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      Towards non-invasive monitoring of pathogen–host interactions during Candida albicans biofilm formation using in vivo bioluminescence

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          Abstract

          Candida albicans is a major human fungal pathogen causing mucosal and deep tissue infections of which the majority is associated with biofilm formation on medical implants. Biofilms have a huge impact on public health, as fungal biofilms are highly resistant against most antimycotics. Animal models of biofilm formation are indispensable for improving our understanding of biofilm development inside the host, their antifungal resistance and their interaction with the host immune defence system. In currently used models, evaluation of biofilm development or the efficacy of antifungal treatment is limited to ex vivo analyses, requiring host sacrifice, which excludes longitudinal monitoring of dynamic processes during biofilm formation in the live host. In this study, we have demonstrated for the first time that non-invasive, dynamic imaging and quantification of in vitro and in vivo C. albicans biofilm formation including morphogenesis from the yeast to hyphae state is feasible by using growth-phase dependent bioluminescent C. albicans strains in a subcutaneous catheter model in rodents. We have shown the defect in biofilm formation of a bioluminescent bcr1 mutant strain. This approach has immediate applications for the screening and validation ofantimycotics under in vivo conditions, for studying host–biofilm interactions in different transgenic mouse models and for testing the virulence of luminescent C. albicans mutants, hereby contributing to a better understanding of the pathogenesis of biofilm-associated yeast infections.

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          Most cited references43

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          Mechanisms of biofilm resistance to antimicrobial agents.

          Biofilms are communities of microorganisms attached to a surface. It has become clear that biofilm-grown cells express properties distinct from planktonic cells, one of which is an increased resistance to antimicrobial agents. Recent work has indicated that slow growth and/or induction of an rpoS-mediated stress response could contribute to biocide resistance. The physical and/or chemical structure of exopolysaccharides or other aspects of biofilm architecture could also confer resistance by exclusion of biocides from the bacterial community. Finally, biofilm-grown bacteria might develop a biofilm-specific biocide-resistant phenotype. Owing to the heterogeneous nature of the biofilm, it is likely that there are multiple resistance mechanisms at work within a single community. Recent research has begun to shed light on how and why surface-attached microbial communities develop resistance to antimicrobial agents.
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            Epidemiology of invasive mycoses in North America.

            The incidence of invasive mycoses is increasing, especially among patients who are immunocompromised or hospitalized with serious underlying diseases. Such infections may be broken into two broad categories: opportunistic and endemic. The most important agents of the opportunistic mycoses are Candida spp., Cryptococcus neoformans, Pneumocystis jirovecii, and Aspergillus spp. (although the list of potential pathogens is ever expanding); while the most commonly encountered endemic mycoses are due to Histoplasma capsulatum, Coccidioides immitis/posadasii, and Blastomyces dermatitidis. This review discusses the epidemiologic profiles of these invasive mycoses in North America, as well as risk factors for infection, and the pathogens' antifungal susceptibility.
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              Environmental sensing and signal transduction pathways regulating morphopathogenic determinants of Candida albicans.

              Candida albicans is an opportunistic fungal pathogen that is found in the normal gastrointestinal flora of most healthy humans. However, under certain environmental conditions, it can become a life-threatening pathogen. The shift from commensal organism to pathogen is often correlated with the capacity to undergo morphogenesis. Indeed, under certain conditions, including growth at ambient temperature, the presence of serum or N-acetylglucosamine, neutral pH, and nutrient starvation, C. albicans can undergo reversible transitions from the yeast form to the mycelial form. This morphological plasticity reflects the interplay of various signal transduction pathways, either stimulating or repressing hyphal formation. In this review, we provide an overview of the different sensing and signaling pathways involved in the morphogenesis and pathogenesis of C. albicans. Where appropriate, we compare the analogous pathways/genes in Saccharomyces cerevisiae in an attempt to highlight the evolution of the different components of the two organisms. The downstream components of these pathways, some of which may be interesting antifungal targets, are also discussed.
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                Author and article information

                Journal
                Cell Microbiol
                Cell. Microbiol
                cmi
                Cellular Microbiology
                BlackWell Publishing Ltd (Oxford, UK )
                1462-5814
                1462-5822
                January 2014
                12 September 2013
                : 16
                : 1
                : 115-130
                Affiliations
                [1 ]Biomedical MRI/MoSAIC, Department Imaging & Pathology, KU Leuven Leuven, Flanders, Belgium
                [2 ]VIB Department of Molecular Microbiology, KU Leuven Leuven, Flanders, Belgium
                [3 ]Laboratory of Molecular Cell Biology, KU Leuven Leuven, Flanders, Belgium
                Author notes
                For correspondence. *E-mail patrick.vandijck@ 123456mmbio.vib-kuleuven.be ; Tel. (+32) 16 321512; Fax (+32) 16 321979.
                **E-mail uwe.himmelreich@ 123456med.kuleuven.be ; Tel. (+32) 16 330925; Fax (+32) 16 330901.
                [†]

                Shared first authors.

                [‡]

                Shared last authors.

                Article
                10.1111/cmi.12184
                4204156
                23962311
                e10209f1-ca51-4b4d-abe7-394017905db9
                © 2013 The Authors. Cellular Microbiology published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 17 July 2013
                : 12 August 2013
                : 21 August 2013
                Categories
                Original Articles

                Microbiology & Virology
                Microbiology & Virology

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