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Review
. 2004 Jan;10(1):14-9.
doi: 10.3201/eid1001.030119.

Fungal biofilms and drug resistance

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Review

Fungal biofilms and drug resistance

Mary Ann Jabra-Rizk et al. Emerg Infect Dis. 2004 Jan.

Abstract

Candida species, including the novel opportunistic pathogen Candida dubliniensis, are now emerging as major agents of nosocomial infections. Many such manifestations of infections associated with the formation of Candida biofilms include those occurring on devices such as indwelling intravascular catheters. Fungal biofilm-associated infections are frequently refractory to conventional therapy because of resistance to antimicrobial agents. This resistance could be in part due to the surface-induced upregulation of drug efflux pumps. Biofilm-associated Candida show uniform resistance to a wide spectrum of the currently available conventional antifungal agents, which implies that antimicrobial drugs that specifically target biofilm-associated infections are needed. The novel classes of antifungal agents, the lipid formulation of amphotericins, and the echinocandins have demonstrated unique antifungal activity against the resistant Candida biofilms, providing a breakthrough in the treatment of life-threatening invasive systemic mycoses. The use of drugs effective in combating biofilm-associated infections could lead to major developments in the treatment of fungal implant infections.

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Figures

Figure 1
Figure 1
Illustration of biofilm development in Candida albicans and C. dubliniensis; A, early 0–11 h; B, intermediate 12–30 h; C, mature 38–72 h; FS, flat surface; YC, yeast cell; H, hyphae; EP, exopolymeric matrix.
Figure 2
Figure 2
Typical field found in scanning electron micrograph of biofilm formed by Candida albicans on intravascular disc prepared from catheter material

References

    1. Calderone RA, ed. Candida and candidiasis. Washington: ASM Press; 2002.
    1. Douglas LJ. Medical importance of biofilms in Candida infections. Rev Iberoam Micol. 2002;19:139–43. - PubMed
    1. Douglas LJ. Candida biofilms and their role in infection. Trends Microbiol. 2003;11:30–6. 10.1016/S0966-842X(02)00002-1 - DOI - PubMed
    1. Baillie GS, Doublas LJ. Matrix polymers of Candida biofilms and their possible role in biofilm resistance to antifungal agents. J Antimicrob Chemother. 2000;46:397–403. 10.1093/jac/46.3.397 - DOI - PubMed
    1. Chandra J, Kuhn DM, Mulherjee PK, Hoyer LL, McCormick T, Ghannoum MA. Biofilm formation by the fungal pathogen Candida albicans: development, architecture, and drug resistance. J Bacteriol. 2001;183:5385–94. 10.1128/JB.183.18.5385-5394.2001 - DOI - PMC - PubMed

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