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Canola (Brassica napus) is the major oilseed crop in Canada. Blackleg (Leptosphaeria maculans) causes yield losses annually, with a larger impact in the last two decades caused by breakdown of resistance in growers' fields. A 4‐year small‐plot field study from 2014 to 2017 in Manitoba investigated the impact of the B. napus–L. maculans interaction on the emergence of virulent isolates towards specific R genes. Doubled haploid B. napus 'Topas' introgression lines carrying single R genes were used, with a 2‐year canola–wheat rotation. Blackleg incidence was reduced by 40% in 2017 compared to 2014 for all R genes tested except Rlm4. In 2017, disease severity was reduced between 21% and 52% compared to 2014 for all R genes tested except Rlm2. There was a significant shift from AvrLm2 and AvrLm4 to virulent alleles avrLm2 and avrLm4, respectively, which led to the gain of virulence toward Rlm2 and Rlm4 Topas introgression lines within a year. Sequencing of the AvrLm2 gene of isolates from 2014 and 2015 revealed a shift of AvrLm2 to avrLm2 allele due to accumulation of point mutations. Masking of AvrLm3 phenotype by the presence of the AvrLm4‐7 allele was also confirmed by analysing phenotypes and genotypes of the isolates collected from 2014 to 2017. Based on these and previous findings, we demonstrate the need for an epidemiological model that takes into account complex molecular mechanisms allowing plant breeders to select appropriate R genes, including balanced cultivar rotation strategies to maintain blackleg resistance in the Canadian Prairies. [ABSTRACT FROM AUTHOR]

Blackleg, caused by the fungal pathogen Leptosphaeria maculans, is one of the most economically important diseases of canola (Brassica napus, oilseed rape) worldwide. This study assessed incidence of blackleg, the avirulence allele, and mating type distributions of L. maculans isolates collected in commercial canola fields in Manitoba, Canada, from 2010 to 2015. A total of 956 L. maculans isolates were collected from 2010 to 2015 to determine the presence of 12 avirulence alleles using differential canola cultivars and/or PCR assays specific for each avirulence allele. AvrLm2, AvrLm4, AvrLm5, AvrLm6, AvrLm7, AvrLm11, and AvrLmS were detected at frequencies ranging from 97 to 33%, where the AvrLm1, AvrLm3, AvrLm9, AvrLepR1, and AvrLepR2 alleles were the least abundant. When the race structure was examined, a total of 170 races were identified among the 956 isolates, with three major races, AvrLm-2-4-5-6-7-11, AvrLm-2-4-5-6-7-11-S, and Avr-1-4-5-6-7-11-(S) accounting for 15, 10, and 6% of the total fungal population, respectively. The distribution of the mating type alleles (MAT1-1 and MAT1-2) indicated that sexual reproduction was not inhibited in any of the nine Manitoba regions in any of the years L. maculans isolates were collected.