TY - JOUR
T1 - How to build a biofilm
T2 - a fungal perspective
AU - Blankenship, Jill R.
AU - Mitchell, Aaron P.
N1 - Funding Information:
We thank all members of the Mitchell laboratory for numerous discussions, particularly Clarissa Nobile for comments on the manuscript. Support from National Institutes of Health/National Institute of Allergy and Infectious Disease (grant R01 AI067703) is gratefully acknowledged. JRB acknowledges support from NIH grant F32 AI 71439.
PY - 2006/12
Y1 - 2006/12
N2 - Biofilms are differentiated masses of microbes that form on surfaces and are surrounded by an extracellular matrix. Fungal biofilms, especially those of the pathogen Candida albicans, are a cause of infections associated with medical devices. Such infections are particularly serious because biofilm cells are relatively resistant to many common antifungal agents. Several in vitro models have been used to elucidate the developmental stages and processes required for C. albicans biofilm formation, and recent studies have begun to define biofilm genetic control. It is clear that cell-substrate and cell-cell interactions, hyphal differentiation and extracellular matrix production are key steps in biofilm development. Drug resistance is acquired early in biofilm formation, and appears to be governed by different mechanisms in early and late biofilms. Quorum sensing might be an important factor in dispersal of biofilm cells. The past two years have seen the emergence of several genomic strategies to uncover global events in biofilm formation and directed studies to understand more specific events, such as hyphal formation, in the biofilm setting.
AB - Biofilms are differentiated masses of microbes that form on surfaces and are surrounded by an extracellular matrix. Fungal biofilms, especially those of the pathogen Candida albicans, are a cause of infections associated with medical devices. Such infections are particularly serious because biofilm cells are relatively resistant to many common antifungal agents. Several in vitro models have been used to elucidate the developmental stages and processes required for C. albicans biofilm formation, and recent studies have begun to define biofilm genetic control. It is clear that cell-substrate and cell-cell interactions, hyphal differentiation and extracellular matrix production are key steps in biofilm development. Drug resistance is acquired early in biofilm formation, and appears to be governed by different mechanisms in early and late biofilms. Quorum sensing might be an important factor in dispersal of biofilm cells. The past two years have seen the emergence of several genomic strategies to uncover global events in biofilm formation and directed studies to understand more specific events, such as hyphal formation, in the biofilm setting.
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U2 - 10.1016/j.mib.2006.10.003
DO - 10.1016/j.mib.2006.10.003
M3 - Review article
C2 - 17055772
AN - SCOPUS:33751235557
SN - 1369-5274
VL - 9
SP - 588
EP - 594
JO - Current Opinion in Microbiology
JF - Current Opinion in Microbiology
IS - 6
ER -