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BACKGROUND: Wheat crown rot (WCR), primarily caused by Fusarium pseudograminearum has become more and more prevalent in winter wheat areas in China. However, limited fungicides have been registered for the control of WCR in China so far. Pyraclostrobin is a representative quinone outside inhibitor (QoI) with excellent activity against Fusarium spp. There is currently limited research on the resistance risk and resistance mechanism of F. pseudograminearum to pyraclostrobin. RESULTS: Here, we determined the activity of pyraclostrobin against F. pseudograminearum. The EC50 values ranged from 0.022 to 0.172 μg mL−1 with an average EC50 value of 0.071 ± 0.030 μg mL−1. Four highly pyraclostrobin‐resistant mutants were obtained from two sensitive strains by ultraviolet (UV) mutagenesis in the laboratory. The mutants showed decreased mycelial growth rate and virulence as compared with the corresponding wild‐type strains, indicating that pyraclostrobin resistance suffered a fitness penalty in F. pseudograminearum. It was found that the high resistance of four mutants was caused by the G143S mutation in Cytb. Molecular docking analysis also further confirms that the G143S mutation in Cytb decreased the binding affinity between pyraclostrobin and Cytb. CONCLUSION: The resistance risk of F. pseudograminearum to pyraclostrobin could be low to medium. Although a mutation at the G143S position of Cytb could potentially occur, this mutation decreases the fitness of the mutant, which may reduce its survival in the environment. Therefore, the negative consequences of a possible mutation are lower. This makes pyraclostrobin a good candidate for controlling crown rot in wheat. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

BACKGROUND: Negative cofactor 2 NC2β (Ncb2 or Dr1) is the beta subunit of a conserved heterodimeric regulator of transcription negative cofactor 2 (NC2) complex that has been identified as key regulator of drug resistance in model fungi. However, its role in plant pathogens is still unclear. RESULTS: We identified an NC2β orthologue, FpNcb2, in Fusarium pseudograminearum, which is not only a significant regulatory function in drug resistance, but also essential for growth, conidiation and penetration. Moreover, FpNcb2 undergoes alternative splicing which creates two mRNA isoforms. As a putative CCAAT binding protein, FpNcb2 concentrates in the nuclei, contributing to the expression of two spliced mRNA of FpNcb2 in hypha, conidiophores and conidia, with exception of FpNcb2ISOA in germlings. Expression of each spliced mRNA of FpNcb2 in Δfpncb2 mutant could full complement the defects on growth, conidiation and fungicides sensitivity to that of wild type. However, FpNcb2ISOA and FpNcb2ISOB have different effects on virulence. FpNcb2 acts as a regulator for the transcription of some genes encoding drug efflux and hydrolases. CONCLUSION: Our analysis showed the existence of alternative mRNA splicing in the NC2β orthologue, which is associated with protein subcellular localization and fungal virulence. The further elucidation of the target genes of NC2β will provide insights into the potential regulation mechanisms in the antifungal resistance and pathogenesis of F. pseudograminearum. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

The worldwide occurrence of wheat crown rot, predominantly caused by the pathogen Fusarium pseudograminearum, has a serious impact on wheat production. Numerous microorganisms have been employed as biocontrol agents, exhibiting effectiveness in addressing a wide array of plant pathogens through various pathways. The mycelium of the white-rot fungus Phanerochaete chrysosporium effectively inhibits the growth of F. pseudograminearum by tightly attaching to it and forming specialized penetrating structures. This process leads to the release of intracellular inclusions and the eventual disintegration of pathogen cells. Furthermore, volatile organic compounds and fermentation products produced by P. chrysosporium exhibit antifungal properties. A comprehensive understanding of the mechanisms and modalities of action will facilitate the advancement and implementation of this biocontrol fungus. In order to gain a deeper understanding of the mycoparasitic behavior of P. chrysosporium, transcriptome analyses were conducted to examine the interactions between P. chrysosporium and F. pseudograminearum at 36, 48, and 84 h. During mycoparasitism, the up-regulation of differentially expressed genes (DEGs) encoding fungal cell-wall-degrading enzymes (CWDEs), iron ion binding, and mycotoxins were mainly observed. Moreover, pot experiments revealed that P. chrysosporium not only promoted the growth and quality of wheat but also hindered the colonization of F. pseudograminearum in wheat seedlings. This led to a delay in the development of stem base rot, a reduction in disease severity and incidence, and the activation of the plant's self-defense mechanisms. Our study provides important insights into the biocontrol mechanisms employed by P. chrysosporium against wheat crown rot caused by F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR), mainly caused by Fusarium pseudograminearum, is a serious fungal disease that affects wheat yield. To determine the inhibitory activity of metconazole to F. pseudograminearum in Henan province, the toxicity of metconazole against three randomly selected isolates (JY2208, HB2201, and XC2116) at different developmental stages was determined from 219 isolates tested. The combined toxicity of metconazole with prochloraz, phenamacril, fluazinam, and fludioxonil against isolate JY2208 was determined according to the mass ratio of 5 : 1, 3 : 1, 1 : 1, 1 : 3, 1 : 5. The indoor control efficacy of metconazole against FCR was determined by the wheat coleoptile inoculation method. The results showed that the average EC50 values of mycelium growth, sporulation quantity, spore germination, and germ tube elongation of three isolates were (0.0397 ± 0.0035) μg/mL, (0.9549 ± 0.1152) μg/mL, (0.6114 ± 0.0393) μg/mL, and (0.0235 ± 0.0015) μg/mL, respectively. The EC50 values of metconazole, inhibiting mycelium growth of 219 isolates of F. pseudograminearum, ranged from 0.0207 to 0.0839 μg/mL, with an average value of (0.0406 ± 0.0114) μg/mL. The sensitivity frequency distribution was a continuous single-peak curve, which could serve as the baseline sensitivity of F. pseudograminearum to metconazole in Henan Province. The synergy ratios (SR) of metconazole combined with prochloraz, phenamacril, fluazinam, and fludioxonil ranged from 0.51 to 2.32. Different combinations and ratios of the mixture demonstrated either additive inhibition or synergistic inhibition efficacy. These results indicated that metconazole can be used in combination with prochloraz, phenamacril, fluazinam, and fludioxonil. Metconazole and fluazinam, with a mass ratio of 5 : 1, exhibited the strongest synergistic inhibition effect, achieving the maximum synergy ratio, with an SR of 2.32. Under laboratory conditions, the combination of 8% metconazole suspension and 50% fluazinam suspension, with the active ingredient of mass ratio of 5 : 1, achieved 100% control efficacy at the concentration of 80 μg/mL. These results could provide a basis for controlling the Fusarium crown rot caused by F. pseudograminearum. [ABSTRACT FROM AUTHOR]

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Fusarium pseudograminearum causes destructive crown disease in wheat. The velvet protein family is a crucial regulator in development, virulence, and secondary metabolism of fungi. We conducted a functional analysis of FpVelB using a gene replacement strategy. The deletion of FpVelB decreased radial growth and enhanced conidial production compared to that of wild type. Furthermore, FpVelB modulates the fungal responses to abiotic stress through diverse mechanisms. Significantly, virulence decreased after the deletion of FpVelB in both the stem base and head of wheat. Genome-wide gene expression profiling revealed that the regulation of genes by FpVelB is associated with several processes related to the aforementioned phenotype, including "immune", "membrane", and "antioxidant activity", particularly with regard to secondary metabolites. Most importantly, we demonstrated that FpVelB regulates pathogen virulence by influencing deoxynivalenol production and modulating the expression of the PKS11 gene. In conclusion, FpVelB is crucial for plant growth, asexual development, and abiotic stress response and is essential for full virulence via secondary metabolism in F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) is an important and devastating disease of wheat (Triticum aestivum) caused by the fungus Fusarium pseudograminearum and related pathogens. Using two distinct susceptible cultivars, we investigated the isolation frequencies of F. pseudograminearum and quantified its biomass accumulation and the levels of the associated toxins deoxynivalenol (DON) and DON-3-glucoside (D3G) in inoculated field-grown wheat plants. We detected F. pseudograminearum in stem, peduncle, rachis, and husk tissues, but not in grains, whereas DON and D3G accumulated in stem, rachis, husk, and grain tissues. Disease severity was positively correlated with the frequency of pathogen isolation, F. pseudograminearum biomass, and mycotoxin levels. The amount of F. pseudograminearum biomass and mycotoxin contents in asymptomatic tissue of diseased plants were associated with the distance of the tissue from the diseased internode and the disease severity of the plant. Thus, apparently healthy tissue may harbor F. pseudograminearum and contain associated mycotoxins. This research helps clarify the relationship between F. pseudograminearum occurrence, F. pseudograminearum biomass, and mycotoxin accumulation in tissues of susceptible wheat cultivars with or without disease symptoms, providing information that can lead to more effective control measures. [ABSTRACT FROM AUTHOR]

ABSTRACT Fusarium pseudograminearum, a soil-borne fungus, is the cause of the devastating wheat disease known as wheat crown rot (WCR). The persistence of this pathogen in the soil and crop residues contributes to the increased occurrence and severity of WCR. Therefore, developing effective strategies to prevent and manage WCR is of great importance. In this study, we isolated a bacterial strain, designated as SR9, from the stem of wheat, that exhibited potent antagonistic effects against F. pseudograminearum, as well as the biocontrol efficacy of SR9 on WCR was quantified at 83.99% ± 0.11%. We identified SR9 as Pseudomonas khavaziana and demonstrated its potential as a plant probiotic. SR9 displayed broad-spectrum antagonism against other fungal pathogens, including Neurospora dictyophora, Botrytis californica, and Botryosphaeria dothidea. Whole-genome sequencing analysis revealed that SR9 harbored genes encoding various cell wall-degrading enzymes, cellulases, and lipases, along with antifungal metabolites, which are responsible for its antagonistic activity. Gene knockout and quantitative PCR analyses reveal that phenazine is the essential factor for antagonism. SR9 possessed genes related to auxin synthesis, flagellar biosynthesis, biofilm adhesion, and the chemotaxis system, which play pivotal roles in plant colonization and growth promotion; we also evaluated the effects of SR9 on plant growth in wheat and Arabidopsis. Our findings strongly suggest that SR9 holds great promise as a biocontrol agent for WCR in sustainable agriculture.IMPORTANCEThe escalating prevalence of wheat crown rot, primarily attributed to Fusarium pseudograminearum, necessitates the development of cost-effective and eco-friendly biocontrol strategies. While plant endophytes are recognized for their biocontrol potential, reports on effective strains targeting wheat crown rot are sparse. This study introduces the Pseudomonas khavaziana SR9 strain as an efficacious antagonist to the wheat crown rot pathogen Fusarium pseudograminearum. Demonstrating a significant reduction in wheat crown rot incidence and notable plant growth promotion, SR9 emerges as a key contributor to plant health and agricultural sustainability. Our study outlines a biological approach to tackle wheat crown rot, establishing a groundwork for innovative sustainable agricultural practices.

Fusarium crown rot (FCR) in wheat is a prevalent soil-borne disease worldwide and poses a significant threat to the production of wheat (Triticum aestivum) in China, with F. pseudograminearum being the dominant pathogen. Currently, there is a shortage of biocontrol resources to control FCR induced by F. pseudograminearum, along with biocontrol mechanisms. In this study, we have identified 37 strains of biocontrol bacteria displaying antagonistic effects against F. pseudograminearum from over 8000 single colonies isolated from soil samples with a high incidence of FCR. Among them, QY43 exhibited remarkable efficacy in controlling FCR. Further analysis identified the isolate QY43 as Pseudomonas aeruginosa, based on its colony morphology and molecular biology. In vitro, QY43 significantly inhibited the growth, conidial germination, and the pathogenicity of F. pseudograminearum. In addition, QY43 exhibited a broad spectrum of antagonistic activities against several plant pathogens. The genomics analysis revealed that there are genes encoding potential biocontrol factors in the genome of QY43. The experimental results confirmed that QY43 secretes biocontrol factor siderophores and pyocyanin. In summary, QY43 exhibits a broad spectrum of antagonistic activities and the capacity to produce diverse biocontrol factors, thereby showing substantial potential for biocontrol applications to plant disease. [ABSTRACT FROM AUTHOR]

In China, Fusarium pseudograminearum has emerged as a major pathogen causing Fusarium crown rot (FCR) and caused significant losses. Studies on the pathogen's properties, especially its mating type and trichothecene chemotypes, are critical with respect to disease epidemiology and food/feed safety. There are currently few available reports on these issues. This study investigated the species composition, mating type idiomorphs, and trichothecene genotypes of Fusarium spp. causing FCR in Henan, China. A significant shift in F. pseudograminearum-induced FCR was found in the present study. Of the 144 purified strains, 143 were F. pseudograminearum, whereas only 1 Fusarium graminearum was identified. Moreover, a significant trichothecene-producing capability of F. pseudograminearum strains from Henan was observed in this work. Among the 143 F. pseudograminearum strains identified, F. pseudograminearum with a 15ADON genotype was found to be predominant (133 isolates), accounting for 92.36% of all strains, followed by F. pseudograminearum with a 3ADON genotype, whereas only one NIV genotype strain was detected. Overall, a relatively well-balanced 1:1 ratio of the F. pseudograminearum population was found in Henan. To the best of our knowledge, this is the first study that has examined the Fusarium populations responsible for FCR across the Henan wheat-growing region. [ABSTRACT FROM AUTHOR]

In the past decade, due to straw incorporation and soil salinization, wheat crown rot (FCR) mainly caused by Fusarium pseudograminearum has become widespread in the Huang-Huai wheat-growing region of China. It poses a serious threat to the high and stable yield of wheat and has brought potential toxin pollution to animal feed made from wheat straw. The phenylpyrrole fungicide fludioxonil is widely used in seed dressing or coating. Previous studies of our research group have shown that fludioxonil has a strong inhibitory effect on the mycelial growth of F. pseudograminearum, but the mechanism of inhibition has remained unclear. In this paper, the inhibitory mechanism of fludioxonil on the mycelial growth of F. pseudograminearum was studied, and the inhibitory effect of fludioxonil on spore germination, germ tube elongation and sporulation were evaluated, and the field control efficacy of fludioxonil on FCR was determined. The results showed that fludioxonil made the mycelium of F. pseudograminearum malformed as follows: the top mycelium branches increased, the mycelium became dense, the mycelium spacing became shorter; mycelial cells in the colony became irregularly enlarged, branches increased but were short and uneven in thickness, had blunt round top or were enlarged. Compared with mycelial growth, the inhibitory effect of fludioxonil on conidial germination was weaker, and the EC50 value to conidial germination was 7.2358–55.3856 μg/mL. However, fludioxonil delayed the germination time of conidia and increased the probability of conidia germination from intermediate cells. Fludioxonil also recorded a strong inhibitory effect on germ tube elongation, and the EC50 to germ tube elongation was only 0.0078 μg/mL. Fludioxonil caused conidial cells enlargement, but the teratogenic effect on the germ tube was not obvious. Fludioxonil could also delay the formation time of conidia. In the mung bean soup liquid medium containing fludioxonil, it took 72 h to form conidia, while 0.8 μg/mL completely inhibited conidia formation. The EC50 values of fludioxonil to sporulation ranged from 0.1439–0.2739 μg/mL. The control efficacies of fludioxonil against FCR at the jointing and filling stages of wheat were better than that of carbendazim, and it reduced the whiteheads rate at the milk stage, but decreased the control efficacy at the filling stage. Fludioxonil could be used as a seed dressing agent in the prevention and control of FCR. [ABSTRACT FROM AUTHOR]

Crown rot (CR; Fusarium pseudograminearum) is a serious disease in winter cereals. Soil type, temperature, nutrients, water availability and stubble‐borne inoculum levels play major roles in determining disease severity. This paper reports the impact of two different watering regimes on the disease severity and gas exchange of F. pseudograminearum infected bread wheat for the first time. Fusarium pseudograminearum inoculated and noninoculated genotypes with different susceptibility to CR were watered to either field capacity or a reduced watering regime in three controlled environment experiments. Rate of photosynthesis, stomatal conductance, internal CO2 concentration and transpiration rate were measured using a portable photosynthesis system, together with disease severity of leaf sheaths at 28 days after planting. Significant differences in disease severity were reported between watering treatments with reduction in CR symptoms in the partially resistant genotypes in the reduced water treatment. Photosynthesis, stomatal conductance and transpiration rate were significantly decreased across most genotypes when inoculated with F. pseudograminearum. Differences in gas exchange between inoculum treatments were more evident in plants watered to field capacity. Water availability has been reported to be one of the crucial factors for initiating F. pseudograminearum infection and subsequent development of CR disease. This research demonstrates significant variation in genotype‐related responses to the complex interactions of F. pseudograminearum infection and water treatment, with a negative impact of both limited soil water availability and CR disease severity on plant gas exchange in bread wheat. [ABSTRACT FROM AUTHOR]

BACKGROUND: Wheat Fusarium crown rot (FCR) is a serious problem primarily caused by Fusarium pseudograminearum, a pathogenic agent known to produce mycotoxins, including deoxynivalenol (DON). Cyclobutrifluram, a novel succinate dehydrogenase inhibitor devised by Syngenta, has immense potential to control both nematodes and Fusarium diseases. However, its efficacy in combating Fusarium species, its ability to prevent and reverse the detrimental effects of FCR, and its impact on the production of DON by F. pseudograminearum are yet to be fully ascertained. RESULTS: Cyclobutrifluram exhibited substantial inhibitory activity against Fusarium species, with half‐maximal effective concentration values ranging from 0.0021–0.0647 μg mL−1. It demonstrated significant inhibitory activity toward three developmental stages of F. pseudograminearum, F. graminearum and F. asiaticum. Furthermore, cyclobutrifluram showed both protective and curative activities against FCR and was rapidly absorbed by roots and transported to wheat stems and leaves. Cyclobutrifluram could also decrease DON production by F. pseudograminearum. CONCLUSION: This investigation has revealed the potential of cyclobutrifluram as a formidable candidate fungicide, particularly in its ability to effectively combat FCR and other Fusarium‐related ailments. This novel compound has exceptional pathogen‐fighting capabilities, coupled with remarkable systemic translocation properties and a notable ability to reduce the production of DON. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Abstract Background Fusarium crown rot (FCR) is one of the most significant diseases limiting crop production in the Huanghuai wheat-growing region of China. Prothioconazole, a triazole sterol 14α-demethylation inhibitor (DMI) fungicide developed by the Bayer Crop Protection Company, is mainly registered for the prevention and control of wheat powdery mildew and stripe rust (China Pesticide Information Network). It is known to exhibit high activity against F. pseudograminearum, but further research, particularly regarding the potential for fungicide resistance, is required before it can be registered for the control of FCR in China. Results The current study found that the baseline sensitivity of 67 field isolates of F. pseudograminearum collected between 2019 and 2021 ranged between 0.016–2.974 μg/mL, with an average EC50 value of 1.191 ± 0.720 μg/mL (mean ± SD). Although none of the field isolates exhibited signs of resistance, three highly resistant mutants were produced by repeated exposure to prothioconazole under laboratory conditions. All of the mutants were found to exhibit significantly reduced growth rates on potato dextrose agar (PDA), as well as reduced levels of sporulation, which indicated that there was a fitness cost associated with the resistance. However, inoculation of wounded wheat coleoptiles revealed that the pathogenicity of the resistant mutants was little affected or actually increased. Molecular analysis of the genes corresponding to the prothioconazole target protein, FpCYP51 (FpCYP51A, FpCYP51B, and FpCYP51C), indicated that the resistant mutants contained three conserved substitutions (M63I, A205S, and I246V) that were present in the FpCYP51C sequence of all three mutants, as well as several non-conserved substations in their FpCYP51A and FpCYP51B sequences. Expression analysis revealed that the presence of prothioconazole (0.1 μg/mL) generally resulted in reduced expression of the three FpCYP51 genes, but that the three mutants exhibited more complex patterns of expression that differed in comparison to their parental isolates. The study found no evidence of cross-resistance between prothioconazole and any of the fungicides tested including three DMI fungicides tebuconazole, prochloraz, and flutriafol. Conclusions Taken together these results not only provide new insight into the resistant mechanism and biological characteristics associated with prothioconazole resistance in F. pseudograminearum, but also strong evidence that prothioconazole could provide effective and sustained control of FCR, especially when applied in combination with other fungicides.

The worldwide occurrence of wheat crown rot, predominantly caused by the pathogen Fusarium pseudograminearum, has a serious impact on wheat production. Numerous microorganisms have been employed as biocontrol agents, exhibiting effectiveness in addressing a wide array of plant pathogens through various pathways. The mycelium of the white-rot fungus Phanerochaete chrysosporium effectively inhibits the growth of F. pseudograminearum by tightly attaching to it and forming specialized penetrating structures. This process leads to the release of intracellular inclusions and the eventual disintegration of pathogen cells. Furthermore, volatile organic compounds and fermentation products produced by P. chrysosporium exhibit antifungal properties. A comprehensive understanding of the mechanisms and modalities of action will facilitate the advancement and implementation of this biocontrol fungus. In order to gain a deeper understanding of the mycoparasitic behavior of P. chrysosporium, transcriptome analyses were conducted to examine the interactions between P. chrysosporium and F. pseudograminearum at 36, 48, and 84 h. During mycoparasitism, the up-regulation of differentially expressed genes (DEGs) encoding fungal cell-wall-degrading enzymes (CWDEs), iron ion binding, and mycotoxins were mainly observed. Moreover, pot experiments revealed that P. chrysosporium not only promoted the growth and quality of wheat but also hindered the colonization of F. pseudograminearum in wheat seedlings. This led to a delay in the development of stem base rot, a reduction in disease severity and incidence, and the activation of the plant’s self-defense mechanisms. Our study provides important insights into the biocontrol mechanisms employed by P. chrysosporium against wheat crown rot caused by F. pseudograminearum.

Fusarium crown rot (FCR) caused by Fusarium pseudograminearum is a serious threat to wheat production worldwide. This study aimed to assess the effects of Talaromyces muroii strain TM28 isolated from root of Panax quinquefolius against F. pseudograminearum. The strain of TM28 inhibited mycelial growth of F. pseudograminearum by 87.8% at 72 h, its cell free fermentation filtrate had a strong antagonistic effect on mycelial growth and conidial germination of F. pseudograminearum by destroying the integrity of the cell membrane. In the greenhouse, TM28 significantly increased wheat fresh weight and height in the presence of pathogen Fp, it enhanced the antioxidant defense activity and ameliorated the negative effects of F. pseudograminearum, including disease severity and pathogen abundance in the rhizosphere soil, root and stem base of wheat. RNAseq of F. pseudograminearum under TM28 antagonistic revealed 2,823 differentially expressed genes (DEGs). Most DEGs related to cell wall and cell membrane synthesis were significantly downregulated, the culture filtrate of TM28 affected the pathways of fatty acid synthesis, steroid synthesis, glycolysis, and the citrate acid cycle. T. muroii TM28 appears to have significant potential in controlling wheat Fusarium crown rot caused by F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Background: Fusarium crown rot (FCR) is one of the most significant diseases limiting crop production in the Huanghuai wheat-growing region of China. Prothioconazole, a triazole sterol 14α-demethylation inhibitor (DMI) fungicide developed by the Bayer Crop Protection Company, is mainly registered for the prevention and control of wheat powdery mildew and stripe rust (China Pesticide Information Network). It is known to exhibit high activity against F. pseudograminearum, but further research, particularly regarding the potential for fungicide resistance, is required before it can be registered for the control of FCR in China. Results: The current study found that the baseline sensitivity of 67 field isolates of F. pseudograminearum collected between 2019 and 2021 ranged between 0.016–2.974 μg/mL, with an average EC50 value of 1.191 ± 0.720 μg/mL (mean ± SD). Although none of the field isolates exhibited signs of resistance, three highly resistant mutants were produced by repeated exposure to prothioconazole under laboratory conditions. All of the mutants were found to exhibit significantly reduced growth rates on potato dextrose agar (PDA), as well as reduced levels of sporulation, which indicated that there was a fitness cost associated with the resistance. However, inoculation of wounded wheat coleoptiles revealed that the pathogenicity of the resistant mutants was little affected or actually increased. Molecular analysis of the genes corresponding to the prothioconazole target protein, FpCYP51 (FpCYP51A, FpCYP51B, and FpCYP51C), indicated that the resistant mutants contained three conserved substitutions (M63I, A205S, and I246V) that were present in the FpCYP51C sequence of all three mutants, as well as several non-conserved substations in their FpCYP51A and FpCYP51B sequences. Expression analysis revealed that the presence of prothioconazole (0.1 μg/mL) generally resulted in reduced expression of the three FpCYP51 genes, but that the three mutants exhibited more complex patterns of expression that differed in comparison to their parental isolates. The study found no evidence of cross-resistance between prothioconazole and any of the fungicides tested including three DMI fungicides tebuconazole, prochloraz, and flutriafol. Conclusions: Taken together these results not only provide new insight into the resistant mechanism and biological characteristics associated with prothioconazole resistance in F. pseudograminearum, but also strong evidence that prothioconazole could provide effective and sustained control of FCR, especially when applied in combination with other fungicides. [ABSTRACT FROM AUTHOR]

BACKGROUND: Fusarium pseudograminearum is one of the dominant pathogens of Fusarium crown rot (FCR) worldwide. Unfortunately, no fungicides have yet been registered for the control of FCR in wheat in China. Pydiflumetofen, a new‐generation succinate dehydrogenase inhibitor, exhibits excellent inhibitory activity to Fusarium spp. A resistance risk assessment of F. pseudograminearum to pydiflumetofen and the resistance mechanism involved have not yet been investigated. RESULTS: The median effective concentration (EC50) value of 103 F. pseudograminearum isolates to pydiflumetofen was 0.0162 μg mL−1, and the sensitivity exhibited a unimodal distribution. Four resistant mutants were generated by fungicide adaption, which possessed similar or impaired fitness compared to corresponding parental isolates based on the results of mycelial growth, conidiation, conidium germination rate, and virulence determination. Pydiflumetofen showed strong positive cross‐resistance with cyclobutrifluram and fluopyram but no cross‐resistance with carbendazim, phenamacril, tebuconazole, fludioxonil, or pyraclostrobin. Sequence alignment revealed that pydiflumetofen‐resistant F. pseudograminearum mutants had two single‐point mutations of A83V or R86K in FpSdhC1. Molecular docking further confirmed that point mutation of A83V or R86K in FpSdhC1 could confer resistance of F. pseudograminearum to pydiflumetofen. CONCLUSION: Fusarium pseudograminearum shows an overall moderate risk of developing resistance to pydiflumetofen, and point mutation FpSdhC1A83V or FpSdhC1R86K could confer pydiflumetofen resistance in F. pseudograminearum. This study provided vital data for monitoring the emergence of resistance and developing resistance management strategies for pydiflumetofen. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Fusarium crown rot of wheat (FCR) is mainly caused by Fusarium pseudograminearum and is a major disease in the Huang-huai wheat growing region in China, leading to a potential yield loss. In order to evaluate the effect of pyraclostrobin on the growth of F. pseudograminearum and its control efficacy, the inhibitory activity of pyraclostrobin against the growth of F. pseudograminearum was studied, and field trials of pyraclostrobin against FCR was carried out. The results showed that pyraclostrobin had strong inhibitory effect on four growth stages of F. pseudograminearum. The EC50 value of pyraclostrobin to mycelial growth was 0.1168–10.3378 μg/mL with an average of (3.5348 ± 3.0044) μg/mL, and with the shortening of branch spacing, the branching number increased as well as the bending of the hyphal apex at the edge of the mycelia. The EC50 value of pyraclostrobin on conidial germination was 0.0052–0.2498 μg/mL with an average of (0.0782 ± 0.0504) μg/mL, and there was an increased chance that conidia will germinate from intermediate cells. The EC50 value of pyraclostrobin on germ tube elongation was 0.0244–0.0605 μg/mL, which could make the middle cells of the conidia to swell and become deformed, but the teratogenic effect on the germ tube was not obvious. Pyraclostrobin can delay conidia sporulation time and make the conidia cells enlarged and deformed. The EC50 value of sporulation was 0.0170–0.0225 μg/mL. The results of field trials in Xin'an County and Yichuan County of Luoyang City showed that compared with carbendazim, pyraclostrobin had higher control effect on FCR at the jointing stage and the filling stage, with the control effect being more than 50%. It also reduced the rate of white spikes of wheat at the milky stage, but the control effect of pyraclostrobin at the filling stage decreased. At the same time, pyraclostrobin soaking increased the plant height, stem girth and 1,000 grain weight of wheat. Pyraclostrobin could be used as an alternative fungicide in the integrated management of FCR. [ABSTRACT FROM AUTHOR]

Fusarium pseudograminearum causes destructive crown disease in wheat. The velvet protein family is a crucial regulator in development, virulence, and secondary metabolism of fungi. We conducted a functional analysis of FpVelB using a gene replacement strategy. The deletion of FpVelB decreased radial growth and enhanced conidial production compared to that of wild type. Furthermore, FpVelB modulates the fungal responses to abiotic stress through diverse mechanisms. Significantly, virulence decreased after the deletion of FpVelB in both the stem base and head of wheat. Genome-wide gene expression profiling revealed that the regulation of genes by FpVelB is associated with several processes related to the aforementioned phenotype, including “immune”, “membrane”, and “antioxidant activity”, particularly with regard to secondary metabolites. Most importantly, we demonstrated that FpVelB regulates pathogen virulence by influencing deoxynivalenol production and modulating the expression of the PKS11 gene. In conclusion, FpVelB is crucial for plant growth, asexual development, and abiotic stress response and is essential for full virulence via secondary metabolism in F. pseudograminearum.

Fusarium crown rot (FCR) in wheat is a prevalent soil-borne disease worldwide and poses a significant threat to the production of wheat (Triticum aestivum) in China, with F. pseudograminearum being the dominant pathogen. Currently, there is a shortage of biocontrol resources to control FCR induced by F. pseudograminearum, along with biocontrol mechanisms. In this study, we have identified 37 strains of biocontrol bacteria displaying antagonistic effects against F. pseudograminearum from over 8000 single colonies isolated from soil samples with a high incidence of FCR. Among them, QY43 exhibited remarkable efficacy in controlling FCR. Further analysis identified the isolate QY43 as Pseudomonas aeruginosa, based on its colony morphology and molecular biology. In vitro, QY43 significantly inhibited the growth, conidial germination, and the pathogenicity of F. pseudograminearum. In addition, QY43 exhibited a broad spectrum of antagonistic activities against several plant pathogens. The genomics analysis revealed that there are genes encoding potential biocontrol factors in the genome of QY43. The experimental results confirmed that QY43 secretes biocontrol factor siderophores and pyocyanin. In summary, QY43 exhibits a broad spectrum of antagonistic activities and the capacity to produce diverse biocontrol factors, thereby showing substantial potential for biocontrol applications to plant disease.

In China, Fusarium pseudograminearum has emerged as a major pathogen causing Fusarium crown rot (FCR) and caused significant losses. Studies on the pathogen’s properties, especially its mating type and trichothecene chemotypes, are critical with respect to disease epidemiology and food/feed safety. There are currently few available reports on these issues. This study investigated the species composition, mating type idiomorphs, and trichothecene genotypes of Fusarium spp. causing FCR in Henan, China. A significant shift in F. pseudograminearum-induced FCR was found in the present study. Of the 144 purified strains, 143 were F. pseudograminearum, whereas only 1 Fusarium graminearum was identified. Moreover, a significant trichothecene-producing capability of F. pseudograminearum strains from Henan was observed in this work. Among the 143 F. pseudograminearum strains identified, F. pseudograminearum with a 15ADON genotype was found to be predominant (133 isolates), accounting for 92.36% of all strains, followed by F. pseudograminearum with a 3ADON genotype, whereas only one NIV genotype strain was detected. Overall, a relatively well-balanced 1:1 ratio of the F. pseudograminearum population was found in Henan. To the best of our knowledge, this is the first study that has examined the Fusarium populations responsible for FCR across the Henan wheat-growing region.

The soil-borne pathogen Fusarium pseudograminearum is capable of causing a highly destructive crown disease in wheat. The purpose of this study was to characterize the biological functions, such as of virulence and secondary metabolites (SMs), of a putative RNA-Pol II transcription elongation factor, FpRtfA, in F. pseudograminearum. The current study revealed that the deletion of FpRtfA reduced radial growth compared to wild type in F. pseudograminearum. In addition, FpRtfA was found important to conidiation and response to metal ions and oxidative stress. More importantly, the virulence to the wheat stem base or head was decreased when FpRtfA was deleted. Using genome-wide gene expression profiling, FpRtfA was found to regulate several processes related to the above phenotype, such as the carbohydrate metabolic process, and the response to oxidative stress and oxidoreductase activity, especially for SMs. Further, we proved that FpRtfA exerts its regulatory effect on the virulence of pathogens by modulating the expression of the PKS gene, but not the generation of DON. In conclusion, FpRtfA has important roles in growth, asexual development, and the response to metal ions and oxidative stress. More importantly, FpRtfA is required for SMs and full virulence in F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Aims: Soil-borne pathogens severely damage the yield and quality of crops worldwide. Plant and soil microbiomes (e.g. in the rhizosphere) intimately interact with the plant, the pathogen and influence outcomes of disease infection. Investigation of how these microbiomes respond to disease infection is critical to develop solutions to control diseases. Methods: Here, we conducted a field experiment and collected healthy and crown rot disease infected (caused by Fusarium pseudograminearum, Fp) wheat plants. We investigated their microbiomes in different compartments, plant immune responses and interactions with the pathogen (Fp) aiming at advancing our knowledge on microbiome-mediated regulation of plant responses to pathogens. Results: We found that Fp colonised wheat plants significantly in terms of relative abundances, accounting for 11.3% and 60.7% of the fungal communities in the rhizosphere and roots, respectively. However, Fp presented with a small fraction of the leaf microbiome, up to 1.2%. Furthermore, Fp-infection led to significant changes in the composition of microbiomes in the rhizosphere and root while had little impact on leaves. We further found that wheat defence signalling pathways, microbiomes and the pathogen intimately correlated with each other in structural equation modelling. As such, we also identified ecological clusters explained changes in the wheat defence signalling pathways. Lastly, microbial co-occurrence network complexity was higher in Fp-infected plants relative to healthy plants, suggesting that Fp-infection may have led to changes in the wheat microbial community structure. Conclusions: We provide novel evidence that soil-borne diseases disrupt belowground plant microbiomes influencing the responses of plant immunity to pathogens. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR), mainly caused by Fusarium pseudograminearum, not only seriously threatens the yield and quality of wheat, but also endangers the health and safety of humans and livestock. Piriformospora indica is a root endophytic fungus that colonizes plant roots extensively and can effectively promote plant growth and improve plant resistance to biotic and abiotic stresses. In this study, the mechanism of FCR resistance mediated by P. indica in wheat was revealed from the phenylpropanoid metabolic pathway. The results showed that the colonization of P. indica significantly reduced the progression of wheat disease, the amount of F. pseudograminearum colonization, and the content of deoxynivalenol (DON) in wheat roots. RNA-seq suggested that P. indica colonization could reduce the number of differentially expressed genes (DEGs) in the transcriptome caused by F. pseudograminearum infection. The DEGs induced by the colonization of P. indica were partially enriched in phenylpropanoid biosynthesis. Transcriptome sequencing and qPCR indicated that the colonization of P. indica up-regulated the expression of genes involved in the phenylpropanoid biosynthesis pathway. The metabolome analysis indicated that the colonization of P. indica increased the metabolites' accumulation in the phenylpropanoid biosynthesis. Consistent with transcriptome and metabolomic analysis, microscopic observations showed enhanced lignin accumulation in the roots of the Piri and Piri+Fp lines, most likely contributing to the arrested infection by F. pseudograminearum. These results suggested that P. indica increased resistance to F. pseudograminearum in wheat by inducing the phenylpropanoid pathway. [ABSTRACT FROM AUTHOR]

Wheat crown rot, caused by Fusarium pseudograminearum, is an emerging soil-borne fungal disease and causes serious damage in areas where water is scarce. However, the interactions between plant, microbiome, and pathogen under different watering regimes are rarely known. In our study, we designed three watering patterns, including the early-drought (DR1), late-drought (DR2), and well-watered (WAT) patterns, and sampled at heading and grain filling, to investigate the effect of different watering regimes on the microbial community and disease severity. These findings showed that well-watered pattern at grain filling decreased the disease index compared to other patterns, and the bacterial community in the WAT and DR2 at grain filling showed higher alpha diversity (rhizosphere and root) and more stable structures (root). For the microbial network, irrespective of compartments, bacterial networks in the WAT and DR2 were more complex and connected with a higher average degree and clustering coefficient than DR1 at both periods. Furthermore, several potential beneficial microbes as biomarkers were enriched under good water conditions, specifically during the heading of DR2 and grain filling of WAT, including operational taxonomic units (OTUs) affiliated with the taxa of Arenimonas, Sphingomonas, Pseudoxanthomonas, Devosia, Lysobacter, Chitinophagaceae, and Gaiellales in the rhizosphere and root. Overall, the microbiome reshaped by good moisture or avoiding early drought should be emphasized and further used in controlling Fp-caused wheat crown rot. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) caused by Fusarium pseudograminearum is one of the most serious soil-borne diseases of wheat. Among 58 bacterial isolates from the rhizosphere soil of winter wheat seedlings, strain YB-1631 was found to have the highest in vitro antagonism to F. pseudograminearum growth. LB cell-free culture filtrates inhibited mycelial growth and conidia germination of F. pseudograminearum by 84.14% and 92.23%, respectively. The culture filtrate caused distortion and disruption of the cells. Using a face-to-face plate assay, volatile substances produced by YB-1631 inhibited F. pseudograminearum growth by 68.16%. In the greenhouse, YB-1631 reduced the incidence of FCR on wheat seedlings by 84.02% and increased root and shoot fresh weights by 20.94% and 9.63%, respectively. YB-1631 was identified as Bacillus siamensis based on the gyrB sequence and average nucleotide identity of the complete genome. The complete genome was 4,090,312 bp with 4357 genes and 45.92% GC content. In the genome, genes were identified for root colonization, including those for chemotaxis and biofilm production, genes for plant growth promotion, including those for phytohormones and nutrient assimilation, and genes for biocontrol activity, including those for siderophores, extracellular hydrolase, volatiles, nonribosomal peptides, polyketide antibiotics, and elicitors of induced systemic resistance. In vitro production of siderophore, β-1, 3-glucanase, amylase, protease, cellulase, phosphorus solubilization, and indole acetic acid were detected. Bacillus siamensis YB-1631 appears to have significant potential in promoting wheat growth and controlling wheat FCR caused by F. pseudograminearum. [ABSTRACT FROM AUTHOR]

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Chaetomium globosum is a common plant endophytic fungi that exhibits great biocontrol potential in plant disease. Fusarium crown rot (FCR) is an important disease in wheat that seriously threatens wheat production worldwide. The control effect of C. globosum against wheat FCR remains unclear. In this study, we introduced an identified C. globosum 12XP1-2-3 and tested its biological control potential against wheat FCR. The hypha and fermentation broth exhibited an antagonistic effect against Fusarium pseudograminearum. Results from indoor experiments showed that C. globosum 12XP1-2-3 might delay the onset of symptoms of brown stem base and significantly reduced the disease index (37.3%). Field trials showed that wheat seeds coated with a spore suspension of 12XP1-2-3 grew better than the control seeds, had control effects of 25.9-73.1% on FCR disease, and increased wheat yield by 3.2-11.9%. Analysis of rhizosphere microorganisms revealed that seeds coated with C. globosum ('Cg' treatment) had a greater effect on fungal rather than on bacterial alpha diversity and may improve the health state of rhizosphere microorganisms, as reflected by the significantly increased fungal Shannon index at Feekes 11 and the increased complexity of the bacterial co-occurrence network but decreased complexity of the fungal network. Moreover, the accumulation of beneficial bacteria such as Bacillus and Rhizobium at Feekes 3, and Sphingomonas at Feekes 7 in the 'Cg' treatment may be the important contributions to healthier wheat growth state, significantly reduced relative abundance of Fusarium at Feekes 11, and reduced occurrence of FCR disease. These results provide a basis for further research on the mechanism of action of C. globosum and its application in the biological control of FCR in the field. [ABSTRACT FROM AUTHOR]

Fusarium pseudograminearum is a major pathogen for the destructive disease Fusarium crown rot (FCR) of wheat (Triticum aestivum). The cytosolic Acetoacetyl-CoA thiolase II (AACT) is the first catalytic enzyme in the mevalonate pathway that biosynthesizes isoprenoids in plants. However, there has been no investigation of wheat cytosolic AACT genes in defense against pathogens including Fusarium pseudograminearum. Herein, we identified a cytosolic AACT-encoding gene from wheat, named TaAACT1, and demonstrated its positively regulatory role in the wheat defense response to F. pseudograminearum. One haplotype of TaAACT1 in analyzed wheat genotypes was associated with wheat resistance to FCR. The TaAACT1 transcript level was elevated after F. pseudograminearum infection, and was higher in FCR-resistant wheat genotypes than in susceptible wheat genotypes. Functional analysis indicated that knock down of TaAACT1 impaired resistance against F. pseudograminearum and reduced the expression of downstream defense genes in wheat. TaAACT1 protein was verified to localize in the cytosol of wheat cells. TaAACT1 and its modulated defense genes were rapidly responsive to exogenous jasmonate treatment. Collectively, TaAACT1 contributes to resistance to F. pseudograminearum through upregulating the expression of defense genes in wheat. This study sheds new light on the molecular mechanisms underlying wheat defense against FCR. [ABSTRACT FROM AUTHOR]

Fusarium pseudograminearum has been identified as a significant pathogen. It causes Fusarium crown rot (FCR), which occurs in several major wheat-producing areas in China. Chemical control is the primary measure with which to control this disease. In this study, transcriptome sequencing (RNA-Seq) was used to determine the different mechanisms of action of four frequently used fungicides including carbendazim, pyraclostrobin, tebuconazole, and phenamacril on F. pseudograminearum. In brief, 381, 1896, 842, and 814 differentially expressed genes (DEGs) were identified under the carbendazim, pyraclostrobin, tebuconazole, and phenamacril treatments, respectively. After the joint analysis, 67 common DEGs were obtained, and further functional analysis showed that the ABC transported pathway was significantly enriched. Moreover, FPSE_04130 (FER6) and FPSE_11895 (MDR1), two important ABC multidrug transporter genes whose expression levels simultaneously increased, were mined under the different treatments, which unambiguously demonstrated the common effects. In addition, Mfuzz clustering analysis and WGCNA analysis revealed that the core DEGs are involved in several critical pathways in each of the four treatment groups. Taken together, these genes may play a crucial function in the mechanisms of F. pseudograminearum's response to the fungicides stress. [ABSTRACT FROM AUTHOR]

Sharp eyespot and Fusarium crown rot, mainly caused by soil-borne fungi Rhizoctonia cerealis and Fusarium pseudograminearum, are destructive diseases of major cereal crops including wheat (Triticum aestivum). However, the mechanisms underlying wheat-resistant responses to the two pathogens are largely elusive. In this study, we performed a genome-wide analysis of wall-associated kinase (WAK) family in wheat. As a result, a total of 140 TaWAK (not TaWAKL) candidate genes were identified from the wheat genome, each of which contains an N-terminal signal peptide, a galacturonan binding domain, an EGF-like domain, a calcium binding EGF domain (EGF-Ca), a transmembrane domain, and an intracellular Serine/Threonine protein kinase domain. By analyzing the RNA-sequencing data of wheat inoculated with R. cerealis and F. pseudograminearum, we found that transcript abundance of TaWAK-5D600 (TraesCS5D02G268600) on chromosome 5D was significantly upregulated, and that its upregulated transcript levels in response to both pathogens were higher compared with other TaWAK genes. Importantly, knock-down of TaWAK-5D600 transcript impaired wheat resistance against the fungal pathogens R. cerealis and F. pseudograminearum, and significantly repressed expression of defense-related genes in wheat, TaSERK1, TaMPK3, TaPR1, TaChitinase3, and TaChitinase4. Thus, this study proposes TaWAK-5D600 as a promising gene for improving wheat broad resistance to sharp eyespot and Fusarium crown rot (FCR) in wheat. [ABSTRACT FROM AUTHOR]

The cereal disease Fusarium crown rot (FCR), caused by the fungal pathogen Fusarium pseudograminearum (Fp), is a major constraint to cereal production worldwide. Nitrogen (N) fertilizer is estimated to be approximately 30% of the input costs for grain growers in Australia and is the primary driver of yield and grain protein levels. When targeting high yield and protein, generous nitrogen fertilizer applications are thought to result in large biomass production, which exacerbates FCR severity, reducing grain yield and quality. This research was undertaken to investigate the effect of temporal N availability in high-protein bread and durum wheat varieties on FCR severity. Laboratory and controlled environment experiments assessed the relationship between FCR and N at a mechanistic and plant level. An in vitro study demonstrated an increase in Fp mycelial growth under increased N availability, especially when N was supplied as urea compared with ammonium nitrate. Similarly, under controlled environmental conditions, increased soil N availability promoted FCR severity within infected plants. Stem N transfer efficiency was significantly decreased under FCR infection in both bread and durum wheat varieties by 4.5% and 10.2%, respectively. This new research demonstrates that FCR not only decreases yield and grain quality but appears to have previously unrecognised detrimental impacts on nitrogen-use efficiency in wheat. This indicates that the current impact of losses from FCR may also decrease N-use inefficiencies, as well as yield and quality penalties. An improved understanding of the interactions and restrictions of FCR infection may allow growers to better manage the disease through manipulation of the soil's temporal N availability. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) on wheat is a soil-borne disease that affects the yield and quality of the produce. In 2020, 297 Fusarium pseudograminearum isolates were isolated from diseased FCR wheat samples from eight regional areas across Hebei Province in China. Baseline sensitivity of F. pseudograminearum to fludioxonil (0.0613 ± 0.0347 mg/mL) and tebuconazole (0.2328 ± 0.0840 mg/mL) were constructed based on the in vitro tests of 71 and 83 isolates, respectively. The resistance index analysis showed no resistance isolate to fludioxonil but two low-resistance isolates to tebuconazole in 2020. There was an increased frequency of resistant isolates from 2021 to 2022 based on the baseline sensitivity for tebuconazole. There was no cross-resistance between fludioxonil and tebuconazole. This study provides a significant theoretical and practical basis for monitoring the resistance of F. pseudograminearum to fungicides, especially the control of FCR. [ABSTRACT FROM AUTHOR]

Wheat crown rot caused by Fusarium pseudograminearum is an important disease of wheat and leads to a severe impact on the yield and quality of wheat. At present, there are no chemical fungicides registered for the control of this disease. In this study, samples were collected from 17 cities in Henan Province and 82 strains of wheat crown rot were isolated and purified, including 76 strains of F. pseudograminearum and 6 strains of Fusarium graminearum. The EC50 values of azoxystrobin on spore germination of F. pseudograminearum 76 strains are 0.02-1.54 μg/mL and the average EC50 value is (0.33 ± 0.29) μg/mL. According to the test of abnormal data, LHWY-6 and SQYC-6 were the abnormal strains. The average EC50 values of azoxystrobin to 74 isolates (97.37%) was (0.30 ± 0.24) μg/mL after discarding the two outliers, which could be used as the sensitivity baseline of F. pseudograminearum to azoxystrobin. The sensitivity of strain from different cities varies. The sensitivity to azoxystrobin is also fluctuant for the strains from the same city. The fold changes of strain sensitivity from Xuchang, Jiaozuo, Luoyang and Shangqiu are all above 20.00, that from Nanyang, Sanmenxia, and Kaifeng are all below 2.00, and from the other cities are between 2.70-12.00. When the sensitivity of F. pseudograminearum spore germination to azoxystrobin was compared with that to prothioconazole, carbendazim, fludioxonil, phenamacril, pyraclostrobin, and tebuconazole, the results showed that the inhibitory effects of 5 fungicides on spore germination are lower than those of azoxystrobin, except pyraclostrobin. The EC50 values of azoxystrobin against 6 strains of F. graminearum are 0.10-0.42 μg/mL and the average EC50 value is (0.19 ± 0.12) μg/mL. The inhibitory activity of azoxystrobin on the mycelial growth of the two species of Fusarium is faint with EC50 of above 7 μg/mL. The 15% azoxystrobin FS agent has a 63.64% control effect against wheat crown rot with a dose of 260 g/(100 kg seeds) in vitro and a control effect of 55.24% with a dose of 220 g/(100 kg seeds) in the greenhouse. Azoxystrobin shows a notable inhibitory effect on spore germination of wheat crown rot fungi, has a good effect on disease control in vitro and greenhouse conditions and can be used as a high-quality alternative fungicide in the field. [ABSTRACT FROM AUTHOR]

Soil-borne fungal diseases are always a threat to wheat production. Developing molecular markers is helpful in early diagnosis and precautionary treatment of these diseases. In this study, a total of 42 Rhizoctonia isolates and 11 Fusarium isolates were obtained from 84 samples of diseased wheat plants collected from 11 locations in China. Rhizoctonia cerealis (Rc) and Fusarium pseudograminearum (Fpg) were the most abundant species in the majority of the sampling regions, accounting for 77.4% and 11.3% of the total isolates, respectively. Eight internal transcribed spacer (ITS) types of Rc were defined based on ITS sequencing identification, among which the ITS type I was the most predominant types isolated in all test regions. Based on the ITS sequences of all isolates, two specific markers were developed to distinguish Rc, Rhizoctonia solani (Rs) and three species of Fusarium at the DNA level. These markers were used to successfully detect 53 isolates of Rc, Rs and Fusarium collected in the study. Identification results by markers developed in this work were further confirmed by ITS sequencing. These markers could be used to detect the specific infective pathogen in diseased wheat seedlings or soil residues in fields, which would then be useful for early prevention and treatment of diseases sharp eyespot (SE) and Fusarium crown rot (FCR). [ABSTRACT FROM AUTHOR]

Abstract Introduction Plant‐associated microorganisms are widely explored for their use as bioinoculants in agriculture. However, the rate and ability of introduced microbes to colonise and interact with indigenous soil microbiomes are largely unknown. Materials & Methods In this study, we constructed a bacterial synthetic community (SynCom) using eight plant‐growth‐promoting bacteria isolated from the wheat (Triticum aestivum) rhizosphere, including three Bacillus spp., two Acinebacter spp., an Enterobacter sp., a Xanthomonas sp. and a Burkholderia sp., which all showed multiple plant growth‐promoting effects including indole‐3‐acetic acid and ammonia production and fungal pathogen suppression. We inoculated this SynCom in a soil with reduced microbial diversity, and investigated the ability of the SynCom to colonise wheat plants, and interact with soil microbes in the presence or absence of a soil‐borne pathogen Fusarium pseudograminearum (Fp). Results We found that SynCom significantly increased the wheat plant growth, root development and biomass production. Fp load in soil was significantly reduced and plant survival rates increased following the SynCom inoculation. Soil microbial community structure was altered by the SynCom, and noticeably, relative abundance of Pseudomonas spp. was induced in the soil. Conclusion This study provides novel evidence that colonisation of a beneficial SynCom promotes plant growth and alters soil microbial community.

Fusarium pseudograminearum , the causal agent of Fusarium crown rot, poses a significant threat to cereal crops. Building upon our previous investigation of the transcriptional response of this pathogen to four key fungicides (carbendazim, phenamacril, pyraclostrobin, and tebuconazole), this study delves into the impact of elevated fungicide concentrations using RNA-seq. Global transcriptomic analysis and gene clustering revealed significant enrichment of genes involved in the ABC transporter pathway. Among these transporters, FPSE_06011 (FpZRA1), a conserved gene in eukaryotes, exhibited consistent upregulation at both low and high fungicide concentrations. Targeted deletion of FpZRA1 resulted in reduced sporulation, spore germination, and tolerance to cell wall stress, osmotic stress, and oxidative stress. Furthermore, the FpZRA1 knockout mutants exhibited decreased pathogenicity on wheat coleoptiles and reduced production of the mycotoxin deoxynivalenol (DON), as evidenced by the markedly down-regulated expression of TRI5 , TRI6 , and TRI10 in the RT-qPCR analysis. In summary, our findings highlight the impact of fungicide concentration on transcriptional reprogramming in F. pseudograminearum and identify FpZRA1 as a critical regulator of fungal development, stress tolerance, and pathogenicity. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) caused by Fusarium pseudograminearum poses a significant threat to wheat production in the Huang-Huai-Hai region of China. However, the pathogenic mechanism of F. pseudograminearum is still poorly understood. Zn 2 Cys 6 transcription factors, which are exclusive to fungi, play pivotal roles in regulating fungal development, drug resistance, pathogenicity, and secondary metabolism. In this study, we present the functional characterization of a Zn 2 Cys 6 transcription factor F. pseudograminearum , designated Fp487. In F. pseudograminearum , Fp487 is shown to be required for mycelial growth through gene knockout and phenotypic analyses. Compared with wild-type CF14047, the ∆ Fp487 mutant displayed a slight reduction in growth rate but a significant decrease in conidiogenesis, pathogenicity and 3-acetyl-deoxynivalenol (3AcDON) production. Moreover, the mutant exhibited heightened sensitivity to oxidative and cytomembrane stress. Furthermore, we synthesized dsRNA from the Fp487 gene in vitro , resulting in a reduction in the growth rate of F. pseudograminearum and its virulence on barley leaves through spray-induced gene silencing (SIGS). Notably, this study makes the first instance of inducing the expression of abundant dsRNA from F. pseudograminearum by engineering the Escherichia coli strain HT115 (DE3) and utilizing the SIGS technique to evaluate the virulence effect of dsRNA on F. pseudograminearum. In conclusion, our findings revealed the crucial role of Fp487 in regulating pathogenicity, stress responses, DON production, and conidiogenesis in F. pseudograminearum. Furthermore, Fp487 is a potential RNAi-based target for FCR control. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) is a major limitation to the wheat (Triticum aestivum L.) industry in the inland Pacific Northwest, United States. Genetic resistance to FCR is poorly understood and major gene resistance is not available in adapted cultivars. Chemical control is ineffective and crop rotations, which disrupt cycles of the disease, are not feasible in the region’s precipitation-limited climate. Cultural control methods are the only realistic option for farmers who struggle to minimize the impact of this disease. It is well established that FCR is favored by moisture-limited environments and an oversupply of plant-available nitrogen in soil. Effects of the supply of phosphorus in soil have not been clearly delineated. We conducted a 2-year FCR experiment at two locations in the low-precipitation zone (

Reliable prediction of the risk of mycotoxin contamination in post-harvest wheat will aid in improvement of the quality and safety. To establish the relationship between Fusarium pseudograminearum mycotoxins and CO2 production, changes in their respective concentrations were monitored for the artificial contamination of wheat under different values of water activities (0.84 aw, 0.92 aw, and 0.97 aw) and temperatures (20 ℃, 25 ℃, and 30 ℃). Water activity played a significant role in all these processes. CO2 concentration together with moisture content and temperature were used as the main parameters to establish DON and ZEN contamination prediction models. The prediction accuracy for DON was 98.15 % (R2 = 0.990) and 90.74 % for ZEN (R2 = 0.982). These models were combined with T/RH/MC/CO2 multi-parameter integrated sensors to form an early warning system, which offers a great prospect to minimise the risk of DON/ZEN contamination in post-harvest wheat.

Fusarium crown rot (FCR) of wheat, an important soil-borne disease, presents a worsening trend year by year, posing a significant threat to wheat production. Fusarium pseudograminearum cv. b was reported to be the dominant pathogen of FCR in China. Peroxisomes are single-membrane organelles in eukaryotes that are involved in many important biochemical metabolic processes, including fatty acid β-oxidation. PEX11 is important proteins in peroxisome proliferation, while less is known in the fungus F. pseudograminearum. The functions of FpPEX11a, FpPEX11b, and FpPEX11c in F. pseudograminearum were studied using reverse genetics, and the results showed that FpPEX11a and FpPEX11b are involved in the regulation of vegetative growth and asexual reproduction. After deleting FpPEX11a and FpPEX11b, cell wall integrity was impaired, cellular metabolism processes including active oxygen metabolism and fatty acid β-oxidation were significantly blocked, and the production ability of deoxynivalenol (DON) decreased. In addition, the deletion of genes of FpPEX11a and FpPEX11b revealed a strongly decreased expression level of peroxisome-proliferation-associated genes and DON-synthesis-related genes. However, deletion of FpPEX11c did not significantly affect these metabolic processes. Deletion of the three protein-coding genes resulted in reduced pathogenicity of F. pseudograminearum. In summary, FpPEX11a and FpPEX11b play crucial roles in the growth and development, asexual reproduction, pathogenicity, active oxygen accumulation, and fatty acid utilization in F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Homeobox transcription factors have been implicated in filamentous growth, conidia formation and virulence in fungal pathogens. However, the presence of the homeobox gene family and their potential influence on pathogenesis in Fusarium pseudograminearum have not been investigated. F. pseudograminearum is an important plant pathogen that causes wheat and barley crown rot. In this study, we performed a genome-wide survey for F. pseudograminearum homeobox genes, and 11 FpHtfs were identified and characterized. Domain analyses revealed that all of these proteins contain a complete homeobox domain that contains three helices. Expression profiles of FpHtf genes at different pathogen stages showed that six FpHtf genes were induced during infection. Further, we generated and characterized FpHtf3 deletion mutants in F. pseudograminearum, showing it was essential for virulence. These results indicated that members of the homeobox gene family are likely involved in F. pseudograminearum pathogenicity. Our work also provides a useful foundation for further studies on the complexity and function of the homeobox gene family in F. pseudograminearum. [ABSTRACT FROM AUTHOR]

Fusarium crown rot (FCR) of wheat has become more and more serious in China in recent years, which not only threatens food security, but also has the potential threat of mycotoxin contamination, which endangers human and animal health. This paper summarizes the damage status of wheat crown rot and the dominant Fusarium spp. that cause the disease in different regions. It is clear that Fusarium pseudograminearum has gradually become the dominant pathogen of FCR in many major wheat producing areas in China. On this basis, the infection cycle and genetic diversity of F. pseudograminearum were further analyzed, revealing the serious occurrence of FCR and the accumulation of F. pseudograminearum in soil, agricultural measures and various environmental and climatic factors, especially drought environment is closely related. This paper also summarized the reported key proteins that regulate the pathogenicity of F. pseudograminearum, revealed the toxin production type of F. pseudograminearum, clarified the biochemical pathway of deoxynivalenol (DON) synthesis, effects of different fungicides on DON synthesis, and the mechanism by which fungicides stimulate or inhibit DON synthesis. With the purpose of "disease control and deoxynivalenol reduction", a variety of comprehensive prevention and control measures for coordinated disease prevention are proposed, which have important reference value for the realization of green prevention and control of FCR. [ABSTRACT FROM AUTHOR]

Fusarium pseudograminearum , a soil-borne fungus, is the cause of the devastating wheat disease known as wheat crown rot (WCR). The persistence of this pathogen in the soil and crop residues contributes to the increased occurrence and severity of WCR. Therefore, developing effective strategies to prevent and manage WCR is of great importance. In this study, we isolated a bacterial strain, designated as SR9, from the stem of wheat, that exhibited potent antagonistic effects against F. pseudograminearum , as well as the biocontrol efficacy of SR9 on WCR was quantified at 83.99% ± 0.11%. We identified SR9 as Pseudomonas khavaziana and demonstrated its potential as a plant probiotic. SR9 displayed broad-spectrum antagonism against other fungal pathogens, including Neurospora dictyophora , Botrytis californica , and Botryosphaeria dothidea . Whole-genome sequencing analysis revealed that SR9 harbored genes encoding various cell wall-degrading enzymes, cellulases, and lipases, along with antifungal metabolites, which are responsible for its antagonistic activity. Gene knockout and quantitative PCR analyses reveal that phenazine is the essential factor for antagonism. SR9 possessed genes related to auxin synthesis, flagellar biosynthesis, biofilm adhesion, and the chemotaxis system, which play pivotal roles in plant colonization and growth promotion; we also evaluated the effects of SR9 on plant growth in wheat and Arabidopsis . Our findings strongly suggest that SR9 holds great promise as a biocontrol agent for WCR in sustainable agriculture.IMPORTANCEThe escalating prevalence of wheat crown rot, primarily attributed to Fusarium pseudograminearum , necessitates the development of cost-effective and eco-friendly biocontrol strategies. While plant endophytes are recognized for their biocontrol potential, reports on effective strains targeting wheat crown rot are sparse. This study introduces the Pseudomonas khavaziana SR9 strain as an efficacious antagonist to the wheat crown rot pathogen Fusarium pseudograminearum . Demonstrating a significant reduction in wheat crown rot incidence and notable plant growth promotion, SR9 emerges as a key contributor to plant health and agricultural sustainability. Our study outlines a biological approach to tackle wheat crown rot, establishing a groundwork for innovative sustainable agricultural practices., Competing Interests: The authors declare no conflict of interest.

Fusarium pseudograminearum is one of the major fungal pathogens that cause Fusarium crown rot (FCR) worldwide and can lead to a substantially reduced grain yield and quality. Transcription factors play an important role in regulating growth and pathogenicity in plant pathogens. In this study, we identified a putative Zn(II)2Cys6 fungal-type domain-containing transcription factor and named it FpUme18. The expression of FpUME18 was induced during the infection of wheat by F. pseudograminearum. The ΔFpume18 deletion mutant showed defects in growth, conidial production, and conidial germination. In the responses to the cell wall, salt and oxidative stresses, the ΔFpume18 mutant inhibited the rate of mycelial growth at a higher rate compared with the wild type. The staining of conidia and mycelia with lipophilic dye FM4-64 revealed a delay in endocytosis when FpUME18 was deleted. FpUME18 also positively regulated the expression of phospholipid-related synthesis genes. The deletion of FpUME18 attenuated the pathogenicity of wheat coleoptiles. FpUME18 also participated in the production of the DON toxin by regulating the expression of TRI genes. Collectively, FpUme18 is required for vegetative growth, conidiation, stress response, endocytosis, and full virulence in F. pseudograminearum.

Fusarium crown rot (FCR), mainly caused by Fusarium pseudograminearum, not only seriously threatens the yield and quality of wheat, but also endangers the health and safety of humans and livestock. Piriformospora indica is a root endophytic fungus that colonizes plant roots extensively and can effectively promote plant growth and improve plant resistance to biotic and abiotic stresses. In this study, the mechanism of FCR resistance mediated by P. indica in wheat was revealed from the phenylpropanoid metabolic pathway. The results showed that the colonization of P. indica significantly reduced the progression of wheat disease, the amount of F. pseudograminearum colonization, and the content of deoxynivalenol (DON) in wheat roots. RNA-seq suggested that P. indica colonization could reduce the number of differentially expressed genes (DEGs) in the transcriptome caused by F. pseudograminearum infection. The DEGs induced by the colonization of P. indica were partially enriched in phenylpropanoid biosynthesis. Transcriptome sequencing and qPCR indicated that the colonization of P. indica up-regulated the expression of genes involved in the phenylpropanoid biosynthesis pathway. The metabolome analysis indicated that the colonization of P. indica increased the metabolites’ accumulation in the phenylpropanoid biosynthesis. Consistent with transcriptome and metabolomic analysis, microscopic observations showed enhanced lignin accumulation in the roots of the Piri and Piri+Fp lines, most likely contributing to the arrested infection by F. pseudograminearum. These results suggested that P. indica increased resistance to F. pseudograminearum in wheat by inducing the phenylpropanoid pathway.

Fusarium crown rot (FCR) caused by Fusarium pseudograminearum is one of the most serious soil-borne diseases of wheat. Among 58 bacterial isolates from the rhizosphere soil of winter wheat seedlings, strain YB-1631 was found to have the highest in vitro antagonism to F. pseudograminearum growth. LB cell-free culture filtrates inhibited mycelial growth and conidia germination of F. pseudograminearum by 84.14% and 92.23%, respectively. The culture filtrate caused distortion and disruption of the cells. Using a face-to-face plate assay, volatile substances produced by YB-1631 inhibited F. pseudograminearum growth by 68.16%. In the greenhouse, YB-1631 reduced the incidence of FCR on wheat seedlings by 84.02% and increased root and shoot fresh weights by 20.94% and 9.63%, respectively. YB-1631 was identified as Bacillus siamensis based on the gyrB sequence and average nucleotide identity of the complete genome. The complete genome was 4,090,312 bp with 4357 genes and 45.92% GC content. In the genome, genes were identified for root colonization, including those for chemotaxis and biofilm production, genes for plant growth promotion, including those for phytohormones and nutrient assimilation, and genes for biocontrol activity, including those for siderophores, extracellular hydrolase, volatiles, nonribosomal peptides, polyketide antibiotics, and elicitors of induced systemic resistance. In vitro production of siderophore, β-1, 3-glucanase, amylase, protease, cellulase, phosphorus solubilization, and indole acetic acid were detected. Bacillus siamensis YB-1631 appears to have significant potential in promoting wheat growth and controlling wheat FCR caused by F. pseudograminearum.

Wheat crown rot, caused by Fusarium pseudograminearum, is an emerging soil-borne fungal disease and causes serious damage in areas where water is scarce. However, the interactions between plant, microbiome, and pathogen under different watering regimes are rarely known. In our study, we designed three watering patterns, including the early-drought (DR1), late-drought (DR2), and well-watered (WAT) patterns, and sampled at heading and grain filling, to investigate the effect of different watering regimes on the microbial community and disease severity. These findings showed that well-watered pattern at grain filling decreased the disease index compared to other patterns, and the bacterial community in the WAT and DR2 at grain filling showed higher alpha diversity (rhizosphere and root) and more stable structures (root). For the microbial network, irrespective of compartments, bacterial networks in the WAT and DR2 were more complex and connected with a higher average degree and clustering coefficient than DR1 at both periods. Furthermore, several potential beneficial microbes as biomarkers were enriched under good water conditions, specifically during the heading of DR2 and grain filling of WAT, including operational taxonomic units (OTUs) affiliated with the taxa of Arenimonas, Sphingomonas, Pseudoxanthomonas, Devosia, Lysobacter, Chitinophagaceae, and Gaiellales in the rhizosphere and root. Overall, the microbiome reshaped by good moisture or avoiding early drought should be emphasized and further used in controlling Fp-caused wheat crown rot.

Yield losses are experienced in corn fields due to stalk and ear rot disease. The fungicides used against the disease can not show the desired effect and the problem of resistance arises over time. For this reason, it is necessary to develop new strategies in the control against the disease. In this study, it was aim to determine the inhibitory effects of essential oils of rosemary, black cumin, cumin and sandalwood, and ginger against Fusarium verticillioides and Fusarium pseudograminearum under in vitro conditions. The essential oils were applied in doses of 0.25, 0.5, 1, 2 and 4 µl mL-1. PDA medium free of essential oils was used as negative control and PDA medium containing commercial fungicide (80 g l-1 Triticonazole, 40 g l-1 Pyraclostrobin-BASF company) was used as positive control. The experiment was carried out in a randomized plot design with three replications. In addition, chemical content analysis of essential oils was determined by GC-MS method. As a result of the study, as the dose of rosemary, black cumin, sandalwood and ginger essential oils increased, their inhibitory effects against both pathogens increased, and these effects were found close to each other. While the highest inhibitory effect against F. verticillioides and F. pseudograminearum was detected in the positive control treatment of cumin essential oil, 82.1% and 78.9%, respectively, this effect was found to be 74.6% and 68.3% in 4 µl mL-1 dose, respectively. However, more detailed studies should be carried out with these essential oils under field conditions. [ABSTRACT FROM AUTHOR]