Abstract

Monilinia fructicola and Monilinia laxa species are the most destructive and economically devastating fungal plant pathogens causing brown rot disease on stone and pome fruits worldwide. Mitochondrial genomes (mitogenomes) play critical roles influencing the mechanisms and directions of the evolution of fungal pathogens. The pan-mitogenomics approach predicts core and accessory regions of the mitochondrial genomes and explains the gain or loss of variation within and between species. The present study is a fungal pan-mitogenome of M. fructicola (N = 8) and M. laxa (N = 8) species. The completely sequenced and annotated mitogenomes showed high variability in size within and between the species. The mitogenomes of M. laxa were larger, ranging from 178,351 to 179,780bp, than the mitogenomes of M. fructicola, ranging from 158,607 to 167,838bp. However, size variation within the species showed that M. fructicola isolates were more variable in the size range than M. laxa isolates. All the mitogenomes included conserved mitochondrial genes, as well as variable regions including different mobile introns encoding homing endonucleases or maturase, non-coding introns, and repetitive elements. The linear model analysis supported the hypothesis that the mitogenome size expansion is due to presence of variable (accessory) regions. Gene synteny was mostly conserved among all samples, with the exception for order of the rps3 in the mitogenome of one isolate. The mitogenomes presented AT richness; however, A/T and G/C skew varied among the mitochondrial genes. The purifying selection was detected in almost all the protein-coding genes (PCGs) between the species. However, cytochrome b was the only gene showing a positive selection signal among the total samples. Combined datasets of amino acid sequences of 14 core mitochondrial PCGs and rps3 obtained from this study together with published mitochondrial genome sequences from some other species from Heliotales were used to infer a maximum likelihood (ML) phylogenetic tree. ML tree indicated that both Monilinia species highly diverged from each other as well as some other fungal species from the same order. Mitogenomes harbor much information about the evolution of fungal plant pathogens, which could be useful to predict pathogenic life strategies.

Highlights

  • Fungi are one of the most remarkable and diverse kingdom, with approximately 720,256 species compared with other eukaryotic organisms worldwide (Blackwell, 2011; Badotti et al, 2017)

  • Amino acid translation of the protein-coding genes (PCGs) in the mitochondrial genomes of M. fructicola and M. laxa isolates were obtained based on the mitochondrial translation code data four using the Geneious 9.1.8 program (Kearse et al, 2012)

  • To strengthen the evolutional relationships between our data and other genera of the Helotiales, amino acid sequences of each of the PCGs and ribosomal protein were included from published mitochondrial genome data

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Summary

Introduction

Fungi are one of the most remarkable and diverse kingdom, with approximately 720,256 species compared with other eukaryotic organisms worldwide (Blackwell, 2011; Badotti et al, 2017). The presence of mitochondrial-encoded ribosomal protein genes, such as rps, and its homologs (var and S5) differs among fungal groups, and these genes may have been transferred to the nuclear genomes in different eukaryotic species (Bullerwell et al, 2000; Smits et al, 2007; Sethuraman et al, 2009; Korovesi et al, 2018; Yildiz and Ozkilinc, 2020). Copy number, gene duplications, gain/loss of introns, and transposable and repetitive elements are the main factors causing mitogenome variations (Basse, 2010; Aguileta et al, 2014). Because of these factors, mitogenome sizes may vary within and among fungal taxonomic groups (Burger et al, 2003). Recent studies showed that homing endonucleases, such as GIY-YIG and LAGLIDADG families, play a significant role in shaping fungal genome structure and contribute to variations within and between species (Sandor et al, 2018; Kolesnikova et al, 2019; Yildiz and Ozkilinc, 2020)

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