Literature DB >> 5970461

Growth and invasiveness of Candida albicans in the germ-free and conventional mouse after oral challenge.

A W Phillips, E Balish.   

Abstract

Candida albicans was established in large numbers throughout the gut after one oral challenge in the germ-free and in the conventional mouse. Of the strains tested, only the germ-free ND 1 mouse appeared to be susceptible to infection, and this was confined to the stomach mucosa; lesions contained large numbers of hyphal and mycelial forms with blastospores. These forms were also seen in the gut of resistant germ-free ND 4 mice after challenge. Only budding yeast forms were seen in the gut contents from conventional animals. The concentration of sulfhydryl-containing compounds was decreased in the stomach contents from germ-free mice. The stomach tissue of conventional animals seemed to be more acidic than that of germ-free animals, and association of C. albicans with conventional mice neutralized some of this acidity. E(h) values of contents from the gut of unchallenged mice were usually higher in conventional than in germ-free animals; after challenge, the E(h) in both groups decreased. Some reciprocal effects of intestinal microorganisms and host are discussed in relation to intestinal candidiasis.

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Year:  1966        PMID: 5970461      PMCID: PMC1058406          DOI: 10.1128/am.14.5.737-741.1966

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


  11 in total

1.  Morphological and physiological characterization of germfree life.

Authors:  H A GORDON
Journal:  Ann N Y Acad Sci       Date:  1959-05-08       Impact factor: 5.691

2.  Studies on peridontal disease in the mouse. 3. The germ-free mouse and its conventional control.

Authors:  P N BAER; W L NEWTON
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1960-09

3.  A spectrophotometric titration for the determination of sulfhydryl groups.

Authors:  I M KLOTZ; B R CARVER
Journal:  Arch Biochem Biophys       Date:  1961-12       Impact factor: 4.013

4.  The experimental pathogenicity of various species of Candida in Swiss mice.

Authors:  Z T MANKOWSKI
Journal:  Trans N Y Acad Sci       Date:  1957-04

5.  Pathogenesis of Candida albicans infection following antibiotic therapy. II. Further studies of the effect of antibiotics on the in vitro growth of Candida albicans.

Authors:  M HUPPERT; J CAZIN
Journal:  J Bacteriol       Date:  1955-10       Impact factor: 3.490

6.  Intradermal test in ankylostomiasis.

Authors:  B G PRASAD; G B MATHUR
Journal:  Indian J Med Res       Date:  1962-01       Impact factor: 2.375

7.  Rearing of germfree and monocontaminated chicks in rigid plastic isolators.

Authors:  A W PHILLIPS; H R NEWCOMB; R LACHAPELLE; E BALISH
Journal:  Appl Microbiol       Date:  1962-05

8.  The enhancement of the virulence of Candida albicans in mice.

Authors:  S B SALVIN; J C CORY; M K BERG
Journal:  J Infect Dis       Date:  1952 Mar-Apr       Impact factor: 5.226

9.  Growth, morphogenesis, and virulence of Candida albicans after oral inoculation in the germ-free and conventional chick.

Authors:  E Balish; A W Phillips
Journal:  J Bacteriol       Date:  1966-05       Impact factor: 3.490

10.  ASSOCIATION OF GERMFREE MICE WITH BACTERIA ISOLATED FROM NORMAL MICE.

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

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  27 in total

1.  Experimental gastrointestinal and disseminated candidiasis in immunocompromised animals.

Authors:  T J Walsh; P A Pizzo
Journal:  Eur J Epidemiol       Date:  1992-05       Impact factor: 8.082

2.  Microbiota signalling through MyD88 is necessary for a systemic neutrophilic inflammatory response.

Authors:  Dipti Karmarkar; Kenneth L Rock
Journal:  Immunology       Date:  2013-12       Impact factor: 7.397

3.  Interplay between the gastric bacterial microbiota and Candida albicans during postantibiotic recolonization and gastritis.

Authors:  Katie L Mason; John R Erb Downward; Nicole R Falkowski; Vincent B Young; John Y Kao; Gary B Huffnagle
Journal:  Infect Immun       Date:  2011-10-10       Impact factor: 3.441

4.  Ecology of Candida albicans gut colonization: inhibition of Candida adhesion, colonization, and dissemination from the gastrointestinal tract by bacterial antagonism.

Authors:  M J Kennedy; P A Volz
Journal:  Infect Immun       Date:  1985-09       Impact factor: 3.441

5.  Colonization of congenitally athymic, gnotobiotic mice by Candida albicans.

Authors:  E Balish; M J Balish; C A Salkowski; K W Lee; K F Bartizal
Journal:  Appl Environ Microbiol       Date:  1984-04       Impact factor: 4.792

6.  Suppression of Candida albicans by human oral streptococci in gnotobiotic mice.

Authors:  W F Liljemark; R J Gibbons
Journal:  Infect Immun       Date:  1973-11       Impact factor: 3.441

7.  Effect of oral tetracycline, the microbial flora, and the athymic state on gastrointestinal colonization and infection of BALB/c mice with Candida albicans.

Authors:  P B Helstrom; E Balish
Journal:  Infect Immun       Date:  1979-03       Impact factor: 3.441

8.  In vitro modification of Candida albicans invasiveness.

Authors:  S E Fontenla de Petrino; M E de Jorrat; A Sirena; J C Valdez; O Mesón
Journal:  Mycopathologia       Date:  1986-05       Impact factor: 2.574

9.  Poly(I.C)-induced interferons enhance susceptibility of SCID mice to systemic candidiasis.

Authors:  J Jensen; A Vazquez-Torres; E Balish
Journal:  Infect Immun       Date:  1992-11       Impact factor: 3.441

10.  Experimental murine candidiasis: pathological and immune responses to cutaneous inoculation with Candida albicans.

Authors:  D K Giger; J E Domer; J T McQuitty
Journal:  Infect Immun       Date:  1978-02       Impact factor: 3.441

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