Evaluation of Fusarium Head Blight Resistance in 410 Chinese Wheat Cultivars Selected for Their Climate Conditions and Ecological Niche Using Natural Infection Across Three Distinct Experimental Sites

Exploiting wheat cultivars with stable resistance to Fusarium Head blight (FHB) and toxin accumulation is a cost-effective and environmentally friendly strategy to reduce the risk of yield losses and contamination with mycotoxins. To facilitate the deployment of stable cultivar resistance, we evaluated FHB resistance and resistance to mycotoxin accumulation in 410 wheat lines bred by local breeders from four major wheat growing regions in China after natural infection at three distinct locations (Hefei, Yangzhou and Nanping). Significant differences in disease index were observed among the three locations. The disease indexes (DI’s) in Nanping were the highest, followed by Yangzhou and Hefei. The distribution of DI’s in Yangzhou showed the best discrimination of FHB resistance in cultivars. Growing region and cultivar had significant effect on DI and mycotoxins. Among the climate factors, relative humidity and rainfall were the key factors resulting in the severe disease. Even though most cultivars were still susceptible to FHB under the strongly conducive conditions applied, the ratio of resistant lines increased in the Upper region of the Yangtze River (UYR) and the Middle and Lower Region of the Yangtze River (MLYR) between 2015 and 2019. Deoxynivalenol (DON) was the dominant mycotoxin found in Hefei and Yangzhou, while NIV was predominant in Nanping. Disease indexes were significantly correlated with DON content in wheat grain.

[1]  Yilin Zhou,et al.  The distribution of Fusarium graminearum and F. asiaticum causing Fusarium head blight of wheat in relation to climate and cropping system. , 2021, Plant disease.

[2]  Á. Mesterházy Updating the Breeding Philosophy of Wheat to Fusarium Head Blight (FHB): Resistance Components, QTL Identification, and Phenotyping—A Review , 2020, Plants.

[3]  S. Chulze,et al.  Fusarium head blight in Argentina: Pathogen aggressiveness, triazole tolerance and biocontrol-cultivar combined strategy to reduce disease and deoxynivalenol in wheat , 2020, Crop Protection.

[4]  L. Herselman,et al.  Molecular breeding of wheat lines for multiple rust and Fusarium head blight resistance , 2020, Euphytica.

[5]  S. Rastelli,et al.  Co-Occurrence of Moniliformin and Regulated Fusarium Toxins in Maize and Wheat Grown in Italy , 2020, Molecules.

[6]  H. Zhang,et al.  Resistance to Fusarium head blight and mycotoxin accumulation among 129 wheat cultivars from different ecological regions in China , 2020 .

[7]  H. Buerstmayr,et al.  Breeding for Fusarium head blight resistance in wheat—Progress and challenges , 2020 .

[8]  Hongxiang Ma,et al.  Breeding for the resistance to Fusarium head blight of wheat in China , 2019, Frontiers of Agricultural Science and Engineering.

[9]  S. Dreisigacker,et al.  Genetics for low correlation between Fusarium head blight disease and deoxynivalenol (DON) content in a bread wheat mapping population , 2019, Theoretical and Applied Genetics.

[10]  G. Drezner,et al.  The Pressure of Fusarium Disease and Its Relation with Mycotoxins in The Wheat Grain and Malt , 2019, Toxins.

[11]  Xiaomin Han,et al.  Co-occurrence of multi-mycotoxins in wheat grains harvested in Anhui province, China , 2019, Food Control.

[12]  Xiangji Kong,et al.  Host and Cropping System Shape the Fusarium Population: 3ADON-Producers Are Ubiquitous in Wheat Whereas NIV-Producers Are More Prevalent in Rice , 2018, Toxins.

[13]  D. Backhouse,et al.  Climate change impacts on the ecology of Fusarium graminearum species complex and susceptibility of wheat to Fusarium head blight: a review , 2016 .

[14]  J. Qiu,et al.  Effect of environmental factors on Fusarium population and associated trichothecenes in wheat grain grown in Jiangsu province, China. , 2016, International journal of food microbiology.

[15]  C. Fanelli,et al.  Climate, Soil Management, and Cultivar Affect Fusarium Head Blight Incidence and Deoxynivalenol Accumulation in Durum Wheat of Southern Italy , 2016, Front. Microbiol..

[16]  M. Lemmens,et al.  Masked mycotoxins: does breeding for enhanced Fusarium head blight resistance result in more deoxynivalenol-3-glucoside in new wheat varieties? , 2016 .

[17]  C. Waalwijk,et al.  Biogeography of Fusarium graminearum species complex and chemotypes: a review , 2015, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment.

[18]  Jianhong Xu,et al.  Natural occurrence of deoxynivalenol and zearalenone in wheat from Jiangsu province, China. , 2014, Food chemistry.

[19]  J. Qiu,et al.  Molecular characterization of the Fusarium graminearum species complex in Eastern China , 2014, European Journal of Plant Pathology.

[20]  Yueju Zhao,et al.  A minor survey of deoxynivalenol in Fusarium infected wheat from Yangtze–Huaihe river basin region in China , 2013 .

[21]  L. Tamburic-Ilincic Effect of 3B, 5A and 3A QTL for Fusarium head blight resistance on agronomic and quality performance of Canadian winter wheat , 2012 .

[22]  H. Zhang,et al.  Population Analysis of the Fusarium graminearum Species Complex from Wheat in China Show a Shift to More Aggressive Isolates , 2012, PloS one.

[23]  B. Bakutis,et al.  Acoustic sensing of deoxynivalenol in co-occurrence with zearalenone and T-2/HT-2 toxin in winter wheat cultivar Sirvinta from Lithuania , 2011 .

[24]  A. Schaafsma,et al.  FHB Resistance of winter wheat from Canada and Europe estimated across multi-environments after inoculation with two deoxynivalenol producing Fusarium species , 2011 .

[25]  G. Bai,et al.  Management and resistance in wheat and barley to fusarium head blight. , 2003, Annual review of phytopathology.

[26]  L. Madden,et al.  Risk assessment models for wheat fusarium head blight epidemics based on within-season weather data. , 2003, Phytopathology.

[27]  Á. Mesterházy,et al.  Nature of wheat resistance to Fusarium head blight and the role of deoxynivalenol for breeding , 1999 .