Antifungal Activities (In vitro) of Some Plant Extracts and Smoke on Four Fungal Pathogens of Different Hosts (2024)

Pakistan Journal of Biological Sciences

Year: 2002 | Volume: 5 | Issue: 3 | Page No.: 307-309

Research Article

Shahidul Alam
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

Nargis Akhter
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

Most. Ferdousi Begum
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

M. Sabina Banu
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

M. Rafiqul Islam
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

Arfatun Nahar Chowdhury
BCSIR-Laboratories, Rajshahi, Bangladesh

M. S. Alam
Department of Botany, Rajshahi University, Rajshahi-6205, Bangladesh

ABSTRACT

Inhibition of spore/conidial germination of four fungi viz., Bipolaris sorokiniana,Fusarium oxysporum f. sp. vasinfectum, Rhizopus artocarpi andBotryodiplodia theobromae was tested using the extracts of different partsof Vinca rosea and Azadirachta indica and smoke of rice straw,wheat straw, tobacco leaf and "dhup" (incense) and showed good resultsin their inhibition. Vinca rosea root extract inhibited 100% spore germinationof Bipolaris sorokiniana and Rhizopus artocarpi when it was immersedfrom 5-30 minutes at 5:1.25 (w/v) concentration. A. indica (leaf, rootand seed) extracts showed good (100%) inhibition results on B. sorokiniana,and R. artocarpi. Smoke of rice straw, wheat straw, tobacco leaf and?dhup? had a great antifungal effect against these fungi. PDFAbstractXMLReferencesCitation

How to cite this article

Shahidul Alam, Nargis Akhter, Most. Ferdousi Begum, M. Sabina Banu, M. Rafiqul Islam, Arfatun Nahar Chowdhury and M. S. Alam, 2002. Antifungal Activities (In vitro) of Some Plant Extracts and Smoke on FourFungal Pathogens of Different Hosts. Pakistan Journal of Biological Sciences, 5: 307-309.

DOI: 10.3923/pjbs.2002.307.309

URL: https://scialert.net/abstract/?doi=pjbs.2002.307.309

Search

INTRODUCTION

Several higher plants and their constituents have shown success in plant disease control and are proved to be harmless and non-phytotoxic unlike chemical fungicides (Spencer et al., 1957; Shekhawat and Prasad, 1971; Appleton and Tansey, 1975; Misra and Dixit, 1976; Singh et al., 1986 and Dubey, 1991). The extracts of plants also exhibited marked effect on germination of fungal spores as well (Singh and Singh, 1981; Singh et al., 1983 and Dubey, 1991). The extracts of plant parts are recommended to control the disease (Dixit et al., 1983; Pandey et al., 1983; Chary et al., 1984 and Singh and Dwivedi, 1990). Smoke has also antifungal activities (Alam et al., 1999). In the present study, an attempt has been made to observe the effect of different plant extracts and smoke as fungicides on Bipolaris sorokiniana, Fusarium oxysporum f. sp. vasinfectum, Rhizopus artocarpi and Botryodiplodia theobromae.

MATERIALS AND METHODS

Bipolaris sorokiniana, Rhizopus artocarpi, Fusarium oxysporum f. sp. vasinfectum and Botryodiplodia theobromae were isolated from leaf blight disease of wheat, fruit rot disease of jackfruit, wilt disease of cotton and bud rot disease of coconut respectively. Fungi were cultured on PDA medium. Extraction of root, seed and leaf tissues of different plants viz., Vinca rosea and Azadirachta indica in alcohol was done following the method described by Mahadevan and Sridhar (1982). Five gram tissues were cut into pieces and immediately plunged in boiling ethyl alcohol (80%) in a beaker and allowed to boil for 5-10 minutes using 5-10 ml of alcohol for each gram of tissue. The extraction was done on top of a steam bath. Then these extracts, were cooled in a pan of cold water. The tissues were crushed thoroughly in a mortar with a pestle and then passed through two layers of cheese-cloth. Re-extracted the ground tissues for 3 minutes in hot 80 per cent alcohol and 2-3 ml of alcohol were used for every gm of tissues. The volume (10 ml) of the extract was evaporated on a steam bath to dryness and 1.25 ml of sterilized distilled water was added for five gm of tissues and the extracts were used as fungicides. Conidia/spore from 10 days old culture on PDA plates were taken and conidial/spore suspensions were made separately with different plant extracts (Leaf and root of V. rosea and leaf, root and seed of A. indica). These suspensions (1.25-ml) were taken in small sterilized petri dishes (65 mm) and were kept at 30±2°C for 5-30 minutes. After that period, a drop of treated conidial/spore suspension (from different plant extracts) was taken on separate slides for 24 hours of incubation. Then a drop of lactophenol cotton blue was placed on the conidial/spore suspension in the slides. The slides were examined under high power (×40) for recording the percentage of conidial/spore germination.

The evaluation of fungitoxicity of smoke in the laboratory was made by Parmeter’s technique (1975) with a modification. Rice straw, wheat straw, tobacco leaf and ‘dhup’ were burnt in a metal pot with a cover fitted with rubber tube, the resulting smoke was cooled to ambient temperature by passing through the rubber tube. The cooled smoke was introduced into petri plates containing PDA with fungal colony. The petri plates containing cultures were placed for varying lengths of time (5, 10 and 15 minutes) in the smoke chamber (a wooden box of 0.5 m × 0.5 m × 0.5 m, where smokes are passed through by rubber tube) and exposed to dense rice straw, wheat straw, tobacco leaf and ‘dhup’ smoke. Aqueous spore/conidial suspension of the pathogen was placed on slides previously exposed to rice straw, wheat straw, tobacco leaf and ‘dhup’ smoke and was incubated in a moist chamber for 24 hours. After that period the slides were examined under high power (×40) microscope for recording the percentage of spore/conidial germination. Statistical analysis of data given as percentage was carried out from angular transformed values and performed using Microsoft Excel software. LSD were determined, whenever, the calculated ‘F’ values were significant at 5% level (Snedecor and Cochran, 1980).

RESULTS AND DISCUSSION

Vinca rosea root extracts inhibited 100% spore/conidial germination of Bipolaris sorokiniana and Rhizopus artocarpi, when immersed from 5-30 minutes at 5:1.25 (w/v) concentration (Table 1). It has moderate to good effect on the inhibition of Botryodiplodia theobromae and Fusarium oxysporum f. sp. vasinfectum (81 and 74%) at 5:1.25 (w/v) concentration and immersion after 30 minutes. Vinca rosea leaf extracts, showed moderate types of inhibition effect on B. sorokiniana, F. oxysporum f. sp. vasinfectum, R. artocarpi and B. theobromae (57, 62, 40 and 59%) with immersion after 30 minutes. Leaf, root and seed extracts of A. indica, showed good results against the inhibition of these fungi. Hundred percent spore germination inhibited on root, leaf and seed extracts of A. indica against R. artocarpi. The extracts of leaf and root of A. indica inhibited 100% spore germination of Bipolaris sorokiniana after 5-30 minutes of immersion. Moderate to good effect showed on the inhibition of spore/conidial germination (67, 56 and 75%) of F. oxysporum f. sp. vasinfectum, immersion after 30 minutes in leaf, root and seed extracts of A. indica. Correlation (r1) value (0.958-0.997) indicates that there was a highly significant relationship between immersion period (5-30 minutes) in plant extracts and inhibition of spore/conidial germination, except R. artocarpi in root, leaf and seed extracts of A. indica and B. sorokiniana in leaf and root extracts of A. indica and root extracts of V. rosea.

Table 1: Effect of different plant extracts as fungicides on the inhibition of spore/conidial germination of four fungi (after immersing 5 - 30 minutes).
Antifungal Activities (In vitro) of Some Plant Extracts and Smoke on Four Fungal Pathogens of Different Hosts (8)
* Mean of three replications. ( ) Parenthesis show the percentage of spore/conidial germination.
r1 =Correlation value between immersion period and germination inhibition of spore/conidia.
Table 2: Effect of smoke on the inhibition of spore/conidial germination of different fungi grown on PDA.
Antifungal Activities (In vitro) of Some Plant Extracts and Smoke on Four Fungal Pathogens of Different Hosts (9)
* Mean of three replications. ( ) Parenthesis show the percentage of spore/conidial germination.
r2 = Correlation value between smoke exposed period and germination inhibition of spore/conidia.

Calculated F value of spore/conidial germination of selected pathogens in different types of plant extracts and immersion period is grater than table value. It indicates a significant role of plant extracts and immersion period on spore/ conidial germination (Table 1). Alam et al. (1999) reported the antifungal effects of leaf and root extracts of Vinca rosea and leaf, root and seed extracts of Azadirachta indica against chilli fruit rot pathogen Alternaria tenuis. Singh et al. (1993) reported the antifungal activities of leaf extracts against Botryodiplodia theobromae, Fusarium oxysporum, Helminthosporium spiciferum, Curvularia lunata, Aspergillus flavus and Trichothecium roseum. They used some medicinal plants such as, Calotropis procera, Vitex negundo, Lantana camara, Azadirachta indica, Ficus religiosa, Ocimum sanctum, Thuja orientalis, Argemone mexicana, Achyranthes aspera, Datura fastuosa and Ricinus communis and observed good control against these pathogens. Of the 11 leaf extracts, those of A. indica and O. sanctum were the most effective in controlling the fungi. The present study indicates the presence of some antifungal compounds in A. indica and V. rosea.

Smoke of rice straw, wheat straw, tobacco leaf and ‘dhup’ were effective for the inhibition of fungi. Hundred per cent spore germination inhibition of R. artocarpi occurred, when this fungus was smoked using wheat straw, rice straw, tobacco leaf and ‘dhup’ smoke for 5-15 minutes in a smoked chamber. Effect of smoke is more or less equal on F. oxysporum f. sp. vasinfectum, but 100% inhibition occurred within 10 – 15 minutes of smoke using rice straw, wheat straw, tobacco leaf and ‘dhup’ smoke. Not only that, Table 2 also indicates the effectiveness of smoke against all the tested fungi. Correlation (r2) value (0.866-0.999) indicates that there was a highly significant relationship between smoke exposed period (5-15 minutes) and inhibition of spore germination, except R. artocarpi. Calculated F value of germination inhibition of tested fungi was greater than table value in all the cases. This result indicates a significant role of smoke from different sources and their exposure period on the inhibition of selected fungi (Table 2). Alam et al. (1999) reported similar results against chilli fruit rot pathogen Alternaria tenuis. They observed that the growth of A. tenuis was totally inhibited when inoculated on the medium exposed to rice straw and ‘dhup’ smoke for 5 to 15 minutes. Tobacco leaf smoke was ineffective against A. tenuis as fungitoxicide.

Application of chemical fungicides is a conventional method to control the diseases caused by fungal pathogens. Tremendous health hazards are reported to occur during the application of fungicides in field conditions (Alam et al., 1999). Present experiment was carried out for the protection of environment and save the health hazards of animal kingdom. This study suggested that all the tested plant extracts and smoke of rice straw, wheat straw, tobacco leaf and ‘dhup’ has antifungal effect and their application in field condition will reduce severity of diseases.

REFERENCES

  1. Alam, S., M.S. Alam and F. Mahal, 1999. Growth inhibition (in vitro) of chilli fruit rot pathogen Alternaria tenuis. J. Asiat. Soc. Bangladesh Sci., 25: 211-216.

  2. Appleton, J.A. and M.R. Tansey, 1975. Inhibition of growth of 200 pathogenic fungi by garlic extract. Mycologia, 67: 882-885.

  3. Chary, M.P., E.J.S. Reddy and S.M. Reddy, 1984. Screening of indigenous plants for their antifungal principle. Pesticides, 17: 17-18.

  4. Dixit, S.N., N.K. Dubey and N.N. Tripathi, 1983. Fungitoxic Essential Oils Vis-A-Vis Disease Control. In: Recent Advances in Plant Pathology, Husain, A., B.R. Singh, K. Singh and V.P. Agnihotri (Eds.). Print House, Lucknow, pp: 521.

  5. Dubey, R.C., 1991. Fungicidal effect of essential oils of three higher plants on sclerotia of Macrophomina phaseolina. Indian Phytopathol., 44: 241-243.

  6. Mahadevan, A. and R. Sridhar, 1982. Methods in Physiological Plant Pathology. 2nd Edn., Sivakami Publications, Madraj, pp: 316.

  7. Misra, S.B. and S.N. Dixit, 1976. Fungicidal spectrum of leaf extracts of Allium sativum. Indian Phytopathol., 29: 448-448.

  8. Pandey, R.S., S.N. Bhargava, D.N. Shukla and D.K. Dwivedi, 1983. Control of pestalotia fruit rot of guava by leaf extracts of two medicinal plants. Revists Mexicana De Fitopatologia, 2: 15-16.

  9. Parmeter, J.R. and B. Uhrenholdt, 1975. Some effects of pine needle and grass smoke on fungi. Phytopathology, 65: 23-31.

  10. Shekhawat, P.S. and R. Prasada, 1971. Antifungal properties of some plant extracts: Inhibition of spore germination. Indian Phytopathol., 24: 800-802.

  11. Singh, H.B. and U.P. Singh, 1981. Effect of volatility of some plants extract on Erysiphe. Indian J. Plant Pathol., 10: 66-67.

  12. Singh, H.N.P., M.M. Prasad and K.K. Shinha, 1993. Efficacy of leaf extracts of some medicinal plants against disease development in banana. Lett. Microbiol., 17: 269-271.
    Direct Link

  13. Singh, R.K. and R.S. Dwivedi, 1990. Fungicidal properties of neem and blue gum against Sclerotium rolfsii Sacc., a foot rot pathogen of barley. Acta Bot. Indica, 18: 260-262.

  14. Singh, R.N., I.R. Sindhu and K. Gupta, 1986. Effect of leaf exudate and extract of Spinach on some phylloplane fungi. Acta Bot. Indica, 14: 104-110.
    Direct Link

  15. Singh, Y., R.D. Tripathi, N.N. Tripathi and S.N. Dixit, 1983. The isolation and properties of fungitoxic principle from Zingiber officinale. Indian J. Plant Pathol., 1: 89-96.

  16. Spencer, D.M., J.N. Topps and R.L. Wain, 1957. Fungistatic properties of tissue: An antifungal substance from the tissue of Vicia faba. Nature, 179: 651-662.

  17. Snedecor, G.W. and W.G. Cochran, 1980. Statistical Methods. 7th Edn., Iowa State University Press, Ames, Iowa, USA., ISBN-13: 9780813815602, Pages: 507.
    Direct Link

Search

Related Articles

Leave a Comment

Your email address will not be published. Required fields are marked *

Antifungal Activities (In vitro) of Some Plant Extracts  and Smoke on  Four 
Fungal  Pathogens of Different Hosts (2024)

FAQs

What is antifungal activity of plant extracts? ›

Sage, due to the highest phenolic content among the tested plant extracts, was also the most effective against pathogenic fungi, inhibiting their growth even by 83.53% (F. culmorum—20% concentration). High antifungal activity was also observed for tansy extracts, especially for the concentration of 20%.

What is antifungal activity? ›

The antifungal activities of monocytes and resident macrophages have been extensively studied. Macrophages from different species and different anatomic sites vary in their capacity to inhibit and kill fungi. For example, activated murine peritoneal macrophages have potent antifungal effects on C. neoformans.

What is the positive control for antifungal activity? ›

Standard antifungal drug Nystatin was used as positive control and sterile distilled water as negative control and incubated at 35°C for 48 hours. The zone of inhibition was measured in millimeter.

What is the strongest antifungal in the world? ›

Amphotericin B is one of medicine's mightiest drugs: a potent, broad-spectrum antifungal antibiotic that kills even some of the most dangerous fungi outright. Despite more than half a century of use, pathogens have formed little resistance to it—a virtual unicorn in the antimicrobial world.

How do you test antifungal activity of bacteria? ›

In order to determine antimicrobial or antifungal activity of a compound being studied, there are existing in vitro methods that can be carried out. Among these, diffusion methods, thin-layer chromatography (TLC)-bioautography and dilution methods are the most commonly used.

What are the 4 types of antifungals? ›

The four main classes of antifungal drugs are the polyenes, azoles, allylamines and echinocandins.

How do you get rid of antifungal infections? ›

Typically, a course of antifungal creams (either prescription or over-the-counter) will clear up the rash and relieve the itchiness. Your healthcare provider can also discuss preventive steps to keep the rash from coming back.

How do you get rid of antifungal resistance? ›

In addition to standardized susceptibility testing and appropriate drug dosing, one of the ways to avoid resistance is the use of combinational antifungal therapy. Combination therapy also offers advantages in increased synergistic action with enhanced spectrum activity.

Can plant fungus affect humans? ›

Those fungal species that are able to grow at 35–37 °C can become a human pathogen or commensal flora [2]. The pathogen enters the human body through damaged skin and the respiratory tract and can causes infection mostly in immunocompromised individuals.

What is the natural enemy of fungus? ›

Fungi, like other organisms, have natural predators, including fungivorous nematodes and arthropods that use them as an important food source. Thus, they require mechanisms to detect and respond to injury.

How can you tell if a plant is fungal or bacterial infection? ›

Leaf wilting is a typical symptom of verticilium wilt, caused by the fungal plant pathogens Verticillium albo-atrum and V. dahliae. Common bacterial blight symptoms include brown, necrotic lesions surrounded by a bright yellow halo at the leaf margin or interior of the leaf on bean plants.

What controls fungal infections? ›

Ways to reduce your risk of various fungal infections include practicing good personal hygiene and protecting yourself from fungi that are found in the environment. Tips for avoiding fungal infections include: Shower after getting dirty or sweaty. Don't let areas of your skin stay damp.

What type of pathogens do antifungals target? ›

Antifungal drugs treat fungal infections by killing or stopping the growth of dangerous fungi in the body. Fungi can develop resistance to antifungal drugs the same way bacteria can develop resistance to antibiotics.

What is a positive fungal test? ›

If your Fungal Culture and Sensitivity test is positive, it means that fungal organisms have been detected in the sample. Your clinican will use this information to guide your treatment and prescribe appropriate antifungal medications.

What phytochemicals have antifungal activity? ›

Phytochemicals show antifungal activity, and they act in a synergistic manner. Polyphenols are effective against important crop pathogenic fungi. Most relevant antifungal thiols are allicin and its derivatives.

What phytochemicals are responsible for antifungal activity? ›

Phytochemicals with antifungal compounds derived from plants. Those with the most promising antifungal activity isolated from natural sources include flavonoids, tannins, coumarins, quinones, lignans, and neolignans [105] (Table 1).

What is an example of a disinfectant with antifungal activity? ›

Chlorine, phenol, sodium dodecyl sulfate and quaternary ammonium salts were the chemical disinfectants, and bifonazole and terbina ne were the antifungal pharmaceutical products tested against clinical isolates of Aspergillus and Candida species. Fungal inocula were obtained from conidial preparations of two A.

What are antifungals in plants? ›

Plants are rich source of bioactive secondary metabolites of wide variety such as tannins, terpenoids, saponins, alkaloids, flavonoids, and other compounds, reported to have in vitro antifungal properties.

Top Articles
Latest Posts
Article information

Author: Greg O'Connell

Last Updated:

Views: 6154

Rating: 4.1 / 5 (42 voted)

Reviews: 81% of readers found this page helpful

Author information

Name: Greg O'Connell

Birthday: 1992-01-10

Address: Suite 517 2436 Jefferey Pass, Shanitaside, UT 27519

Phone: +2614651609714

Job: Education Developer

Hobby: Cooking, Gambling, Pottery, Shooting, Baseball, Singing, Snowboarding

Introduction: My name is Greg O'Connell, I am a delightful, colorful, talented, kind, lively, modern, tender person who loves writing and wants to share my knowledge and understanding with you.