Disease assessment was conducted in 30 oil palm growing communities in six districts in Central, Eastern and Western Regions of Ghana, two districts per region and five farming communities per district. For the purpose of this study, the selected districts surveyed were renamed as K29B, K37-1, K31-1, K37-2, K30, and K4. The K29B and K37-1 represent Denkyembour and Fateakwa districts from the Eastern region, K31-1 and K37-2 represent Nzema West and Mpohor districts from the Western region, while K30 and K4 represent Twifo-Atti Morkwa and Gomoa East districts from Central Region.

The districts visited in Eastern region, lie within latitudes 6°.10871′ N to 6°.38431′ N and longitudes 0°.35047′ W - 0°.30′ W and 0°10′E to 0°30 E. They cover land areas ranging from 1500 km ² to 2050 km ² of the region. In the Western region, the two districts lie within latitudes 4.8520°N to 5.2 609°N and -2.2377° W to 1.5021°W and covered land areas ranging between 1,200 km ² to 6,231 km ². Twifo-Atti Morkwa (K30) and Gomoa East (K4) districts from the Central region lie within latitudes 5°3.209′ N to 5°7.891′ N and longitudes 1°23.200′ W - 1° 54.360′ W. They cover land areas ranging from 1,160 km ² and 5,231 km ² of the region. All these regions are located within the semi-deciduous forest zone in Ghana. The areas are characterized by a double maxima rainfall pattern followed by a prolonged dry season. The minimum temperature during the study period (October 2022 to February 2024) ranged between 22.6°C and 25.2°C and the maximum varied between 31.4°C and 36.0°C. The relative humidity varied from 45% to 75%.

Intensive BSR disease scouting was carried out based on the single-point disease assessment using the standard operating procedure (SOP) of the Ganoderma census published by the Malaysian Palm Oil Board (MPOB, 2014). The process was done by counting the number of infected trees using a block of a hundred trees along a diagonal on each plantation for proper disease representation. A total of 3000 palms were assessed, 100 palms per plantation.

Disease incidence was computed using modified version of Vicent’s formula ( Lekete-Lawson et al., 2024). % BSR Disease Incidence ( DI ) on the field = Number of BSR infected oil palm per Plantation Total number of selected oil palm per Plantation × 100

Disease severity was scored on a scale of 0-4 ( Lekete-Lawson et al., 2024)

where, 0 = no symptom, and 4 ≥ 9 Maximum number of fruiting bodies per palm or foliar symptoms > 4 fronds/palm

Ninety symptomatic samples, including fruiting bodies (Basidiocarps) and Ganoderma sp. (Dikaryotic), were collected from infected life palms across all three regions ( Figure 1).

Media compositions were as follows: PDA for one litre of distilled water included: 39 g of Pre-mixed, Dehydrated PDA powder (Supplier: Thermo Fisher Scientific, Catalog code: CM0139B amended with 3 g of peptone (supplier: Clinichem Ltd, catalogue code: 70161), pH: 5. Malt extract agar (MEA: supplier: Thermo Fisher Scientific, Catalogue code: CM0059B); composition per liter of distilled water: 30 g of malt extract, 3 g of peptone, and 15 g of agar (Supplier: Millipore Sigma, Catalogue number: 05040); pH: 5.6. The diseased samples collected from both the infected oil palm trunk and the Basidiocarps were cut into approximately 1 cm pieces with a scalpel blade and rinsed three times in sterilized distilled water, surface sterilized in a 10% sodium hypochlorite (solution, and blotting on tissue paper ( Goh et al., 2014). The samples that were sterilized were aseptically inoculated onto PDA (powder (Supplier: Thermo Fisher Scientific, Catalog code: CM0139B) and incubated at 28±1 °C for four days and later sub-cultured on Malt Malt extract agar (MEA: supplier: Thermo Fisher Scientific, Catalogue code: CM0059B) till pure cultures of isolated fungi were obtained. The pure fungal cultures were maintained on Malt Extract agar (MEA) Malt extract agar (MEA: supplier: Thermo Fisher Scientific, Catalogue code: CM0059B) as stock cultures in Petri dishes in dark conditions at room temperature (28 ± 1°C) for further analysis.

Macro-morphological identification and confirmation were done using colony characteristics (shape, colour and texture of the mycelia) and micrograph description. Cultures from various plantations were grouped based on their morphological resemblances. There were three replications per isolate. Sporulation was assessed on glass slides by mounting a small portion of mycelia in sterilized distilled water with a blue stain and observed under a Leizer microscope of lens magnification of 40X. Mycelia, obtained from the various samples, were preserved in the biological incubation chamber (Thermostatic Cabinet ST 1 POL-EKO2; ST 1/1/1, Manufacturer: POL-EKO . Registered trademark ( ^{® ,}™): POL-EKO ^® sp.k of POL-EKO-APARATURA sp.j.) at 20 °C for 12 days, for pathogenicity tests and other clinical analyses.

Infected BSR samples, fruiting bodies and isolated fungi were taken to CABI Microbial Identification Service, Bakeham Lane, UK for Molecular identification and confirmation.

2.8.1 Procedure as follows

All original samples ( Ganoderma fruiting bodies and isolated fungi) were tested for purity. Molecular assays were conducted on all samples with nucleic acid as the template. A total of 29 basidiocarps and 24 Ganoderma pure cultures were investigated. Microzone, UK, proprietary formulation microLYSIS ^®-PLUS (MLP) underwent rapid thermal cycling for cell lysis and release of DNA. Polymerase Chain Reaction (PCR) was used to amplify the rDNA in vitro after DNA extraction. The DNA quality of the PCR products was then evaluated. The samples were electrophoresis using a 2% agarose gel (Supplier of agarose gel: Thermo Fisher Scientific, Catalogue Number: UltraPure™ Agarose, 500 g – 165005001) and GelRed-stained (supplier: Biotium, Inc., Catalogue Number: GelRed ^® Nucleic Acid Stain, 10,000X in water - 41003/41003-1). An additional PCR purification step was performed to eliminate excess dNTPs, primers, polymerase, and other constituents of the PCR mix, in order to obtain an extremely pure DNA template for sequencing. PCR amplicons were later characterized by sequencing with the BigDye ^® Terminator v3.1 kit from Applied Biosystems (Life Technologies, UK,) and a pair of primers: ITS1 (TCC GTA GGT GAA CCT GCG G) and ITS4 (TCC GCT TAT TGA TAT GC GTAC) ( Gašparcová et al., 2017). The basidiomycete-selective primer GanET (GCGTTACAT GAG CGCAATACAA) was also used to prevent the potential co-amplification of contaminant non-basidiomycetous fungi.

Sequencing reactions were carried out with the use of fluorescently tagged chain terminator dNTPs. Sample processing was executed with the AB 3130 Genetic Analyzer for the examination of the sequence of nucleotide bases (adenine, guanine, cytosine, and thymine) in the DNA oligonucleotide. Preliminary identification was made by matching the sequenced data with the sequences in the European Molecular Biology Laboratory (EMBL) database via the European Bioinformatics Institute (EBI). For verification, the samples were re-identified by ITS sequence analysis using the FASTA algorithm and the Fungus database from EBI and the BLAST algorithm with the NCBI standard database (Report on molecular work: https://figshare.com/s/86864d9d08393658fb20) (Accessed: 07.02.2025).

2.8.2.0 Phylogenetic analysis

2.8.2.1 Sequence alignment

Sequences of newly identified species were analysed using standard BLAST searches in GenBank: [ Lekete-Lawson, (2025a), ( https://doi.org/10.6084/m9.figshare.28389083)] to identify more similar sequences. In addition to sequences obtained in this study, all sequences used for phylogenetic analysis were retrieved from GenBank: ( ftp://ftp.ncbi.nlm.nih.gov/pub/agarwala/indexed_megablast). The sequence multiple alignments were done using the online version of MAFFT (v7.511) https://mafft.cbrc.jp/alignment/software/ and open access online version of Geneious Bioinformatics Software for sequence Data analysis R9 v. 2019.2.3 ( https://www.geneious.com/): Rozewicki et al. (2019) manually formatted with Clustal-Omega 1.2.4 (open access available: http://www.clustal.org/omega/) pairwise sequence alignment tools to minimise gaps and ensure proper alignment.

For the purpose of this study, three-weeks-old healthy germinated palm seeds of commercial standard crosses of (Dura × Pisifera, (D × P)) obtained from Ghana Sumatra Ltd were used for the pathogenicity test. A volume of 250 ml Beatson glass jars (R3/83 mm 4 Doz) containing a mixture of planting media (black soil, bio-cha, and treated plant biostimulant) at 2:2:1 100 g per glass was used. The jars were autoclaved for 45 minutes at 121°C. The mixtures were left to cool for three days. After three days, healthy germinated seeds with uniform growth were sown into the glass jar containing the sterilized growth medium for artificial inoculation ( Goh et al., 2014). A total of Hundred and forty-four (144) germinated palm seeds germinated palm seeds (three treatment and control, 6 seeds per replicate) were arranged in a randomised complete block design (RCBD) in the growth chamber and maintained for one week under laboratory conditions at CSIR-OPRI Plant Pathology laboratory, (6°.10871′N, 0°.35047′W and 0°10′E) with relative humidity and temperature regulated at 70 % and 28±1°C, respectively.

2.9.1 Inoculum preparation

Research has shown that Ganoderma species are wood-decomposing fungi that thrive on decaying wood, which provides essential nutrients and moisture ( Kumar et al., 2022; Mangaiha et al., 2019; Chang et al., 2002). Thus, techniques by Angel et al. (2021) and Bivi et al. (2016), with slight modifications, were used in Ganoderma inoculum preparation using Woodblocks made from Triplochitan scleroxylon (Wawa), which was previously tested in preliminary studies (Anonymous, 2024-unpublished) to be an effective growth medium for Ganoderma fungi. The Wawa Woodblock (WWBs) incubation time was 15 days ( Breton et al., 2005, 2006).

2.9.2 Artificial inoculation of germinated oil palm seeds

Inoculation of germinated seeds was performed in 250 ml Beatson glass jars (R3/83 mm 4 Doz) with WWBs previously colonized by Ganoderma isolates. Glasses (components) were incubated according to the method described by Lo et al. (2023) with slight modification. The set-up was maintained under lab conditions with relative humidity and temperature regulated at 70% and 28±1°C, respectively. The infection process was monitored and recorded daily. Germinated seed nuts with WWBs without inoculum served as a negative control.

Re-isolation of inoculated fungi from the destructive samples was performed following the techniques by Agrios (2005) and Idris et al. (2006). The roots were treated and plated on Malt extract agar and subcultured until a pure culture was obtained and identified by Lo et al. (2023)

2.9.3 Symptoms recording

Disease development based on external and internal symptoms was recorded every three days. External symptoms were based on visual estimation of the proportion of tissues damaged by inoculated fungi, using the scale established by Breton et al. (2006). Internal symptoms were recorded by splitting the inoculated seed nuts in two cross-sections and through the root. Other symptoms which were not visible were confirmed using molecular tools. All the signs and symptoms recorded were used for disease rating.

2.9.4 Disease rating

Disease rating in vitro was computed as: % BSR Disease Incidence ( DI ) per germinated seed nut = Number of infected oil palm seed nuts Total number of inoculated seed nuts × 100

The results for interpreting pathogenicity tests were based on the percentage of infection on test seed nuts. These were subjected to an ANOVA, and treatment means were separated with the least significant difference (LSD) at 5% after rating (R-Software data analysis: Lekete-Lawson, E. (2025a) https://figshare.com/authors/Emmanuellah_Lekete-Lawson/20618918). The data on different parameters were also compiled and analysed using the R-Stat version 2021 statistical package ( R Core team (2021) https://www.R-project.org, accessed 10/8/2024). The LSD at 1% was also used to separate the means of treatment fungi and the control.

Out of 3000 palm trees assessed, 341 palms were identified as Ganoderma-infected palms representing 11.3% of disease incidence. However, the level of infection differs. The number of fruiting bodies (basidiocarps) counted on each infected palm varied between 2 and 274, and severity scores were between 2 and 4, with 4 being the highest recorded on the 9-year-old palm. District K29-B in the Eastern region showed the highest percentage of infection, with 161 infected palms and 274 basidiocarps. District K4 has the least, with 2 infected palms and 4 basidiocarps representing a severity score of one.

This study revealed a higher infection rate in the Eastern region compared to the other two regions surveyed. Figure 1 shows the total number of palms affected and the severity score range of BSR disease in the selected oil palm growing Districts in Ghana.

Basal stem rot disease observed on the fields depicts the basidiocarps which first appeared as small white buttons ( Figure 2B) of tissue on the stem and later developed into a bracket shape mainly on the base ( Figure 2Dii) or at the upper side ( Figure 2Di) causing Basal Stem Rot (BSR) or Upper Stem Rot (USR) disease. These basidiocarps are woody, perennial and dimidiate; their cap (pileus) is concave, and some are circular with rough and irregular margins/blades (lamellae/gills). Pileus measured from 4-17 cm in diameter ( Figure 2Di); and 7 cm to 19 cm in length. Surface glabrous; crisped; shiny; dry and smooth. Their upper surfaces also took on a variety of white to yellowish-brown colours and was with concentric zonations ( Figure 2Dii). Also, the underside/gills are white ( Figure 2), gills adnexed, crowded (8-14 attached lamellae) with 8 series of lamellae, narrow and crisped. Most of the BSR basidiocarps lacked a stipe. However, in some upper-stem rot mushrooms, a short, wide, and noticeable stipe was present ( Figure 2Di). This stipe was lateral, compressed, and uniform in width, with a bulbous base and distinct longitudinal striations. The hymenophore is woody and dark-brown with no volva. No basidiospores, basidia, and basidioles were observed. The substrates were observed in live mature oil palms ( Figure 2).

Many of the heavily infected palms were seen full of basidiocarps growing from the base ( Figure 2 A, B, C & Dii; some deteriorated and others fractured and collapsed ( Figure 2C).

3.3.1 Isolation and identification of causal agent(s) of the BSR disease on oil palm

Out of 90 symptomatic samples collected from the field, 60 of them were screened for fungal isolation. 29 categories of fungal cultures were obtained and identified, 24 of them were identified as suspected Ganoderma fungi, and grouped into three (GA, GD2B and TD2B) ( Figure 4). Other fungi isolated and identified include Trichoderma, Xylaria, Fusarium, Phytophthora, and others (moulds; Rhizopus, Aspergillus spp.). These fungal isolates were grouped based on their macromorphological characteristics and micrograph features. They were further ranked based on their taxonomy and percentage of occurrences ( Figure 3).

Overall, suspected Ganoderma fungi were identified 24 times, representing 66% of the total isolates. This was followed by Trichoderma sp. (13%) with saprophytic fungi (others) recording the least (2%). These suspected Ganoderma fungi were also categorised into three based on colony similarities in culture media, growth rate and their place of origin. Isolates GA from the Eastern, GD ₂B from the Central and TD ₂B from the Western regions ( Figure 4).

All cultures in Figure 4A were produced simultaneously. GA had the fastest growth rate, followed by TD ₂B and GD ₂B. These three groups of the Ganoderma isolates produced white, velvety, fluffy and cottony colonies on Malt extract agar medium ( Figure 4A). GA colonies appeared white, stranded, cottony and fluffy ( Table 1). GD ₂B produced white and stranded mycelium, velvety with concentric cottony and hyphal-knot structure ( Table 1). TD ₂B appeared white, fluffy, cottony and velvety but turned yellowish-brown as it progressed ( Figure 4). Their mycelium micrograph also shows hollow, septate and clamp connections ( Figure 4B) when viewed under a compound microscope with a magnification of 40X. No spore was seen on the artificial medium. Table 1 shows macromorphological features of the three groups of Ganoderma fungi isolated.

3.4.1 Source of inoculum

The study showed that the three isolated Ganoderma fungi (GA, TD ₂B and GD ₂B) were able to colonise the inoculated WWBs. The first sign of growth was observed after seven days of inoculation with GA isolate, TD ₂B isolates after 12 days and GD ₂B appeared after 16 days of inoculation. The total incubation time of the WWB inoculum was 17 days. The growth chamber was maintained at a temperature of 28±1°C and relative humidity of 60-75% suitable for the fungal growth.

3.4.2 In vitro artificial inoculation

This research presents an in vitro artificial inoculation test on oil palm germinated seed nuts, in a controlled environment resulting in the first symptoms development within 2-3 weeks. The first symptoms on inoculated seeds appeared after eight days of inoculation and differences between the inoculates and inoculated germinated seeds and control ( Figure 5dii) became noticeable around 14 to 16 days ( Figure 5aii and Figure 5bii).

After 21 days of artificial inoculation, germinated seed nuts inoculated with WWBs inoculum showed physiological symptoms of disease including root decay ( Figure 5(aii and cii), necrosis ( Figure 5(aii, bii and cii)), leaf withering ( Figure 5(aii, and cii)), decaying bole tissue ( Figure 5bii) and other lesions that were absent in the control group of seed nuts ( Figure 5dii).

3.4.3 External and internal symptoms evaluation

The percentage infection was determined by considering both external and internal disease indices ( Table 2). The external infections were recorded based on visual symptoms observed in the inoculated seedlings while internal infections were evaluated based on endophytic symptoms analysis and re-confirmation of pathogenicity using molecular tools.

Table 2 shows the results of the pathogenicity tests of different Ganoderma isolates (T1:GA, T2:GD ₂B, T3:TD ₂B) from BSR-infected oil palms in Ghana. Each isolate (GA, GD ₂B TD ₂B,) and the control group were analyzed with estimated effects, standard errors, t-values, and p-values to measure their relative impact on the test seed nuts. Out of 144 seedlings tested, 58.3 % were infected. Data showed that GA fungi from the Eastern Region exhibited severe pathogenic effects (t-value: 8.221680) on the germinated seed nuts and caused 26.1% of seedling deaths ( Figure 6). Its treatment against the control showed a highly significant (p<0.01) difference with adjusted p-value (p adj) of (0.0000004)***).

3.5.1 Pathogenicity variation and treatment comparisons

The treatment GD ₂B isolates showed a significant increase of 44.433 units with a t-value; (5.059787) and a p-value of 0.0003237 compared to the control. Isolates from the Western region (TD ₂B) showed a relatively strong effect (t-value = 6.957682), on the treated seed nuts compared to the control group. GD ₂B shows a decrease of -27.77 difference with a weak pathogenicity effect (p-value: 0.0233249), confidence Interval (lower, upper): (-52.35, -3.19) and a low percentage (2 %) seedling death ( Figure 6) ( Table 3). Isolate TD ₂B shows a decrease in virulence effect (-11.1 units) compared to the GA isolates, with an adjusted p-value (p adj): of 0.5952326 and a confidence interval (lower and upper): (-35.68, 13.48) of which is not significant. Comparing the pathogenicity effect of TD ₂B and GD ₂B isolates, TD ₂B shows an increase of 16.67 difference with the confidence Interval (lower and upper): (-7.91, 41.25) compared to GD ₂B, but this difference is not significant (p-value = 0.2604245).

3.5.2 Symptoms recording

The highest external symptoms (62.21%) and seedling death were observed in the seed nuts inoculated with GA and TD ₂B fungi ( Figure 6) and the lowest severity (4.23 %) was observed in the GD ₂B treated seed nuts. None of the other isolated fungi ( Trichoderma, Xylaria, Fusarium and Phytophthora and saprophytes (moulds) produced similar BSR symptoms when tested under Koch’s postulate.

3.6.1 Real-time PCR assay

A total of 53 samples (24 pure culture-based isolates and 29 Ganoderma Basidiocarps) were amplified. ITS/18rRNA gene sequencing and MLST (multilocus sequence typing) were subsequently used to further characterize and identify the Ganoderma fungi isolated from the initial infected samples. DNA extracted from the basidiocarps and the Ganoderma isolates from the infected oil palm were amplified using ITS/GanET gene sequencing primer pair. Multilocus sequence typing (MLST) produced a 320 bp fragment and sequenced as the DNA amplicon. A single separation line was observed in Temperature gradient gel Electrophoresis (TGGE) ( Figure 7) at the standard band corresponding to the ITS regions of Ganoderma sp. showing consistent results. There was no significant difference between the bands produced by the 29 genotypes of basidiocarps ( Figure 7B) and those of the culture-based samples ( Figure 7A) except for sample numbers (20) and (35) whose bands were very faint.

3.6.2 Sequence results

The ITS/ITS4/GanET gene sequence primer pair from the amplified samples showed top matches of >97% to sequences assigned to members of the genus Ganoderma. Fully (and validly) named matches of >98% included 99.3% identity to three sequences of Ganoderma sp. (HM138671; HM138670 and HM138672) generated from strains assigned to Ganoderma ryvardenii (syn. Ganoderma ryvardense). Sequence HM138671 is from the type strain of G. ryvardenii. (HKAS58053). A match of 99% was also obtained to sequence MN809325 from Ganoderma wiiroense strain LDCMY02. Other best matches notified to published strains were only at 92.0-95.6% identity to sequences assigned to G . boninense. Out of total sample amplified, 89% of the sequence obtained matches G. ryvardenii, 7 % to G. wiiroense and 4 % matches G. boninense.

3.6.3 Proof of Koch’s postulate

3.6.3.1 Re-isolation and Molecular confirmation of Ganoderma fungi after pathogenicity test

Amplification of the DNA extracted from the bole and root tissues of the artificially inoculated oil palm seedlings using the ITS1/ITS4 primer pair produced similar base pairs (320 bp) of DNA fragment, which was the same size sequenced as the amplicon of DNA ( Figure 7B) from Ganoderma pure culture ( Figure 4). The identity of the fungi was confirmed again as Ganoderma ryvardenii via the sequencing of the ITS primer pair amplified products. All the isolates obtained after artificial inoculation had their ITS region sequences that were split into a single line and belonged to the taxon Ganoderma which has 99.3% of its gene sequence similarities with the strain of G. ryvardenii.

3.6.4 Phylogenetic results

The standard band quality of the overall amplification most likely corresponds to a novel species of Ganoderma.

The phylogenetic analyses using ITS sequences and their accession numbers confirmed the identification of a new Ganoderma species ( Figure 8B). Additionally, the majority of the obtained sequences were associated with Ganoderma ryvadenii with their corresponding accession numbers as indicated by the arrows in Figure 8B.

Field observations and percentage infection rates of Ganoderma in the selected oil palm plantations provide important information about the disease's spread, effects, and mechanism of transmission. Although BSR was initially found in palms older than 25–30 years old, it has recently been reported that the disease can affect younger palms, including those as young as one year old ( Zakaria, 2023).

This study showed a higher infection rate in the Eastern region than in the other two Regions surveyed. Despite the low disease incidence in the selected districts compared with the total number of palm trees analysed, the rate of disease spread was of grave concern. A similar observation was made by Lekete-Lawson et al. (2024) in a separate study on oil palm in Ghana.

The physiological features portrayed by the pathogen in this study, shared similar characteristics of Ganoderma species described by Bharudin et al. (2022) and Chong et al. (2017). According to these authors, basal stem rot (BSR) in oil palm is a disease caused by bracket fungi, producing basidiocarps which are perennial hard-knot and pinhead-like when immature; fan-shaped and large when mature; with irregular margins/blades (lamellae/gills). They are called Ganoderma fungi and are members of the phylum Basidiomycota and the family Ganodermataceae. Hushiarian et al. (2013) and Pilotti (2005) also reiterated that the basidiocarp is a typical characteristic feature of Ganoderma fungi. These basidiocarps are lignicolous and leathery and sometimes grow in a hoof-like form on the trunks of infected palms, just as observed in the present study ( Figure 2). Some of the heavily infected palms that were seen full of basidiocarps were rotten, fractured and collapsed as a result of the infection. Similarly, Siddiqui et al. (2021) and Josephin et al. (2024) observed that after the oil palm tree becomes infected, the fungus quickly spreads throughout the trunk tissues, causing the internal structures to deteriorate leading to the collapse and the death of the infected palms.

4.3.1 Macromorphological characteristic of culture of Ganoderma fungi

The isolated fungi were grouped based on their macromorphological characteristics and micrograph features. They were further ranked based on their taxonomy and percentage of occurrences. Research has shown that most Ganoderma species identified in the past were based on morphological characteristics ( Latiffah & Ho, 2005). However, studies by Mohd Rakib et al. (2014) showed that Ganoderma species are genetically heterogeneous and different based on their geographical origin, thus resulting in genetic variations even within the same species ( Hong et al., 2001). This was evident in the present study when the macromorphological characteristics of colonies of Ganoderma fungi isolated from the three regions appeared different.

The study showed slight differences in culture characteristics among the three Ganoderma isolates (GA, GD ₂B and TD ₂B) regarding their colony colour, texture and growth rate. The white and stranded mycelium, velvety with concentric cottony and hyphal-knot structure produced by GD ₂B isolates were similar to what was found in the studies conducted by Beck et al. (2018) and Badalyan et al. (2015) on several Ganoderma species, in which some species of Ganoderma appeared as cottony texture with powdery radiating parallel hyphae which were white and later changed to lemon yellowish. TD ₂B appeared white, fluffy, cottony and velvety but turned yellowish-brown as it progressed. Mohanty et al. (2011) discovered that some Ganoderma species age as their colonies turn yellowish to brown.

The varied growth rate observed among the isolates with GA exhibiting the fastest growth rate could depend on several variables, including the culture's duration, the media's composition, the ambient temperature and the media composition. According to Gáperová and Petrýdesová (2009) several elements, including light, temperature, medium volume, nutritional component ratio, and others, might influence the properties of mycelia under study. Although our findings suggest that the macromorphological traits of cultures and the mycelium's growth rate may be utilised to identify specific Ganoderma species, more research is needed to distinguish individual species.

4.4.1 Source of inoculum

Triplochiton scleroxylon (Wawa woodblocks-(WWBs)) used for inoculum in this study helped to retain the survival of isolated fungi for the inoculation. The studied Ganoderma fungi (GA, TD ₂B and GD ₂B) were able to colonise the inoculated WWBs but at varied degrees of myceliation. According to Mangaiha et al. (2019), woody debris (inoculum) plays an important role in the long-term survival of Ganoderma fungi. They enhance the resistance of the growth of Ganoderma fungi against environmental stress ( Loyd et al., 2018). Woodblocks (WWBs), as a source of inoculum, produced successful infection on oil palm germinated seeds.

Although, research revealed that Rubberwood block (RWB) is an ideal substrate that improves the long-term survival, biological yield and productivity of Ganoderma fungi ( Breton et al. (2006); Alexander, (2017) and Nusaibah et al. (2016)), however, an experiment conducted by Angel et al., (2021) showed that if RWB becomes scarce, other substrates, including sawdust and wood chippings, could be used as a source of inoculum, through non-invasive tissue culture techniques. This was confirmed in this study when Wawa woodblock (WWB) as a substrate and inoculum source, was able to establish Ganoderma infection on the oil palm germinated seed nuts marking the first successful attempt at using the tissue culture technique for establishing Ganoderma infections on oil palm germinated seed nuts in Ghana. Nonetheless, other isolated fungi such as Trichoderma, Phytophthora, Fusarium, Xylaria, and others (moulds) were not able to colonise the substrate (WWBs).

Breton et al . (2005, 2006) showed a positive correlation between germinated seeds and 3-month-old seedlings in the discrimination between progenies for their susceptibility to Ganoderma. Although the formation of Ganoderma basidiocarps was not observed in this experiment probably due to the short time allocation and the substrate used, the disease symptoms, displayed by GA, GD2B and TD2B isolates were similar to those of a typical BSR disease in young seedlings. Similar features were also observed by Angel et al. (2021) after post-inoculation of plantlets with sawdust inoculum which displayed physiological symptoms of the disease that resembled those of a typical BSR infection. Unlike inoculation tests on 3-month-old seedlings that had been conducted by previous researchers including Idris et al. (2004) and Rees et al. (2007), the results of this study have shown that in vitro inoculation test can be used as an alternative to reduce the age needed for inoculation techniques, shortening inoculation duration, and ensure consistency in experimental results.

4.6.1 Pathogenicity variation

The results suggest robust evidence against the null hypothesis, indicating that all isolates tested in this study exhibit a higher degree of pathogenicity. However, some disparities were observed in the aggressiveness of isolated Ganoderma fungi from the Eastern, Western, and Central regions of Ghana comparing their pathogenicity against control. GA isolate has the most virulent pathogenic effect causing the highest disease infection and death of the test seed nuts. This points to the fact that GA is likely responsible for the majority of BSR infections in the selected oil palm plantations in Ghana. The variations in the level of pathogenicity identified among the Ganoderma isolates in this study correspond to findings by Lo et al. (2023), Goh et al. (2014), Mohd Rakib et al. (2014) and Breton et al. (2006). These individual authors also observed some differences in the degree of pathogenicity of Ganoderma pathogens on oil palms from different geographical locations. For instance, Lo et al. (2023) and Mohd Rakib et al. (2014), observed that there were some variations in aggressiveness within the species of Ganoderma boninense obtained from infected oil palms at different estates in Sarawak.

Breton et al. (2006) discovered that G. boninense isolates from different plantations in Indonesia had varying levels of aggressiveness. Likewise, in Malaysia, the transmission rate of Ganoderma disease varies by estate, potentially indicating differences in G. boninense aggressiveness across isolates from different regions ( Goh et al., 2014). Mohd Rakib et al. (2014) also revealed similar observations about the significant variation in the aggressiveness levels of Ganoderma species isolated from different areas. The authors observed that G. boninense and G. zonatum isolated from Betong and Miri differed in their aggressiveness. This was demonstrated when all the Ganoderma isolates obtained from various oil palm growing areas in Ghana showed varied responsiveness in their disease establishment.

The gradual decline of growth among the germinated seed nuts after being inoculated with Ganoderma isolates was observed. From day 14, the virulence factor of GA isolates from the Eastern region could be clearly distinguished from the others (TD ₂B and GD ₂B). The effect of the isolated fungi appeared after 15 days of incubation with initial infection of lesions forming on the roots of the inoculated seed nuts. This corresponds with the characteristic infection pattern by Ganoderma spp. as reported by Rees et al. (2007) and Breton et al. (2006). According to Rees et al. (2007), Ganoderma infection usually starts from the root system of the infected palms when in direct contact with the inoculum. Isolate GA has the strongest pathogenic effect on the test seed nuts, compared to isolate TD ₂B. However, the pathogenic effect of TD ₂B isolate is still highly significant (p<0.05).

The highest external symptoms and seedling death was observed in the seed nuts inoculated with GA and TD ₂B fungi whereas the lowest severity was observed in the GD ₂B treated seed nuts. Apparently, none of the other isolated fungi ( Trichoderma, Xylaria, Fusarium and Phytophthora and saprophytes (moulds) were able to produce similar BSR symptoms observed on the original samples when tested under Koch’s postulate.

4.7.1 Real-time PCR assay

Despite the weak fragment shown in the band formation of samples 20 and 35, probably due to PCR inhibitors, the standard band quality of the overall amplification most likely corresponds to a novel species of Ganoderma. He et al ., (2022) predicted that approximately 1.4 to 4.2 million species of Basidiomycota will be discovered worldwide by 2030, as over 54,000 have already been reported. Since the coming of the molecular age, several species previously described morphologically are now redefined as new taxa in addition to the finding of new taxa. To this effect, there are now over 36,000 Basidiomycota species, according to a comprehensive systematic survey using molecular data ( Begerow et al. 2018).

The molecular tools employed in this experiment allowed us to differentiate between numerous fungal species of Ganoderma disease that are present in Ghana's oil palm fields. Sequences of other phylogenetic markers useful in the phylogeny of Ganoderma fungi supported our hypothesis that the isolates most likely represent a novel species of Ganoderma. For instance, the majority of the ITS sequences of Ganoderma sp. [HM138671; HM138670 and HM138672] generated from strains assigned to Ganoderma ryvardenii (syn. Ganoderma ryvardense) HM138671; HM138670 and HM138672 published in Mycosphere 2 (2): 179–188. Of these, sequence HM138671 is from the type of strain of G. ryvardenii. (HKAS58053). There was a single match of 100% to sequence MN809325 from Ganoderma wiiroense strain LDCMY02 but this has not been published in a peer-reviewed publication and is quite distinct from other sequences of G. wiiroense in GenBank, so it is discounted here. Thereafter, the third-best matches to published strains were also identified to sequences assigned to G. boninense.

Additionally, the sequence alignment in phylogenetic tree building also revealed high similarities among Ganoderma strains identified in Cameroon (HKAS58053) and the new strains identified in Ghana (HM138671; HM138670 and HM138672). As such the phylogenetic analyses based on ITS sequences and their accession numbers confirmed the novelty of this Ganoderma species on oil palm in Ghana. This finding enhances our understanding of the diversity and distribution of specific Ganoderma species within African mycobiota. This also confirms the initial discovery made by Kinge and Mih (2011), who first reported the pathogen on oil palm in Cameroon and gave the species name as Ganoderma ryvardense with the specific epithet in honour of Lief Ryvarden, a distinguished mycologist who has contributed significantly to genus Ganoderma and African mycobiota. (Mycosphere 2 (2): 179–188). Evidently, this is the first report of G. ryvardenii causing BSR disease on oil palm in Ghana and possibly second in West Africa.