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Eukaryotic Cell, December 2007, p. 2240-2250, Vol. 6, No. 12
1535-9778/07/$08.00+0     doi:10.1128/EC.00104-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

A Rho3 Homolog Is Essential for Appressorium Development and Pathogenicity of Magnaporthe grisea

Wu Zheng ,^, Jisheng Chen, Wende Liu, Shiqin Zheng, Jie Zhou, Guodong Lu,^* and Zonghua Wang^*

The Key Laboratory of Biopesticide and Chemistry Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou 350002, People's Republic of China

Received 2 April 2007/ Accepted 1 October 2007

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The small GTPase Rho3 is conserved in fungi and plays a key role in the control of cell polarity and exocytosis in yeast. In this report, we show that a Rho3 homolog, MgRho3, is dispensable for polarized hyphal growth in the rice blast fungus Magnaporthe grisea. However, MgRho3 is required for plant infection. Appressoria formed by the Mgrho3 deletion mutants are morphologically abnormal and defective in plant penetration. Conidia of the Mgrho3 deletion mutants are narrower than those of the wild-type strain and delayed in germination. Transformants expressing a dominant negative Mgrho3 allele exhibit similar phenotypes as the Mgrho3 deletion mutant, while transformants expressing a constitutively active allele of MgRho3 can produce normal conidia but remain defective in appressorium formation and plant infection. In contrast, overexpression of wild-type MgRho3 increases the infectivity of M. grisea. Our results reveal a new role for the conserved Rho3 as a critical regulator of developmental processes and pathogenicity of M. grisea.

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Magnaporthe grisea is an ascomycete pathogen of important cereal crops, such as rice, barley, and wheat. It causes rice blast, one of the most severe fungal diseases of rice throughout the world (33, 35). The fungus infects rice plants in a sophisticated manner, like many other foliar pathogens. Germ tubes produced from conidia differentiate into specialized infection structures called appressoria and then use the enormous turgor pressure generated in appressoria for plant penetration (8). Mature appressoria develop thin penetration pegs to physically pierce the host surface and enter plant epidermal cells. At early stages, the penetration peg contains high concentrations of actin filaments (3) and recruits the rice cell membrane to form the extrainvasive hyphal membrane, while infection hyphal growth and its co-opt plasmodesmata for cell-to-cell movement (18). It has been hypothesized that actin and cytoskeleton elements may be involved in the reestablishment of polarized growth by determining the penetration site and in stabilizing the tip of the penetration peg (15). After penetration, the peg differentiates into infectious hyphae that grow inter- and intracellularly and result in development of blast lesions.

Signal transduction pathways that regulate infection-related morphogenesis have been extensively studied in M. grisea during the past few years (34, 41). In general, cyclic AMP (cAMP) signaling is involved in surface recognition and initiation of appressorium formation (1, 20, 22, 44). However, appressorium formation is regulated by the Pmk1 mitogen-activated protein kinase pathway (25, 42, 46). The pmk1 deletion mutant fails to form appressoria and is nonpathogenic. One putative transcription factor regulated by PMK1 is MST12, which is homologous to Saccharomyces cerevisiae Ste12 and essential for pathogenesis (27). The mst12 deletion mutant forms melanized appressoria that have normal appressorium turgor but fail to develop penetration pegs, probably due to cytoskeleton defects in mature appressoria (26). MST12 may function downstream of PMK1 to regulate genes involved in appressorial penetration and infectious growth, but other factors must exist in M. grisea to regulate appressorium formation. Other M. grisea mutants that are known to form melanized appressoria but that fail to penetrate plant cells include PLS1 (encoding a tetraspanin-like protein) (6) and MPS1 (encoding a mitogen-activated protein kinase) mutants (43). The mps1 mutant appears to have weaker cell walls, but the penetration defect of the pls1 mutant may be related to cytoskeleton changes associated with appressorial penetration.

Besides the importance of infection structure differentiation, it is also known that secretion of elicitor proteins plays a key role in the pathogenesis of most pathogenic fungi. For example, genome analysis has revealed that the plant fungal pathogen M. grisea has 739 secreted proteins, nearly twice the proteins found in the nonpathogenic fungus Neurospora crassa (7). It is very important to understand how these proteins are secreted into the host cells. However, the mechanisms that regulate protein secretion in pathogenic fungi are still unknown.

The Rho family of small GTPases regulate a wide spectrum of cellular functions, especially those involving the actin cytoskeleton (36). However, different members in the Rho family have specific functions. Rho3, one of the Rho family members, first isolated in S. cerevisiae (21), has been shown to act as a key regulator of cell polarity and exocytosis through modulating vesicle delivery function, mediated by the unconventional myosin Myo2, and vesicle docking and fusion functions, which are mediated by the exocytosis component Exo70 (2, 16, 23, 29). In Rho3 promoter shutdown experiments, a strong cell polarity defect and a partially depolarized actin cytoskeleton were observed in Candida albicans (10). Rho3-regulated exocytosis also is critical for cell division, cell separation, and polarized cell growth in Schizosaccharomyces pombe (38). In filamentous fungi, both growth and protein secretion of Trichoderma reesei in cellulose cultures are remarkably decreased in rho3 disruptant strains (37). Deletion of AgRho3 caused early lysis of emerging germ tubes and characteristic swellings at the hyphal tips of Ashbya gossypii (40). Recently, it has been shown that AgRho3p is able to directly activate formin-driven actin cable nucleation through its interaction with the SH3/PH domain-containing protein AgBoi1/2p (19).

In this study, we identified and characterized the Rho3 homolog in M. grisea (named MgRho3) and determined its role in pathogenesis. The Mgrho3 deletion mutant was viable and had a normal growth rate. Slender conidia from the Mgrho3 mutant were delayed in germination and defective in appressorium formation. Appressoria formed by the Mgrho3 deletion mutant were morphologically abnormal and defective in plant penetration. Expression of a dominant active or dominant negative Mgrho3 also resulted in defects in appressorium formation and plant penetration, but overexpression of wild-type MgRho3 resulted in more efficient plant infection. These results indicate that MgRho3 is dispensable for polarized hyphal growth but required for pathogenesis in M. grisea.

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Fungal strains, culture, and transformation. Magnaporthe grisea (Herbert) Barr strain 70-15 (7) and its derivative strains described in this paper were maintained on sterile filter paper and cultured in complete medium. For sporulation, oatmeal agar or rice polish agar medium was used. Fungal transformations were performed as described by Sweigard et al. (32), using hygromycin B (at a final concentration of 400 µg/ml; Roche Applied Science, Mannheim, Germany) or glufosinate ammonium (at a final concentration of 300 µg/ml; Sigma-Aldrich Co., St. Louis, MO) as a selective marker, depending on the selection marker gene on the plasmid vector to be transformed.

Isolation of MgRho3. Primers P6f and P6r (Table 1) were used to amplify MgRho3 from 70-15 genomic DNA by PCR consisting of 30 cycles of 45 s at 94°C, 45 s at 58°C, and 2 min at 72°C, followed by 7 min at 72°C. PCR products were then cloned in the pGEM-T Easy vector (Promega Corp., Madison, WI) and sequenced. Corresponding cDNA was isolated by reverse transcription-PCR (RT-PCR) with primers P6f and P6r, cloned in the pGEM-T Easy vector, and sequenced. Total RNA and cDNA used in the study were all isolated with the SuperScript first-strand synthesis system for RT-PCR (Invitrogen Corp., Carlsbad, CA).

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TABLE 1. Primers used for this study

MgRho3 replacement and mutants. To generate the MgRho3 gene replacement vector, a 2.0-kb fragment of MgRho3 was amplified with primers P1f and P1r and cloned between KpnI and SacI sites on pCSN43 as pRHO3. The hph gene was released from pCSN43 with XhoI and EcoRV sites and cloned into the XhoI and SmaI sites of pRHO3 as the MgRho3 gene replacement vector pKOR3. To construct the complementation vector pCOR3, a 3.03-kb fragment including a native promoter and open reading frame (ORF) of MgRho3 was amplified with primers P2f and P2r and then cloned between SacI and BamHI sites of pBARKS1 containing the Basta resistance gene.

Site-directed mutagenesis was used to generate dominant MgRho3 mutants (MgRho3-CA [constitutively active] and MgRho3-DN [dominant negative]) by PCR-mediated amplification from cDNA of strain 70-15. Two primers including the forward primer P3f and reverse primer P3r were used to generate MgRho3-CA by replacing the glycine (G22) of MgRho3 with valine, and a dominant negative MgRho3 mutant (MgRho3-DN) was generated by replacement of the aspartic acid (D128) with alanine by recombinant PCR with primers P4f, P5r, P5f, and P4r. All mutated DNA fragments were amplified with Pfu polymerase (Stratagene) and sequenced. Expression of MgRho-CA and MgRho3-DN was driven by the constitutive RP27 promoter built within pTE11. The MgRho3 genomic DNA fragment amplified from 70-15 with primers P4F and P4R was also cloned into the site of XhoI in pTE4 and driven by the promoter RP27 to generate the overexpression vector pROE3.

Reverse transcription-PCR and real-time PCR analysis. Total RNA samples were prepared using an SV total RNA isolation system (Promega Corp.) from growing hyphae of M. grisea. cDNAs were synthesized as described above. For reverse transcription-PCR, a 0.76-kb PCR fragment for the β-tubulin gene MgTUB (MGG_00604.5) was amplified as an internal control using primers P7f and P7r. MgRho3 was amplified through RT-PCR with the primers P6f and P6r.

In a real-time PCR, primers P8f and P8r were used to amplify a 92-bp amplicon of MgRho3. As an endogenous control, an 85-bp amplicon of the β-tubulin gene was amplified with primers P9f and P9r. Quantitative real-time RT-PCR was performed with the MJ Research Opticon real-time detection system using TaKaRa SYBR Premix Ex Taq (Perfect Real Time; Takara, Japan). To verify that the amplification efficiencies of MgRho3 and MgTUB1 were approximately equal, PCRs were performed with serial dilutions of cDNA templates. The relative quantification of the MgRho3 transcript was calculated by the 2 – Ct method (20a).

Analysis of hyphal morphology, conidium germination, appressorium formation, and penetration. Conidial suspensions (5 x 10⁴ conidia/ml) were prepared from 10-day-old oatmeal agar cultures, and aliquots (50 µl) were applied to either the hydrophobic or hydrophilic side of a GelBond film (Cambrex BioScience, Rockland, ME). The conidial droplets were incubated in a moist petri dish at room temperature. Conidial germination and appressorium formation were examined at 1, 2, 4, 8, and 24 h postincubation. Appressorium penetration on onion epidermal cells was assayed as described elsewhere (44). Photographs were taken with an Olympus BX51 universal research microscope. Cell wall and septum of hyphae were visualized by calcofluor white staining as described previously (13). To observe the Spitzenkörper localization, FM4-64 staining of hyphal tips was conducted following the procedure described by Fischer-Parton et al. (11). Mycelia of MgRho3 mutants were stained with a 7.5 µM aqueous working solution of FM4-64 and observed immediately. Confocal images were acquired using a Zeiss Axioskop 2 microscope equipped with a Zeiss LSM 510 Meta system. Spectral data were collected with 514-nm excitation using 1-mW helium-neon lasers. The appressorium turgor was examined with the incipient cytorrhysis technique using 2 M glycerol (14). For intracellular cAMP measurements, mycelia were collected from 3-day-old liquid complete medium cultures by filtering through Miracloth and frozen in liquid nitrogen immediately. All fungal samples were lyophilized for 16 h and weighed. Dry fungal tissues (100 µg) were ground to a powder in liquid nitrogen and resuspended in 1 ml ice-cold 6% (wt/vol) trichloroacetic acid (24) and then centrifuged in Eppendorf tubes at 12,000 rpm for 5 min at 4°C. The supernatant (200 µl) was transferred to a new tube and extracted five times with an equal volume of chloroform. The concentration of intracellular cAMP was determined with the enzyme immunoassay system (Amersham-Pharmacia Biotech) according to the manufacturer's instructions.

Infection assays. Rice (Oryza sativa L.), cultivar CO39, was grown under greenhouse conditions. Fifteen-day-old seedlings were used for infection assays. Conidial suspensions (1 x 10⁵ conidia/ml in 0.02% Tween solution) were prepared from rice polish agar cultures and spray inoculated onto plant seedlings as described elsewhere (44). Root infection assays were carried out as described previously (9).

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MgRho3 encodes a homolog of Rho GTPases. In the M. grisea genome sequence (7), there is one Cdc42 gene homolog, one Rac1 gene homolog, and five other Rho-GTPase-encoding genes. The predicted gene MGG_10323.5 encodes a protein that shares 88%, 87%, 66%, and 65% identity with Rho3 homologs from N. crassa, Hypocrea jecorina, S. cerevisiae, and S. pombe, respectively. It contains all the consensus domains characteristic of Rho GTPases, including a GTP/GDP binding domain, an effector binding site, a Rho insert domain, and a membrane localization domain CAAX box (Fig. 1A). Thus, we named the gene product MgRho3 (for M. grisea Rho3). Phylogenetic analysis revealed that MgRho3 is closely related to Rho3 homologs from other fungi (Fig. 1B).

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FIG. 1. Alignment and phylogenetic analysis of MgRho3 with other fungal Rho3 homologs. (A) An alignment of Rho3 homologs in fungi based on their amino acid sequences. Five GTP/GDP binding or hydrolysis domains are highlighted and labeled as G1 through G5. G1, GXXXXGKS/T; G2, core effector domain T; G3, DXXGQ/H/T; G4, T/NKXD; G5, C/SAK/L/T); CAAX box, a posttranslational prenylation motif. (B) Phylogenetic relationship of Rho3 homologs in fungi, calculated using the neighbor-joining method of parsimony distance in PHYLIP 3.65 (bootstrap values [percentages] are indicated at the nodes). The fungal source and accession number of each sequence are represented as follows: AfRho3, Aspergillus fumigatus, AAG12157; AnRho3, Aspergillus nidulans, XP_660291; CaRho3, Candida albicans, EAK95917; EgRho3, Eremothecium gossypii, AAG41252; EnRho3, Emericella nidulans, AAK55443; FgRho3, Fusarium graminearum, XP_380346; HjRho3, Hypocrea jecorina, CAC20376; MgRho3, Magnaporthe grisea, MG07176.4); NcRho3, Neurospora crassa, CAE76595; ScRho1, Saccharomyces cerevisiae, BAA00897; SccRho3, Schizophyllum commune, Q9P8J9; SpRho1, Schizosaccharomyces pombe, O13928; UmRho3, Ustilago maydis, XP_401685. The tree was rooted with AtROP1 (Arabidopsis thaliana, NP190698) as an outgroup member.

MgRho3 is dispensable for vegetative growth in M. grisea. To study the function of MgRho3, the 728-bp fragment of the MgRho3 ORF was replaced with the hygromycin phosphotransferase (hph) gene in strain 70-15. Three putative Mgrho3 deletion mutants, Mgrho3-5, Mgrho3-9, and Mgrho3-22, were identified by PCR with primers Phf and P2r and confirmed by Southern blot analysis (Fig. 2A and B). No MgRho3 transcripts could be detected by RT-PCR in the deletion mutant Mgrho3-22 (Fig. 2C). Two additional Mgrho3 deletion mutants, Mgrho3-5 and Mgrho3-9, had similar hybridization patterns as Mgrho3-22 in a Southern blot analysis (data not shown).

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FIG. 2. The MgRho3 knockout construct and molecular confirmation. (A) Restriction map of the MgRho3 genomic region and knockout construct. Thick arrows indicate orientations of the MgRho3 and phosphotransferase (hph) genes. Restriction enzymes are abbreviated as follows: K, KpnI; S, SmaI; Sa, SalI; X, XhoI. The MgRho3 knockout construct pKOR3 was constructed by replacing the XhoI/SmaI 774-bp fragment of the MgRho3 ORF with the hph gene. (B) Total genomic DNA samples (5 µg per lane) isolated from M. grisea 70-15 (wild type [WT]), Mgrho3-22 (deletion mutant), MgRho3-Com (complemented transformant), and MgRho3-Ect (ectopic transformant) were digested with PstI and subjected to Southern blot analysis. The probe, a 599-bp PCR fragment amplified from 70-15 genomic DNA using primers S1 and S2, is part of the 0.7-kb MgRho3 fragment replaced by the 2.4-kb hph gene (top). The same blot (at the top of the panel) was stripped and rehybridized with a 421-bp probe amplified from 70-15 genomic DNA by primers S3/P1r (lower portion of the panels). This probe is located downstream of the SmaI gene deletion site (see Materials and Methods). (C) Total RNA samples (approximately 2 µg per reaction mixture) isolated from mycelia of M. grisea strains 70-15 (WT), Mgrho3-22 and MgRho3-Com were subjected to RT-PCR using gene-specific primers P6f/P6r. The RT-PCR product is 633 bp, as predicted.

The growth rate of the Mgrho3 deletion mutant was similar to that of the wild-type strain, but conidiation was significantly reduced in the mutant Mgrho3-22 (see Table 2). Conidia formed by the Mgrho3 deletion mutant were three celled and similar in length to those of 70-15. However, conidia produced by the mutant Mgrho3-22 had reduced widths (Table 2) and appeared to be ellipsoid instead of pyriform (Fig. 3A). We also found that the Mgrho3 mutant appeared to have the hyperbranching phenotype in aerial hyphae and became curly and slightly swollen at the tip compared to those of 70-15 (Fig. 3B and C). Similar to 70-15, the Mgrho3 deletion mutant had one nucleus in each hyphal compartment (data not shown), suggesting that nuclear division and cytokinesis were normal in the Mgrho3 deletion mutant. Although MgRho3 is dispensable for septum formation in M. grisea, the average length of hyphal compartments (distance between two septa) was reduced in Mgrho3-22 (Fig. 3C). FM4-64 staining of hyphae in the wild type and the Mgrho3 deletion mutant showed that Spitzenkörper was still present at the hyphal tips, as shown in Fig. 4. This result matched our preliminary result (data not shown), that the total secreted protein was not affected in the mutant.

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TABLE 2. Phenotypic analysis of MgRho3 mutants of M. griseaa

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FIG. 3. Spore morphology, hyphal branching, and septation. (A) Conidia cultured on an oatmeal agar plate at day 10 after incubation were examined with differential interference contrast microscopy. (B) Branching patterns of mycelia of a complete medium culture at day 3 after incubation. Frequent branching happened at the terminal mycelia of Mgrho3-22. (C) Calcofluor staining of mycelia to show the distance between septa.

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FIG. 4. Spitzenkörper localization of the Mgrho3 deletion mutant. Young growing mycelia were stained with aqueous FM4-64 solution (7.5 µM) and observed immediately under a confocal microscope. Arrows show the Spitzenkörper localization at the hyphal tips of both WT and Mgrho3 deletion mutants.

MgRho3 is essential for plant infection. To determine whether MgRho3 is involved in pathogenesis, we conducted infection assays with 2-week-old rice seedlings. Rice leaves inoculated with the wild-type strain 70-15 developed typical blast lesions 7 days after inoculation (Fig. 5A). Under the same conditions, the Mgrho3 deletion mutant Mgrho3-22 showed dramatically reduced virulence, although a small proportion of inoculated leaves still produced a few lesions (Fig. 5A and Table 2). However, these brown lesions failed to produce any conidia when leaves were detached and incubated under high-moisture conditions for a prolonged period in a petri dish. So, these lesions are hypersensitive reaction-like lesions. The Mgrho3 deletion mutants were further confirmed to be nonpathogenic in wounding leaf (Fig. 5B) and root infection (Fig. 5C) assays. Under the same conditions, both the ectopic transformant (MgRho3-Ect) and the wild-type strain caused typical blast lesions on inoculated rice leaves (Fig. 5A). The other two Mgrho3 deletion mutants, Mgrho3-5 and Mgrho3-9, displayed the same defects in pathogenicity as Mgrho3-22 (data not shown).

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FIG. 5. Infection assays of Mgrho3 deletion mutants. (A) Rice leaves of cultivar CO39 were sprayed with conidium suspensions from the wild-type strain (70-15), Mgrho3-22, MgRho3-Ect, and MgRho3-Com. Typical leaves were scanned 7 days after inoculation. (B) Wounded rice leaves of cultivar CO39 were inoculated with conidia (5 x 104 conidia/ml) from strains 70-15, Mgrho3-22, and MgRho3-Com. Typical leaves were photographed 5 days after inoculation. (C) A root infection assay was carried out as described elsewhere (9).

We reintroduced the wild-type MgRho3 gene carried by plasmid pCOR3 into the mutant Mgrho3-22 and obtained three Basta-resistant transformants carrying the transforming vector by PCR analysis. One of the resulting transformants, MgRho3-Com, contained a single copy of pCOR3 integrated into the genome (Fig. 2B) and was selected for further analysis. Similar to the wild-type strain, the transformant MgRho3-Com was able to penetrate and develop infectious hyphae in onion epidermal cells. This was further confirmed by its fully recovered pathogenicity in rice (Fig. 5; see also Fig. 7, below). These data indicated that deletion of MgRho3 was directly responsible for the defects of the Mgrho3 deletion mutants in plant infection.

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FIG. 7. Penetration assays of the Mgrho3 deletion mutant on onion epidermal cells. Conidial suspensions (around 1,000 conidia in 20 µl) of wild-type strain 70-15 (WT), Mgrho3-22, MgRho3-Com, and MgRho3-Ect were inoculated on strips of onion epidermis as described by Xu et al. (44). Infectious hyphae were photographed 1 day after inoculation (top panel) and 2 days after inoculation (lower panel) by using differential interference contrast microscopy. A, appressorium; C, conidium; H, hypha; IF, infectious hypha.

MgRho3 is essential for the development of functional appressoria. To further determine the defects of the Mgrho3 deletion mutants, we assayed spore germination and appressorium development on the hydrophobic side of GelBond membranes. Almost all 70-15 conidia had germinated by 4 h, but only 66.5% of conidia of the mutant Mgrho3-22 produced germ tubes in the same time period under the same conditions, followed by 76.4% at 8 h and 100% at 24 h. At 8 h, all germ tubes had formed melanized appressoria in 70-15 and MgRho3-Com cultures, but only about 15.7% of the germ tubes of the Mgrho3 deletion mutant differentiated into appressoria. At 24 h, about 60% of the Mgrho3-22 germ tubes formed appressoria but were not fully melanized (Fig. 6A and B). More appressoria developed upon prolonged incubation for up to 48 h; however, most of these germ tubes produced deformed and less-melanized appressoria. Most appressoria of the mutant Mgrho3-22 were aberrant in morphology, more elongated, and less swollen than the wild type. Only about 9% of appressoria appeared to be normal (swollen and rounded) in morphology (Fig. 6A), but they were smaller in size (Fig. 6A). We further examined the turgor pressure of appressoria of Mgrho3-22 with the incipient cytorrhysis technique. Appressoria of Mgrho3-22 were more osmotically sensitive and 72.8% ± 10.6% of appressoria collapsed when they were treated with 2 M glycerol for 20 min, but only 12.7% ± 5.7% appressoria of the wild-type 70-15 collapsed under the same conditions. The complemented strain was normal in germination and appressorium formation and turgor pressure establishment (Fig. 6A, B, and C). Furthermore, we measured the endogenous cAMP levels in Mgrho3 mutants. Interestingly, the intracellular cAMP level in the Mgrho3 deletion mutants was 3,455.1 ± 254.8 fmol/mg of mycelia, which was 67% of that detected in the wild-type strain 70-15 (5,201.9 ± 199.1 fmol/mg of mycelia).

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FIG. 6. Appressorium formation of the Mgrho3 deletion mutant on artificial hydrophobic surfaces. Conidia were incubated on the surface of hydrophobic GelBond films as described in Materials and Methods. Healthy appressoria from the wild-type strain (WT) and MgRho3-Com versus abnormal appressoria from the Mgrho3-22 strain were examined with differential interference contrast microscopy.

In penetration assays with onion epidermal cells, we also observed that most appressoria formed on onion epidermis were aberrant in morphology and defective in plant penetration (Fig. 7). Only about 12% of the appressoria formed by the mutant Mgrho3-22 were able to penetrate and form limited infectious hyphae in onion epidermal cells. Even after prolonged incubation for up to 72 h, penetration frequency and infectious hyphal growth were not increased in the Mgrho3 deletion mutant. Under the same conditions, over 85% of appressoria formed by the wild-type strain 70-15 penetrated into epidermal cells, and invasive hyphae had grown prosperously by 48 h (Fig. 7). The results indicate that the Mgrho3 deletion mutant is defective in developing functional appressoria and infectious hyphae. When 10 mM exogenous cAMP was supplied, defects of Mgrho3 deletion mutants for appressorium morphology, penetration, and plant infection could not be rescued (data not shown). It is likely that these defects are directly responsible for the loss of pathogenicity in the Mgrho3 deletion mutant.

Overexpression of MgRho3 enhances pathogenicity. To demonstrate that the expression level of MgRho3 affects its function, we used the RP27 promoter derived from the M. grisea ribosomal protein 27 gene constructed in pSM565 (4) to express MgRho3 in the wild-type strain 70-15 of M. grisea. Three MgRho3 overexpression mutants were identified by real-time PCR (Fig. 8A), showing a 6- to 10-fold increase in transcripts compared with the wild-type strain at vegetative hyphal stage and a 2-fold increase in infected rice leaves. All three overexpression transformants had similar phenotypes, but only data of transformant MgRho3OE-16 are presented here. In contrast to the MgRho3 deletion mutant Mgrho3-22, conidiation increased in transformant MgRho3OE-16, about three times more than that of the wild-type 70-15 strain (Table 2). Conidial morphology (Fig. 8C) and germination appeared to be normal in the transformant MgRho3OE-16. Interestingly, appressorium formation was faster in MgRho3OE-16 than in the wild-type strain. All the germ tubes formed appressoria after 4 h of incubation on the GelBond hydrophobic surface, which was significantly faster than that with the wild type. Infectious growth of MgRho3 overexpression mutants on onion epidermal cells was accelerated, and appressorium development and infectious growth were also advanced (Fig. 8D). On 2-week-old seedlings of rice cultivar CO39, MgRho3OE-16 caused more and larger lesions than the wild-type strain (Fig. 8B), with 94.8 ± 20.3 lesions on a 5-cm-long rice leaf tip, while the wild type produced only 26.04 ± 6.4 lesions (Table 2), suggesting that overexpression of MgRho3 increased the fungal virulence. The other two MgRho3 overexpression transformants had similar phenotypes and displayed enhanced virulence.

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FIG. 8. Morphology of MgRho3 overexpression mutants. (A) Total RNA samples (approximately 5 µg per reaction mixture) isolated from mycelia of M. grisea strains 70-15 (wild type [WT]) and MgRho3 overexpression transformants (MgRho3OE-8, -12, and -16) were subjected to real-time PCR. (B) Rice leaves of cultivar CO39 were sprayed with conidial suspensions from the wild-type strain (70-15) and MgRho3OE-16. Typical leaves were scanned 7 days after inoculation. (C) Appressoria examined with differential interference contrast microscopy 8 h after conidia were incubated on the surface of hydrophobic GelBond films as described in Materials and Methods. (D) Conidial suspensions (around 1,000 condia in 20 µl) of M. grisea strain 70-15 (WT) and MgRho3OE-16 were inoculated on strips of onion epidermis. Infectious hyphae were photographed 2 days after inoculation.

Expression of MgRho3-CA and -DN alleles results in distinct defects in appressorium development and pathogenicity. To further investigate the biological function of MgRho3, we constructed the MgRho3-CA and MgRho3-DN alleles and transformed them into the wild-type 70-15 strain. Conidia produced by transformants expressing MgRho3-CA had normal morphology but were defective in appressorium formation (Fig. 9A). Similar to the MgRho3 deletion mutant Mgrho3-22, transformants expressing the MgRho3-DN allele produced slender conidia (Fig. 9A) and deformed appressoria. Interestingly, both MgRho3-CA and MgRho3-DN transformants were defective in plant infection (Fig. 9). These results suggest that proper regulation of MgRho3 activity is critical for appressorium formation and plant infection.

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FIG. 9. Morphology and infection assay of MgRho3 dominant mutants. (A) Conidia of 70-15 (wild type [WT]), MgRho3-CA, and MgRho3-DN cultured on oatmeal agar plates for 10 days. (B) Conidial suspensions (around 1,000 conidia in 20 µl) of M. grisea strain 70-15 (WT) and MgRho3 dominant mutants were inoculated on strips of onion epidermis. Infectious hyphae were photographed 2 days after inoculation. (C) Rice leaves of cultivar CO39 were sprayed with conidial suspensions from the wild-type strain (70-15), MgRho3-CA, and MgRho3-DN. A, appressorium; C, conidium; H, hypha; IF, infectious hypha. All were examined with differential interference contrast microscopy.

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Rho3 is a member of the Ras superfamily of monomeric GTPases. It is known to be involved in the regulation of cell polarity, exocytosis, and vesicle secretion through its functional characterization in S. cerevisiae (2, 21, 23, 29). In S. pombe, Rho3 regulates cell division, cell separation, and polarized cell growth (38). In filamentous fungi, Rho3 homologs are not essential for establishing and maintaining polarized hyphal tip growth. Deletion of Rho3 reduces vegetative growth and protein secretion in T. reesei (37). In M. grisea, we showed that Mgrho3 deletion mutants have no obvious defects in vegetative growth. In contrast to irregular swelling observed in an Agrho3 mutant (19, 40), germ tubes and vegetative hyphae of the Mgrho3 mutants had basically normal morphology. However, conidia produced by the Mgrho3 mutants were narrower and appeared more slender than those of the wild-type strain (Fig. 3A). Conidium germination was delayed, but the germination pattern remained the same.

The Mgrho3 deletion mutant still formed appressoria, which were morphologically abnormal and defective in plant penetration. In rice infection assays, the Mgrho3 deletion mutant is nonpathogenic, indicating that MgRho3 is a key regulator in appressorium penetration and infectious growth in M. grisea. To our knowledge, this is the first report that links the Rho3 protein with fungal pathogenesis. The Rho3 homologs are well conserved in other plant pathogenic fungi (Fig. 1) and may be involved in various plant infection processes. Appressorium formation and invasive growth are two key steps in the infection cycle of many plant pathogenic fungi.

Two signaling pathways, the cAMP/protein kinase A (PKA) and PMK1 mitogen-activated protein kinase pathways, are known to regulate these processes in M. grisea (20, 42, 46). Unlike the cpkA and pmk1 mutants, the Mgrho3 mutants produce slender conidia (Fig. 3A) and abnormal appressoria (Fig. 6A). Our data showed that although the intracellular cAMP level in the Mgrho3 deletion mutant is lower than that of the wild-type strain, exogenous cAMP failed to rescue defects in appressorium development, penetration, and plant infection. These data suggest that the Mgrho3 mutant differs from the cpkA mutant (deleted of the catalytic subunit of PKA) in appressorial penetration and plant infection. About 12% of appressoria formed by the Mgrho3 mutants are able to penetrate and form infectious hyphae. Black specks were observed on rice leaves sprayed with the Mgrho3 mutants. The cpkA mutant, however, is blocked in penetration and causes rare blast lesions, possibly by penetrating through wounds (44). These data suggest that Rho3 may not directly activate the cAMP/PKA pathway in regulation of appressorium development and normal turgor pressure establishment.

The cytorrhysis assay indicated that the Mgrho3 mutant had reduced appressorium turgor, which plays a key role in plant penetration in M. grisea (8). One possible explanation is that the slender conidia of the Mgrho3 mutant may have less carbon storage than normal pyriform conidia. In M. grisea, carbon storage, such as in glycogen and lipid bodies, plays an important role in appressorium turgor generation (12, 39). Therefore, it is likely that appressoria formed by the Mgrho3 mutants are defective in penetration because of the reduced turgor pressure.

However, it remains possible that failure in appressorial penetration in the Mgrho3 mutant is caused by defects in cytoskeleton reorganization associated with formation of the penetration peg. Small GTPases are well known to regulate actin cytoskeleton organization. In M. grisea, actin accumulates at the base of the appressorium and in the penetration peg (3), suggesting a reorganization of the actin cytoskeleton during such polarized growth. Mutants deleted of MST12, one of the putative downstream transcription factors of Pmk1, form melanized appressoria and have normal appressorium turgor pressure (26). Appressoria formed by the mst12 mutant are defective in microtubule reorganization associated with penetration peg formation at late stages of appressorium formation. Clergeot et al. (6) speculated that PLS1 could be involved in a similar signaling pathway in fungi that controls actin cytoskeleton reorganization at the base of the appressorium before penetration peg emergence. MgRho3 may also play a role in regulation of the actin cytoskeleton, as in other organisms (36). It is well documented that Rho3 controls polarized cell growth in yeast through regulation of actin cytoskeleton and membrane trafficking, and a number of Rho3 effectors have been identified and are known to play an important role in these regulatory functions, including formin (For3), Myo2, Exo70, and Rgd1 (23, 28, 29, 30). In M. grisea, all these genes are well conserved, but none of them has been functionally characterized, so that results in S. cerevisiae will facilitate the study of MgRho3 effectors in M. grisea.

Finally, our results indicated that overexpression of wild-type MgRho3 increases the fungal virulence in rice. Interestingly, overexpression of wild-type Cdc42 has no morphological consequences in Penicillium marneffei (5) and no effects on pathogenicity in Claviceps purpurea (31). In contrast, overexpression of Cdc42 disturbs the normal pattern of budding site selection in S. cerevisiae (17) and induces growth tip enlargement in Wangiella dermatitidis (45). In M. grisea, MgRho3 is constitutively expressed in vegetative hyphae, conidia, germ tubes, and appressoria. Its expression peaks at the conidium germination stage (47). Our real-time PCR data showed that there was a twofold increase in infected rice leaves with the MgRho3 overexpression transformants, suggesting that the expression level of MgRho3 may be related to the fungal infectivity. Expression of either the dominant active or dominant negative MgRho3 allele caused dramatic defects in appressorium formation and plant penetration, and dominant negative MgRho3 also resulted in deformed conidia. In S. cerevisiae, transformants expressing a dominant active Rho3 displayed cold sensitivity and produced elongated, bent cells (2, 16). However, expression of a dominant negative Rho3 allele abolished its interaction with Exo70 and Myo2 and caused defects both in the actin cytoskeleton and exocytosis (29). In M. grisea, overexpression of wild-type MgRho3 only increases its expression level but still maintains the equilibrium between GTP- and GDP-bound forms. However, overexpression of a dominant active allele of MgRho3 may bypass the upstream activation signals and disturb the activation status.

 
We thank Zhenbiao Yang at the University of California, Riverside, and Guangpu Li at the University of Oklahoma Health Sciences Center, Oklahoma City, for their critical reading and suggestions on the manuscript, and Shengcheng Wu at the University of Georgia, Athens, and Bo Liu at the University of California, Davis, for their helpful discussions.

This work was supported by the 973 Program (2006CB1019001), National Science Foundation, China (project numbers 30070030 and 30470066), and the Fujian Natural Science Foundation (B0520002).

 
* Corresponding author. Mailing address: The Key Laboratory of Biopesticide and Chemistry Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou 350002, People's Republic of China. Phone: 86-591-83790312. Fax: 86-591-83727618. E-mail for Zonghua Wang: zonghuaw{at}163.com. E-mail for Guodong Lu: lgd{at}fjau.edu.cn

Published ahead of print on 12 October 2007.

W.Z. and J.C. contributed equally to this work.

Present address: Fuzhou Criminal Science & Technology Institute, Fuzhou 350003, People's Republic of China.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

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Eukaryotic Cell, December 2007, p. 2240-2250, Vol. 6, No. 12
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