Genome Comparisons between <i>Botrytis fabae</i> and the Closely Related Gray Mold Fungus <i>Botrytis cinerea</i> Reveal Possible Explanations for Their Contrasting Host Ranges
Klaus Klug | Pinkuan Zhu | Patrick Pattar | Tobias Mueller | Nassim Safari | Frederik Sommer | Claudio A. Valero-Jiménez | Jan A. L. van Kan | Bruno Huettel | Kurt Stueber | David Scheuring | Michael Schroda | Matthias Hahn
While <i>Botrytis cinerea</i> causes gray mold on many plants, its close relative, <i>Botrytis fabae</i>, is host-specifically infecting predominantly faba bean plants. To explore the basis for its narrow host range, a gapless genome sequence of <i>B. fabae</i> strain G12 (BfabG12) was generated. The BfabG12 genome encompasses 45.0 Mb, with 16 chromosomal telomere-to-telomere contigs that show high synteny and sequence similarity to the corresponding <i>B. cinerea</i> B05.10 (BcB0510) chromosomes. Compared to BcB0510, it is 6% larger, due to many AT-rich regions containing remnants of transposable elements, but encodes fewer genes (11,420 vs. 11,707), due to losses of chromosomal segments with up to 20 genes. The coding capacity of BfabG12 is further reduced by nearly 400 genes that had been inactivated by mutations leading to truncations compared to their BcB0510 orthologues. Several species-specific gene clusters for secondary metabolite biosynthesis with stage-specific expression were identified. Comparison of the proteins secreted during infection revealed high similarities, including 17 phytotoxic proteins that were detected in both species. Our data indicate that evolution of the host-specific <i>B. fabae</i> occurred from an ancestral pathogen with wide host range similar to <i>B. cinerea</i> and was accompanied by losses and degeneration of genes, thereby reducing its pathogenic flexibility.
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