Literature DB >> 354525

Antagonism among the normal anaerobic bacteria of the mouse gastrointestinal tract determined by immunofluorescence.

R D Berg.   

Abstract

Strictly anaerobic Bacteroides sp., Eubacterium sp., and Fusobacterium sp. were isolated from the cecum of a conventional mouse. An immunofluorescent method utilizing rabbit antisera specific for each of these three strains was developed to determine their population levels in the gastrointestinal tracts of gnotobiotic mice. Population levels of these anaerobes in groups of gnotobiotic mice colonized with either Bacteroides, Eubacterium, or Fusobacterium were compared with those of gnotobiotes colonized with all three strains. Bacteroides population levels in gnotobiotes colonized with all three strains were 100-fold less than the Bacteroides population level in gnotobiotes colonized with only the Bacteroides strain. Eubacterium or Fusobacterium population levels were not reduced by the presence of the other anaerobic strains. Thus, strictly anaerobic Eubacterium sp. and Fusobacterium sp. that colonized gnotobiotic mice caused a reduction in the in vivo population levels of a strictly anaerobic Bacteroides sp.

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Year:  1978        PMID: 354525      PMCID: PMC242986          DOI: 10.1128/aem.35.6.1066-1073.1978

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  22 in total

1.  Bacterial interference by oropharynegeal and clinical isolates of anaerobic bacteria.

Authors:  P R Murray; J E Rosenblatt
Journal:  J Infect Dis       Date:  1976-09       Impact factor: 5.226

Review 2.  Immunological responses and microorganisms indigenous to the gastrointestinal tract.

Authors:  R D Berg; D C Savage
Journal:  Am J Clin Nutr       Date:  1972-12       Impact factor: 7.045

3.  Use of anaerobic glove boxes for the cultivation of strictly anaerobic bacteria.

Authors:  A Aranki; R Freter
Journal:  Am J Clin Nutr       Date:  1972-12       Impact factor: 7.045

4.  Interactions between mechanisms controlling the intestinal microflora.

Authors:  R Freter
Journal:  Am J Clin Nutr       Date:  1974-12       Impact factor: 7.045

5.  Synergism between ecologic and immunologic control mechanisms of intestinal flora.

Authors:  S Shedlofsky; R Freter
Journal:  J Infect Dis       Date:  1974-03       Impact factor: 5.226

6.  Immune responses of specific pathogen-free and gnotobiotic mice to antigens of indigenous and nonindigenous microorganisms.

Authors:  R D Berg; D C Savage
Journal:  Infect Immun       Date:  1975-02       Impact factor: 3.441

7.  Effect of colon flora and short-chain fatty acids on growth in vitro of Pseudomonas aeruginsoa and Enterobacteriaceae.

Authors:  M E Levison
Journal:  Infect Immun       Date:  1973-07       Impact factor: 3.441

8.  Shigella flexneri inhibition by acetic acid.

Authors:  R C Baskett; D J Hentges
Journal:  Infect Immun       Date:  1973-07       Impact factor: 3.441

9.  Determination of the optimal ammonium sulfate concentration for the fractionation of rabbit, sheep, horse, and goat antisera.

Authors:  G A Hebert; P L Pelham; B Pittman
Journal:  Appl Microbiol       Date:  1973-01

10.  Function of various intestinal bacteria in converting germfree mice to the normal state.

Authors:  R Freter; G D Abrams
Journal:  Infect Immun       Date:  1972-08       Impact factor: 3.441

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  10 in total

1.  Bacterial interference by anaerobic species isolated from human feces.

Authors:  M P Wilhelm; D T Lee; J E Rosenblatt
Journal:  Eur J Clin Microbiol       Date:  1987-06       Impact factor: 3.267

2.  New semisolid agar for the detection of motile salmonellae.

Authors:  E A Hine; E K Stefen; J E Wagner
Journal:  J Clin Microbiol       Date:  1988-05       Impact factor: 5.948

3.  Colonization of gnotobiotic mice by Roseburia cecicola, a motile, obligately anaerobic bacterium from murine ceca.

Authors:  T B Stanton; D C Savage
Journal:  Appl Environ Microbiol       Date:  1983-05       Impact factor: 4.792

4.  Bacterial translocation from the gastrointestinal tracts of rats receiving thermal injury.

Authors:  K Maejima; E A Deitch; R D Berg
Journal:  Infect Immun       Date:  1984-01       Impact factor: 3.441

5.  Inhibition of translocation of viable Escherichia coli from the gastrointestinal tract of mice by bacterial antagonism.

Authors:  R D Berg; W E Owens
Journal:  Infect Immun       Date:  1979-09       Impact factor: 3.441

6.  Translocation of certain indigenous bacteria from the gastrointestinal tract to the mesenteric lymph nodes and other organs in a gnotobiotic mouse model.

Authors:  R D Berg; A W Garlington
Journal:  Infect Immun       Date:  1979-02       Impact factor: 3.441

7.  Inhibition of Escherichia coli translocation from the gastrointestinal tract by normal cecal flora in gnotobiotic or antibiotic-decontaminated mice.

Authors:  R D Berg
Journal:  Infect Immun       Date:  1980-09       Impact factor: 3.441

8.  Bacterial translocation from the gastrointestinal tract of athymic (nu/nu) mice.

Authors:  W E Owens; R D Berg
Journal:  Infect Immun       Date:  1980-02       Impact factor: 3.441

9.  Translocation of Escherichia coli from the gastrointestinal tract to the mesenteric lymph nodes in gnotobiotic mice receiving Escherichia coli vaccines before colonization.

Authors:  R D Berg; A W Garlington
Journal:  Infect Immun       Date:  1980-12       Impact factor: 3.441

10.  Promotion of the translocation of enteric bacteria from the gastrointestinal tracts of mice by oral treatment with penicillin, clindamycin, or metronidazole.

Authors:  R D Berg
Journal:  Infect Immun       Date:  1981-09       Impact factor: 3.441

  10 in total

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