We isolated an MgATG1 gene encoding a serine/threonine protein kinase from the rice blast fungus Magnaporthe grisea. In the ⌬Mgatg1 mutant, in which the MgATG1 gene had been deleted, autophagy was blocked; the mutant also showed fewer lipid droplets in its conidia, lower turgor pressure of the appressorium, and such defects in morphogenesis as delayed initiation and slower germination of conidia. As a result of lower turgor pressure of the appressorium, the ⌬Mgatg1 mutant lost its ability to penetrate and infect the two host plants, namely, rice and barley. However, normal values of the parameters and infective abilities were restored on reintroducing an intact copy of the MgATG1 gene into the mutant. Autophagy is thus necessary for turnover of organic matter during the formation of conidia and appressoria and for normal development and pathogenicity in M. grisea.Magnaporthe grisea, a filamentous ascomycete fungus, is best known as the causal agent of rice blast, the most serious disease of cultivated rice throughout the world (15), and has been developed as a model organism for investigating fungus-host interactions (4, 27). The appressorium, a specialized cell necessary for infection by the rice blast fungus, generates tremendous intracellular turgor pressure (as much as 8.0 MPa) to penetrate the leaf cuticle (5, 26). Such enormous turgor in the appressorium is a consequence of accumulation of very large quantities of glycerol in the cell, and potential sources of glycerol biosynthesis are lipid, glycogen, and two sugars, trehalose and mannitol, in the conidium (21).The process of development from the conidium to the appressorium, and then from the appressorium to the penetration peg or infectious hypha, requires a cell to undergo significant phenotypic changes accompanied by the breakdown and recycling of old cellular components in about 30 h (21). In M. grisea, appressorium formation involves autophagy, but nuclei in conidia of the ⌬Mgatg8 mutant were not degraded during appressorium formation, and the mutant failed to infect the plant through the appressoria (29). Also, the mutant produced far fewer conidia. Autophagy is a common and evolutionarily preserved process that degrades and recycles old proteins and organelles in all eukaryotic cells (8,9,18,31). For many years, autophagy was believed to be involved in changes in cellular architecture during differentiation and development, presumably through its role in the turnover of organelles and proteins (9). Our study sought to find out whether autophagy has a role in the turnover of organic matter that enables a hypha to form a conidium, which then goes on to develop an appressorium, and in generating the turgor pressure in the appressorium required for successful infection.An expressed sequence tag (clone s197; GenBank accession no. CK828251) for MgATG1 (autophagy-related gene 1), homologous to ATG1 of yeast in its protein sequence, was found in the appressorium of the rice blast fungus (10). Because the fungus is used as a primary model for host-pathogen...