TY - JOUR
T1 - A C. elegans-based, whole animal, in vivo screen for the identification of antifungal compounds.
AU - Tampakakis, Emmanouil
AU - Okoli, Ikechukwu
AU - Mylonakis, Eleftherios
N1 - Funding Information:
ACKNOWLEDGMENTS Support was provided by NIH R01 award AI075286 (E.M.). We are grateful to Melanie de Silva of Broad Institute of Massachusetts Institute of Technology, USA, for technical assistance.
Copyright:
This record is sourced from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
PY - 2008
Y1 - 2008
N2 - Traditional antimicrobial screens focus on compounds that block the growth of microbial organisms. A new Caenorhabditis elegans-based bioassay can be used for the identification of antifungal compounds that are effective against Candida albicans. According to the protocol, adult nematodes are infected with C. albicans and moved to 96-well plates containing the tested compounds. In the presence of compounds with no antifungal activity, the fungus kills the worms and develops filaments that penetrate through the cuticle. In contrast to traditional screening methods and mammalian models, this facile, time-efficient and less costly assay allows the study of Candida cells in nonplanktonic form and may allow the concurrent evaluation of toxicity and antifungal activity and identify compounds that target virulence factors or modify host immune response. The screening assay takes about 5-6 d depending on the experimental design.
AB - Traditional antimicrobial screens focus on compounds that block the growth of microbial organisms. A new Caenorhabditis elegans-based bioassay can be used for the identification of antifungal compounds that are effective against Candida albicans. According to the protocol, adult nematodes are infected with C. albicans and moved to 96-well plates containing the tested compounds. In the presence of compounds with no antifungal activity, the fungus kills the worms and develops filaments that penetrate through the cuticle. In contrast to traditional screening methods and mammalian models, this facile, time-efficient and less costly assay allows the study of Candida cells in nonplanktonic form and may allow the concurrent evaluation of toxicity and antifungal activity and identify compounds that target virulence factors or modify host immune response. The screening assay takes about 5-6 d depending on the experimental design.
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U2 - 10.1038/nprot.2008.193
DO - 10.1038/nprot.2008.193
M3 - Article
C2 - 19180076
AN - SCOPUS:63349109504
SN - 1754-2189
VL - 3
SP - 1925
EP - 1931
JO - Nature protocols
JF - Nature protocols
IS - 12
ER -