Inducible antibacterial defense system in C-elegans

被引:355
作者
Mallo, GV
Kurz, CL
Couillault, C
Pujol, N
Granjeaud, S
Kohara, Y
Ewbank, JJ
机构
[1] Univ Mediterranee, CNRS, INSERM, Ctr Immunol Marseille Luminy, F-13288 Marseille 9, France
[2] Univ Mediterranee, CNRS, INSERM, Lab Genet & Physiol Dev, F-13288 Marseille, France
[3] Natl Inst Genet, Mishima, Shizuoka 411, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1016/S0960-9822(02)00928-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The term innate immunity refers to a number of evolutionary ancient mechanisms that serve to defend animals and plants against infection. Genetically tractable model organisms, especially Drosophila, have contributed greatly to advances in our understanding of mammalian innate immunity [1, 2]. Essentially, nothing is known about immune responses in the nematode Caenorhabditis elegans [3,4]. Using high-density cDNA microarrays, we show here that infection of C. elegans by the Gram-negative bacterium Serratia marcescens provokes a marked upregulation of the expression of many genes. Among the most robustly induced are genes encoding lectins and lysozymes, known to be involved in immune responses in other organisms. Certain infection-inducible genes are under the control of the DBL-1/TGFbeta pathway [5]. We found that dbl-1 mutants exhibit increased susceptibility to infection. Conversely, overexpression of the lysozyme gene lys-1 augments the resistance of C. elegrans to S. marcescens. These results constitute the first demonstration of inducible antibacterial defenses in C. elegans and open new avenues for the investigation of evolutionary conserved mechanisms of innate immunity.
引用
收藏
页码:1209 / 1214
页数:6
相关论文
共 28 条
[1]   Caenorhabditis elegans as a host for the study of host-pathogen interactions [J].
Aballay, A ;
Ausubel, FM .
CURRENT OPINION IN MICROBIOLOGY, 2002, 5 (01) :97-101
[2]   Sugar binding properties of the two lectin domains of the tandem repeat-type galectin LEC-1 (N32) of Caenorhabditis elegans -: Detailed analysis by an improved frontal affinity chromatography method [J].
Arata, Y ;
Hirabayashi, J ;
Kasai, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (05) :3068-3077
[3]   Caenorhabditis elegans has scores of hedgehog-related genes:: Sequence and expression analysis [J].
Aspöck, G ;
Kagoshima, H ;
Niklaus, G ;
Bürglin, TR .
GENOME RESEARCH, 1999, 9 (10) :909-923
[4]   Amoebapore homologs of Caenorhabditis elegans [J].
Bányai, L ;
Patthy, L .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1998, 1429 (01) :259-264
[5]   INDUCIBLE ANTIBACTERIAL DEFENCE SYSTEM IN DROSOPHILA [J].
BOMAN, HG ;
NILSSON, I ;
RASMUSON, B .
NATURE, 1972, 237 (5352) :232-+
[6]  
BORGONIE G, 1995, FUND APPL NEMATOL, V18, P123
[7]   Plant pathogens and integrated defence responses to infection [J].
Dangl, JL ;
Jones, JDG .
NATURE, 2001, 411 (6839) :826-833
[8]   Genome-wide analysis of the Drosophila immune response by using oligonucleotide microarrays [J].
De Gregorio, E ;
Spellman, PT ;
Rubin, GM ;
Lemaitre, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) :12590-12595
[9]   C-type lectin-like domains in Caenorhabditis elegans:: predictions from the complete genome sequence [J].
Drickamer, K ;
Dodd, RB .
GLYCOBIOLOGY, 1999, 9 (12) :1357-1369
[10]   Tackling both sides of the host-pathogen equation with Caenorhabditis elegans [J].
Ewbank, JJ .
MICROBES AND INFECTION, 2002, 4 (02) :247-256