Abstract

In this study, clubroot resistance in the resynthesized European winter Brassica napus cv. ‘Tosca’ was introgressed into a Canadian spring canola line ‘11SR0099’, which was then crossed with the clubroot susceptible spring line ‘12DH0001’ to produce F1 seeds. The F1 plants were used to develop a doubled haploid (DH) mapping population. The parents and the DH lines were screened against ‘old’ pathotypes 2F, 3H, 5I, 6M and 8N of the clubroot pathogen, Plasmodiophora brassicae, as well as against the ‘new’ pathotypes 5X, 5L, 2B, 3A, 3D, 5G, 8E, 5C, 8J, 5K, 3O and 8P. Genotyping was conducted using a Brassica 15K SNP array. The clubroot screening showed that ‘Tosca, ‘11SR0099’ and the resistant DH lines were resistant to three (2F, 3H and 5I) of the five ‘old’ pathotypes and four (2B, 3O, 8E and 8P) of the 12 ‘new’ pathotypes, while being moderately resistant to the ‘old’ pathotype 8N and the ‘new’ pathotypes 3D and 5G. ‘Tosca’ was susceptible to isolates representing pathotype 3A (the most common among the ‘new’ pathotypes) as well as pathotypes 6M, 5X, 5L, 5K and 8J. Linkage analysis and QTL mapping identified a ca. 0.88–0.95 Mb genomic region on the A03 chromosome of ‘Tosca’ as conferring resistance to pathotypes 2F, 3H, 5I, 2B, 3D, 5G, 8E, 3O and 8P. The identified QTL genomic region housed the CRk, Crr3 and CRd gene(s). However, the susceptibility of ‘Tosca’ to most of the common virulent pathotypes makes it unattractive as a sole CR donor in the breeding of commercial canola varieties in western Canada.

Highlights

  • Rapeseed (Brassica napus and B. rapa) was the second most important oilseed crop (71.9 MMT) after soybeans (362.0 MMT) worldwide in 2018–20191

  • Clubroot resistance in Canadian canola varieties was derived from the European winter B. napus cultivar ‘Mendel’[17,18]

  • A doubled haploid mapping population developed from F­ 1 plants of the clubroot resistant spring line and a clubroot susceptible Canadian spring canola line was genotyped with a Brassica 15K SNP array, and linkage analysis and Quantitative trait loci (QTL) mapping were conducted to identify genomic regions associated with clubroot resistance from ‘Tosca’

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Summary

Introduction

Rapeseed (Brassica napus and B. rapa) was the second most important oilseed crop (71.9 MMT) after soybeans (362.0 MMT) worldwide in 2018–20191. Clubroot resistance in Canadian canola varieties was derived from the European winter B. napus cultivar ‘Mendel’[17,18]. Since most current commercial canola varieties do not possess resistance to isolates representing the ‘new’ P. brassicae pathotypes, there is a need to identify and utilize additional resistance sources for development of the generation of clubroot resistant cultivars. This task is especially daunting in Alberta, where various novel pathotypes have become w­ idespread[8,15,16]. A doubled haploid mapping population developed from F­ 1 plants of the clubroot resistant spring line and a clubroot susceptible Canadian spring canola line was genotyped with a Brassica 15K SNP array, and linkage analysis and QTL mapping were conducted to identify genomic regions associated with clubroot resistance from ‘Tosca’

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