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Nox Complex signal and MAPK cascade pathway are cross-linked and essential for pathogenicity and conidiation of mycoparasite Coniothyrium minitans
research-article
Author(s):
Wei Wei
1
,
2 ,
Wenjun Zhu
1
,
2 ,
Jiasen Cheng
2 ,
Jiatao Xie
2 ,
Daohong Jiang
1
,
2 ,
Guoqing Li
1
,
2 ,
Weidong Chen
3 ,
Yanping Fu
a
,
2
Publication date (Electronic):
12 April 2016
Journal:
Scientific Reports
Publisher:
Nature Publishing Group
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Abstract
The NADPH oxidase complex of a sclerotial mycoparasite Coniothyrium minitans, an important biocontrol agent against crop diseases caused by Sclerotinia sclerotiorum, was identified and its functions involved in conidiation and mycoparasitism were studied. Gene knock-out and complementary experiments indicated that CmNox1, but not CmNox2, is necessary for conidiation and parasitism, and its expression could be significantly induced by its host fungus. CmNox1 is regulated by CmRac1-CmNoxR and interacts with CmSlt2, a homolog of Saccharomyces cerevisiae Slt2 encoding cell wall integrity-related MAP kinase. In Δ CmNox1, CmSlt2-GFP fusion protein lost the ability to localize to the cell nucleus accurately. The defect of conidiation in Δ CmRac1 could be partially restored by over-expressing CmSlt2, indicating that CmSlt2 was a downstream regulatory factor of CmNox1 and was involved in conidiation and parasitism. The expressions of mycoparasitism-related genes CmPks1, Cmg1 and CH1 were suppressed in the knock-out mutants of the genes in CmNox1-CmSlt2 signal pathway when cultivated either on PDA. Therefore, our study infers that CmRac1-CmNoxR regulates CmNox1-CmSlt2 pathway in regulating conidiation and pathogenicity of C. minitans.
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Most cited references46
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Sclerotinia sclerotiorum (Lib.) de Bary: biology and molecular traits of a cosmopolitan pathogen.
Melvin D Bolton, Bart Thomma, Berlin D. Nelson (2006)
SUMMARY Sclerotinia sclerotiorum (Lib.) de Bary is a necrotrophic fungal pathogen causing disease in a wide range of plants. This review summarizes current knowledge of mechanisms employed by the fungus to parasitize its host with emphasis on biology, physiology and molecular aspects of pathogenicity. In addition, current tools for research and strategies to combat S. sclerotiorum are discussed. Sclerotinia sclerotiorum (Lib.) de Bary: kingdom Fungi, phylum Ascomycota, class Discomycetes, order Helotiales, family Sclerotiniaceae, genus Sclerotinia. Hyphae are hyaline, septate, branched and multinucleate. Mycelium may appear white to tan in culture and in planta. No asexual conidia are produced. Long-term survival is mediated through the sclerotium; a pigmented, multi-hyphal structure that can remain viable over long periods of time under unfavourable conditions for growth. Sclerotia can germinate to produce mycelia or apothecia depending on environmental conditions. Apothecia produce ascospores, which are the primary means of infection in most host plants. S. sclerotiorum is capable of colonizing over 400 plant species found worldwide. The majority of these species are dicotyledonous, although a number of agriculturally significant monocotyledonous plants are also hosts. Disease symptoms: Leaves usually have water-soaked lesions that expand rapidly and move down the petiole into the stem. Infected stems of some species will first develop dark lesions whereas the initial indication in other hosts is the appearance of water-soaked stem lesions. Lesions usually develop into necrotic tissues that subsequently develop patches of fluffy white mycelium, often with sclerotia, which is the most obvious sign of plants infected with S. sclerotiorum. http://www.whitemoldresearch.com; http://www.broad.mit.edu/annotation/fungi/sclerotinia_sclerotiorum.
- Record: found
- Abstract: found
- Article: found
Functional Analysis of the Kinome of the Wheat Scab Fungus Fusarium graminearum
Chenfang Wang, Shijie Zhang, Rui Hou … (2011)
Introduction In eukaryotic organisms, reversible protein phosphorylation by protein kinase (PK) is involved in the regulation of various growth and developmental processes and responses to environmental stimuli. Approximately 30% of cellular proteins are phosphorylated [1]. The eukaryotic PK superfamily consists of conventional and atypical protein kinases. Conventional PKs (ePKs) have been classified into eight groups, AGC, CAMK, CK1, CMGC, RGC, STE, TK, and TKL, based on their similarities in amino acid sequences, domain structures, and modes of regulation [2], [3]. Protein kinases with a conserved kinase domain (PF00069) but not classified into these eight groups are categorized as the ‘other’ group of ePKs. Atypical PKs (aPKs) lack significant sequence similarity with ePKs. Four groups of aPKs, Alpha, PIKK, PDHK, and RIO, are known to possess protein kinase activity [2], [3]. In general, approximately 1% of predicted genes encode protein kinases in higher eukaryotes, such as human, mouse, rice, and Arabidopsis [4]–[6]. In the budding yeast Saccharomyces cerevisiae, 127 PK genes have been identified, which is approximately 2% of its genome. Many of them play critical roles in signal transduction, cell division, sexual reproduction, and stress responses. The genome of Schizosaccharomyces pombe contains 117 PK genes. Approximately 85% of its kinome is shared with S. cerevisiae, indicating that these two yeasts have a high degree of homology in their PK genes [7]. To date, genomes of over 40 filamentous fungi have been sequenced. Besides the model filamentous fungi Neurospora crassa and Aspergillus nidulans, genome sequences are available for a number of plant pathogenic fungi, including Magnaporthe oryzae, Ustilago maydis, and four Fusarium species. In general, less than 1% of the predicted genes in filamentous fungi encode protein kinases [8], [9]. In addition to the well conserved cell-cycle related genes, several PK genes are known by classical genetic studies to be important for hyphal growth in N. crassa and A. nidulans [10], [11]. In plant pathogenic fungi, a number of PK genes are known to be important for pathogenesis, including the key components of well-conserved MAP kinase (MAPK), calcium, and cAMP signaling pathways [12]–[14]. However, a systematic functional characterization of the kinomes of filamentous fungi or fungal pathogens has not been reported. Fusarium head blight (FHB) or scab, caused by Fusarium graminearum, is one of the most important diseases on wheat and barley [15], [16]. In addition to causing severe yield losses under favorable environmental conditions, this pathogen produces harmful mycotoxins, such as deoxynivalenol (DON) and zearalenone. DON is an important virulence factor in the wheat scab fungus [17], [18]. In addition to its economic importance, F. graminearum is a tractable genetic system amenable to molecular and genomic studies. Gene replacement with the split-marker approach is highly efficient [19]. To date, three PK genes, GPMK1, MGV1, and SNF1, have been shown by targeted deletion to be important for various developmental and plant infection processes [20]–[24]. In this study, we identified 116 putative PK genes in F. graminearum. Although 20 of them appear to be essential, mutants were generated for the other 96 PK genes and characterized for defects in growth, conidiation, colony and conidium morphology, germination, stress responses, plant infection, DON production, and sexual reproduction. In total, 42 PK mutants were significantly reduced in virulence or non-pathogenic, and 45 mutant were defective in sexual reproduction. A number of these protein kinase genes, including two that are unique to filamentous fungi, are dispensable for hyphal growth and likely encode novel fungal virulence factors. We used the interlog method [25] to predict the PK-PK and PK-protein interaction networks of F. graminearum, which has two Cdc2 kinase and two aurora kinase genes. Results from this study indicate that PK genes are important for various developmental and plant infection processes in F. graminearum. The functions of some well conserved PK genes, such as IME2 and BUB1, differ significantly between F. graminearum and S. cerevisiae. Results Identification of Protein Kinase Genes in F. graminearum Among the 13,321 predicted genes of F. graminearum, 116 encode putative protein kinases (Table S1; Figure 1). Eight of them are atypical PKs. All of the PK genes were manually annotated. Problems with the open reading frame prediction were identified and corrected for 22 of them (Table S1). In comparison with S. cerevisiae, F. graminearum has fewer PK genes (Table S1). It lacks distinct orthologs of 19 yeast PK genes, including DBF4, SMK1, MEK1, NNK1, ELM1, ALK1, YGK3, NPR1, ISR1, and HAL5. None of them are essential in yeast but some, such as ALK1 and ELM1, are involved in mitosis or cytokinesis. For 22 single copy PK genes in F. graminearum, S. cerevisiae has two or more paralogs, including TOR1/TOR2, CKA1/CKA2, DBF2/DBF20, YPK1/YPK2, PKH1/PKH2, and RIO1/RIO2 (Table S1). In contrast, F. graminearum has two orthologs of IPL1 (Fg06959 and Fg02399) and CDC28 (Fg08468 and Fg03132), which are single copy genes in yeast. It also contains 28 putative PK genes, including Fg01058, Fg02488, Fg00792, and Fg01559, that have no distinct orthologs in S. cerevisiae (Table S1). Many of them are unique to filamentous fungi. 10.1371/journal.ppat.1002460.g001 Figure 1 Phylogenetic analysis with the conventional protein kinase (ePK) genes of Fusarium graminearum. The unrooted maximum likelihood tree was constructed with the catalytic domain sequences. Different protein kinase groups, AGC (PKA, PKG, PKC, βARK, ribosomal S6 family PKs and their close relatives), CAMK (calmodulin-regulated kinases), CK1 (casein kinase 1 and close relatives), CMGC (CDKs, MAPKs, GSK, and CDK-like kinases), STE (many kinases involved in the MAPK cascades), and Other (with a conserved kinase domain but could not be classified) are labeled with different colors. Fg05135 contains two catalytic domains (a and b). Interestingly, several PK genes are closely linked in F. graminearum (Table S2). For examples, Fg04053 and Fg04054 are only 7626-bp apart. Their chromosomal positions are conserved in F. verticillioides, F. oxysporum, and A. nidulans but not in M. oryzae and N. crassa. Fg06939 and Fg06940 encode kinases orthologous to yeast Sat4 (Hal4) and Tos3, respectively. Their orthologs also are closely linked in F. verticillioides, F. oxysporum, M. oryzae, A. nidulans, and N. crassa (Table S2). We searched the PlexDB database (www.plexdb.org) that contains published microarray data of F. graminearum [26], [27] to compare expression levels of different PK genes. During barley infection, the expression of 12 PK genes, including Fg06385 (Gpmk1), Fg07295 (Mmk2), Fg07329 (Gsk3), Fg08691 (Pbs2), Fg09660 (Pkc1), and Fg10228 (Swe1) was increased 48 hpi (Table S3). By 144 hpi, their expression levels were up-regulated 5-fold or more. In contrast, no PK genes were reduced over 5-fold during barley infection, although the expression of Fg01559, Fg07745, Fg09150, and Fg07344 was reduced approximately 2-fold at 144 hpi (Table S3). During spore germination, Fg03132 is highly expressed at early stages. In comparison with ungerminated conidia, it was up-regulated over 11- and 8-fold at 2 and 8 h, respectively. The other CDC28 ortholog, Fg08468, also was up-regulated but to a lesser extent. Its expression was increased 2.9- and 2.0-fold at 2 and 8 h, respectively (Table S3). The expression of Fg06502 (Rio1), Fg01347 (Bub1), and Fg00472 (Sch9) also peaked at 2 h. These genes may play a role in the establishment of polarized growth. Fg01271 (Cdc5), Fg13318 (Mec1), Fg09408 (Kin3), and Fg08635 (Dbf2) were up-regulated at 2 and 8 h, when cell division and cytokinesis are activated during germination. Knockout Mutants of Predicted PK Genes The gpmk1 and mgv1 mutants were generated in previous studies [20], [22], [24]. For all of the other PK genes, gene replacement constructs were generated by the split-marker approach [19] and transformed into protoplasts of the wild-type strain PH-1. The resulting hygromycin-resistant transformants were screened by PCR with primers F5 and R6 (Figure S1) located in the deleted region. All putative knockout mutants were further confirmed by PCR with primer pairs F7/H855R and R8/H856F [28]. Primers F7 and R8 were located outside the flanking sequences of the gene replacement constructs (Figure S1). Only transformants that underwent homologous recombination in the flanking sequences contain PCR products of expected sizes. A total of 20 PK knockout mutants (Table S1) were selected for verification by Southern blot hybridizations. All of them, including the Fg00362, Fg04053, Fg08701, Fg08906, Fg10228, and Fg10381 mutants (Table S1), were confirmed to be true deletion mutants. For 96 PK genes, we were able to identify at least two or more knockout mutants with similar phenotypes described below. Twelve of them are orthologous to essential genes in S. cerevisiae or S. pombe (Table 1), indicating that these protein kinases are not required for hyphal growth in F. graminearum. However, many of these mutants grew poorly. Of the 20 PK genes for which we failed to identify knockout mutants, at least 35 transformants from three or more independent transformations were screened (Table 1), indicating that knockout mutants may be nonviable. Sixteen of them are orthologous to essential genes in S. cerevisiae, including FgPKC1 (Fg09660), FgTRA1 (Fg06089), FgKIN28 (Fg07423), and FgHRR25 (Fg08731). For the Fg05306, Fg05775, Fg06637, and Fg05393 genes, their orthologs in yeast are not essential but we failed to identify knockout mutants after screening over 60 transformants from at least three independent transformations (Table 1). Deletion of these genes may be lethal because of the gene replacement efficiency of the split-marker approach in F. graminearum. 10.1371/journal.ppat.1002460.t001 Table 1 Protein kinase genes essential in S. cerevisiae, S. pombe, or F. graminearum. F. graminearum S. cerevisiae S. pombe Transformants screened Mutants identified PK genes essential in the fission or budding yeast but not in F. graminearum Fg02399 a IPL1 ark1 20 14 Fg00433 RAD53 cds1 20 11 Fg04947 CAK1 - 16 6 Fg13318 MEC1 SPBC216.05 20 10 Fg10381 CDC15 cdc7 20 3 Fg08468 a CDC28 cdc2 18 12 Fg03132 a CDC28 cdc2 20 8 Fg01188 CBK1 orb6 c 87 7 Fg05734 KIC1 nak1 c 20 5 Fg07344 - sid1 20 15 Fg08906 - SPCC70.05C 20 10 Fg04053 - prp4 70 7 PK genes essential in F. graminearum and other fungi Fg00677 CKA1, CKA2 cka1 75 0 Fg01137 MPS1 mph1 40 0 Fg01271 CDC5 plo1 36 0 Fg04054 VHS1, SKS1 ran1 85 0 Fg05845 YPK1, YPK2 gad8 52 0 Fg06089 TEL1 tel1 105 0 Fg06502 RIO1, RIO2 SPAC10F6.10,SPBC1703.05 46 0 Fg06959 a IPL1 ark1 37 0 Fg07409 SGV1 cdk9 64 0 Fg07423 KIN28 crk1, mcs6 38 0 Fg07855 CDC7 hsk1, spo4 50 0 Fg08133 TOR1, TOR2 tor1, tor2 100 0 Fg08731 HRR25 hhp1, hhp2 37 0 Fg09408 (nimA)b KIN3 fin1 36 0 Fg09660 PKC1 pck1, pck2 40 0 Fg10725 PKH1,PKH2 ksg1 42 0 Fg05393 PHO85 d pef1 141 0 Fg06637 KNS1 d lkh1 95 0 Fg05775 IRE1 d ppk4 117 0 Fg05306 VPS15 d ppk19 64 0 a One of the two paralogs in F. graminearum. -, no distinct ortholog. b Orthologous to nimA, an essential gene in A. nidulans. c In S. pombe, orb6, nak1, and sid1 are essential genes. KIC1 and CBK1 are essential genes in the wild-type but no ssd1 mutant strains of S. cerevisiae. Fg07344 and Fg05734 are orthologous to Sid1 and Nak1 of S. pombe, respectively. Sid1 has no distinct ortholog in S. cerevisiae. d PHO85, KNS1, IRE1, and VPS15 are not essential genes in S. cerevisiae. All of the knockout mutants were characterized for defects in vegetative growth, colony morphology, pigmentation, conidiation, conidium morphology, conidium germination and germ tube growth, hyphal tip growth and branching, perithecium formation, ascospore production, ascospore dispersal, DON production, wheat and corn infection, and responses to treatments with 0.05% H2O2, and 0.7 M NaCl. The resulting phenotypic data were deposited in a searchable database available at fgkinome.nwsuaf.edu.cn. Overall, deletion of 64 non-essential PK genes (66.7%) resulted in at least one of the 17 phenotypes examined. Because of the importance of protein kinases in fungal growth and differentiation, many of these mutants have pleiotropic defects, and we were able to isolate at least one PK mutant defective in each phenotype examined in this study. When analyzed for the association between different phenotypes by Pearson correlation efficient, defects in plant infection and vegetative growth had the highest correlation efficient followed by the correlation between sexual reproduction and growth rate or virulence (Table S4). Although phenotypes of at least two knockout mutants were examined for each gene, we have selected nine genes (Fg04053, Fg05734, Fg07251, Fg02795, Fg07329, Fg07344, Fg08906, and Fg10381) for complementation assays. For all of them, the reintroduction of the wild-type allele rescued the defects observed in the corresponding mutants. PK Genes Important for Hyphal Growth Among the 96 non-essential PK genes, 32 of them (66.7%) were found to play critical roles in vegetative growth. Deletion of any one of these genes, including GzSNF1 and MGV1 [20], [29], resulted in over 30% reduction in growth rate (Table 2). Many of these mutants had abnormal colony morphology, growth, or branching patterns (Figure 2A; fgkinome.nwsuaf.edu.cn). The Fg00362, Fg01188 (Cbk1), and Fg04053 mutants had the most significant reduction in growth (>90%) and formed compact colonies with limited hyphal growth (Figure S2). The Fg00362 and Fg01188 mutants had similar morphological defects and produced densely aggregated vegetative hyphae that were wider and had shorter compartments and fewer branches. Their orthologs in N. crassa are the POD-6 (polarity-defective 6) and COT-1 genes that are functionally related in regulating hyphal growth [10]. The Fg04053 mutant appeared to have less severe defects in hyphal morphology and branching (Figure S2). It formed non-pigmented colonies with rare aerial hyphae. Like Fg00362, Fg04053 lacks a distinct ortholog in S. cerevisiae. 10.1371/journal.ppat.1002460.g002 Figure 2 Representative PK mutants with defects in colony morphology and hyphal growth. A. Three-day-old PDA cultures of PH-1 and the Fg10037, Fg06957, Fg10066, Fg10381, Fg08635, Fg07344, and Fg08468. B. Hyphae of PH-1 and the Fg10066, Fg06957, Fg04947, Fg10037, and Fg10381 mutants grown on CM slab agars for 36 h. Bar = 100 µm. 10.1371/journal.ppat.1002460.t002 Table 2 Protein kinase genes important for vegetative growth and/or pathogenesis. Strainsa Growth rate (%)b Conidiation (%)b Disease Indexc PH-1 (WT) 100.0 100.0 13.6 Fg04484 (Srb10) 69.4 59.9 1.0 Fg05547 (Atg1) 67.8 45.9 2.0 Fg04382 (Kin82) 67.4 69.4 7.5 Fg08468 (Cdc28) 66.7 131.6 1.5 Fg09903 (Ste7) 65.9 151.0 1.0 Fg06939 (Sat4) 64.4 52.3 4.5 Fg05734 (Kic1) 63.9 38.5 1.8 Fg13318 (Mec1) 62.4 65.0 1.2 Fg06878 (Cmk1/Cmk2) 60.4 73.9 2.1 Fg08701 (Gin4-like)c 58.1 50.0 8.5 Fg10228 (Swe1) 55.9 27.1 1.3 Fg10381 (Cdc15) 52.8 17.8 0.9 Fg08635 (Dbf2/Dbf20) 50.4 14. 0.8 Fg01641 (Sak1) 49.4 10.0 1.2 Fg06385 (Gpmk1) 47.0 32.6 0.5 Fg08691 (Pbs2) 64.41 41.2 0.8 Fg05484 (Ste11) 45.6 73.6 1.0 Fg04947 (Cak1) 39.0 22.4 1.7 Fg02795 (Sky1) 38.9 62.2 0.5 Fg07295 (Mkk1/Mkk2) 30.0 50.9 0.7 Fg06326 (Bck1) 29.3 21.5 0.0 Fg10313 (Mgv1) 28.2 69.7 0.0 Fg09897 (Snf1) 25.3 55.9 1.0 Fg00408 (Ssk2/Ssk22) 42.4 54.5 0.5 Fg07251 (Tpk2) 17.1 47.9 1.0 Fg07329 (Gsk3) 15.7 2.7 0.5 Fg10037 (Bud32) 15.3 1.4 0.0 Fg06957 (Cla4) 15.2 53.0 2.1 Fg10066 (Yck1/2/3) 14.8 0.0 0.9 Fg01188 (Cbk1) 4.4 0.0 0.1 Fg00362 2.8 0.0 0.0 Fg04053 2.0 1.3 0.0 Fg09274 (Kin1/Kin2) 80.7 29.6 3.5 Fg00472 (Sch9) 86.1 58.9 2.6 Fg04770 94.7 111.8 2.5 Fg10095 78.8 70.0 2.3 Fg06793 (Ctk1) 74.5 52.9 2.0 Fg01312 (Rim15) 103.7 3.2 2.0 Fg09612 (Hog1) 44.9 90.6 1.5 Fg03284 (Cka1/Cka2) 89.3 105.9 1.5 Fg05418 (Yak1) 101.2 30.5 1.3 Fg08906 (Prr2) 103.9 62.5 1.4 Fg07344 74.0 16.8 1.0 Fg11812 (Kin4) 80.9 52.0 1.0 a Mutants deleted of the predicted PK genes. Yeast orthologs, if exist, were listed in the bracket. b Percentage of growth rate and conidiation of the mutants in comparison with that of PH-1. c Diseased spikelets per wheat head examined 14 dpi. Only mutants with >30% reduction in growth rate or a disease index 400 ppm) in infested kernels (Table S7). However, DON production was reduced in many of these PK mutants. In 22 mutants, the level of DON in infested wheat kernels was less than 900 ppm. Among them, eight mutants had a disease index less than 5 (Table S7). These results indicate that reduction in DON production was positively correlated with changes in virulence in most of these PK mutants, which is consistent with the importance of DON in plant infection [17], [18]. However, a few PK mutants had no significant changes in DON production, such as the Fg06957 and Fg05547 mutants, but were drastically reduced in virulence (Table S7). Factors other than DON production, such as defects in growth and stress responses, may be responsible for reduced virulence in these mutants. Predicted Networks of PK-PK and PK-Protein Interactions For the protein kinase genes with distinct orthologs in S. cerevisiae, we used the interlog approach to predict their interaction networks in F. graminearum. A total of 231 interactions were identified based on their yeast interlogs (Figure 8). Among them are three MAPK cascades, Fg05484-Fg09903- Fg06385, Fg00408-Fg08691-Fg09612, and Fg06326-Fg07295-Fg10313. Mutants of each MAPK pathway expressed similar phenotypes. Other predicted PK-PK interactions include the Fg04484-Fg09897, Fg10228-Fg08468, and Fg11812-Fg10313 interactions (Figure 9A). Both the Fg04484 and Fg09897 mutants grew faster in the presence of 0.7 M NaCl (Figure 5). 10.1371/journal.ppat.1002460.g008 Figure 8 The predicted interactome of protein kinases in F. graminearum. Orthologs of yeast protein kinases (PKs) were identified and used for the prediction of protein-protein interactions. The PK-PK interaction map was generated with Cytoscape. Three MAP kinase pathways are highlighted in green. 10.1371/journal.ppat.1002460.g009 Figure 9 Verification of predicted PK-PK interactions. A. Different concentrations of yeast cells (cells/ml) of the transformants expressing the labeled bait and prey constructs were assayed for growth on SD-Leu-Trp-His plates. P and N were the positive and negative controls provided in the BD Matchmaker library construct kit. B. The same set of yeast transformants were assayed for β-galactosidase activities. C. Co-IP assays. Western blots of total proteins isolated from transformants expressing the GFP and 3xFLAG fusion constructs as labeled and proteins eluted from anti-FLAG beads were detected with a monoclonal anti-GFP antibody. The same approach was used to predict the interactions of protein kinases with other proteins of F. graminearum. The predicted PK-protein interactome consists of 763 pairs of interactions (Figure S3). The main hubs of predicted networks include Fg08468 (Cdc28), Fg08731 (Hrr25), Fg07855 (Cdc7), Fg01271 (Cdc5), Fg10313 (Mgv1), Fg09897 (Snf1), Fg05393 (Pho85), and Fg10037 (Bud32) (Figure S3). For the two putative Cdc2/Cdc28 orthologs, only Fg08468 was included in this analysis as the representative. It was predicted to interact with 22 protein kinases and 85 other proteins. In S. cerevisiae, HRR25 is involved in regulating diverse events, including vesicular trafficking, DNA repair, and chromosome segregation. FgHrr25 also was predicted to interact with 59 proteins. To verify the predicted interactions, components of the Gpmk1 and Mgv1 MAPK pathway were selected for yeast two-hybrid and co-immunoprecipitation (co-IP) assays. In yeast two-hybrid assays, the FgSte50-Fst7, FgSte50-Fst11, Fst11-Fst7, Fst7-Gpmk1, and FgMmk2 (Fg07295)-Mgv1 interactions were confirmed by growth on SD-His (Figure 9A) and LacZ activities (Figure 9B). FgSte50 was included in this experiment because its ortholog interacts with Ste7 and Ste11 in other fungi [35], [36]. As predicted, the interaction of Fst11 with Gpmk1, Pbs2, or Hog1 was not detected. The FgMmk2-Mgv1 and FgSte7-Gpmk1 interactions were further verified by co-immunoprecipitation (co-IP) assays (Figure 9C). We also used co-IP assays to confirm the predicted interaction between FgKIN4 (Fg11812) and Mgv1 (Figure 9C). Discussion Protein kinases play key regulatory roles in various biological functions in eukaryotic organisms. To systematically characterize the kinome of F. graminearum, we attempted to generate PK gene knockout mutants with the split-marker approach. Among the 96 PK genes that are not essential for vegetative growth, 42 and 45 of them were found to be important for plant infection (Table 2) and sexual reproduction, respectively (Table 3). Before this study, only three protein kinase genes, Mgv1, Gpmk1, and GzSnf1, were known to be important for plant infection in F. graminearum [20], [21], [24]. In this study, we found that the FgSTE11 (Fg05484) and FgSTE7 (Fg09903) genes functioning upstream from GPMK1 (Fg06385) also are important for pathogenesis and sexual reproduction (Table 2; Figure 7). In yeast, the PAK kinase Ste20 functions upstream from the pheromone response pathway. While the Fgste11 and Fgste7 mutants had similar phenotypes with the Gpmk1 mutant, deletion of FgSTE20 (Fg09492) had no obvious phenotypic effect. Interestingly, deletion of FgCLA4 (Fg06957), the only other PAK kinase gene in F. graminearum, resulted in a significant reduction in virulence. However, the Fgcla4 mutant still produced ascospores and was defective in vegetative growth. These results indicate that neither of these two PAK kinases functions upstream from the Gpmk1 pathway. Orthologs of Cla4 are known to function independently of MAPK pathways in plant infection and asexual reproduction in M. oryzae, U. maydis, and Claviceps purpurea [37]–[39]. The Other Two MAPK Pathways also Are Important for Plant Infection and Sexual Reproduction in F. graminearum The FgBck1 (Fg06326)-FgMmk2 (Fg07295)-Mgv1 (Fg10313) MAPK cascade is orthologous to the cell integrity pathway in yeast. Similar to the mgv1 mutant, the Fgbck1 and Fgmmk2 mutants formed small, whitish colonies and were defective in plant infection (Figure 7) as well as production of perithecia (Table 3). They also were defective in hyphal fusion and tended to produce wavy hyphae. In S. cerevisiae, the Pkc1 protein kinase C functions upstream from the yeast cell wall integrity pathway. Like Pkc1 in yeast, FgPKC1 (Fg06268) is an essential gene in F. graminearum. According to the predicted PK-protein interaction networks, Mgv1 have more interacting proteins than the other two MAPKs (Figure S3). Mgv1 may regulate a number of downstream targets, such as the Mig1 and Swi4 orthologs [40], [41] in F. graminearum. The interactions of Mgv1 with FgMmk2 and FgKin4 were confirmed by yeast two-hybrid or co-IP assays. The MAPK cascade orthologous to the yeast HOG pathway [42] also is well conserved in F. graminearum. As expected, the Fgssk2 (Fg00408), Fgpbs2 (Fg08691), and Fghog1 (Fg09612) mutants were hypersensitive to hyperosmotic stresses (Figure 5). These mutants also were significantly reduced in virulence and blocked in sexual reproduction. This MAPK pathway is dispensable for plant infection in M. oryzae but is essential for pathogenesis in Botrytis cinerea and Alternaria alternata [43], [44]. The Fgssk2, Fgpbs2, and Fghog1 mutants had increased sensitivities to H2O2 and reduced growth rate, which may contribute to its defects in plant infection. Interestingly, the osmoregulation pathway appears to regulate the development of aerial hyphae and fruiting bodies in F. graminearum. The Fgssk2, Fgpbs2, and Fghog1 mutants were sterile and rarely produced aerial hyphae on agar pates. Hyphae of these mutants had smaller branching angles and tended to grow in parallel on the surface (Figure S4). These phenotypic effects have not been reported in other fungi. Therefore, it will be important to determine the role of this MAPK pathway in aerial hyphal growth, sexual reproduction, and pathogenesis. Other PK Genes Important for Plant Infection Besides PK genes related to the MAPK and cAMP signaling pathways, over 30 PK mutants were significantly reduced in virulence (Table 2). However, many of them had severe growth defects, which may be directly responsible for reduced virulence. Among the PK mutants with a disease index less than 5, only the Fgyak1 (Fg05418), Fgrim15 (Fg01312), Fgprr2 (Fg08906), and Fg04770 mutants had no significant changes in growth rate. Although these genes are conserved in filamentous ascomycetes, none of them has been reported to be important for pathogenesis in plant pathogens. The Fgrim15 and Fg04770 mutants were reduced in the production of DON (Table S7), which is a critical virulence factor in Fusarium head blight [17]. The Fgyak1 and Fgprr2 mutants rarely spread from the inoculated kernels to nearby spikelets on wheat heads (disease index<1.5). The Fgyak1 mutant had increased sensitivity to H2O2 (Table S6), 0.01% SDS, and 200 µg/ml Congo Red. In S. cerevisiae, Yak1 is known to regulate the stress-responsive transcription factors Hsf1 and Msn2. Fg05418 may have similar functions in F. graminearum. Interestingly, the Fgprr2 mutant had increased tolerance to hyperosmotic and oxidative stresses but was reduced in virulence (Figure 5; 6). The Fgkin4 (Fg11812), Fgsch9 (Fg00472), Fg10095, Fgctk1 (Fg06793), Fgcka1 (Fg03284), Fg07344, Fgsrb10 (Fg04484), and Fgapg1 (Fg05547) mutants had approximately 30% reduction in growth rate but a disease index less than 2.6 (Table 2). None of their orthologs except APG1 is known to be important for plant infection in fungal pathogens. In A. nidulans, the Kin4-related kinase KfsA is implicated in regulating septum formation [45]. The Fgkin4 mutant, similar to the Fgcdc15 mutant, was defective in septum formation (Figure 10), conidiation, and sexual reproduction, further indicating that septation plays a critical role in pathogenesis and development in F. graminearum. In M. oryzae, the ortholog of CDC15 is an important virulence factor [46]. The Fgsch9 mutant was reduced in DON production (Table S7) and had increased sensitivity to oxidative stress (Table S6), which may be related to its reduced virulence. In yeast, Sch9 is functionally related to the PKA and TORC pathways. The role of TOR pathway is not clear in plant pathogenic fungi. The only TOR kinase gene in F. graminearum, Fg08133, is essential (Table 1). 10.1371/journal.ppat.1002460.g010 Figure 10 Septation defects in the Fg10228, Fg11812, and Fg10381 mutants. Germ tubes of the wild type and mutant strains were incubated at 25°C for 18 h. The same fields were observed under DIC (left) and epifluoresence (UV) microscopy. Bar = 20 µm. Arrows point to septa. Septum formation was irregular in the Fg11812 mutant, but the Fg10381 and Fg10228 mutants rarely produced septa. Orthologs of APG1 and autophagy are known to be important for pathogenesis in M. oryzae and U. maydis [47], [48]. It is likely that the Fgapg1 mutant had similar defects in autophagy and infectious growth. Orthologs of CTK1 and SRB10 are involved in cell division in S. cerevisiae but have not been characterized in plant pathogenic fungi. The Fgctk1 and Fgsrb10 mutants all had pleiotropic defects in growth, conidiation, sexual reproduction, and plant infection (Tables 3). These two genes are likely involved in basic cellular processes, such as cell cycle or cytokinesis in F. graminearum. Protein Kinase Genes and Sexual Reproduction Because ascospores are the primary inoculum, sexual reproduction is a critical stage of wheat scab disease cycle. A total of 45 PK genes, including all 12 members of the STE group, were found to be important for sexual reproduction. Many of these mutants also were defective in vegetative growth and plant infection. However, several PK genes, including Fg01058, Fg01347, and Fg06970 appear to play more specific or important roles in sexual reproduction. Deletion of these genes had no other significant phenotypic changes. Although deletion of Fg01058 or Fg01347 only resulted in defects in ascospore release, the Fg06970 mutant failed to produce perithecia (Table 3). Whereas Fg01058 is unique to filamentous fungi, Fg01347 is orthologous to yeast Bub1, a protein kinase phosphorylated by Cdc28 and involved in cell cycle checkpoint. Fg06970 is orthologous to yeast Psk1 and Psk2, two PAS domain-containing protein kinases that regulate protein synthesis and carbohydrate metabolism and storage [49]. Besides the Fg06970 mutant, 19 additional mutants that were blocked in perithecium formation. These mutants may be defective in female fertility or in the switch from vegetative growth to sexual reproduction. In the budding yeast, the Smk1, Mek1, Sak1, and Ime2 kinases are required for sporulation. F. graminearum and other filamentous ascomyctes lack Smk1 and Mek1 orthologs. MEK1 is a meiosis-specific protein kinase, and Smk1 MAPK regulates late stages of ascospore formation. Whereas the yeast ime2 and sak1 mutants are defective in sporulation, the Fgime2 (Fg04418) and Fgsak1 (Fg01641) mutants still produced ascospores, although the latter two mutants had pleiotropic defects. These observations indicate that ascospore formation is regulated by different mechanisms in F. graminearum than in S. cerevisiae. However, the Fgctk1 (Fg06973), Fgcak1 (Fg04947), Fgkic1 (Fg05734), Fgswe1 (Fg10228), and Fgdbf1 (Fg08635) mutants were aborted in ascus or ascospore development (Table 3). Their orthologs also are involved in sexual reproduction in yeast. Therefore, some genetic elements are conserved between yeast and filamentous fungi for sexual reproduction. Essential PK Genes in F. graminearum Among the 20 PK genes for which we failed to isolate knockout mutants in F. graminearum, most of their orthologs are essential genes in S. cerevisiae, S. pombe, or A. nidulans (Table 1). The CBK1, KIC1, and other RAM complex genes are essential in the wild type but not in the ssd1 mutant of S. cerevisiae [50]. F. graminearum has an ortholog of SSD1 (Fg07009), but deletion of FgCBK1 or FgKIC1 is not lethal (Table 1). Although deletion of individual genes is not lethal, the phk1 phk2 and ypk1 ypk2 double mutants are not viable. Fg10725 and Fg05845 are orthologs of the yeast Pkh1/Pkh2 and Ypk1/Ypk2 kinases, respectively. The downstream targets of Pkh1 and Pkh2 include Pkc1, Ypk1, and Ypk2. Ypk1 phosphorylates and down-regulates the Fpk1 kinase, a known flippase activator [51]. In F. graminearum, the Fgfpk1 (Fg04382) deletion mutant was reduced in growth and had increased sensitivities to hyperosmotic and oxidative stresses. Deletion of PHO85, IRE1, KNS1, or VPS1 is not lethal in S. cerevisiae, but we failed to identify knockout mutants of their orthologs in F. graminearum (Fg05393, Fg05775, Fg06637, and Fg05306). The ortholog of VPS1 in A. nidulans, VPSA, is involved in vacuole biogenesis. The vpsA mutant is viable but has poor vegetative growth [52]. In yeast, PHO85 encodes a cyclin-dependent kinase (CDK) involved in the regulation of cellular responses to nutrient levels and environmental conditions. In A. nidulans, phoA and phoB are two CDKs homologous to PHO85. Although deletion of phoA or phoB is not lethal, the phoA phoB double mutant is not viable, suggesting an essential role for PhoA and PhoB in cell cycle control and morphogenesis [53]. F. graminearum and many other filamentous fungi have only one PHO85 ortholog. In U. maydis and C. neoformans, deletion of the PHO85 ortholog is lethal [54], [55]. F. graminearum Uniquely Has Two Aurora Kinase Genes Aurora kinases regulate chromosome condensation and segregation during cellular division. In S. cerevisiae, deletion of the IPL1 gene is lethal. The aurora kinase gene ark1 also is essential in S. pombe. Similar to the yeasts, all of the sequenced filamentous fungi, including F. verticillioides and F. oxysporum, have a single aurora kinase gene. In contrast, F. graminearum has two aurora kinase genes, Fg06959 and Fg02399. Whereas Fg06959 appears to be an essential gene, deletion of Fg02399 had no significant phenotypic effects other than reduced conidiation (Table 2). Cell Cycle- or Cytokinesis-related Kinase Genes Important for Pathogenesis Similar to their orthologs in yeast, the FgCDC5 (Fg01271), FgCDC7 (Fg07855), FgTEL1 (Fg06089), FgMPS1 (Fg01137), FgSGV1 (Fg07409), and FgNIMA (Fg09408) genes are essential in F. graminearum. Most likely, they have conserved functions in F. graminearum. While Kin3 is not essential in S. cerevisiae, its ortholog, NimA, is required for the regulation of mitosis in A. nidulans [56]. In contrast, CDC15 is essential in yeast but deletion of its ortholog in A. nidulans (SEPH) is not lethal [57]. In F. graminearum, the Fgcdc15 (Fg10381) deletion mutant was reduced in vegetative growth and conidiation. It was significantly reduced by not blocked in septation in conidia (Figure 3C) and hyphae (Figure 10). Both Fg00677 and Fg03284 are orthologous to CKA1, which encodes the alpha catalytic subunit of casein kinase 2 (CK2) that is essential for cell cycle progression and proliferation in yeast. Although Fg00677 is essential in F. graminearum, the Fg03284 deletion mutant had no obvious defects in growth and conidiation but was significantly reduced in virulence. In C. albicans, the homozygous cka2 but not cka1 mutant has attenuated virulence in the mouse model of oropharyngeal candidiasis [58]. However, the phenotype of the cka2 mutant can be suppressed by overexpression of CKA1. It is possible that Fg00677 and Fg03284 have similar functional relationship in F. graminearum. In S. cerevisiae, SWE1 is not essential but plays important roles in the cell cycle. The ANKA kinase gene, an ortholog of SWE1, also is involved in the regulation of septation and cell cycle checkpoint responses [59]. In F. graminearum, the Fgswe1 (Fg10228) mutant was reduced in septation (Figure 10). However, it had pleiotropic defects hyphal growth, conidiation, and plant infection. In yeast, Swe1-mediated inhibition of Cdc28 is important for its checkpoint functions and pseudohyphal growth. FgSWE1 may be important for infectious growth in planta in F. graminearum. The SWE1 ortholog is essential in U. maydis [60]. Only One of the PK Genes Related to DNA Damage Response Is Important for Plant Infection in F. graminearum In S. cerevisiae, Rad53 is required for cell-cycle arrest in response to DNA damage. Two of the downstream targets of Rad53 are Dun1 and Dbf4. In F. graminearum, the Fgrad53 (Fg00433) mutant had no obvious defects other than reduced conidiation. Whereas the Fgdun1 (Fg07121) mutant had no detectable phenotypes, F. graminearum, like many other filamentous fungi, lacks a distinct ortholog of Dbf4, an essential gene required for the initiation of DNA replication. Chk1 is the other kinase functional as a DNA damage checkpoint effector in yeast and other eukaryotes [61]. Similar to the Fgrad53 mutant, the Fgchk1 (Fg01506) deletion mutant were normal in growth and plant infection but had increased sensitivity to UV irradiation. It appears that FgRad53 and FgChk1 kinases are important for DNA damage repair but dispensable for pathogenesis in F. graminearum. In yeast, both Rad53 and Chk1 are phosphorylated by Mec1, an essential gene involved in the cell cycle checkpoint control in response to DNA damage. In F. graminearum, deletion of FgMEC1 (Fg13318) was not lethal but the Fgmec1 mutant was significantly reduced in virulence. It also was reduced in growth rate, conidiation, had increased sensitivity to H2O2. In A. nidulans, the AtmA and UvsB kinases, orthologs of Tel1 and Mec1, also are functionally related in regulating DNA damage responses and act upstream from the ChkA and ChkB check point kinases [62]. PK Genes with No Distinct Orthologs in S. cerevisiae Among the 28 F. graminearum PK genes that lack distinct orthologs in S. cerevisiae, four of them have orthologs in S. pombe (Table S8). Whereas the function of ppk23 is not clear, the intracellular gradient of Pom1 is used as the sensor for cell length in S. pombe [63]. In F. graminearum, the Fgppk23 (Fg05406) mutant had no phenotype other than reduced conidiation. The Fgpom1 (Fg10095) mutant was defective in plant infection, DON synthesis, and sexual reproduction although it was only slightly reduced in conidiation and vegetative growth. Although prp4 and sid1 are essential genes in S. pombe, the Fgsid1 (Fg07344) and Fgprp4 (Fg04053) mutants were viable but displayed pleiotrophic defects. The Fgprp4 mutant has severe growth defects. Prp4 is involved in spliceosome functions in S. pombe [64]. Interestingly, the Fgprp4 mutant was unstable. We had identified over a dozen spontaneous suppressor mutants with faster growth rate. Further characterization of the Fgprp4 mutant and suppressor mutations will be useful to determine the role this protein kinase in RNA splicing and fungal pathogenesis. For 15 of the other 24 PK genes that appear to be specific for filamentous fungi, their knockout mutants had no obvious phenotypic changes (Table S7). Some of them may be not true PK genes. Among the rest 9 genes, deletion of Fg09150 resulted in approximately 80% reduction in conidiation but had no other detectable phenotypic effect. In contrast, the Fg01058 mutant was defective only in ascospore morphology and release, suggesting that these two PK genes have specific functions during asexual and sexual reproduction, respectively. The Fg00792, Fg01559, Fg02488, and Fg06420 mutants were slightly reduced in DON production but had no significant defects in plant infection. Therefore, Fg00362, Fg03146, and Fg04770 are the only three PK genes that are absent in the yeasts but important for plant infection in F. graminearum (Table S8). The Fg00362 mutant grew poorly (Table 2). POD-6, an ortholog of Fg00362, has been functionally characterized in N. crassa [10]. It interacts with COT-1 and plays a critical role in hyphal growth. Their orthologs likely have conserved functions in F. graminearum because the Fgpod6 and Fgcot1 mutants had the same growth defects (Figure S2). In contrast, the Fg03146 and Fg04770 mutants had no obvious defects in growth. Orthologs of Fg03146 and Fg04770 have not been characterized in filamentous fungi. It will be important to further characterize these two novel fungal virulence factors. Materials and Methods Identification of PK Genes Protein sequences of F. graminearum were searched against the Kinomer v.1.0 HMM library using the HMMSCAN program from the HMM software suite HMMer (version 3.0 for windows) to identify and classify protein kinases as described [3], [65]. The cut off value was set to 20. We also searched for additional putative PK genes that are predicted by the Broad Institute (www.broadinstitute.org/annotation/genome/fusarium_graminearum) or MIPS (mips.helmholtz-muenchen.de/genre/proj/FGDB) to contain the protein kinase domain (Pkinase, PF00069). Phylogenetic analysis was conducted with MEGA version 5 [66]. The catalytic domain sequences were aligned with COBALT [67] and trimmed with trimAl [68]. The maximum likelihood phylogeny tree was visualized using Interactive Tree Of Life Version 1.9 (http://itol.embl.de/#). Generation of the Knockout Mutants The split-marker approach [19] was used to generate the gene replacement constructs for the PK genes. The primers used to amplify the flanking sequences for each gene are available at fgkinome.nwsfau.edu.cn. The resulting PCR products were transformed into protoplasts of the wild-type strain PH-1 [69] as described [17], [20]. Hygromycin B (Calbiochem, La Jolla, CA) was added to a final concentration of 250 µg/ml for transformant selection. Putative knockout mutants identified by screening with primers F5 and R6 were further analyzed by PCR with primers F7 and H856R or primers H855F and R8 to confirm the gene replacement events (Figure S1). All of the mutants generated in this study were preserved in 15% glycerol at −80°C. Assays for Growth and Conidiation Defects Colony morphology and growth rate were assayed with potato dextrose agar (PDA) cultures grown at 25°C for three days. Conidiation was assayed with 5-day-old CMC cultures as described [20], [70]. Conidium morphology was examined and photographed with an Olympus BX-51 microscope. For assaying conidium germination and germ tube growth, freshly harvested conidia were cultured in liquid YEPD medium for 12 h. Slab cultures grown on a thin layer of complete medium (CM) for 36 h were examined for defects in hyphal tip growth and branching [20], [70]. Assays for Defects in Sexual Reproduction and Stress Responses Aerial hyphae of 7-day-old carrot agar cultures were pressed down with 300 µl of sterile 0.1% Tween 20. Perithecium formation and cirrhi production were assayed after incubation at 25°C for 2 weeks. For mutants that formed perithecia but failed to produce cirrhi 3-4 weeks after fertilization, at least 10 perithecia were examined for ascospores and ascogenous hyphae. For assaying sensitivities to various stresses, vegetative growth was assayed on PDA plates with 0.7 M NaCl, 0.05% H2O2, 0.01% SDS, or 200 µg/ml Congo Red [71]. Plant Infection and DON Production Assays Conidia harvested from 5-day-old CMC cultures were resuspended to 106 spores/ml. Flowering wheat heads of cultivar Xiaoyan 22 were drop-inoculated with 10 µl of conidium suspensions at the fifth spikelet from the base of the inflorescence [72], [73]. After the inoculation, wheat heads were capped with a plastic bag for 48 h to maintain the moisture. Spikelets with typical symptoms were examined 14 days post-inoculation (dpi). Diseased wheat kernels were pooled to assay for DON production as described [20]. For stalk rot assays, 8-week-old corn plants of cultivar Pioneer 2375 were inoculated as described [70], [74] and assayed for symptoms 14 dpi. Infection assays with corn silks were conducted as described [20]. Prediction of Protein-Protein Interactions (PPIs) The protein-protein interaction (PPI) networks of S. cerevisiae were downloaded from the Database of Interacting Proteins (DIP, dip.doe-mbi.ucla.edu/dip) and SGD (www.yeastgenome.org). Orthologous pairs of F. graminearum and S. cerevisiae genes were obtained from the Inparanoid database [75] and by BlastP searches. To strengthen the reliability of predicted interactions, the bit score cut off value was set to 200. The predicted PPI interaction map was generated with the Cytoscape program [76]. Yeast Two-Hybrid Assays Protein-protein interactions were assayed with the Matchmaker yeast two-hybrid system (Clontech, Mountain View, CA). ORFs of the GPMK1, FgSTE50 (Fg04101), and FgSTE7 (Fg09903) were amplified from first-strand cDNA of PH-1 and cloned into pGBK7 (Clontech) as the bait constructs. For the FgSTE11 (Fg05484), FgHOG1 (Fg09612), and FgPBS2 (Fg08691) genes, their ORFs were amplified and cloned into pGADT7 as the prey constructs. Prey constructs also were generated for the GPMK1 and FgSTE50 genes. The resulting bait and prey vectors were co-transformed in pairs into yeast strain AH109 (Clontech). The Leu+ and Trp+ transformants were isolated and assayed for growth on SD-Trp-Leu-His medium and galactosidase activities with filter lift assays as described [77]. The positive and negative controls were provided in the Matchmaker Library Construction & Screening Kits (Clontech). Co-immunoprecipitation (co-IP) Assays The GPMK1 and MGV1 genes were amplified and cloned into pDL2 by the yeast gap repair approach [78], [79] to generate the 3xFLAG fusion constructs. Similar approaches were used to generate the GFP fusion constructs for the FgMMK2 (Fg07295), FgKIN4 (Fg11812),and FgSTE7 (Fg09903) genes with the pFL3 vector [80]. The resulting fusion constructs were verified by DNA sequencing and transformed in pairs into PH-1. Transformants expressing pairs of fusion constructs were confirmed by western blot analysis. For co-IP assays, total proteins were isolated and incubated with the anti-FLAG M2 beads as described [81]. Proteins eluted from beads were analyzed by western blot detection with a monoclonal anti-GFP (Roche, Indianapolis, IN) antibody. Supporting Information Figure S1 PCR primers used for the generation and identification of gene replacement mutants. The arrows indicate the directions of the primers. (EPS) Click here for additional data file. Figure S2 Growth defects of the Fgcot1 (Fg01188), Fgpod6 (Fg00362), and Fgprp4 (Fg04053) mutants. Colony morphology (colony), hyphal growth on complete medium (CM) slab agar (agar), and hyphae cultured in liquid CM (liquid). (EPS) Click here for additional data file. Figure S3 Predicted interactions of protein kinases with other proteins of F. graminearum. Orthologs of interacting proteins in S. cerevisiae were identified and used for the prediction of protein kinase (PK)-protein interactions. The PK-protein interaction map was generated with Cytoscape. (EPS) Click here for additional data file. Figure S4 Defects of the osmoregulation MAPK pathway mutants in aerial hyphal growth and branching. (EPS) Click here for additional data file. Table S1 Putative protein kinase genes in Fusarium graminearum. (DOC) Click here for additional data file. Table S2 Protein kinase genes that are closely linked to each other in F. graminearum. (DOC) Click here for additional data file. Table S3 Expression profiles of protein kinase genes during barley infection, sexual development, and conidium germination. (DOC) Click here for additional data file. Table S4 The Pearson correlation efficient between major phenotypes. (DOC) Click here for additional data file. Table S5 Mutants with defects in germ tube (GT) growth. (DOC) Click here for additional data file. Table S6 Mutants with altered responses to stresses. (DOC) Click here for additional data file. Table S7 Kinase mutants with 30% reduction in DON production. (DOC) Click here for additional data file. Table S8 Mutant phenotypes of 28 F graminearum PK genes with no distinct orthologs in S. cerevisiae. (DOC) Click here for additional data file.
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Generation of reactive oxygen species by fungal NADPH oxidases is required for rice blast disease.
Martin J. Egan, Zheng-Yi Wang, Mark Jones … (2007)
One of the first responses of plants to microbial attack is the production of extracellular superoxide surrounding infection sites. Here, we report that Magnaporthe grisea, the causal agent of rice blast disease, undergoes an oxidative burst of its own during plant infection, which is associated with its development of specialized infection structures called appressoria. Scavenging of these oxygen radicals significantly delayed the development of appressoria and altered their morphology. We targeted two superoxide-generating NADPH oxidase-encoding genes, Nox1 and Nox2, and demonstrated genetically, that each is independently required for pathogenicity of M. grisea. Deltanox1 and Deltanox2 mutants are incapable of causing plant disease because of an inability to bring about appressorium-mediated cuticle penetration. The initiation of rice blast disease therefore requires production of superoxide by the invading pathogen.
Author and article information
Journal
Journal ID (nlm-ta): Sci Rep
Journal ID (iso-abbrev): Sci Rep
Title:
Scientific Reports
Publisher:
Nature Publishing Group
ISSN
(Electronic):
2045-2322
Publication date
(Electronic):
12
April
2016
Publication date Collection: 2016
Volume: 6
Electronic Location Identifier: 24325
Affiliations
[1
]State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University , Wuhan 430070, Hubei Province, P R China
Author notes
Article
Publisher Item ID: srep24325DOI: 10.1038/srep24325
PMC ID: 4828707
PubMed ID: 27066837
SO-VID: a72e726f-2935-4cd1-b178-044d6f7b33fa
Copyright © Copyright © 2016, Macmillan Publishers Limited
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This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
History
Date
received
: 30
October
2015
Date
accepted
: 24
March
2016
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Subject:
Article
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