The Imd Pathway Is Involved in Antiviral Immune Responses in Drosophila

被引:191
作者
Costa, Alexandre
Jan, Eric
Sarnow, Peter
Schneider, David
机构
[1] Department of Microbiology and Immunology, Stanford University, Stanford, CA
[2] School of Public Health, University of California, Berkeley, CA
[3] Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, BC
来源
PLOS ONE | 2009年 / 4卷 / 10期
关键词
CRICKET PARALYSIS VIRUS; NF-KAPPA-B; HOST-DEFENSE; PGRP-LC; MELANOGASTER; ACTIVATION; INFECTION; PROTEIN; TOLL; BACTERIAL;
D O I
10.1371/journal.pone.0007436
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cricket Paralysis virus (CrPV) is a member of the Dicistroviridae family of RNA viruses, which infect a broad range of insect hosts, including the fruit fly Drosophila melanogaster. Drosophila has emerged as an effective system for studying innate immunity because of its powerful genetic techniques and the high degree of gene and pathway conservation. Intra-abdominal injection of CrPV into adult flies causes a lethal infection that provides a robust assay for the identification of mutants with altered sensitivity to viral infection. To gain insight into the interactions between viruses and the innate immune system, we injected wild type flies with CrPV and observed that antimicrobial peptides (AMPs) were not induced and hemocytes were depleted in the course of infection. To investigate the contribution of conserved immune signaling pathways to antiviral innate immune responses, CrPV was injected into isogenic mutants of the Immune Deficiency (Imd) pathway, which resembles the mammalian Tumor Necrosis Factor Receptor (TNFR) pathway. Loss-of-function mutations in several Imd pathway genes displayed increased sensitivity to CrPV infection and higher CrPV loads. Our data show that antiviral innate immune responses in flies infected with CrPV depend upon hemocytes and signaling through the Imd pathway.
引用
收藏
页数:9
相关论文
共 72 条
[1]   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
[2]   Genetic variation affecting host-parasite interactions:: Different genes affect different aspects of sigma virus replication and transmission in Drosophila melanogaster [J].
Bangham, Jenny ;
Kim, Kang-Wook ;
Webster, Claire L. ;
Jiggins, Francis M. .
GENETICS, 2008, 178 (04) :2191-2199
[3]   The phytopathogenic bacteria Erwinia carotovora infects Drosophila and activates an immune response [J].
Basset, A ;
Khush, RS ;
Braun, A ;
Gardan, L ;
Boccard, F ;
Hoffmann, JA ;
Lemaitre, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3376-3381
[4]   Death and survival: viral regulation of TNF signaling pathways [J].
Benedict, CA ;
Banks, TA ;
Ware, CF .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (01) :59-65
[5]  
Braun A, 1997, GENETICS, V147, P623
[6]   Analysis of the Drosophila host defense in domino mutant larvae, which are devoid of hemocytes [J].
Braun, A ;
Hoffmann, JA ;
Meister, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14337-14342
[7]   Psidin is required in Drosophila blood cells for both phagocytic degradation and immune activation of the fat body [J].
Brennan, Catherine A. ;
Delaney, Joseph R. ;
Schneider, David S. ;
Anderson, Kathryn V. .
CURRENT BIOLOGY, 2007, 17 (01) :67-72
[8]   Entry is a rate-limiting step for viral infection in a Drosophila melanogaster model of pathogenesis [J].
Cherry, S ;
Perrimon, N .
NATURE IMMUNOLOGY, 2004, 5 (01) :81-87
[9]   Host-pathogen interactions in drosophila: new tricks from an old friend [J].
Cherry, Sara ;
Silverman, Neal .
NATURE IMMUNOLOGY, 2006, 7 (09) :911-917
[10]   Drosophila peptidoglycan recognition protein LC (PGRP-LC) acts as a signal-transducing innate immune receptor [J].
Choe, KM ;
Lee, H ;
Anderson, KV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (04) :1122-1126