H. C. Douglas. 1951 The fermentation of purines by Micrococcus lactilyticus J. Bacteriol. 61 605–616
Willems, A., and M. D. Collins. 1995 Phylogenetic placement of Dialister pneumosintes (formerly Bacteroides pneumosintes) within the Sporomusa subbranch of the Clostridium subphylum of the Gram-positive bacteria Int. J. Syst. Bacteriol. 45 403–405
Williams, B. L., R. M. Pantalone, and J. C. Sherris. 1976 Subgingival microflora and periodontitis J. Periodont. Res. 11 1–18
Williams, B. L., S. K. Osterberg, and J. Jorgensen. 1979 Subgingival microflora of periodontal patients on tetracycline therapy J. Clin. Periodontol. 6 210–221
Williams, B. L., J. L. Ebersole, M. D. Spektor, and R. C. Page. 1985 Assessment of serum antibody patterns and analysis of subgingival microflora of members of a family with a high prevalence of early-onset periodontitis Infect. Immun. 49 742–750
Williams, B. T. 1977 Pelvic abscess associated with repeated recovery of veillonella Am. J. Obstet. Gynecol. 129 342–343
Winter, P. F., and E. A. Delwiche. 1975 Cell wall composition and incorporation of radio-labelled compounds by Veillonella alcalescens Can. J. Microbiol. 21 2039–2047
Wittenberger, C. L., A. J. Beaman, L. N. Lee, R. M. McCabe, and J. A. Donkersloot. 1977 Possible role of Streptococcus salivarius glucosyltransferase in adherence of Veillonella to smooth surfaces In: D. Schlessinger (Ed.) Microbiology American Society for Microbiology Washington, DC 417–421
Wolff, L. F., M. J. Krupp, and W. F. Liljemark. 1985 Microbial changes associated with advancing periodontitis in STR/N mice J. Periodontal Res. 20 378–385
Yordy, D. M., and E. A. Delwiche. 1979 Nitrite reduction in Veillonella alcalescens J. Bacteriol. 137 905–911
Zambon, J. J., H. Reynolds, J. G. Fisher, M. Shlossman, R. Dunford, and R. J. Genco. 1988 Microbiological and immunological studies of adult periodontitis in patients with noninsulin-dependent diabetes mellitus J. Periodontol. 59 23–31
Zussa, C., P. Ius, F. Cesari, C. Valfre, O. Totis, C. Canova, and P. Pugina. 1994 Fortuitous detection of prosthetic valve endocarditis caused by an uncommon etiologic agent (letter) J. Thorac. Cardiovasc. Surg. 107 1167–1168
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Kolenbrander, P. (2006). The Genus Veillonella . In: Dworkin, M., Falkow, S., Rosenberg, E., Schleifer, KH., Stackebrandt, E. (eds) The Prokaryotes. Springer, New York, NY. https://doi.org/10.1007/0-387-30744-3_36
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