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Effects of non-adapted quantitative trait loci (QTL) for Fusarium head blight resistance on European winter wheat and Fusarium isolates
(2010) Ohe, Christiane von der; Miedaner, Thomas
Fusarium head blight (FHB), caused by Fusarium graminearum and F. culmorum, is a devastating disease responsible for tremendous damage in wheat fields and contamination of grain with mycotoxins deoxynivalenol (DON) and nivalenol (NIV), rendering the harvest unsafe for human and animal consumption. The variability of Fusarium populations is high and changes in aggressiveness, chemotypes or species within and among Fusarium populations are known. Stable FHB resistance combined with high yield is one main target in wheat breeding programs. Mapping studies detected several quantitative trait loci (QTL) for FHB resistance in non-adapted sources, such as Sumai3 from China. The two most important and commonly used major QTL are located on chromosome 3BS (Fhb1) und 5A (Qfhs.ifa-5A). However, negative side effects of non-adapted resistance sources introgressed in elite winter wheat material are feared in Europe. Furthermore, the stability of the QTL effect against changing Fusarium populations is unknown. The objectives of this research were to analyze whether (1) the QTL Fhb1 and Qfhs.ifa-5A introgressed from a non-adapted resistance source into two winter wheat varieties have possible side effects on agronomic and quality performance, (2) 3-ADON and 15-ADON chemotypes are significantly different in their aggressiveness and DON production, (3) competition among Fusarium isolates in mixtures exists, and if so, how the resistant host will influence this competition. In conclusion, both resistance QTL are effective and stable in elite spring and winter wheat backgrounds. For improvement of FHB resistance both QTL are valuable, but Qfhs.ifa-5A would suffice for European breeding programs. Due to chemotype shifts, 3-ADON isolates could pose a greater risk to food safety than 15-ADON but breeding and use of highly resistant lines can reduce the risks associated with DON in wheat. Accordingly, resistant spring wheat lines were less affected by the tested Fusarium isolates and mixtures and, therefore, confirmed a high stability of these QTL. Directed selection of highly aggressive isolates due to the resistance QTL seems to be unlikely in the short term.
Inheritance of quantitative resistance and aggressiveness in the wheat/Fusarium pathosystem with emphasis on Rht dwarfing genes
(2010) Voß, Hans-Henning; Miedaner, Thomas
Fusarium head blight (FHB), or scab, is one of the most devastating fungal diseases affecting small-grain cereals and maize, causing severe yield losses and contamination of grain with mycotoxins such as deoxynivalenol (DON) worldwide. Fusarium graminearum (teleomorph Gibberella zeae) and Fusarium culmorum are the most prevalent Fusarium species in wheat production in Central and Northern Europe. Breeding for increased resistance to FHB in wheat is considered the most effective strategy for large scale disease management and mycotoxin reduction. Height reducing Rht genes are extensively used in wheat breeding programmes worldwide in order to improve lodging resistance and yield potential, with Rht-D1b being the most important Rht allele in Northern Europe. However, their individual effects on FHB resistance are yet unclear. Due to the incremental approach to increase host resistance the question arises whether the Fusarium pathogen has the capability to adapt by increased aggressiveness and/or increased mycotoxin production. Therefore, the objectives of the present study were to investigate the effects on FHB resistance of Rht-D1b and additional Rht alleles, the segregation variance for FHB resistance and identification of FHB resistance QTL in subsequent mapping analyses in three crossing populations segregating for the semi-dwarfing Rht-D1b allele and two sets of isogenic wheat lines. Regarding the pathogen, the study aims to determine the segregation variance in two F. graminearum crosses of highly aggressive parental isolates and to examine the stability of host FHB resistance, pathogen aggressiveness and the complex host-pathogen-environment interactions in a factorial field trial. All experiments were conducted on the basis of multienvironmental field trials including artificial inoculation of spores. The presence of Rht-D1b resulted in 7-18% reduction in plant height, but considerably increased FHB severity by 22-53% within progenies from three tested European elite winter wheat crosses. In the following QTL mapping analyses the QTL with the strongest additive effects was located at the Rht-D1 locus on chromosome arm 4DS and accordingly coincided with a major QTL for plant height in all three wheat populations. On total, a high number of 8 to 14 minor QTL for FHB reaction that were found in the three populations which emphasised the quantitative inheritance of FHB resistance in European winter wheat. The detected QTL mostly showed significant QTL-by-environment interactions and often coincided with QTL for plant height. By means of isogenic lines in the genetic background of the variety Mercia, Rht-D1b and Rht-B1d significantly increased mean FHB severity by 52 and 35%, respectively, compared to the wild-type (rht). Among the Maris Huntsman data set, the Rht alleles increased mean FHB severity by 22 up to 83%, but only the very short lines carrying Rht-B1c or Rht-B1b+Rht-D1b showed significance. The analyses of 120 progenies of the crosses from each of the highly aggressive parental F. graminearum isolates revealed significant genetic variation for aggressiveness, DON and fungal mycelium production following sexual recombination. This variation resulted in stable transgressive segregants towards increased aggressiveness in one of the two progeny. The factorial field trial, including eleven F. graminearum and F. culmorum isolates varying in aggressiveness and seven European elite winter wheat varieties, varying in their FHB resistance level, displayed no significant wheat variety × isolate interaction. Nevertheless, isolates possessing increased aggressiveness significantly increased FHB severity and DON production at a progressive rate on varieties with reduced FHB resistance. In conclusion, the analysed Rht alleles led to differently pronounced negative effects on FHB resistance that strongly depended on the genetic background. However, significant genetic variation for FHB resistance exists for selection and, thus, to largely counteract these effects by accumulating major and minor FHB resistance QTL. Significant genetic variation for aggressiveness among F. graminearum and the capability to increase its level of aggressiveness beyond yet known levels simply by sexual recombination may lead to long term erosion of FHB resistance. The rate at which increased aggressiveness develops will depend on the selection intensity and whether it is of constant, episodic or balanced nature. Consequently, the selection pressure imposed on the pathogen should be minimized by creating and maintaining a broad genetic base of FHB resistance that relies on more than one genetically unrelated resistance source by combining phenotypic and marker-assisted selection to achieve a sustainably improved FHB resistance in wheat breeding.
Molecular and phenotypic analyses of pathogenicity, aggressiveness, mycotoxin production, and colonization in the wheat-Gibberella zeae pathosystem
(2004) Cumagun, Christian Joseph R.; Miedaner, Thomas
Fusarium head blight (FHB), caused by Gibberella zeae (Schwein.) Petch (anamorph: Fusarium graminearum Schwabe), is one of the principal diseases responsible for extensive damage in wheat fields and contamination of grain with the mycotoxins deoxynivalenol (DON) and nivalenol (NIV), rendering the harvest unsafe for human and animal consumption. Control of FHB is difficult because of the complex nature of host-pathogen-environment interaction and the nonavailability of highly effective fungicides. Agronomic practices and resistance breeding, therefore, offer the best strategies for disease management. Mapping by molecular markers provides an accurate approach for genetic analyses of simple and complex traits particularly pathogenicity, aggressiveness, and mycotoxin production. Pathogenicity, as defined here, is the ability to cause disease whereas aggressiveness is the quantity of disease induced by a pathogenic isolate on a susceptible host in which isolates do not interact differentially with host cultivars. The project aims to (1) map pathogenicity and aggressiveness of G. zeae based on a published genetic map (2) estimate genetic diversity of four parent isolates by PCR-based markers (3) examine the inheritance of pathogenicity, aggressiveness, mycotoxin type (DON/NIV), and DON production on a phenotypic basis, (4) analyse genetic covariation among aggressiveness, DON, and fungal colonization, (5) and compare aggressiveness of 42 isolates in greenhouse and field environments. Two crosses of G. zeae using nit (nitrate nonutilizing) marker technique were performed: (1) pathogenic DON-producing Z-3639 (Kansas, USA) x nonpathogenic NIV-producing R-5470 (Japan) belonging to lineage 7 and 6, respectively, and (2) DON-producing FG24 (Hungary) x FG3211 (Germany), both aggressive lineage 7 isolates. For the first cross, 99 progeny segregated in a consistent 61:38 for pathogenicity: nonpathogenicity in a two-year greenhouse experiment. Among the 61 pathogenic progeny, disease severity, measured as percentage infected spikelets, varied significantly (P = 0.01). Heritability for aggressiveness was high. Pathogenicity locus was mapped on linkage group IV near loci PIG1 (red pigment production), TOX1 (trichothecene toxin amount), and PER1 (perithecial production) explaining 60%, 43%, and 51% of the phenotypic variation, respectively. Two large aggressiveness QTLs were mapped on linkage group I linked to the locus TRI5 (trichodiene synthase in the trichothecene gene cluster) and an amplified fragment length polymorphism (AFLP) marker (EAAMTG0655K), explaining 51% and 29% of the observed phenotypic variation, respectively. These unlinked loci suggest that genetic basis between pathogenicity and aggressiveness were different. TRI5 is located in the same gene cluster as a previously identified gene known as TRI13, which determines whether DON or NIV will be produced. DON-producing progeny were, on average, twice as aggressive as were those producing NIV. Loci were only detected in the two linkage groups mentioned from the nine linkage groups present in the map. For the second cross FG24 x FG3211 with 153 progeny, head blight rating and relative plot yield were used as aggressiveness traits. DON production was measured by a commercial kit enzyme immunoassay. These three traits were quantitatively inherited among 153 progeny across three environments. Repeatabilities within each environment were medium to high but heritabilities across environments were medium only due to high progeny-environment interaction. DON was a less environmentally stable trait than aggressiveness. Transgressive segregants were detected frequently. This implies that even a cross within a lineage could lead to an increase in aggressiveness. Mapping of this cross was not initiated because the parents were not polymorphic enough to construct a genetic map. Instead, the parents were analysed for polymorphism in comparison to the parents of the first cross using 31 AFLP primer combinations and 56 random amplified polymorphic DNA (RAPD) primers. Polymorphism between Z-3639 and R-5470 was about three to four times higher than between FG24 and FG3211. Cluster analysis revealed that R-5470 was genetically separated from the other three parents, thus confirming the lineage assignments. Among preselected 50 progeny from the same field experiments that showed normal distribution for aggressiveness - head blight rating, fungal colonization, and DON production were correlated (r = 0.7, P = 0.01). Fungal colonization measured as Fusarium exoantigen (ExAg) content using enzyme-linked immunosorbent assay (ELISA) varied also quantitatively, but heritability was lower due to high progeny-environment interaction and error. Strong correlations among all traits indicate control by similar genes or gene complexes. No significant variation was observed for DON/ExAg ratio. Aggressiveness traits and DON production were more environmentally stable compared to Fusarium ExAg content. Our findings imply that aggressiveness may have other components apart from mycotoxin production. Genotypic variation for aggressiveness among the 42 progeny in one greenhouse and three field environments was significant and their correlation was moderate (r = 0.7, P = 0.01). High heritability in both environments again indicates that aggressiveness was a relatively stable trait, although methods of inoculation differed, i.e., injection for greenhouse and spraying for field experiments. Greenhouse aggressiveness could predict aggressiveness in the field, and thereby should reduce costs for resistance and phytopathological studies. In conclusion, we consider G. zeae as medium-risk pathogen with the potential to evolve to a higher level of aggressiveness due to sexual recombination. Erosion of quantitative resistance in FHB cannot be ignored, especially if host resistances with oligogenic inheritance, e.g. Sumai 3 from China, are used on a large acreage. Consequently, the rather simple inheritance of pathogenicity and aggressiveness in G. zeae could lead to a gradual increase of aggressiveness. These results should enhance efforts of plant breeders to use several, genetic distinct sources of resistance in order to avoid possible FHB outbreaks in the future.

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