Resistance of Candida albicans Biofilms to Drugs and the Host Immune System

is a commensal fungus that resides on mucosal surfaces and in the gastrointestinal and genitourinary tracts in humans. However, it can cause an infection when the immune system of the host is impaired or if a niche becomes available. Many infections are due to the organism's ability to form a b...

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Bibliographic Details
Published in:Jundishapur journal of microbiology 2016-11, Vol.9 (11), p.e37385-e37385
Main Authors: Sandai, Doblin, Tabana, Yasser M, Ouweini, Ahmad El, Ayodeji, Ishola Oluwaseun
Format: Article
Language:English
Subjects:
Review
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Summary:is a commensal fungus that resides on mucosal surfaces and in the gastrointestinal and genitourinary tracts in humans. However, it can cause an infection when the immune system of the host is impaired or if a niche becomes available. Many infections are due to the organism's ability to form a biofilm on implanted medical devices. A biofilm represents an optimal medium for the growth of as it allows cells to be enclosed by a self-produced extracellular matrix (ECM). The present work investigated certain aspects of the resistance of biofilms to drugs and the host immune system. An ECM was found to provide the infrastructure for biofilm formation, prevent disaggregation, and shield encapsulated cells from antifungal drugs and the host's immune system. By influencing and upregulating multiple glucan modification genes, β-1, 3-glucan, an important component of ECM, was shown to be responsible for many of the biofilm's drug-resistant properties. On being engulfed by ECM, the fungal cell was found to switch from glycolysis to gluconeogenesis. Resembling the cellular response to starvation, this was followed by the activation of the glyoxylate cycle that allowed the use of simple molecules as energy sources. Mature biofilms were found to be much more resistant to antifungal agents and the host immune system than free cells. The factors responsible for high resistance included the complex architecture of biofilms, ECM, increased expression of drug efflux pumps, and metabolic plasticity.
ISSN:2008-3645
2008-4161
DOI:10.5812/jjm.37385