Medical Mycology · 1985 · 132 citations · 29 references
Life SciencesInfectious DiseasesMicrobiologyMedical MicrobiologyMicrobial EcologyMicrobial PathogenesisGastrointestinal InfectionsGut MicrobiomeGut MicrobiotaMucosal Microbiota InteractionsMucosal PathogenesisAdhesion To Intestinal MucosaCandida Albicans InfectionGut Microbiota EffectsIntestinal Microbiota EcologyIntestinal Microbiota EffectsIntestinal Microbiota ModulationMicrobial Ecology Of The GutMucosal Microbiota
Mice were treated orally with various antibiotics to determine which members of the indigenous intestinal microflora normally suppress Candida albicans colonization and dissemination from the gastrointestinal (GI) tract. The mice were given penicillin, clindamycin, vancomycin, erythromycin, or gentamicin for 3 days, and then challenged orally with C. albicans. Penicillin, clindamycin, and vancomycin, but not gentamicin or erythromycin, decreased the total anaerobic bacterial populations in the animals ceca, and increased the enteric bacilli population levels. All three of the former antibiotics allowed C. albicans to proliferate in the gut and, subsequently, disseminate from the GI tract to visceral organs. The ability of C. albicans to associate with intestinal mucosal surfaces was also tested. It was found that antibiotics which reduced anaerobic population levels, but not enteric bacilli or aerobes, also predisposed animals to mucosal association by C. albicans. It is suggested that the strictly anaerobic bacterial populations which predominate in the gut ecosystem are responsible for the inhibition of C. albicans adhesion, colonization and dissemination from the GI tract.
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FUNGÆMIA AND FUNGURIA AFTER ORAL ADMINISTRATION OF CANDIDA ALBICANS
W. Kŕause, H. Matheis, Karin Wulf · The Lancet · 1969 · 353 citations
H. Harlan Stone, LAURA D. KOLB, CAMILLA A. CURRIE et al. · Annals of Surgery · 1974 · 227 citations · Full text