Genetic diversity of Australian Fusarium pseudograminearum populations causing crown rot in wheat

被引:7
|
作者
Khudhair, Mohammed [1 ,2 ]
Obanor, F. [3 ]
Kazan, K. [1 ]
Gardiner, D. M. [1 ]
Aitken, E. [2 ]
McKay, A. [4 ]
Giblot-Ducray, D. [4 ]
Simpfendorfer, S. [5 ]
Thatcher, L. F. [6 ]
机构
[1] CSIRO Agr & Food, 306 Carmody Rd, St Lucia, Qld 4067, Australia
[2] Univ Queensland, Sch Agr & Food Sci, St Lucia, Qld 4072, Australia
[3] Grains Res & Dev Corp, 4 Natl Circuit, Barton, ACT 2600, Australia
[4] South Australian Res & Dev Inst, Primary Ind & Reg South Australia, Urrbrae, SA 5064, Australia
[5] Tamworth Agr Inst, New South Wales Dept Primary Ind, 4 Marsden Pk Rd, Calala, NSW 2340, Australia
[6] CSIRO Agr & Food, 147 Underwood Ave, Floreat, WA 6014, Australia
关键词
Fusarium pseudograminearum; Fusarium crown rot; Western Australia; Eastern Australian states; Wheat; STUBBLE MANAGEMENT; NATURAL OCCURRENCE; PACIFIC-NORTHWEST; GRAMINEARUM; AGGRESSIVENESS; PATHOGENS; RECOMBINATION; FIELDS; YIELD; MAP;
D O I
10.1007/s10658-020-02198-0
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Fusarium crown rot (FCR) caused by the fungus Fusarium pseudograminearum (Fp) is an important disease of wheat that reduces yield and grain quality in many countries, including Australia. In this study, we investigated mating type idiomorph composition, putative chemotype and population genotypic structure of 98 Fp isolates from Western Australia (WA) and the eastern Australian states of New South Wales, Victoria and South Australia. Our results revealed the expected 1:1 mating type ratio for isolates from the eastern states while there was significant variation to a 1:1 mating type composition with isolates from WA. A chemotype-specific PCR assay indicated that all Fp isolates from eastern states and WA segregated for the 3-ADON trichothecene chemotype. Genetic diversity assessed using 21 cleaved amplified polymorphic sequence markers revealed a high level of genotypic variation within and between Fp populations from eastern Australian states and WA. Analysis of molecular variance (AMOVA) showed significant difference between populations from eastern states and WA. The genetic diversity measured by Shannon index ranged from 0.95 to 2.30 with the lowest and highest values detected in Hart and Rowena populations, respectively in the eastern states. Index of association analysis showed no significant linkage of markers among isolates within 60% of the populations, suggesting that sexual reproduction may be occurring in the pathogen from those locations. These results improve understanding of Fp population dynamics across Australia and highlight the importance of monitoring for shifts in the population which could have implications for disease management.
引用
收藏
页码:741 / 753
页数:13
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