scholarly journals Test Antifungal Phatogen Extract Secondary Metabolites Of Endophytic Fungi Raru Plant (Cotylelobium melanoxylon)

2016 ◽  
Vol 1 (2) ◽  
pp. 6
Author(s):  
Uswatun Hasanah ◽  
Riwayati Riwayati ◽  
Idramsa Idramsa

This study aims to determine the ability of extracts  secondary metabolites of endophytic fungi raru plant Siarang (Cotylelobium melanoxylon) in inhibiting the growth of pathogenic fungi. Pathogenic fungi tested were Collectotrichum, Fusarium oxysporum, Candida albicans and Sclerotium rolfsii. Test antifungal pathogens carried out by using the method of Kirby-Bour, ie by measuring the clear zone located around the paper disc which is the zone of growth inhibition of pathogenic fungi. Measurement of inhibition zone is done by using a caliper or ruler. The results showed that the secondary metabolites of endophytic fungi extracts could inhibit the growth of pathogenic fungus Candida albicans is the clear zone of 10.23 mm. Keywords : endophytic fungus, Cotylelobium melanoxylon, extract of secondary metabolites, fungal pathogens, inhibition zone

2021 ◽  
Vol 21 (1) ◽  
pp. 72
Author(s):  
Muhammad Hasan Basri ◽  
Lalu Zulkifli ◽  
Abdul Syukur

Plant damage by pathogenic fungi is often found in plants, one of which is caused by Sclerotium rolfsii. Biological control strategy offers a promising alternative for managing disease in plants because they are environmental friendly compared to pesticides application. One of the biological control offered is by using endophytic fungi isolated from Vitex trivolia L. The aim of the study was to isolate, to identify macroscopic and microscopic endophytic fungi from Vitex trifolia L and to test their antagonism potency against the pathogenic fungus Sclerotium rolfsii in vitro. The isolation obtained 7 endophytic fungi isolates identified based on their genus characteristics, nsmely Periconia sp, Aspergillussp, Dendrophoma  sp, Geotrichum  sp, Ampulliferina  sp, Chalara  sp, dan Bispora sp and 2 isolates have not been identified. The Antibacterial test of the fungi isolate on the 4 tested bacteria showed that of all the fungi isolate have low activity. The antagonism test using the direct opposition method with the PIRG formula, showed that the 3 isolates had high percentage of growth inhibition, in which ALJ1, BLJ5, and ALJ3 isolate has  85%, 90%, and 100% respectively. This potency could be used as biological agents on the pathogenic fungus Sclerotium rolfsii.


2021 ◽  
Vol 7 (4) ◽  
pp. 301
Author(s):  
Nurul Farizah Azuddin ◽  
Masratul Hawa Mohd ◽  
Nik Fadzly N. Rosely ◽  
Asyraf Mansor ◽  
Latiffah Zakaria

Calamus castaneus is a common rattan palm species in the tropical forests of Peninsular Malaysia and is noticeable by the yellow-based spines that cover the stems. This study aimed to determine the prevalence of fungal endophytes within C. castaneus spines and whether they inhibit the growth of fungal pathogens. Twenty-one genera with 40 species of fungal endophytes were isolated and identified from rattan palm spines. Based on molecular identification, the most common isolates recovered from the spines were Colletotrichum (n = 19) and Diaporthe spp. (n = 18), followed by Phyllosticta spp., Xylaria sp., Trichoderma spp., Helminthosporium spp., Penicillium spp., Fusarium spp., Neopestalotiopsis spp., Arthrinium sp., Cyphellophora sp., Cladosporium spp., Curvularia sp., Bionectria sp., and Acremonium spp. Non-sporulating fungi were also identified, namely Nemania primolutea, Pidoplitchkoviella terricola, Muyocopron laterale, Acrocalymma fici, Acrocalymma medicaginis, and Endomelanconiopsis endophytica. The isolation of these endophytes showed that the spines harbor endophytic fungi. Most of the fungal endophytes inhibited the growth of several plant pathogenic fungi, with 68% of the interactions resulting in mutual inhibition, producing a clear inhibition zone of <2 mm. Our findings demonstrate the potential of the fungal endophytes from C. castaneus spines as biocontrol agents.


2022 ◽  
Vol 2 ◽  
Author(s):  
Sefinew Tilahun ◽  
Marye Alemu ◽  
Mesfin Tsegaw ◽  
Nega Berhane

Ginger diseases caused by fungal pathogens have become one of the most serious problems causing reduced production around the world. It has also caused a major problem among farmers in different parts of Ethiopia resulting in a huge decline in rhizome yield. However, the exact causative agents of this disease have not been identified in the state. Although there are few studies related to pathogenic fungus identification, molecular level identification of fungal pathogen was not done in the area. Therefore, this study was undertaken to isolate and characterized the fungal causative agent of ginger disease from the diseased plant and the soil samples collected around the diseased plant from Chilga district, Gondar, Ethiopia. Samples from infected ginger plants and the soil around the infected plant were collected. Culturing and purification of isolates were made using Potato Dextrose Agar supplemented with antibacterial agent chloramphenicol. The morphological characterization was done by structural identification of the isolates under the microscope using lactophenol cotton blue stains. Isolated fungi were cultured and molecular identification was done using an internal transcribed spacer (ITS) of ribosomal DNA (rDNA). A total of 15 fungal morphotypes including 11 Aspergillus spp. (73.3%), 2 Penicillium spp. (13.3%), and single uncultured fungus clone S23 were isolated from the samples representing all the plant organs and the soil. Aspergillus spp. (73.3%) was the most common and seems to be the major causative agent. To the best of our knowledge, this is the first report of ginger pathogenic fungi in Ethiopia identified using ITS rDNA molecular techniques. This study will lay foundation for the development of management strategies for fungal diseases infecting ginger.


EUGENIA ◽  
2011 ◽  
Vol 17 (3) ◽  
Author(s):  
Emmy Senewe ◽  
Guntur Manengkey

ABSTRACT Leptocorisa oratorius is one major pest of rice in North Sulawesi. Hence, it is necessary to control the pest. The research objective was to identify and to test pathogenicity of local  entomopathogen fungi which infected  Leptocorisa oratorius. The pathogens were collected through sampling of L. oratorius which had been infected by the fungi in the field. The pathogenic fungi was isolated using PDA medium, identified followed by inoculation for pathogenecity test.  During several sampling pest, it was found that  L. oratorius was attacked by fungal pathogens in the field. The identification revelead that the fungal pathogens were Beauveria sp and Fusarium sp. Both the fungal pathogen produced white mycelium and could only be distinguished using microscope in the laboratory. Result of pathogenicity tests showed that the two fungal pathogens caused different mortality of the L. oratorius. Mortality of  L. oratorius caused by pathogenic fungus Beauveria sp was  30.3% . Whereas, mortality of  L. oratorius caused by Fusarium sp was only 3.33%. Keywords : pathogenic fungi, entomopathogen, pathogenicity tests, L. oratorius


mSphere ◽  
2018 ◽  
Vol 3 (2) ◽  
Author(s):  
Eric H. Jung ◽  
David J. Meyers ◽  
Jürgen Bosch ◽  
Arturo Casadevall

ABSTRACTSimilarities in fungal and animal cells make antifungal discovery efforts more difficult than those for other classes of antimicrobial drugs. Currently, there are only three major classes of antifungal drugs used for the treatment of systemic fungal diseases: polyenes, azoles, and echinocandins. Even in situations where the offending fungal organism is susceptible to the available drugs, treatment courses can be lengthy and unsatisfactory, since eradication of infection is often very difficult, especially in individuals with impaired immunity. Consequently, there is a need for new and more effective antifungal drugs. We have identified compounds with significant antifungal activity in the Malaria Box (Medicines for Malaria Ventures, Geneva, Switzerland) that have higher efficacy than some of the currently used antifungal drugs. Our best candidate, MMV665943 (IUPAC name 4-[6-[[2-(4-aminophenyl)-3H-benzimidazol-5-yl]methyl]-1H-benzimidazol-2-yl]aniline), here referred to as DM262, showed 16- to 32-fold-higher activity than fluconazole againstCryptococcus neoformans. There was also significant antifungal activity in other fungal species with known antifungal resistance, such asLomentospora prolificansandCryptococcus gattii. Antifungal activity was also observed against a common fungus,Candida albicans. These results are important because they offer a potentially new class of antifungal drugs and the repurposing of currently available therapeutics.IMPORTANCEMuch like the recent increase in drug-resistant bacteria, there is a rise in antifungal-resistant strains of pathogenic fungi. There is a need for novel and more potent antifungal therapeutics. Consequently, we investigated a mixed library of drug-like and probe-like compounds with activity inPlasmodiumspp. for activity against two common fungal pathogens,Cryptococcus neoformansandCandida albicans, along with two less common pathogenic species,Lomentospora prolificansandCryptococcus gattii. We uncover a previously uncharacterized drug with higher broad-spectrum antifungal activity than some current treatments. Our findings may eventually lead to a compound added to the arsenal of antifungal therapeutics.


2021 ◽  
Vol 12 (5) ◽  
pp. 523-531
Author(s):  
Anjali Singh ◽  
◽  
Ratna U. Thosar ◽  
Vijayshree Chavan ◽  
Sujoy Saha ◽  
...  

In vitro bio-efficacy of the novel copper (NC101 and NCP102) and phosphonate (PN103 and PMN104) based fungicides against various soil borne and grape vine pathogens was evaluated at ICAR-National Research Centre for Grapes, Pune, Maharashtra, India during February - April 2021. The fungicides were screened against five bacterial pathogens viz. Xanthomonas campestris pv. citri, X. campestris pv. campestris, X. campestris pv. punicae, X. campestris pv. viticola and X. oryzae pv. oryzae and 10 fungal pathogens viz. Rhizoctonia bataticola, Sclerotium rolfsii, Cladosporium sp, Alternaria alternata, Colletotrichum gloeosporioides, Penicillium notatum, Magnaporthe oryzae, Fusarium oxysporium, Macrophomina phaseolina (Soyabean isolate) and Macrophomina phaseolina (Jute isolate) at different concentrations. Results indicated that among all the tested fungicides viz. NC101, NCP102, PN103 and PMN104, phosphonate based fungicides (PN103 and PMN104) were highly effective against bacterial isolates with zone of inhibition ranging between 8.75 - 31.12 mm in which X. campestris pv. viticola was found to express least inhibition zone. In case of pathogenic fungal isolates, similar trend was observed, most of the isolates showed cent percent inhibition at higher concentration of PN103 and PMN104. However Sclerotium rolfsii showed least or no inhibition when tested at different concentrations of fungicides. The chemicals exhibited wide range of inhibition and it was found to increase steadily with increase in concentrations of the test fungicides.


Plant Disease ◽  
2013 ◽  
Vol 97 (7) ◽  
pp. 1000-1000 ◽  
Author(s):  
J.-H. Kwon ◽  
D.-W. Kang ◽  
J. Kim

Taro (Colocasia esculenta L.) is grown throughout the world primarily for its tubers, which become edible after cooking. Taro stems are often used in a traditional soup in South Korea. In September 2012, a suspected white rot of taro occurred in a farmer's fields in Jinju, South Korea. Infected plants gradually withered, a white mycelial mat appeared, and numerous sclerotia developed on the surface of petioles near the soil line. The heavily infected petioles rotted and the entire plant eventually died. The freshly isolated pathogenic fungus was grown on potato dextrose agar (PDA) and examined microscopically. Aerial mycelia usually formed many narrow hyphal strands 4 to 8 μm wide. The white mycelia formed a typical clamp connection structure after 6 days growth at 25°C. The sclerotia were white at first, gradually turned dark brown, and were 1 to 3 mm in diameter. Small globoid sclerotia formed abundantly on PDA after 18 days of growth. Ten 2-month-old potted taro plants were inoculated with S. rolfsii-colonized agar discs directly at the base of each plant and kept at 25°C in a greenhouse to test pathogenicity. Three taro plants were inoculated similarly with uncolonized agar discs as controls. Eight days after inoculation, blight symptoms were observed, and S. rolfsii was reisolated from the artificially inoculated plants. The control taro plants remained healthy. We amplified and sequenced an internal transcribed spacer (ITS) rDNA region of the isolate using the ITS1 (5′-TCCGTAGGTGAACCTGCGG-3′) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′) primers to confirm the identity of the fungus (2). The resulting 684-bp sequence was deposited in GenBank (Accession No. KC491876). A comparison with other sequences available in the GenBank database revealed that the ITS sequence shared 100% similarity with Sclerotium rolfsii sequences (HQ420816 and JN017199). Based on the symptoms, mycological characteristics, ITS sequence analysis, and host plant pathogenicity, this fungus was identified as S. rolfsii Saccardo (1). To our knowledge, this is the first report of white rot in taro caused by S. rolfsii in Korea. References: (1) J. E. Mordue. CMI Descriptions of Pathogenic Fungi and Bacteria. No. 410, 1974. (2) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, New York, 1990.


2017 ◽  
Vol 2 (1) ◽  
pp. 33-35
Author(s):  
Prasetyo Handrianto

ABSTRAKJamur Lingzhi (Ganoderma lucidum) merupakan herbal yang memiliki aktivitas antibiotik atau antibakteri. Triterpenoid dalam Jamur Lingzhi mengandung senyawa yang menunjukkan aktivitas antibakteri melaluimekanisme pengikatan polimer yang kuat terhadap porin (protein transmembran) pada membran luar dari dinding sel bakteri sehingga menyebabkan kerusakan pada porin. Tujuan penelitian ini adalah menentukan efek ekstrak etanol Jamur Lingzhi dalam menghambat pertumbuhan bakteri Escherichia coli. Metode yang digunakan adalah metode cakram dengan mengamati zona hambat yang muncul disekitar cakram. Kosentrasi ekstrak yang digunakan adalah 20 µg / ml, 40 µg / ml, 60 µg / ml, 80 µg / ml, 100 µg / ml. Kosentrasi ekstrak 20µg / ml dan 40 µg / ml menghasilkan zona hambat masing-masing 10,5 mm dan 12,4 mm yang dikategorikan sebagai kurang aktif, sedangkan kosentrasi 60 µg / ml, 80 µg / ml, dan 100 µg / ml menghasilkan zona hambat 13,65 mm, 14,9 mm, dan 16,5 mm yang dikategorikan sebagai aktif. Hasil menunjukkan ekstrak etanol Jamur Lingzhi dapat  menghambat pertumbuhan bakteri Escherichia coli.Kata kunci : Ganoderma lucidum, Escherichia coli, Ekstrak etanol, Antibakteri.ABSTRACTLingzhi mushroom (Ganoderma lucidum) is a herbal remedy that has as an antibiotic or antibacterial activity. Lingzhi mushroom triterpenoids containing compounds which possess antibacterial activity by reacting with porin mechanisms (transmembrane protein) on the outer membrane of the bacterial cell wall, forming a strong bond polymers that cause damage porin. The purpose of this study was to was to determine the effect of Lingzhi mushroom extract (Ganoderma lucidum) using ethanol in inhibiting the growth of bacteria Escherichia coli. The method used was paper disc method by observing the clear zone that is visible around the paper disc. And concentration used was 20 µg / ml, 40 µg / ml, 60 µg / ml, 80 µg / ml, 100 µg / ml. At a concentration of 20 µg /ml and 40 µg / ml produce inhibition zone of 10.5 mm and 12.4 mm by category inhibition zone less active and at a concentration of 60 µg / ml, 80 µg / ml, 100 µg / ml produce inhibition zone 13.65 mm by 14.9 mm and 16.5 mm in the active category. The results obtained show that the extract of lingzhi mushroom (Ganoderma lucidum) using ethanol effect on the growth of the bacterium Escherichia coli.Keywords: Ganoderma lucidum , Escherichia coli, Ethanol extract, Antibacterial.


Author(s):  
Leenah Alaalm ◽  
Julia L. Crunden ◽  
Mark Butcher ◽  
Ulrike Obst ◽  
Ryann Whealy ◽  
...  

The highly conserved, ubiquitous molecular chaperone Hsp90 is a key regulator of cellular proteostasis and environmental stress responses. In human pathogenic fungi, which kill more than 1.6 million patients each year worldwide, Hsp90 governs cellular morphogenesis, drug resistance, and virulence. Yet, our understanding of the regulatory mechanisms governing fungal Hsp90 function remains sparse. Post-translational modifications are powerful components of nature’s toolbox to regulate protein abundance and function. Phosphorylation in particular is critical in many cellular signaling pathways and errant phosphorylation can have dire consequences for the cell. In the case of Hsp90, phosphorylation affects its stability and governs its interactions with co-chaperones and clients. Thereby modulating the cell’s ability to cope with environmental stress. Candida albicans, one of the leading human fungal pathogens, causes ~750,000 life-threatening invasive infections worldwide with unacceptably high mortality rates. Yet, it remains unknown if and how Hsp90 phosphorylation affects C. albicans virulence traits. Here, we show that phosphorylation of Hsp90 is critical for expression of virulence traits. We combined proteomics, molecular evolution analyses and structural modeling with molecular biology to characterize the role of Hsp90 phosphorylation in this non-model pathogen. We demonstrated that phosphorylation negatively affects key virulence traits, such as the thermal stress response, morphogenesis, and drug susceptibility. Our results provide the first record of a specific Hsp90 phosphorylation site acting as modulator of fungal virulence. Post-translational modifications of Hsp90 could prove valuable in future exploitations as antifungal drug targets.


2018 ◽  
Vol 6 (2) ◽  
Author(s):  
Dafid Lauluw ◽  
Reni L. Kreckhoff ◽  
Sammy N.J. Longdong ◽  
Desy M. Mantiri ◽  
Juliaan Ch. Watung ◽  
...  

The objective of this study was to determine the minimum concentration of extract in inhibiting motile motile aeromonad septicaemia. The material used was the stems and leaves of the plant P. grandiflora as much as 10 g. The crushed simplicia was then macerated with aquades with a ratio of 1:10,  then filtered with filter paper and, put in an Erlenmeyer, and evaporated in an incubator at temperature of 30°C. The sensitivity test was performed by placing a paper disc containing extract on the agar medium that had been scratched with bacterial colonies. Clear zone formed around the paper disc was compared with standard classification table for clarifying the inhibition level.  The results showed that stem and leaf extract had inhibition zone against Aeromonas hydrophila bacteria that caused motile aeromonad septicaemia. The best result was obtain at concentration of extract 3.25 mg / L) with an average diameter of 22.67 mm and for leaf extract had a moderate to strong zone for all treatments. These proved that stem and leaf extract of P. grandiflora plant had antibacterial activity and can be used as control of MAS disease caused by A. hydrophila bacteria. Keywords:  Portulaca grandiflora plant, motile aeromonad septicemia,  minimum       inbibition concentration


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