Exploring the Biocontrol Efficacy of Trichoderma spp. against Rigidoporus microporus, the Causal Agent of White Root Rot Disease in Rubber Trees (Hevea brasiliensis)

Rigidoporus microporus, which causes white root rot disease (WRD) in Hevea brasiliensis, is a looming threat to rubber plantation in Malaysia. The current study was conducted to determine and evaluate the efficiency of fungal antagonists (Ascomycota) against R. microporus in rubber trees under laboratory and nursery conditions. A total of 35 fungal isolates established from the rubber tree rhizosphere soil were assessed for their antagonism against R. microporus by the dual culture technique. Trichoderma isolates can inhibit the radial growth of R. microporus by 75% or more in the dual culture test. Strains of T. asperellum, T. koningiopsis, T. spirale, and T. reesei were selected to assess the metabolites involved in their antifungal activity. Results indicated that T. asperellum exhibited an inhibitory effect against R. microporus in both volatile and non-volatile metabolite tests. All Trichoderma isolates were then tested for their ability in producing hydrolytic enzymes such as chitinase, cellulase and glucanase, indole acetic acid (IAA), siderophores production, and phosphate solubilization. From the positive results of the biochemical assays, T. asperellum and T. spirale were selected as the biocontrol candidates to be further tested in vivo against R. microporus. The nursery assessments revealed that rubber tree clone RRIM600 pretreated with only T. asperellum or with the combination of T. asperellum and T. spirale was able to reduce the disease severity index (DSI) and exert higher suppression of R. microporus compared to other pretreated samples, with the average DSI below 30%. Collectively, the present study demonstrates that T. asperellum represents a potential biocontrol agent that should be further explored to control R. microporus infection on rubber trees.


Introduction
In Malaysia, rubber (Hevea brasiliensis) leaves, stems, and roots are afflicted by a great number of diseases associated with fungal pathogens. Among these fungal infections, Rigidoporus microporus, which causes white root rot disease (WRD), is reported to be the most serious, as it often fatal to the tree and brings a severe reduction of latex production and economic loss [1][2][3]. WRD has caused a major loss of yield of up to 50% in old plantations with a great impact on the investors of rubber tree farming [4].
The white root rot pathogen, R. microporus, causes severe damage to the woody tissues of H. brasiliensis, which results in substantial death of the trees and sometimes in the loss of a whole stand [5]. This soil-borne pathogen can survive for years in the field by creating white mycelia that can stick to the surface of the root. The ability of mycelia to develop several meters long and spread through the soil infecting the neighboring healthy trees has been the main concern to rubber growers over the past decades [6,7].
R. microporus attacks plants at different stages. It appears in young rubber plantations as early as two years old plants and also in five-or six-years old plants, not limited to old rubber plantation trees which are also suffering from this disease [8]. Once the rubber tree is infected by the pathogen, the mycelium or white rhizomorphs of R. microporus can be seen attaching to the roots when exposed. As the disease infection progresses, the leaves show general discoloration, proceeded by premature flowering and fruiting of the trees. In the advanced stage, a large, firm, semi-fleshy, often tier-up, and brownish-orange bracket forms on the collar of infected rubber trees. The formations of the sporocarp normally appear only after the trees have been dead for a while [1].
For the past 20 years, higher success in controlling the WRD disease is achieved through the use of fungicides with different active ingredients such as triadimenol, triadimefon, propiconazole, terbuconazole, hexaconazole, and myclobutanil [9,10]. Utilizing chemical control is not only uneconomical, but it often does not display the much-needed efficacy against soil pathogens. The continuous usage of chemical control approaches fosters the development of resistant pathogens [11] while also destructively affecting the quality of food resources and the environment. Furthermore, agrochemical applications, particularly urea, fungicides, and herbicides, under extensive usage are likely to boost populations of root rot pathogens in field soils [12][13][14]. The search for a suitable strain of biological control agents (BCAs) with greater biocontrol activities is necessary for alternative strategies against R. microporus, as the cultural and chemical practices used by the farmers are less practical.
BCAs, as a sustainable alternative to chemical control for plant diseases, are a popular research topic in this modern agricultural practice [3,15,16]. BCAs that are most extensively used belong to the genus Trichoderma for fungi and Pseudomonas and Bacillus for bacteria [17,18]. Numerous species of non-pathogenic rhizosphere fungi have been reported to be capable to control WRD in rubber trees caused by R. microporus in Thailand, Sri Lanka, Indonesia, and Nigeria [4,5,[19][20][21]. Trichoderma spp. (division: ascomycota), a non-pathogenic rhizosphere fungus, has been receiving great attention in biological control research in the tropics [22][23][24]. T. harzianum, T. hamatum, T. virens, T. atroviridis, and T. viride are among the Trichoderma species which have been reported to control plant fungal diseases in Thailand and Indonesia [25,26].
In vitro screenings of antagonists have been widely used to select potential BCAs and elucidate their biocontrol mechanisms. There are numerous modes of action have been reported to be applied by Trichoderma spp. against plant pathogens. Generally, mechanisms comprised the biocontrol activities of fungal antagonists are presented in two ways: (i) the direct interaction (produce toxic compounds or antibiotics, synthesis of hydrolytic enzymes, and competition) and (ii) indirect interaction (induce resistance in the host plant) [27,28]. It was suggested by Suryanto et al. [21] that the application of BCAs prior to the pathogen infection will give a better result whereby the BCAs provide protective rather than curative treatment.
In this study, selected Trichoderma isolates were tested for their efficacy as potential BCAs against R. microporus. Antagonistic efficiency was evaluated as in vitro production of volatile and non-volatile substances, hydrolytic enzymes (chitinase, cellulase, and glucanase), and plant growth-promoting traits, e.g., indole acetic acid (IAA), siderophores and phosphate solubilization. Nursery assessments were also conducted to provide insight into the natural interactions of host-pathogen-environment to ensure its effective use as a BCA in rubber plantations.

Pathogen and Potential Antagonists
The pure isolate of R. microporus RL21 (accession number MN103602) was obtained from the Laboratory of Crop Improvement and Protection Unit, Rubber Research Institute of Malaysia (RRIM), and the virulence of this isolate against the rubber tree clone RRIM600 was published by Go et al. [29].
Searching for potential antagonistic fungi was performed through the collection of soil samples from the rhizosphere of healthy and WRD-infected rubber trees located in the Hevea Germplasm, Field 23, the Rubber Research Institute of Malaysia (RRIM), Sungai Buloh. Soil samples were collected from holes dug around healthy and WRD-infected rubber trees. The isolation of the soil-borne fungi was performed via the soil dilution plating method performed on the potato dextrose agar (PDA) (DifcoTM, Detroit, MI, USA), as described by Go et al. [30]. A serial dilution of the soil was performed for up to 10 −4 using 1 g of soil added into 9 mL of distilled water. A total of 200 µL of the solution from the serial dilutions of 10 −3 and 10 −4 was spread onto PDA plates. Each dilution consisted of three replicates. The Petri dishes were placed in the incubator at 28 ± 2 • C for one week. Single spore isolation was performed on new plates of PDA to obtain a pure culture of the fungi.
For the DNA extraction, a fungal mass of approximately 100 mg was used. After the one-week incubation period, a fine sterilized spatula was used to scrape the actively growing fungal mass from the culture plate. The genomic DNA was extracted according to the method described by Lin et al. [31], with minor modifications. The primers ITS1 (5 -TCCGTAGGTGAACCTGCGG-3 ) and ITS4 (5 -TCCTCCGCTTATTGAT ATGC-3 ) were used for amplifying the ITS region [32]. The reaction system contained 12.5 µL of Taq Polymerase (1st BASE Biochemicals), 1.0 µL of template DNA, 1.0 µL of each forward and reverse primer, and 9.5 µL distilled water to a final volume of 25 µL. The amplification was carried out using Vapoprotect ® (Eppendorf, Hamburg, Germany) with the following protocol of cycling parameters: 98 • C for 2 min, followed by 25 cycles of 98 • C for 15 s, tempering at 60 • C for 30 s, extension at 72 • C for 30 s, and the final extension at 72 • C for 10 min. A total of 1% (w/v) agarose gel with FloroSafe DNA gel dye (1st BASE) was used to electrophorese the PCR products. At 70 V, electrophoresis was performed for 45 min and DNA fragments were visualized under a UV Transilluminator. The PCR products were then purified for direct DNA sequencing using the BigDye ® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Waltham, MA, USA). The sequences of the fungal isolates were identified using Basic Local Alignment Search Tool (BLAST) searches (http://www.ncbi.nlm.nih.gov/BLAST, accessed 29 October 2021). All the sequence data of the isolated soil-borne fungi were deposited in the GenBank nucleotide sequence databases.

In Vitro Dual Culture Bioassays
The antagonistic potential of 35 soil-borne fungal isolates against R. microporus, isolate RL21) was verified in a dual culture assay with 90 mm Petri plates containing the PDA medium, referring to the method published by Fokkema [33]. Pure cultures of actively growing pathogens and potential antagonists that were ten days old, were each cut on the edge side to obtain a 7 mm diameter mycelial disc for plate seeding. R. microporus and antagonist plugs were positioned together on opposite sides in the same plate 1 cm away from the side of the Petri dish. To compensate for the faster growth, antagonist isolates were placed in the plate a day after the pathogen has been placed. For control samples, only a pathogen plug was placed on the plate. Inoculated plates were then sealed with Parafilm and incubated in the dark at 28 ± 2 • C. All dual cultures and control were replicated four times. On day 5 after the antagonists were inoculated, the pathogen radial growth in each plate was recorded using a caliper. The percentage inhibition of radial growth (PIRG) was calculated using Equation (1) adapted from Korsten et al. [34]: where r1 = the colony radius of the pathogen in control and r2 = the colony radius of the pathogen in treatment.

Antifungal Activities Non-Volatile Compounds
Non-volatile substances produced by Trichoderma isolates were analyzed using the method published by Dennis and Webster [35] with slight modifications. The culture plates of Trichoderma isolates were incubated for seven days at 28 ± 2 • C for growth and metabolite production. A 7 mm diameter disc of the bioagents was then cut from an actively growing region of the culture and seeded in 100 mL of potato dextrose broth (PDB) (Oxoid Limited, Loughborough, Leics, UK). The PDB cultures were placed in a rotary shaker (Lab Line, USA) with agitation rates at 150 rpm at 28 ± 2 • C for seven days. After this time, the culture broth was strained through a sterilized Whatman filter paper No. 1 (Merck, Darmstadt, HE, Germany) and passed through a sterile membrane filter with a pore size of 0.45 µm. The filtrates were combined into a primarily prepared PDA medium which was sterilized by autoclaving and later maintained at 50 • C to avoid solidification. Three different concentrations of culture filtrate at 25%, 50%, and 75% were prepared by utilizing the PDA medium as a solvent and were then poured and solidified in Petri plates. A one-week actively grown R. microporus with a mycelial disc of approximately 7 mm in diameter was then transferred to the solidified agar plates containing culture filtrates of different concentrations. The inoculated agar plates were later incubated at 28 ± 2 • C. Agar plates without culture filtrates served as the control. Four replications were conducted for each treatment. The radial growth of R. microporus was recorded daily for the duration of one week and the PIRG value was calculated using Equation (1).

Volatile Compound
The effect of volatiles released from Trichoderma isolates in suppressing the fungal growth of plant pathogens was determined using an overlapping plate assay adapted from Boubekeur et al. [36] and Dennis and Webster [35]. A mycelial plug (7 mm in diameter) of R. microporus isolate RL21 was removed from the mother culture plate and inserted centrally onto the PDA Petri plate and incubated for three days. After three days, culture plates inoculated with R. microporus were inverted on top of the culture plates containing seven-day-old actively growing Trichoderma isolates. Under aseptic conditions, the Petri plates were sealed with parafilm tape and incubated in the dark at 28 ± 2 • C. For the control, the culture plate inoculated with R. microporus was inverted on top of the plate containing just PDA. Four replications were conducted for each treatment and the radial growth of R. microporus was documented daily. The inhibition rate was calculated using Equation (1).

Identification of Antifungal Metabolites
Trichoderma isolates were characterized for their secondary metabolite productions through Gas Chromatography-Mass Spectrometry (GC-MS), as described by Siddiquee et al. [37] with slight modification. For metabolite production, the flasks containing 100 mL of PDB were seeded with Trichoderma plugs (7 mm in diameter) and incubated at 28 ± 2 • C on a rotary shaker at 150 rpm for 21 days. The culture filtrates of Trichoderma isolates were collected by straining them through Whatman filter paper No. 1 (Merck, Germany) and then they passed through a sterile membrane filter with a pore size of 0.45 µm. Ethyl acetate (100 mL) with equal volume was added to the culture filtrate in a 250 mL Erlenmeyer flask, and the mixture was allowed to stand overnight to make sure the cells were dead.
The next day, the ethyl acetate phase was separated from the broth (water phase) using a separatory funnel to remove residual salts and other polar components. The separatory funnel was rinsed twice with ethyl acetate. Approximately 1-2 g of sodium sulfate salt was added to the collected ethyl acetate phase to remove excess water. It was then separated from the ethyl acetate phase using Whatman filter paper No. 1 (Merck, Germany). The ethyl acetate phase was further evaporated using a rotary evaporator at 40 • C in a 250 mL round bottom flask. The crude extract was then diluted with 100 mL of 90% methanol and 100 mL of n-hexane. n-hexane was added to remove fatty acids and other non-polar components. The two different layers that formed were then separated using a separatory funnel. The methanol phase formed at the bottom was collected and further evaporated in a 250 mL round bottom flask at 40 • C using a rotary evaporator. Extracted compounds formed in the round bottom flasks were then diluted with 10 mL of high-performance liquid chromatography (HPLC) grade methanol. The extracted compounds were stored in a −20 • C freezer until further use.
Hydrocarbons and other volatile compounds were separated using the TSQ Quantum Instrument Method (Thermo Scientific, Waltham, MA, USA). GC-MS analysis was performed at an ionization energy of 70 eV. A TG-5MS column (Thermo Scientific, USA) (30 m × 0.25 mm ID, 0.25 µm film thickness) was used to separate volatile compounds produced by Trichoderma isolates at a temperature of 260 • C. The oven conditions were 1 min for equilibration time and 40 • C for 2 min, and the program was further ramped to 200 • C at a rate of 10 • C/min and 25 • C/min to 260 • C for 25 min, with a total run time of 45.40 min. Identified volatile compounds produced by Trichoderma isolates were compared with the mass spectra from a reference library (NIST-17 Mass Spectra Library, National Institute of Standards and Technology).

Production of Extracellular Hydrolytic Enzymes Chitinase
For the quantitative assessment of chitinase activity, the crude extracts of Trichoderma isolates were prepared by culturing the antagonists in 100 mL of Trichoderma Liquid Enzyme (TLE), which comprised KH 2 PO 4 (0.2 g/L), (NH 4 ) 2 SO 4 (0.14 g/L), bactopeptone (0.1 g/L), urea (0.03 g/L), MgSO 4 ·7H 2 O (0.03 g/L), CaCl 2 ·6H 2 O (0.03 g/L), and 1 mL of a 0.01% trace elements solution (Fe 2+ , Mn 2+ , Zn 2+ , and Co 2+ ). A total of 1 g of colloidal chitin was added to the TLE as a source of carbon. The fungal cultures were incubated for 72 h at 28 ± 2 • C with an agitation rate of 150 rpm. All microbial cultivation was performed in triplicate for each of the isolates. At the end of the incubation, the culture supernatants and mycelia were separated by filtration through Whatman filter paper No. 1 (Merck, Germany). The chitinase activities of Trichoderma isolates were determined using 1% (w/v) colloidal chitin dissolved in a 0.05 M sodium acetate buffer (pH 5.2)). The reaction mixtures which contained 50 µL of enzyme solution (culture supernatants) and 100 µL of colloidal chitin dissolved in the buffer were used to run the enzyme detection. The mixtures were then incubated for 15 min at 37 ± 2 • C. At the end of the incubation, 0.5 mL of 3,5-dinitrosalicylic acid (DNS reagent) was added and heated at 95 • C for 10 min to stop the enzyme-substrate reaction. N-acetylglucosamine was used for the preparation of the standard curves. The series of N-acetylglucosamine solutions were added with 1.0 mL of the DNS reagent and placed in a boiling water bath for 5 min. The absorbance values of the solutions were read at a 540 nm wavelength using Varian Cary 50 UV-Vis spectrophotometer (Varian, Mulgrave, Victoria, Australia). The concentration of reducing sugar for each sample was calculated using the standard curves regression equation and the results are expressed in mg/mL. The qualitative analysis of chitinase production by Trichoderma isolates was conducted based on the protocol published by Murthy and Bleakley [38], with slight modifications. Purified chitin powder (R & M chemicals, Essex, MA, UK) was used to prepare colloidal chitin and incorporated into the chitinase agar medium as a sole carbon source. About 5 g of chitin powder was slowly added into 60 mL of concentrated HCl (Fisher Scientific, Loughborough, Leics, UK) and stirred vigorously at room temperature for 1 h. The solution was then filtered using glass wool in a glass funnel. A total of 200 mL of 50% ethanol was added to the filtrate with vigorous stirring to precipitate the filtrate. The precipitate was then collected by passing through Whatman filter paper No. 1 (Merck, Germany). Colloidal chitin was collected from the filter paper and stored at 4 • C in the dark until further used. The chitinase detection medium, which consisted of a mixture of colloidal chitin (4.5 g/L), MgSO 4 ·7H2O (0.3 g/L), (NH 4 ) 2 SO 4 (3.0 g/L), KH 2 PO 4 (2.0 g/L), citric acid monohydrate (1.0 g/L), Bacto agar (15 g/L), bromocresol purple (0.15 g/L), and Tween-80 (200 µL/L) was adjusted to pH 4.7 and then autoclaved at 121 • C for 15 min. Seven-day-old culture plugs (7 mm) were seeded in the center of the respective medium and incubated at 28 ± 2 • C, with four replications per isolate. The Color intensity and diameter of the purple-colored zone (chitinolytic activity) around the colony of Trichoderma isolates were observed. The enzyme activity was ranked using a scale from 0, the isolate showing no activity to 4, the isolate showing the highest activity.

Cellulase
For the quantitative assessment of cellulase activity, the crude extracts of Trichoderma isolates were prepared by culturing the antagonists in a liquid basal medium containing 10 g of glucose, 5 g of yeast extract, 0.6 g of KH 2 PO 4 , 0.5 g of MgSO 4 ·7H 2 O, 0.4 g of K 2 HPO 4 , 0.25 g of CuSO 4 , 0.05 g of FeSO 4 ·7H 2 O, 0.05 g MnSO 4 , and 0.001 g of ZnSO 4 prepared in 1 L of distilled water, as described by Tellez-Tellez et al. [39]. The fungal cultures were incubated for 72 h at 28 ± 2 • C with an agitation rate of 150 rpm. All microbial cultivation was performed in triplicate for each of the isolates. At the end of the incubation, the culture supernatants and mycelia were separated by filtration through Whatman filter paper No. 1 (Merck, Germany). The cellulase activities of Trichoderma isolates were determined using 1% (w/v) carboxymethyl cellulose (CMC) dissolved in a 0.05 M citrate buffer (pH 4.0). The reaction mixtures, which contained 50 µL of enzyme solution (culture supernatants) and 100 µL of CMC dissolved in a citrate buffer, were used to conduct the cellulase activities. The mixtures were then incubated for 15 min at 37 ± 2 • C. At the end of the incubation, 0.5 mL of 3,5-dinitrosalicylic acid (DNS reagent) was added and heated at 95 • C for 10 min to stop the enzyme-substrate reaction. Glucose was used for the preparation of the standard curves. The series of glucose solutions were added with 1.0 mL of the DNS reagent and placed in a boiling water bath for 5 min. The absorbance values of the solutions were read at a 540 nm wavelength using Varian Cary 50 UV-Vis spectrophotometer (Varian, Mulgrave, Victoria, Australia). The concentration of reducing sugar for each sample was calculated using the standard curves regression equation and the results are expressed in mg/mL.
The qualitative analysis of cellulase production by Trichoderma isolates was determined by referring to the method described by Zehra et al. [40]. The (CMC) agar was prepared in 1 L of distilled water consisting of 16 g of the Bacto agar, 0.5 g of CMC, 0.5 g of bactopeptone, 0.2 g of Congo red, and 0.1 g of yeast extract. The antagonists (7 mm plugs) were inoculated on the respective media and incubated at 28 ± 2 • C for 4-7 days with four replications each. CMC agar plates were observed for the yellow, opaque, or discolored zone (cellulase activity) around the colony. The enzyme activity was ranked using the score as described in the chitinase assay.

β-1,3-glucanase
For the quantitative assessment of β-1,3-glucanase activity, the crude extracts of Trichoderma isolates were prepared by culturing the antagonists in 100 mL of Trichoderma Liquid Enzyme (TLE), which comprised KH 2 PO 4 (0.2 g/L), (NH 4 ) 2 SO 4 (0.14 g/L), bactopeptone (0.1 g/L), urea (0.03 g/L), MgSO 4 ·7H 2 O (0.03 g/L), CaCl 2 ·6H 2 O (0.03 g/L), and 1 mL of 0.01% trace element solution (Fe 2+ , Mn 2+ , Zn 2+ , and Co 2+ ). A total of 0.3 g of glucose and 0.5 g of colloidal chitin were added to the TLE as a source of carbon. The fungal cultures were incubated for 72 h at 28 ± 2 • C with an agitation rate of 150 rpm. All microbial cultivation was performed in triplicate for each of the isolates. At the end of the incubation, the culture supernatants and mycelia were separated by filtration through Whatman filter paper No. 1 (Merck, Germany). The β-1,3-glucanase activities of Trichoderma isolates were determined using 0.75% (w/v) laminarin dissolved in a 0.05 M sodium acetate buffer (pH 5.2). The reaction mixtures, which contained 50 µL enzyme solution (culture supernatants) and 100 µL substrates dissolved in respective buffers, were used to run the enzyme detection. The mixtures were then incubated for 15 min at 37 ± 2 • C. At the end of the incubation, 0.5 mL of 3,5-dinitrosalicylic acid (the DNS reagent) was added and heated at 95 • C for 10 min to stop the enzyme-substrate reaction. Glucose was used for the preparation of the standard curves. The series of glucose solutions were added with 1.0 mL of the DNS reagent and placed in a boiling water bath for 5 min. The absorbance values of the solutions were read at a 540 nm wavelength using a spectrophotometer (Varian Cary 50 Conc, Australia). The concentration of reducing sugar for each sample was calculated using the standard curves regression equation and the results are expressed in mg/mL.

Plant Growth Promotion Activity Indole Acetic Acid Production
Indole acetic acid (IAA) produced by Trichoderma isolates was quantified by following the protocol as described by Noori and Saud [41]. Trichoderma isolates were grown in sterile PDB with 5 mL of 0.2% (w/v) L-tryptophan, incubated at 28 ± 2 • C, and allowed to grow for 72 h. A conical flask without a fungal plug served as the control. Culture supernatants were filtered with Whatman filter paper No. 1 (Merck, Germany) after the optimum period (72 h). A total of 1 mL of filtrate was mixed with 2 mL of Salkowski reagent (35% perchloric acid, 1 mL 0.5 M FeCl 3 ). After 20 min incubation, the color density formed was read using a UV spectrophotometer at a 540 nm absorbance. The appearance of red or pink color indicated IAA production. To determine the amount of IAA produced from Trichoderma isolates, a series of IAA dilutions generated at 0, 5, 10, 20, 50, and 100 µg/mL was prepared to plot a standard curve. The presence of IAA in the culture filtrate was compared to the standard graph and expressed as µg/mL.

Siderophores Production
The chrome azurol S (CAS) assay described by Schwyn and Neilands was used to detect the production of siderophores. The CAS agar was prepared by mixing 900 mL of King's B medium and 100 mL of a CAS-HDTMA solution. King's B medium was prepared using 20 g of the Bacto agar, 20 g protease peptone, 1.5 g MgSO 4 ·7H 2 O, and 1.5 g K 2 HPO 4 , in 1 L of distilled water. The CAS-HDTMA solution was prepared using 0.062 g of CAS in 50 mL dH 2 O, 0.072 g hexa decyl tri methyl-ammonium bromide (HDTMA) in 40 mL dH 2 O, and 10 mL of iron (III) solution (1 mM FeCl 3 in 10 mM HCl). The CAS agar medium was sterilized by autoclaving at 121 • C for 15 min. Fungal plugs (7 mm in diameter) were plated on the CAS agar medium and incubated for 4-7 days at 28 ± 2 • C. Four replications were conducted per isolate. The amount of siderophore production activity was evaluated based on the orange zone developed around the fungal colony, according to Cherkupally et al. [42].

Biochemical Properties Index
A scoring system was assigned based on the mode of action which includes mycoparasitism, antifungal activities, production of extracellular hydrolytic enzymes, and plant growth-promoting activities associated with Trichoderma isolates against R. microporus. A scale order was used to objectively rank the activity of each Trichoderma isolate ranging from 0 to 4, with 4 indicating the isolate showing the highest activity, 3 showing the isolate with the second highest activity, 2 indicating the isolate at third place, 1 indicating the isolate showing the lowest activity, and 0 indicating the isolate showing no activity. Isolates with identical values were assigned an identical rank score. If a pair of isolates tie for the highest score, both isolates were assigned under scale 4 and the next isolate activity value will not be ranked under scale 3 but instead ranked under scale 2. The scoring results were used to select the potential Trichoderma isolates and further explored as BCAs for the evaluation of their efficiency against R. microporus under a nursery experimental plot.

Nursery Experiments 2.4.1. Biocontrol and Pathogen Inoculum Preparation
Trichoderma asperellum ST011 and T. spirale HT009 isolates were selected as potential BCAs to evaluate their capability against R. microporus in vivo. The Trichoderma isolates were grown on a PDA medium at 28 ± 2 • C for one week. Sterilized distilled water was added onto the PDA plate of Trichoderma asperellum ST011 and T. spirale HT009, and the fungal mass was scraped from the culture plate using a fine sterilized spatula to prepare a stock solution for serial dilution. A serial dilution was performed to quantify the total number of spores on a single plate. The colony-forming units (cfu) for each of the dilutions were determined by spore counting using a hemocytometer under the microscope. At the time of application, the spore concentration of each BCAs was adjusted to 10 8 cfu/mL using sterilized distilled water.
Wood for inoculation was obtained from a freshly cut rubber tree in UPM. The logs were then cut into smaller blocks with dimensions of 6 cm × 6 cm × 6 cm. Wood blocks were first washed with tap water and autoclaved twice at 121 • C, 15 psi for 30 min. A melted (liquefied by heat) malt extract agar (MEA) (Oxoid, UK) of 60 mL was poured into a high-performance plastic (HPP) bag (7" × 10" dimension) containing a rubber block. A MEA was added as a supplementary nutrient for the growth of R. microporus. Cotton plugs were used to plug the open end of the bags to allow the passage of air, but prevent any contamination of the blocks. The bags containing wood blocks and melted MEA were autoclaved at 121 • C and 15 psi for 20 min.
During the cooling process, the HPP bags were rotated frequently to ensure the wood blocks were well coated with the melted agar before the agar solidified. Each of the rubber wood blocks coated with MEA was inoculated with a 1 cm 2 fungal plug taken from a plate of one-week-old R. microporus culture. The inoculated blocks were incubated in dark conditions for one month at 28 ± 2 • C until the blocks were fully colonized by R. microporus mycelium.

Rubber Seedlings Inoculation
RRIM600 was selected as the host plant due to its high susceptibility to R. microporus [29] which favored WRD development. Four-month-old H. brasiliensis, clone RRIM600 seedlings, were bought from Sendayan Nursery, Seremban. The seedlings were maintained in nursery plots of the Faculty of Forestry, Universiti Putra Malaysia (UPM) for two months prior to the nursery assessment. The rubber seedlings were watered daily and fertilized once with NPK (15:15:15). Neem oil was applied to the plant surface using a 5 L garden pressure sprayer to eliminate any pest infestation.
In vivo study was carried out at the nursery of the Faculty of Forestry, UPM. The study was carried out using randomized complete block design with four blocks and six treatments ( Table 1) for six replicates randomized within each block (n = 4). The six-monthold rubber seedlings of the clone RRIM600 were maintained in polybags (10-inch × 12-inch) which contained a 7 kg/polybag mixture of soil, sand, and compost at a ratio of 8:8:2 as a growth substrate. The planting media mixture for the seedlings in all treatments was autoclaved twice at 121 • C for 1 h. For treatment T3 (T. asperellum ST011), treatment T4 (T. spirale HT009), and treatment T5 (T. asperellum + T. spirale), biocontrol suspensions of 100 mL per polybag were poured evenly into the sterilized planting media once a week for a period of one month before R. microporus inoculation. For chemical treatment (T6), the fungicide Kentil propiconazole 250 EC (Kenso Corporation, Petaling Jaya, Selangor, Malaysia) was diluted with distilled water at a ratio of 1:100 and 100 mL of the dilution was poured evenly into the soil once a week for a period of one month before R. microporus inoculation. Table 1. Type of treatments on rubber seedlings using Trichoderma suspensions and chemical fungicide for white root rot disease assessment in the nursery.

T1
Tree without inoculation of R. microporus T2 Tree inoculated with R. microporus and without application of biocontrol suspension or chemical fungicide T3 Biocontrol application with 100 mL of 10 8 cfu/mL suspension of T. asperellum ST011 to the planting media once a week for a month before the tree is inoculated with an R. microporus wood block T4 Biocontrol application with 100 mL of 10 8 cfu/mL suspension of T. spirale HT009 to the planting media once a week for a month before the tree is inoculated with an R. microporus wood block T5 Biocontrol application with 100 mL of 10 8 cfu/mL suspension of T. asperellum ST011 + T. spirale HT009 to the planting media once a week for a month before the tree is inoculated with an R. microporus wood block T6 Chemical application with 100 mL Kentil propiconazole 250 EC in a diluted form of 1% to the planting media once a week for a month before the tree is inoculated with an R. microporus wood block The inoculations of R. microporus were started 7 days after the last biocontrol suspension or fungicide dilution was added to the planting media. The inoculation was performed by placing R. microporus inoculum (rubber blocks colonized by R. microporus mycelium) at the bottom of the polybag, which was in direct contact with the roots of the rubber seedlings. The polybags were then filled up with the planting media treated with biocontrol suspension/fungicide for treatments 3-6. Planting medium inoculated with the pathogen but without biocontrol suspension/fungicide served as positive control and seedlings without R. microporus inoculum served as a negative control. The seedlings were then placed on benches in the nursery and were watered daily.

Disease Severity Assessment
The disease assessment was adapted from the method published by Wattanasilakorn et al. [43]. The plants challenged with R. microporus were observed for the growth of fungal rhizomorphs at the root and collar region of the plants. The symptoms developed on the roots (rotted) and the leaves (yellowing) were recorded. Observations were conducted at one-month intervals for six months after one month of the preliminary incubation period. The time to establish the disease symptoms and signs was also recorded. Four seedlings from each treatment, with one plant per block, were harvested at monthly intervals for disease assessment. For each isolate, the disease severity index (DSI) was determined using Equation (2) based on the infection scores, which include justifications of above-and below-ground symptoms, as shown in Table 2.
Disease severity index (DSI) % = (S 0 × X S0 ) + (S 1 × X S1 ) + (S 2 × X S2 ) + . . . (S H × X SH ) × 100 (2) X sum × S H where S 0 , S 1 , and S 2 , . . . , S H are the disease severity scores (0 to 4 for above-ground symptoms and 0 to 5 for below-ground symptoms), X S1 , X S2 , and X S3 , . . . , X SH are number of plants that are classified under the specific disease severity scoring, X sum is the total of plants, and S H is the the highest scoring of disease severity classification: 4 for above-ground symptoms or 5 for below-ground symptoms.
The classification scheme used in the disease severity index (DSI) was categorized with four disease severity scorings for above-ground symptoms and five disease severity scorings for below-ground symptoms ( Table 2). The efficacy of biocontrol or chemical application was then calculated based on the average DSI obtained from each of the treatments using Equation (3), as described by Gafni et al. [44]: where s1 = Disease severity index in the positive control and s2 = Disease severity index in the biocontrol or chemical treatment.

Transmission Electron Microscopy (TEM) Observation
The tissue processing method for the TEM was adapted from Kim and Kremer [39] with slight modifications. Small root fragments of about 2 mm long x 1 mm thickness were excised from the harvested plant. Healthy and infected root tissues were fixed in 2.5% glutaraldehyde at 4 • C overnight. The root tissues were again fixed in 2.5% glutaraldehyde at 4 • C for 2 h. The samples were then washed with a 0.1 M sodium cacodylate buffer for 10 min and the washing step was repeated three times. This was followed by a post-fixed in 1% osmium tetroxide at 4 • C for 2 h. The samples were subsequently washed again with a 0.1 M sodium cacodylate buffer for 10 min and repeated three times. The dehydration process was performed in a crescent series of acetone solutions (35,50,75,95, and 100%) for 10 min each up to 95% concentration, followed by 15 min with 100% concentration and repeated three times. The preparation process was continued by infiltration of the samples with an acetone and resin mixture. The resin was made up of 10 mL of agar 100 resin, 6 mL of dodecenylsuccinic anhydride, 5.5 mL of methyl nadic anhydride, and 0.5 mL benzyldimethylamine. The samples were immersed in the acetone and resin mixture at a ratio of 1:1 for 4 h, followed by 1:3 overnight, and immersed overnight with resin. The samples were then kept in beam capsules and filled with resin. Next, polymerization was performed in the oven at 60 • C for 48 h. Thin sections (1 µm) were sliced using an ultramicrotome with a diamond knife. The sections were stained with uranyl acetate for 15 min and washed with double-distilled water (ddH 2 O), followed by lead citrate for 10 min and washed with ddH 2 O. The sections were examined with a JEOL JEM2100F Field Emission Transmission electron microscope (JOEL, Japan). The root vascular system of the rubber seedlings and white root rot pathogen colonization patterns were observed by TEM.

Statistical Analysis
Statistical analyses were conducted using the statistical package SPSS for Windows, version 23.0 (SPSS, Chicago, IL, USA), which was used to evaluate the quantitative data of the PIRG values for a dual culture assay, non-volatile, and volatile metabolites; and the biochemical assays which include chitinase, cellulase, β-1, 3-glucanase enzymes, and IAA productions for analysis of variance (ANOVA) at a 95% confident level (p ≤ 0.05). Results were analyzed using one-way ANOVA, followed by Tukey's test as a post hoc test. The Tukey-Kramer multiple comparisons test was applied to analyze the differences between the treatment effects when significance was observed. The effects were considered to be not statistically significant when the p-value was higher than 0.05 at a 95% confidence level.

Identification and Selection of Potential Antagonistic Fungi through Dual Culture Assays
A total of 35 fungal isolates were successfully established from the soil samples obtained from the rhizosphere of rubber trees located at RRIM, Sungai Buloh. The sequence data of the fungal species associated with the soil sampled in this study was deposited in the GenBank nucleotide sequence databases (Table 3).   Figure 1 shows the direct competitive interaction by a dual culture assay of 35 fungal isolates against the growth of an R. microporus isolate RL21. The isolates HT007 and ST011, which were identified as Cunninghamella bainieri and T. asperellum, revealed an aggressive inhibitory result on the hyphal growth of R. microporus after five days of incubation, with significantly, the highest PIRG value recorded by Cunninghamella bainieri at 93.18% (Table 4). This was followed by T. asperellum (ST011) and L. theobromae (ST010). Other isolates that performed strong antagonism with PIRG values of more than 75% against R. microporus were identified as T. koningiopsis (isolates HT001 and ST014) and T. spirale (HT009).  Table 4 for the fungalnumber association. The first apparent physical contact between the above isolates and the pathogen R. microporus occurred within the first 2-3 days, followed by growth inhibition. Figure 1 shows that the isolates HT007, ST011, HT001, ST014, HT009, and ST010 have fully occupied the PDA medium and overgrowth the pathogen on the 5th day after inoculation (DAI). This caused a space limitation for R. microporus, preventing any radial expansion on the culture plate. The present study showed that there were four Trichoderma spp., namely T. asperellum, T. koningiopsis, T. reesei, and T. spirale, together with C. bainieri, Lasiodiplodia theobromae, Aspergillus nomius, Byssochlamys spectabilis, and Penicillium sp. categorized under R1 and R2 (Table 4). With these scores (R1 and R2), the mentioned isolates were considered antagonistic to the pathogen, with a substantial PIRG result achieved by the isolates HT007 and ST011.
Moderate antifungal activities were found in the other ten isolates, which include T. koningiopsis (HT015), A. nomius (HT016), Penicillium sp. (HT017 and ST003), B. spectabilis (HT018 and ST017), T. spirale (ST004 and ST006), Fusarium oxysporum (ST005), and T. reesei (ST013). These isolates inhibited the growth of R. microporus by 52.18-70.35% within five DAI. Among these, F. oxysporum (ST005) created the most distinct growth inhibition zone at the line of contact with the pathogen. However, some changes were observed in the physical interactions between isolate ST005 with R. microporus after a growing period of 15 days. The pathogen was not just capable to circumvent parasitism but also formed mycelial strands to grow over the mycelia of isolate ST005.
Despite the promising results demonstrated by C. bainieri and L. theobromae for their antagonism against R. microporus, both isolates were not taken into consideration as potential biocontrol agents. This is due to the genus of the species Cunninghamella being reported to cause infections, especially to the immunocompromised hosts [45], and L. theobromae to cause diseases, such as die-back, blight, and root rot to different crops in the tropical and subtropical regions, which includes guava, coconut, papaya, and grapevine [46].

Non-Volatile Compounds
The results of the study revealed a significant interaction (p ≤ 0.05) between the Trichoderma species and the concentration of non-volatile filtrate (Trichoderma isolates x the concentration of culture filtrate) on the growth inhibition of R. microporus (Figure 2). Isolate T. asperellum extracts with 75% and 50% concentrations of culture filtrates exhibited the highest inhibition activity against R. microporus after five DAI, with the inhibition rate recorded at 78.80% and 77.41%, respectively ( Table 5). The non-volatile filtrate of T. koningiopsis HT001 and T. reesei ST013 was recorded to have the least effect against R. microporus, with minimal inhibition rates at 10.20% and 5.90%, respectively, even with a 75% concentration. No inhibition activity was observed against the pathogen in the plates incorporated, with 50% and 25% of the culture filtrate produced by T. koningiopsis HT001 and T. reesei ST013. Table 5. Effects of three different concentrations of culture filtrate containing non-volatile metabolites produced by four Trichoderma isolates on Rigidoporus microporus radial growth and the percentage inhibition of radial growth (PIRG) after 5 days of growth at 28 ± 2 • C, in the dark.    Figure 2 shows the effect of non-volatile filtrates produced by Trichoderma spp. on the morphological characteristic of R. microporus. Distorted shapes on the growth patterns and sparse mycelial growth were clearly seen, especially in the non-volatile filtrate plates of T. spirale HT009 and T. asperellum ST011, as compared to the control at five DAI (Figure 2d). The study documented by Dixit et al. [47] demonstrated the abnormal morphological characters of the pathogenic fungi, i.e., the reduced number of sclerotia and sparse mycelial growth was due to the presence of an inhibiting substance produced by the Trichoderma spp. The lack of inhibitory effects against R. microporus with a non-volatile compound in T. koningiopsis HT001 and T. reesei ST013 isolates indicated that their antagonism activities were performed using other mechanisms rather than in non-volatile compound production.

Volatile Compounds
Volatile compounds produced by Trichoderma isolates induced a slight inhibition of the pathogen growth ( Table 6). The inhibition of R. microporus demonstrated by Trichoderma isolates was moderate to weak, at which T. asperellum ST011 performed at 55.77%, followed by T. spirale HT009 (37.77%), T. koningiopsis HT001 (33.42%), and T. reesei ST013 (26.76%), respectively (Table 6). Table 6. Effects of volatile organic compounds produced by four Trichoderma isolates on Rigidoporus microporus radial growth and the percentage inhibition of radial growth (PIRG) using the overlapping plate assay after 5 days of growth at 28 ± 2 • C, in the dark.
Undoubtedly, the chemical profiles varied among different isolates. The common compound 13-Docosenamide,(Z)-identified in the present study was reported to have an antimicrobial function when it was extracted from the seeds of Mucuna pruriens Linn [46] and Zhang et al. [49] also stated that 13-Docosenamide,(Z)-was one of the key bioactive compounds produced by T. longibrachiatum, with its antifungal activity recorded at 7.69%.
The compound 4-hydroxy-benzeneethanol identified in the crude culture of T. asperellum ST011 and T. reesei ST013 was previously reported to decrease the root-knot nematode egg hatchability to less than 10% with a 9.6 mM or higher concentration of the active compound extracted from Welsh onion root exudates [52].

Production of Extracellular Hydrolytic Enzymes
T. asperellum ST011 had the highest activity of all the enzymes tested ( Table 8). The result of the chitinase plate assay from T. asperellum ST011 demonstrated a rapid and the highest response, with quantitative results at 0.04 µmol/min. The fastest reaction of color changed and the darkest purplish zone formation by T. asperellum ST011 was evident (Figure 3c). The other three isolates exhibited similar results for chitinase activity (0.02 µmol/min) after 72 h of incubation at 28 • C. In general, all the Trichoderma isolates fully changed the chitinase detection agar to purple color at five DAI.  T. asperellum ST011 was significantly the highest in cellulase activity (0.26 µmol/min), followed by T. spirale HT009 (0.18 µmol/min), T. koningiopsis HT001 (0.11 µmol/min), and T. reesei ST013 (0.04 µmol/min) ( Table 8). This corresponded with the results obtained from the cellulase plate assay, at which T. asperellum ST011 showed a distinct yellowopaque hydrolyzing zone on the CMC plate (Figure 3c). From the quantitative results of glucanase presented in Table 8, the highest activity was exhibited by T. asperellum ST011 (0.06 µmol/min), followed by T. koningiopsis HT001 (0.03 µmol/min), and T. reesei ST013 (0.02 µmol/min). No glucanase activity was shown by T. spirale HT009.
Chitinase and glucanase enzymes secreted by Trichoderma species are known to act synergistically in degrading the cell wall of the fungi pathogens so as to obtain nutrients for their own growth [55]. The present study shows that some of the Trichoderma isolates presented higher ability in hydrolyzing chitin, cellulose, and glucan with isolate T. asperellum ST011 achieving the highest score for all the enzyme activities tested. As the main component of the fungal cell wall is made up of chitin, glucan, and proteins [56], Trichoderma isolates that possessed higher enzyme activities have a higher capability to hydrolyze these elements, which is one of the key mechanisms in antagonistic activity for the isolate against the plant pathogenic fungi. Hence, chitinase, glucanase, and cellulase are essential in the hyperparasitic system.

Plant Growth Promotion Activity
Significant differences were observed in the mean values of IAA production between T. asperellum ST011 and T. reesei ST013. The highest amount of IAA was produced by T. asperellum ST011 (1.68 µg/mL) followed by T. reesei ST013 (0.83 µg/mL), and was absent in T. koningiopsis HT001 and T. spirale HT009 (Table 9). IAA is essential for plant growth development [57] and enhances the fitness of plant-microbe interactions by increasing the amount of lateral and adventitious roots. This facilitates nutrient absorption and promotes root exudation, which in turn provides more opportunities for root-microbe interaction [58]. In the present study, both T. asperellum and T. reesei showed positive IAA production. A similar finding was reported by Muniroh et al. [59], stating that T. asperellum was able to produce IAA in lower amounts. Brummell and Hall [60] claimed that even small amounts of IAA could directly enhance plant growth by stimulating cell division or elongation. Table 9. Indole acetic acid (IAA) produced by Trichoderma isolates, T. koningiopsis HT001, T. spirale HT009, T. asperellum ST011, and T. reesei ST013.
The Trichoderma isolates were verified on phosphate solubilizing using a PVK agar plate. The ability to solubilize phosphate was positively exhibited by T. spirale HT009, T. asperellum ST011, and T. reesei ST013 to different extents ( Figure 4). Phosphate solubilization was not detected from T. koningiopsis HT001. Phosphorus (P) is one of the important plant nutrients that has a significant impact on plant growth. In the present study, T. koningiopsis HT001 was the only isolate that was not able to solubilize the inorganic phosphate. The key process responsible for the release of insoluble phosphate was the generation of organic acids by the phosphate-solubilizing microbes. Phosphate-solubilizing microbes, such as fungi and bacteria, play an important role in transforming insoluble P to soluble P forms that can easily be assimilated by plants [59]. Although the nutrients required by plants are abundant in nature, only a small amount of P is readily available in the form for plant uptake [59]. All tested Trichoderma isolates were found to produce siderophores that changed color from green to orange on the CAS agar plates (Figure 4). The fastest color change was observed in T. spirale HT009 (Figure 4b) at five DAI, while the other three Trichoderma isolates took 8-10 days. Siderophores are ferric ion-specific chelating agents formed by microorganisms to combat low iron stress [61]. In order to make the ferric ion [Fe(III)] available to microbials and plants, siderophores play a crucial role in chelating it from the surrounding environment [62]. According to Kobayashi and Nishiwaza [63], Fe is an essential micronutrient for plant growth. Many of the BCAs with significant antagonistic characteristics produce siderophores that chelate the available iron and prevent iron uptake by the respective pathogen which indirectly limits the proliferation and root colonization of the pathogen [64].

Scoring of the Biochemical Properties Index
The scoring system presented in Table 10 was developed to summarize the biochemical assays performed by Trichoderma isolates for their antifungal activities, lytic enzyme production, and plant growth-promoting activity. T. asperellum ST011 ranked the most activity in all assays, except siderophore production, and a total score of 30 was recorded. T. spirale (HT009) performed high activity in all assays, except β-1,3 glucanase and IAA production. Based on the biochemical assays, the isolates T. asperellum ST011 and T. spirale HT009 were selected to perform in vivo assays against R. microporus.

Disease assessment
In this study, (-) the control plants of T1 without R. microporus inoculation showed no symptoms until the end of the experiment. Plants inoculated with R. microporus, (+) control plants of T2 (without pretreatment), plants pretreated with biocontrol suspensions (T3, T4, and T5), and plants pretreated with chemical fungicide (T6) showed above and below-ground symptoms of WRD at various degrees, i.e yellowing of the leaves followed by wilting and root rotting incidence (Figures 5 and 6). Six months after inoculation (MAI) of R. microporus, (+) the control plants in T2 showed the greatest disease severity index of 68.54 based on the above-and below-ground scorings (Table 11). A lower disease severity index (DSI) value for T3, T4, T5, and T6 indicated that the disease suppression was effective with the biocontrol and chemical applications. The DSI of plants pretreated with the Trichoderma biocontrol suspension in T3, T4, and T5 was recorded at 28.44%, 42.71%, and 27.92%, respectively, after six MAI of R. microporus inoculation (Table 11). The investigation showed that biocontrol suspension of just T. asperellum alone and a combination of T. asperellum + T. spirale reflected higher efficacy against R. microporus, with their efficiency percentage recorded at 58.51% and 59.27%, respectively (Table 11). Thus, the biocontrol suspensions were effective, with a reduction of DSI by almost 40% compared to (+) the control T2. Despite the promising results shown by Trichoderma isolates, the application of T. spirale alone is less effective when compared to applying T. asperellum (T3) alone or with the combination of both Trichoderma suspensions (T5), suggesting that T. asperellum played a more important role in suppressing WRD in the present study. There was no significant difference between the DSI value in plants treated with just T. asperellum (T3) and the one with the combination of T. asperellum and T. spirale (T5).   On the other hand, the formation of rhizomorphs in the rubber seedlings of T6 (the treatment with chemical fungicide) was noticeably lesser when compared to (+) the control T2, with a DSI of 33.54% recorded. Despite the positive effect of propiconazole on the WRD development for the first three MAI, the rhizomorph formation was increasing gradually thereafter. The mycelia of R. microporus appeared to grow rapidly and spread again with the white rhizomorphs noticeable on the root surface. Table 12, the mortality of the rubber seedlings clone RRIM600 revealed that the plants in T2 which served as (+) the control have caused serious damage, as the survival rate was only recorded at 33.33% in the six MAI of R. microporus. The greatest survival rate of 66.67% was achieved by plants treated with T3 and T5. This was followed by T6 and T4, with the survival rate of plants recorded being 58.33% and 50.00%, respectively. The present study demonstrated that Trichoderma isolates have the potential to improve soil health and compete with R. microporus when the host plants were challenged with the respective pathogen at which their applications were aimed to function as a protective approach. The nursery trial demonstrated that the rubber clone RRIM600 challenged with R. microporus without any biocontrol or chemical treatments had serious damage, with a mortality rate as high as 66.67%, which indicated that the rubber clone RRIM600 was susceptible to R. microporus.

As shown in
Prior application of the BCAs could not completely eliminate the presence of R. microporus rhizomorphs. It was observed that pretreated soil with selected Trichoderma isolates prior to the inoculation of R. microporus was only able to reduce the disease severity by 27-43%, as the infected plants were not completely free of R. microporus infection even after 60 days. Although, it was reported by Suryanto et al. [21] that BCAs work best as a preventive measure rather than a curative. Systematic inoculation of Trichoderma isolates in the soil even after infection may help to limit the further spread of R. microporus by securing Trichoderma as the dominating role in suppressing the pathogen.

Transmission Electron Microscopy (TEM) Observation
The TEM observation revealed that the root tissues of the healthy seedling in T1 were normal and free from R. microporus, with thick and smooth cell walls (Figure 7a). The results showed the presence of the pathogen hyphae penetrated the root tissues of the plant in T2 (Figure 7b). The cell walls of roots infected with R. microporus were extensively degraded and ruptured. Cells of the infected root were severely compressed compared to the healthy root in T1, which were still firm in shape. The penetration of R. microporus hyphae into the root tissues was noticeable in plants treated with Trichoderma suspension and fungicide (Figure 7c-f), yet a lesser amount of hyphae penetration was observed, particularly in T3, T5, and T6. Therefore, cell damage was reduced compared to T2 root tissue. Reduced penetration of R. microporus hyphae into host root systems may be related to the ability of the biocontrol agents, Trichoderma spp. in producing cell wall degrading enzymes acting on the hyphae of R. microporus, thus weakening the pathogen. Biocontrol suspensions of T. asperellum and T. spirale were effective in slowing disease progression, which is believed to have reduced disease severity.

Conclusions
In this study, a total of 35 fungal isolates were successfully established from the rubber tree rhizosphere soil and further screened for their antagonistic potential against R. microporus in dual culture plates. Four Trichoderma isolates represented by T. asperellum, T. koningiopsis, T. spirale, and T. reesei showed high antagonistic potential in the inhibition of radial growth of R. microporus of 75% or more. In vitro results clearly demonstrated that T. asperellum and T. spirale isolates showed high antifungal activity in reducing mycelia growth of the pathogen R. microporus through volatile and non-volatile productions. Moreover, the screening of enzymes revealed their capability to excrete extracellular lytic enzymes, such as chitinase, cellulase, and glucanase, at different levels. Positive results demonstrated by the Trichoderma isolates in the plant growth-promoting activities, such as indole acetic acid, siderophores productions, and phosphate solubilization have further supported the use of selected Trichoderma isolates against R. microporus in vivo. In nursery assessments, studies have shown that soil pretreated with T. asperellum ST013 as a single treatment or combination with T. spirale HT009 was able to reduce the disease severity index of R. microporus to a similar extent as in the propiconazole chemical treatment. Further studies should focus on the potential adverse effects of T. asperellum ST011 by assessing the knowledge of its environmental fate and behavior in terms of persistence, survival, and dispersion in different soil types.