Marco Papageorgiou
Proposal
The oil palm crop was brought to South East Asia via the British in the 1870s, from its original location in West
Africa (Hushiarian et al., 2013). Oil palm (Elaeis guineensis) production from Malaysia and Indonesia, the two
largest producers (Durand-Gasselin et al., 2005), contribute between 84-85% of the worlds production
(Hushiarian et al., 2013; Ho et al., 2014). Further, oil palm is agriculturally vital to Malaysia, producing a range
of products from vegetable oil, cosmetics and biofuels (Paterson et al., 2008), and, consisting a nationwide total
of 5 million hectares, which concurrently contributes 31.4% of the world’s oil palm (Rakib et al., 2014).
Oil palm is subsequently affected by several pests and diseases; basal stem rot (BSR) and upper stem rot (USR)
are such oil palm diseases (Rakib et al., 2014; Sahebi et al., 2014; Lim et al., 2005), caused from the
basidiomycete, Ganoderma boninense (Pilotti et al., 2003). The source of BSR has been linked to
basidiospores, in which high numbers are capable of long distance travelling from their initial release from
basidiocarps; ultimately entering oil palm wounds hitherto created from planting, harvesting and crop
management practices (Ho et al., 2015; Rees et al., 2009). It has also ben suggested that another source of
Ganoderma spp. infections occur through previous palm plantation debris, in which Ganoderma utilise in order
to initiate oil palm root infection (Ho et al., 2015).
Although there are indeed several different species of Ganoderma, Ganoderma boninense has been labelled as
a major oil palm virulent, which continues on to be the causative agent of BSR; with several other species
attributes to diseases in grapevines, pal, rubber, and tea (Ho et al., 2015; Sahebi et al., 2014). Collectively, a
total of 15 Ganoderma species have been detected in oil palm (Ho et al., 2015). The severity of these stem rot
diseases is further exacerbated from the lack of understanding and clarity of this pathogen. From an economical
perspective, G. boninense has caused financial losses from between RM225 million to RM1.5 billion each year
(Husharian et al., 2013). With these facts taken into consideration, the oil palm pathogenic infection has
lowered the overall productivity of the crop. To date, there is still no economically feasible approach at
controlling disease caused by G. boninense (Durand-Gasselin et al., 2005).
The fungus, caused by Ganoderma boninense, consequently causes white rot of the wood from the breakdown
of lignin, thus exposing spongy and fibrous cellulose (Tan et al., 2013; Paterson 2007). Ganoderma spp.
produce and secrete several key compounds that work to degrade this host cell lignin (syringyl uniting oil palm
trunks), lowering the shielding effect from microbial attack.
A plant will recognise and respond to pathogenic attack through means pertaining to the expression of
molecular effectors and other molecules. The mode of Ganoderma invasion begins with a oil palm root
invasion of fungal mycelia which penetrate and spread to the shoots (Sahebi et al., 2014). This is followed by
the collapse of the trunk. Ganoderma can be spread via airborne basidiospores, insects, spore transfer, and
mycelial root contact (Kwan et al., 2014); and, it is considered that infection of oil palm by Ganoderma occurs
via contact of palm roots with colonised debris living within soil (Pilotti et al., 2003). Additionally, and
secondary to this mode of infectivity by Ganoderma, is the spreading of Ganoderma pathogens through the
contact of living palm roots with each-other (Pilotti et al., 2003).
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Marco Papageorgiou
Next Generation Sequencing (NGS) technologies, such as Genome-wide associations studies (GWAS) can be
readily employed in order to map and identify a magnitude of allelic variations (Yano et al., 2016). Current
methods to control basal stem rot (BSR) involve the use of fungicides, along with conventional cultural
practices which include elimination and burning of those infected oil palm crops (Tan et al., 2013). Oil palm
genes relating to the tolerance and resistance of G. boninense are yet to be fully characterised; and this places a
clear emphasis and need to profile those differentially expressed genes, and their transcripts, which are
associated with molecular events that occur between the host and G. boninense virulent.
This profiling can be undertaken by the incorporation of next-generation sequencing methodologies. As a result,
from generating and charactering molecular interactions, several biomarkers may help the process of detecting
BSR. These studies could also facilitate, and incorporate, the use of conventional PCR and qPCR to quantify
molecular biomarker candidates based on G. boninense - oil palm interactions. A molecular screening approach,
also referred to as an oil palm genetic improvement programs (Kwan et al., 2014), can be classified as a more
targeted and effective option when compared to current disease management practices, in place to eradicate the
BSR disease.
Gene-to-function using functional genomics (Robinson et al., 2009); the incorporation of mutagenised oil palm
lines could provide by utilised to show those genes which have a multipurpose role during inception with G.
boninense. By creating mutant phenotypes of oil palm genes, before treatment with G. boninense, a more
targeted approach, based on gene mutants, could facilitate a map of genetic pathways that are enabled through
infection from G. boninense providing a narrative built upon a gene or gene sets which have been inactivated.
Oil palm resistance could be a strategy (Ho et al., 2015) whereby an alteration of lignin biosynthesis is
facilitated (Paterson et al., 2008); these genetic manipulations would require changes in key enzymes that lead
to strengthened lignin, however would presume an additional layer of public discourse from the marketing of
GM palm oil products. Nonetheless, approaches to creating mutagenesis within oil palm genes could include:
•
•
•
•
RNAi
T-DNA inserts
Transposon inserts
EMS
At this stage, it would be advantageous to uncover the molecules representing defence mechanisms/pathways of
Ganoderma and oil palm interactions which can provide data pertaining to transcript abundance levels. This can
be assisted, and sped up, with appropriate screening and marker-assisted breeding programs which will
subsequently expose DNA makers, inherently associated with these defence-related transcripts (Ho et al.,
2015). Molecular markers, identified through application of marker technologies, can be utilised against a
criterion which considers high value traits (Appleby et al., 2009) associated with Ganoderma and oil palm
interactions.
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Marco Papageorgiou
A new approach is currently underway; a genetic/molecular approach to identify those genes involved in
defence against Ganoderma spp; specifically G. boninense.
By utilising large-scale genetic screening on oil palm - Ganoderma interactions, the downstream expression of
genes associated with this plant-pathogen will provide insights as to which oil palm species are more tolerable
and/or resistant to G. boninense infections. The next steps of oil palm research will require a closer focus and
analysis of oil palm defence pathways, in G. boninense infections, in alignment with those already established
and outlined. This disease-resistance of oil palm research should also consider hormonal responses to other
Ganodema species at different infection phases (Ho et al., 2015). In addition to pinning the exact expressed
genes, and their mRNA transcript abundances, involved in oil palm - Ganoderma spp, it could also be
beneficial to apply structural biology studies to determine the biological processes that unfold at the protein
interaction level. This not only adds value by more precisely illustrating gene function from comparative
studies on non-inoculated and inoculated oil palm with Ganoderma; but also contributes to oil palm gene
databases (Hrmova et al., 2009).
Digging deeper, 3D structural studies on oil palm defence molecules can help define the possibility of any
complex interactions between gene/protein and pathogenic protein from assemblies transcription complexes,
and/or plant membrane-bound transporters, and signalling transduction (Hrmova et al., 2009). The merging of
functional genomics, withs structural biology and plant cell biology will be better positioned to model oil palm
defence pathways in reaction to Ganoderma infection; this can be practically applied within the purview of
generating oil palm genomics programs that seek to label, compare, and clearly describe those oil palm
products associated with mRNA transcript data, based on Ganoderma inoculation, with their respective
function at the protein-protein interaction level.
This combination of NGS, transcript abundance data, and subsequent 3D structural information, should be
appropriately included and carried out within the context of comparative studies based on G. boninense stage
infection on oil palm.
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Marco Papageorgiou
References:
Nikki Appleby, David Edwards, and Jacqueline Batley, 2009. New Technologies for Ultra-High Throughput
Genotyping in Plants. Methods in Molecular Biology, Plant Genomics, vol. 513.
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Possible sources of genetic resistance in oil palm (Elaeis guineensis Jacq.) to basal stem rot caused by
Ganoderma boninense - prospects for future breeding. Mycopathologia, vol. 159, pp. 93-100.
Maria Hrmova and Geoffrey B. Fincher, 2009. Functional Genomics and Structural Biology in the Definition of
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Marco Papageorgiou
Mahbod Sahebi, Mohammad M. Hanafi, Mui-Yun Wong, A.S. Idris, Parisa Azizi, Mohammad Faseleh Jahromi,
Parisa Shokryazdan, Rambod Abiri, Hasmah Mohidin, 2015. Towards immunity of oil palm against Ganoderma
fungus infection. Acta Physiology Plant, vol. 37, no. 195.
Yung-Chie Tan, Mui-Yun Wong, Chai-Ling Ho, 2015. Expression profiles of defence related cDNAs in oil palm
(Elaeis guineensis Jacq.) inoculated with mycorrhizae and Trichoderma harzianum Rifai T32. Plant Physiology
and Biochemistry, Vol. 96, pp. 296-300.
Yung-Chie Tan, Keat-Ai Yeoh, Mui-Yun Wong, Chai-Ling Ho, 2013. Expression profiles of putative defencerelated proteins in oil palm (Elaeis guineensis) colonised by Ganoderma boninense. Journal of Plant
Physiology, vol. 170, pp-.
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