Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1978 Dec;8(6):629–634. doi: 10.1128/jcm.8.6.629-634.1978

Metabolically deficient dwarf-colony mutants of Escherichia coli: deficiency and resistance to antibiotics of strains isolated from urine culture.

E Borderon, T Horodniceanu
PMCID: PMC275315  PMID: 370140

Abstract

Sixteen metabolically deficient dwarf-colony mutants of Escherichia coli were isolated from urine culture and represented about 2% of all E. coli isolated during the same period. In 14 cases, mutants were isolated from debilitated patients: elderly persons or patients in the terminal stages of a chronic disease. In 15 of these subjects, deficient dwarf-colony mutants appeared to be the true cause of urinary tract infection, since there was leukocyturia and important bacteriuria, and organisms were obtained in pure culture. Study of metabolic deficiencies on Davis synthetic medium and nutritive agar resulted in the identification of eleven deficiencies in cysteine, two in thiamine, two in thymidine, and one in glutamine. Study of resistance to antibiotics revealed that nine were susceptible to all antibiotics, three were resistant to tetracycline alone, two were resistant to two antibiotics (chloramphenicol-tetracycline, streptomycin-tetracycline), and two were resistant to three antibiotics (ampicillin-chloramphenicol-tetracycline, ampicillin-streptomycin-tetracycline). Resistance was coded for by conjugative plasmids in five strains.

Full text

PDF
629

Selected References

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

  1. BARBOUR R. G. H. Small colony variants ("G" forms) produced by Staph. pyogenes during the development of resistance to streptomycin. Aust J Exp Biol Med Sci. 1950 Jul;28(4):411–414. doi: 10.1038/icb.1950.41. [DOI] [PubMed] [Google Scholar]
  2. Borderon E., Horodniceanu T., Buissiere J., Barthez J. P. Mutants déficients à colonies naines de Escherichia coli: étude d'une souche thiamine-déficiente isolée d'une uroculture. Ann Microbiol (Paris) 1977 May-Jun;128A(4):413–417. [PubMed] [Google Scholar]
  3. Borderon E., Horodniceanu T. Mutants déficients à colonies naines de Staphylococcus: étude de trois souches isolées chez des malades porteurs d'ostéosynthèses. Ann Microbiol (Paris) 1976 May-Jun;127(4):503–514. [PubMed] [Google Scholar]
  4. Brumfitt W., Faiers M. C., Reeves D. S., Datta N. Antibiotic-resistant Escherichia coli causing urinary-tract infection in general practice: relation to faecal flora. Lancet. 1971 Feb 13;1(7694):315–317. doi: 10.1016/s0140-6736(71)91043-9. [DOI] [PubMed] [Google Scholar]
  5. CHABBERT Y. A., PATTE J. C. Cellophane transfer: application to the study of activity of combinations of antibiotics. Appl Microbiol. 1960 Jul;8:193–199. doi: 10.1128/am.8.4.193-199.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Charles H. P., Roberts G. A. Carbon dioxide as a growth factor for mutants of Escherichia coli. J Gen Microbiol. 1968 Apr;51(2):211–224. doi: 10.1099/00221287-51-2-211. [DOI] [PubMed] [Google Scholar]
  7. Cox G. B., Gibson F. The role of shikimic acid in the biosynthesis of vitamin K2. Biochem J. 1966 Jul;100(1):1–6. doi: 10.1042/bj1000001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cox G. B., Newton N. A., Gibson F., Snoswell A. M., Hamilton J. A. The function of ubiquinone in Escherichia coli. Biochem J. 1970 Apr;117(3):551–562. doi: 10.1042/bj1170551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dennison S. Naturally occurring R factor, derepressed for pilus synthesis, belonging to the same compatibility group as the sex factor F of Escherichia coli K-12. J Bacteriol. 1972 Jan;109(1):416–422. doi: 10.1128/jb.109.1.416-422.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Devriese L. A. Hemin-dependent mutants isolated from methicillin-resistant Staphylococcus aureus strains. Antonie Van Leeuwenhoek. 1973;39(1):33–40. doi: 10.1007/BF02578839. [DOI] [PubMed] [Google Scholar]
  11. GOUDIE J. G., GOUDIE R. B. Recurrent infections by a stable dwarf-colony variant of Staphylococcus aureus. J Clin Pathol. 1955 Nov;8(4):284–287. doi: 10.1136/jcp.8.4.284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gibson F., Pittard J. Pathways of biosynthesis of aromatic amino acids and vitamins and their control in microorganisms. Bacteriol Rev. 1968 Dec;32(4 Pt 2):465–492. [PMC free article] [PubMed] [Google Scholar]
  13. HALE J. H. Studies on staphylococcus mutation: a naturally occurring "G" gonidial variant and its carbon dioxide requirements. Br J Exp Pathol. 1951 Aug;32(4):307–313. [PMC free article] [PubMed] [Google Scholar]
  14. Horodniceanu T., Bouanchaud D. H., Bieth G., Chabbert Y. A. R plasmids in Streptococcus agalactiae (group B). Antimicrob Agents Chemother. 1976 Nov;10(5):795–801. doi: 10.1128/aac.10.5.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Horodniceanu T., Bouanchaud D. H. Genetic and physical studies of recombinant plasmids formed between an R plasmid of compatibility group FI and sex factor F of HfrH. J Bacteriol. 1976 Jan;125(1):58–67. doi: 10.1128/jb.125.1.58-67.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lacey R. W. Dwarf-colony variants of Staphylococcus aureus resistant to aminoglucoside antibiotics and to a fatty acid. J Med Microbiol. 1969 Aug;2(3):187–197. doi: 10.1099/00222615-2-3-187. [DOI] [PubMed] [Google Scholar]
  17. Maskell R., Okubadejo O. A., Payne R. H., Pead L. Human infections with thymine-requiring bacteria. J Med Microbiol. 1978 Feb;11(1):33–45. doi: 10.1099/00222615-11-1-33. [DOI] [PubMed] [Google Scholar]
  18. Quie P. G. Microcolonies (G-variants) of Staphylococcus aureus. Yale J Biol Med. 1969 Apr;41(5):394–403. [PMC free article] [PubMed] [Google Scholar]
  19. Rettger L. F., Gillespie H. B. Bacterial Variation, with Special Reference to Pleomorphism and Filtrability. J Bacteriol. 1933 Sep;26(3):289–319. doi: 10.1128/jb.26.3.289-319.1933. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. SASARMAN A., HORODNICEANU T. L'UTILISATION DE LA N'EOMYCINE POUR L'OBTENTION DE VARIANTES AVEC DES PETITES COLONIES (NAINES) CHEZ LE GENRE SALMONELLA. Arch Roum Pathol Exp Microbiol. 1963 Sep-Dec;22:1101–1110. [PubMed] [Google Scholar]
  21. Sasarman A., Surdeanu M., Szabados J., Greceanu V., Horodniceanu T. Menaphthone-requiring mutants of Staphylococcus aureus. Rev Can Biol. 1968 Dec;27(4):333–339. [PubMed] [Google Scholar]
  22. Sompolinsky D., Cohen M., Ziv G. Epidemiological and biochemical studies on thiamine-less dwarf-colony variants of Staphylococcus aureus as etiological agents of bovine mastitis. Infect Immun. 1974 Feb;9(2):217–228. doi: 10.1128/iai.9.2.217-228.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sompolinsky D., Ernst-Geller Z., Segal S. Metabolic disorders in thiamineless dwarf strains of Staphylococcus aureus. J Gen Microbiol. 1967 Aug;48(2):205–213. doi: 10.1099/00221287-48-2-205. [DOI] [PubMed] [Google Scholar]
  24. Sompolinsky D., Gluskin I., Ziv G. Pantothenate-requiring dwarf colony variants of Staphylococcus aureus as the etiological agent in bovine mastitis. J Hyg (Lond) 1969 Sep;67(3):511–516. doi: 10.1017/s0022172400041930. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Săsărman A., Chartrand P., Proschek R., Desrochers M., Tardif D., Lapointe C. Uroporphyrin-accumulating mutant of Escherichia coli K-12. J Bacteriol. 1975 Dec;124(3):1205–1212. doi: 10.1128/jb.124.3.1205-1212.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Săsărman A., Greceanu V., Szégli G., Surdeanu M. Complémentation biochimique des mutants NcF- de Bacillus subtilis et de Staphylococcus aureus. Arch Roum Pathol Exp Microbiol. 1968 Jun;27(2):455–462. [PubMed] [Google Scholar]
  27. Săsărman A., Horodniceanu T. Locus determining normal colony formation on the chromosome of Escherichia coli K-12. J Bacteriol. 1967 Oct;94(4):1268–1269. doi: 10.1128/jb.94.4.1268-1269.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Săsărman A., Sanderson K. E., Surdeanu M., Sonea S. Hemin-deficient mutants of Salmonella typhimurium. J Bacteriol. 1970 May;102(2):531–536. doi: 10.1128/jb.102.2.531-536.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Săsărman A., Surdeanu M., Horodniceanu T. Locus determining the synthesis of delta-aminolevulinic acid in Escherichia coli K-12. J Bacteriol. 1968 Nov;96(5):1882–1884. doi: 10.1128/jb.96.5.1882-1884.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Săsărman A., Surdeanu M., Portelance V., Dobardzic R., Sonea S. Classification of vitamin K-deficient mutants of Staphylococcus aureus. J Gen Microbiol. 1971 Feb;65(2):125–130. doi: 10.1099/00221287-65-2-125. [DOI] [PubMed] [Google Scholar]
  31. VOUREKA A. Bacterial variants in patients treated with chloramphenicol. Lancet. 1951 Jan 6;1(6645):27–28. doi: 10.1016/s0140-6736(51)93498-8. [DOI] [PubMed] [Google Scholar]
  32. WISE R. I., SPINK W. W. The influence of antibiotics on the origin of small colonies (G variants) of Micrococcus pyogenes var. aureus. J Clin Invest. 1954 Dec;33(12):1611–1622. doi: 10.1172/JCI103041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wulff D. L. Delta-aminolevulinic acid-requiring mutant from Escherichia coli. J Bacteriol. 1967 Apr;93(4):1473–1474. doi: 10.1128/jb.93.4.1473-1474.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. YEGIAN D., GALLO G., TOLL M. W. Kanamycin resistant staphylococcus mutant requiring heme for growth. J Bacteriol. 1959 Jul;78(1):10–12. doi: 10.1128/jb.78.1.10-12.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES