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      Multiple Plant Surface Signals are Sensed by Different Mechanisms in the Rice Blast Fungus for Appressorium Formation

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          Abstract

          Surface recognition and penetration are among the most critical plant infection processes in foliar pathogens. In Magnaporthe oryzae, the Pmk1 MAP kinase regulates appressorium formation and penetration. Its orthologs also are known to be required for various plant infection processes in other phytopathogenic fungi. Although a number of upstream components of this important pathway have been characterized, the upstream sensors for surface signals have not been well characterized. Pmk1 is orthologous to Kss1 in yeast that functions downstream from Msb2 and Sho1 for filamentous growth. Because of the conserved nature of the Pmk1 and Kss1 pathways and reduced expression of MoMSB2 in the pmk1 mutant, in this study we functionally characterized the MoMSB2 and MoSHO1 genes. Whereas the Momsb2 mutant was significantly reduced in appressorium formation and virulence, the Mosho1 mutant was only slightly reduced. The Mosho1 Momsb2 double mutant rarely formed appressoria on artificial hydrophobic surfaces, had a reduced Pmk1 phosphorylation level, and was nonresponsive to cutin monomers. However, it still formed appressoria and caused rare, restricted lesions on rice leaves. On artificial hydrophilic surfaces, leaf surface waxes and primary alcohols-but not paraffin waxes and alkanes- stimulated appressorium formation in the Mosho1 Momsb2 mutant, but more efficiently in the Momsb2 mutant. Furthermore, expression of a dominant active MST7 allele partially suppressed the defects of the Momsb2 mutant. These results indicate that, besides surface hydrophobicity and cutin monomers, primary alcohols, a major component of epicuticular leaf waxes in grasses, are recognized by M. oryzae as signals for appressorium formation. Our data also suggest that MoMsb2 and MoSho1 may have overlapping functions in recognizing various surface signals for Pmk1 activation and appressorium formation. While MoMsb2 is critical for sensing surface hydrophobicity and cutin monomers, MoSho1 may play a more important role in recognizing rice leaf waxes.

          Author Summary

          The rice blast fungus is a major pathogen of rice and a model for studying fungal-plant interactions. Like many other fungal pathogens, it can recognize physical and chemical signals present on the rice leaf surface and form a highly specialized infection structure known as appressorium. A well conserved signal transduction pathway involving the protein kinase gene PMK1 is known to regulate appressorium formation and plant penetration in this pathogen. However, it is not clear about the sensor genes that are involved in recognizing various plant surface signals. In this study we functionally characterize two putative sensor genes called MoMSB2 and MoSHO1. Genetic and biochemical analyses indicated that these two genes have overlapping functions in recognizing different physical and chemical signals present on the rice leaf surface for the activation of the Pmk1 pathway and appressorium formation. We found that primary alcohols, a major component of leaf waxes in grasses, can be recognized by the rice blast fungus as chemical cues. While MoMSB2 is critical for sensing hydrophobicity and precursors of cutin molecules of rice leaves, MoSHO1 appears to be more important than MoMSB2 for recognizing wax components.

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          Most cited references41

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          Structure and function of the cell surface (tethered) mucins.

          Cell surface mucins are large transmembrane glycoproteins involved in diverse functions ranging from shielding the airway epithelium against pathogenic infection to regulating cellular signaling and transcription. Although hampered by the relatively recent characterization of cell surface mucins and the difficulties inherent in working with molecules of their size, numerous studies have placed the tethered mucins in the thick of normal and diseased lung physiology. This review focuses on the three best-characterized cell surface mucins expressed in the respiratory tract: MUC1, MUC4, and MUC16.
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            Identification and characterization of MPG1, a gene involved in pathogenicity from the rice blast fungus Magnaporthe grisea.

            Differential cDNA cloning was used to identify genes expressed during infectious growth of the fungal pathogen Magnaporthe grisea in its host, the rice plant. We characterized one of these genes, MPG1, in detail. Using a novel assay to determine the proportion of fungal biomass present in the plant, we determined that the MPG1 transcript was 60-fold more abundant during growth in the plant than in culture. Mpg1 mutants have a reduced ability to cause disease symptoms that appears to result from an impaired ability to undergo appressorium formation. MPG1 mRNA was highly abundant very early in plant infection concomitant with appressorium formation and was also abundant at the time of symptom development. The MPG1 mRNA was also expressed during conidiation and in mycelial cultures starved for nitrogen or carbon. MPG1 potentially encodes a small, secreted, cysteine-rich, moderately hydrophobic protein with the characteristics of a fungal hydrophobin. Consistent with the role of the MPG1 gene product as a hydrophobin, Mpg1 mutants show an "easily wettable" phenotype. Our results suggest that hydrophobins may have a role in the elaboration of infective structures by fungi and may fulfill other functions in fungal phytopathogenesis.
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              Roles for rice membrane dynamics and plasmodesmata during biotrophic invasion by the blast fungus.

              Rice blast disease is caused by the hemibiotrophic fungus Magnaporthe oryzae, which invades living plant cells using intracellular invasive hyphae (IH) that grow from one cell to the next. The cellular and molecular processes by which this occurs are not understood. We applied live-cell imaging to characterize the spatial and temporal development of IH and plant responses inside successively invaded rice (Oryza sativa) cells. Loading experiments with the endocytotic tracker FM4-64 showed dynamic plant membranes around IH. IH were sealed in a plant membrane, termed the extra-invasive hyphal membrane (EIHM), which showed multiple connections to peripheral rice cell membranes. The IH switched between pseudohyphal and filamentous growth. Successive cell invasions were biotrophic, although each invaded cell appeared to have lost viability when the fungus moved into adjacent cells. EIHM formed distinct membrane caps at the tips of IH that initially grew in neighboring cells. Time-lapse imaging showed IH scanning plant cell walls before crossing, and transmission electron microscopy showed IH preferentially contacting or crossing cell walls at pit fields. This and additional evidence strongly suggest that IH co-opt plasmodesmata for cell-to-cell movement. Analysis of biotrophic blast invasion will significantly contribute to our understanding of normal plant processes and allow the characterization of secreted fungal effectors that affect these processes.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Pathog
                plos
                plospath
                PLoS Pathogens
                Public Library of Science (San Francisco, USA )
                1553-7366
                1553-7374
                January 2011
                January 2011
                20 January 2011
                : 7
                : 1
                : e1001261
                Affiliations
                [1 ]Purdue-NWAFU Joint Research Center, Northwest A&F University, Yangling, Shaanxi, China
                [2 ]Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana, United States of America
                University of Melbourne, Australia
                Author notes

                Conceived and designed the experiments: WL XZ JRX. Performed the experiments: WL XZ GL LL LK CW HZ. Analyzed the data: WL XZ JRX. Wrote the paper: WL XZ JRX.

                Article
                10-PLPA-RA-4143R3
                10.1371/journal.ppat.1001261
                3024261
                21283781
                bf738020-b88a-499b-b29b-7a0a724d38e2
                Liu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 8 September 2010
                : 15 December 2010
                Page count
                Pages: 13
                Categories
                Research Article
                Cell Biology/Cell Signaling
                Microbiology/Cellular Microbiology and Pathogenesis
                Microbiology/Microbial Growth and Development

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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