Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1981 Jun;146(3):1075–1082. doi: 10.1128/jb.146.3.1075-1082.1981

Nutritionally variant streptococci from patients with endocarditis: growth parameters in a semisynthetic medium and demonstration of a chromophore.

A Bouvet, I van de Rijn, M McCarty
PMCID: PMC216963  PMID: 7240084

Abstract

Nutritionally variant streptococci have been characterized in the past by their growth as satellite colonies and by their nutrient requirements of cysteine or vitamin B6 for growth in complex media. To further understand the growth characteristics of these strains, we studied fresh isolates from patients with endocarditis by using chemically defined medium enriched with 2% Todd-Hewitt dialysate. Under anaerobic conditions, growth yields of the strains in this medium were comparable to those obtained from a complex medium supplemented with vitamin B6, whereas under aerobic conditions, most of the strains had higher growth yields in the semisynthetic medium. Furthermore, the requirement for cysteine and vitamin B6 in the semisynthetic medium was no greater than that of other Streptococcus species. Electron microscopic studies demonstrated normal cell wall structures in organisms grown in the semisynthetic medium as compared with abnormal and irregular cell wall thickening in organisms grown in supplemented complex medium. Finally, these strains appeared to contain a common component when grown in the semisynthetic medium as demonstrated by the appearance of a chromophore after boiling the bacteria at pH 2. Therefore, the demonstration of a medium which permits adequate growth with a normal ultrastructure of nutritionally variant streptococci will permit the further study of this group of important streptococci.

Full text

PDF
1075

Images in this article

Selected References

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

  1. Berman K. S., Gibbons R. J., Nalbandian J. Localization of intracellular polysaccharide granules in Streptococcus mitis. Arch Oral Biol. 1967 Oct;12(10):1133–1138. doi: 10.1016/0003-9969(67)90061-1. [DOI] [PubMed] [Google Scholar]
  2. Bouvet A., Ryter A., Fréhel C., Acar J. F. Nutritionally deficient streptococci: electron microscopic study of 14 strains isolated in bacterial endocarditis. Ann Microbiol (Paris) 1980 Sep-Oct;131B(2):101–120. [PubMed] [Google Scholar]
  3. Carey R. B., Gross K. C., Roberts R. B. Vitamin B6-dependent Streptococcus mitior (mitis) isolated from patients with systemic infections. J Infect Dis. 1975 Jun;131(6):722–726. doi: 10.1093/infdis/131.6.722. [DOI] [PubMed] [Google Scholar]
  4. Cayeux P., Acar J. F., Chabbert Y. A. Bacterial persistence in streptococcal endocarditis due to thiol-requiring mutants. J Infect Dis. 1971 Sep;124(3):247–254. doi: 10.1093/infdis/124.3.247. [DOI] [PubMed] [Google Scholar]
  5. Cooksey R. C., Thompson F. S., Facklam R. R. Physiological characterization of nutritionally variant streptococci. J Clin Microbiol. 1979 Sep;10(3):326–330. doi: 10.1128/jcm.10.3.326-330.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. FRENKEL A., HIRSCH W. Spontaneous development of L forms of streptococci requiring secretions of other bacteria or sulphydryl compounds for normal growth. Nature. 1961 Aug 12;191:728–730. doi: 10.1038/191728a0. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. George R. H. The isolation of symbiotic streptococci. J Med Microbiol. 1974 Feb;7(1):77–83. doi: 10.1099/00222615-7-1-77. [DOI] [PubMed] [Google Scholar]
  9. Higgins M. L., Daneo-Moore L., Boothby D., Shockman G. D. Effect of inhibition of deoxyribonucleic acid and protein synthesis on the direction of cell wall growth in Streptococcus faecalis. J Bacteriol. 1974 May;118(2):681–692. doi: 10.1128/jb.118.2.681-692.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Higgins M. L., Daneo-Moore L. Factors influencing the frequency of mesosomes observed in fixed and unfixed cells of Streptococcus faecalis. J Cell Biol. 1974 May;61(2):288–300. doi: 10.1083/jcb.61.2.288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Higgins M. L., Shockman G. D. Procaryotic cell division with respect to wall and membranes. CRC Crit Rev Microbiol. 1971 May;1(1):29–72. doi: 10.3109/10408417109104477. [DOI] [PubMed] [Google Scholar]
  12. KELLENBERGER E., RYTER A., SECHAUD J. Electron microscope study of DNA-containing plasms. II. Vegetative and mature phage DNA as compared with normal bacterial nucleoids in different physiological states. J Biophys Biochem Cytol. 1958 Nov 25;4(6):671–678. doi: 10.1083/jcb.4.6.671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kessler R. E., van de Rijn I., McCarty M. Characterization and localization of the enzymatic deacylation of lipoteichoic acid in group A streptococci. J Exp Med. 1979 Dec 1;150(6):1498–1509. doi: 10.1084/jem.150.6.1498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Koshi G., Lalitha M. K. Satelliting streptococci causing infective endocarditis--a short communication. Indian J Med Res. 1978 Apr;67:538–541. [PubMed] [Google Scholar]
  15. 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]
  16. McCarthy L. R., Bottone E. J. Bacteremia and endocarditis caused by satelliting streptococci. Am J Clin Pathol. 1974 May;61(5):585–591. doi: 10.1093/ajcp/61.5.585. [DOI] [PubMed] [Google Scholar]
  17. Narasimhan S. L., Weinstein A. J. Infective endocarditis due to a nutritionally deficient streptococcus. J Pediatr. 1980 Jan;96(1):61–62. doi: 10.1016/s0022-3476(80)80327-1. [DOI] [PubMed] [Google Scholar]
  18. Niven C. F., Smiley K. L., Sherman J. M. The Hydrolysis of Arginine by Streptococci. J Bacteriol. 1942 Jun;43(6):651–660. doi: 10.1128/jb.43.6.651-660.1942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Roberts K. B., Sidlak M. J. Satellite streptococci. A major cause of "negative" blood cultures in bacterial endocarditis? JAMA. 1979 May 25;241(21):2293–2294. doi: 10.1001/jama.241.21.2293. [DOI] [PubMed] [Google Scholar]
  20. Roberts R. B., Krieger A. G., Schiller N. L., Gross K. C. Viridans streptococcal endocarditis: the role of various species, including pyridoxal-dependent streptococci. Rev Infect Dis. 1979 Nov-Dec;1(6):955–966. doi: 10.1093/clinids/1.6.955. [DOI] [PubMed] [Google Scholar]
  21. 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]
  22. Rosan B. Relationship of the cell wall composition of group H streptococci and Streptococcus sanguis to their serological properties. Infect Immun. 1976 Apr;13(4):1144–1153. doi: 10.1128/iai.13.4.1144-1153.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sherman S. P., Washington J. A., 2nd Pyridoxine inhibition of a symbiotic streptococcus. Am J Clin Pathol. 1978 Oct;70(4):689–690. doi: 10.1093/ajcp/70.4.689. [DOI] [PubMed] [Google Scholar]
  24. Von Handrick W., Meister E. M., Köhler W. Uber einen Fall von Sepsis lenta durch Streptococcus cremoris. Kinderarztl Prax. 1974 Nov;42(11):509–513. [PubMed] [Google Scholar]
  25. Wicken A. J., Gibbens J. W., Knox K. W. Comparative studies on the isolation of membrane lipoteichoic acid from Lactobacillus fermenti. J Bacteriol. 1973 Jan;113(1):365–372. doi: 10.1128/jb.113.1.365-372.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. van de Rijn I., Kessler R. E. Growth characteristics of group A streptococci in a new chemically defined medium. Infect Immun. 1980 Feb;27(2):444–448. doi: 10.1128/iai.27.2.444-448.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES