3. Bilsel International Efes Scientific Researches and Innovatıon Congress, İzmir, Türkiye, 22 Mart 2024, ss.349, (Özet Bildiri)
Fusarium head blight (FHB) is one of the most devastating diseases of cereals worldwide. Genomic plasticity
and the relatively high level of polymorphisms in chromosomal and mitochondrial genomes (mitogenome,
"mtDNA") of FHB pathogens are important reasons for failure to control FHB. In this study, mtDNA genome
based phylogenetic analysis were carried out in causal agents of FHB with totally 20 accessions (Fusarium
graminearum with 15 members, F. culmorum, F. avenaceum, F. pseudograminearum, F. poae, F. proliferatum,
and F. solani-F.oxysporum as outer groups). Nucleotide sequences of mtDNA were obtained from GenBank.
Sequence similarity and UPGMA trees were constructed by MAFFT software. R/RStudio (with packages of
"ape", "phangorn", and "factoextra") was used to obtain distance matrix, maximum likelihood (ML)
dendrogram, and principal component (PCA) analysis-derived data of FHB pathogens. Bayesian topology
analysis was carried out using MrBayes software via Ubuntu-Linux terminal. Individuals belonging to different
species showed markedly different clustering via ML and UPGMA dendrograms which included F.
graminearum members within the same sub-cluster. Distance matrix also supported this cluster profiling with
mean distance value as 41.75%. In PCA analysis, FHB pathogens were clustered together in Dim1 and Dim2
whereas F. solani and F.oxysporum (not FHB pathogens) were clustered distinctly. Percentages of dimensions
were as 93% and 6% for x and y axes meaning that FHB causal agents were genetically so similar for their
mtDNA phylogeny. Bayesian topology analysis showed that members of F. graminearum and remaining FHB
pathogens were genetically dissimilar with F. solani and F. oxysporum. It was found that mitogenome can
strongly differentiate Fusarium spp. not only at the species-specific level, but also in terms of pathogen
characteristics. Specific and potential marker genes located in mtDNA of FHB pathogens can also be
investigated in future studies for detailed characterization of FHB pathogens.