Tion might occur under nitrogen starvation conditions, but the content and abundance of nitrogenous compounds encountered during biotrophy is understudied [4]. The goal of this work was to understand what genetic approaches could be developed to determine the available or accessible nutrient content of host plants during infection. We reasoned that biochemical mutants, requiring nutrient supplementation for growth on plates, would only establish infection in plants if they received the samenutrient(s) from 1676428 the host. Conversely, biochemical mutants that could not access the required nutrients in the host would enter the plant but fail to establish disease. As proof-of-principle, we generated a methionine auxotrophic mutant strain of M. oryzae, Dstr3, which had a strict requirement for methionine or aspartate on GMM (homocysteine supported somewhat poorer growth of both Guy11 and Dstr3 strains on GMM). In addition, nitrogenous components of CM, including sources of partially digested peptides, also permitted growth. When applied to plants, Dstr3 strains were greatly reduced in lesion development, although livecell-imaging demonstrated they produced functional appressoria and could invade host cells. However, Dstr3 strains were unable to sustain invasive hyphal growth in rice cells and largely failed to progress to cells adjacent to the 
point of infection. This suggests both that Dstr3 strains are unable to obtain sources of methionine or aspartate during infection, and that the limited growth of Dstr3 strains in host plant cells represents the point at which endogenous methionine and aspartate sources might be finally exhausted following the successful formation of appressorium, plant penetration and IH elaboration. These observations are consistent with the appressorial transcriptional profiling studies of Soanes and co-Nutrient Conditions during Rice InfectionFigure 5. Disrupting MoSTR3 function abolishes infection but not appressorium formation. (A) Dstr3 strains cannot infect rice leaves. Conidial spores were applied to three-week old plants of the susceptible cultivar CO-39 at a rate of 56104 spores ml21. Images were taken after 144 hpi. (B) Although unable to infect rice leaves, Dstr3 strains could form appressoria on hydrophobic 842-07-9 web plastic cover slips, shown here after 24 hr. Scale bar is 10 mm. (C) The rate of appressorium formation for Dstr3 strains was compared to Guy11. Three plastic coverslips per strain were inoculated with 200 ml of a spore suspension containing 16105 spores ml21. After 24 hr, the number of appressoria formed by 50 conidia was counted on each cover slip, and a mean value generated. Error bars are standard deviation. Closed bars are values for Guy11 and grey bars are values for Dstr3 strains. Bars with the same letter are not significantly different (Student9s t-test p#0.05). doi:10.1371/journal.pone.0047392.gworkers [26] that suggested amino acid uptake is not a significant process during appressorium development and the initial TBHQ web stages of plant infection, and also supports recent work which showed proteasome-mediated turnover of endogenous proteins is required for appressorium development and pathogenicity in M. oryzae [27]. Taken together, this work demonstrates that de novo methionine biosynthesis is essential for infection because the Dstr3 suppressing metabolites shown in Figure 3 and 4 ?such as free sources of aspartate and methionine or mixtures of peptides 
?are not readily available to the fungus during.Tion might occur under nitrogen starvation conditions, but the content and abundance of nitrogenous compounds encountered during biotrophy is understudied [4]. The goal of this work was to understand what genetic approaches could be developed to determine the available or accessible nutrient content of host plants during infection. We reasoned that biochemical mutants, requiring nutrient supplementation for growth on plates, would only establish infection in plants if they received the samenutrient(s) from 1676428 the host. Conversely, biochemical mutants that could not access the required nutrients in the host would enter the plant but fail to establish disease. As proof-of-principle, we generated a methionine auxotrophic mutant strain of M. oryzae, Dstr3, which had a strict requirement for methionine or aspartate on GMM (homocysteine supported somewhat poorer growth of both Guy11 and Dstr3 strains on GMM). In addition, nitrogenous components of CM, including sources of partially digested peptides, also permitted growth. When applied to plants, Dstr3 strains were greatly reduced in lesion development, although livecell-imaging demonstrated they produced functional appressoria and could invade host cells. However, Dstr3 strains were unable to sustain invasive hyphal growth in rice cells and largely failed to progress to cells adjacent to the point of infection. This suggests both that Dstr3 strains are unable to obtain sources of methionine or aspartate during infection, and that the limited growth of Dstr3 strains in host plant cells represents the point at which endogenous methionine and aspartate sources might be finally exhausted following the successful formation of appressorium, plant penetration and IH elaboration. These observations are consistent with the appressorial transcriptional profiling studies of Soanes and co-Nutrient Conditions during Rice InfectionFigure 5. Disrupting MoSTR3 function abolishes infection but not appressorium formation. (A) Dstr3 strains cannot infect rice leaves. Conidial spores were applied to three-week old plants of the susceptible cultivar CO-39 at a rate of 56104 spores ml21. Images were taken after 144 hpi. (B) Although unable to infect rice leaves, Dstr3 strains could form appressoria on hydrophobic plastic cover slips, shown here after 24 hr. Scale bar is 10 mm. (C) The rate of appressorium formation for Dstr3 strains was compared to Guy11. Three plastic coverslips per strain were inoculated with 200 ml of a spore suspension containing 16105 spores ml21. After 24 hr, the number of appressoria formed by 50 conidia was counted on each cover slip, and a mean value generated. Error bars are standard deviation. Closed bars are values for Guy11 and grey bars are values for Dstr3 strains. Bars with the same letter are not significantly different (Student9s t-test p#0.05). doi:10.1371/journal.pone.0047392.gworkers [26] that suggested amino acid uptake is not a significant process during appressorium development and the initial stages of plant infection, and also supports recent work which showed proteasome-mediated turnover of endogenous proteins is required for appressorium development and pathogenicity in M. oryzae [27]. Taken together, this work demonstrates that de novo methionine biosynthesis is essential for infection because the Dstr3 suppressing metabolites shown in Figure 3 and 4 ?such as free sources of aspartate and methionine or mixtures of peptides ?are not readily available to the fungus during.