TY - JOUR
T1 - The art of serendipity
T2 - Killing of Caenorhabditis elegans by human pathogens as a model of bacterial and fungal pathogenesis
AU - Mylonakis, Eleftherios
AU - Ausubel, Frederick M.
AU - Tang, Robin Jian
AU - Calderwood, Stephen B.
N1 - Funding Information:
This work was supported by a grant from Aventis, SA to FMA. and SBC and by a postdoctoral fellowship from the Howard Hughes Medical Institute to EM.
PY - 2003/6
Y1 - 2003/6
N2 - The nematode worm, Caenorhabditis elegans, has been used to develop a facile model system of host-pathogen interactions to identify basic evolutionarily conserved pathways associated with microbial pathogenesis. The model involves the killing of Coenorhabditis elegans by a variety of human pathogens. Several virulence-related genes in a variety of pathogens previously shown to be involved in mammalian infection have also been shown to play a role in Caenorhabditis elegans killing. Screening of large numbers of microbial mutants for attenuation in a mammalian model would require thousands of mice, rats or rabbits. In contrast, the Caenorhabditis elegans model allows rapid identification of mutants in microbial genes associated with pathogenesis and then these phenotypes can be confirmed in a relevant mammalian model.
AB - The nematode worm, Caenorhabditis elegans, has been used to develop a facile model system of host-pathogen interactions to identify basic evolutionarily conserved pathways associated with microbial pathogenesis. The model involves the killing of Coenorhabditis elegans by a variety of human pathogens. Several virulence-related genes in a variety of pathogens previously shown to be involved in mammalian infection have also been shown to play a role in Caenorhabditis elegans killing. Screening of large numbers of microbial mutants for attenuation in a mammalian model would require thousands of mice, rats or rabbits. In contrast, the Caenorhabditis elegans model allows rapid identification of mutants in microbial genes associated with pathogenesis and then these phenotypes can be confirmed in a relevant mammalian model.
KW - AIDS
KW - Burkholderia pseudomallei
KW - Caenorhabditis elegans
KW - Cryptococcus neoformans
KW - Enterococus faecalis
KW - HIV
KW - MAP-kinase
KW - Pseudomonas aeruginosa
KW - Salmonella enterica
KW - Serratia marcescens
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U2 - 10.1586/14787210.1.1.167
DO - 10.1586/14787210.1.1.167
M3 - Review article
C2 - 15482109
AN - SCOPUS:2942596325
VL - 1
SP - 167
EP - 173
JO - Expert Review of Anti-Infective Therapy
JF - Expert Review of Anti-Infective Therapy
SN - 1478-7210
IS - 1
ER -