Literature DB >> 4160825

Growth and virulence of Candida albicans after oral inoculation in the chick with a monoflora of either Escherichia coli or Streptococcus faecalis.

E Balish, A W Phillips.   

Abstract

Balish, Edward (Syracuse University, Syracuse, N.Y.), and A. W. Phillips. Growth and virulence of Candida albicans after oral inoculation in the chick with a monoflora of either Escherichia coli or Streptococcus faecalis. J. Bacteriol. 91:1744-1749. 1966.-Bacterial protection against intestinal infection by Candida albicans was investigated in chicks with a monoflora of either Escherichia coli or Streptococcus faecalis. These animals were obtained by orally inoculating germ-free chicks (3 days old) with pure cultures of bacteria. Each bacterial species was established in large numbers in the gut of separate groups of animals within 24 hr of inoculation; these numbers were similar in chicks examined 34 days later, at which time all animals were killed. The numbers of bacteria from contents of the crop, small intestine, and ceca were similar in chicks with the E. coli monoflora. Comparable results were obtained in chicks with the S. faecalis monoflora, except for decreased numbers in the duodenum and jejunum. Some of the monoflora chicks (7 days old) were transferred into separate isolators, orally inoculated with C. albicans, and observed for 34 days. All chicks grew well and appeared healthy. However, examinations at autopsy revealed severe crop infections in chicks with a diflora containing S. faecalis. Preferential growth of hyphae (C. albicans) occurred in the lesions and throughout the gut. The numbers of S. faecalis in the gut were comparable to those found in unchallenged animals. Agglutinins against C. albicans were not detected in our test or control chicks. Chicks with a diflora containing E. coli and C. albicans had a few microscopic crop lesions containing small numbers of hyphae. C. albicans was well established in the gut of these animals, largely as the yeast form. The numbers of E. coli in the gut were similar to those in control chicks. Thus, it was concluded that E. coli provided protection against crop infection by C. albicans. In crop contents from unchallenged animals, chicks with S. faecalis monoflora were about pH 5, whereas birds with E. coli monoflora were about pH 7. The challenge did not greatly change the former value, and the latter was slightly decreased. In the crop of unchallenged birds, negative E(h) values were found in chicks with S. faecalis and positive E(h) values in those with E. coli. Challenge did not greatly change these values. These data on pH and E(h) were related to conditions for morphogenesis of C. albicans and virulence. No major difference in the concentrations of serum proteins was seen in chicks with E. coli or S. faecalis after challenge with C. albicans. Possible mechanisms of the protective effect of E. coli are discussed.

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Year:  1966        PMID: 4160825      PMCID: PMC316116          DOI: 10.1128/jb.91.5.1744-1749.1966

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


  13 in total

1.  SYMPOSIUM ON BIOCHEMICAL BASES OF MORPHOGENESIS IN FUNGI. IV. MOLECULAR BASES OF FORM IN YEASTS.

Authors:  W J NICKERSON
Journal:  Bacteriol Rev       Date:  1963-09

2.  A protein disulphide reductase from pea seeds.

Authors:  M D HATCH; J F TURNER
Journal:  Biochem J       Date:  1960-09       Impact factor: 3.857

3.  Enzymatic reduction of disulfide bonds in cell wall protein of baker's yeast.

Authors:  W J NICKERSON; G FALCONE
Journal:  Science       Date:  1956-08-17       Impact factor: 47.728

4.  MICROORGANISMS IN THE INTESTINAL TRACT OF NORMAL CHICKENS.

Authors:  S K Shapiro; W B Sarles
Journal:  J Bacteriol       Date:  1949-10       Impact factor: 3.490

5.  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

6.  Experimental Shigella infections. V. Studies in germ-free guinea pigs.

Authors:  S B FORMAL; G DAMMIN; H SPRINZ; D KUNDEL; H SCHNEIDER; R E HOROWITZ; M FORBES
Journal:  J Bacteriol       Date:  1961-08       Impact factor: 3.490

7.  ESTABLISHMENT OF HUMAN INDIGENOUS BACTERIA IN GERM-FREE MICE.

Authors:  R J GIBBONS; S S SOCRANSKY; B KAPSIMALIS
Journal:  J Bacteriol       Date:  1964-11       Impact factor: 3.490

8.  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

9.  Production of tolerance to the toxicity of Candida albicans by nonfungal materials.

Authors:  H F HASENCLEVER; W O MITCHELL
Journal:  J Bacteriol       Date:  1962-12       Impact factor: 3.490

10.  Experimental enteric Shigella and Vibrio infections in mice and guinea pigs.

Authors:  R FRETER
Journal:  J Exp Med       Date:  1956-09-01       Impact factor: 14.307

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  13 in total

1.  Immunity to Candida albicans.

Authors:  T J Rogers; E Balish
Journal:  Microbiol Rev       Date:  1980-12

Review 2.  The gnotobiotic animal as a tool in the study of host microbial relationships.

Authors:  H A Gordon; L Pesti
Journal:  Bacteriol Rev       Date:  1971-12

Review 3.  Budding off: bringing functional genomics to Candida albicans.

Authors:  Matthew Z Anderson; Richard J Bennett
Journal:  Brief Funct Genomics       Date:  2015-09-30       Impact factor: 4.241

4.  An anaerobic continuous-flow culture model of interactions between intestinal microflora and Candida albicans.

Authors:  M J Kennedy; A L Rogers; R J Yancey
Journal:  Mycopathologia       Date:  1988-09       Impact factor: 2.574

5.  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

6.  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

7.  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

8.  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

9.  Gastrointestinal candidiasis in rats treated with antibiotics, cortisone, and azathioprine.

Authors:  A DeMaria; H Buckley; F von Lichtenberg
Journal:  Infect Immun       Date:  1976-06       Impact factor: 3.441

10.  Influence of antibiotics or certain intestinal bacteria on orally administered Candida albicans in germ-free and conventional mice.

Authors:  J D Clark
Journal:  Infect Immun       Date:  1971-12       Impact factor: 3.441

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