Qiang Zhang†
Hanna Dandena
Madison McCausland
Wen Xu
Genyi Li- Department of Plant Science, University of Manitoba, Winnipeg, MB, Canada
Leptosphaeria maculans causes blackleg disease in Brassica napus. The blackleg disease is mainly controlled by resistance genes in B. napus. Previous studies have shown that the blackleg resistant BLMR2 locus that conferred horizontal resistance under field conditions, is located on chromosome A10 of B. napus. The purpose of this study is to fine map this locus and hence identify a candidate gene underlying horizontal resistance. The spectrum of resistance to L. maculans isolates of the resistance locus BLMR2 was analyzed using near isogenic lines, resistant, and susceptible cultivars. The results showed that this locus was horizontally resistant to all isolates tested. Sequence characterized amplified regions (SCAR), simple sequence repeats (SSR), and single nucleotide polymorphism (SNP) markers were developed in the chromosome region of BLMR2 and a fine genetic map was constructed. Two molecular markers narrowed BLMR2 in a 53.37 kb region where six genes were annotated. Among the six annotated genes, BnaA10g11280D/BnaA10g11290D encoding a cytochrome P450 protein were predicted as the candidate of BLMR2. Based on the profiling of pathogen induced transcriptome, three expressed genes in the six annotated genes were identified while only cytochrome P450 showed upregulation. The candidate corresponds to the gene involved in the indole glucosinolate biosynthesis pathway and plant basal defense in Arabidopsis thaliana. The molecular markers identified in this study will allow the quick incorporation of the BLMR2 allele in rapeseed cultivars to enhance blackleg resistance.
Introduction
Brassica napus (oilseed rape/canola) is an important crop used for edible oil production worldwide. Blackleg, caused by Leptosphaeria maculans, is one of the most devastating diseases in B. napus (canola, oilseed, and rapeseed) production. There are both qualitative and quantitative types of resistance to fungal pathogens like L. maculans (Rouxel et al., 2003; Raman et al., 2012, 2013). Qualitative resistance is race-specific and depends on the presence of a single resistance (R) gene in plant and corresponding avirulence (Avr) genes in pathogen (Ansan-Melayah et al., 1998). In contrast, quantitative resistance or horizontal resistance is race non-specific, which may be mediated by several genes and expressed from the seedling to adult plant stages, conferring only partial resistance to all races of the pathogen (Delourme et al., 2006; Rimmer, 2006). Identification and incorporation of resistance genes in Brassica species to produce resistant cultivars is an efficient approach to combat blackleg disease in B. napus (Hayward et al., 2012).
To date, over a dozen loci including Rlm1-10, LepR1 to LepR4, BLMR1, and BLMR2 conferring resistance to L. maculans have been mapped in the cultivated Brassica species (Yu et al., 2005, 2008, 2013; Delourme et al., 2006; Rimmer, 2006; Long et al., 2011; Larkan et al., 2013). However, the effectiveness of these resistance genes is decreased after they are used in production for a few years, and the genes need to be replaced with other novel genes (Li et al., 2003; Rouxel et al., 2003; Kutcher et al., 2007). For example, LepR3 in Surpass 400 that provides race-specific resistance to the fungal pathogen L. maculans suffered a major defeat in Australia in 2004 (Li et al., 2003; Sprague et al., 2006). On the other hand, studies on rice (Maeda et al., 2006) and barley (Van Berloo et al., 2001) have confirmed that quantitative genes conferred effective resistance. Quantitative resistance likely remains effective over time than qualitative resistance (Kaur et al., 2009; Brun et al., 2010; Zhang et al., 2016). Therefore, it is important and necessary to identify and combine qualitative and quantitative genes for durable blackleg resistance.
It is very difficult to identify the genes for quantitative trait loci in the complex genome of B. napus because little information is available on the genetic control of quantitative resistance to L. maculans. In previous study, the blackleg quantitative resistance gene BLMR2 identified in Surpass 400 showed horizontal resistance under field conditions (Dandena et al., 2019). A few blackleg resistance genes including Rlm2, LepR3, BLMR2, and LepR2 have been mapped on B. napus chromosome A10. Among these the highly resistant Rlm2 and LepR3 are allelic and function as receptors (Larkan et al., 2013, 2014, 2015). Characterization of the BLMR2 and LepR2 need further studies although these genes are likely different from the other R genes based on the map position and phenotype (Long et al., 2011; Larkan et al., 2016). BLMR2 segregated as a single dominant allele and has a distinctly intermediate phenotype when cotyledon inoculated with the L. maculans isolate 87-41 (Long et al., 2011). This allowed the development of NILs (W + BLMR2) using molecular marker assisted backcrossing along with progeny testing of recombinants.
In this report, BLMR2 was fine mapped in B. napus with the use of sequence characterized amplified regions (SCAR) and simple sequence repeats (SSR) markers. Furthermore, inoculation assay with individual isolates showed that BLMR2 has race non-specific resistance to all the isolates tested. These results lay a foundation for utilizing the blackleg resistance BLMR2 allele in developing resistant B. napus cultivars that effectively control L. maculans.
Materials and Methods
Materials for Testing Horizontal Resistance
Three near isogenic lines containing resistance BLMR1, BLMR2, and Rlm2 alleles were developed using the two resistant cultivars Surpass 400 and Glacier, and a susceptible cultivar Westar. BLMR1 and BLMR2 were derived from the cross between Surpass 400 and Westar (Long et al., 2011) while Rlm2 was derived from the cross between Glacier and Westar. BLMR1 and BLMR2 were separated at BC1F3 based on differential phenotypic interaction with the L. maculans isolate 87-41 and molecular marker data (Long et al., 2011). From crosses of Surpass 400 × Westar and Glacier × Westar, F3 and F1 progeny, respectively, were backcrossed to Westar four to five times and molecular marker assisted selection (MAS) was implemented during backcrossing (Dandena et al., 2019). Individuals containing homozygous BLMR1, BLMR2, or Rlm2 alleles were selected based on molecular markers and inoculation assays to obtain three isogenic lines in Westar background, named as W + BLMR1 (BC4F4), W + BLMR2 (BC4F4), and W + Rlm2 (BC4F2), respectively. The near isogenic lines, together with two resistant cultivars Glacier and Quinta, and the susceptible Westar were used to perform interaction analysis.
Mapping Populations
The BC1F3 plants carrying BLMR2/blmr2 alleles from the cross of B. napus cultivar Surpass 400 and Westar were backcrossed to Westar (blmr2/blmr2) to produce BC2, BC3, and BC4 populations, and the BC4 was selfed to obtain BC4F4. All plants used in backcrossing and selfing were phenotyped through inoculation and genotyped using the flanking molecular markers. The BC4 F3 and BC4F4 were inoculated with L. maculans isolate 87-41 to test cotyledon resistance. Segregation ratios of resistant to susceptible individuals in the F4 and BC4 were analyzed with χ2 test of goodness of fit. A total of 5,952 BC3 individuals were used to fine map the resistance locus.
Preparation of L. maculans Inoculum
To test the horizontal and race-non-specific resistance of BLMR2, 24 L. maculans isolates were used in cotyledon assay. These pathogen isolates were selected from the collection at the University of Manitoba. The inoculum of all isolates was prepared, and cotyledons were wounded and inoculated as described previously (Long et al., 2011). Disease reactions were rated in 12–16 days after inoculation according to the classification of 0–9 (Chen and Fernando, 2006).
DNA Extraction and Development of SSR and SCAR
A modified CTAB extraction procedure as described by Li and Quiros (2001) was used to extract DNA. The Brassica rapa genomic sequence1 was used to identify SSR loci and primers covering SSR were designed to amplify the specific loci in B. napus. SCAR loci were developed using a similar procedure as SSR markers except sequencing the targets from Surpass 400 and Westar. The A genome-specific primers were used to amplify Surpass 400 and Westar to identify insertions/deletions of the targets which were used to develop SCAR markers.
Detection of SCAR and SSR
A five fluorescent dye color set 6-FAM, VIC, NED, PET and LIZ was used for signal detection with an ABI 3100xl Genetic Analyzer (Thermo Fisher Scientific, Toronto, ON, Canada). The LIZ color was the standard and other four were used to label primers of SSR and SCAR. For SSR and SCAR detection, the genome-specific primers were used to obtain PCR products containing SSR or deletion/insertion positions. A 10 μl PCR mixture contained two genome-specific primers and one labeled M13 primer, 50 ng of genomic DNA, 0.375 mM dNTP, 1X PCR buffer, 1.5 mM MgCl2 and 1 U of Taq polymerase. The PCR running program was 94°C, 3 min; 94°C, 1 min; 58°C with −0.8°C each cycle 1 min and 72°C, 1 min for 5 cycles; 94°C, 1 min; 57°C, 1 min and 72°C, 1 min for 25 cycles. The PCR products were separated in the ABI 3100 Genetic analyzer. The data were collected and analyzed with ABI GenScan software and further transferred into images for scoring using Genographer software.
Sequencing of the Candidate Gene
Fully expanded cotyledons were inoculated using L. maculans isolate 87-41 (isolate-inoculated) or water (mock-inoculation). Four days after inoculation, cotyledon samples from eight individual plants per sample were pooled and ground in liquid nitrogen. Total RNA was extracted using Trizol reagent (Thermo Fisher Scientific, Toronto, ON, Canada). RNA quality was determined using 1% agarose gel and Nanodrop. cDNA was synthesized using total RNA and the SuperScriptTM III kit following manufacturer’s protocol (Thermo Fisher Scientific, Toronto, ON, Canada). Then, primers (Table 1) were used to amply the full-length cDNA of the candidate gene of BLMR2 and cloned into the TA cloning vector with the TOPO® TA Cloning® Kit (Thermo Fisher Scientific, Toronto, ON, Canada). Positive clones were selected to extract plasmid DNA using the standard mini preparation protocol. The plasmid DNA was sequenced using the BigDyeTM terminator v3.1 cycle sequencing kit (Thermo Fisher Scientific, Toronto, ON, Canada). Full length cDNA sequence was assembled using SeqMan software.
Table 1. Primers for all applications.
Quantitative Analysis of Candidate Gene Expression
Total RNA was extracted from cotyledon samples of NIL, W + BLMR2 and Westar inoculated with L. maculans isolate 87-41 at 4 days after inoculation (dai). cDNA was synthesized using the SuperScript IV First-Strand Synthesis kit (Thermo Fisher Scientific, Toronto, ON, Canada). Quantitative real-time PCR (qRT-PCR) was conducted using SYBR Green Master Mix (Bio-Rad) according to manufacturer’s recommendation (Bio-Rad). The P450 gene specific primers were used to amplify the gene (Table 1). The actin gene (BnaA01g19850D) was used as a control for normalization. Relative gene expression was calculated by the 2–ΔΔCT method.
Results
Resistance to L. maculans Isolates
Three near isogenic lines W + BLMR1, W + BLMR2, and W + Rlm2, along with Wester, Glacier, and Quinta were inoculated with 24 isolates. The results showed that only W + BLMR2 was resistant to all tested isolates, indicating that the resistance of BLMR2 was horizontal and race non-specific. BLMR1 and Rlm2 showed differential interactions with the tested isolates and the two resistant cultivars Glacier and Quinta also showed different resistant spectra while Westar was susceptible to all isolates as expected (Table 2).
Table 2. Testing of resistance spectra of three near isogenic lines and three cultivars in Brassica napus using 24 isolates of Leptosphaeria maculans*.
Segregation of BLMR2 in the Mapping Populations
In the mapping populations of BLMR2, 656 F4 individuals were used to confirm the segregation ratio of BLMR2. There were 513 resistant plants and 143 susceptible plants showing a 3:1 segregation ratio (χ2 test, p > 0.05). In the BC4 mapping population of 831 individuals, there were 438 resistant plants and 393 susceptible plants showing a 1:1 segregation ratio (χ2 test, p > 0.05), suggesting that one dominant resistance allele is responsible for the BLMR2 resistance to blackleg (Figure 1).
Figure 1. Cotyledons of Surpass 400, near isogenic line W + BLMR2 and Westar, 14 days after inoculation (dai) of the pycnidiospore suspension (2 × 107 spores/mL) of Leptosphaeria maculans isolate 87-41. Surpass 400 showing high resistance (A); W + BLMR2 showing intermedium resistance (B); and Westar with the susceptible phenotype (C).
Fine Mapping of the Resistance Gene
Sequence characterized amplified region (SCAR) and SSR markers were used to map BLMR2 on chromosome A10. Using 1,632 BC4 plants, six recombinant individuals were obtained. Their selfed progeny was inoculated with L. maculans isolate 87-41 to confirm recombinants. Then, more sequence-based SCAR and SSR were developed to fine map the BLMR2 locus. Another 4,320 BC4 individuals were inoculated with L. maculans isolate 87-41 to identify another 14 recombinants. Using all 20 recombinants, BLMR2 was narrowed in a small region between molecular markers N10-47 and N10-43 after their phenotypes and genotypes were analyzed (Table 3 and Figure 2). Selfed progeny of all recombinants was also tested to confirm the recombination in the BC4F4. The chromosome region of molecular markers N10-47 and N10-43 was located from 9494993 to 9548367 in the reference genome sequence of chromosome A102, spanning a 53.37 kb region. In the reference sequence, seven genes are annotated while two genes BnaA10g11280D and BnaA10g11290D were re-annotated into one gene based on the full length of cDNA.
Table 3. Phenotypesand genotypes of 20 recombinants in the BC3 population of Brassica napus*.
Figure 2. Genetic and physical map of BLMR2 locus on Chromosome A10 of Brassica napus. Genetic map showing BLMR1 and BLMR2 (Long et al., 2011; A). The flanking SSR and SCAR markers used in the fine mapping of BLMR2 (B). Molecular marker data of the recombinants with resistant phenotype showing overlapping BLMR2 region corresponding to 57.3 kb physical interval. The candidate BLMR2 gene is indicated (C).
Full length cDNA of the candidate gene was sequenced from both the near isogenic line W + BLMR2 with BLMR2 in Westar background and Westar. Comparison of the cDNA sequences showed that there are six polymorphisms in W + BLMR2 compared to the background genotype Westar while only one of these six nucleotide changes results in one difference of amino acid (AA) (Supplementary Data 1). RNA-seq data in the previous report (NCBI Archive under the BioProject accession number PRJNA378851, Zhou et al., 2019) were analyzed to compare the expression of the six genes in the fine mapped region of BLMR2 and the results showed that three of the six genes were expressed while only the candidate gene was upregulated after inoculation (Supplementary Data 2).
Analysis of Expression of the Candidate Gene by qPCR
In addition, qRT-PCR was used to determine the relative gene expression of the candidate gene in the resistant W + BLMR2 and Westar. The relative fold change in the accumulation of B. napus CYP450 transcript was significantly higher in the pathogen (L. maculans isolate 87-41) inoculated resistant W + BLMR2 at 4 dai compared to pathogen inoculated Westar or mock checks (Figure 3). Our results suggest that CYP450 possibly plays a role in L. maculans induced defense response in B. napus.
Figure 3. Validation of the expression of Brassica napus CYP81F2 gene in the resistant near isogenic line (NIL) W + BLMR2 and susceptible Westar using qRT-PCR at 4 days after inoculation (dai) with Leptosphaeria maculans isolate 87-41. Samples d-Wes is water check of Westar; Wes, inoculated Westar; d-NIL, water check of NIL; NIL, inoculated NIL. The relative gene expression value is normalized using the Actin gene (BnaA01g19850D). Error bar shows standard deviation of the mean based on three biological replicates. The asterisk (∗) represents significant difference from all the other samples based on Tukey test, p < 0.05.
Discussion
It is hypothesized that quantitative resistance genes work by a complex interaction of many response genes to pathogens, and any individual gene does not show strong effect, therefore there is less selective pressure on the fungus (Zhu et al., 1993; Delourme et al., 2008). Mapping and eventually cloning these genes will facilitate the transfer and pyramiding of multiple resistance genes with different resistance spectra through molecular marker-assisted selection in B. napus (Long et al., 2011). In this paper, the disease reactions of BLMR2 to a range of isolates of L. maculans were analyzed. The results showed that BLMR2 is a horizontal resistance locus to all the isolates of the blackleg pathogen, compared to typical R genes and resistant cultivars. In the previous study, the results in field testing showed that BLMR2 conferred resistance to blackleg under field conditions, suggesting that this resistance gene is very useful to the breeding of resistant cultivars in B. napus (Dandena et al., 2019).
In this study, BLMR2 was fine mapped in a 53.37 kb region where six genes were annotated. Of these six genes, one was identified as the candidate gene of BLMR2 based on the analysis of gene expression. The candidate is homologous to CYP81F2 in Arabidopsis thaliana. Several studies showed that CYP81F2 catalyzes the modification of indole glucosinolate (IGS) which involves the accumulation of defensive secondary metabolites (Abdel-farid et al., 2010; Wiesner et al., 2013). In Arabidopsis, its hydrolytic products produced by myrosinases (PEN2 and PEN3) are involved in innate immune response to pathogens (Bednarek et al., 2009; Clay et al., 2009). The CYP81F2 and PEN2 dependent hydrolytic products are also associated with callose deposition in FLG22-triggered basal immunity (Bednarek et al., 2009; Clay et al., 2009). While it remains elusive whether genes involving the glucosinolate biosynthesis are linked to defense response induced by L. maculans in B. napus, a complex pattern of IGS accumulation in B. rapa – L. maculans interaction was observed (Abdel-farid et al., 2010). Furthermore, Robin et al. (2017) associated upregulation of CYP81F2 (Bol026044) gene in the moderate blackleg resistant cabbage cultivar with increased IGS accumulation at the seedling stage. Recent global transcriptomic studies identified multiple genes involved in the IGS biosynthesis in B. napus – L. maculans incompatible interaction (Becker et al., 2017; Zhou et al., 2019). However, the mechanisms underlying horizontal resistance are rarely reported, and hence the findings in this study suggest that secondary metabolic pathways such as the biosynthetic pathways of glucosinolates may play a role in plant resistance to various diseases. However, how the change of AA in the DNA sequence confers the horizontal resistance in this study need to be investigated in the future.
Plant disease resistance is classified in many ways, vertical vs horizontal, qualitative vs quantitative, race-specific vs race-non-specific, a high vs an intermediate level of resistance. Typical R genes such as NBS-LRR, receptor like proteins (RLP) and receptor like kinases (RLK) have been cloned since their phenotypes can be easily observed (Dangl and Jones, 2001). For some diseases such as sclerotinia diseases in rapeseed, sunflower and soybean and fusarium head blight in cereal crops, no vertical, qualitative or race-specific resistance has been identified so no typical R genes for these diseases has been cloned (Behla et al., 2017; Mesterhazy, 2020). In this study, the horizontal resistance of BLMR2 has been stressed since it conferred intermediate resistance under field conditions (Dandena et al., 2019) and showed intermediate resistance to all isolated tested under controlled environmental conditions. Several characteristics of the resistance of the BLMR2 locus need to be addressed. First, its resistance is race-non-specific and intermediate while the resistance is dominant and resistant in all heterozygous genotypes tested. Second, single allele of this locus confers relatively strong resistance, so the phenotypes of this locus were relatively easy to be scored (Figure 1). The accurate scores of phenotypes made it possible to perform fine mapping and narrow the gene into a small chromosome region. Third, this kind of resistance is assumed to be controlled by polygenes and very difficult to be transferred from cultivar to cultivar while the BLMR2 locus can be easily transferred using molecular markers targeting the six mutations in the DNA sequence (Supplementary Data 1). Finally, unlike all previous reports where horizontal resistance is hypothesized to have a minor effect of one locus in resistance controlled by multiple loci (Tian et al., 2006; Skowrońska et al., 2020), the resistance locus BLMR2 confers a relative strong effect so the near isogenic lines showed the level of resistance which can meet the standard of blackleg resistance in Canada field trials (Canola Council of Canada).
Conclusion
The availability of accurate phenotypes and a large population aided in the precise mapping of the BLMR2 locus. With a combination of BLMR2 fine-mapping, molecular marker assisted development of NILs and comparative physical mapping, the candidate gene for BLMR2 as a homolog of CYP81F2 (At5g57220) in Arabidopsis was identified. Markers identified in this study can be used to transfer this horizontal resistance from cultivar to cultivar using MAS or gene pyramiding for resistance durability.
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/, PRJNA378851.
Author Contributions
QZ, HD, and GL designed the experiment and wrote the manuscript. QZ and HD finished the most experiments. MM, HL, ZL, and WX collected the data of some experiments. All authors contributed to the article and approved the submitted version.
Funding
This research was supported by the Natural Sciences and Engineering Research Council (NSERC) CRD project (CRDPJ 523840 – 18).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to acknowledge Dilantha Fernando who offered most isolates used in this study.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2021.663868/full#supplementary-material
Footnotes
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Keywords: Brassica napus, Leptosphaeria maculans, BLMR2, cytochrome p450, fine mapping
Citation: Zhang Q, Dandena H, McCausland M, Liu H, Liu Z, Xu W and Li G (2021) Genetic Analysis of a Horizontal Resistance Locus BLMR2 in Brassica napus. Front. Plant Sci. 12:663868. doi: 10.3389/fpls.2021.663868
Received: 03 February 2021; Accepted: 12 April 2021;
Published: 25 May 2021.
Edited by:
Jacqueline Batley, University of Western Australia, AustraliaReviewed by:
Alexander Idnurm, The University of Melbourne, AustraliaXiaodong Wang, Jiangsu Academy of Agricultural Sciences (JAAS), China
Copyright © 2021 Zhang, Dandena, McCausland, Liu, Liu, Xu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Genyi Li, genyi.li@ad.umanitoba.ca
†These authors have contributed equally to this work and share first authorship