Theoretical and Applied Genetics

, Volume 109, Issue 1, pp 215–224 | Cite as

Molecular mapping of resistance to Fusarium head blight in the spring wheat cultivar Frontana

  • B. Steiner
  • M. Lemmens
  • M. Griesser
  • U. Scholz
  • J. Schondelmaier
  • H. BuerstmayrEmail author
Original Paper


Fusarium head blight (FHB) is a destructive disease of wheat. The objective of this study was to characterise the FHB resistance of the Brazilian spring wheat cultivar Frontana through molecular mapping. A population of 210 doubled-haploid lines from a cross of Frontana (partially resistant) and Remus (susceptible) was evaluated for FHB resistance during three seasons. Spray and single-spikelet inoculations were applied. The severity, incidence and spread of the disease were assessed by visual scoring. The population was genotyped with 566 DNA markers. The major QTL effect associated with FHB resistance mapped to chromosome 3A near the centromere, explaining 16% of the phenotypic variation for disease severity over 3 years. The most likely position is in the Xgwm720–Xdupw227 interval. The genomic region on 3A was significantly associated with FHB severity and incidence in all years evaluated, but not with FHB spread, indicating the prominent contribution of this QTL to resistance against initial infection. The map interval Xgwm129–Xbarc197 on chromosome 5A also showed consistent association with FHB severity and accounted for 9% of the phenotypic variation. In addition, smaller effects for FHB severity were identified on chromosomes 1B, 2A, 2B, 4B, 5A and 6B in single years. Individual QTLs for resistance to FHB spread accounted for less than 10% of the variation in trait expression. The present study indicates that FHB resistance of Frontana primarily inhibits fungal penetration (type I resistance), but has a minor effect on fungal spread after infection (type II resistance).


Plant Height Fusarium Head Blight Composite Interval Mapping Fusarium Head Blight Resistance Fusarium Head Blight Severity 
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We thank M. Roeder (IPK Gatersleben, Germany) for screening SSR markers and P. Cregan and Q. Song (USDA ARS, Beltsville, USA) for supplying unpublished ‘BARC’ SSR primers. The excellent technical assistance of M. Stierschneider and M. Fidesser (IFA-Tulln, Austria) is gratefully acknowledged. We thank M. Skrzypczak (Winnipeg, Canada) and B. Hackauf (Gross Luesewitz, Germany) for providing PCR protocols for ‘M13-tailed’ primers and thank B.S. Gill (Kansas State University, USA) and M.E. Sorrells (Cornell University, USA) for allowing us the use of their RFLP clones. We are also grateful to H. Toubia-Rahme (IFA-Tulln, Austria) and D. Mather (McGill University, Canada) for their suggestions to improve the manuscript. This work was supported by the Austrian Federal Ministry for Education, Science and Culture project GZ 309.006/3-VIII/B/8/2000 and by the EU-funded FUCOMYR project, contract QLRT-2001–02044: ‘Novel tools for developing Fusarium-resistant and toxin-free wheat for Europe’.


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Copyright information

© Springer-Verlag 2004

Authors and Affiliations

  • B. Steiner
    • 1
  • M. Lemmens
    • 1
  • M. Griesser
    • 1
  • U. Scholz
    • 1
  • J. Schondelmaier
    • 2
  • H. Buerstmayr
    • 1
    Email author
  1. 1.Department of Biotechnology in Plant ProductionIFA-Tulln, Institute for AgrobiotechnologyTullnAustria
  2. 2.Saaten-Union Resistenzlabor GmbHLeopoldshoeheGermany

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