Drosophila eiger mutants are sensitive to extracellular pathogens

被引:87
作者
Schneider, David S. [1 ]
Ayres, Janelle S. [1 ]
Brandt, Stephanie M. [1 ]
Costa, Alexandre [1 ]
Dionne, Marc S. [1 ]
Gordon, Michael D. [1 ]
Mabery, Eric M. [1 ]
Moule, Madeleine G. [1 ]
Pham, Linh N. [1 ]
Shirasu-Hiza, Mimi M. [1 ]
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
D O I
10.1371/journal.ppat.0030041
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We showed previously that eiger, the Drosophila tumor necrosis factor homolog, contributes to the pathology induced by infection with Salmonella typhimurium. We were curious whether eiger is always detrimental in the context of infection or if it plays a role in fighting some types of microbes. We challenged wild-type and eiger mutant flies with a collection of facultative intracellular and extracellular pathogens, including a fungus and Gram-positive and Gramnegative bacteria. The response of eiger mutants divided these microbes into two groups: eiger mutants are immunocompromised with respect to extracellular pathogens but show no change or reduced sensitivity to facultative intracellular pathogens. Hence, eiger helps fight infections but also can cause pathology. We propose that eiger activates the cellular immune response of the fly to aid clearance of extracellular pathogens. Intracellular pathogens, which can already defeat professional phagocytes, are unaffected by eiger.
引用
收藏
页数:7
相关论文
共 25 条
[1]   Hemolymph coagulation and phenoloxidase in Drosophila larvae [J].
Bidla, G ;
Lindgren, M ;
Theopold, U ;
Dushay, MS .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2005, 29 (08) :669-679
[2]   Downregulation of the Drosophila immune response by peptidoglycan-recognition proteins SC1 and SC2 [J].
Bischoff, Vincent ;
Vignal, Cecile ;
Duvic, Bernard ;
Boneca, Ivo G. ;
Hoffmann, Jules A. ;
Royet, Julien .
PLOS PATHOGENS, 2006, 2 (02) :139-147
[3]   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
[4]   Drosophila:: The genetics of innate immune recognition and response [J].
Brennan, CA ;
Anderson, KV .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :457-483
[5]   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
[6]   Akt and foxo dysregulation contribute to infection-induced wasting in Drosophila [J].
Dionne, Marc S. ;
Pham, Linh N. ;
Shirasu-Hiza, Mimi ;
Schneider, David S. .
CURRENT BIOLOGY, 2006, 16 (20) :1977-1985
[7]   Drosophila melanogaster is a genetically tractable model host for Mycobacterium marinum [J].
Dionne, MS ;
Ghori, N ;
Schneider, DS .
INFECTION AND IMMUNITY, 2003, 71 (06) :3540-3550
[8]   Interactions between the cellular and humoral immune responses in Drosophila [J].
Elrod-Erickson, M ;
Mishra, S ;
Schneider, D .
CURRENT BIOLOGY, 2000, 10 (13) :781-784
[9]   Functional dissection of an innate immune response by a genome-wide RNAi screen [J].
Foley, E ;
O'Farrell, PH .
PLOS BIOLOGY, 2004, 2 (08) :1091-1106
[10]   WntD is a feedback inhibitor of Dorsal/NF-κB in Drosophila development and immunity [J].
Gordon, MD ;
Dionne, MS ;
Schneider, DS ;
Nusse, R .
NATURE, 2005, 437 (7059) :746-749