Literature DB >> 4914569

Selective outgrowth of fimbriate bacteria in static liquid medium.

D C Old, J P Duguid.   

Abstract

Competitive mixed cultures were grown from inocula of a large number of bacteria of a genotypically nonfimbriate (fim(-)) strain of Salmonella typhimurium and a small number of a genotypically fimbriate (fim(+)) variant strain that formed type 1 fimbriae and had been derived from the fim(-) strain by phage transduction. The fim(+) strain differed from the fim(-) strain in fermenting l-rhamnose (rha(+)), and the viable fim(+) and fim(-) bacteria present in the cultures after different periods at 37 C were counted differentially in platings on rhamnose media. When the cultures were grown under aerobic static conditions in tubes of nutrient broth, the fim(+) bacteria rapidly outgrew the fim(-) bacteria, so that, although starting as a small minority (e.g., 1 in 10(7)), they approached or surpassed the number of the fim(-) in 48 hr. A pellicle consisting of fimbriate bacteria was formed on the surface of the broth between 6 and 24 hr, and it is thought that the advantage of access to atmospheric oxygen enjoyed by these bacteria in the pellicle enabled them to outgrow the fim(-) bacteria confined in the oxygen-depleted broth. The fim(+) bacteria did not show selective outgrowth in mixed cultures grown in broth aerated by continuous shaking, in static broth incubated anaerobically in hydrogen, and on aerobic agar plates, i.e., under conditions not allowing an advantage from pellicle formation. The outgrowth of fim(+) bacteria in aerobic static broth was prevented by the addition of alpha-methylmannoside, a substance that inhibits the adhesive and early pellicle-forming properties of bacteria with type 1 fimbriae. A motile flagellate (fla(+)) variant of a fim(-)fla(-) strain of S. typhimurium outgrew its parent strain in mixed cultures in aerobic static broth, but the selective advantage conferred by motility was weaker than that conferred by fimbriation.

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Year:  1970        PMID: 4914569      PMCID: PMC248102          DOI: 10.1128/jb.103.2.447-456.1970

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  15 in total

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2.  Non-flagellar filamentous appendages (fimbriae) and haemagglutinating activity in Bacterium coli.

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3.  Transduction of flagellar characters in Salmonella.

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4.  Genetic exchange in Salmonella.

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5.  Mutants of Escherichia coli requiring methionine or vitamin B12.

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6.  Fimbriation, pellicle formation and the amount of growth of salmonellas in broth.

Authors:  D C Old; I Corneil; L F Gibson; A D Thomson; J P Duguid
Journal:  J Gen Microbiol       Date:  1968-04

7.  The function of bacterial fimbriae.

Authors:  J P Duguid
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  1968       Impact factor: 4.291

8.  Fimbriae and adhesive properties in Salmonellae.

Authors:  J P Duguid; E S Anderson; I Campbell
Journal:  J Pathol Bacteriol       Date:  1966-07

9.  Studies on negative chemotaxis and the survival value of motility in Pseudomonas fluorescens.

Authors:  J L Smith; R N Doetsch
Journal:  J Gen Microbiol       Date:  1969-03

10.  Terminology of bacterial fimbriae, or pili, and their types.

Authors:  J P Duguid; E S Anderson
Journal:  Nature       Date:  1967-07-01       Impact factor: 49.962

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  90 in total

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2.  Type 1 fimbriation and phase switching in a natural Escherichia coli fimB null strain, Nissle 1917.

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Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

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4.  Osmolarity and pH growth conditions regulate fim gene transcription and type 1 pilus expression in uropathogenic Escherichia coli.

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5.  FimA, FimF, and FimH are necessary for assembly of type 1 fimbriae on Salmonella enterica serovar Typhimurium.

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6.  Utilization of d-tartaric acid by Salmonella paratyphi B and Salmonella java: comparison of anaerobic plate test, lead acetate test and turbidity test.

Authors:  R M Barker
Journal:  J Hyg (Lond)       Date:  1985-08

7.  Functional heterogeneity of intestinal Escherichia coli strains expressing type 1 somatic pili (fimbriae): assessment of bacterial adherence to intestinal membranes and surface hydrophobicity.

Authors:  P M Sherman; W L Houston; E C Boedeker
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8.  Role of type 1 pili and effects of phase variation on lower urinary tract infections produced by Escherichia coli.

Authors:  S J Hultgren; T N Porter; A J Schaeffer; J L Duncan
Journal:  Infect Immun       Date:  1985-11       Impact factor: 3.441

9.  A whole-organ perfusion model of Bordetella pertussis adherence to mouse tracheal epithelium.

Authors:  L O Bakaletz; M S Rheins
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10.  Genetic complementation analysis of Escherichia coli type 1 somatic pilus mutants.

Authors:  L M Swaney; Y P Liu; K Ippen-Ihler; C C Brinton
Journal:  J Bacteriol       Date:  1977-04       Impact factor: 3.490

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