scholarly journals Biocontrol Efficacy of Different Isolates of Trichoderma against Soil Born Pathogen Rhizoctonia solani

2014 ◽  
Vol 63 (1) ◽  
pp. 95-103 ◽  
Author(s):  
SAEED AHMAD ASAD ◽  
NAEEM ALI ◽  
ABDUL HAMEED ◽  
SABAZ ALI KHAN ◽  
RAFIQ AHMAD ◽  
...  
Keyword(s):  
Rhizoctonia Solani ◽  
Disease Incidence ◽  
Antagonistic Activity ◽  
Water Soluble ◽  
Trichoderma Spp ◽  
Volatile Metabolites ◽  
Bean Plants ◽  
First Time

In this study, the biocontrol abilities of water-soluble and volatile metabolites of three different isolates of Trichoderma (T. asperellum, T. harzianum and Trichoderma spp.) against soil borne plant pathogen Rhizoctonia solani were investigated both in vitro and in vivo. The results showed for the first time that mycelial growth inhibition of the pathogen was 74.4-67.8% with water-soluble metabolites as compared to 15.3-10.6% with volatile metabolites in vitro. In vivo antagonistic activity of Trichoderma isolates against R. solani was evaluated on bean plants under laboratory and greenhouse conditions. We observed that T. asperellum was more effective and consistent, lowering disease incidence up to 19.3% in laboratory and 30.5% in green house conditions. These results showed that three isolates of Trichoderma could be used as effective biocontrol agents against R. solani.

Antitumor Activities of Extracts and Compounds from Water Decoctions of Taxus cuspidata

2010 ◽  
Vol 38 (06) ◽  
pp. 1107-1114 ◽  
Author(s):  
Shougang Jiang ◽  
Yu Zhang ◽  
Yuangang Zu ◽  
Zhuo Wang ◽  
Yujie Fu
Keyword(s):  
Antitumor Activity ◽  
Water Soluble ◽  
Taxus Cuspidata ◽  
Antitumor Activities ◽  
Antitumor Effects ◽  
Anticancer Properties ◽  
Specific Host ◽  
First Time

Water decoctions from the leaves of Taxus cuspidata are used in traditional Chinese medicine to treat cancer, suggesting that water soluble constituents from these leaves may possess anticancer properties. Interestingly, hydrophilic paclitaxel derivatives, as opposed to paclitaxel itself, can be detected by high pressure liquid chromatography in water decoctions from these leaves. The remainder extracts, which are free of paclitaxel and hydrophilic paclitaxel derivatives, from the T. cuspidata leaves were investigated for antitumor activity in vivo and in vitro for the first time in this study. EE80B, 7-xylosyl-10-deacetylpaclitaxel and 7-xylosyl-10-deacetylpaclitaxel C displayed the most antitumor activity in vivo. However, in vitro studies with tumor cell lines showed that EE80B had a significantly smaller antitumor effect than paclitaxel. We hypothesize that water decoctions from T. cuspidata leaves exhibit antitumor effects in vivo, which may be aided by the activation of specific host mechanisms (e.g. stimulation of antitumor immunity) which are not present in vitro.

scholarly journals Biocontrol potential of Trichoderma harzianum in controlling wilt disease of pistachio caused by Verticillium dahliae

2017 ◽  
Vol 57 (2) ◽  
pp. 185-193 ◽  
Author(s):  
Zeinab Fotoohiyan ◽  
Saeed Rezaee ◽  
Gholam Hosein Shahidi Bonjar ◽  
Amir Hossein Mohammadi ◽  
Mohammad Moradi
Keyword(s):  
Verticillium Dahliae ◽  
Trichoderma Harzianum ◽  
Pathogenic Fungus ◽  
Antagonistic Activity ◽  
Wilt Disease ◽  
Dual Culture ◽  
Volatile Metabolites ◽  
Biocontrol Potential

Abstract Verticillium wilt caused by Verticillium dahliae, is one of the most devastating diseases in pistachio orchards in the world including Iran. In search for an effective non-chemical strategy for the management of this disease, we evaluated the biocontrol potential of Trichoderma harzianum isolates obtained from the rhizosphere of healthy pistachio trees in different locations of the Kerman province of Iran against V. dahliae under laboratory and greenhouse conditions. Dual culture tests in the laboratory were conducted in a completely randomized design using 72 T. harzianum isolates. Twenty isolates showed the highest in vitro antagonistic activity. The results indicated that all 20 isolates were capable of inhibiting the mycelial growth of V. dahliae significantly. Among them, isolates Tr8 and Tr19 were the most effective by 88.89% and 85.12% inhibition, respectively. Extracted cell free metabolites of all effective isolates also inhibited the growth of V. dahliae in the culture medium significantly. According to the results, isolates Tr4 and Tr6 inhibited fungal pathogen growth by 94.94% and 88.15% respectively, through production of non-volatile metabolites. In the evaluation of volatile metabolites, isolates Tr5 and Tr4 were the most effective by 26.27% and 24.49% growth inhibition, respectively. Based on the results of the in vitro experiments, the five most effective isolates were selected for evaluation under greenhouse conditions for their biocontrol potential in controlling Verticillium wilt of pistachio. Results of the greenhouse, (in vivo) experiments were positive and indicated that the occurrence of wilt disease in plants treated with the antagonists alone or in combination with pathogenic fungus was lower than in plants inoculated with pathogen alone. The overall results of this study suggest that Trichoderma fungal antagonist may be an effective biocontrol agent for the control of Verticillium wilt of pistachio.

scholarly journals Biological Management of Colocasia Blight Incited by Phytophthora colocasiae using Native Strains of Antagonists in North Western Himalayas

2021 ◽  
Author(s):  
Divya Bhandhari ◽  
Amar Singh ◽  
J.V. Patel ◽  
D.K. Banyal
Keyword(s):  
Growth Inhibition ◽  
Disease Control ◽  
Pseudomonas Fluorescens ◽  
Mycelial Growth ◽  
Antagonistic Activity ◽  
Trichoderma Spp ◽  
Phytophthora Colocasiae ◽  
Biological Management

Background: Colocasia is cultivated globally for its edible corm and leaves. Leaf blight incited by Phytophthora colocasiae is the most destructive disease of colocasia. The current study aims at biological management of the disease. Methods: Nine Trichoderma isolates from the colocasia rhizosphere soil along with five designated isolates of Trichoderma spp. already available in the Department of Plant Pathology, CSK HPKV, Palampur were tested in vitro for antagonistic activity against P. colocasiae. Similarly, six unidentified bacterial strains isolated from colocasia phylloplane and available Pseudomonas fluorescens were evaluated for antagonistic activity against P. colocasiae under in vitro conditions. The bioagents found best under in vitro conditions were evaluated in vivo. Result: Trichoderma isolate Ti-6 was found significantly superior bioagent as it resulted in 72.9 per cent mycelial growth inhibition of P. colocasiae followed by Ti-5 (63.2%), Ti-4 (60.1%) and Ti-1 (54.5%). Amongst bacterial antagonists, Pseudomonas fluorescens gave maximum mycelial growth inhibition of 50.5 per cent followed by Pb-3 (31.4%) and Pb-6 (30.5%). The efficacy of five Trichoderma spp isolates viz., Ti-6, Ti-5, Ti-4, Ti-1, T. viride and one bacterial isolate of P. fluorescens found effective under in vitro were also evaluated in vivo using three delivery systems under net house condition. Corm treatment with bioagents was found superior for management of colocasia blight. Corm treatment with Ti-6 was found to be significantly superior to other treatments as 93.74 per cent of disease control was observed. For drenching, bioagent Ti-6 was proved best in managing blight disease (88.91%) followed by Ti-5 (88.90%). However, Ti-5 isolate of Trichoderma sp. as soil application was found superior with 90.02 per cent disease control.

Management of Root Rot of Fenugreek Caused by Rhizoctonia solani using Plant Extracts and Bio-agents

2020 ◽  
Author(s):  
Shankar Lal Yadav ◽  
R.P. Ghasolia
Keyword(s):  
Rhizoctonia Solani ◽  
Pseudomonas Fluorescens ◽  
Seed Yield ◽  
Plant Extracts ◽  
Trichoderma Harzianum ◽  
Root Rot ◽  
Disease Incidence ◽  
Clove Extract

Background: Root rot of fenugreek (Trigonella foenum-graecum L.) caused by Rhizoctonia solani is an important constraint to the crop and causes significant economic losses in Rajasthan as well as India and fungicides are the major tool to overcome the disease incidence. As per environment and health issues and demand of organically produced fenugreek green leaves and seeds, it is a major concerned to control it by eco-friendly approaches. The current study aimed to find the most effective control measure of this dreaded disease through eco-friendly approaches.Methods: The present field-laboratory investigations were conducted during 2016-17 and 2017-18, to evaluate six plant extracts in vitro and in vivo, namely neem (Azadirachta indica), Alstonia (Alstonia scholaris), garlic (Allium sativum), datura (Datura stramonium), tulsi (Ocimum tenuiflorum), aak (Calotropis gigantea) and four bio-agents (Trichoderma harzianum, T. viride, Bacillus subtilis and Pseudomonas fluorescens) in vivo through seed treatment alone and/or in combination for two consecutive years. Result: Our investigations in vitro with botanicals cleared that garlic clove extract was highly antimycotic to the pathogen (79.52%) followed by aak (62.48%) and neem extract (53.37%). Under field conditions, seed soaking with garlic clove extract (@10%) for 30 minutes was observed the most effective in reducing disease incidence (62.02%) and in increasing seed yield (65.35%) followed by aak (56.56% and 59.82%, respectively). In bio-agents, Trichoderma harzianum + Pseudomonas fluorescens (@ 3+3 g/kg seeds) was found superior in reducing disease incidence (66.81%) and in increasing seed yield (73.06%) and the next best was T. viride + P. fluorescens. The findings of this study can be utilized to manage the disease effectively and eco-friendly and also to obtain organic produce of the fenugreek.

scholarly journals Biological and chemical control of Sclerotinia sclerotiorum using Trichoderma spp. and Ulocladium atrum and pathogenicity to bean plants

2010 ◽  
Vol 53 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Girlene Soares de Figueirêdo ◽  
Lívio Carvalho de Figueirêdo ◽  
Francinete Carla Nunes Cavalcanti ◽  
Angela Coimbra dos Santos ◽  
Antonio Felix da Costa ◽  
...  
Keyword(s):  
Sclerotinia Sclerotiorum ◽  
Chemical Control ◽  
Statistical Difference ◽  
Phaseolus Vulgaris L ◽  
Trichoderma Spp ◽  
Thiophanate Methyl ◽  
Bean Plants ◽  
Antagonistic Potential

Four isolates of Sclerotinia sclerotiorum were tested for pathogenicity in IPA-10 variety bean plants (Phaseolus vulgaris L.), and all were pathogenic. Biological control in vitro was evaluated using eight isolates of Trichoderma spp. and, one of Ulocladium atrum. Chemical control in vitro with fungicides Thiophanate methyl, Iprodione and Carbendazim was also tested. Except U. atrum, all Trichoderma isolates showed antagonistic potential against S. sclerotiorum, where isolate 3601 presented the best performance. Thiophanate methyl chemical control was the most efficient. This fungicide and isolate 3601were compared in vivo in greenhouse. There was statistical difference between the treatments, and the application of fungicide and antagonist before the pathogen was the most efficient approach, reducing the percentage of pathogenicity to 32.94% and 37.04%, respectively.

scholarly journals Effect of Two Biological Formulations Based onBacillus subtilisandPseudomonas fluorescenson Control ofDidymella applanata, the Causal Agent of Red Raspberry Cane Spur Blight

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Margarita Shternshis ◽  
Tatyana Shpatova ◽  
Anatoly Belyaev
Keyword(s):  
Weather Conditions ◽  
Field Trials ◽  
Antagonistic Activity ◽  
Rubus Idaeus ◽  
Causal Agent ◽  
Red Raspberry ◽  
Natural Conditions ◽  
First Time

In vitroandin vivostudies were conducted to estimate the efficacy of the two microbial formulations based onBacillus subtilisCohn. andPseudomonas fluorescensMig. on the fungusDidymella applanata(Niessl.) Sacc., the causal agent of red raspberry (Rubus idaeusL.) spur blight.In vitro, both bacteria reduced the growth ofD. applanata. In inoculation experiments with raspberry canes in two cultivars with different susceptibility toD. applanata, these antagonistic bacteria suppressed fungal development by reducing the lesions area and the number ofD. applanatafruiting bodies. Field trials of two biological formulations under natural conditions showed a significant suppression of the disease.B. subtilisandP. fluorescensincluded in the formulations revealed antagonistic activity towardsD. applanatathat depended on the red raspberry cultivar and weather conditions. In all cases,B. subtilisshowed better results thanP. fluorescensin biocontrol of the raspberry spur blight. This study demonstrated for the first time the ability of the biocontrol agentsB. subtilisandP. fluorescensto suppress red raspberry cane spur blight, a serious worldwide disease.

scholarly journals Ubisol-Q10, a Nanomicellar and Water-Dispersible Formulation of Coenzyme-Q10 as a Potential Treatment for Alzheimer’s and Parkinson’s Disease

Antioxidants ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 764
Author(s):  
Darcy Wear ◽  
Caleb Vegh ◽  
Jagdeep K. Sandhu ◽  
Marianna Sikorska ◽  
Jerome Cohen ◽  
...  
Keyword(s):  
Coenzyme Q10 ◽  
Water Soluble ◽  
In Vivo Models ◽  
Federal Drug Administration ◽  
Water Dispersible ◽  
Therapeutic Value ◽  
Effective Doses ◽  
First Time

The world continues a desperate search for therapies that could bring hope and relief to millions suffering from progressive neurodegenerative diseases such as Alzheimer’s (AD) and Parkinson’s (PD). With oxidative stress thought to be a core stressor, interests have long been focused on applying redox therapies including coenzyme-Q10. Therapeutic use has failed to show efficacy in human clinical trials due to poor bioavailability of this lipophilic compound. A nanomicellar, water-dispersible formulation of coenzyme-Q10, Ubisol-Q10, has been developed by combining coenzyme-Q10 with an amphiphilic, self-emulsifying molecule of polyoxyethanyl α-tocopheryl sebacate (derivatized vitamin E). This discovery made possible, for the first time, a proper assessment of the true therapeutic value of coenzyme-Q10. Micromolar concentrations of Ubisol-Q10 show unprecedented neuroprotection against neurotoxin exposure in in vitro and in vivo models of neurodegeneration and was extremely effective when delivered either prior to, at the time of, and most significantly, post-neurotoxin exposure. These findings indicate a possible way forward for clinical development due to effective doses well within Federal Drug Administration guidelines. Ubisol-Q10 is a potent mobilizer of astroglia, antioxidant, senescence preventer, autophagy activator, anti-inflammatory, and mitochondrial stabilizer. Here we summarize the work with oil-soluble coenzyme-Q10, its limitations, and focus mainly on efficacy of water-soluble coenzyme-Q10 in neurodegeneration.

An Attempt at Biological Control of Blossom Blight of Rose Caused by Botrytis cinerea Using some Local Trichoderma spp. Strains

2020 ◽  
Vol 55 (1) ◽  
pp. 27-34
Author(s):  
G. Zadehdabagh ◽  
K. Karimi ◽  
M. Rezabaigi ◽  
F. Ajamgard
Keyword(s):  
Botrytis Cinerea ◽  
Mycelial Growth ◽  
Limiting Factor ◽  
Dual Culture ◽  
Trichoderma Spp ◽  
Khuzestan Province ◽  
Inhibitory Potential ◽  
Cut Rose

The northern of Khuzestan province in Iran is mainly considered as one of the major areas of miniature rose production. Blossom blight caused by Botrytis cinerea has recently become a serious limiting factor in rose production in pre and post-harvest. In current study, an attempt was made to evaluate the inhibitory potential of some local Trichoderma spp. strains against B. cinerea under in vitro and in vivo conditions. The in vitro results showed that all Trichoderma spp. strains were significantly able to reduce the mycelial growth of the pathogen in dual culture, volatile and non-volatile compounds tests compared with control, with superiority of T. atroviride Tsafi than others. Under in vivo condition, the selected strain of T. atroviride Tsafi had much better performance than T. harzianum IRAN 523C in reduction of disease severity compared with the untreated control. Overall, the findings of this study showed that the application of Trichoderma-based biocontrol agents such as T. atroviride Tsafi can be effective to protect cut rose flowers against blossom blight.

Fenofibrate Solid Dispersion for Improving Oral Bioavailability: Preparation, and Characterization and in vivo Evaluation

2020 ◽  
Vol 13 (5) ◽  
pp. 5102-5109
Author(s):  
Venu Madhav K ◽  
Somnath De ◽  
Chandra Shekar Bonagiri ◽  
Sridhar Babu Gummadi
Keyword(s):  
Oral Bioavailability ◽  
Oral Delivery ◽  
Solid Dispersions ◽  
In Vitro Release ◽  
Aqueous Solubility ◽  
Water Soluble ◽  
Scanning Calorimetry ◽  
In Vivo Evaluation

Fenofibrate (FN) is used in the treatment of hypercholesterolemia. It shows poor dissolution and poor oral bioavailability after oral administration due to high liphophilicity and low aqueous solubility. Hence, solid dispersions (SDs) of FN (FN-SDs) were develop that might enhance the dissolution and subsequently oral bioavailability. FN-SDs were prepared by solvent casting method using different carriers (PEG 4000, PEG 6000, β cyclodextrin and HP β cyclodextrin) in different proportions (0.25%, 0.5%, 0.75% and 1% w/v). FN-SDs were evaluated solubility, assay and in vitro release studies for the optimization of SD formulation. Differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) analysis was performed for crystalline and morphology analysis, respectively. Further, optimized FN-SD formulation evaluated for pharmacokinetic performance in Wistar rats, in vivo in comparison with FN suspension.  From the results, FN-SD3 and FN-SD6 have showed 102.9 ±1.3% and 105.5±3.1% drug release, respectively in 2 h. DSC and PXRD studies revealed that conversion of crystalline to amorphous nature of FN from FT-SD formulation. SEM studies revealed the change in the orientation of FN when incorporated in SDs. The oral bioavailability FN-SD3 and FN-SD6 formulations exhibited 2.5-folds and 3.1-folds improvement when compared to FN suspension as control. Overall, SD of FN could be considered as an alternative dosage form for the enhancement of oral delivery of poorly water-soluble FN.

Chemosensitizing Activity of Histone Deacetylases Inhibitory Cyclic Hydroxamic Acids for Combination Chemotherapy of Lymphatic Leukemia

2018 ◽  
Vol 18 (4) ◽  
pp. 365-371 ◽  
Author(s):  
Denis V. Mishchenko ◽  
Margarita E. Neganova ◽  
Elena N. Klimanova ◽  
Tatyana E. Sashenkova ◽  
Sergey G. Klochkov ◽  
...  
Keyword(s):  
Lipid Peroxidation ◽  
Acute Toxicity ◽  
Histone Deacetylases ◽  
Hydroxamic Acids ◽  
Water Soluble ◽  
Male Rat ◽  
Hybrid Male ◽  
Cyclic Hydroxamic Acids

Background: Anti-tumor effect of hydroxamic acid derivatives is largely connected with its properties as efficient inhibitors of histone deacetylases, and other metalloenzymes involved in carcinogenesis. Objective: The work was aimed to (i) determine the anti-tumor and chemosensitizing activity of the novel racemic spirocyclic hydroxamic acids using experimental drug sensitive leukemia P388 of mice, and (ii) determine the structure-activity relationships as metal chelating and HDAC inhibitory agents. Method: Outbreed male rat of 200-220 g weights were used in biochemical experiments. In vivo experiments were performed using the BDF1 hybrid male mice of 22-24 g weight. Lipid peroxidation, Fe (II) -chelating activity, HDAC fluorescent activity, anti-tumor and anti-metastatic activity, acute toxicity techniques were used in this study. Results: Chemosensitizing properties of water soluble cyclic hydroxamic acids (CHA) are evaluated using in vitro activities and in vivo methods and found significant results. These compounds possess iron (II) chelating properties, and slightly inhibit lipid peroxidation. CHA prepared from triacetonamine (1a-e) are more effective Fe (II) ions cheaters, as compared to CHA prepared from 1- methylpiperidone (2a-e). The histone deacetylase (HDAC) inhibitory activity, lipophilicity and acute toxicity were influenced by the length amino acids (size) (Glycine < Alanine < Valine < Leucine < Phenylalanine). All compounds bearing spiro-N-methylpiperidine ring (2a-e) are non-toxic up to 1250 mg/kg dose, while compounds bearing spiro-tetramethylpiperidine ring (1a-e) exhibit moderate toxicity which increases with increasing lipophility, but not excite at 400 mg/kg. Conclusion: It was shown that the use of combination of non-toxic doses of cisplatin (cPt) or cyclophosphamide with CHA in most cases result in the appearance of a considerable anti-tumor effect of cytostatics. The highest chemosensitizing activity with respect to leukemia Р388 is demonstrated by the CHA derivatives of Valine 1c or 2c.

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