Entry of oomycete and fungal effectors into plant and animal host cells

被引:83
作者
Kale, Shiv D. [1 ]
Tyler, Brett M. [1 ]
机构
[1] Virginia Tech, Virginia Bioinformat Inst, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
PYRENOPHORA-TRITICI-REPENTIS; RICE BLAST RESISTANCE; PHYTOPHTHORA-SOJAE; FLAX RUST; PTR TOXA; MAGNAPORTHE-ORYZAE; GENE ONTOLOGY; PATHOGEN PHYTOPHTHORA; AVIRULENCE PROTEINS; DISEASE RESISTANCE;
D O I
10.1111/j.1462-5822.2011.01659.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fungal and oomycete pathogens cause many destructive diseases of plants and important diseases of humans and other animals. Fungal and oomycete plant pathogens secrete numerous effector proteins that can enter inside host cells to condition susceptibility. Until recently it has been unknown if these effectors enter via pathogen-encoded translocons or via pathogen-independent mechanisms. Here we review recent evidence that many fungal and oomycete effectors enter via receptor-mediated endocytosis, and can do so in the absence of the pathogen. Surprisingly, a large number of these effectors utilize cell surface phosphatidyinositol-3-phosphate (PI-3-P) as a receptor, a molecule previously known only inside cells. Binding of effectors to PI-3-P appears to be mediated by the cell entry motif RXLR in oomycetes, and by diverse RXLR-like variants in fungi. PI-3-P appears to be present on the surface of animal cells also, suggesting that it may mediate entry of effectors of fungal and oomycete animal pathogens, for example, RXLR effectors found in the oomycete fish pathogen, Saprolegnia parasitica. Reagents that can block PI-3-P-mediated entry have been identified, suggesting new therapeutic strategies.
引用
收藏
页码:1839 / 1848
页数:10
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