Literature DB >> 14325475

ASSOCIATION OF GERMFREE MICE WITH BACTERIA ISOLATED FROM NORMAL MICE.

R W SCHAEDLER, R DUBS, R COSTELLO.   

Abstract

Germfree mice were given food contaminated with pure cultures of various bacterial species isolated from ordinary healthy mice. The cultures were given singly, or in association, or consecutively at weekly intervals. Whatever the technique of administration, the lactobacilli and anaerobic streptococci immediately established themselves throughout the gastrointestinal tract, and became closely associated with the walls of the organs. In contrast, the organisms of the bacteroides group were found in large numbers only in the large intestine. Within a week after exposure, the populations of these three bacterial species reached levels similar to those found in ordinary mice. They remained at these characteristic levels throughout the period of observation (several months). Their presence resulted in a progressive decrease in the size of the cecum which eventually became normal in gross appearance. Coliform bacilli multiplied extensively and persisted at high levels in all parts of the gastrointestinal tract of germfree mice, even after these had become colonized with lactobacilli, anaerobic streptococci and bacteroides. However, the coliform population fell precipitously within a few days after the animals were fed the intestinal contents of healthy pathogen-free mice.

Entities:  

Keywords:  BACTEROIDES; CECUM; EXPERIMENTAL LAB STUDY; GERM-FREE LIFE; INTESTINE, SMALL; LACTOBACILLUS; MICE; STOMACH; STREPTOCOCCUS

Mesh:

Year:  1965        PMID: 14325475      PMCID: PMC2138033          DOI: 10.1084/jem.122.1.77

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  7 in total

1.  GENERATION CYCLE IN THE DUODENAL CRYPT CELLS OF GERM-FREE AND CONVENTIONAL MICE.

Authors:  S LESHER; H E WALBURG; G A SACHER
Journal:  Nature       Date:  1964-05-30       Impact factor: 49.962

2.  BACTERIA INDUCED MORPHOLOGIC CHANGES.

Authors:  J A HUDSON; T D LUCKEY
Journal:  Proc Soc Exp Biol Med       Date:  1964-07

Review 3.  NORMAL BACTERIAL POPULATIONS OF THE INTESTINE AND THEIR RELATION TO INTESTINAL FUNCTION.

Authors:  R M DONALDSON
Journal:  N Engl J Med       Date:  1964-05-14       Impact factor: 91.245

4.  COMPOSITION, ALTERATION, AND EFFECTS OF THE INTESTINAL FLORA.

Authors:  R DUOBOS; R W SCHAEDLER; R COSTELLO
Journal:  Fed Proc       Date:  1963 Nov-Dec

5.  Effect of a Clostridium species upon cecal size of gnotobiotic mice.

Authors:  B J SKELLY; P C TREXLER; J TANAMI
Journal:  Proc Soc Exp Biol Med       Date:  1962-07

6.  Flexible film apparatus for the rearing and use of germfree animals.

Authors:  P C TREXLER; L I REYNOLDS
Journal:  Appl Microbiol       Date:  1957-11

7.  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

  7 in total
  83 in total

1.  Colonization dynamics of altered Schaedler flora is influenced by gender, aging, and Helicobacter hepaticus infection in the intestines of Swiss Webster mice.

Authors:  Zhongming Ge; Yang Feng; Nancy S Taylor; Masahiro Ohtani; Martin F Polz; David B Schauer; James G Fox
Journal:  Appl Environ Microbiol       Date:  2006-07       Impact factor: 4.792

2.  Immunity to enteric infection in mice.

Authors:  F M Collins
Journal:  Infect Immun       Date:  1970-03       Impact factor: 3.441

3.  Influence of the indigenous gastrointestinal microbial flora on duodenal Mg2+ -dependent and (Na+ + K+) -stimulated adenosine triphosphatase activities in mice.

Authors:  D P Yolton; D C Savage
Journal:  Infect Immun       Date:  1976-04       Impact factor: 3.441

Review 4.  Helicobacter bilis: bacterial provocateur orchestrates host immune responses to commensal flora in a model of inflammatory bowel disease.

Authors:  J G Fox
Journal:  Gut       Date:  2007-07       Impact factor: 23.059

5.  Response to Fungal Dysbiosis by Gut-Resident CX3CR1+ Mononuclear Phagocytes Aggravates Allergic Airway Disease.

Authors:  Xin Li; Irina Leonardi; Alexa Semon; Itai Doron; Iris H Gao; Gregory Garbès Putzel; Youngjun Kim; Hiroki Kabata; David Artis; William D Fiers; Amanda E Ramer-Tait; Iliyan D Iliev
Journal:  Cell Host Microbe       Date:  2018-11-29       Impact factor: 21.023

6.  Distribution and effects of a defined six-member murine-derived microflora in gnotobiotic gerbils.

Authors:  K F Bartizal; B S Wostmann; M Wagner
Journal:  Appl Environ Microbiol       Date:  1984-04       Impact factor: 4.792

7.  The mouse intestinal microflora with emphasis on the strict anaerobes.

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

8.  Enterococcus faecalis readily colonizes the entire gastrointestinal tract and forms biofilms in a germ-free mouse model.

Authors:  Aaron M T Barnes; Jennifer L Dale; Yuqing Chen; Dawn A Manias; Kerryl E Greenwood Quaintance; Melissa K Karau; Purna C Kashyap; Robin Patel; Carol L Wells; Gary M Dunny
Journal:  Virulence       Date:  2016-08-25       Impact factor: 5.882

9.  A real-time PCR assay for accurate quantification of the individual members of the Altered Schaedler Flora microbiota in gnotobiotic mice.

Authors:  João Carlos Gomes-Neto; Sara Mantz; Kyler Held; Rohita Sinha; Rafael R Segura Munoz; Robert Schmaltz; Andrew K Benson; Jens Walter; Amanda E Ramer-Tait
Journal:  J Microbiol Methods       Date:  2017-02-09       Impact factor: 2.363

10.  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

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