Transfer of Fusarium Head Blight Resistance from Thinopyrum elongatum to bread wheat cultivar Chinese Spring

Genome ◽  
2021 ◽  
Author(s):  
George Fedak ◽  
Dawn Chi ◽  
Danielle Wolfe ◽  
Thérèse Ouellet ◽  
Wenguang Cao ◽  
...  

The diploid form of Tall Wheatgrass, Thinopyrum elongatum (Host) D. R. Dewey (2n = 2x = 14, EE genome) has a high level of resistance to Fusarium head blight. The symptoms do not spread beyond the inoculated floret following point inoculation. Using the series of E genome chromosome additions in a bread wheat cultivar Chinese Spring (CS) background, the resistance was found to be localized to the long arm of chromosome 7E. CS mutant ph1b was used to induce recombination between chromosome 7E, present in the 7E(7D) substitution and homoeologous wheat chromosomes. Multivalent chromosome associations were detected in BC1 hybrids attesting to the effectiveness of the ph1b mutant. Genetic markers specific for chromosome 7E were used to estimate the size of the 7E introgression in the wheat genome. Using single sequence repeat (SSR) markers specific for homoeologous wheat chromosome 7, introgressions were detected on wheat chromosomes 7A, 7B and 7D. Some of the introgression lines were resistant to Fusarium head blight.

2019 ◽  
Vol 139 (2) ◽  
pp. 251-262 ◽  
Author(s):  
David Sewordor Gaikpa ◽  
Bärbel Lieberherr ◽  
Hans Peter Maurer ◽  
C. Friedrich H. Longin ◽  
Thomas Miedaner

2021 ◽  
Author(s):  
Xianrui Guo ◽  
Qinghua Shi ◽  
Jing Yuan ◽  
Mian Wang ◽  
Jing Wang ◽  
...  

AbstractFusarium head blight (FHB), caused by Fusarium species, seriously threaten global wheat production. Three wheat-Th.elongatum FHB resistant translocation lines have been developed and used for breeding. Transcriptomic analysis identified a derivative glutathione S-transferase transcript T26102, which was homologous to Fhb7 and induced dramatically by Fusarium graminearum. Homologs of Fhb7 were detected in several genera in Triticeae, including Thinopyrum, Elymus, Leymus, Pseudoroegeria and Roegeria. Several wheat-Thinopyrum translocation lines carrying Fhb7 remain susceptible to FHB, and transgenic plants overexpressing the T26102 on different backgrounds did not improve the FHB resistance. Taken as a whole, we show the application of the chromatin derived from diploid Thinopyrum elongatum successfully conferring wheat with high level FHB resistance independent of the Fhb7.One Sentence SummaryThinopyrum elongatum chromatin from 7EL was successfully applied to wheat FHB resistance breeding, but the resistant gene other than the reported Fhb7 remained unknown.


Euphytica ◽  
2015 ◽  
Vol 208 (2) ◽  
pp. 367-375 ◽  
Author(s):  
Zhanwang Zhu ◽  
David Bonnett ◽  
Marc Ellis ◽  
Xinyao He ◽  
Nicolas Heslot ◽  
...  

Crop Science ◽  
2016 ◽  
Vol 56 (4) ◽  
pp. 1473-1483 ◽  
Author(s):  
Stine Petersen ◽  
Jeanette H. Lyerly ◽  
Peter V. Maloney ◽  
Gina Brown-Guedira ◽  
Christina Cowger ◽  
...  

Crop Science ◽  
2020 ◽  
Vol 60 (6) ◽  
pp. 2919-2930 ◽  
Author(s):  
Neal R. Carpenter ◽  
Emily Wright ◽  
Subas Malla ◽  
Lovepreet Singh ◽  
David Van Sanford ◽  
...  

2020 ◽  
Vol 71 (16) ◽  
pp. 4703-4714 ◽  
Author(s):  
Benjamin Hales ◽  
Andrew Steed ◽  
Vincenzo Giovannelli ◽  
Christopher Burt ◽  
Marc Lemmens ◽  
...  

Abstract Fusarium head blight (FHB) causes significant grain yield and quality reductions in wheat and barley. Most wheat varieties are incapable of preventing FHB spread through the rachis, but disease is typically limited to individually infected spikelets in barley. We point-inoculated wheat lines possessing barley chromosome introgressions to test whether FHB resistance could be observed in a wheat genetic background. The most striking differential was between 4H(4D) substitution and 4H addition lines. The 4H addition line was similarly susceptible to the wheat parent, but the 4H(4D) substitution line was highly resistant, which suggests that there is an FHB susceptibility factor on wheat chromosome 4D. Point inoculation of Chinese Spring 4D ditelosomic lines demonstrated that removing 4DS results in high FHB resistance. We genotyped four Chinese Spring 4DS terminal deletion lines to better characterize the deletions in each line. FHB phenotyping indicated that lines del4DS-2 and del4DS-4, containing smaller deletions, were susceptible and had retained the susceptibility factor. Lines del4DS-3 and del4DS-1 contain larger deletions and were both significantly more resistant, and hence had presumably lost the susceptibility factor. Combining the genotyping and phenotyping results allowed us to refine the susceptibility factor to a 31.7 Mbp interval on 4DS.


Genome ◽  
2003 ◽  
Vol 46 (5) ◽  
pp. 817-823 ◽  
Author(s):  
Sixin Liu ◽  
James A Anderson

A major QTL for resistance to Fusarium head blight (FHB) in wheat, Qfhs.ndsu-3BS, has been identified and verified by several research groups. The objective of this study was to increase the marker density in this QTL region using STS (sequence-tagged site) markers developed from wheat expressed sequence tags (ESTs) near Qfhs.ndsu-3BS. Because wheat chromosome 3BS and rice chromosome 1S are syntenous, the sequences of P1-derived artificial chromosome (PAC) and (or) bacterial artificial chromosome (BAC) clones covering the sub-distal portion of rice chromosome 1S were used as queries for a BLASTn search to identify wheat ESTs most likely near Qfhs.ndsu-3BS. Sixty-eight out of 79 STS primer pairs designed from wheat ESTs amplified PCR products from the genomic DNA of Triticum aestivum 'Chinese Spring'. Twenty-eight STS markers were localized on chromosome 3BS by aneuploid analysis. Six out of the nine STS markers that could be mapped in the T. aestivum 'Sumai 3'/T. aestivum 'Stoa' population had higher R2 and LOD values for this QTL than the most significant marker reported previously. Therefore, leveraging genome sequence information available in rice for wheat genetics is an effective strategy to develop DNA markers for Qfhs.ndsu-3BS, and this strategy may have broad applications for targeted mapping of other traits in cereal crops.Key words: comparative mapping, genomics.


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