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Updated: Aug 24, 2026

Understanding the Development of Compensatory Pathways in a Mutant Malaria Parasite Harbouring Hypomorphic Allele of Plant-Like Kinases
Published on: November 22, 2024
Two PAK kinase genes, CHM1 and MST20, have distinct functions in Magnaporthe grisea
Lei Li1, Chaoyang Xue, Kenneth Bruno
1Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907, USA.
Abstract:
In the rice blast fungus Magnaporthe grisea, the Pmk1 mitogen-activated protein (MAP) kinase is essential for appressorium formation and infectious growth. PMK1 is homologous to yeast Fus3 and Kss1 MAP kinases that are known to be regulated by the Ste20 PAK kinase for activating the pheromone response and filamentation pathways. In this study, we isolated and characterized two PAK genes, CHM1 and MST20, in M. grisea. Mutants disrupted in MST20 were reduced in aerial hyphae growth and conidiation, but normal in growth rate, appressorium formation, penetration, and plant infection. In chm1 deletion mutants, growth, conidiation, and appressorium formation were reduced significantly. Even though appressoria formed by chm1 mutants were defective in penetration, chm1 mutants were able to grow invasively on rice leaves and colonize through wounds. The chm1 mutants were altered in conidiogenesis and produced conidia with abnormal morphology. Hyphae of chm1 mutants had normal septation, but the length of hyphal compartments was reduced. On nutritionally poor oatmeal agar, chm1 mutants were unstable and produced sectors that differed from original chm1 mutants in growth rate, conidiation, or colony morphology. However, none of the monoconidial cultures derived from these spontaneous sectors were normal in appressorial penetration and fungal pathogenesis. These data suggest that MST20 is dispensable for plant infection in M. grisea, but CHM1 plays a critical role in appressorium formation and penetration. Both mst20 and chm1 deletion mutants were phenotypically different from the pmk1 mutant that is defective in appressorium formation and infectious hyphae growth. It is likely that MST20 and CHM1 individually play no critical role in activating the PMK1 MAP kinase pathway during appressorium formation and infectious hyphae growth. However, CHM1 appears to be essential for appressorial penetration and CHM1 and MST20 may have redundant functions in M. grisea.
Insights
In Magnaporthe grisea, CHM1 is crucial for appressorium formation and penetration, while MST20 is dispensable for infection. These PAK genes may have redundant roles, but CHM1 is essential for rice blast fungus pathogenesis.
Area of Science:
- Molecular biology
- Plant pathology
- Mycology
Background:
- The Pmk1 mitogen-activated protein (MAP) kinase pathway is vital for rice blast fungus (Magnaporthe grisea) infection.
- PAK kinases regulate MAP kinase pathways in other fungi, suggesting a similar role in M. grisea.
Purpose of the Study:
- To isolate and characterize PAK genes (CHM1 and MST20) in M. grisea.
- To investigate the roles of CHM1 and MST20 in fungal development and pathogenesis.
Main Methods:
- Gene deletion and mutant characterization.
- Phenotypic analysis of growth, conidiation, and appressorium formation.
- Pathogenicity assays on rice plants.
Main Results:
- MST20 mutants showed reduced aerial hyphae growth and conidiation but were otherwise normal.
- CHM1 mutants exhibited defects in growth, conidiation, appressorium formation, and penetration, yet could colonize wounded leaves.
- CHM1 mutants produced abnormal conidia and had reduced hyphal compartment length. Spontaneous sectors from CHM1 mutants remained defective in pathogenesis.
Conclusions:
- MST20 is not essential for M. grisea plant infection.
- CHM1 plays a critical role in appressorium formation and penetration, essential for pathogenesis.
- CHM1 and MST20 may possess redundant functions, and neither appears individually critical for activating the Pmk1 MAP kinase pathway during infection stages.
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