Comparative analysis of genetic structures and aggressiveness of Fusarium pseudograminearum populations from two surveys undertaken in 2008 and 2015 at two sites in the wheat belt of Western Australia

• Published in: Plant pathology Vol. 68; no. 7; pp. 1337 - 1349
• Main Authors: Khudhair, M., Thatcher, L. F., Gardiner, D. M., Kazan, K., Roper, M. M., Aitken, E., Obanor, F.
• Format: Journal Article
• Language: English
• Published: Oxford Wiley Subscription Services, Inc 01-09-2019
• Subjects: Barley; Comparative analysis; Crop yield; Crown rot; Disease control; Fungal diseases; Fungi; Fusarium; fusarium crown rot; Fusarium pseudograminearum; Genetic analysis; Genetic diversity; Genetic structure; Mating; population dynamics; Population genetics; Population studies; Populations; Toxins; Western Australia; Wheat; Australia; Western Australia Australia
• ISSN: 0032-0862; 1365-3059
• DOI: 10.1111/ppa.13056

Fusarium crown rot (FCR), caused predominantly by Fusarium pseudograminearum (Fp) in Australia, is an important fungal disease of wheat and barley. FCR causes significant yield losses and reduced grain quality worldwide. This study investigated the population dynamics of FCR‐causing F. pseudograminearum isolates from Western Australia (WA), a major wheat‐growing region. Wheat samples were collected from a total of seven different sites in 2008 and 2015. Two sites, Tammin and Karlgarin, with moderate to high FCR incidence, were intensively sampled in both years. The results revealed significant increase in Fp isolation frequency between 2008 and 2015. Over 86% of 1100 Fusarium isolates were Fp in 2015 compared with 59% of 639 isolates from 2008. Mating type idiomorphs, toxin chemotypes and population genetic structures were determined for a subset of 279 Fp isolates (132 isolates from 2008 and 165 from 2015). Mating type analysis revealed differences in MAT1‐1 and MAT1‐2 distributions between Tammin and Karlgarin for both years. Results also showed that 97.6% of Fp isolates analysed had the 3‐ADON trichothecene chemotype. Additionally, for the first time in Australia, the 15‐ADON chemotype was identified in 2.3% and 2.4% of Fp isolates from 2008 and 2015, respectively. The genetic structure of Fp population determined using 21 cleaved amplified polymorphic sequence (CAPS) markers revealed a high level of genetic variation within and between populations. In addition, 2015 isolates from Tammin and Karlgarin were significantly more aggressive (P < 0.0001) than 2008 isolates. This finding may have implications in managing this significant fungal disease.