Fungicidal activity of marine actinomycetes against ... - NOPR

3 downloads 0 Views 164KB Size Report
Of 160 isolates, 10 showed a potent activity against all the fungi tested. ... best carbon and nitrogen sources, respectively and 17.5 ppt was the best salinity level.
Indian Journal of Biotechnology Vol. 4, April 2005, pp. 271-276

Fungicidal activity of marine actinomycetes against phytopathogenic fungi K Kathiresan1*, R Balagurunathan2 and M Masilamani Selvam1 1

Centre of Advanced Study in Marine Biology, Annamalai University, Parangipettai 608 502, India 2

Department of Microbiology, Sri Sankara College, Kanchipuram 631 561, India Received14 July 2003; revised 1 April 2004; accepted 15 April 2005

A total of 160 isolates of marine actinomycetes were isolated from the sediment samples drawn from mangroves, estuary, sand dune, and industrially polluted coast. Of these, mangrove sediments were rich sources of marine actinomycetes. Each isolate was tested against four phytopathogenic fungi, viz. Rhizoctonia solani, Pyricularia oryzae, Helminthosporium oryzae (causing sheath blight, blast and leaf spot diseases of rice) and Colletotrichum falcatum (causing red rot disease of sugar cane). About 51% of isolates were found effective against H. oryzae and P. oryzae, 31% against R. solani, and 12.5% against C. falcatum. Of 160 isolates, 10 showed a potent activity against all the fungi tested. These isolates appeared to produce high antifungal compounds at 120 hrs of incubation period of production medium culture. Glucose and soybean meal were the best carbon and nitrogen sources, respectively and 17.5 ppt was the best salinity level for maximum antibiotic production. Cylinder plate method was found better for antifungal assay than the disc diffusion method. Based on the morphological and culture characteristics, the potent strains were identified as the species belonged to the genus Streptomyces. These strains may prove to be the potent source for isolation of agrobased fungicides. Keywords: antifungal activity, fungicides, marine actinomycetes, plant pathogens, Streptomyces IPC Code: Int.Cl.7 C12N1/02,1/04; C12R1:01

Introduction Fungal diseases in agriculture crops pose a great challenge. The currently used fungicides are either less effective or of great environmental concern1-3. Hence, it is necessary to develop environmentally safer and potent fungicides of natural origin. Microbial metabolites have been expected to minimize the deleterious side effects caused by synthetic fungicides4. In this regard, actinomycetes deserve to be studied, as they are known to produce potent antibiotics. Compared to terrestrial species, marine actinomycetes are important sources of novel antibiotics5,6 (Newman et al, l989; Okami, 1986). The actinomycetes found in the marine and coastal ecosystems may be viewed as a rich gene pool possibly containing isolates capable of producing useful metabolites6,7. However, only few attempts have been made out to isolate marine actinomycetes especially for their antifungal activity8-15. In the present study, the isolated actinomycetes from marine samples have been tested against four fungal pathogens that cause economically important diseases in crops, like rice and sugarcane, to identify potent antagonistic strains. __________ *Author for correspondence: Tel: 91-4144-243223: Fax: 91-4144-243555 E-mail: [email protected]

Materials and Methods Collection of Samples

Sediment samples were collected in sterile vials from the industrially polluted marine environment of Cuddalore; the sand dune vegetation of Spinifex; the Vellar estuary of Porto Novo; and from the mangrove vegetation that exists along the Indian coastline in the Gulf of Kutch (Gujarat), Kalpadevi, Narayanamali (Ratnagiri, Maharashtra), Charo Island (Goa), Kundapur (Karnataka), Kumarakam (Kerala), Poomarichan Island, Manoli Island (Gulf of Mannar, Tamilnadu), Muthupet (Tamilnadu), Pichavaram (Tamilnadu), Kakinada Bay (Andhra Pradesh), Bhitarkanika (Orissa), and Sundarbans (West Bengal). Isolation of Marine Actinomycetes

The sediment samples collected were air-dried for one week and kept at 45°C for 1 hr to minimize the bacterial contaminants. About 1 g of sample was then transferred to an Erlenmeyer's flask containing 99 ml of sterile 50% seawater. The sediment suspension was further diluted to 10–5 dilution level. One ml of the diluted suspension was spread over the surface of starch-casein agar medium16 prepared in 50% seawater to enhance the isolation of marine actinomycetes. The pH of the selected media used was adjusted to 7.2. To prevent the fungal and

272

INDIAN J BIOTECHNOL, APRIL 2005

bacterial contaminants, cycloheximide (100 mg/l) and nalidixic acid (20 mg/l) were added to the medium. The Petri plates were then incubated at 28±2°C and the colonies were observed from 5th day onwards for 1 month. Strains of marine actinomycetes were picked out and purified by repeated streaking on yeast extract-malt extract agar (ISP 2) medium. The pure cultures of the actinomycetes were transferred to ISP 2 slants and preserved at 4±2°C. Phytopathogenic fungi, viz. Rhizoctonia solani, Pyricularia oryzae, Helminthosporium oryzae (causing sheath blight, blast and leaf spot diseases of rice), and Colletotrichum falcatum (causing red rot disease of sugarcane), isolated from the diseased crop plants, were used as test fungi. These pathogens were obtained from the Department of Plant Pathology, Faculty of Agriculture, Annamalai University and maintained on potato dextrose agar medium. Screening of Actinomycete Isolates for Antifungal Activity Primary Screening

A modified ‘cross-streak’ method was used for the primary screening of actinomycete isolates16. Yeast extract-glucose agar plates were inoculated at the center with a 5 mm plug of the actinomycete isolate to be tested. The plates were incubated at 28±2°C for 5 days. Five replicates were made for each of the actinomycete isolates. After 5 days of incubation, 4 mm plugs of four-day-old cultures of R. solani, P. oryzae, H. oryzae and C. falcatum were ‘crossplugged’ 15 mm away on either side to the original plug of actinomycete isolate. The control plates were also maintained with cultures of test fungi without the actinomycete isolates. The plates were then incubated at 28±2°C and the inhibition zone of fungal growth, if any, was measured at 72 hr. From this screening, strains of high antifungal activity were selected. Secondary Screening

The selected isolates were further tested in the secondary screening by shake flask studies12,17 to confirm their antifungal activity. The spore suspension of the selected isolates were inoculated into soybean medium and kept in a shaker. After 96 hrs, the culture broth was separated from the mycelium by centrifugation at 5000 rpm and tested for antifungal activity by the paper disc method. Spore suspensions of 4-day-old cultures of the test fungi growing in potato dextrose medium were prepared. The concentration of the spore suspension was adjusted to 106 spores/ml. About 0.1 ml of the

spore suspension was then inoculated on potato dextrose agar medium in Petri plates. The sterile paper disc impregnated with 0.1 ml of the culture filtrate of the each strain was placed in the centre of the agar plate and incubated at 28±2°C for 48 hrs. The diameter of the inhibition zone for each strain was recorded. Five replicates were maintained for each treatment. Optimization of Cultural Conditions for Antifungal Activity

Modified method of Sambamurthy & Ellaiah18 was used. To study the influence of incubation period, the culture was maintained in the production medium for up to 7 days. The broth drawn at 48, 96, 120 and 168 hrs was tested for antifungal activity. To study the influence of carbon and nitrogen sources on the antifungal activity, different carbon sources, viz. glycerol, glucose, lactose and maltose each at 1% of the production medium separately were used, and different nitrogen sources, namely soybean meal, yeast extract, malt extract, peptone and sodium nitrate each at 1% of the production medium were used separately. The broth drawn at 120 hrs of incubation was tested for antifungal activity. Salinity Induced Antifungal Activity

Fresh spores of Streptomyces spp. were inoculated into the medium and shaken in a rotary shaker. After two days, inoculated medium was incorporated at 10% into the production medium containing different salinities, viz. 0, 5, 17.5 and 35 ppt. The culture was kept in a shaker for 5 days. The cultured broth was taken for antifungal assay by measuring the inhibition zone. Antifungal Assay Systems

The culture broth from the production medium was extracted with ethyl acetate at pH 7.0 and concentrated in a vacuum rotary evaporator. The extract was tested against fungal strains by disc diffusion method and/or cylinder plate (well) method. In the former method, filter paper disc was dipped one time or two times in the extract and tested. In the second method, the extract was taken in a well with dimension of 3 mm diam and 3 mm depth on the potato dextrose agar medium contained in Petri dishes. The diameter of the inhibition zone was measured after 48 hrs. Identification of Marine Actinomycetes

The 10 isolates found to be potent antagonists were identified based on the following characteristics, viz.

KATHIRESAN et al: FUNGICIDES FROM MARINE ACTINOMYCETES

aerial mass colour, melanoid pigment, reverse side pigment, spore chain morphology and assimilation of carbon sources, and also by comparing the characteristics with the keys given by Nonomura19 (l974). Results and Discussion Actinomycetes from Marine Samples

As other reports have recorded the occurrence of actinomycetes in the sediment of marine and estuarine environments, in the present study also, high numbers of actinomycetes were isolated. A total of 160 isolates were obtained from different marine sediment samples (Table 1). The maximum number of isolates was obtained from the coastal mangrove sediments and the minimum from industrially polluted coastal samples, which cannot be attributed to the difference in number of samplings as it was maintained constant. Thus, the mangrove sediments can be a potential source for isolating diversified marine actinomycetes, rather than other marine samples. This might be due to the favourable niche of the mangrove habitat that provides nutrients for saprophytic actinomycetes. About 100 strains were isolated from a mangrove stand of Morib, Selangor, Malaysia in an earlier study12. Patil et al14 also isolated a total of 133 actinomycetes out of 129 marine sediment samples from Tuticorin coast in Southeast coast of India. However, the samples yielded high number of antagonistic actinomycetes in polluted sites followed by mangrove swamps. The high incidence of antagonistic actinomycetes in the polluted sites was attributed to the discharge of domestic sewage by the fishermen community living nearby. Thus, a relationship between the high incidence of actinomycetes and the polluted environments has been established20. Contrary to the above report, the polluted marine sediments provided less actinomycete isolates in the present study. This might be due to the industrial pollutants that are deleterious to the actinomycetes existing in the polluted samples. Table 1—Isolates obtained from different marine samples No.

1 2 3 4

Type of marine sample

Mangrove sediments around the coastline Estuarine sediment, Vellar estuary Soil around sand dune plant (Spinifex sp.) in Porto Novo Industrially polluted marine sediment, Cuddalore

No. of isolates 118 29 8 5

273

Antifungal Activity of Marine Actinomycetes

The antifungal activities of marine actinomycetes against four phytopathogenic fungi in the primary screening are presented in Fig. 1. The isolates termed as ‘effective’ showed inhibition zone of >10 mm, and those as ‘non effective’ exhibited inhibition zone of 20 mm against all the four fungi tested. Four strains (RH 1, MP 1, MIII 1, SEA 5) exhibited inhibition zone of >20 mm against H. oryzae and P. oryzae. Other isolates exhibited moderate activity.

Fig. 1—Percentage of antagonistic actinomycetes, of the 160 isolates tested against phytopathogenic fungi in the primary screening. Table 2—Antifungal activity of selected actinomycetes in the secondary screening No.

Isolate No.

Inhibition zone (mm) H. oryzae C. falcatum R. solani

1 RH 1 20 27.5 2 MP 1 20 11 3 MIII 1 22 11 4 MI 1 9 5 5 SEA 5 21 10 6 BC 3 11 6 7 BC 1 7 5 8 SD 3 9 3 9 AN 1C 15.5 12 10 AN 1CR 10.5 11.5 Each value is an average of 5 replicates and strains/test fungi are significant at 5%

P. oryzae

20 15 12 10 14 11 5 9 10 12 the values

25 22 20 11 21 12 7 7 13.5 13.5 between

INDIAN J BIOTECHNOL, APRIL 2005

274

Antifungal Activity Influenced by Incubation Period

The potent strains were incubated in the broth culture for its production of antibiotics at different incubation periods of 48, 96, 120 and 168 hrs. The broth was then extracted in ethyl acetate and tested against the test fungus F. solani. The results are shown in Fig. 2. For all the cultures, it was observed that inhibition zone was increased with the increase in incubation period in the production medium and a maximum inhibition was achieved for cultures incubated at 120 hrs. However, further increase in incubation period (at 168 hrs) showed a declining trend in inhibition zone. Antifungal Activity Influenced by Carbon and Nitrogen Source

Fig. 3—Influence of various nitrogen sources on antifungal activity of Streptomyces fradiae against Collectotrichum falcatum.

Of the nitrogen sources, viz. soybean meal, yeast extract, malt extract, peptone and sodium nitrate, soybean was found to be the best (Fig. 3). Of the carbon sources, viz. glycerol, glucose, lactose and maltose, glucose was found to be the best (Fig. 4). Salinity Effect on Antifungal Activity

Among the various salinity levels tested, 17.5 ppt showed the highest antifungal activity against all the test fungi, followed by 5 ppt (Table 3). However, 30 ppt showed the least antifungal activity. Antifungal Activity under Different Methods

The results of antifungal activity under different systems are shown in Fig. 5. The best antifungal

Fig. 2—Influence of incubation period on antifungal activity of marine actinomycete strains (BC 1, BC 3, SD 3, AN 1C, AN 1CR) against Fusarium solani.

Fig. 4—Influence of various carbon sources on antifungal activity of Streptomyces fradiae against Collectotrichum falcatum.

Fig. 5—Influence of various assay systems on antifungal activity of Streptomyces fradiae against five phytopathogenic fungi

Table 3—Salinity induced antifungal activity of the marine actinomycete strain (RH 1) Salinity (ppt)

Fusarium solani (IZ in mm)

R. solani (IZ in mm)

C. falcatum (IZ in mm)

H. oryzae (IZ in mm)

P. oryzae (IZ in mm)

0 9 10 10 12 12 5 14 16 15 17 17 17.5 16 16 18 17 18 35 12 14 14 13 14 Each value is an average of 5 replicates and the values between salinity and/test fungi are significant at 5%

KATHIRESAN et al: FUNGICIDES FROM MARINE ACTINOMYCETES

275

Table 4—Isolates of marine actinomycetes identified and their characteristic features Isolate code

Name of species identified as per Nonomura19 key

Colour of aerial mycelium, melonoid pigment, reverse side colour

Spore chain, spore surface, growth

Source of carbon assimilated

RHI 1

Streptomyces fradiae

Pink, nil, yellow to brown,

Retinaculum-Apertum, smooth, good

Arabinose, glucose

MP 1

Streptomyces roseolilacinus

Pink, nil, white to brown

Spirals-Spira, smooth, good

Arabinose, glucose

M III 1

Streptomyces helvaticus

White, nil, yellow

Straight-Rectus, smooth, good

Arabinose, glucose, xylose

MI1

Actinomyces auriomonopodiales

White, nil, yellow

Straight-Rectus, smooth, good

Arabinose, fructose, inositol, mannitol, raffinose,glucose, xylose

SEA 5

Streptomyces albidoflavus

White, nil, pale yellow to black

Variable flexible-Flexibilis, smooth, good

Arabinose, fructose, mannitol, glucose, xylose

BC 3

Streptomyces orientalis

White, nil, pale yellow

Open loops-Retinaculum Apertum, smooth, good

Arabinose, fructose, inositol, mannitol, rhamnose, glucose, xylose

BC 1

Srteptomyces roseiscleroticus

Black to white, nil, pale yellow to white

Spirals-Spria, smooth, good

Arabinose, fructose, mannitol, rhamnose, glucose, xylose

SD 3

Streptomyces sclerotialus

White, nil, light-yellow to white

Spirals-Spira, smooth, good

Arabinose, fructose, inositol, mannitol, rhamnose, sucrose, glucose, xylose

AN 1C

Streptomyces galtieri

White, nil, white, nil

Straight Rectus, smooth, good

Glucose

AN 1CR

Streptomyces sp.

White, nil, white

Straight Rectus, smooth, good

Glucose

assay system was cylinder plate method. This showed consistently higher activity in all the cases than the disc diffusion method with single or double dips. However, double dip was better than single dip disc diffusion method. Identification of Strains

The 10 antagonistic isolates of marine actinomycetes were identified as different species of the genus Streptomyces However, one Streptomyces sp. could not be identified and is under further investigation. The characteristic features of the isolated species are given in Table 4. Most of the species have white colour mycelium and their reverse side colour of cultures was yellow as none of them produced melanin pigments. Vanajakumar et al24 have also reported that white colour series of actinomycetes were the dominant forms, followed by the grey, yellow and red colour series. These different colour series were also recorded in soil, marine and river sediments25-27. In the present study, the isolates belong to green or blue colour series failed to show potent antagonistic properties against the test fungi. The strains also varied in the utilization of carbon source

(Table 4). Two strains (AN 1C, AN 1CR) utilized only glucose, while others utilized several sugars. Strain SD 3 utilized eight sugars except raffinose, which was utilized only by MI 1. Likewise, sucrose was utilized only by SD 3. So far, only few active compounds isolated from actinomycetes are known to be the potential biopesticides with broad spectral activity10 but they are not yet available in the market. In this context, 10 strains of Streptomyces selected in the present study have shown considerable antifungal activity against the economically important pathogens of rice and sugarcane. Therefore, these strains may be taken up for further investigation and to characterize the active compounds for agrochemical uses. Acknowledgement The authors are thankful to the authorities of Annamalai University for providing facilities, Prof. K. Ramanujam, Head of Plant Pathology, Annamalai University for supplying the fungal cultures, and the Department of Ocean Development, Govt. of India for financial assistance.

INDIAN J BIOTECHNOL, APRIL 2005

276 References 1 2

3

4

5

6 7

8

9

10

11

12

13

14

Cohen Y & Coffy M D, Systemic fungicides and the control of oomycetes, Annu Rev Phytopathol, 24 (1986) 311-338. Fruh T, Chemla P, Ehrler J & Farooq S, Natural products as pesticides: Two examples of strereoselective synthesis, Pestic Sci, 46 (1996) 37-47. Knight S C, Anthony V M, Brady A M, Greenland A J, Heaney S P et al, Rationale and perspectives on the development of fungicides, Annu Rev Phytopathol, 35 (1997) 349-372. Porter N, Physiochemical and biophysical panel symposium biologically active secondary metabolites, Pestic Sci, 16 (1985) 422-427. Newman D J, Jensen P R, Clement J J & Acebal C, Novel activities from marine derived microorganisms, in Novel microbial products for medicine and agriculture, edited by A L Demain, Somkuti J C, Hunter-Cevera J C & Rossmore J C (Elsevier Press, Amsterdam) 1989, 239-251. Okami Y, Martine microorganisms as a source of bioactive agents, Microb Ecol, 12 (1986) 6578. Goodfellow M & Haynes J A, Actinomycetes in marine sediments, in Biological, biochemical and biomedical aspects of Actinomytes, edited by L Ortiz-Ortiz, L F Bojahil & V Yakoleff (Academic Press, New York) 1984, 453-472. Ellaiah P & Reddy A P C, Isolation of actinomycetes from marine sediments off Visakhapatnam, East Coast of India, Indian J Mar Sci, 16 (1987) 134-135. Rao V P, Chaudhuri S & Nair L N, Actinomycetes from mangrove rhizosphere and their antagonistic activities, in Mangroves of Sundarbans and elsewhere (Proc Nat Symp on Conserv & Manage of Mangroves). 1991, 232-234. Balagurunathan R, Studies on antagonistic actinomycetes from Indian shallow sea sediments with references to γlactone type of antibiotic from Streptomyces griseobrunneus (P-33). Ph D Thesis, Annamalai University, India, 1992. Kala R & Chandrika V, Microbial production of antibiotics from mangrove ecosystem, CMFRI Spl Publ, 61 (1995) 117122. Vikineswary S, Nadaraj P, Wong W H & Balabaskaran S, Actinomycetes from a tropical mangrove ecosystem— Antifungal activity of selected strains, Asian Pac J Mol Biol Biotechnol, 5 (1997) 81-86. Balagurunathan R & Subramanian A, In vitro inhibition of fish pathogens by an antibiotic from Streptomyces griseobrunneus (P-33), Malays Appl Biol, 27 (1998) 149-150. Patil R, Jeyasekaran G, Shanmugam S A & Jeya Shakila R, Control of bacterial pathogens, associated with fish diseases,

15

16

17

18

19

20

21

22

23

24

25

26

27

by antagonistic marine actinimyctes isolated from marine sediments, Indian J Mar Sci, 30 (2001) 264-267. Sivakumar K, Actinomycetes of an Indian mangrove (Pichavaram) environment: An inventory. Ph D Thesis, Annamalai University, India, 2001. Nadaraj P, Isolation and characterization of an antifungal agent from an indigenous Streptomyces sp. M Sc, Thesis, University of Malaya, Kuala Lumpur, Malaysia, 1996. Balagurunathan R & Subramanian A, Studies on marine Streptomyces nigrifaciens (P-9). I. Taxonomy and standardization of antibiotic production, Cienc Mar, 19 (1993) 435-443. Sambamurthy K & Ellaiah P, Neomycin (B & C) production by a new streptomyces species S. marinensis. Part II, Hind Antibiot Bull, 17 (1974) 41-42. Nonomura H, Key for the classification and identification of 458 species of streptomycetes included in the ISP, J Ferment Technol, 52 (1974) 78-92. Walker J D & Colwell R R, Factors affecting enumeration and isolation of actinomycetes from Chesapeake Bay and South Eastern Atlantic Ocean sediments, Mar Biol, 30 (l975) l93-201. Okazaki T & Okami Y, Studies on marine organisms II. Actinomycetes in Sagami Bay and their antibiotic substances, J Antibiotics, 25 (1972) 461-466. Okazaki T & Okami Y, Studies on actinomycetes isolated from shallow sea and their antibiotic substances, in Actinomycetes: The boundary microorganisms, edited by T Arai (Toppan Co. Ltd., Tokyo) 1976, 123-162. Pisano M A, Sommer M J & Brancaccio L, Isolation of bioactive actinomycetes from marine sediments using rifampicin, Appl Microbiol Biotechnol, 31 (1989) 609-612. Vanajakumar, Selvakumar N & Natarajan R, Antagonistic properties of Actinomycetes isolated from mollusks of the Porto Novo region, South India, in Bioactive compounds from marine organisms, edited by M Thompson et al (Oxford & IBH Publishing Co. Pvt. Ltd., New Delhi) 1995, 267-274. Rangaswamy G, Oblisami G & Swaminathan R, Antagonistic actinomycetes in the soils of South India (Phoenix Press, Visveswarapuram, Bangalore) 1967, 156. Davis F L & Williams S T, Studies on the ecology of actinomycetes in soil. I The occurrence and distribution of actinomycetes in a pine forest soil, Soil Biol Biochem, 2 (1970) 227-238. Batra K, Sahani H V & Srivastava M, Distribution pattern of Streptomyces from flooded Ganga waters, Indian J Exp Biol, 10 (1972) 439-441.

Suggest Documents