TY - JOUR
T1 - Fusarium pathogenesis investigated using Galleria mellonella as a heterologous host
AU - Coleman, Jeffrey J.
AU - Muhammed, Maged
AU - Kasperkovitz, Pia V.
AU - Vyas, Jatin M.
AU - Mylonakis, Eleftherios
N1 - Funding Information:
We would like to thank Evan Mojica in the MGH clinical mycology laboratory for kindly providing Fusarium isolates and Beth Burgwyn Fuchs for insightful discussions. This research was supported by a National Institutes of Health R01 award ( AI075286 ) and a R21 award ( AI079569 ) to EM and a T32 award ( AI07061 ) to JJC.
PY - 2011/12
Y1 - 2011/12
N2 - Members of the fungal genus Fusarium are capable of manifesting in a multitude of clinical infections, most commonly in immunocompromised patients. In order to better understand the interaction between the fungus and host, we have developed the larvae of the greater wax moth, Galleria mellonella, as a heterologous host for fusaria. When conidia are injected into the haemocoel of this Lepidopteran system, both clinical and environmental isolates of the fungus are able to kill the larvae at 37 °C, although killing occurs more rapidly when incubated at 30 °C. This killing was dependent on several other factors besides temperature, including the Fusarium strain, the number of conidia injected, and the conidia morphology, where macroconidia are more virulent than their microconidia counterpart. There was a correlation in the killing rate of Fusarium spp. when evaluated in G. mellonella and a murine model. In vivo studies indicated G. mellonella haemocytes were capable of initially phagocytosing both conidial morphologies. The G. mellonella system was also used to evaluate antifungal agents, and amphotericin B was able to confer a significant increase in survival to Fusarium-infected larvae. The G. mellonella-Fusarium pathogenicity system revealed that virulence of Fusarium spp. is similar, regardless of the origin of the isolate, and that mammalian endothermy is a major deterrent for Fusarium infection and therefore provides a suitable alternative to mammalian models to investigate the interaction between the host and this increasingly important fungal pathogen.
AB - Members of the fungal genus Fusarium are capable of manifesting in a multitude of clinical infections, most commonly in immunocompromised patients. In order to better understand the interaction between the fungus and host, we have developed the larvae of the greater wax moth, Galleria mellonella, as a heterologous host for fusaria. When conidia are injected into the haemocoel of this Lepidopteran system, both clinical and environmental isolates of the fungus are able to kill the larvae at 37 °C, although killing occurs more rapidly when incubated at 30 °C. This killing was dependent on several other factors besides temperature, including the Fusarium strain, the number of conidia injected, and the conidia morphology, where macroconidia are more virulent than their microconidia counterpart. There was a correlation in the killing rate of Fusarium spp. when evaluated in G. mellonella and a murine model. In vivo studies indicated G. mellonella haemocytes were capable of initially phagocytosing both conidial morphologies. The G. mellonella system was also used to evaluate antifungal agents, and amphotericin B was able to confer a significant increase in survival to Fusarium-infected larvae. The G. mellonella-Fusarium pathogenicity system revealed that virulence of Fusarium spp. is similar, regardless of the origin of the isolate, and that mammalian endothermy is a major deterrent for Fusarium infection and therefore provides a suitable alternative to mammalian models to investigate the interaction between the host and this increasingly important fungal pathogen.
KW - Antifungal agent
KW - Fusariosis
KW - Fusarium
KW - Galleria
KW - Heterologous host
KW - Thermotolerance
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U2 - 10.1016/j.funbio.2011.09.005
DO - 10.1016/j.funbio.2011.09.005
M3 - Article
C2 - 22115447
AN - SCOPUS:81955164780
SN - 1878-6146
VL - 115
SP - 1279
EP - 1289
JO - Fungal Biology
JF - Fungal Biology
IS - 12
ER -