Literature DB >> 4586864

Microbial colonization of the intestinal epithelium in suckling mice.

C P Davis, J S McAllister, D C Savage.   

Abstract

Colonization by indigenous microorganisms of the mucosal epithelia of the large bowels of suckling mice was followed by microbial culture techniques and by light, fluorescence, and electron microscopy. Certain microbes colonize in distinctive patterns the cecal and colonic epithelia in these mice. Coliforms and enterococci colonize the large bowel 7 to 9 days after birth and reach high population levels during the second week. During that period, these facultative anaerobes can be detected by immunofluorescence techniques in microcolonies in the mucin on the epithelium. During the third week, however, after their populations decline to the low levels characteristic of adult mice, coliforms and enteroccoci can be observed only infrequently in the mucous layer. Anaerobic fusiform-shaped bacteria appear in the mucous layers along with the microcolonies of enterococci and coliforms during the second week after birth. These anaerobes increase in numbers in the mucin until they form thick layers on the mucosal epithelium by the end of the third week. They remain in the mucous layer throughout the life of the normal mouse. Anaerobic spiral-shaped microbes also colonize the mucous layer on the cecal and colonic epithelium. But these organisms can be detected by immunofluorescence in 1-week-old mice, well in advance of the time the fusiform-shaped bacteria can be found. In the second week, the latter microbes co-inhabit the mucous layer with the spiral-shaped organisms. The fusiform- and spiral-shaped microbes remain associated in the mucin on the cecal and colonic mucosal epithelia into the adult life of mice.

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Year:  1973        PMID: 4586864      PMCID: PMC422740          DOI: 10.1128/iai.7.4.666-672.1973

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  6 in total

1.  Enumeration of the oxygen sensitive bacteria usually present in the intestine of healthy mice.

Authors:  A Lee; J Gordon; R Dubos
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Authors:  D C Savage; J S McAllister; C P Davis
Journal:  Infect Immun       Date:  1971-10       Impact factor: 3.441

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Authors:  A Lee; J Gordon; C J Lee; R Dubos
Journal:  J Exp Med       Date:  1971-02-01       Impact factor: 14.307

4.  The fecal flora of various strains of mice. Its bearing on their susceptibility to endotoxin.

Authors:  R W SCHAEDLER; R J DUBOS
Journal:  J Exp Med       Date:  1962-06-01       Impact factor: 14.307

5.  THE DEVELOPMENT OF THE BACTERIAL FLORA IN THE GASTROINTESTINAL TRACT OF MICE.

Authors:  R W SCHAEDLER; R DUBOS; R COSTELLO
Journal:  J Exp Med       Date:  1965-07-01       Impact factor: 14.307

6.  The anaerobic bacterial flora of the mouse cecum.

Authors:  J H Gordon; R Dubos
Journal:  J Exp Med       Date:  1970-08-01       Impact factor: 14.307

  6 in total
  33 in total

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3.  Bacterial association in the gastrointestinal tract of beagle dogs.

Authors:  C P Davis; D Cleven; E Balish; C E Yale
Journal:  Appl Environ Microbiol       Date:  1977-08       Impact factor: 4.792

4.  Types and distribution of anaerobic bacteria in the large intestine of pigs.

Authors:  E G Russell
Journal:  Appl Environ Microbiol       Date:  1979-02       Impact factor: 4.792

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Authors:  H Marcotte; M C Lavoie
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6.  Fecal Indole as a Biomarker of Susceptibility to Cryptosporidium Infection.

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Authors:  M J Kennedy; P A Volz
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8.  Resistance of calves to Cryptosporidium parvum: effects of age and previous exposure.

Authors:  J A Harp; D B Woodmansee; H W Moon
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9.  Colonization of gnotobiotic mice by Roseburia cecicola, a motile, obligately anaerobic bacterium from murine ceca.

Authors:  T B Stanton; D C Savage
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10.  Isolation and cultivation of spirochetes and other spiral-shaped bacteria associated with the cecal mucosa of rats and mice.

Authors:  A Lee; M Phillips
Journal:  Appl Environ Microbiol       Date:  1978-03       Impact factor: 4.792

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