Specific host genes required for the killing of Klebsiella bacteria by phagocytes

被引:107
作者
Benghezal, M
Fauvarque, MO
Tournebize, R
Froquet, R
Marchetti, A
Bergeret, E
Lardy, B
Klein, G
Sansonetti, P
Charette, SJ
Cosson, P
机构
[1] Univ Geneva, Ctr Med Univ, Dept Physiol Cellulaire & Metab, CH-1211 Geneva, Switzerland
[2] Athelas SA, CH-1228 Geneva, Switzerland
[3] UJF, CNRS, CEA, UMR5092,Lab Biochim & Biophys Syst Integres, F-38054 Grenoble, France
[4] Inst Pasteur, F-75724 Paris, France
[5] Ctr Hosp Univ Grenoble, Enzymol Lab, GREPI, EA2938, Grenoble, France
关键词
D O I
10.1111/j.1462-5822.2005.00607.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The amoeba Dictyostelium discoideum shares many traits with mammalian macrophages, in particular the ability to phagocytose and kill bacteria. In response, pathogenic bacteria use conserved mechanisms to fight amoebae and mammalian phagocytes. Here we developed an assay using Dictyostelium to monitor phagocyte-bacteria interactions. Genetic analysis revealed that the virulence of Klebsiella pneumoniae measured by this test is very similar to that observed in a mouse pneumonia model. Using this assay, two new host resistance genes (PHG1 and KIL1) were identified and shown to be involved in intracellular killing of K. pneumoniae by phagocytes. Phg1 is a member of the 9TM family of proteins, and Kil1 is a sulphotransferase. The loss of PHG1 resulted in Dictyostelium susceptibility to a small subset of bacterial species including K. pneumoniae. Remarkably, Drosophila mutants deficient for PHG1 also exhibited a specific susceptibility to K. pneumoniae infections. Systematic analysis of several additional Dictyostelium mutants created a two-dimensional virulence array, where the complex interactions between host and bacteria are visualized.
引用
收藏
页码:139 / 148
页数:10
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共 47 条
[21]  
HASHIMOTO Y, 1992, J BIOL CHEM, V267, P15744
[22]   The immune response of Drosophila [J].
Hoffmann, JA .
NATURE, 2003, 426 (6962) :33-38
[23]   Heparin is essential for the storage of specific granule proteases in mast cells [J].
Humphries, DE ;
Wong, GW ;
Friend, DS ;
Gurish, MF ;
Qiu, WT ;
Huang, CF ;
Sharpe, AH ;
Stevens, RL .
NATURE, 1999, 400 (6746) :769-772
[24]   Sulfation and sulfotransferases .5. The importance of 3'-phosphoadenosine 5'-phosphosulfate (PAPS) in the regulation of sulfation [J].
Klaassen, CD ;
Boles, JW .
FASEB JOURNAL, 1997, 11 (06) :404-418
[25]   A microchip implant system as a method to determine body temperature of terminally ill rats and mice [J].
Kort, WJ ;
Hekking-Weijma, JM ;
TenKate, MT ;
Sorm, V ;
VanStrik, R .
LABORATORY ANIMALS, 1998, 32 (03) :260-269
[26]   NADPH oxidase homologs are required for normal cell differentiation and morphogenesis in Dictyostelium discoideum [J].
Lardy, B ;
Bof, M ;
Aubry, L ;
Paclet, MH ;
Morel, F ;
Satre, M ;
Klein, G .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2005, 1744 (02) :199-212
[27]   Constitutive and inducible green fluorescent protein expression in Bartonella henselae [J].
Lee, AK ;
Falkow, S .
INFECTION AND IMMUNITY, 1998, 66 (08) :3964-3967
[28]  
Lemansky P, 2001, J CELL SCI, V114, P345
[29]   Roles of DNA adenine methylation in regulating bacterial gene expression and virulence [J].
Low, DA ;
Weyand, NJ ;
Mahan, MJ .
INFECTION AND IMMUNITY, 2001, 69 (12) :7197-7204
[30]   Identification of Staphylococcus aureus virulence genes in a murine model of bacteraemia using signature-tagged mutagenesis [J].
Mei, JM ;
Nourbakhsh, F ;
Ford, CW ;
Holden, DW .
MOLECULAR MICROBIOLOGY, 1997, 26 (02) :399-407