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. 1980 Jan;27(1):235–245. doi: 10.1128/iai.27.1.235-245.1980

Characterization of tufted streptococci isolated from the "corn cob" configuration of human dental plaque.

C Mouton, H S Reynolds, R J Genco
PMCID: PMC550750  PMID: 6987171

Abstract

Streptococci isolated from "corn cob" configurations of human dental plaque possess a polar fibrillar tuft extending 100 to 150 nm from one pole of the cell. The two strains studied were physiologically related to the Streptococcus sanguis-Streptococcus mitior group and were most similar to Streptococcus mitis ATCC 903. The corn cob streptococci were serologically related to S. sanguis serotype 1. The polar tuft contained at least two antigenically distinct components, one serologically related to the glycerol phosphate backbone of teichoic acid. The other was an electrophoretically slow-moving antigen similar to a component of S. mitis ATCC 903. It is suggested that the corn cob streptococci in vivo adhere to Bacterionema matruchotii by means of the polar tuft.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amako K., Umeda A. Scanning electron microscopy of Staphylococcus. J Ultrastruct Res. 1977 Jan;58(1):34–40. doi: 10.1016/s0022-5320(77)80005-1. [DOI] [PubMed] [Google Scholar]
  2. Bratthall D., Carlsson J. Oral streptococci and commercial grouping sera. Odontol Revy. 1968;19(2):205–209. [PubMed] [Google Scholar]
  3. Breznak J. A., Pankratz H. S. In situ morphology of the gut microbiota of wood-eating termites [Reticulitermes flavipes (Kollar) and Coptotermes formosanus Shiraki]. Appl Environ Microbiol. 1977 Feb;33(2):406–426. doi: 10.1128/aem.33.2.406-426.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Carlsson J. A medium for isolation of Streptococcus mutans. Arch Oral Biol. 1967 Dec;12(12):1657–1658. doi: 10.1016/0003-9969(67)90201-4. [DOI] [PubMed] [Google Scholar]
  5. Carlsson J. A numerical taxonomic study of human oral streptococci. Odontol Revy. 1968;19(2):137–160. [PubMed] [Google Scholar]
  6. Carlsson J. Presence of various types of non-haemolytic streptococci in dental plaque and in other sites of the oral cavity in man. Odontol Revy. 1967;18(1):55–74. [PubMed] [Google Scholar]
  7. Carlsson J. Zooglea-forming streptococci, resembling Streptococcus sanguis, isolated from dental plaque in man. Odontol Revy. 1965;16(4):348–358. [PubMed] [Google Scholar]
  8. DEIBEL R. H., EVANS J. B. Modified benzidine test for the detection of cytochrome-containing respiratory systems in microorganisms. J Bacteriol. 1960 Mar;79:356–360. doi: 10.1128/jb.79.3.356-360.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Facklam R. R. Physiological differentiation of viridans streptococci. J Clin Microbiol. 1977 Feb;5(2):184–201. doi: 10.1128/jcm.5.2.184-201.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. GIBBONS R. J., SOCRANSKY S. S. Intracellular polysaccharide storage by organisms in dental plaques. Its relation to dental caries and microbial ecology of the oral cavity. Arch Oral Biol. 1962 Jan-Feb;7:73–79. doi: 10.1016/0003-9969(62)90050-x. [DOI] [PubMed] [Google Scholar]
  11. HAHN J. J., COLE R. M. STREPTOCOCCAL M ANTIGEN LOCATION AND SYNTHESIS, STUDIED BY IMMUNOFLUORESCENCE. J Exp Med. 1963 Nov 1;118:659–666. doi: 10.1084/jem.118.5.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Markham J. L., Knox K. W., Wicken A. J., Hewett M. J. Formation of extracellular lipoteichoic acid by oral streptococci and lactobacilli. Infect Immun. 1975 Aug;12(2):378–386. doi: 10.1128/iai.12.2.378-386.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mejàre B., Edwardsson S. Streptococcus milleri (Guthof); an indigenous organism of the human oral cavity. Arch Oral Biol. 1975 Nov;20(11):757–762. doi: 10.1016/0003-9969(75)90048-5. [DOI] [PubMed] [Google Scholar]
  14. Mouton C., Reynolds H., Genco R. J. Combined micromanipulation, culture and immunofluorescent techniques for isolation of the coccal organisms comprising the "corn cob" configuration of human dental plaque. J Biol Buccale. 1977 Dec;5(4):321–332. [PubMed] [Google Scholar]
  15. RANTZ L. A., RANDALL E. Use of autoclaved extracts of hemolytic streptococci for serological grouping. Stanford Med Bull. 1955 May;13(2):290–291. [PubMed] [Google Scholar]
  16. Rosan B. Absence of glycerol teichoic acids in certain oral streptococci. Science. 1978 Sep 8;201(4359):918–920. doi: 10.1126/science.684416. [DOI] [PubMed] [Google Scholar]
  17. Rosan B. Antigens of Streptococcus sanguis. Infect Immun. 1973 Feb;7(2):205–211. doi: 10.1128/iai.7.2.205-211.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Sherman J. M., Niven C. F., Smiley K. L. Streptococcus salivarius and Other Non-hemolytic Streptococci of the Human Throat. J Bacteriol. 1943 Mar;45(3):249–263. doi: 10.1128/jb.45.3.249-263.1943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Van Driel D., Wicken A. J., Dickson M. R., Knox K. W. Cellular location of the lipoteichoic acids of Lactobacillus fermenti NCTC 6991 and Lactobacillus casei NCTC 6375. J Ultrastruct Res. 1973 Jun;43(5):483–497. doi: 10.1016/s0022-5320(73)90025-7. [DOI] [PubMed] [Google Scholar]
  20. Weiss R. L. The structure and occurrence of pili (fimbriae) on Pseudomonas aeruginosa. J Gen Microbiol. 1971 Aug;67(2):135–143. doi: 10.1099/00221287-67-2-135. [DOI] [PubMed] [Google Scholar]
  21. Wilkinson S. G. Glycosyl diglycerides from Pseudomonas rubescens. Biochim Biophys Acta. 1968 Oct 22;164(2):148–156. doi: 10.1016/0005-2760(68)90141-0. [DOI] [PubMed] [Google Scholar]

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