Poster
Rei Kida
Graduate school of Science and Technology, Tokyo University of Science, Japan
Noda, Chiba, Japan
Kohtetsu Kita
Graduate school of Science and Technology, Tokyo University of Science, Japan
Noda, Chiba, Japan
Momotaka Uchida
Medical Mycology Research Center, Chiba University, Japan
Chiba, Chiba, Japan
Lassagne Alexandre
CIRAD, UMR PHIM, F-34398 Montpellier, France; PHIM Plant Health Institute, Univ Montpellier, INRAE, CIRAD, Institut Agro, IRD, Montpellier, France
Montpellier, Languedoc-Roussillon, France
Didier Tharreau
CIRAD, UMR PHIM, F-34398 Montpellier, France; PHIM Plant Health Institute, Univ Montpellier, INRAE, CIRAD, Institut Agro, IRD, Montpellier, France
Montpellier, Languedoc-Roussillon, France
Elisabeth Fournier
PHIM Plant Health Institute, Univ Montpellier, INRAE, CIRAD, Institut Agro, IRD, Montpellier, France
Montpellier, Languedoc-Roussillon, France
Tsutomu Arie
Professor
United Graduate School of Agricultural Science, Tokyo University of Agriculture and Technology, Japan
fuchu, Tokyo, Japan
Takashi Kamakura
Graduate school of Science and Technology, Tokyo University of Science, Japan
Noda, Chiba, Japan
Takayuki Arazoe
Graduate school of Science and Technology, Tokyo University of Science, Japan
Noda, Chiba, Japan
The rice blast fungus Pyricularia oryzae (Magnaporthe oryzae) is a heterothallic ascomycete that causes destructive disease in cultivated rice. The infection cycle of this fungus consists of asexual reproduction, and most field isolates lost female fertility. Several isolates collected in one population from the area of the origin of this pathogen (South East Asia) retained female fertility, suggesting that female fertility has been lost during spread of the pathogen in various ecosystems all around the world. We previously showed that functional mutations in Pro1, a global transcriptional regulator, cause the loss of female fertility in nature. In this study, we found that partial morphological changes, velvet-like mycelia, of female-fertile isolates occurred during long-term culture (2–4 weeks) on agar media. We also showed that isolated lines from the modified mycelia lost female fertility due to mutations in the velvet family gene VeA. To investigate whether Pro1 is involved in mycelial morphology, female-sterile isolates with dysfunctional Pro1 were complemented by functional Pro1. The transformants showed mycelial morphology similar to that of female-fertile isolates, and modified mycelia appeared during long-term culture. In addition, Pro1-deletion mutants of female-fertile isolates showed velvet-like mycelia. These results suggest that Pro1 regulates both female fertility and mycelial morphology but may trigger appearance of modified mycelia during long-term culture.