scholarly journals Antifungal activity of extracts of Melia azedarach and Ageratum conyzoides against Lasiodiplodia pseudotheobromae through in vitro test

2021 ◽  
Vol 886 (1) ◽  
pp. 012007
Author(s):  
Asman Asman ◽  
A B Cahyani ◽  
A H Nufus ◽  
A Rosmana ◽  
A Fakhruddin ◽  
...  
Keyword(s):  
Fungal Biomass ◽  
Solid Medium ◽  
Colony Growth ◽  
Melia Azedarach ◽  
In Vitro Test ◽  
Ageratum Conyzoides ◽  
Wet Biomass ◽  
Dry Biomass ◽  
Dieback Disease

Abstract Lasiodiplodia pseudotheobromae is one of the pathogens of the cocoa dieback disease. Currently, the disease is considered a significant disease in cocoa, which is a newly emerging disease in Sulawesi. The control tools and methods remain unexplored comprehensively. The main objective of this study was to evaluate Melia azedarach and Ageratum conyzoides leaf extract to inhibit the growth of the L. pseudotheobromae. Three different concentrations were applied for each weed extract, namely: 1%, 3%, and 5%. The experiment was conducted through the poison food technique method both in solid medium and liquid medium. M. azedarach and A. conyzoides were significantly inhibited the colony growth of L. pseudotheobromae in all concentrations in solid medium. However, A. conyzoides 5% performed well to suppress the colony growth of L. pseudotheobromae (42.7%), followed by M. azedarach 5% (16.0%). The mycelium biomass of L. pseudotheobromae was significantly inhibited by M. azedarach and A. conyzoides as well. A. conyzoides 5% showed a higher inhibition of the fungal biomass either wet biomass (90.3%) or dry biomass (95.5%), followed by M. azedarach 5% both wet biomass (85.6%) and dry biomass (78.1%). M. azedarach and A. conyzoides remain to inhibit the colony growth and fungal biomass regardless of the type of concentrations. M. azedarach and A. conyzoides can potentially be an option for controlling dieback disease caused by L. pseudotheobromae.

scholarly journals Antifungal activity of crude extracts of Ageratum conyzoides and Chromolaena odorata for management of Lasiodiplodia theobromae and Lasiodiplodia pseudotheobromae through in vitro evaluation

2021 ◽  
Vol 886 (1) ◽  
pp. 012008
Author(s):  
Asman Asman ◽  
Adelvia ◽  
Ade Rosmana ◽  
Sylvia Sjam ◽  
Hamdayanty ◽  
...  
Keyword(s):  
Fungal Biomass ◽  
Synthetic Medium ◽  
Dry Weight ◽  
Colony Growth ◽  
Chromolaena Odorata ◽  
Ageratum Conyzoides ◽  
Lasiodiplodia Theobromae ◽  
Wet Weight ◽  
Poison Food Technique

Abstract Lasiodiplodia is an important genus of fungi causing destructive diseases on perennial crops, including cocoa. Two crucial species of Lasiodiplodia that cause diseases in cocoa are Lasiodiplodia theobromae and Lasiodiplodia pseutheobromae. A variety of weeds is the potential to be applied as botanical fungicides to control the pathogens. The main objective of this study was to evaluate Ageratum conyzoides and Chromolaena odorata leaf extract to inhibit the growth of L. theobromae and L. pseudotheobromae on a synthetic medium. Solvent organic was methanol for weed extraction with a ratio of 1:5. The experiment was conducted through the poison food technique method, both in the solid and liquid medium in three different concentrations, 1, 3, and 5%. The result showed that A. conyzoides and C. odorata were significantly inhibited the colony growth of both Lasiodiplodia in all concentrations in a solid medium. A. conyzoides performed better than C. odorata in all concentrations of both Lasiodiplodia in inhibition. A. conyzoides 5% performed well to suppress the colony growth of L. pseudotheobromae (100%), followed by A. conyzoides 3% and A. conyzoides 1%. A. conyzoides 5% able to inhibit the colony growth of L. theobromae until 100%, followed by A. conyzoides 3% and 1%. Meanwhile, A. conyzoides and C. odorata extract tested on PDB medium at 1, 3, and 5% reduced the fungal biomass significantly at all concentrations. C. odorata was found most effective in inhibiting fungal biomass of both pathogens either on wet weight or on dry weight at 1, 3, and 5% %. A. conyzoides and C. odorata can manage the growth of L. theobromae and L. pseudotheobromae through in vitro conditions.

scholarly journals Potensi Cendawan Endofit pada Tanaman Binahong (Anredera cordifolia (Ten.) Steenis) untuk Mengendalikan Botryodiplodia theobromae Pat. Penyebab Mati Pucuk pada Bibit Jabon (Anthocephalus cadamba (Roxb.) Miq)

2019 ◽  
Vol 10 (2) ◽  
pp. 114-118
Author(s):  
Yunik Istikorini
Keyword(s):  
Medicinal Plant ◽  
Endophytic Fungi ◽  
Disease Incidence ◽  
Colony Growth ◽  
Colony Development ◽  
Botryodiplodia Theobromae ◽  
Antifungal Effect ◽  
Dieback Disease ◽  
Anthocephalus Cadamba

Endophytic fungi provides potential advantages as biocontrol agents in the plant. Binahong (Anredera cordifolia) is a medicinal plant which can potentially overcome many kinds of diseases. The dieback disease is caused by Botryodiplodia theobromae Pat. that may lead the death of the host. The objective of this research was to analyze the potency of endophytic fungi from binahong leaves to control the fungus B. theobromae as causal agent of dieback disease on jabon (Anthocepalus cadamba). The isolates of endophytic fungi from binahong used were bnh1.1, bnh1.2, bnh1.3, bnh4.2, bnh4.5, bnh3.3 and bnh3.4. The antifungal effect of endophytic fungi againts colony growth of virulent B. theobromae were tested in vitro. The results showed that all endophytic fungus (7 isolates) inhibited the colony development of B. theobromae ranging from 28.52%-52.22%. Treatment with endophytic fungi bnh4.5 and bnh4.2 had protected jabon from virulent B. theobromae. It has been expressed by the delay of the incubation period and the decreasing of disease severity (respectively 33.34% and 40.84%. Key words: Anredera cordifolia, Botryodiplodia theobromae, disease incidence, endophytic fungi

scholarly journals GROWTH OF FOUR TREE SPECIES ON MEDIA CONTAINING GOLD MINE TAILING OF PT ANTAM UBPE PONGKOR

2016 ◽  
Vol 7 (3) ◽  
pp. S72-S76
Author(s):  
Ulfah Juniarti Siregar ◽  
Roisatuz Zakiyah
Keyword(s):  
Growth Parameters ◽  
Average Diameter ◽  
Melia Azedarach ◽  
High Concentration ◽  
Shoot Ratio ◽  
Root Shoot Ratio ◽  
Wet Biomass ◽  
Dry Biomass ◽  
Two Factors ◽  
Media Types

PT Antam UBPE Pongkor is a gold mining company that produces waste in the from of tailing mud which contains heavy metal with sufficiently high concentration. The aim of this research was to study the growth of four types of plant, i.e. Casuarina junghuniana, Pinus merkusii, Melia azedarach, and Gmelina arborea in a media containing tailing mud. This research used a completely randomized factorial design with two factors, i.e. types of plant and media. Two kinds of media was used i.e. 1200g tailing and a mixture of 900g tailing and 300g compost. Growth parameters observed were plant diameter, height, number of leaf, leaf lenght and widht, total wet and dry biomass, root-shoot-ratio and number of stomata. Soil and plant analysis was done after four months of experiment. The results showed that plant types have significant effects on all parameters except root-shoot-ratio and plant height. Media types significantly affect plant diameter, wet and dry biomass. Interaction between plant types and media gave sifnificant effect on diameter, wet and dry biomass. G. arborea had the best growth response on all parameters except root-shoot-ratio and plant heigh. Its average diameter was 4.56 mm, leaf lenght 3.67 cm, leaf widht 3.000 cm, total wet biomass 50.21 g, total dry biomass 32.19 g and number of stomata is 89.Key words: C. junghuniana, G. arborea, metal, M. azedarach, tailing, P. merkusii.

Haemostatic Platelet Plug Formation in the Isolated Rabbit Mesenteric Preparation - An Analysis of Red Blood Cell Participation

1980 ◽  
Vol 44 (01) ◽  
pp. 006-008 ◽  
Author(s):  
D Bergqvist ◽  
K-E Arfors
Keyword(s):  
Whole Blood ◽  
Platelet Rich Plasma ◽  
Adenosine Diphosphate ◽  
In Vitro Test ◽  
Pharmacological Agents ◽  
Vitro Test ◽  
Releasing Effect ◽  
Plug Formation

SummaryIn a model using an isolated rabbit mesenteric preparation microvessels were transected and the time until haemostatic plugs formed was registered. Perfusion of platelet rich plasma gave no haemostasis whereas whole blood did. Addition of chlorpromazine or adenosine to the whole blood significantly prolonged the time for haemostasis, and addition of ADP to the platelet rich plasma significantly shortened it. It is concluded that red cells are necessary for a normal haemostasis in this model, probably by a combination of a haemodynamic and ADP releasing effect.The fundamental role of platelets in haemostatic plug formation is unquestionable but there are still problems concerning the stimulus for this process to start. Three platelet aggregating substances have been discussed – thrombin, adenosine diphosphate (ADP) and collagen. Evidence speaking in favour of thrombin is, however, very minimal, and the discussion has to be focused on collagen and ADP. In an in vitro system using polyethylene tubings we have shown that "haemostasis" can be obtained without the presence of collagen but against these results can be argued that it is only another in vitro test for platelet aggregation (1).To be able to induce haemostasis in this model, however, the presence of red blood cells is necessary. To further study this problem we have developed a model where haemostatic plug formation can be studied in the isolated rabbit mesentery and we have briefly reported on this (2).Thus, it is possible to perfuse the vessels with whole blood as well as with platelet rich plasma (PRP) and different pharmacological agents of importance.

First Fluorescent Acetylspermidine Deacetylation Assay for HDAC10 Identifies Inhibitors of Neuroblastoma Cell Colony Growth That Increase Lysosome Accumulation

2020 ◽  
Author(s):  
Daniel Herp ◽  
Johannes Ridinger ◽  
Dina Robaa ◽  
Stephen A. Shinsky ◽  
Karin Schmidtkunz ◽  
...  
Keyword(s):  
Histone Deacetylases ◽  
High Throughput Screening ◽  
Neuroblastoma Cell ◽  
Hdac Inhibitors ◽  
Anticancer Therapy ◽  
Colony Growth ◽  
Autophagic Flux ◽  
Enzymatic Conversion ◽  
Lysine Deacetylase

Histone deacetylases (HDACs) are important epigenetic regulators involved in many diseases, esp. cancer. First HDAC inhibitors have been approved for anticancer therapy and many are in clinical trials. Among the 11 zinc-dependent HDACs, HDAC10 has received relatively little attention by drug discovery campaigns, despite its involvement e.g. in the pathogenesis of neuroblastoma. This is due in part to a lack of robust enzymatic conversion assays. In contrast to the protein lysine deacetylase and deacylase activity of the other HDAC subtypes, it has recently been shown that HDAC10 has strong preferences for deacetylation of oligoamine substrates like spermine or spermidine. Hence, it also termed a polyamine deacetylase (PDAC). Here, we present the first fluorescent enzymatic conversion assay for HDAC10 using an aminocoumarin labelled acetyl spermidine derivative to measure its PDAC activity, which is suitable for high-throughput screening. Using this assay, we identified potent inhibitors of HDAC10 mediated spermidine deacetylation in-vitro. Among those are potent inhibitors of neuroblastoma colony growth in culture that show accumulation of lysosomes, implicating disturbance of autophagic flux.

scholarly journals In Vitro Newly Isolated Environmental Phage Activity against Biofilms Preformed by Pseudomonas aeruginosa from Patients with Cystic Fibrosis

2021 ◽  
Vol 9 (3) ◽  
pp. 478
Author(s):  
Ersilia Vita Fiscarelli ◽  
Martina Rossitto ◽  
Paola Rosati ◽  
Nour Essa ◽  
Valentina Crocetta ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Pseudomonas Aeruginosa ◽  
Multidrug Resistant ◽  
In Vitro Test ◽  
Chronic Infections ◽  
Hospital Environments ◽  
Vitro Test ◽  
General Reliability ◽  
Phage Activity

As disease worsens in patients with cystic fibrosis (CF), Pseudomonas aeruginosa (PA) colonizes the lungs, causing pulmonary failure and mortality. Progressively, PA forms typical biofilms, and antibiotic treatments determine multidrug-resistant (MDR) PA strains. To advance new therapies against MDR PA, research has reappraised bacteriophages (phages), viruses naturally infecting bacteria. Because few in vitro studies have tested phages on CF PA biofilms, general reliability remains unclear. This study aimed to test in vitro newly isolated environmental phage activity against PA isolates from patients with CF at Bambino Gesù Children’s Hospital (OBG), Rome, Italy. After testing in vitro phage activities, we combined phages with amikacin, meropenem, and tobramycin against CF PA pre-formed biofilms. We also investigated new emerging morphotypes and bacterial regrowth. We obtained 22 newly isolated phages from various environments, including OBG. In about 94% of 32 CF PA isolates tested, these phages showed in vitro PA lysis. Despite poor efficacy against chronic CF PA, five selected-lytic-phages (Φ4_ZP1, Φ9_ZP2, Φ14_OBG, Φ17_OBG, and Φ19_OBG) showed wide host activity. The Φ4_ZP1-meropenem and Φ14_OBG-tobramycin combinations significantly reduced CF PA biofilms (p < 0.001). To advance potential combined phage-antibiotic therapy, we envisage further in vitro test combinations with newly isolated phages, including those from hospital environments, against CF PA biofilms from early and chronic infections.

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