A 20-kb lineage-specific genomic region tames virulence in pathogenic amphidiploid Verticillium longisporum
Harting, Rebekka; Starke, Jessica; Kusch, Harald; Pöggeler, Stefanie; Maurus, Isabel; Schlüter, Rabea; Landesfeind, Manuel; Bulla, Ingo; Nowrousian, Minou; de Jonge, Ronnie; Stahlhut, Gertrud; Hoff, Katharina J; Aßhauer, Kathrin P; Thürmer, Andrea; Stanke, Mario; Daniel, Rolf; Morgenstern, Burkhard; Thomma, Bart P H J; Kronstad, James W; Braus-Stromeyer, Susanna A; Braus, Gerhard H
(2021) Molecular Plant Pathology, volume 22, issue 8, pp. 939 - 953
(Article)
Abstract
Amphidiploid fungal Verticillium longisporum strains Vl43 and Vl32 colonize the plant host Brassica napus but differ in their ability to cause disease symptoms. These strains represent two V. longisporum lineages derived from different hybridization events of haploid parental Verticillium strains. Vl32 and Vl43 carry same-sex mating-type genes derived from both
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parental lineages. Vl32 and Vl43 similarly colonize and penetrate plant roots, but asymptomatic Vl32 proliferation in planta is lower than virulent Vl43. The highly conserved Vl43 and Vl32 genomes include less than 1% unique genes, and the karyotypes of 15 or 16 chromosomes display changed genetic synteny due to substantial genomic reshuffling. A 20 kb Vl43 lineage-specific (LS) region apparently originating from the Verticillium dahliae-related ancestor is specific for symptomatic Vl43 and encodes seven genes, including two putative transcription factors. Either partial or complete deletion of this LS region in Vl43 did not reduce virulence but led to induction of even more severe disease symptoms in rapeseed. This suggests that the LS insertion in the genome of symptomatic V. longisporum Vl43 mediates virulence-reducing functions, limits damage on the host plant, and therefore tames Vl43 from being even more virulent.
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Keywords: Verticillium longisporum, genome comparison, hybridization, lineage-specific region, pathogenicity, Molecular Biology, Agronomy and Crop Science, Soil Science, Plant Science
ISSN: 1464-6722
Publisher: Wiley-Blackwell
Note: Funding Information: The authors thank Nicole Scheiter, Anne Reinhard, and Stefan Bock for excellent technical assistance, Clara Hoppenau, Kai Nesemann, and Christian Timpner for genomic DNA, Luigi Faino for PacBio annotation support, Andreas von Tiedemann, Derek Barbara, and Riccardo Baroncelli for V.?longisporum strains, the Norddeutsche Pflanzenzucht for B. napus seeds, and Miriam Leonard, Annalena H?fer, and Alexandra Nagel for support. J.S. and I.M. were supported by IRTG 2172 PRoTECT and CREATE (co-directed by J.W.K.) from the Natural Sciences and Engineering Research Council of Canada. Funding was provided by DFG grant BR1502-15-1 and the BMBF BioFung project. M.N. was supported by DFG grant NO407/5-1 and thanks Ulrich K?ck and Christopher Grefen for support at Ruhr-Universit?t Bochum. Open-access funding enabled and organized by ProjektDEAL. Funding Information: The authors thank Nicole Scheiter, Anne Reinhard, and Stefan Bock for excellent technical assistance, Clara Hoppenau, Kai Nesemann, and Christian Timpner for genomic DNA, Luigi Faino for PacBio annotation support, Andreas von Tiedemann, Derek Barbara, and Riccardo Baroncelli for . strains, the Norddeutsche Pflanzenzucht for . seeds, and Miriam Leonard, Annalena Höfer, and Alexandra Nagel for support. J.S. and I.M. were supported by IRTG 2172 PRoTECT and CREATE (co‐directed by J.W.K.) from the Natural Sciences and Engineering Research Council of Canada. Funding was provided by DFG grant BR1502‐15‐1 and the BMBF BioFung project. M.N. was supported by DFG grant NO407/5‐1 and thanks Ulrich Kück and Christopher Grefen for support at Ruhr‐Universität Bochum. Open‐access funding enabled and organized by ProjektDEAL. V longisporum B napus Publisher Copyright: © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd
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