Galleria mellonella as a model system to study Cryptococcus neoformans pathogenesis

被引:354
作者
Mylonakis, E
Moreno, R
El Khoury, JB
Idnurm, A
Heitman, J
Calderwood, SB
Ausubel, FM
Diener, A
机构
[1] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Biol Mol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Ctr Immunol & Inflammatory Dis, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02114 USA
[5] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[6] Duke Univ, Med Ctr, Div Infect Dis, Durham, NC 27710 USA
[7] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[8] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
[9] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
[10] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
D O I
10.1128/IAI.73.7.3842-3850.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Evaluation of Cryptococcus neoformans virulence in a number of nomnammalian hosts suggests that C neoformans is a nonspecific pathogen. We used the killing of Galleria mellonella (the greater wax moth) caterpillar by C neoformans to develop an invertebrate host model system that can be used to study cryptococcal virulence, host immune responses to infection, and the effects of antifungal compounds. All varieties of C neoformans killed G. mellonella. After injection into the insect hemocoel, C neoformans proliferated and, despite successful phagocytosis by host hemocytes, killed caterpillars both at 37 degrees C and 30 degrees C. The rate and extent of killing depended on the cryptococcal strain and the number of fungal cells injected. The sequenced C. neoformans clinical strain H99 was the most virulent of the strains tested and killed caterpillars with inocula as low as 20 CFU/caterpillar. Several C. neoformans genes previously shown to be involved in mammalian virulence (CAP59, GPA1, X4S1, and PKA1) also played a role in G. mellonella killing. Combination antifungal therapy (amphotericin B plus flucytosine) administered before or after inoculation was more effective than monotherapy in prolonging survival and in decreasing the tissue burden of cryptococci in the hemocoel. The G. mellonella-C. neoformans pathogenicity model may be a substitute for mammalian models of infection with C. neoformans and may facilitate the in vivo study of fungal virulence and efficacy of antifungal therapies.
引用
收藏
页码:3842 / 3850
页数:9
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