Search

Maize, one of the most important cereal crops in Bangladesh, is severely contaminated by fumonisin, a carcinogenic secondary metabolite produced by Fusarium including Fusarium proliferatum. Biocontrol with Bacillus strains is an effective approach to controlling this F. proliferatum as Bacillus has proven antagonistic properties against this fungus. Therefore, the present study aimed to determine how native Bacillus strains can reduce fumonisin in maize cultivated in Bangladesh, where BDISO76MR (Bacillus subtilis) strains showed the highest efficacy both in vitro in detached cob and in planta under field conditions. The BDISO76MR strain could reduce the fumonisin concentration in detached cob at 98.52% over untreated control, by inhibiting the conidia germination and spore formation of F. proliferatum at 61.56% and 77.01%, respectively in vitro. On the other hand, seed treatment with formulated BDISO76MR showed higher efficacy with a reduction of 97.27% fumonisin contamination compared to the in planta cob inoculation (95.45%) over untreated control. This implies that Bacillus-based formulation might be a potential approach in mitigating fumonisin contamination in maize to ensure safe food and feed. [ABSTRACT FROM AUTHOR]

Copyright of Mycosystema is the property of Mycosystema Editorial Board and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Fusarium proliferatum is associated with the root rot of many plant species, but knowledge of its impact on western Canadian field crops is limited. This study assessed the host range of this fungus and its effect on plant emergence, plant height, and shoot and root dry weights in repeated greenhouse experiments with wheat, barley, faba beans, peas, lentils, canola, lupine, and soybeans. Infection was confirmed via PCR, and principal component analysis determined the utility of different parameters in assessing host responses. All crops were at least partly susceptible, developing mild to severe disease at the seedling and adult stages, and showing significant reductions in growth. In general, the barley and wheat demonstrated higher tolerances to infection, followed by the faba bean and the pea. The soybean, canola, lupine, and lentil were most susceptible. The canola and the soybean were particularly vulnerable to F. proliferatum at the pre-emergence stage, while infection greatly reduced the lentil's biomass. Reductions in the barley's emergence and other growth parameters, however, occurred only under a high inoculum concentration. Variability in root rot severity among cultivars of the same crop indicated some diversity in host reactions within species. Nonetheless, the absence of fully-resistant crops may pose challenges in managing F. proliferatum in western Canadian cropping systems. [ABSTRACT FROM AUTHOR]

Abstract O-GlcNAcylation, an important post-translational modification catalyzed by O-GlcNAc transferase (OGT), plays critical roles in several biological processes. In this study, we present our findings on the function of FpOGT in regulating physiological processes and pathogenicity of Fusarium proliferatum (Fp), the alfalfa root rot fungus. The deletion of FpOGT impaired mycelial growth and altered macroconidia morphology in Fp. Furthermore, ΔFpOGT mutant displayed altered tolerance to various stressors, including cell wall perturbing agents, osmotic stressors, metal ionic stressors, and fungicides. Deletion of FpOGT significantly decreased Fp virulence toward alfalfa. The transcriptome analysis demonstrated that FpOGT plays a regulatory role in glucose metabolic pathways, including glycolysis, tricarboxylic acid (TCA) cycle, and hexosamine biosynthesis pathway (HBP), by influencing the expression of relevant genes. The downregulation of the glucokinase gene, FpGCK, was observed in ΔFpOGT, and the disruption of FpGCK led to a decrease in Fp virulence. Additionally, FpOGT affected the expression levels of the FpGCK-AS1 isoform, thereby impacting glucokinase function. The molecular docking analysis elucidated the plausible physical interaction between FpOGT and FpGCK, thereby offering valuable insights into their interrelationship. These findings underscore the indispensable involvement of FpOGT, the sole O-GlcNAc transferase in Fp, in various biological processes and the pathogenicity through its regulation of fundamental metabolic processes. Consequently, this study emphasizes the significance and elucidates the molecular mechanism underlying the role of O-GlcNAc transferase in diverse fundamental biological processes and the pathogenicity of phytopathogenic fungi.

Stalk rot is a prevalent disease of maize (Zea mays L.) that severely affects maize yield and quality worldwide. The ascomycete fungus Fusarium spp. is the most common pathogen of maize stalk rot. At present, the molecular mechanism of Fusarium proliferation during the maize stalk infection that causes maize stalk rot has rarely been reported. In this study, we investigated the response of maize to F. proliferatum infestation by analyzing the phenotypic, transcriptomic, and metabolomic data of inbred lines ZC17 (resistant) and CH72 (susceptible) with different levels of resistance to stalk rot. Physiological and phenotypic results showed that the infection CH72 was significantly more severe than ZC17 after inoculation. Transcriptome analysis showed that after inoculation, the number of differentially expressed genes (DEGs) was higher in CH72 than in ZC17. Nearly half of these DEGs showed the same expression trend in the two inbred lines. Functional annotation and enrichment analyses indicated that the major pathways enriched for DEGs and DEMs included the biosynthesis of plant secondary metabolites, phenylalanine metabolism, biosynthesis of plant hormones, and plant–pathogen interactions. The comprehensive analysis of transcriptome and metabolome data indicated that phenylalanine metabolism and the phenylalanine, tyrosine, and tryptophan biosynthesis pathways played a crucial role in maize resistance to F. proliferatum infection. In addition, a transcription factor (TF) analysis of the DEGs showed that several TF families, including MYB, bHLH, NAC, and WRKY, were significantly activated after inoculation, suggesting that these TFs play important roles in the molecular regulatory network of maize disease resistance. The findings of this study provide valuable insights into the molecular basis of the response of maize to Fusarium proliferatum infection and highlight the importance of combining multiple approaches, such as phenotyping, transcriptomics, and metabolomics, to gain a comprehensive understanding of plant–pathogen interactions. [ABSTRACT FROM AUTHOR]

O-GlcNAcylation, an important post-translational modification catalyzed by O-GlcNAc transferase (OGT), plays critical roles in several biological processes. In this study, we present our findings on the function of FpOGT in regulating physiological processes and pathogenicity of Fusarium proliferatum (Fp), the alfalfa root rot fungus. The deletion of FpOGT impaired mycelial growth and altered macroconidia morphology in Fp. Furthermore, ΔFpOGT mutant displayed altered tolerance to various stressors, including cell wall perturbing agents, osmotic stressors, metal ionic stressors, and fungicides. Deletion of FpOGT significantly decreased Fp virulence toward alfalfa. The transcriptome analysis demonstrated that FpOGT plays a regulatory role in glucose metabolic pathways, including glycolysis, tricarboxylic acid (TCA) cycle, and hexosamine biosynthesis pathway (HBP), by influencing the expression of relevant genes. The downregulation of the glucokinase gene, FpGCK, was observed in ΔFpOGT, and the disruption of FpGCK led to a decrease in Fp virulence. Additionally, FpOGT affected the expression levels of the FpGCK-AS1 isoform, thereby impacting glucokinase function. The molecular docking analysis elucidated the plausible physical interaction between FpOGT and FpGCK, thereby offering valuable insights into their interrelationship. These findings underscore the indispensable involvement of FpOGT, the sole O-GlcNAc transferase in Fp, in various biological processes and the pathogenicity through its regulation of fundamental metabolic processes. Consequently, this study emphasizes the significance and elucidates the molecular mechanism underlying the role of O-GlcNAc transferase in diverse fundamental biological processes and the pathogenicity of phytopathogenic fungi. [ABSTRACT FROM AUTHOR]

During the survey in greenhouse‐cut flower carnation (Dianthus caryophyllus L.) areas in Izmir, wilted carnation samples were collected from 92 greenhouses. A total of 95 Fusarium spp. isolates were obtained from carnation greenhouses, 80 had been identified as Fusarium oxysporum f.sp. dianthi and published earlier, while the remaining 15 were identified as Fusarium proliferatum (Fp) based on morphological and molecular analysis using TEF1‐α gene sequences in this study. The prevalence of wilting disease of carnation caused by Fp was estimated to be 16.3% of the total area. Pathogenicity tests were conducted by dipping the carnation roots (cv. Turbo) in a spore suspension of monoconidial isolates and transplanting them into pots. Pathogenicity studies confirmed the ability of all Fp to cause symptoms of wilting, leaves and stems shriving. Phylogenetic analysis of sequences from the translation elongation factor 1α (TEF‐1 α) region of the 15 Fp isolates obtained from carnation formed a large clade of isolates originating from carnation and a wide range of other hosts in different geographical locations worldwide. To our knowledge, this is the first report of F. proliferatum causing wilt disease of carnation based on molecular identification in Türkiye. [ABSTRACT FROM AUTHOR]

This study investigates the reactions of four summer pumpkin cultivars (cvs. Çağlayan, Mert Bey, Sena Hanım, TG38) to root and crown rot caused by Fusarium proliferatum by taking into account criteria such as disease severity, plant growth (number of leaves, height, dry and fresh weight of shoot) and the accumulation of phenolic compounds in the roots. Seeds of each cultivar were inoculated with the pathogen and left to develop for 1 month at 25oC in a controlled climate room. The content of phenolic compounds in ethanolic root extracts was determined using high-performance liquid chromatography (HPLC). Cv. Sena Hanım had the lowest disease severity (4.40%) among the cultivars, followed by cvs. Çağlayan (10.62%) and Mert Bey (11.07%). Plants developed from inoculated seeds of cvs. Çağlayan and Sena Hanım had no decrease in the number of leaves and in length, fresh and dry weight of shoots in comparison to the control (plants from non-inoculated seeds), while cv. Mert Bey demonstrated a decrease at very low rates in shoot fresh and dry weight (2.24% and 0.77%, respectively). The phenolic compound that exhibited the highest increase in root extracts of cv. Sena Hanım compared to the control among the cultivars was p-coumaric acid (6.57-fold). This study demonstrates that p-coumaric acid can play an important role in the resistance of pumpkin to seed infestation by F. proliferatum.

Maize, one of the most important cereal crops in Bangladesh, is severely contaminated by fumonisin, a carcinogenic secondary metabolite produced by Fusarium including Fusarium proliferatum. Biocontrol with Bacillus strains is an effective approach to controlling this F. proliferatum as Bacillus has proven antagonistic properties against this fungus. Therefore, the present study aimed to determine how native Bacillus strains can reduce fumonisin in maize cultivated in Bangladesh, where BDISO76MR (Bacillus subtilis) strains showed the highest efficacy both in vitro in detached cob and in planta under field conditions. The BDISO76MR strain could reduce the fumonisin concentration in detached cob at 98.52% over untreated control, by inhibiting the conidia germination and spore formation of F. proliferatum at 61.56% and 77.01%, respectively in vitro. On the other hand, seed treatment with formulated BDISO76MR showed higher efficacy with a reduction of 97.27% fumonisin contamination compared to the in planta cob inoculation (95.45%) over untreated control. This implies that Bacillus-based formulation might be a potential approach in mitigating fumonisin contamination in maize to ensure safe food and feed.

Fusarium proliferatum decreases the productivity of shallot (Allium cepa L.). Endophytic bacteria are potential biocontrol agents in controlling the growth of F. proliferatum. This study aimed to select and characterize endophytic bacteria producing bioactive compounds that inhibit the growth of F. proliferatum. The endophytic bacteria used were isolated from the roots, stems, leaves, and soil of shallot plants from healthy and diseased shallot farming fields. The endophytic bacteria were selected using the dual culture method and extracted using ethyl acetate solvent. The results of the 16S rRNA identification suggested that isolate ABP5.2 is similar to Pseudomonas aeruginosa, while isolates BBP5.2 and DBP4.1 are similar to Myroides profundi. Isolate BBP5.2 was found to have the highest ability (68.15%) to inhibit the growth of F. proliferatum by using its antifungal compounds through a direct mechanism. In addition, the results of the Gas Chromatography-Mass Spectrophotometry analysis suggested that the compounds produced by the crude extracts of BBP5.2 isolate are hexadecanoic acid, 9-octadecenoic acid, linoleic acid, and piperine. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum is associated with the root rot of many plant species, but knowledge of its impact on western Canadian field crops is limited. This study assessed the host range of this fungus and its effect on plant emergence, plant height, and shoot and root dry weights in repeated greenhouse experiments with wheat, barley, faba beans, peas, lentils, canola, lupine, and soybeans. Infection was confirmed via PCR, and principal component analysis determined the utility of different parameters in assessing host responses. All crops were at least partly susceptible, developing mild to severe disease at the seedling and adult stages, and showing significant reductions in growth. In general, the barley and wheat demonstrated higher tolerances to infection, followed by the faba bean and the pea. The soybean, canola, lupine, and lentil were most susceptible. The canola and the soybean were particularly vulnerable to F. proliferatum at the pre-emergence stage, while infection greatly reduced the lentil’s biomass. Reductions in the barley’s emergence and other growth parameters, however, occurred only under a high inoculum concentration. Variability in root rot severity among cultivars of the same crop indicated some diversity in host reactions within species. Nonetheless, the absence of fully-resistant crops may pose challenges in managing F. proliferatum in western Canadian cropping systems.

2012 Elsevier Ltd. All rights reserved.Subcutaneous infections caused by two unusual fungi are rare. Here we report an elderly woman with long-term glucocorticoid use who was infected with Fusarium proliferatum on the right dorsum of the hand presenting with a verrucous plaque and Prototheca wickerhamii on the left dorsum of the hand presenting with geographic ulcers with erythematous plaques. The diagnosis was made through histopathological examination of skin samples and fungal culture, with identification through molecular examination. She was successfully treated with voriconazole.

The search for new drug-producing microorganisms is one of the most promising situations in current world scientific scenarios. The use of molecular biology as well as the cloning of protein and compound genes is already well established as the gold standard method of increasing productivity. Aiming at this increase in productivity, this work aims at the cloning, purification and in silico analysis of l-asparaginase from Fusarium proliferatum in Komagataella phaffii (Pichia pastoris) protein expression systems. The l-asparaginase gene (NCBI OQ439985) has been cloned into Pichia pastoris strains. Enzyme production was analyzed via the quantification of aspartic B-hydroxamate, followed by purification on a DEAE FF ion exchange column. The in silico analysis was proposed based on the combined use of various technological tools. The enzymatic activity found intracellularly was 2.84 IU/g. A purification factor of 1.18 was observed. The in silico analysis revealed the position of five important amino acid residues for enzymatic activity, and likewise, it was possible to predict a monomeric structure with a C-score of 1.59. The production of the enzyme l-asparaginase from F. proliferatum in P. pastoris was demonstrated in this work, being of great importance for the analysis of new methodologies in search of the production of important drugs in therapy. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum and Fusarium fujikuroi are the causative pathogens of stem rot in red-fleshed dragon fruit (Hylocereus polyrhizus). Both species are toxigenic fungi that produce several mycotoxins, including fumonisin B1 (FB1), moniliformin (MON), and beauvericin (BEA). These mycotoxins exert phytotoxic effects and are involved in pathogenesis in the host plants. In this study, we investigated the ability of F. proliferatum and F. fujikuroi to produce FB1, MON, and BEA. Polymerase chain reaction amplification using FUM1-specific primers detected the gene in all 44 isolates tested, indicating that all isolates produced FB1. Isolates of F. proliferatum and F. fujikuroi produced variable concentrations of FB1, ranging from 11.97-236.80 µg/g. MON and BEA were also produced at 0.48-174.84 µg/g and 0.28-70.02 µg/g, respectively by isolates of F. proliferatum and F. fujikuroi. These results suggest that the three mycotoxins play roles in stem rot disease development and symptom manifestation, as all isolates tested were pathogenic and led to stem rot in H. polyrhizus. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum causes yield loss in many agricultural crops. The chemicals used to control it bring problems due to phytotoxicity, residues, environmental pollution and harmful effects on human health. In recent years, the use of environmentally friendly control practices has increased due to the development of environmental and human health awareness. This study was carried out to determine antifungal activities of 52 candidate bioagent bacterial strains and two fungal isolates against F. proliferatum isolated from red pepper on petri plate assay. The activities of five bacterial strains and 2 fungal isolates that showed the highest inhibitory effect on F. proliferatum in in vitro were also determined in the dark at 25 ± 2 °C. In pot assay, the experiment was established with the most effective five bacterial strains (FDG-37, 70.63%; PM-18, 69.44%; Jumbo A, 66.07%; TV-13B, 64.00%; TV-15B, 60.71%) and two fungal isolates (ET 4 and ET 14, 74.35%). As a result, it was determined that Bacillus subtilis, Pseudomonas chlororaphis, Bacillus sp. and T. harzianum can be candidate in the biological control of F. proliferatum on red peppers. [ABSTRACT FROM AUTHOR]

Pineapple (Ananas comosus L. Merr) is a plant that can live well on nutrient-poor lands such as peatlands. However, plant resistance to nutrient-poor conditions is caused by symbiosis with endophytic bacteria capable of plant growth-promoting bacteria (PGPB) through biostimulant and bioprotective mechanisms. This study aims to characterize the potential of endophytic bacteria from pineapple roots from peatlands as biostimulants and bioprotective agents. Thirteen endophytic bacteria from pineapple root were characterized by their ability as biostimulants through phosphate dissolution tests using Pikovskaya media qualitatively and quantitatively, and the production of indole-3-acetic acid (IAA) upon additional 0.1% tryptophan. Furthermore, bacteria as bioprotectors were characterized by qualitative production of chitinase enzyme and antifungal tests against Fusarium proliferatum using dual culture techniques. The results showed the presence of 2 positive bacteria in all tests, namely the ANAP3 and ANAP5 isolates. ANPA3 bacteria show the highest activity in IAA production (26.3 ppm), and the highest antifungal activity in inhibiting F. proliferatum, with an inhibitory index reaching 52.6%. Meanwhile, ANAP5 is an endophytic bacterium with the highest phosphate dissolving activity, with a dissolved phosphate value of 253.5 ppm. This finding shows that some endophytic bacteria from pineapple roots on peatlands can be biostimulants and bioprotectors that can be developed as PGPB. [ABSTRACT FROM AUTHOR]

Stalk rot is a prevalent disease of maize (Zea mays L.) that severely affects maize yield and quality worldwide. The ascomycete fungus Fusarium spp. is the most common pathogen of maize stalk rot. At present, the molecular mechanism of Fusarium proliferation during the maize stalk infection that causes maize stalk rot has rarely been reported. In this study, we investigated the response of maize to F. proliferatum infestation by analyzing the phenotypic, transcriptomic, and metabolomic data of inbred lines ZC17 (resistant) and CH72 (susceptible) with different levels of resistance to stalk rot. Physiological and phenotypic results showed that the infection CH72 was significantly more severe than ZC17 after inoculation. Transcriptome analysis showed that after inoculation, the number of differentially expressed genes (DEGs) was higher in CH72 than in ZC17. Nearly half of these DEGs showed the same expression trend in the two inbred lines. Functional annotation and enrichment analyses indicated that the major pathways enriched for DEGs and DEMs included the biosynthesis of plant secondary metabolites, phenylalanine metabolism, biosynthesis of plant hormones, and plant–pathogen interactions. The comprehensive analysis of transcriptome and metabolome data indicated that phenylalanine metabolism and the phenylalanine, tyrosine, and tryptophan biosynthesis pathways played a crucial role in maize resistance to F. proliferatum infection. In addition, a transcription factor (TF) analysis of the DEGs showed that several TF families, including MYB, bHLH, NAC, and WRKY, were significantly activated after inoculation, suggesting that these TFs play important roles in the molecular regulatory network of maize disease resistance. The findings of this study provide valuable insights into the molecular basis of the response of maize to Fusarium proliferatum infection and highlight the importance of combining multiple approaches, such as phenotyping, transcriptomics, and metabolomics, to gain a comprehensive understanding of plant–pathogen interactions.

Copyright of Journal of Henan Agricultural Sciences is the property of Editorial Board of Journal of Henan Agricultural Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Two filamentous endophytic ascomycete fungi with different phenotypes were isolated and characterized from the vegetative tissue of Rheum spiciforme, a threatened and endemic trans-Himalayan medicinal herb. The visible morphological characteristics and microscopic features allowed the recognition of the endophytes as Fusarium proliferatum and Aureobasidium pullulans. Molecular identification involved partial DNA sequence analyses of internal transcribed spacer (ITS), elongation factor 1α (EF-1α), and calmodulin (CAL) regions of F. proliferatum DNA, and ITS and large subunit (LSU) of the nuclear ribosomal DNA (rDNA) of A. pullulans. The respective phylogenetic analyses by the Maximum Likelihood Method based on the combined ITS-EF-1α-CAL and ITS-LSU sequences showed that the former isolate is closest to F. proliferatum and the latter to A. pullulans. Moreover, using the LC-QTOF-MS technique, selected populations of R. spiciforme (one population with endophytes and another showing no apparent colonization), as well as the isolated endophytes, were evaluated for various specialized chemical constituents belonging to anthraquinone (rhein, physcion, emodin, and aloe-emodin), stilbenoid (piceatannol and resveratrol), and flavonoid (rutin, quercetin, and naringenin) class of compounds. Except for rutin, the results demonstrated that the identified endophytes possibly play an important role in sharing the metabolite synthesis machinery of the host. The current study may contribute to a better comprehension of the host-endophyte relation and open the door to the cost-effective synthesis of highly-valuable bioactive chemicals from microbial sources. [ABSTRACT FROM AUTHOR]

Background: Excessive inflammation results in severe tissue damage aswell as serious acute or chronic disorders, and extensive research has focused on finding new anti-inflammatory hit compounds with safety and efficacy profiles from natural products. As promising therapeutic entities for the treatment of inflammation-related diseases, fusaproliferin and its analogs have attracted great interest. However, the underlying anti-inflammatory mechanism is still poorly understood and deserves to be further investigated. Methods: For the estimation of the anti-inflammatory activity of fusaproliferin (1) and its analogs (2-4) in vitro and in vivo, lipopolysaccharide (LPS)-induced RAW264.7 macrophages and zebrafish embryos were employed. Then, transcriptome analysis was applied to guide subsequent western blot analysis of critical proteins in related signaling pathways. Surface plasmon resonance assays (SPR) combined with molecular docking analyses were finally applied to evaluate the affinity interactions between 1-4 and TLR4 and provide a possible interpretation of the downregulation of related signaling pathways. Results: 1-4 significantly attenuated the production of inflammatory messengers, including nitric oxide (NO), reactive oxygen species (ROS), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β), as well as nitric oxide synthase (iNOS) andcyclooxygenase-2 (COX-2), in LPS-induced RAW264.7 macrophages. Transcriptome analyses based on RNA-seq indicated the ability of compound 1 to reverse LPS stimulation and the nuclear factor kappa-B (NF-κB) and mitogen-activated protein kinase (MAPKs) signaling pathways contribute to the anti-inflammatory process. Experimental verification at the protein level revealed that 1 can inhibit the activation of inhibitor of NF-κB kinase (IKK), degradation of inhibitor of NF-κB (IκB), and phosphorylation of NF-κB and reduce nuclear translocation of NF-κB. 1 also decreased the phosphorylation of MAPKs, including p38, extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK). SPR assays andmolecular docking results indicated that 1-4 exhibited affinity for the TLR4 protein with KD values of 23.5-29.3 μM. Conclusion: Fusaproliferin and its analogs can be hit compounds for the treatment of inflammation-associated diseases. [ABSTRACT FROM AUTHOR]

Abstract Background Fusarium species are saprophytic fungi with a worldwide distribution. These fungi cause various infections among immunocompromised patients; however, they can also involve immunocompetent individuals. Case presentation We report a case of a 41-year-old Iranian woman who presented with ulcerative lesions on her lips 10 months ago. She had a long history of anxiety but had no history of classical risk factors such as trauma, cosmetic lip tattoo, burning in her lips, smoking or use of alcohol and opium. A skin biopsy from the lower lip was performed and sent for microbiological examinations. Hyaline septate hyphae were seen on direct microscopy with potassium hydroxide. The clinical specimen was subcultured on sabouraud dextrose agar with chloramphenicol and prepared for antifungal susceptibility testing and molecular identification. Considering the minimum inhibitory concentrations (MIC) for antifungals, itraconazole (100 mg orally twice a day) was started for her, and after 2 months, the lesions were treated. She followed up for 3 months, and no signs of disease recurrence were observed. Conclusions Selecting an appropriate treatment strategy according to the laboratory assessments is essential in clinical practice and the management of rare infections to prevent related mortality and morbidity of opportunistic fungal infections.

The aim of the current study was to isolate endophytes from the roots of Rhazya stricta and assess their potential to improve the growth of drought-stressed sunflower seedlings. The potential role of the isolated endophytic fungus was initially screened by using two rice varieties (mutant rice cultivar Waito-C: Gibberellins deficient; and Dongji byeo: Gibberellins-producing normal cultivar). A significant (p < 0.05) increase in various growth attributes of both rice varieties associated with one of the isolates i.e., N4 was noticed. Furthermore, the N4 isolate was tested for its role in improving the agronomic attributes of sunflowers under drought stress. The symbiotic association significantly (p < 0.05) improved the host growth and protection from PEG-induced drought stress. The drought mitigation in N4-associated sunflower seedlings can be linked with the regulation of phytohormones, stress-related metabolites, low-molecular-weight proteins and sugars, and scavenging of reactive oxygen species (ROS). Microscopic analysis revealed that the potent endophytic fungal strain consisted of thin and hyaline hyphae, forming dense olive-green mycelia (4–5 cm in dm) with black flask-shaped fruiting bodies. Based on the ITS sequence homology and phylogeny, the strain was identified as Fusarium proliferatum (MG251448). The results of this study concluded that this phytohormone-secreting endophyte can improve crop productivity in dry areas where drought stress is the main challenge faced by crops. [ABSTRACT FROM AUTHOR]

Chitosan is a natural polysaccharide and, when applied externally, is able to stimulate both growth and defense of the plant, enhancing its resistance to abiotic stresses and suppressing the development of many phytopathogens. Immune response includes the activation of defense proteins, carbohydrases such as chitinases and glucanases, which are also known to participate in the regulation of morphogenesis. In this study, for the first time, the effect of treatment with unfractionated (hydrolysate) chitosan of low (CH1) and medium (CH2) molecular weight on chitinase and glucanase activities, as well as on the expression of chitinase and β-1,3-glucanase genes in the roots of two cultivars of garlic Allium sativum L. differing by resistance to Fusarium rot was examined. It was shown that the effect of chitosans on the enzymatic activity and expression of the genes encoding β-1,3-glucanases (AsPR2a, AsPR2b, and AsPR2c) and chitinases (AsCHI1, AsCHI3, AsCHI7, AsCHI17, and AsCHI23) is cultivar-specific, which may be due to different susceptibility of the cultivars to Fusarium. The expression pattern of chitinase genes AsCHI10, AsCHI27, and AsCHI34, similar between varieties, suggested their involvement in root tissue morphogenesis. The results indicated a greater stimulatory effect of CH2 in comparison with CH1 on chitinase and glucanase activity. The stronger inhibitory influence of CH2 (as compared with CH1) on the expression of chitinase and β-1,3-glucanase genes correlated with the lower fungicidal effect of CH2 on Fusarium proliferatum. The findings may be used in breeding biotechnology to increase the resistance of garlic to Fusarium. [ABSTRACT FROM AUTHOR]

In 2018 and 2019, taro (Colocasia esculenta) plants presenting symptoms including a reddish-brown dry rot of the corms and wilting of the leaves were found in several fields in Kagoshima, Japan. Fusarium solani, F. proliferatum and F. oxysporum were isolated and identified based on morphological and molecular characteristics. Among the three fungal species F. solani was the most frequently found. We inoculated taro cv. Dotare corms with representative isolates of each species, and all three isolates reproduced the original symptoms. This is the first report of F. proliferatum as a causal agent of taro dry rot in Japan. [ABSTRACT FROM AUTHOR]

Polysaccharides from fungal source have been proved to be effective in different plethora of biomedical fields. The present study was carried out on exopolysaccharide (EPS) production by Fusarium proliferatum, considered novel fungus as no reports on its EPS production capability has been reported yet. The main objective of this study was to optimize media for better EPS production extracellularly under submerged culture conditions. Among all malt extract broth was selected as favorable medium for EPS yielding 81.4 ± 0.48 mg/l. Optimization revealed 9 days of incubation period, pH 6.0 and temperature 25 °C best for the growth and EPS yield. The medium 12 out of sixteen media was selected as best for the EPS yield which was ensured by various permutation and combinations of chemical factors. The optimized medium includes: malt extract medium (basal medium), xylose 4%, glucose 4%, tryptophan 0.1%, olive oil 3%, Tween 80 0.2%, vitamin C 0.2%, K2HPO4 0.2%, CaCl2 0.5%, pH 6.0, incubation period of 9 days at temperature 25 °C yielding 4067 ± 153.08 mg/l of EPS. HPTLC, FTIR and LCMS analysis exhibited the monomeric composition of maltose, fructose, xylose, galactose, glucose, raffinose and sorbose with functional group of –OH, C=O, C–O–C, C–O, –C–H, COO– with glycosidic likanges and suggested the production of glycan by these fungi. Owing to the existing reports of anti-cancerous property of β-Glycan an in-silico investigation was carried out to which indicatedits higher reactivity and lower binding affinityin comparison to imatinib, an oral chemotherapy drug to treat cancer.

Dry rot is an emerging issue for garlic production worldwide and Fusarium proliferatum is its major causal agent. Since the disease is seed-transmitted, sowing healthy cloves is crucial. In this study, some disinfection strategies were tested on garlic seeds, including steam, dry heat, chemical disinfectants and gaseous ozone (O3). Steam reduced the Colony Forming Units·g−1 (CFUs·g−1) by up to 92% in garlic seeds, but, at the same time, it affected their germination (−36%). Similarly, hydrogen peroxide (H2O2) and peracetic acid (C2H4O3) reduced the CFUs·g−1 by up to 83%; however, these methods also severely impaired germination (−40%). Dry heat did not negatively impact germination, but fungal contamination was not significantly reduced. The most promising strategy was gaseous O3 treatment; it decreased CFUs·g−1 by up to 96%, without causing any reduction of germination. The treatments applied were partially effective because the fungus is predominantly located in the outer layer of the seed, although it is also found in the inner portions. Some of these treatments can contribute to garlic protection from seed-borne pathogens and possibly reduce the occurrence of garlic dry rot. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Henan Agricultural Sciences is the property of Editorial Board of Journal of Henan Agricultural Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Microbial remediation, utilizing reduction of Cr(VI) to Cr(III), is considered a promising method for lowering toxic environmental chromium levels. In this study, a Cr(VI)-resistant fungal strain, Fusarium proliferatum S4 (F. proliferatum), was isolated from seriously chromium-polluted soil at Haibei Chemical Plant, China. This strain for treatment chromium-containing solution resulted in 100.00%, 93%, and 74% removal at initial concentrations of 10, 30, and 50 mg L−1 Cr(VI), respectively, after 12 days of treatment in a batch mode. Contributions of different cell fractions to Cr(VI) removal were explored. The Cr(VI) removal capacity of various cell components from strong to weak was as follows: cytoplasm, cell secretions, and cell debris. Observations obtained by scanning electron microscopy and transmission electron microscopy with energy dispersive X-ray spectroscopy revealed that not only the cell surfaces but also the intracellular contents were involved Cr through adsorption, reduction, or accumulation. Fourier transform infrared spectra indicated that a large number of functional groups (amino, carbonyl, carboxyl, and phosphate groups) participated in chromium binding on the cell surface. X-ray photoelectron spectroscopy confirmed the presence of Cr on the cell surface only as Cr(III). The results have important implications for an in-depth understanding of microbial chromate reduction by F. proliferatum. This study provides an insight into the microbial Cr(VI) bioreduction efficiency, and mechanisms in the chromium-contaminated environment. [ABSTRACT FROM AUTHOR]

In Bangladesh, Fusarium proliferatum is a prevalent pathogen of maize plants that poses a significant threat to human health and livestock by producing carcinogenic fumonisin. However, the use of the Bacillus species, which can colonize the infected plant parts, has been practiced globally to mitigate fumonisin contamination in maize. In this study, B. subtilis MMM1, a native isolate from the maize rhizosphere, was found to be the most effective antagonist against F. proliferatum, which reduced their mycelial growth and total fumonisin accumulation by 85.31% and 85.12%, respectively, over control through a fivefold reduction in fungal population (1.1 × 104 CFU/g maize grain) in vitro. Furthermore, out of the five bacilli used in this study, B. subtilis MMM1 was able to increase the root and, shoot length, and the vigor index of maize seedlings, by colonizing the fresh roots at 82 × 106 CFU/g root tissue. This suggests that B. subtilis MMM1 might be put forth both as a biocontrol agent and a plant growth promoter in Bangladesh to combat F. proliferatum. Nevertheless, evaluation of its efficacy in reducing fumonisin contamination in maize should be investigated under field conditions. [ABSTRACT FROM AUTHOR]

Onychomycosis, a nail fungal infection, is normally caused by dermatophytes. However, yeasts and non‐dermatophyte moulds (NDM) are among pathogens that cause nail disease. Regarding, this study aimed to describe the molecular epidemiology of Fusarium onychomycosis in the North of Iran. Two hundred and fifty seven nail samples collected from the patients clinically suspected of onychomycosis were subjected to direct microscopy, calcofluor white staining and culture. Fusarium isolates were identified at a species level through determination of multi‐locus sequences for internal transcribed spacer and translation elongation factor 1 alpha. Based on the findings, Fusarium species were isolated from onychomycosis patients (n = 27). According to a previous partial genes analysis, the species in the recent study belonged to the members of F. fujikuroi species complex (n = 14), Fusarium incarnatum‐equiseti species complex (n = 1) and F. solani species complex (n = 12). In this study, F. proliferatum was the dominant Fusarium species collected from the samples. The correct identification of Fusarium species is essential regarding the increased prevalence of Fusarium onychomycosis and the inherent resistance of these agents to a wide spectrum of antifungals. The obtained results indicated variation in the epidemiology of Fusarium species isolated from onychomycosis. Moreover, the minimum inhibitory concentration (MIC) of luliconazole and lanoconazole was in the range of 0.001–1 μg/ml, with the geometric mean of MICs obtained at 0.0103 and 0.0343 μg/ml against Fusarium species, respectively. These findings can increase researchers' knowledge regarding diversity of species, distribution of onychomycosis and the choice of a proper treatment. [ABSTRACT FROM AUTHOR]

The search for new drug-producing microorganisms is one of the most promising situations in current world scientific scenarios. The use of molecular biology as well as the cloning of protein and compound genes is already well established as the gold standard method of increasing productivity. Aiming at this increase in productivity, this work aims at the cloning, purification and in silico analysis of l-asparaginase from Fusarium proliferatum in Komagataella phaffii (Pichia pastoris) protein expression systems. The l-asparaginase gene (NCBI OQ439985) has been cloned into Pichia pastoris strains. Enzyme production was analyzed via the quantification of aspartic B-hydroxamate, followed by purification on a DEAE FF ion exchange column. The in silico analysis was proposed based on the combined use of various technological tools. The enzymatic activity found intracellularly was 2.84 IU/g. A purification factor of 1.18 was observed. The in silico analysis revealed the position of five important amino acid residues for enzymatic activity, and likewise, it was possible to predict a monomeric structure with a C-score of 1.59. The production of the enzyme l-asparaginase from F. proliferatum in P. pastoris was demonstrated in this work, being of great importance for the analysis of new methodologies in search of the production of important drugs in therapy.

Background: Fusarium species are saprophytic fungi with a worldwide distribution. These fungi cause various infections among immunocompromised patients; however, they can also involve immunocompetent individuals.Case Presentation: We report a case of a 41-year-old Iranian woman who presented with ulcerative lesions on her lips 10 months ago. She had a long history of anxiety but had no history of classical risk factors such as trauma, cosmetic lip tattoo, burning in her lips, smoking or use of alcohol and opium. A skin biopsy from the lower lip was performed and sent for microbiological examinations. Hyaline septate hyphae were seen on direct microscopy with potassium hydroxide. The clinical specimen was subcultured on sabouraud dextrose agar with chloramphenicol and prepared for antifungal susceptibility testing and molecular identification. Considering the minimum inhibitory concentrations (MIC) for antifungals, itraconazole (100 mg orally twice a day) was started for her, and after 2 months, the lesions were treated. She followed up for 3 months, and no signs of disease recurrence were observed.Conclusions: Selecting an appropriate treatment strategy according to the laboratory assessments is essential in clinical practice and the management of rare infections to prevent related mortality and morbidity of opportunistic fungal infections. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum is the principal etiological agent of rice spikelet rot disease (RSRD) in China, causing yield losses and fumonisins contamination in rice. The intraspecific variability and evolution pattern of the pathogen is poorly understood. Here, we performed whole-genome resequencing of 67 F. proliferatum strains collected from major rice-growing regions in China. Population structure indicated that eastern population of F. proliferatum located in Yangtze River with the high genetic diversity and recombinant mode that was predicted as the putative center of origin. Southern population and northeast population were likely been introduced into local populations through gene flow, and genetic differentiation between them might be shaped by rice-driven domestication. A total of 121 distinct genomic loci implicated 85 candidate genes were suggestively associated with variation of fumonisin B1 (FB1) production by genome-wide association study (GWAS). We subsequently tested the function of five candidate genes (gabap, chsD, palA, hxk1, and isw2) mapped in our association study by FB1 quantification of deletion strains, and mutants showed the impact on FB1 production as compared to the wide-type strain. Together, this is the first study to provide insights into the evolution and adaptation in natural populations of F. proliferatum on rice, as well as the complex genetic architecture for fumonisins biosynthesis. [ABSTRACT FROM AUTHOR]

Aims: This study evaluated the control effect of the endophytic fungus Phomopsis liquidambaris B3 against rice bakanae disease (RBD) caused by Fusarium proliferatum and the disease control result of different inoculation times of beneficial micro‐organisms. Methods and Results: Rice seedlings preinoculated, coinoculated and noninoculated with B3 were exposed to F. proliferatum stress and grown under controlled conditions. Greenhouse experimental results showed that rice preinoculation with B3 significantly reduced rice bakanae disease by 21.45%, inhibited the colonization of F. proliferatum, increased defence‐related enzyme activities, upregulated the expression of defence genes and promoted plant photosynthesis. However, bakanae disease in rice coinoculation with B3 increased by 11.45%, resulted in excessive reactive oxygen species (ROS) bursts and plant cell death. Conclusions: Preinoculation with the endophytic fungus P. liquidambaris B3 significantly reduced rice bakanae disease by triggering the SA‐dependent defence pathways of plants, and promoted plant growth. However, coinoculatiton with P. liquidambaris B3 activated excessive defence responses, resulting in plants cell death and aggravation of bakanae disease. Significance and Impact of the Study: This study indicated that P. liquidambaris B3 was an effective method for agricultural control against rice bakanae disease caused by F. proliferatum, and provides an experimental basis for the development of sustainable endophytic fungal resources to effectively control plant diseases caused by pathogenic fungi, and suggests that precise application of beneficial micro‐organisms may be become a key factor in farmland crop disease management. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum is the primary cause of spikelet rot disease in rice (Oryza sativa L.) in China. The pathogen not only infects a wide range of cereals, causing severe yield losses but also contaminates grains by producing various mycotoxins that are hazardous to humans and animals. Here, we firstly reported the whole-genome sequence of F. proliferatum strain Fp9 isolated from the rice spikelet. The genome was approximately 43.9 Mb with an average GC content of 48.28%, and it was assembled into 12 scaffolds with an N50 length of 4,402,342 bp. There is a close phylogenetic relationship between F. proliferatum and Fusarium fujikuroi, the causal agent of the bakanae disease of rice. The expansion of genes encoding cell wall-degrading enzymes and major facilitator superfamily (MFS) transporters was observed in F. proliferatum relative to other fungi with different nutritional lifestyles. Species-specific genes responsible for mycotoxins biosynthesis were identified among F. proliferatum and other Fusarium species. The expanded and unique genes were supposed to promote F. proliferatum adaptation and the rapid response to the host's infection. The high-quality genome of F. proliferatum strain Fp9 provides a valuable resource for deciphering the mechanisms of pathogenicity and secondary metabolism, and therefore shed light on development of the disease management strategies and detoxification of mycotoxins contamination for spikelet rot disease in rice. [ABSTRACT FROM AUTHOR]

Monodehydroascorbate reductase (MDHAR) catalyzes the reduction of monodehydroascorbic acid, formed as a result of reactive oxygen species neutralization to ascorbic acid, which is one of the main mechanisms for maintaining the intracellular redox status. Three MDHAR genes encoding monodehydroascorbate reductases of different cellular localization are identified in the garlic genome (Allium sativum L.). The Pyr_redox_2 domain, the domains of binding with FAD and NAD(P)H cofactors, and a unique long loop motif required for the enzyme active site formation were identified in the amino acid sequences AsMDHAR1, AsMDHAR4, and AsMDHAR5. The expression profiles of MDHAR1, MDHAR4, and MDHAR5 genes in various organs of a garlic plant were determined, and the alteration in the transcription levels of AsMDHARs in response to infection with the pathogen Fusarium proliferatum was studied. The maximum AsMDHARs transcription was shown in leaves, pseudostem, and, in the case of AsMDHAR1, in roots. In response to infection with F. proliferatum, an increase in the transcription of all three AsMDHAR genes in the roots of garlic plants was revealed, while the activation of the genes was similar and did not depend on the degree of cultivar resistance to Fusarium rot. [ABSTRACT FROM AUTHOR]

Sugars and organic acids are important factors associated with the postharvest quality of fruits and vegetables, but respiratory metabolism effects the metabolite contents. The objectives of this study were to explore the affects of Fusarium proliferatum infection on the postharvest quality and respiratory metabolism of green asparagus. It was found that F. proliferatum caused the soluble sugar concentration of asparagus to increase over the first 2 d of storage and then decrease again to become significantly lower than the control at 4 d. The titratable acidity (TA) of infected asparagus also increased from day 2 to day 6 and then decreased to become significantly lower than the control. Similarly, the key enzyme activities of the Embden-Meyerhof-Parnas (EMP) pathway, tricarboxylic acid (TCA) cycle, and pentose phosphate pathway (PPP) increased in pathogen-infected asparagus at the beginning of storage and then decreased to become lower than the control at the end. These findings demonstrate that F. proliferatum caused quality deterioration and an impairment of respiratory metabolism in postharvest asparagus. This research helps to clarify the relationships between pathogen infection, physiological metabolism, and asparagus quality and will provide valuable information for the control of postharvest diseases of asparagus. [ABSTRACT FROM AUTHOR]

Background: Excessive inflammation results in severe tissue damage as well as serious acute or chronic disorders, and extensive research has focused on finding new anti-inflammatory hit compounds with safety and efficacy profiles from natural products. As promising therapeutic entities for the treatment of inflammation-related diseases, fusaproliferin and its analogs have attracted great interest. However, the underlying anti-inflammatory mechanism is still poorly understood and deserves to be further investigated. Methods: For the estimation of the anti-inflammatory activity of fusaproliferin (1) and its analogs (2 - 4) in vitro and in vivo , lipopolysaccharide (LPS)-induced RAW264.7 macrophages and zebrafish embryos were employed. Then, transcriptome analysis was applied to guide subsequent western blot analysis of critical proteins in related signaling pathways. Surface plasmon resonance assays (SPR) combined with molecular docking analyses were finally applied to evaluate the affinity interactions between 1 - 4 and TLR4 and provide a possible interpretation of the downregulation of related signaling pathways. Results: 1 - 4 significantly attenuated the production of inflammatory messengers, including nitric oxide (NO), reactive oxygen species (ROS), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β), as well as nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), in LPS-induced RAW264.7 macrophages. Transcriptome analyses based on RNA-seq indicated the ability of compound 1 to reverse LPS stimulation and the nuclear factor kappa-B (NF-κB) and mitogen-activated protein kinase (MAPKs) signaling pathways contribute to the anti-inflammatory process. Experimental verification at the protein level revealed that 1 can inhibit the activation of inhibitor of NF-κB kinase (IKK), degradation of inhibitor of NF-κB (IκB), and phosphorylation of NF-κB and reduce nuclear translocation of NF-κB. 1 also decreased the phosphorylation of MAPKs, including p38, extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK). SPR assays and molecular docking results indicated that 1 - 4 exhibited affinity for the TLR4 protein with KD values of 23.5–29.3 μM. Conclusion: Fusaproliferin and its analogs can be hit compounds for the treatment of inflammation-associated diseases. [ABSTRACT FROM AUTHOR]

• Fusarium-Dendrobium interactions were studied under greenhouse cultivation • Fusarium proliferatum strains behave differently with the orchid host plants • F. proliferatum ET1 shows endophytic lifestyle in D. nobile and D. moschatum roots • Non-myccorhizal endophytic fungi include non-pathogenic Fusarium isolates • Direct plant assays are needed to determine endophytism of orchid-associated fungi Orchids reveal a complexity of interactions with their microbial partners, particularly with mycorrhizal fungi. Orchid roots are also colonized by a number of associated endophytic fungi, whose activity and role is as yet insufficiently known. Here we studied the relations between two epiphytic orchids, Dendrobium moshatum and D. nobile , and several strains of the genus Fusarium – two pathogenic, F. fujikuroi (IMI58289) and F. proliferatum (NRRL 62905), and an orchid-associated, Fusarium proliferatum ET1. Recent reports indicate that F. proliferatum shows a high phenotypic variation in causing symptoms on one or different hosts. In this study, in contrast to the pathogenic species, an orchid-associated F. proliferatum ET1 strain showed its neutral endophytic lifestyle strategy towards the host-orchids. Despite an invasive and aggressive distribution of both phytopathogens, causing the root and leaf symptoms, the moderate colonization of F. proliferatum ET1 did not cause any negative effects on the adult plants during the experimental period. The quantitative characteristic of the fungal growth assessed by counting colony forming units confirmed the results of the bioassay, supporting the strain-specificity of the orchid-fungal interactions and a pattern of balanced relations with the non-mycorrhizal endophytic Fusarium isolate. [ABSTRACT FROM AUTHOR]

Fusarium proliferatum known as a pathogen of sheath rot disease. This study aims to determine the genetic diversity by rep-PCR and determine the relationship between the molecular diversity data and the in vitro environmental treatment by using light, pH and temperature and rice variety test. The rep-PCR amplification demonstrated that F. proliferatum was categorized into two groups. Based on the mycelial weight and the growth rate parameters, the 12light/12dark, pH 8, and 25 °C sub-treatments showed the highest outcomes, while in continuous light, pH 6, and 25 °C sub-treatments got the highest spore production. The Inpari 30 rice variety showed the highest disease severity results for F. proliferatum infection. Both the results of the F. proliferatum groups did not affect the fungal growth and fungal infection in several tested rice varieties. These findings suggest that each isolate has a different ability to grow, produce mycelium and spores, and infect a specific rice variety. [ABSTRACT FROM AUTHOR]

Infections by Fusarium and Fusarium-like species on cacti and other succulent plants cause the syndrome known as Fusarium dry rot and soft rot. There are only few records of Fusarium species as pathogens of cacti and other succulent plants from Iran. The objective of this study was the identification and characterization of fusarioid species recovered from ornamental succulents in Shiraz County, Iran. Three fusarioid species, including F. oxysporum, F. proliferatum, and Neocosmospora falciformis (formerly F. falciforme), were recovered from 29 diverse species of cacti and other succulents with symptoms of Fusarium dry rot and soft rot. The three fungal species were identified on the basis of morphological characters and the phylogenetic analysis of the translation elongation factor1-α (tef1) nuclear gene. The F. oxysporum isolates were identified as F. oxysporum f. sp. opuntiarum. The pathogenicity of the three fusarioid species was tested on a range of economically important ornamental succulents, mostly in the Cactaceae family. The three species showed a broad host spectrum and induced different types of symptoms on inoculated plants, including soft and dry rot, chlorosis, necrotic spots, wilt, drying, root and crown rot. This is the first report of N. falciformis as a pathogen of succulent plants worldwide. [ABSTRACT FROM AUTHOR]

Relevance and methods. Losses of agricultural crops are associated not only with the development of diseases during the growing season, but also during post-harvest storage. Garlic is a popular vegetable and aromatic crop in world. Significant losses in garlic yield during cultivation and storage are associated with fungal pathogens, the most harmful of which are representatives of the genus Fusarium. In the Moscow region, the defeat of garlic by Fusarium occurs annually, but with varying intensity. At the Federal Scientific Vegetable Center (FSVC), it was shown that rot and wilting of garlic plants is caused by a complex of pathogenic fungi, including mainly different species of Fusarium. At the same time, the ratio of Fusarium species in the pathogenic complex changes from year to year, new Fusarium species and their races are registered. The aim of this study was to identify fungal phytopathogens causing dry rot of garlic cloves during post-harvest storage. To carry out the work, garlic bulbs of cultivars Dubkovsky and Strelets were taken from the FSVC storage.Results. As a result of visual examination, cloves with symptoms of dry rot were identified. The diseased cloves tissues were plated on potato dextrose agar to obtain fungal colonies. Analysis of the morphological and cultural characteristics of fungal isolates, as well as the nucleotide sequences of four DNA regions (ITS spacers, genes EF1α, RPB1, and RPB2) showed that the causative agent of dry rot of garlic cloves is the pathogenic fungus Fusarium proliferatum. In addition, in the field, identification was carried out based on the analysis of the sequences of spacers ITS and the EF1αgene of phytopathogenic fungi inhabiting the root zone of garlic plants. As a result, two species of fungi of the genus Fusarium (F. proliferatum and F. oxysporum f. sp. cepae), as well as the species Rhizoctonia solani, Volutella rosea, and Ceratobasidium sp. were found in the root zone of garlic cultivars.

Background: Excessive inflammation results in severe tissue damage as well as serious acute or chronic disorders, and extensive research has focused on finding new anti-inflammatory hit compounds with safety and efficacy profiles from natural products. As promising therapeutic entities for the treatment of inflammation-related diseases, fusaproliferin and its analogs have attracted great interest. However, the underlying anti-inflammatory mechanism is still poorly understood and deserves to be further investigated.Methods: For the estimation of the anti-inflammatory activity of fusaproliferin (1) and its analogs (2-4)in vitro and in vivo, lipopolysaccharide (LPS)-induced RAW264.7 macrophages and zebrafish embryos were employed. Then, transcriptome analysis was applied to guide subsequent western blot analysis of critical proteins in related signaling pathways. Surface plasmon resonance assays (SPR) combined with molecular docking analyses were finally applied to evaluate the affinity interactions between 1-4 and TLR4 and provide a possible interpretation of the downregulation of related signaling pathways.Results: 1-4 significantly attenuated the production of inflammatory messengers, including nitric oxide (NO), reactive oxygen species (ROS), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β), as well as nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), in LPS-induced RAW264.7 macrophages. Transcriptome analyses based on RNA-seq indicated the ability of compound 1 to reverse LPS stimulation and the nuclear factor kappa-B (NF-κB) and mitogen-activated protein kinase (MAPKs) signaling pathways contribute to the anti-inflammatory process. Experimental verification at the protein level revealed that 1 can inhibit the activation of inhibitor of NF-κB kinase (IKK), degradation of inhibitor of NF-κB (IκB), and phosphorylation of NF-κB and reduce nuclear translocation of NF-κB. 1 also decreased the phosphorylation of MAPKs, including p38, extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK). SPR assays and molecular docking results indicated that 1-4 exhibited affinity for the TLR4 protein with KD values of 23.5–29.3 μM.Conclusion: Fusaproliferin and its analogs can be hit compounds for the treatment of inflammation-associated diseases.

Fusarium proliferatum has been identified as the causal pathogen of Fusarium root rot of Ba kich (Morinda officinalis) (FRRBK). No studies are available regarding the effectiveness of chemical treatments on the disease incidence of FRRBK. The efficacy of five active ingredients (metconazole, prochloraz, tebuconazole, kresoximmethyl, and pyraclostrobin) from two chemical groups (demethylation inhibitors and quinone outside inhibitors) in reducing three isolates (BKVN, BKDT, and BKPL) of F. proliferatum mycelial growth was tested in vitro. The results indicate that only metconazole, prochloraz, and tebuconazole are highly effective in inhibiting the mycelial growth of F. proliferatum. These were selected for investigation of their efficacy with regard to the disease incidence of FRRBK in pot and in field conditions. Prochloraz and metconazole showed the highest efficacy and significantly suppressed the disease incidence of FRRBK in pot and in field conditions.

In this study, 13 previously undescribed acorane sesquiterpenoids, namely, proliferacorins A–M, were isolated from the solid fermentation of Fusarium proliferatum. Their structures and absolute configurations were confirmed via spectroscopic analyses, quantum-chemical NMR calculations with DP4+ probability analyses, ECD calculations and comparisons, and single-crystal X-ray diffraction techniques. Proliferacorins A–E (1 – 5) have a 7-oxa-tricyclo[6.3.1.01,5]tridecane decorated with a rare ether bridge between C-7 and C-11, while proliferacorin F (6) possesses a 7-oxa-tricyclic[6.4.0.01,5]dodecane skeleton with an unusual ether bond between C-6 and C-11. Proliferacorins C and D (3 and 4) are a pair of isomers at the carbon bridge between C-5 and C-7, whereas proliferacorins H and I (8 and 9) are a pair of spiro carbon isomers. All isolates were tested for their cytotoxic, anti-inflammatory, and immunosuppressive activities. Proliferacorins A−M (1 − 13), thirteen undescribed acorane sesquiterpenoids, were isolated from Fusarium proliferatum. Proliferacorins A−E (1 − 5) have a 7-oxa-tricyclo[6.3.1.01,5]tridecane decorated with a rare ether bridge between C-7 and C-11, while proliferacorin F (6) possesses a 7-oxa-tricyclic[6.4.0.01,5]dodecane skeleton with an unusual ether bond between C-6 and C-11. Proliferacorins C and D (3 and 4) are a pair of isomers at the carbon bridge between C-5 and C-7, whereas proliferacorins H and I (8 and 9) are a pair of spiro carbon isomers. [Display omitted] • Thirteen undescribed sesquiterpenoids were isolated from Fusarium proliferatum. • Proliferacorins A−E have a 7-oxa-tricyclo[6.3.1.01,5]tridecane tricyclic skeleton. • Proliferacorin F possesses a 7-oxa-tricyclic[6.4.0.01,5]dodecane tricyclic system. • Proliferacorins C and D are a pair of isomers at the carbon bridge. • Proliferacorins H and I are a pair of C-5 spiro carbon isomers. [ABSTRACT FROM AUTHOR]

In the present investigation, the effect of cinnamon oil (CO) (10, 30, 50 and 70 %) on the growth rate (mm/day) and aflatoxin B1 (AFB1) and fumonisin B1 (FB1) production of Aspergillus flavus (AF01) and Fusarium proliferatum (FP01) isolates, respectively was determined at optimum water activities (0.95 and 0.99 a w) and temperatures (25, 30 and 35 °C) on paddy and polished rice grains. The results showed that the growth rate, AFB1 and FB1 production of all the fungal isolates decreased with an increase in CO concentrations on both matrices. AF01 and FP01 failed to grow under all conditions on paddy at 50 % of CO concentration whereas both fungi were completely inhibited (No Growth-NG) at 70 % of CO on polished rice. Regarding mycotoxin production, 30 % of CO concentrations could inhibit AFB1 and FB1 production in both matrices (No Detection-ND). In this study, the production of mycotoxins was significantly influenced by cinnamon oil compared to the growth of both fungi. These results indicated the promising potential of CO in improving the quality of rice preservation in post-harvest; however, further investigations should be evaluated on the effects on the qualitative characteristics of grains. Especially, the prospective application of CO in rice storage in industry scales to mitigate mycotoxin contamination need also to be further researched. Moreover, collaboration between researchers, agricultural experts, and food industry should be set up to achieve effective and sustainable strategies for preserving rice. • Cinnamon oil (CO) was used to minimize A. flavus and F. proliferatum growth and mycotoxins. • CO significantly inhibited both fungi and their toxins on paddy and polished rice. • FB1 and F. proliferatum growth was strongly inhibited compared to AFB1 and A. flavus growth by CO. [ABSTRACT FROM AUTHOR]

The aim of the current study was to isolate endophytes from the roots of Rhazya stricta and assess their potential to improve the growth of drought-stressed sunflower seedlings. The potential role of the isolated endophytic fungus was initially screened by using two rice varieties (mutant rice cultivar Waito-C: Gibberellins deficient; and Dongji byeo: Gibberellins-producing normal cultivar). A significant (p < 0.05) increase in various growth attributes of both rice varieties associated with one of the isolates i.e., N4 was noticed. Furthermore, the N4 isolate was tested for its role in improving the agronomic attributes of sunflowers under drought stress. The symbiotic association significantly (p < 0.05) improved the host growth and protection from PEG-induced drought stress. The drought mitigation in N4-associated sunflower seedlings can be linked with the regulation of phytohormones, stress-related metabolites, low-molecular-weight proteins and sugars, and scavenging of reactive oxygen species (ROS). Microscopic analysis revealed that the potent endophytic fungal strain consisted of thin and hyaline hyphae, forming dense olive-green mycelia (4–5 cm in dm) with black flask-shaped fruiting bodies. Based on the ITS sequence homology and phylogeny, the strain was identified as Fusarium proliferatum (MG251448). The results of this study concluded that this phytohormone-secreting endophyte can improve crop productivity in dry areas where drought stress is the main challenge faced by crops.

Plant antifungal proteins include the pathogenesis-related (PR)-5 family of fungi- and other stress-responsive thaumatin-like proteins (TLPs). However, the information on the TLPs of garlic (Allium sativum L.), which is often infected with soil Fusarium fungi, is very limited. In the present study, we identified 32 TLP homologs in the A. sativum cv. Ershuizao genome, which may function in the defense against Fusarium attack. The promoters of A. sativumTLP (AsTLP) genes contained cis-acting elements associated with hormone signaling and response to various types of stress, including those caused by fungal pathogens and their elicitors. The expression of AsTLP genes in Fusarium-resistant and -susceptible garlic cultivars was differently regulated by F. proliferatum infection. Thus, in the roots the mRNA levels of AsTLP7–9 and 21 genes were increased in resistant and decreased in susceptible A. sativum cultivars, suggesting the involvement of these genes in the garlic response to F. proliferatum attack. Our results provide insights into the role of TLPs in garlic and may be useful for breeding programs to increase the resistance of Allium crops to Fusarium infections. [ABSTRACT FROM AUTHOR]