Models of infectious diseases in the fruit fly Drosophila melanogaster

被引:89
作者
Dionne, Marc S. [2 ,3 ]
Schneider, David S. [1 ]
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Kings Coll London, Dept Craniofacial Dev, London SE1 9RT, England
[3] Kings Coll London, Dept Microbiol, London SE1 9RT, England
关键词
D O I
10.1242/dmm.000307
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
We examined the immune response of a fly as physicians might, by looking at the genesis of diseases caused by microorganisms. Fly infections are complex and there are few simple rules that can predict how an infected fly might fare. As we observed the finer details of the infections, we found that almost every microbe caused a different type of pathology in the fly. Two pattern recognition pathways, Toll and immune deficiency (lmd), were found to detect, and respond to, infections. The physiological response of the fly was modified further by Eiger, insulin, Wnt inhibitor of dorsal (WntD) and nitric oxide (NO) signaling. As in humans, some of the damage that occurred during the fly immune response was caused by an over-aggressive response rather than by the microbes themselves. When looking at the matrix of signaling pathways and the microbes being tested, it was immediately obvious that most of the pathways would need to be studied in more detail before defining the rules that govern their role in pathogenesis. This detailed analysis of signaling and pathogenesis has the potential to allow the fly to be used as a model patient instead of as simply an innate immune system model.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 49 条
[1]
Signaling role of hemocytes in Drosophila JAK/STAT-dependent response to septic injury [J].
Agaisse, H ;
Petersen, UM ;
Boutros, M ;
Mathey-Prevot, B ;
Perrimon, N .
DEVELOPMENTAL CELL, 2003, 5 (03) :441-450
[2]
ESTABLISHMENT OF DORSAL-VENTRAL POLARITY IN THE DROSOPHILA EMBRYO - THE INDUCTION OF POLARITY BY THE TOLL GENE-PRODUCT [J].
ANDERSON, KV ;
BOKLA, L ;
NUSSLEINVOLHARD, C .
CELL, 1985, 42 (03) :791-798
[3]
Identification of drosophila mutants altering defense of and endurance to Listeria monocytogenes infection [J].
Ayres, Janelle S. ;
Freitag, Nancy ;
Schneider, David S. .
GENETICS, 2008, 178 (03) :1807-1815
[4]
Crystal cell rupture after injury in Drosophila requires the JNK pathway, small GTPases and the TNF homolog Eiger [J].
Bidla, Gawa ;
Dushay, Mitchell S. ;
Theopold, Ulrich .
JOURNAL OF CELL SCIENCE, 2007, 120 (07) :1209-1215
[5]
INDUCIBLE ANTIBACTERIAL DEFENCE SYSTEM IN DROSOPHILA [J].
BOMAN, HG ;
NILSSON, I ;
RASMUSON, B .
NATURE, 1972, 237 (5352) :232-+
[6]
Secreted bacterial effectors and host-produced eiger/TNF drive death in a Salmonella-infected fruit fly [J].
Brandt, SM ;
Dionne, MS ;
Khush, RS ;
Pham, LN ;
Vigdal, TJ ;
Schneider, DS .
PLOS BIOLOGY, 2004, 2 (12) :2067-2075
[7]
Drosophila:: The genetics of innate immune recognition and response [J].
Brennan, CA ;
Anderson, KV .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :457-483
[8]
Alternative measures of response to Pseudomonas aeruginosa infection in Drosophila melanogaster [J].
Corby-Harris, V. ;
Habel, K. E. ;
Ali, F. G. ;
Promislow, D. E. L. .
JOURNAL OF EVOLUTIONARY BIOLOGY, 2007, 20 (02) :526-533
[9]
The Toll and Imd pathways are the major regulators of the immune response in Drosophila [J].
De Gregorio, E ;
Spellman, PT ;
Tzou, P ;
Rubin, GM ;
Lemaitre, B .
EMBO JOURNAL, 2002, 21 (11) :2568-2579
[10]
Drosophila calcineurin promotes induction of innate immune responses [J].
Dijkers, Pascale F. ;
O'Farrell, Patrick H. .
CURRENT BIOLOGY, 2007, 17 (23) :2087-2093