共 269 条
Drosophila as a Model for Human Viral Neuroinfections
被引:4
作者:

Benoit, Ilena
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机构:
Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada
St Boniface Gen Hosp, Div Neurodegenerat Disorders, Albrechtsen Res Ctr, 351 Tache Ave, Winnipeg, MB R2H 2A6, Canada Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada

Di Curzio, Domenico
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St Boniface Gen Hosp, Div Neurodegenerat Disorders, Albrechtsen Res Ctr, 351 Tache Ave, Winnipeg, MB R2H 2A6, Canada Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada

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Douville, Renee N.
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Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada
St Boniface Gen Hosp, Div Neurodegenerat Disorders, Albrechtsen Res Ctr, 351 Tache Ave, Winnipeg, MB R2H 2A6, Canada Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada
机构:
[1] Univ Winnipeg, Dept Biol, 599 Portage Ave, Winnipeg, MB R3B 2G3, Canada
[2] St Boniface Gen Hosp, Div Neurodegenerat Disorders, Albrechtsen Res Ctr, 351 Tache Ave, Winnipeg, MB R2H 2A6, Canada
来源:
关键词:
Drosophila (fruit fly);
virus;
transposable elements (TEs);
neurological;
infection;
immunity;
human;
models;
transgenic;
homologue;
NF-KAPPA-B;
EPSTEIN-BARR-VIRUS;
VESICULAR STOMATITIS-VIRUS;
IMMUNE-DEFICIENCY IMD;
TATA-BINDING PROTEIN;
TOLL-LIKE RECEPTORS;
ANTIVIRAL IMMUNITY;
GENE-EXPRESSION;
X PROTEIN;
S2;
CELLS;
D O I:
10.3390/cells11172685
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The study of human neurological infection faces many technical and ethical challenges. While not as common as mammalian models, the use of Drosophila (fruit fly) in the investigation of virus-host dynamics is a powerful research tool. In this review, we focus on the benefits and caveats of using Drosophila as a model for neurological infections and neuroimmunity. Through the examination of in vitro, in vivo and transgenic systems, we highlight select examples to illustrate the use of flies for the study of exogenous and endogenous viruses associated with neurological disease. In each case, phenotypes in Drosophila are compared to those in human conditions. In addition, we discuss antiviral drug screening in flies and how investigating virus-host interactions may lead to novel antiviral drug targets. Together, we highlight standardized and reproducible readouts of fly behaviour, motor function and neurodegeneration that permit an accurate assessment of neurological outcomes for the study of viral infection in fly models. Adoption of Drosophila as a valuable model system for neurological infections has and will continue to guide the discovery of many novel virus-host interactions.
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