Literature DB >> 4905032

Selection of media for the isolation of common bacterial L-phase organisms from a clinical specimen.

L N Nimmo, D J Blazevic.   

Abstract

The L-phase of 13 bacteria commonly associated with disease were induced by penicillin and inoculated into various solid and broth media; their growth was recorded for a period of 14 days. Plates containing highly purified agar and sucrose as the stabilizing agent and those incubated under aerobic conditions gave the best results. Magnesium seems to be necessary for growth in broth media on primary isolation, although it may not be necessary on multiple transfers after a more stable state has been reached. Growth in broth media is much more difficult to achieve. Reversion is aided by using a higher concentration of agar in plates, by decreasing the sucrose concentration, and by omitting the antibiotics and horse serum. A procedure has been outlined for the routine culture and identification of L-phase organisms from a clinical specimen.

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Year:  1969        PMID: 4905032      PMCID: PMC378030          DOI: 10.1128/am.18.4.535-541.1969

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  16 in total

1.  Bacterial L-phase growth as a possible complicating factor in certain bacteriological procedures.

Authors:  C W GODZESKI; G BRIER; D E PAVEY
Journal:  Life Sci (1962)       Date:  1962-11

2.  Isolation and reversion of L forms of beta-hemolytic streptococci.

Authors:  Y E CRAWFORD; P F FRANK; B SULLIVAN
Journal:  J Infect Dis       Date:  1958 Jan-Feb       Impact factor: 5.226

3.  Significance of bacterial variants in urine of patients with chronic bacteriuria.

Authors:  L T Gutman; M Turck; R G Petersdorf; R J Wedgwood
Journal:  J Clin Invest       Date:  1965-12       Impact factor: 14.808

4.  L form of Neisseria gonorrhoeae.

Authors:  R B Roberts
Journal:  J Bacteriol       Date:  1966-12       Impact factor: 3.490

5.  L-phase bacteria in human heart tissue.

Authors:  C Godzeski; G Brier; W Glenn
Journal:  Life Sci       Date:  1968-01-15       Impact factor: 5.037

6.  Kinetics of the transformation of Gram-negative rods to spheroplasts and ghosts by serum.

Authors:  S D Davis; D Gemsa; R J Wedgwood
Journal:  J Immunol       Date:  1966-04       Impact factor: 5.422

7.  Comparison of the morphology of PPLO and L-forms of bacteria with light and electron microscopy.

Authors:  L Dienes; S Bullivant
Journal:  Ann N Y Acad Sci       Date:  1967-07-28       Impact factor: 5.691

8.  Large bodies of Mycoplasma and L-form organisms.

Authors:  K S Kang; L E Casida
Journal:  J Bacteriol       Date:  1967-03       Impact factor: 3.490

9.  Staphylococcal spheroplasts and L colonies. II. Conditions conducive to reversion of spheroplasts to vegetative staphylococci.

Authors:  M Hamburger; J Carleton
Journal:  J Infect Dis       Date:  1966-12       Impact factor: 5.226

10.  Staphylococcal spheroplasts and L colonies. I. Population curves of vegetative staphylococci and spheroplasts in methicillin-containing broth over long periods.

Authors:  M Hamburger; J Carleton
Journal:  J Infect Dis       Date:  1966-04       Impact factor: 5.226

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  3 in total

1.  Isolation of L-forms by blood culture.

Authors:  O Brogan
Journal:  J Clin Pathol       Date:  1976-10       Impact factor: 3.411

2.  Growth of cell wall-defective variants of Escherichia coli: comparison of aerobic and anaerobic induction frequencies.

Authors:  T W Huber; A W Brinkley
Journal:  J Clin Microbiol       Date:  1977-08       Impact factor: 5.948

3.  Isolation of L-forms in a clinical microbiology laboratory.

Authors:  J A Swierczewski; P Reyes
Journal:  Appl Microbiol       Date:  1970-09
  3 in total

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