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AbstractChickpea wilt, caused by a complex of soilborne fungi (Fusarium spp. Macrophomina phaseolina, Rhizoctonia solani, Sclerotium rolfsii, and Sclerotinia sclerotiorum), is the most important disease of chickpeas (Cicer arietinum) in Mexico. The aims of this study were to characterize Trichoderma isolates using a combination of phenotypic and molecular approaches and to evaluate their antagonistic activity against soilborne fungi associated with chickpea wilt. A total of 30 Trichoderma isolates were obtained from rhizospheric soil samples collected from chickpea fields in different locations of Sinaloa, Mexico. Dual confrontation assays showed the potential antagonistic effect of Trichoderma isolates against F. languescens, M. phaseolina, R. solani, S. rolfsii, and S. sclerotiorum. Five Trichoderma isolates (FAVF335, FAVF340, FAVF345, FAVF349, and FAVF351) exhibited mycelial growth inhibition of the five pathogens that ranged from 56 to 71%. These isolates were characterized using cultural, morphological, and molecular studies and tested in vivo for their ability to control soilborne pathogens in two chickpea cultivars (Blanco Sinaloa-92 and P2245) under greenhouse conditions. Phylogenetic analysis based on a combined ITS, EF-1α, and rpb2 sequence dataset identified T. afroharzianum (FAVF345, FAVF349, and FAVF351) and T. longibrachiatum (FAVF335 and FAVF340). Coating of chickpea seeds with T. longibrachiatum (FAVF335 and FAVF340) significantly reduced the disease severity and improved the plant growth-promoting attributes. [ABSTRACT FROM AUTHOR]

Trichoderma longibrachiatum UN32 is a well-documented mutant strain known to produce dendrobine-type total alkaloids (DTTAs). It was serendipitously observed that the addition of Co2+ to the medium resulted in a notable enhancement in DTTAs production in the T. longibrachiatum UN32 strain, accompanied by an upregulating effect on the expression of antioxidase-related genes. Hence, the objective of the present work was to ascertain whether ROS (intracellular levels of hydrogen peroxide) induced by Co2+ treatment has a beneficial or detrimental impact on DTTAs biosynthesis. A comparison of the intracellular levels of hydrogen peroxide (H2O2) and DTTAs treated with CoCl2 and CH3COOH revealed that CoCl2 was the optimal inducer for investigating the relationship between ROS formation and DTTAs production. This was due to the observation that ROS formation was reduced by approximately 4% and DTTAs production was increased by 12.55% in comparison to the CH3COOH treatment. The physiological results revealed that the introduction of Co2+ resulted in the oxidative damage and activation of the expression of intracellular superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD). Furthermore, it was confirmed that ROS induced by Co2+ was beneficial to DTTAs production by adding exogenous ROS scavengers. The inclusion of all ROS scavengers, including vitamin C, tocopherol, melatonin, mannitol, and sesamol, resulted in a reduction in ROS accumulation and a concomitant decrease in DTTAs production. Specifically, the addition of melatonin at a concentration of 0.4 mg/L demonstrated significant effects, resulting in a 32.53% (P < 0.01) decrease in ROS accumulation and a 45.22% (P < 0.01) reduction in DTTAs production. Subsequently, the timelines of accumulation of intracellular H2O2 and DTTAs content indicated that ROS are also crucial for normal fermentation without CoCl2 addition. Specifically, the proper H2O2 dose for DTTAs accumulation is between 8.82 and 18.86 μmol/g. The present study offers the initial experimental evidence indicating that CoCl2 enhance DTTAs production during the culture of T. longibrachiatum UN32 via leading an increase in intracellular ROS, which is conductive to DTTAs production and can be inhibited by the ROS scavengers. Our results provide insights into the mechanistic study of DTTAs biosynthesis. [ABSTRACT FROM AUTHOR]

Forestry residues (FR) and medicinal-aromatic plant waste (MAPW) are considered potential resources for energy recovery. In this context, we explore the bioethanol production potential of three microbial strains Aspergillus niger, Zymomonas mobilis, and Trichoderma longibrachiatum using this lignocellulosic hydrolysate as a substrate. The blend of FR and MAPW was pretreated by different methods like acid sulfuric (AS), steam explosion (SE), and enzymatic (E). The ethanol yield was measured by gas chromatography (GC). Zymomonas mobilis demonstrated the highest ethanol yield of 5.95% on untreated substrate. Conversely, Aspergillus niger exhibited peak performance with an ethanol yield of 10.78% following AS, SE and E combined pretreatment. Trichoderma longibrachiatum, yielded ethanol ranging from 1.27% to 2.47%. Furthermore, the use of immobilized d' Aspergillus niger strains revealed a small decrease in ethanol yield from 11.34% in the first cycle to only 5.02% in the sixth cycle. In conclusion, Aspergillus niger emerges as a promising candidate due to its dual functionality in pretreatment and ethanol fermentation, offering pathways for advancing sustainable biofuel technologies. [ABSTRACT FROM AUTHOR]

Copyright of Acta Agriculturae Zhejiangensis is the property of Acta Agriculturae Zhejiangensis Editorial Office 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.)

Fungal diseases are a major threat to the horticultural industry and cause substantial postharvest losses. While secondary metabolites from Trichoderma sp. have been explored for their antifungal properties, limited information exists on the phenolic compounds produced by less studied species like Trichoderma longibrachiatum. In this study, phenolic compounds were extracted from a liquid culture of T. longibrachiatum using various solvents and methods (conventional and ultrasonic-assisted). Phenolic compounds were quantified by spectrophotometry and identified by high-performance liquid chromatography with diode array detection (HPLC-DAD). The antifungal activity against Alternaria alternata and Fusarium oxysporum was determined by mycelial growth inhibition assays, maximum growth rate (µmax) by the Gompertz equation, and spore germination tests. Although no significant differences (p ≥ 0.05) were found between the extraction methods, the type of solvent significantly influenced the phenolic content (p ≤ 0.05). Extraction with 70% ethanol showed the highest content of phenolic compounds and flavonoids. More than eight phenolic compounds were detected. Further, this is the first report of the phenolics ferulic, chlorogenic and p-coumaric acids identification in T. longibrachiatum, along with flavonoids such as epicatechin and quercetin, among others. The 70% ethanolic extracts notably inhibited the mycelial growth of A. alternata and F. oxysporum, reducing their maximum growth rate by 1.5 and 1.4 mm/h, respectively. Furthermore, p-coumaric and ferulic acids significantly inhibited spore germination of both pathogens, with a minimum inhibitory concentration (MIC) of 1.5 mg/mL and a minimum fungicidal concentration (MFC) of 2 mg/mL. These findings demonstrate the potential of T. longibrachiatum and its phenolic compounds as viable alternatives for biological control in horticulture and postharvest disease management.

The examination of fungal secretomes has garnered attention for its potential to unveil the repertoire of secreted proteins, notably CAZymes (Carbohydrate-Active enzymes), across various microorganisms. This study presents findings on categorizing the secretome profile of CAZymes by their function and family, derived from the filamentous fungus Trichoderma longibrachiatum LMBC 172. The cultivation was performed through submerged fermentation with three distinct carbon sources: sugarcane bagasse, tamarind seeds, and a control simulating hemicellulose containing 0.5% beechwood xylan plus 0.5% oat spelt xylan. The secretome analysis revealed 206 distinct CAZymes. Each carbon source showed particularities and differences. Of these, 89 proteins were produced simultaneously with all the carbon sources; specifically, 41 proteins using only the hemicellulose simulation, 29 proteins when sugarcane bagasse was used as a carbon source, and only 3 when tamarind seeds were used. However, in this last condition, there was a high intensity of xyloglucanase GH74 production, thus reaffirming the richness of xyloglucan in the constitution of these seeds. When evaluating the proteins found in two conditions, 18 proteins were shown between the simulation of hemicellulose and sugarcane bagasse, 11 proteins between the simulation of hemicellulose and tamarind seeds, and 15 proteins between sugarcane bagasse and tamarind seeds. Among the proteins found, there are representatives of different families such as glycosyl hydrolases (GHs) that cleave cellulose, hemicellulose, pectin, or other components; carbohydrate esterases (CEs); polysaccharide lyases (PLs); carbohydrate-binding modules (CBMs); and auxiliary activity enzymes (AAs). These results demonstrate the importance of analyzing CAZymes secreted by microorganisms under different culture conditions.

Abstract Fusarium oxysporum (Schl.) f.sp. melonis, which causes muskmelon wilt disease, is a destructive filamentous fungal pathogen, attracting more attention to the search for effective fungicides against this pathogen. In particular, Silver nanoparticles (AgNPs) have strong antimicrobial properties and they are not easy to develop drug resistance, which provides new ideas for the prevention and control of muskmelon Fusarium wilt (MFW). This paper studied the effects of AgNPs on the growth and development of muskmelon, the control efficacy on Fusarium wilt of muskmelon and the antifungal mechanism of AgNPs to F. oxysporum. The results showed that AgNPs could inhibit the growth of F. oxysporum on the PDA and in the PDB medium at 100–200 mg/L and the low concentration of 25 mg/L AgNPs could promote the seed germination and growth of muskmelon seedlings and reduce the incidence of muskmelon Fusarium wilt. Further studies on the antifungal mechanism showed that AgNPs could impair the development, damage cell structure, and interrupt cellular metabolism pathways of this fungus. TEM observation revealed that AgNPs treatment led to damage to the cell wall and membrane and accumulation of vacuoles and vessels, causing the leakage of intracellular contents. AgNPs treatment significantly hampered the growth of mycelia in the PDB medium, even causing a decrease in biomass. Biochemical properties showed that AgNPs treatment stimulated the generation of reactive oxygen species (ROS) in 6 h, subsequently producing malondialdehyde (MDA) and increasing protective enzyme activity. After 6 h, the protective enzyme activity decreased. These results indicated that AgNPs destroy the cell structure and affect the metabolisms, eventually leading to the death of fungus.

Fungal diseases are a major threat to the horticultural industry and cause substantial postharvest losses. While secondary metabolites from Trichoderma sp. have been explored for their antifungal properties, limited information exists on the phenolic compounds produced by less studied species like Trichoderma longibrachiatum. In this study, phenolic compounds were extracted from a liquid culture of T. longibrachiatum using various solvents and methods (conventional and ultrasonic-assisted). Phenolic compounds were quantified by spectrophotometry and identified by high-performance liquid chromatography with diode array detection (HPLC-DAD). The antifungal activity against Alternaria alternata and Fusarium oxysporum was determined by mycelial growth inhibition assays, maximum growth rate (µmax) by the Gompertz equation, and spore germination tests. Although no significant differences (p ≥ 0.05) were found between the extraction methods, the type of solvent significantly influenced the phenolic content (p ≤ 0.05). Extraction with 70% ethanol showed the highest content of phenolic compounds and flavonoids. More than eight phenolic compounds were detected. Further, this is the first report of the phenolics ferulic, chlorogenic and p-coumaric acids identification in T. longibrachiatum, along with flavonoids such as epicatechin and quercetin, among others. The 70% ethanolic extracts notably inhibited the mycelial growth of A. alternata and F. oxysporum, reducing their maximum growth rate by 1.5 and 1.4 mm/h, respectively. Furthermore, p-coumaric and ferulic acids significantly inhibited spore germination of both pathogens, with a minimum inhibitory concentration (MIC) of 1.5 mg/mL and a minimum fungicidal concentration (MFC) of 2 mg/mL. These findings demonstrate the potential of T. longibrachiatum and its phenolic compounds as viable alternatives for biological control in horticulture and postharvest disease management. [ABSTRACT FROM AUTHOR]

The examination of fungal secretomes has garnered attention for its potential to unveil the repertoire of secreted proteins, notably CAZymes (Carbohydrate-Active enzymes), across various microorganisms. This study presents findings on categorizing the secretome profile of CAZymes by their function and family, derived from the filamentous fungus Trichoderma longibrachiatum LMBC 172. The cultivation was performed through submerged fermentation with three distinct carbon sources: sugarcane bagasse, tamarind seeds, and a control simulating hemicellulose containing 0.5% beechwood xylan plus 0.5% oat spelt xylan. The secretome analysis revealed 206 distinct CAZymes. Each carbon source showed particularities and differences. Of these, 89 proteins were produced simultaneously with all the carbon sources; specifically, 41 proteins using only the hemicellulose simulation, 29 proteins when sugarcane bagasse was used as a carbon source, and only 3 when tamarind seeds were used. However, in this last condition, there was a high intensity of xyloglucanase GH74 production, thus reaffirming the richness of xyloglucan in the constitution of these seeds. When evaluating the proteins found in two conditions, 18 proteins were shown between the simulation of hemicellulose and sugarcane bagasse, 11 proteins between the simulation of hemicellulose and tamarind seeds, and 15 proteins between sugarcane bagasse and tamarind seeds. Among the proteins found, there are representatives of different families such as glycosyl hydrolases (GHs) that cleave cellulose, hemicellulose, pectin, or other components; carbohydrate esterases (CEs); polysaccharide lyases (PLs); carbohydrate-binding modules (CBMs); and auxiliary activity enzymes (AAs). These results demonstrate the importance of analyzing CAZymes secreted by microorganisms under different culture conditions. [ABSTRACT FROM AUTHOR]

Aims: Damping-off disease, caused by Fusarium oxysporum, affects the growth of Pinus massoniana seedlings. Plant growth-promoting fungi and rhizobacteria (PGPF and PGPR) are widely used in agriculture to control plant soil-borne disease, however, the joint mechanism by which they inhibit damping-off disease in forestry requires further exploration. Methods: The current study screened for the ability of antagonistic PGPF and PGPR strains to inhibit the pathogen, and used soil microbiome and plant transcriptome technologies to characterize the biocontrol mechanism. Results: PGPF strain 3Y, identified as Trichoderma longibrachiatum, and PGPR strain K29, identified as Burkholderia stabilis, were screened and found to strongly inhibit the growth of F. oxysporum through direct contact with the hyphae. The combined use of T. longibrachiatum and B. stabilis effectively reduced disease incidence and severity, and promoted the growth of P. massoniana seedlings, and enhanced soluble sugar, proline, SOD and POD activities. Compound strains treatment impacted the structure of rhizosphere bacterial microbial community, causing significant differences in the relative abundances of some key phyla and genera, promoting the enrichment of some beneficial microorganisms. Transcriptome profiles showed that combination treatment with the biocontrol strains induced the expressions of 8541 differentially expressed genes (DEGs). These genes participated in key biological pathways associated with starch and sucrose metabolism, plant hormone signal transduction, photosynthesis, antioxidant enzymes, and proline synthesis. Conclusion: The combined use of PGPF and PGPR strains controlled F. oxysporum infection of P. massoniana seedlings by regulating physiological responses and soil microbial community. [ABSTRACT FROM AUTHOR]

Invasive fungal infection is a life-threatening complication of chemotherapy and neutropaenia in the haematology population. Trichoderma species rarely cause human disease but have been reported to cause invasive infection in the immunosuppressed. We present a case of invasive Trichoderma longibrachiatum pulmonary infection with fatal outcome in a neutropaenic patient with acute myeloid leukaemia. 2012 Elsevier Ltd. All rights reserved.

Copyright of Food & Fermentation Industries is the property of Food & Fermentation Industries 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.)

ABSTRACT The objective was to evaluate the inoculation with Aspergillus terreus and/or Trichoderma longibrachiatum on fermentation, chemical and microbiological composition of elephant grass ‘Cameroon’ silage (Cenchrus purpureus). Treatments were A. terreus at 105 colony forming units (CFU)/g (AT15), T. longibrachiatum at 105 CFU/g (TL20), a mixture of both at 105 CFU/g (MIX), and a control group without inoculation (CONTR). The design was completely randomized with seven replicates. The MIX silage was most stable, while CONTR, AT15, and TL20, had lower dry matter losses. There was no effect of inoculation in the chemical composition of silages. Only MIX silage (4.40) had pH above the minimum of 4.2 for humid grass silage and above the control (4.05). Bacteria from Diplococcus genus was identified at the opening of TL20 and CONTR silages. After air exposure, the population of rods, Lactobacillus, and total lactic acid bacteria was higher in theTL20 and MIX. The inclusion of a T. longibrachiatum and A. terreus mixture increases dry mater loss and silage pH. T. longibrachiatum was more efficient in maintaining populations of total lactic acid bacteria after opening; therefore, this strain has potential as an additive for elephant grass ‘Cameroon’ silage.

Trichoderma longibrachiatum rarely reported can cause disease in plants. The present study investigates the pathogenicity of T. longibrachiatum isolate UPMT14 on the red leaf lettuce (Lactuca sativa L.) plants grown in sterile soil under a controlled growth room environment. The fungal isolate was initially characterized morphologically as Trichoderma sp. and was then further characterized by (ITS) region sequencing and BLAST comparison identified as T. longibrachiatum. To observe the response of Trichoderma isolate UPMT14 when imposed on lettuce plants. The injection was made and repeated five times, and then the lettuce growth followed for 36 days. On day 36, the present study found that the red leaf lettuce plants expressed foliar symptoms that began as chlorotic, reduced plant height, reduced leaf length and diameter, wilt, and dried up before it collapsed at day 45 compared to untreated control lettuce plants. Microscopic observation on lettuce roots showed that the Trichoderma spores invading the root system by mass sporulation and spatial competition possibly impaired plant water uptake and eventually caused plant wilting. Therefore, this study indicates that T. longibrachiatum is among the causal agents of wilt disease in the lettuce plant. [ABSTRACT FROM AUTHOR]

Lipases are abundantly used in a wide range of industries. Currently, microbial lipases are the most popular source of industrial lipases, of which fungal lipases stand out due to their low cost of production, catalytic activity, and extracellular nature. The demand for lipases has kept researchers exploring new lipolytic fungi. However, the success of such studies lies in the optimization of the growth medium to maximize lipase secretion and the characterization of the enzyme to achieve its highest activity. Therefore, this research was undertaken to identify a lipolytic fungus that was isolated from soil, optimize its lipase secretion, and characterize it. Based on the results of the current study, the lipolytic fungus was identified as Trichoderma longibrachiatum. Its lipase secretion was maximal when it was cultured in a medium containing olive oil and ammonium sulfate as carbon and nitrogen sources, respectively, at a pH of 7.0. Further, the Trichoderma lipase showed its highest activity at a pH of 6.0 and 40 °C. Moreover, preincubation of the lipase with Ca2+ increased its activity. The enzyme characterization revealed that the extracted Trichoderma lipase has industrially desirable properties. The research results showed that the lipolytic Trichoderma longibrachiatum could be focused on industrial applications.

Abstract Background Lentil (Lens culinaris Medik.) is one of the major pulse crops in the world. The present study aimed to evaluate the effect of Trichoderma isolates to control the charcoal rot disease caused by Macrophomina pseudophaseolina recently reported on lentil plants. Results In this study, antagonistic effects of seven isolates of Trichoderma spp. isolated from the rhizosphere of lentil were evaluated in vitro against Macrophomina pseudophaseolina M1. All isolates of Trichoderma significantly reduced the mycelial growth of M1 in vitro. Maximum reduction of the pathogen growth was observed at T10 (72.53%), followed by T5 (63.7%) and T6 (62.88%), while T2 caused the minimum reduction (37.33%). Likewise, Trichoderma isolates significantly reduced the size and number microsclerotia. M1 produced the minimum number of microsclerotia in the presence of T10, followed by T1 causing reduction of 68.56 and 53.37% over control, respectively. The maximum reduction of microsclerotia’s size was observed in the presence of T10 (54.92%), followed by T1 (49.84) and T8 (48.68%). Results also revealed that production of volatile metabolite, components and inhibition of the test pathogen by volatile metabolites varied among different antagonistic Trichoderma. T1 produced the most volatile compounds, followed by T2 and T3 and T10 causing mycelial growth inhibition of 41.66, 33.88, 30.55 and 30.37%, respectively. The efficacy of the antagonistic biocontrol agents on charcoal rot was evaluated in vivo. Seed treatment with T10 significantly protected lentil seedlings from M. pseudophaseolina as compared to untreated plants and also improved their growth. T10 isolate was identified based on molecular tools, using internal transcribed spaces and Translation elongation factor of ribosomal DNA. The results identified T10 as Trichoderma longibrachiatum with accession number MW818102 and OK500004 deposited in NCBI GenBank database. Conclusion The study revealed the first report of using Trichoderma longibrachiatum as a promising biological agent against M. pseudophaseolina causing charcoal rot disease of lentil.

AbstractThe benefits that Trichoderma species provide to plants are numerous and have already been extensively studied. However, the information about the intervention of some factors in the association between fungi and plants is limited. Therefore, this study evaluated the impact of ten isolates of Trichoderma longibrachiatum endophytes and epiphytes added to hydrogel substrate and inoculated on banana plants in vitro for acclimatization. The experiment was conducted using a completely randomize design and the effect of the treatments was assessed with an analysis of variance (ANOVA), and a Tukey’s range test. Then, the relationship between the persistence of spores of endophytic fungi in the substrate with hydrogel and endophytism was determined by a Pearson correlation. The results indicated significant differences in endophytism, persistence, root, plant length, and fresh weight (P < 0.05). Treatment O III 3 M 3 with a previous epiphytic lifestyle had (55.5%) endophytism, followed by O I 3.2 and V IV 2.1 with (44.4%) which had a previous endophytic lifestyle, the latter also had higher persistence, however, endophytic lifestyle did not influence persistence (r = 0.5, r2 = 0.2). All hydrogel isolates promoted root length as opposed to applying hydrogel alone, but isolate VIV2.1, which had higher persistence and root length, and a high percentage of endophytism, did not affect plant length, stem diameter, number of leaves, and fresh weight. A combination of hydrogel and T. longibrachiatum, which can grow inside or outside banana plant tissues, can provide positive effects on acclimatization.

The present study was intended to optimize the culture conditions for secondary metabolite production by endophytic fungi. Based on the morphology and phylogeny, the fungus was identified as Trichoderma longibrachiatum isolated from brinjal leaf based on morphological characterization. The antifungal activity was evaluated against phytopathogens such as Macrophomina phaseolina, Phytopthora infestans, Colletotrichum falcatum and Colletotrichum gloeosporioides through the overlapping method, culture filtrate and organic fraction from Potato dextrose both as a growth medium. The organic fraction exhibited a significant antifungal activity, while modifications in medium composition may possess a major impact on the quantity and quality of secondary metabolites production. To achieve maximum metabolite production, the growth of the culture was optimized with screening of basal media, carbon, nitrogen, pH, trace elements and incubation period. The final optimized fermentation conditions were Minimal ereavis broth as basal media; glucose and sucrose as carbon source; Peptone and Yeast extract as nitrogen source, sodium nitrate as precursor; pH as 6; and incubation period as 7 days at 28°C. This optimization resulted in antifungal activity of 47.19-60.67% against M. phaseolina, P. infestans, C. falcatum, and C. gloeosporioides which was higher than that before optimization (43.80%). GCMS revealed distinct metabolites of T. longibrachiatum, comprising antifungal metabolites and molecules with additional bioactivities. These results strengthen ongoing research on disease control in agriculture by emphasizing the biocontrol potential of T. longibrachiatum isolated from brinjal phyllosphere against plant pathogenic fungi. [ABSTRACT FROM AUTHOR]

Objectives: The aim of the present work was to perform the co-culture between Trichoderma longibrachiatum LMBC 172, a mesophilic fungus, with Thermothelomyces thermophilus LMBC 162, a thermophilic fungus, by submerged fermentation in a bioreactor. Results: There was an increase in protein production, reaching the value of 35.60 ± 3.76 µg/ml at 72 h. An increase in the amount of proteins of 27.5% in relation to the isolated cultivation of T. longibrachiatum and 19.7% in comparison when T. thermophilus was isolated and cultivated. After that, the saccharification profile of three varieties of sugarcane (sugarcane in natura, culms of sugarcane SP80-3280, and culms of Energy cane) submitted in two pretreatments (autohydrolysis and chemical) was performed. The (e) chemical pretreatment was the better in generating of fermentable sugars from sugarcane bagasse and culms of Energy cane, while with the autohydrolysis pretreatment was obtained the better values to culms of SP80-3280 sugarcane. The sugars found were glucose, xylose, arabinose, and cellobiose. Conclusion: These results suggest that the co-culture between these microorganisms has the potential to produce an enzymatic cocktail with high performance in the hydrolysis of materials from the sugar-alcohol industry. [ABSTRACT FROM AUTHOR]

Botrytis cinerea, a causal agent of gray mold disease, is one of the most destructive fungal pathogens that leads to substantial global economic crop losses, especially for tomato plants. The present study aims to investigate the inhibitory effect of two microbial culture filtrates (BCA filtrate alone and combined with salicylic acid) of Trichoderma longibrachiatum and Pseudomonas sp. against the phytopathogenic fungus B. cinerea on tomato plants. The biochemical modifications, gray mold disease incidence, and fruit quality parameters of the tomatoes were determined according to tested treatments. The results showed that both fungi and bacteria were able to solubilize phosphate and produce IAA and HCN. T. longibrachiatum could produce hydrolytic enzymes (chitinase, protease, and glucanase). Otherwise, Pseudomonas sp. showed the capacity to produce catalase and amylase enzymes. Both microbial culture filtrates inhibited the hyphae growth of B. cinerea. The biocontrol efficacy, in vitro, was significant: up to 50% in terms of the growth inhibition rate at a concentration of 40%. The tomato seedlings' growth was promoted by the separate preventive treatments of each micro-organism culture filtrate. In addition, disease severity in the tomato seedlings and fruit was significantly reduced. Furthermore, the combined treatment of tomato fruit with culture filtrates and salicylic acid induced significant biochemical and physiological changes in fruit firmness, juice yield, total protein, and ROS enzyme activities. The culture filtrates of T. longibrachiatum and Pseudomonas sp. can be recommended as an effective microbial biofungicide to control gray mold disease under storage conditions. [ABSTRACT FROM AUTHOR]

Drought stress poses a serious threat to Pinus massoniana seedling growth in southern China. Trichoderma species, as beneficial microorganisms, have been widely used in agriculture to enhance plant growth and drought tolerance, but the interaction mechanisms remain unclear. To investigate the effect of drought-resistant Trichoderma longibrachiatum inoculation on P. massoniana growth under drought stress, the plant physiological indicators and rhizosphere microbiome diversity were measured to identify Trichoderma-activated mechanisms. Trichoderma longibrachiatum inoculation significantly promoted P. massoniana growth under drought treatment, and enhanced nitrogen, phosphorus, and potassium absorption compared with those of non-inoculated seedlings. Trichoderma longibrachiatum treatment alleviated the damage to cell membranes and needle tissue structure, and significantly increased antioxidant enzyme activities, osmotic substance contents, and photosynthesis in P. massoniana in response to drought stress. Soil nutrient contents, activities of sucrase, phosphatase, and urease as well as the relative abundances of the dominant genera Burkholderia, Rhodanobacter, and Trichoderma were elevated in the rhizosphere soil of P. massoniana inoculated with T. longibrachiatum under drought stress. A network analysis showed that certain crucial dominant taxa driven by T. longibrachiatum inoculation, including Penicillium, Trichoderma, Simplicillium, Saitozyma, Burkholderia, Bradyrhizobium, Sinomonas, and Mycobacterium, had more correlations with other microorganisms in the soil. Trichoderma longibrachiatum enhanced P. massoniana seedling growth under drought stress by regulating physiological responses and soil microbial community. [ABSTRACT FROM AUTHOR]

Differential scanning calorimetry (DSC) was used as an efficient and rapid tool in studying the conformational transitions between the folded and unfolded structures of cellulolytic enzymes. The thermal properties of two crude hydrolytic enzyme cocktails containing extracellular cellulases from Trichoderma longibrachiatum DIBAF-10 were analyzed and compared with three commercial cellulase preparations. Differences in the thermal behavior of fungal cellulases in the liquid phase, freeze-dried state, liquid formulations in sodium citrate buffer (pH 4.8), and contact with cellulose, carboxymethyl cellulose, and cellobiose were evaluated. DSC profiles of cellulases from the DIBAF-10 strain provided important thermodynamic information about the thermal stability of the included proteins. Crude enzyme cocktails underwent a reproducible and irreversible exothermic aggregation phenomenon at 52.45 ± 0.90 °C like commercial β-glucosidase. Freeze-dried and resuspended in a sodium citrate buffer, cellulases from T. longibrachiatum showed an endothermic peak dependent on buffer and enzyme concentration. In the enzyme-substrates systems, a shift of the same peak was recorded for all substrates tested. The thermal analysis of freeze-dried cellulase samples in the range of 20–150 °C gave information on the denaturation process. In conclusion, we demonstrated that DSC is a cost-effective tool for obtaining "conformational fingerprinting" of crude fungal cellulase preparations. [ABSTRACT FROM AUTHOR]

Background: Lentil (Lens culinaris Medik.) is one of the major pulse crops in the world. The present study aimed to evaluate the effect of Trichoderma isolates to control the charcoal rot disease caused by Macrophomina pseudophaseolina recently reported on lentil plants. Results: In this study, antagonistic effects of seven isolates of Trichoderma spp. isolated from the rhizosphere of lentil were evaluated in vitro against Macrophomina pseudophaseolina M1. All isolates of Trichoderma significantly reduced the mycelial growth of M1 in vitro. Maximum reduction of the pathogen growth was observed at T10 (72.53%), followed by T5 (63.7%) and T6 (62.88%), while T2 caused the minimum reduction (37.33%). Likewise, Trichoderma isolates significantly reduced the size and number microsclerotia. M1 produced the minimum number of microsclerotia in the presence of T10, followed by T1 causing reduction of 68.56 and 53.37% over control, respectively. The maximum reduction of microsclerotia's size was observed in the presence of T10 (54.92%), followed by T1 (49.84) and T8 (48.68%). Results also revealed that production of volatile metabolite, components and inhibition of the test pathogen by volatile metabolites varied among different antagonistic Trichoderma. T1 produced the most volatile compounds, followed by T2 and T3 and T10 causing mycelial growth inhibition of 41.66, 33.88, 30.55 and 30.37%, respectively. The efficacy of the antagonistic biocontrol agents on charcoal rot was evaluated in vivo. Seed treatment with T10 significantly protected lentil seedlings from M. pseudophaseolina as compared to untreated plants and also improved their growth. T10 isolate was identified based on molecular tools, using internal transcribed spaces and Translation elongation factor of ribosomal DNA. The results identified T10 as Trichoderma longibrachiatum with accession number MW818102 and OK500004 deposited in NCBI GenBank database. Conclusion: The study revealed the first report of using Trichoderma longibrachiatum as a promising biological agent against M. pseudophaseolina causing charcoal rot disease of lentil. [ABSTRACT FROM AUTHOR]

In this study, four species of Trichoderma,T. koningiopsis, T. virens, T. spirale and T. longibrachiatum, which are endophytic in Pinus massoniana,were studied for their drought resistance. The effects of simulated drought, using polyethylene glycol 6 000 (PEG-6 000), on the growth of four Trichoderma species were evaluated, and the physiological responses of drought-resistant strains to stress were analyzed. The results showed that T. longibrachiatum had the strongest adaptability to PEG-6 000 stress among the four species of Trichoderma, and its hyphal and spore growth were less affected by the stress. With the increase in PEG-6 000 concentration, the antioxidant enzyme activities of T. longibrachiatum tendedto increase first and then decrease, the superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) activities reached peaks under 200 and 300 g·L-1 PEG-6 000s, and showed activity levels of 0.922, 98.136 and 4.516 U·g-1, respectively; the osmotic regulatory substances increased with rise in the contents of soluble sugars (SS) and soluble proteins (SP) after the PEG-6 000 concentration increased, reaching peaks of 35.317 and 29.554 mg·g-1 under 200 and 300 g·L-1 PEG-6 000s, respectively. Meanwhile, the proline (Pro) content of T. longibrachiatum showed an increase under PEG-6 000 stress. Correlation analysis showed that under PEG-6 000 stress, antioxidant enzymes and cell osmotic regulators play an essential role in maintaining the normal life activities of T. longibrachiatum. The study findings can be used as a reference for screening drought-resistant strains and improving plant drought resistance. [ABSTRACT FROM AUTHOR]

In the ancient agriculture practices to present day farmers are using leguminous plants in field to enhance of soil fertility, which possess Rhizobium bacteria that has mechanism to acquire nitrogen from air to soluble form. In addition, in this research isolated strain Trichoderma longibrachiatum GFT2 act as biofertilizer and biocontrol agent which has been characterized by performing chitinase (18.56 U/ml), glucanase (13.82U/ml) and IAA production (7.3000μg/ml), PO4 solubilization (10.7142 μg/ml), siderophore production (77.5%). Root colonization assay performed for detection of Trichoderma longibrachiatum GFT2 which colonized over the root or not, further compability test isolated Rhizobium pusense PR4 and Trichoderma longibrachiatum GFT2 for capable to each other on same environment or not. Moreover, Application of Trichoderma longibrachiatum GFT2 and Rhizobium pusense PR4 on peanut plant (Arachis hypogaea) seed germination and nodule formation. Maximum seed germination rate was shown in seed treated with PR4+GFT2 (39%), whereas least number (01) of nodules formed in plant treated with dual culture Trichoderma longibrachiatum GFT2 and Rhizobium pusense PR4. Maximum Sixteen nodules formation in plant treated with in Rhizobium pusense PR4 was observed. In this paper, we analyzed the how Trichoderma longibrachiatum GFT2 effected on peanut plant (Arachis hypogaea) nodulation process when applying in soil and reduced the number of nodules by indirectly inhibit or decline the growth of nodulation bacteria. Plant growth is facilitated by Trichoderma strain, but nitrogen fixation is insufficient in leguminous plants. We can determine the precise interaction between Trichoderma longibrachiatum GFT2 and whether their alteration of soil profiles is due to them by analysing soil samples for meta transcriptomics. [ABSTRACT FROM AUTHOR]

Abstract Background The major challenge of facing the efficient utilization of biomass is the high cost of cellulolytic enzyme, while the Trichoderma longibrachiatum plays an essential role in the production of industrial enzymes and biomass recycling. Results The cellulase hyper‑producing mutants of LC-M4 and LC-M16 derived from the wild type T. longibrachiatum LC strain through heavy ion mutagenesis exhibited the high-efficiency secretion ability of cellulase and hemicellulose. The FPase activities of LC-M4 (4.51 IU/mL) and LC-M16 (4.16 IU/mL) mutants increased by 46.91% and 35.5% when compared to the LC strain, respectively. Moreover, these two cellulase hyper-producing mutants showed faster growth rate on the cellulosic substrates (Avicel and CMC-Na) plate than that of LC strain. Therefore, an integrative transcriptome and proteome profiling analysis of T. longibrachiatum LC and its cellulase hyper‑producing mutant LC-M4 and LC-M16 were employed to reveal the key genes involved in cellulolytic enzymes regulation. It was showed that the transcriptome and proteome profiles changed dramatically between the wild strain and mutant strains. Notably, the overlapped genes obtained from integrative analysis identified that the protein processing in ER involved in protein secretory pathway, starch and sucrose metabolism pathway and N-glycan biosynthesis pathway were significantly changed both in cellulase hyper-producing mutants and thereby improving the enzyme secretion efficiency, which maybe the main reason of cellulase hyper-production in LC-M4 and LC-M16 mutants. In addition, the three DEGs/DEPs (PDI, Sec61, VIP36) related with protein secretion in ER and two DEGs/DEPs (OST, MOGS) related with N-glycan biosynthesis were identified as key candidate genes participating in enzyme protein biosynthesis and secretion. Conclusions In this study, a hypothetical secretory model of cellulase protein in filamentous fungi was established on the basis of DEGs/DEPs and key genes identified from the omics analysis, which were of great guidance on the rational genetic engineering and/or breeding of filamentous fungi for improving cellulase production.

The study aimed to investigate the effect of the bioagent Trichoderma longibrachiatum on cucumber root rot disease. Two pathogenic fungi named Rhizoctonia solani and Fusarium oxysporum were isolated from the roots of cucumber plants infected with root rot disease. The pathogenicity of these fungi was tested in pots and observed that pot of them are pathogenic fungi. The results showed that the germination percentage was significantly reduced to 46.7% and 50% in response to the treatment with R. solani and F. oxysporum, respectively compared to control treatment which was 80%. The results also showed that the disease severity increased in the treatment of R. solani which reached 72.7%, followed by 62% with the treatment of F. oxysporum compared to control treatment which was 86.7%. Furthermore, the results indicated that R. solani and F. oxysporum led to increase damping off to 40.4 % and 22 %, respectively compared to the control treatment (0 %). It was also found that the exydates of R. solani and F. oxysporum significantly reduced the percentage of germination to 33.3 % and 43.3%, respectively compared to the control treatment which was 86.7%. Moreover, the interaction between T. longibrachiatum and each of two pathogenic fungi R. solani and F. oxysporum significantly reduced disease severity to 20.33 and 22.33%, respectively compared to the pathogenic fungi alone which were 80.33 and 69.67%,respectively. [ABSTRACT FROM AUTHOR]

This study was conducted to evaluate the efficiency of the bioagent Trichoderma longibrachiatum in controlling cucumber root rot disease caused by Fusarium solani. The pathogenic fungus was isolated from the roots of cucumber plant infected with root rot disease. The pathogenicity of F. solani was tested in Petri dishes and it was found that it reduced the germination percentage to 50% compared to the control treatment, which was 90%. The results of dual culture showed that the bioagent T. longibrachiatum inhibited the growth of F. solani and the degree of antagonism reached 1 according to Bell scale. The results of the field experiment which conducted in the greenhouse showed that the bioagent T. longibrachiatum led to increase the germination percentage of cucumber plants, reaching 96.7%, which significantly differed from the pathogenic fungus treatment, which amounted to 63.3%. The results indicated that the bioagent T. longibrachiatum significantly reduced the percentage of disease severity to 20.33%, compared with the treatment of the pathogenic fungus F. solani alone, which reached 65.67%. bioagent T. longibrachiatum also increased the plant height significantly up to 177 cm, compared to control treatment and pathogenic fungus treatment, which were 142 and 116 cm, respectively. It was also found that bioagent T. longibrachiatum when it was interacted with the pathogenic fungus led to increase the plant height up to 167 cm, compared with the treatment of pathogenic fungi alone, which was 116 cm. Fresh and dry weight of shoot and root systems also increased significantly in the treatment of T. longibrachiatum compared to the treatment of pathogenic fungus, followed by the treatment of the interaction between T. longibrachiatum and the pathogenic fungus treatments. The results also revealed the efficiency of T. longibrachiatum in increasing plant productivity represented by the number of fruits, the average weight of the fruits and the fruit yield per plant, which were significantly differed from the pathogenic fungus treatment alone. [ABSTRACT FROM AUTHOR]

A study was conducted to isolate efficient biocontrol agent against agriculturally important plant pathogens. Isolated fungus was identified using morphological and molecular characters and evaluated against plant pathogens. Isolated culture was identified as Trichoderma longibrachiatum based on morphological and cultural characteristics. The isolate (TL-RD-01) was able to solubilize the zinc and able to produce the indole 3 acetic acid of about 32.01 μg/ml. To optimize the growth media different carbon and nitrogen sources were studied. Maltose, Corn flour, Peptone and Yeast Extract used media attained maximum growth of T. longibrachiatum. The pH (5 to 6) and temperature (25 °C to 30 °C) was optimized for the growth of T. longibrachiatum TL-RD-01. Molecular identification based on internal transcribed spacer 1 and 2 region (ITS1 and ITS2) sequence analysis have been further confirmed as T. longibrachiatum. The phylogenetic analysis of above ITS gene sequences were carried out. T. longibrachiatum isolate was clearly separated with ITS sequence's analysis with other species of Trichoderma. Mycoparasitic effect of T. longibrachiatum was carried out by dual plate technique against agriculturally important plant pathogens viz., Macrophomina phaseolina, Phytopthora infestans, Collectrotrichum gleosporides (Mango) and Colletotrichum falcatum. Pathogen inhibition effect of T. longibrachiatum isolate was in between 50% to 81.94%. As per the investigation, Trichoderma longibrachiatum (TL-RD-01) could be deployed as a biocontrol agent and a biostimulant. [ABSTRACT FROM AUTHOR]

Xyloglucan (XG) is the predominant hemicellulose in the primary cell wall of superior plants. It has a fundamental role in controlling the stretching and expansion of the plant cell wall. There are five types of enzymes known to cleave the linear chain of xyloglucan, and the most well-known is xyloglucanase (XEG). The immobilization process can be used to solve problems related to stability, besides the economic benefits brought by the possibility of its repeated use and recovery. Therefore, this study aims at the optimization of the xyloglucanase production of Trichoderma longibrachiatum using a central composite rotatable design (CCRD) with tamarind and jatoba seeds as carbon sources, as well as XEG immobilization on ionic supports, such as MANAE (monoamine-N-aminoethyl), DEAE (diethylaminoethyl)-cellulose, CM (carboxymethyl)-cellulose, and PEI (polyethyleneimine). High concentrations of carbon sources (1.705%), at a temperature of 30 °C and under agitation for 72 h, were the most favorable conditions for the XEG activity from T. longibrachiatum with respect to both carbon sources. However, the tamarind seeds showed 23.5% higher activity compared to the jatoba seeds. Therefore, this carbon source was chosen to continue the experiments. The scaling up from Erlenmeyer flasks to the bioreactor increased the XEG activity 1.27-fold (1.040 ± 0.088 U/mL). Regarding the biochemical characterization of the crude extract, the optimal temperature range was 50–55 °C, and the optimal pH was 5.0. Regarding the stabilities with respect to pH and temperature, XEG was not stable for prolonged periods, which was crucial to immobilizing it on ionic resins. XEG showed the best immobilization efficiency on CM-cellulose and DEAE-cellulose, with activities of 1.16 and 0.89 U/g of the derivative (enzyme plus support), respectively. This study describes, for the first time in the literature, the immobilization of a fungal xyloglucanase using these supports. [ABSTRACT FROM AUTHOR]

Twenty isolates of Trichoderma were recovered from lignocellulosic agriculture wastes-rich soil collected from different Egyptian cities (Sadat, Tala, Abo Hamad, Belbeis, Zagazig, Mansoura, Belqas, Kafer-Elshikh, Bella, Tanta, Borg El Arab, Banha, Kafr Shoker, Qalyoub, Shebien Elqanater, Damanhur, Abu al-Matamir, Damietta, Kafr al-Battikh, and Kafr Saad). The Trichoderma isolates were first identified morphologically using conidiophore branching type and conidium morphology. Furthermore, molecular identification based on the ITS (internal transcribed spacers) barcode differentiated between Trichoderma isolates having 98.6% to 100% identity with two Trichoderma species: T. asperellum and T. longibrachiatum. Qualitative and quantitative tests were used for screening the cellulolytic activity of these isolates. The isolates were screened for cellulase production based on the clearing zone diameters and calorimetrically tested on minimal media supplemented with sugar cane bagasse and rice straw as sole carbon sources. The isolates TM41 (T. longibrachiatum) and TM35 (T. asperellum) exhibited the highest diameters of clear zones and showed higher Fpase and CMCase activities. Moreover, the isolate TM18 of T. asperellum displayed the highest diameters of clear zones and showed higher Fpase and Xylanase activities. [ABSTRACT FROM AUTHOR]

A field evaluation test of the compatibility effect of the pesticide Dominante with different concentrations of T. longibrachiatum and M.anisopliae spore suspensions on the mortality rate of various stages of green peach on the cold pepper showed the superiority of the treatment M9 (M.anisopliae 1010 + Dominante (0.5 g/L)) followed by T9 (T. longibrachiatum 1010 + Dominate (0.5 g/L)) with mortality rate reached to 100 and 99.1%, respectively, after 7 days from the treatment. The results showed that the highest values of plant height, root length and dry weight of shoot and root systems were recorded at treatments T6 (T. longibrachiatum 1010 + Dominante (0.25 g/L)) and T5 (T. longibrachiatum 108 + Dominante (0.25g /L)), as the height of the plant reached (34.33 and 32,) cm respectively, the length of the root system reached to (16 and 14) cm, respectively, while the dry weights of the shoot system were (7.81and 7.69) g and the dry root weights were (5.89 and 5.22) g, respectively, compared with the lowest values for these makers in the control which were 17.12 cm, 7.73 cm, 2.89 g and 3.71 g, respectively. The results also showed the compatibility effect of the pesticide Dominante with different concentrations of the T.longibrachiatum and M.anisopliae spores on the number and weight of the of cold pepper fruits under the conditions of green peach insect Myzus persicae. The treatments T6 (T.longibrachiatum 1010 + Dominante (0.25 g/L)) and T5(T.longibrachiatum 108+Dominante (0.25 g/L)) were recorded the highest number of fruits reached (20.33 and 18.33) fruits, respectively, compared with the lowest fruits number 8.63 in the control, while the highest fruit weight were 609.17 and 588.5g in treatments M3 (M.anisopliae 1010) and T6 (T. longibrachiatum 1010 + Dominante (0.25 g/L)), respectively, compared with the lowest fruits weight 244 g in the control.

Drought stress poses a serious threat to Pinus massoniana seedling growth in southern China. Trichoderma species, as beneficial microorganisms, have been widely used in agriculture to enhance plant growth and drought tolerance, but the interaction mechanisms remain unclear. To investigate the effect of drought-resistant Trichoderma longibrachiatum inoculation on P. massoniana growth under drought stress, the plant physiological indicators and rhizosphere microbiome diversity were measured to identify Trichoderma-activated mechanisms. Trichoderma longibrachiatum inoculation significantly promoted P. massoniana growth under drought treatment, and enhanced nitrogen, phosphorus, and potassium absorption compared with those of non-inoculated seedlings. Trichoderma longibrachiatum treatment alleviated the damage to cell membranes and needle tissue structure, and significantly increased antioxidant enzyme activities, osmotic substance contents, and photosynthesis in P. massoniana in response to drought stress. Soil nutrient contents, activities of sucrase, phosphatase, and urease as well as the relative abundances of the dominant genera Burkholderia, Rhodanobacter, and Trichoderma were elevated in the rhizosphere soil of P. massoniana inoculated with T. longibrachiatum under drought stress. A network analysis showed that certain crucial dominant taxa driven by T. longibrachiatum inoculation, including Penicillium, Trichoderma, Simplicillium, Saitozyma, Burkholderia, Bradyrhizobium, Sinomonas, and Mycobacterium, had more correlations with other microorganisms in the soil. Trichoderma longibrachiatum enhanced P. massoniana seedling growth under drought stress by regulating physiological responses and soil microbial community.

Botrytis cinerea, a causal agent of gray mold disease, is one of the most destructive fungal pathogens that leads to substantial global economic crop losses, especially for tomato plants. The present study aims to investigate the inhibitory effect of two microbial culture filtrates (BCA filtrate alone and combined with salicylic acid) of Trichoderma longibrachiatum and Pseudomonas sp. against the phytopathogenic fungus B. cinerea on tomato plants. The biochemical modifications, gray mold disease incidence, and fruit quality parameters of the tomatoes were determined according to tested treatments. The results showed that both fungi and bacteria were able to solubilize phosphate and produce IAA and HCN. T. longibrachiatum could produce hydrolytic enzymes (chitinase, protease, and glucanase). Otherwise, Pseudomonas sp. showed the capacity to produce catalase and amylase enzymes. Both microbial culture filtrates inhibited the hyphae growth of B. cinerea. The biocontrol efficacy, in vitro, was significant: up to 50% in terms of the growth inhibition rate at a concentration of 40%. The tomato seedlings’ growth was promoted by the separate preventive treatments of each micro-organism culture filtrate. In addition, disease severity in the tomato seedlings and fruit was significantly reduced. Furthermore, the combined treatment of tomato fruit with culture filtrates and salicylic acid induced significant biochemical and physiological changes in fruit firmness, juice yield, total protein, and ROS enzyme activities. The culture filtrates of T. longibrachiatum and Pseudomonas sp. can be recommended as an effective microbial biofungicide to control gray mold disease under storage conditions.

Invasive fungal infection is a life-threatening complication of chemotherapy and neutropaenia in the haematology population. Trichoderma species rarely cause human disease but have been reported to cause invasive infection in the immunosuppressed. We present a case of invasive Trichoderma longibrachiatum pulmonary infection with fatal outcome in a neutropaenic patient with acute myeloid leukaemia. 2012 Elsevier Ltd. All rights reserved. [ABSTRACT FROM AUTHOR]

Trichoderma longibrachiatum sp. are free-living filamentous fungi which are common in agro-ecosystems. However, few studies thus far have examined the interaction between Trichoderma longibrachiatum and arbuscular mycorrhizal (AM) fungi in saline soil and their potential for improving plant stress tolerance. Here, single, dual-inoculated (T. longibrachiatum MF, AM fungal community or Glomus sp.), and non-inoculated maize (Zea may L.) were subjected to different salinity levels (0, 75, 150, and 225 mM NaCl) to test the synergistic effects of dual inoculants on maize plants in different salt stress conditions. Plant performance and metabolic profiles were compared to find the molecular mechanisms underlying plant protection against salt stress. The first experiment revealed that dual inoculation of an AM fungal community and T. longibrachiatum MF improved the biomass and K+/Na+ ratio in maize under non-saline conditions, and generally enhanced AM fungal growth in root and soil under all but the 225 mM NaCl conditions. However, MF inoculant did not influence the structure of AM fungal communities in maize roots. In the second experiment, dual inoculation of Glomus sp. and T. longibrachiatum MF increased maize plant biomass, K+/Na+ ratio, and AM fungal growth in root and soil significantly at both 0 and 75 mM NaCl conditions. We identified metabolic compounds differentially accumulated in dual-inoculated maize that may underline their enhanced maize plant tolerance to increasing soil salinity. Our data suggested that the combination of Glomus sp. and T.longibrachiatum leads to interactions, which may play a potential role in alleviating the stress and improve crop productivity in salt-affected soils. [ABSTRACT FROM AUTHOR]

Pepper is vulnerable to soil-borne fungal pathogens such as Rhizoctonia solani and Fusarium oxysporum. The potential of beneficial rhizosphere microorganisms to control R. solani and F. oxysporum f.sp. capsici was evaluated in pepper plants. Paenibacillus polymyxa and Trichoderma longibrachiatum were isolated from rhizospheric soil samples of healthy pepper plants. In vitro, both isolates caused clear reductions in the radial growth of root rot and wilt pathogens. Scanning electron microscopy displayed lysis and abnormal shape of the pathogens in dual cultures with P. polymyxa and T. longibrachiatum. The incidence and severity of root rot and wilt diseases were significantly reduced in pepper plants treated with the growth-promoting fungi (PGPF isolates; Fusarium equiseti GF19-1, Fusarium equiseti GF18-3, and Phoma sp. GS8-3), P. polymyxa, or T. longibrachiatum in comparison to the control. Moreover, the induction treatments led to increased pepper growth compared with their control. The defense related gene (CaPR4) expression was shown to be significantly higher in the treated plants than in the control plants. In conclusion, the antagonistic isolates (P. polymyxa and T. longibrachiatum) and PGPF isolates have a clear impact on the prevention of root rot and wilt diseases in pepper plants incited by R. solani and F. oxysporum f.sp. capsici. The expression of the CaPR4 gene added to the evidence that PGPF isolates generate systemic resistance to pathogen infections. [ABSTRACT FROM AUTHOR]

BackgroundThe relationship between infection and tumors has attracted increasing attention. Trichoderma spp. are often isolated from tumors. However, their potential role remains unclear. We recently reported the isolation of Trichoderma longibrachiatum from a patient with pulmonary spindle cell carcinoma that was confirmed as primary infection by application of laser capture microdissection and polymerase chain reaction. To explore whether the strain is pathogenic and whether it can cause atypical cell proliferation and infiltration of NK cells and T cells, we designed a mouse infection experiment.MethodsTwelve ICR mice were randomly separated into three groups. Cyclophosphamide was used to inhibit the immunity of mice. A mouse model of Trichoderma infection was successfully established by intracutaneous injection on the back skin with a suspension of strain PKUT180420015. The pathological manifestations of Trichoderma infection and the interaction between immune cells and fungi were observed by histopathology, immunohistochemistry and intensive fungal staining. Reisolation of the fungus was observed by infected tissue culture. The inoculated sites exhibited swelling 3 days after inoculation, and ulcers developed at approximately 14 days. Skin specimens were obtained and then cultured at 3, 7, and 14 days after inoculation. We selected mice 14 days after inoculation in Group 3, whose ulcers were the most typical, for histological analysis.ResultsInflammation, angioinvasion and necrosis were observed. Immunohistochemistry showed positive markers of Ki67, CD3, CD56, GZMB, and PRF. Periodic acid-Schiff staining, periodic acid-silver methenamine staining, and Calcofluor staining showed fungal spores in the vascular lumen, vascular walls and around the blood vessels.ConclusionsOur studies showed that a T. longibrachiatum strain (PKUT180420015) isolated from a biopsy specimen in a patient with pulmonary spindle cell carcinoma could induce atypical hyperplasia, with the expression of Ki67, CD3, CD56, GZMB, and PRF in mice. These data indicate that the fungus may be involved in inducing atypical hyperplasia or tumorigenesis.

Summary: Meloidogyne enterolobii is a species capable of overcoming plant resistance moderated by the Mi -1 gene, which is effective against most species of root-knot nematode. This study evaluated the effect of induced resistance in tomato plants (Solanum lycopersicum 'H-9553') with the Mi -1 gene against the development and reproduction of M. enterolobii. Seedlings of tomato 'H-9553' were transplanted into pots, inoculated with 2000 eggs and second-stage juveniles (J2) of M. enterolobii and treated with Acibenzolar-S-Methyl, Bacillus subtilis , B. subtilis + B. licheniformis + Trichoderma longibrachiatum and extract of Reynoutria sachalinensis. The plants were collected at 5, 10, 15, 20, 25 and 30 days after inoculation (DAI) for the analyses of nematode penetration and development, and at 30 DAI for nematode reproduction. The use of B. subtilis increased fresh root weight when compared to the other treatments (20 DAI). There was a reduction in penetration of J2 in the roots of plants subjected to different resistance inducers. The population density of M. enterolobii was significantly reduced only when plants were treated with R. sachalinensis , indicating it as a potential resistance-inducing agent in tomato plants. [ABSTRACT FROM AUTHOR]

An unusual sesquiterpene glycoside trichoacorside A (1) and two novel sorbicillinoid glycosides sorbicillisides A (2) and B (3), together with a known compound sorbicillin (4), were isolated and identified from the culture extract of an endophytic fungus Trichoderma longibrachiatum EN-586, obtained from the marine red alga Laurencia obtusa. Trichoacorside A (1) is the first representative of a glucosamine-coupled acorane-type sesquiterpenoid. Their structures were elucidated based on detailed interpretation of NMR and mass spectroscopic data. The absolute configurations were determined by X-ray crystallographic analysis, chemical derivatization, and DP4+ probability analysis. The antimicrobial activities of compounds 1–4 against several human, aquatic, and plant pathogens were evaluated. [ABSTRACT FROM AUTHOR]

Trichoderma longibrachiatum is a filamentous fungus used as a biological control agent against different plant diseases. The multifunctional secondary metabolites synthesized by Trichoderma , called peptaibols, have emerged as key elicitors in plant innate immunity. This study obtained a high-quality genome sequence for the T. longibrachiatum strain 40418 and identified two peptaibol biosynthetic gene clusters using knockout techniques. The two gene cluster products were confirmed as trilongin AIV a (11-residue) and trilongin BI (20-residue) using liquid chromatography coupled with tandem mass spectrometry. Further investigations revealed that these peptaibols induce plant resistance to Pseudomonas syringae pv tomato ( Pst ) DC3000 infection while triggering plant immunity and cell death. Notably, the two peptaibols exhibit synergistic effects in plant-microbe signaling interactions, with trilongin BI having a predominant role. Moreover, the induction of tomato resistance against Meloidogyne incognita showed similarly promising results.

Trichoderma longibrachiatum MD33, a sesquiterpene alkaloid-producing endophyte isolated from Dendrobium nobile , shows potential medical and industrial applications. To understand the molecular mechanisms of sesquiterpene alkaloids production, a comparative transcriptome analysis was performed on strain MD33 and its positive mutant UN32, which was created using Ultraviolet (UV) mutagenesis and nitrogen ion (N+) implantation. The alkaloid production of UN32 was 2.62 times more than that of MD33. One thousand twenty-four differentially expressed genes (DEGs), including 519 up-regulated and 505 down-regulated genes, were identified. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed 139 GO terms and 87 biosynthesis pathways. Dendrobine, arguably the main sesquiterpene alkaloid the strain MD33 produced, might start synthesis through the mevalonate (MVA) pathway. Several MVA pathway enzyme-coding genes (hydroxy-methylglutaryl-CoA synthase, mevalonate kinase, and farnesyl diphosphate synthase) were found to be differentially expressed, suggesting that physical mutagenesis can disrupt genome integrity and gene expression. Some backbone post-modification enzymes and transcript factors were either discovered, suggesting the sesquiterpene alkaloid metabolism in T. longibrachiatum is a complex genetic network. Our findings help to shed light on the underlying molecular regulatory mechanism of sesquiterpene alkaloids production in T. longibrachiatum. [ABSTRACT FROM AUTHOR]

This study was conducted to evaluate the efficiency of the bioagents Trichoderma harzianum and T. longibrachiatum and the fungicide Topsin-M and their interaction in controlling root rot disease of eggplant caused by Fusarium oxysporum. The results of the laboratory experiment showed the antagonistic ability of the two bioagents factors T.harzianum and T.longibrachiatum in inhibiting the growth of pathogenic fungi by dual culture method, where the antagonism was of degree 1 and 2, respectively according to the Bell scale. The results of the laboratory experiment also showed that the fungicide Topsin-M inhibited the growth of pathogenic fungi by 100% when used at the recommended concentration of 1 g.L-1, while the fungicide inhibited the bioagents T.harzianum and T.longibrachiatum by 16.63 and 26.80%, respectively. In the field experiment, the results showed that there were significant differences in the infection severity with the pathogenic fungus, so the least infection severity was observed in the treatment that contained the pathogenic fungus with one of the bioagents T.harzianum and T.longibrachiatum separately and the fungicide Topsin-M (Fo + Th + TM and Fo + Tl + TM), which amounted to 18.33 and 24.00%, respectively, compared to the treatment of pathogenic fungi (Fo), which amounted to 61.67%. The above two treatments also achieved a significant increase in plant height, reaching 77.33 and 74.67 cm, respectively. Also, these two treatments led to an increase in the fresh weight of the shoot and root systems, which amounted to 530, 515, 70 and 67 g, respectively compared to the treatment of pathogenic fungus, which amounted to 380 and 30.7g, respectively and the average dry weight of the shoot and root systems also increased in these two treatments to 79.58, 76.17, 17.50 and 16.92g, respectively compared to the treatment of pathogenic fungi, which amounted to 42.75 and 7.83g, respectively. The results of the experiment also explained that the largest leaf area and the largest yield of the plant were recorded in the same two treatments, as the leaf area reached 781.3 and 729 cm2, respectively and the yield reached 1864 and 1762 gm, respectively. [ABSTRACT FROM AUTHOR]

Trichoderma longibrachiatum MD33, a sesquiterpene alkaloid-producing endophyte isolated from Dendrobium nobile, shows potential medical and industrial applications. To understand the molecular mechanisms of sesquiterpene alkaloids production, a comparative transcriptome analysis was performed on strain MD33 and its positive mutant UN32, which was created using Ultraviolet (UV) mutagenesis and nitrogen ion (N+) implantation. The alkaloid production of UN32 was 2.62 times more than that of MD33. One thousand twenty-four differentially expressed genes (DEGs), including 519 up-regulated and 505 down-regulated genes, were identified. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed 139 GO terms and 87 biosynthesis pathways. Dendrobine, arguably the main sesquiterpene alkaloid the strain MD33 produced, might start synthesis through the mevalonate (MVA) pathway. Several MVA pathway enzyme-coding genes (hydroxy-methylglutaryl-CoA synthase, mevalonate kinase, and farnesyl diphosphate synthase) were found to be differentially expressed, suggesting that physical mutagenesis can disrupt genome integrity and gene expression. Some backbone post-modification enzymes and transcript factors were either discovered, suggesting the sesquiterpene alkaloid metabolism in T. longibrachiatum is a complex genetic network. Our findings help to shed light on the underlying molecular regulatory mechanism of sesquiterpene alkaloids production in T. longibrachiatum.

Xyloglucan (XG) is the predominant hemicellulose in the primary cell wall of superior plants. It has a fundamental role in controlling the stretching and expansion of the plant cell wall. There are five types of enzymes known to cleave the linear chain of xyloglucan, and the most well-known is xyloglucanase (XEG). The immobilization process can be used to solve problems related to stability, besides the economic benefits brought by the possibility of its repeated use and recovery. Therefore, this study aims at the optimization of the xyloglucanase production of Trichoderma longibrachiatum using a central composite rotatable design (CCRD) with tamarind and jatoba seeds as carbon sources, as well as XEG immobilization on ionic supports, such as MANAE (monoamine-N-aminoethyl), DEAE (diethylaminoethyl)-cellulose, CM (carboxymethyl)-cellulose, and PEI (polyethyleneimine). High concentrations of carbon sources (1.705%), at a temperature of 30 °C and under agitation for 72 h, were the most favorable conditions for the XEG activity from T. longibrachiatum with respect to both carbon sources. However, the tamarind seeds showed 23.5% higher activity compared to the jatoba seeds. Therefore, this carbon source was chosen to continue the experiments. The scaling up from Erlenmeyer flasks to the bioreactor increased the XEG activity 1.27-fold (1.040 ± 0.088 U/mL). Regarding the biochemical characterization of the crude extract, the optimal temperature range was 50–55 °C, and the optimal pH was 5.0. Regarding the stabilities with respect to pH and temperature, XEG was not stable for prolonged periods, which was crucial to immobilizing it on ionic resins. XEG showed the best immobilization efficiency on CM-cellulose and DEAE-cellulose, with activities of 1.16 and 0.89 U/g of the derivative (enzyme plus support), respectively. This study describes, for the first time in the literature, the immobilization of a fungal xyloglucanase using these supports.

Plant diseases caused by Pseudomonas syringae are essentially controlled in the field with the use of copper-based products and antibiotics, raising environmental and safety concerns. Antimicrobial peptides (AMPs) derived from fungi may represent a sustainable alternative to those chemicals. Trichogin GA IV, a non-ribosomal, 11-residue long AMP naturally produced by the fungus Trichoderma longibrachiatum has the ability to insert into phospholipidic membranes and form water-filled pores, thereby perturbing membrane integrity and permeability. In previous studies, peptide analogs modified at the level of specific residues were designed to be water-soluble and active against plant pathogens. Here, we studied the role of glycine-to-lysine substitutions and of the presence of a C-terminal leucine amide on bioactivity against Pseudomonas syringae bacteria. P. syringae diseases affect a wide range of crops worldwide, including tomato and kiwifruit. Our results show that trichogin GA IV analogs containing two or three Gly-to-Lys substitutions are highly effective in vitro against P. syringae pv. tomato (Pst), displaying minimal inhibitory and minimal bactericidal concentrations in the low micromolar range. The same analogs are also able to inhibit in vitro the kiwifruit pathogen P. syringae pv. actinidiae (Psa) biovar 3. When sprayed on tomato plants 24 h before Pst inoculation, only tri-lysine containing analogs were able to significantly reduce bacterial titers and symptom development in infected plants. Our results point to a positive correlation between the number of lysine substitutions and the antibacterial activity. This correlation was supported by microscopy analyses performed with mono-, di- and tri-Lys containing analogs that showed a different degree of interaction with Pst cells and ultrastructural changes that culminated in cell lysis. [Display omitted] • Trichogin GA IV analogs bearing targeted amino acid substitutions were synthesized. • The antimicrobial activity of the analogs was assessed on two P. syringae pathovars. • Gly-to-Lys substitutions enhanced cell interaction and antibacterial activity. • Tri-substituted analogs showed the greatest efficacy against infection in tomato. • The C-terminal leucine amide did not considerably affect the efficacy in planta. [ABSTRACT FROM AUTHOR]

The Himalayan region is conferred by diverse wealth in term of flora and fauna. Among Himalayan plant biodiversity, Saussurea obvallata (common name Brahma Kamal) has an immense spiritual and medicinal significance. Owing to high demand, this herb is on the verge of extinction. Numerous studies have been carried out for preservation and in vitro regeneration of Saussurea obvallata. In view of above, this is the first study which aims to isolate and identify rhizospheric fungi associated with this plant. Soil samples were collected from three locations in Kedarnath valley and total 34 fungal isolates were isolated. Out of 34, three fungal isolates i.e. MaHaD1, MaHaD2 and MaHaD3 were selected for morphological and molecular characterization. The 16S rDNA sequencing identified MaHaD1, MaHaD2 and MaHaD3 as Phanerochaete chrysosporium, Trichoderma longibrachiatum and Aspergillus fumigatus respectively. The presence of these three dominant fungi in rhizospheric region seems to be results of climatic conditions and plant physiology. Results indicate that the presence of fungal microflora may play a vital role in survival and proliferation of Saussurea obvallata plant by providing tolerance and resistance to abiotic stress and fungal/nematode pathogens respectively.