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��ࡱ�>��	:=����789�����������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������_�	���ubjbj	s�bb�m+��������	�	LLLLL$����pppP��t�pVN�:BXXX333�M�M�M�M�M�M�M$<P��RZ�ML�33���MLLXX�N�?�?�?�rLXLX�M�?��M�?�?r
H�UIX������b^�.�����J3��H�M&N0VN�H�HS(8�HSUIUIHSLiIX3Z�@�?�4�333�M�M�;�333VN������������������������������������������������������������������������HS333333333�	 :	Formulation of Trichoderma harzianum based biofungicide against seedling disease of cabbage using different substrates

Md. Iqbal Faruk1 and Md. Lutfur Rahman2

1 Senior Scientific Officer, Plant Pathology Division, BARI, HYPERLINK "mailto:mifaruk2012@yahoo.com"mifaruk2012@yahoo.com
2 Chief Scientific Officer, Training and Communication Wing, BARI, HYPERLINK "mailto:lutfur@bari.gov.bd"lutfur@bari.gov.bd


Running Title: Formulation of Trichoderma harzianum   on seedling disease of cabbage
Table: 4



 Corresponding Author: Dr. Md. Iqbal Faruk 
Senior Scientific Officer
Plant Pathology Division
Bangladesh Agricultural Research Institute
Joydebpur, Gazipur-1701, Bangladesh
Tel.  88-02-9294605
Mobile. 88-01732587563
E-mail.  HYPERLINK "mailto:mifaruk2012@yahoo.com" mifaruk2012@yahoo.com
Abstract
Efficacy of three different substrates viz. rice bran, wheat bran, grass pea bran and their combination along with or without mustard oilcake (MOC) were tested to formulate Trichoderma harzianum based bio-fungicides for the management seedling disease (Fusarium oxysporum) of cabbage in seedbed. All combinations substrates were equally suitable for mass culturing and preparing of T. harzianum bio-fungicides and all the T. harzianum based bio-fungicides were effective in increasing seedling emergence and reducing pre-emergence and post-emergence mortality of cabbage seedling under F. oxysporum inoculated seed bed soils. The shoot length, shoot weight, root length and root weight of cabbage seedling were enhanced significantly by the application of different substrates based T. harzianum bio-fungicides under F. oxysporum inoculated soil under seed bed conditions. The individual (rice bran, wheat bran, grasspea bran) and combination of substrates (rice bran + wheat bran, rice bran + grasspea bran, rice bran + mustard oilcake, rice bran + wheat bran + MOC and wheat bran + grass pea bran + MOC) were equally suitable for formulation of effective T. harzianum based bio-fungicides for the management of foot and root rot disease of cabbage seedling in seed bed condition.
Key word: Rice bran, wheat bran; grasspea ban; mustard oilcake; Trichoderma harzianum; Fusarium oxysporum; cabbage.

Introduction
Availability of quality food and nutrition are the major challenges to achieve healthy and prosperous Bangladesh like other developing countries of the world. Bangladesh is yet to be self-sufficient in quality food and nutrition. In the country vegetables play a vital role in everyday diet to a huge population in general. Among the vegetables, cabbage (Brassica oleracea) is one of the popular herbaceous annual or biennial vegetable that has achieves tremendous popularity over the last century. The crop attacked by several diseases mostly caused by fungi and bacteria leading to severe crop losses. Among the diseases germination failure, seedling mortality, foot and root-rot disease caused by the soil borne pathogen Fusarium oxysporum, is one of the major constraints for seedling production of vegetable crops in seed bed (Najar et al., 2011). Control measures like host resistance has not yet become a viable measure. No resistant variety of cabbage has yet been developed and released against this soil borne pathogen F. oxysporum of vegetable crops in Bangladesh. Soil solarization and organic soil amendment have been used to control the disease but less effective. On the other hand, application of chemical fungicides is expensive and also hazardous to health and environment (Brown and Hendrix 1980, Punja et. al. 1982). Biological methods, on the other hand can be economical, sustainable and free from residual effects and also consider as a potentially powerful alternative method (Kulkarni et al., 2007; Anand and Reddy, 2009). The beneficial microbes are used as biological agents that effectively control soil borne plant pathogens, and about 90% of such bio-control agents are different strains of T. harzianum, T. virens, T. viride (Elad et al., 1983; Roy, 1989; Ben�tez et al., 2004). The fungus Trichoderma possesses different mechanisms to combat the targeted pathogen such as mycoparasitism, competition for space and nutrients, secretion of antibiotics and fungal cell wall degrading enzymes for the inhibition of growth and reproduction of phytopathogens (Kubicek et al., 2001; Howell, 2003; Ben�tez et al., 2004; Harman et al., 2004). In addition, Trichoderma have a stimulatory effect on plant growth (Naseby et al. 2000) as a result of modification of soil conditions. The native bio-control agents usually remain in low population density in most of the agricultural soil, so up- scaling of their density to a higher stability level in soil through artificial inoculation is necessary for successful management of soil borne pathogens in cabbage seed bed. The major limitation is the lack of appropriate mass culturing techniques and inadequate information on the suitable substrate materials of T. harzianum (Harman et al., 1991). Several research report revealed that T. harzianum has been formulated as bio-fungicides in various substrates including wheat bran, rice bran, maize bran, sawdust (Das et al., 1997); rice straw, chickpea bran, grass pea bran, rice course powder, black gram bran (Shamsuzzaman et al., 2003); cow dung, poultry manure, ground nut shell, black ash, coir waste, spent straw from mushroom bed, talc, vermiculite (Rettinassababady and Ramadoss, 2000); and jaggery, groundnut cake, neem cake, niger cake, pongamia (Shamarao et al., 1998). All of these substrate materials are available in Bangladesh but their potentialities to use in the formulation of T. harzianum bio-fungicide have not yet been studied in the country. Therefore, the present study was undertaken to find out the effective local substrates to formulate the suitable medium for mass culturing of T. harzianum to be used as effective bio-fungicides against F. oxysporum causing seedling disease of cabbage under seed bed condition.

Materials and Methods
Efficacy of three organic substrates viz. rice bran, wheat bran, grasspea bran and their combinations mixed with or without mustard oilcake (MOC) was evaluated to formulate T. harzianum based bio-fungicides for the management of foot and root rot disease of cabbage caused by F. oxysporum. The experiment was conducted in the seedbed of Plant Pathology Division, Bangladesh Agricultural Research Institute (BARl), Gazipur during three consecutive years from 2011-12 to 2013-14. The seedbed was inoculated with the fungal isolate F. oxysporum multiplied on the barley grains @ 100g/m2 soil. The pathogen was allowed to colonize the soil in seedbed for 10 days. A pure culture of T. harzianum (TM7) isolated from the native soil was grown in potato dextrose agar (PDA) medium which was used as inocula for preparation bio-fungicides. The treatments in the experiment were T1= Rice bran, T2= Wheat bran, T3= Grasspea bran, T4= Rice bran + Wheat bran (1:1), T5=Rice bran + Grasspea bran (1:1), T6= Rice bran + Mustard oilcake (1:1), T7=  Rice bran + Wheat bran + MOC (1:1:1), T8= Rice bran + Grasspea bran + MOC (1:1:1), T9= Wheat bran + Grasspea bran + MOC (1:1:1), T10= Rice bran + Wheat bran + Grass pea bran+ MOC(1:1:1:1), T11=Seed treatment with provax and T12= Control. According to the treatment combinations 600 g of individual or combination of substrate materials were taken separately in 1000 ml Erlenmeyer flask. The flask with substrate materials were sterilized in an autoclave at 1210C for 15 minutes and cooled down to make it ready for inoculation. The sterilized substrate was inoculated individually with 5 mm diameter mycelia disc of five-day old culture of T. harzianum grown on PDA and then incubated at room temperature (25�2 0C) for 15 days. After incubation the colonized substrates were removed from the flasks, air dried and finally preserved in refrigerator at 10 0C. The inoculum of T. harzianum, colonized on different substrates, were incorporated to the previously F. oxysporum inoculated seedbed soils @ 100 g/m2 soil and kept for 7 days maintaining proper soil moisture to establish T. harzianum in the soils. The control bed did not receive any colonized substrate of T. harzianum except the inoculum of F. oxysporum. The seeds of cabbage variety Atlas were sown in the seedbed @ 200 seeds per treatment. The initial germination of the seeds was 99% as per blotter test result. The percent emergence of the seedling was calculated on the basis of initial germination status of the seeds. The experiment was laid out in completely randomized design (CRD) with four replications. Proper weeding, irrigation and intercultural operations were done to raise cabbage seedlings in the seedbed. Data were collected on seedling emergence after 15 days of seed sowing. Similarly seedling mortality was recorded at an interval of 7 days starting from seedling emergence and it was continued up to 35 days of seedling age. The height and weight of shoot and length and weight of root of tomato seedlings were recorded at 35 days of seedling age. The percent data were converted into arcsine transformation values before statistical analysis. Data were analyzed statistically by using the MSTATC program. The treatment effects were compared by applying the least significant different (LSD) test at P=0.05 level.
Results and Discussion
a) Seedling emergence and pre-emergence mortality 
Every year, the seedling emergence of cabbage was significantly increased over control due to treatment of F. oxysporum inoculated seedbed soil with T harzianum bio-fungicides. Under control the emergence was 49.33, 64.00 and 66.00% in 1st, 2nd and 3rd year, respectively. The seedling emergence increased range from 58.00- 67.00, 80.33-86.67 and 79.00-91.00% due treatment of seedbed soil with the bio-fungicides in 1st, 2nd and 3rd year, respectively. Seedling emergence under various treatments with the bio-fungicides was not significantly different (Table 1). 
On the contrary, the pre-emergence seedling mortality of cabbage under control was 50.67, 36.00 and 34.00% in 1st, 2nd and 3rd year, respectively. The corresponding mortality under treatment of seedbed soils with the bio-fungicides was 33.00-42.00% in first year, 13.33-19.67% in second year and 09.00-21.00% in third year. It was reduced to 17.11-34.87, 45.36-62.97 and 38.23-73.53% in first, second and third year, respectively due to treatments of seedbed soils with various bio-fungicides tested in the present investigation (Table 1). However, efficacy of all bio-fungicides was more or less similar (Table 1). 
b) Post-emergence mortality 
Post-emergence mortality of cabbage in F. oxysporum inoculated seedbed soil was 21.33, 33.67 and 24.67% under control treatment in 1st, 2nd and 3rd year of study, respectively. Treatment of seedbed soil with different substrates based T. harzianum bio-fungicides reduced the disease incidence to 64.04-73.42, 60.41-66.35 and 60.80-72.96% in 1st, 2nd and 3rd year, respectively compared to untreated control. The reduction was significant under every bio-fungicide. Efficacy of all treatments with the bio-fungicides to reduce the disease incidence was not significantly different (Table 2). 
Shoot growth 
Shoot length and shoot weight of cabbage seedlings were increased significantly by different substrates based T. harzianum bio-fungicides over Provax and untreated control in the F. oxysporum inoculated seed bed soil (Table 3). Under control, shoot length was 13.03 cm in first year, 4.90 cm in second year and 10.87 cm in third year. Treatment of seedbed soils with T harzianum based bio-fungicides multiplied on rice bran, wheat bran, grasspea bran alone or in different combinations increased the shoot length to 17.07-18.13, 8.30-10.13 and 16.33-22.07 cm in 1st, 2nd and 3rd year, respectively. The shoot weight under control was 3.75, 3.97 and 6.57 gplant-1 in first, second and third year, respectively. T. harzianum based bio-fungicidal treatments of seedbed soils increased the parameter to 5.53- 5.81, 7.11-8.53 and 8.88-12.40 gplant-1, respectively. Every year, the increase in length and weight of shoot of cabbage seedling due to bio-fungicidal seedbed soil treatment was significant compared to control. Effect of all the treatments on shoot growth was more or less similar (Table 3). 
Root growth 
Every year, the root length of cabbage seedling was significantly lower in non-treated seedbed (control) compared to bio-fungicide and Provax treated beds. In first, second and third year, the root length of cabbage seedlings ranged 7.07-7.87, 7.17- 8.37 and 5.67-8.00 cm under different treatments and 5.46, 4.47 and 4.27 cm in control seedbeds, respectively (Table 4).
In first, second and third year, the ranges of root weight were 0.58-0.62, 0.52-0.61 and 0.65-0.91 gplant-1, respectively in seedbed treated with bio-fungicides multiplied on various substrate materials and  0.43, 0.32 and 0.60 gplant-1 in control seedbeds, respectively (Table 4). The root weight was significantly higher compared to seedbeds received no bio-fungicide or Provax. Effect of the treatments on root growth was more or less similar (Table 4). 
Effect of Provax 
Seed treatment with Provax also effective to reduce the incidence of foot and root rot disease and increased shoot and root growth of cabbage seedlings over control in seedbed soil infested with F oxysporum. However, its efficacy was lower compared to bio-fungicides (Tables 1- 4). 
Results of the present experiment revealed that biological control agent T harzianum multiplied on different substrates materials, rice bran, wheat bran, grasspea bran used alone or in different combinations mixed with or without MOC are effective against foot and root disease of cabbage caused by F oxysporum under seedbed condition. The bio-fungicides achieved satisfactory increase in seed germination, pre- and post-emergence seedling mortality and also growth of cabbage seedling. Similar findings have been reported by other researchers (Bentez et al., 2004; Mausam et al., 2007; Prasad and Anes, 2008; John et al., 2010). Enhanced seed germination due to Trichoderma species was also reported by Mukhtar (2008). The well-known antagonistic fungus Trichoderma spp. are directly parasitizing a diversity of fungi as they are capable of detecting other fungi in the soil and its destroyed other plant pathogenic fungi through expression of cell wall degrading enzymes, mostly chitinases, glucanases and proteases (Harman et al., 2004). The fungus T. harzianum prevailing in the soil and being used in many crops, like lettuce, tomato, onion, cotton, grapes, peas, apples, sweet corn and carrots to control various diseases caused by Phytophthora, Pythium, Sclerotinia, Botrytis, Rhizoctonia and Fusarium (Ben�tez et al., 2004; Mausam et al., 2007).  It was reported that T. harzianum remarkably proliferated the root system and accelerated biological nitrogen fixation in addition to the reduction of diseases caused by F. oxysporum and Pythium spp. in legume crops (John et al., 2010). This findings are in accordance with the observation of the present study where soil is treated with different substrates based T. harzianum bio-fungicides that enhanced the growth of cabbage seedling in F. oxysporum inoculated seedbed soils though the degree of shoot and root growth varied among the treatments. Harman (2006) and Manju and Mall, (2008) also reported positive role of Trichoderma species in increasing plant growth and productivity. In present experiment there is significant increase in emergence, shoot and root length and also shoot and root weights of tomato seedling due to T. harzianum bio-fungicides which is supported by the findings of many investigators (Prasad and Anes, 2008; Mishra and Sinha, 2000; Chaur-Tsuen and Chien-Yih, 2002. It has been reported that Trichoderma isolates possesses the ability to compete for key exudates from seeds that stimulate germination of propagules of plant pathogenic fungi in the soil as they compete with microorganisms for nutrient and space. The three well known mechanisms associated with pathogen control by Trichoderma were competition for nutrients, antibiosis, and myco-parasitism (Chet, 1987). It has been noticed by Tjamos et al. (1992) that T. harzianum controls F. oxysporum by competing for both rhizosphere colonization and nutrients. The study confirm the reports of other researchers regarding the role of T. harzianum to enhance seed germination and root and shoot growth of seedlings (Dubey et al., 2007) as well as increasing the frequency of healthy plants (Rojo et al., 2007). Shoresh et al. (2005) stated that Trichoderma spp. were effective bio-control agents for a number of soil borne plant pathogens and induced a potentate state in the plant enabling it to be more resistant to subsequent pathogen infection. 

Acknowledgement
The authors thankfully acknowledged BAS-USDA who provided financial support and Bangladesh Agricultural Research Institute, Gazipur for extending necessary logistic support for smooth running of this research. Special thanks to Dr. M. A. Rahman, former Chief Scientific Officer Plant Pathology Division, BARI for his fruitful counsel and directives. Thanks also go to the Scientific Assistant Mr.  Md. Abdur Razzak and Mr. Zamil Akter for their sincere assistance in this research work.
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Table-1. Effect of carrier material based T. harzianum bio-fungicides on the emergence and mortality of cabbage seedling in F. oxysporum inoculated soils in seedbed
Name of substratesEmergence (%) of cabbage seedling in seedbed soilPre-emergence mortality (%) of cabbage seedling in seedbed1st year2nd year3rd year1st year2nd year3rd yearT1=Rice bran63.00 85.3386.0037.00 (26.98)14.67 (59.25)14.00 (58.82)T2=Wheat bran62.67 82.3385.0037.33 (26.33)17.67 (50.92)15.00 (55.88)T3=Grasspea bran61.67 83.3390.0038.33 (24.35)16.67 (53.69)10.00 (70.58)T4=Rice bran + Wheat bran63.33 84.3389.0036.67 (27.63)15.67 (56.47)11.00 (67.65)T5=Rice bran + Grass pea bran 66.00 82.0091.0034.00 (32.89)18.00 (50.00)09.00 (73.53)T6=Rice bran + Mustard oilcake59.67 82.0083.0040.33 (20.41)18.00 (50.00)17.00 (50.00)T7=Rice bran + Wheat bran + MOC61.00 86.0085.0039.00 (23.03)14.00 (61.11)15.00 (55.88)T8=Rice bran + Grasspea bran + MOC67.00 80.6786.0033.00 (34.87)19.33 (46.30)14.00 (58.82)T9=Wheat bran + Grass pea bran + MOC59.33 80.3388.0040.67 (19.74)19.67 (45.36)12.00 (64.70)T10=Wheat bran + Grass pea bran+ Rice bran + MOC58.00 86.6779.0042.00 (17.11)13.33 (62.97)21.00 (38.23)T11=Seed treatment with Provax57.67 79.0083.0042.33 (16.46)21.00 (41.67)17.00 (50.00)T12=Control49.33 64.0066.0050.6736.0034.00Values with in the parenthesis are percentage of reduction in pre-emergence mortality due to treatments over control
Table-2. Reduction of cabbage seedling mortality by different carrier material based T. harzianum bio-fungicides in F. oxysporum inoculated soils in seedbed
Name of substratesPost-emergence cabbage seedling mortality (%) in seedbed soilReduction  of cabbage seedling mortality (%) over control in seedbed soil1st year2nd year3rd year1st year2nd year3rd yearT1=Rice bran7.33 b13.33 b7.67 b65.6460.4168.91T2=Wheat bran7.67 b11.67 b7.67 b64.0465.3468.91T3=Grasspea bran7.00 b11.67 b9.33 b67.1865.3462.18T4=Rice bran + Wheat bran5.67 b12.00 b6.67 b73.4264.3672.96T5=Rice bran + Grass pea bran 7.00 b12.00 b7.67 b67.1864.3668.91T6=Rice bran + Mustard oilcake7.00 b11.33 b7.33 b67.1866.3570.29T7=Rice bran + Wheat bran + MOC7.00 b11.67 b8.33 b67.1865.3466.23T8=Rice bran + Grasspea bran + MOC7.67 b11.67 b7.67 b64.0465.3468.91T9=Wheat bran + Grass pea bran + MOC7.33 b12.67 b9.67 b65.6462.3760.80T10=Wheat bran + Grass pea bran+ Rice bran + MOC6.33 b12.67 b8.33 b70.3262.3766.23T11=Seed treatment with Provax5.67 b13.00 b9.67 b73.4261.3960.80T12=Control21.33 a33.67 a24.67 a---Table-3. Effect of different carrier material based T. harzianum bio-fungicides on the shoot growth of cabbage seedling in F. oxysporum inoculated seedbed soil
Name of substratesShoot length in consecutive three years (cm)Shoot weight in consecutive three years (gplant-1)1st year2nd year3rd year1st year2nd year3rd yearT1=Rice bran17.07 b8.53 cd16.97 c5.78 ab7.18 b8.88 cdT2=Wheat bran17.70 ab8.50 cd16.33 cd5.60 ab7.40 b9.58 bcdT3=Grasspea bran17.60 ab8.30 d16.33 cd5.67 ab7.11 b9.28 bcdT4=Rice bran + Wheat bran18.17 ab8.67 cd20.00 ab5.56 ab8.57 a10.88 abcT5=Rice bran + Grass pea bran 17.80 ab8.93 bcd22.07 a5.73 ab8.47 a12.40 aT6=Rice bran + Mustard oilcake18.13 ab9.63 abc20.67 ab5.74 ab8.85 a11.08 abT7=Rice bran + Wheat bran + MOC17.83 ab9.67 abc20.73 ab5.81 a8.73 a11.90 abT8=Rice bran + Grasspea bran + MOC18.13 ab9.87 ab20.13 ab5.60 ab8.73 a10.77 abcT9=Wheat bran + Grass pea bran + MOC17.13 b10.07 ab19.73 b5.67 ab7.45 b10.38 abcT10=Wheat bran + Grass pea bran+ Rice bran + MOC19.13 a10.13 a21.10 ab5.53 b7.57 b10.50 abcT11=Seed treatment with Provax14.97 c5.83 e14.27 d4.74 c4.88 c7.70 deT12=Control13.03 d4.90 e10.87 e3.75 d3.97 d6.57 eValues in a column having same letter did not differ significantly (p=0.05) by LSD.
Table-4. Effect of different carrier material based T. harzianum bio-fungicides on the root growth of cabbage seedling in F. oxysporum inoculated seedbed soil
Name of substratesRoot length of cabbage seedling in consecutive three years (cm) Root weight of cabbage seedling in consecutive three years (mgplant-1)1st year2nd year3rd year1st year2nd year3rd yearT1=Rice bran7.13 a7.33 ab6.07 bcd610 a600 ab660 bT2=Wheat bran7.13 a7.20 ab5.67 d620 a540 ab680 bT3=Grasspea bran7.07 a7.17 b 5.93 cd590 ab560 ab650 bT4=Rice bran + Wheat bran7.37 a7.17 b7.33 a590 ab610 a830 aT5=Rice bran + Grass pea bran 7.76 a7.60 ab8.00 a610 a550 ab870 aT6=Rice bran + Mustard oilcake7.40 a8.50 ab7.07 abc570 b570 ab860 aT7=Rice bran + Wheat bran + MOC7.53 a8.73 a7.20 ab610 a580 ab830 aT8=Rice bran + Grasspea bran + MOC7.47 a8.47 ab7.53 a580 ab610 a890 aT9=Wheat bran + Grass pea bran + MOC7.87 a8.27 ab7.07 abc610 a600 ab910 aT10=Wheat bran + Grass pea bran+ Rice bran + MOC7.53  a8.40 ab7.33 a610 a520 b830 aT11=Seed treatment with Provax6.25 b5.23 c5.13 de480 c400 c650 bT12=Control5.46 b4.47 c4.27 e430 d320 d600 bValues in a column having same letter did not differ significantly (p=0.05) by LSD.
 









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