Abstract
Strains of Streptococcus salivarius were screened by negative staining for the presence of surface structures. Two structural subgroups were found, carrying either fibrils or fimbriae, projecting from the cell surface. Eight strains carried a very dense peritrichous array of fibrils of two distinct lengths. Long fibrils had an average length of 175 nm, and short fibrils had an average length of 95 nm. Two strains carried only long fibrils, one strain carried only short fibrils, and another strain carried a lateral tuft of very prominent fibrils of two lengths, with a fibrillar fuzz covering the remainder of the cell surface. In all the strains in which they were present, the long fibrils were unaffected by protease or trypsin treatment. In contrast, the short fibrils were completely digested by protease and partially removed by trypsin. Neither long nor short fibrils were affected structurally by mild pepsin digestion or by lipase. The Lancefield extraction procedure removed both long and short fibrils. These twelve fibrillar strains were therefore divisible into four structural subgroups. Extracts of all the fibrillar strains reacted with group K antiserum. The second main structural subgroup consisted of nine strains of S. salivarius, all of which carried morphologically identical, flexible fimbriae arranged peritrichously over the cell surface. The fimbriae were structurally distinct from fibrils and measured 0.5 to 1.0 micron long and 3 to 4 nm wide, with an irregular outline and no obvious substructure. There was no obvious reduction in the number of fimbriae after protease or trypsin treatment. Extracts of the fimbriated strains did not react with the group K antiserum. The two serological and structural subgroups could also be distinguished by colony morphology.
Full text
PDF








Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Beachey E. H., Ofek I. Epithelial cell binding of group A streptococci by lipoteichoic acid on fimbriae denuded of M protein. J Exp Med. 1976 Apr 1;143(4):759–771. doi: 10.1084/jem.143.4.759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carlsson J., Grahnén H., Jonsson G., Wikner S. Early establishment of Streptococcus salivarius in the mouth of infants. J Dent Res. 1970 Mar-Apr;49(2):415–418. doi: 10.1177/00220345700490023601. [DOI] [PubMed] [Google Scholar]
- DUGUID J. P., SMITH I. W., DEMPSTER G., EDMUNDS P. N. Non-flagellar filamentous appendages (fimbriae) and haemagglutinating activity in Bacterium coli. J Pathol Bacteriol. 1955 Oct;70(2):335–348. doi: 10.1002/path.1700700210. [DOI] [PubMed] [Google Scholar]
- Ellen R. P., Gibbons R. J. M protein-associated adherence of Streptococcus pyogenes to epithelial surfaces: prerequisite for virulence. Infect Immun. 1972 May;5(5):826–830. doi: 10.1128/iai.5.5.826-830.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons R. J., Houte J. V. Bacterial adherence in oral microbial ecology. Annu Rev Microbiol. 1975;29:19–44. doi: 10.1146/annurev.mi.29.100175.000315. [DOI] [PubMed] [Google Scholar]
- Gibbons R. J., Van Houte J., Liljemark W. F. Parameters that effect the adherence of Streptococcus salivarius to oral epithelial surfaces. J Dent Res. 1972 Mar-Apr;51(2):424–435. doi: 10.1177/00220345720510023101. [DOI] [PubMed] [Google Scholar]
- Gibbons R. J., van Houte J. Selective bacterial adherence to oral epithelial surfaces and its role as an ecological determinant. Infect Immun. 1971 Apr;3(4):567–573. doi: 10.1128/iai.3.4.567-573.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HORSFALL F. L., Jr Studies on non-hemolytic streptococci isolated from the respiratory tract of man; the antigenic basis for type specific reactions with streptococcus salivarius and non-levan-forming streptococci. J Exp Med. 1951 Mar;93(3):229–245. doi: 10.1084/jem.93.3.229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Handley P. S., Jacob A. E. Some structural and physiological properties of fimbriae of Streptococcus faecalis. J Gen Microbiol. 1981 Dec;127(2):289–293. doi: 10.1099/00221287-127-2-289. [DOI] [PubMed] [Google Scholar]
- Henriksen S. D., Henrichsen J. Twitching motility and possession of polar fimbriae in spreading Streptococcus sanguis isolates from the human throat. Acta Pathol Microbiol Scand B. 1975 Apr;83(2):133–140. doi: 10.1111/j.1699-0463.1975.tb00083.x. [DOI] [PubMed] [Google Scholar]
- Hogg S. D., Handley P. S., Embery G. Surface fibrils may be responsible for the salivary glycoprotein-mediated aggregation of the oral bacterium Streptococcus sanguis. Arch Oral Biol. 1981;26(11):945–949. doi: 10.1016/0003-9969(81)90156-4. [DOI] [PubMed] [Google Scholar]
- KRASSE B. The proportional distribution of Streptococcus salivarius and other streptococci in various parts of the mouth. Odontol Revy. 1954;5(3):203–211. [PubMed] [Google Scholar]
- Liljemark W. F., Gibbons R. J. Proportional distribution and relative adherence of Streptococcus miteor (mitis) on various surfaces in the human oral cavity. Infect Immun. 1972 Nov;6(5):852–859. doi: 10.1128/iai.6.5.852-859.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Montague E. A., Knox K. W. Antigenic components of the cell wall of Streptococcus salivarius. J Gen Microbiol. 1968 Dec;54(2):237–246. doi: 10.1099/00221287-54-2-237. [DOI] [PubMed] [Google Scholar]
- Mouton C., Reynolds H. S., Genco R. J. Characterization of tufted streptococci isolated from the "corn cob" configuration of human dental plaque. Infect Immun. 1980 Jan;27(1):235–245. doi: 10.1128/iai.27.1.235-245.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nalbandian J., Freedman M. L., Tanzer J. M., Lovelace S. M. Ultrastructure of Mutants of Streptococcus mutans with Reference to Agglutination, Adhesion, and Extracellular Polysaccharide. Infect Immun. 1974 Nov;10(5):1170–1179. doi: 10.1128/iai.10.5.1170-1179.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ottow J. C. Ecology, physiology, and genetics of fimbriae and pili. Annu Rev Microbiol. 1975;29:79–108. doi: 10.1146/annurev.mi.29.100175.000455. [DOI] [PubMed] [Google Scholar]
- 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]
- STEWART F. S., McKEEVER J. D. Serological definition of Lancefield group K. J Pathol Bacteriol. 1963 Apr;85:383–388. doi: 10.1002/path.1700850216. [DOI] [PubMed] [Google Scholar]
- Sklavounou A., Germaine G. R. Adherence of oral streptococci to keratinized and nonkeratinized human oral epithelial cells. Infect Immun. 1980 Feb;27(2):686–689. doi: 10.1128/iai.27.2.686-689.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WILLIAMS R. E. Streptococcus salivarius (vel hominis) and its relation to Lancefield's group K. J Pathol Bacteriol. 1956 Jul;72(1):15–25. doi: 10.1002/path.1700720103. [DOI] [PubMed] [Google Scholar]
- Weerkamp A. H., Jacobs T. Cell wall-associated protein antigens of Streptococcus salivarius: purification, properties, and function in adherence. Infect Immun. 1982 Oct;38(1):233–242. doi: 10.1128/iai.38.1.233-242.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weerkamp A. H., McBride B. C. Adherence of Streptococcus salivarius HB and HB-7 to oral surfaces and saliva-coated hydroxyapatite. Infect Immun. 1980 Oct;30(1):150–158. doi: 10.1128/iai.30.1.150-158.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weerkamp A. H., McBride B. C. Characterization of the adherence properties of Streptococcus salivarius. Infect Immun. 1980 Aug;29(2):459–468. doi: 10.1128/iai.29.2.459-468.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weerkamp A. H., McBride B. C. Identification of a Streptococcus salivarius cell wall component mediating coaggregation with Veillonella alcalescens V1. Infect Immun. 1981 May;32(2):723–730. doi: 10.1128/iai.32.2.723-730.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]




