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Ecology of Candida albicans gut colonization: inhibition of Candida adhesion, colonization, and dissemination from the gastrointestinal tract by bacterial antagonism
Open accessAbstract
Antibiotic-treated and untreated Syrian hamsters were inoculated intragastrically with Candida albicans to determine whether C. albicans could opportunistically colonize the gastrointestinal tract and disseminate to visceral organs. Antibiotic treatment decreased the total population levels of the indigenous bacterial flora and predisposed hamsters to gastrointestinal overgrowth and subsequent systemic dissemination by C. albicans in 86% of the animals. Both control hamsters not given antibiotics and antibiotic-treated animals reconventionalized with an indigenous microflora showed significantly lower gut populations of C. albicans, and C. albicans organisms were cultured from the visceral organs of 0 and 10% of the animals, respectively. Conversely, non-antibiotic-treated hamsters inoculated repeatedly with C. albicans had high numbers of C. albicans in the gut, and viable C. albicans was recovered from the visceral organs of 53% of the animals. Examination of the mucosal surfaces from test and control animals indicated further that animals which contained a complex indigenous microflora had significantly lower numbers of C. albicans associated with their gut walls than did antibiotic-treated animals. The ability of C. albicans to associate with intestinal mucosal surfaces also was tested by an in vitro adhesion assay. The results indicate that the indigenous microflora reduced the mucosal association of C. albicans by forming a dense layer of bacteria in the mucus gel, out-competing yeast cells for adhesion sites, and producing inhibitor substances (possibly volatile fatty acids, secondary bile acids, or both) that reduced C. albicans adhesion. It is suggested, therefore, that the indigenous intestinal microflora suppresses C. albicans colonization and dissemination from the gut by inhibiting Candida-mucosal association and reducing C. albicans population levels in the gut.
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“It is a member of the healthy microbiota, asymptomatically colonizing the gastrointestinal (GI) tract, reproductive tract, oral cavity, and skin of most humans (1, 64, 87, 97, 99).”
From Candida albicans Biofilms and Human Disease (2015) · cites this paper as [87]
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Warris, A. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780198755388.003.0035 · Cited by 1
Animal Models of Mucosal Candida Infections
Bernardis, F. D., Arancia, S., & Sandini, S. (2010) · Methods in microbiology · doi:10.1016/s0580-9517(10)37014-0
Adhension of Candida albicans to host cells in culutre.
Maiter, A. I. (1989) · ResearchSpace (University of KwaZulu-Natal)
Aislamiento de Candida en la infección de sitio quirúrgico en un servicio de cirugía general
Iñigo, J. J., Calvo, A., Miranda, C., Montón, S., Pérez, F., Echeverría, E., & Lera, J. M. (2002) · Cirugía Española · doi:10.1016/s0009-739x(02)72039-3
Identification and Characterization of Genetic Factors Involved in Candida-Bacterial Interactions
Fox, S. (2013) · Digital Commons - East Tennessee State University (East Tennessee State University)
Gazda - patogén kölcsönhatás vizsgálata Candida fertőzések során
Németh, T. (2014) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2021
Candida albicans: sex and survival in a rat model of colonisation
Rodrigues, E. (2013) · Otago University Research Archive (University of Otago)
Fungicide as Potential Vaccine: Current Research and Future Challenges
Verma, G., Kumar, B., Sharma, A. K., & Yadav, A. N. (2021) · Fungal biology · doi:10.1007/978-3-030-85603-8_22
Metadata
- Authors
- Kennedy, M. J., & Volz, P. A.
- Venue
- Infection and Immunity
- Publisher
- American Society for Microbiology
- Published
- 1985-09
- Volume
- 49
- Issue
- 3
- Pages
- 654-663
- ISSN
- 0019-9567 (ISSN-L)
- 1098-5522
- PMC
- PMC261235
- OpenAlex
- W1907372042
- Cited by
- 208
- References
- 65
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 4 · 2022: 8 · 2021: 6 · 2020: 12 · 2019: 5 · 2018: 3 · 2017: 7 · 2016: 4 · 2015: 6 · 2014: 6 · 2013: 9 · 2012: 2
- FWCI
- 7.45
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Infection and Immunity (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Keywords
- Candida albicans, intestinal colonization, bacterial antagonism, antibiotic-induced dysbiosis, systemic candidiasis, mucosal colonization, secondary bile acids, volatile fatty acids, Syrian hamster model, opportunistic fungal infection
- MeSH terms
- Adhesiveness, Animals, Antibiosis, Anti-Bacterial Agents, Candida albicans, Cecum, Digestive System, Ecology, Cricetinae, Intestinal Mucosa, Male, Mesocricetus, Microscopy, Electron, Scanning, Bacterial Physiological Phenomena
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