Original Research ARTICLE
Genetics of Greenbug Resistance in Synthetic Hexaploid Wheat Derived Germplasm
- 1Centro Internacional de Mejoramiento de Maíz y Trigo (CIMMYT), Global Wheat Program, Mexico, Mexico
- 2Campo Experimental Valle de Mexico, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (INIFAP), Chapingo, Mexico
The greenbug, Schizaphis graminum Rondani, significantly reduces wheat, Triticum aestivum L., grain yields if not controlled. Host plant resistance (HPR) can protect yield, is environmentally friendly and easy to use. Our objectives were to: (1) identify genomic regions associated with S. graminum resistance in a recombinant inbred line (RIL) population derived from a cross of “Sokoll” (resistant) and “Weebill1” (moderately susceptible), (2) evaluate Sokoll derived breeding germplasm for resistance, and (3) conduct allelism tests between Sokoll and sources carrying resistance genes Gba, Gbb, and Gbd. Resistance was measured quantitatively and qualitatively using a SPAD meter and visual assessments, respectively. We identified a large effect resistance gene on chromosome arm 7DL of Sokoll, herein referred as GbSkl, which contributed up to 24% of the phenotypic variation. Other minor QTL on chromosomes 2B, 3A, and 7B were also identified. The QTL on 2B and 3A originated from Weebill1. Of the Sokoll derived germplasm, 13% displayed resistance. Allelism tests indicated that GbSkl could be allelic or tightly linked to the temporarily designated genes Gba, Gbb, and Gbd. Utility of SPAD to determine quantitative variation in resistance phenotyping is demonstrated and breeding efforts are underway to transfer the resistance from Sokoll to new CIMMYT elite germplasm.
Wheat (Triticum aestivum L.) is one of the most important cereal crops globally. The production and cultivated area in 2016 were 749 million tons and 220 million hectares, respectively (FAO, 2018). One third (72 million ha) of the total harvested area is accounted by South and Central Asia and North and East Africa (FAO, 2018). These regions contribute to about 25% of the global wheat production with 30% less yield than the global average (FAO, 2018). Major efforts are ongoing worldwide to increase productivity considering climate change and increasing demand scenarios. Wheat production is constrained by abiotic and biotic factors, and climate change can increase the incidence of pests and diseases in addition to heat and drought stresses (Porter et al., 2014).
Among the biotic constraints that severely affect wheat production are aphids; small insects that feed from the phloem sap. The aphid species Schizaphis graminum Rondani, commonly known as greenbug, is widely distributed worldwide (Blackman and Eastop, 2007; Leach and Hobbs, 2013; CABI-EPPO, 2018) and can reduce wheat yield by 40–50% especially if infestations occur at early growth stages. Chemical control is widely used, however, smallholder farmers often do not have timely access to insecticides nor have resources, and consequently their crop is more prone to aphid damage. Insecticides are often handled improperly by the smallholder farmers and can have negative effects on non-targeted organisms, including humans (Dewar and Foster, 2017; Mitchell et al., 2017; Woodcock et al., 2017; Bondori et al., 2018).
Host plant resistance (HPR) can significantly contribute to yield protection from aphids and reduce the insecticides usage. Additionally, HPR can reduce production costs thus benefiting farmers more from their crop. This control method, is one of the key component of the integrated pest management, and is the most easily applied method by the farmers, as it is already present in the seeds that they sow and has no additional cost to them.
Host plant resistance to insects is classified in categories that describe the way plants react to insect exposures. Essentially, HPR to insects is composed by three categories: antibiosis, antixenosis and tolerance (Painter, 1941; Kogan and Ortman, 1978; Smith, 2005). Tolerance to aphids is considered more complex than the other categories of resistance, as various plant mechanisms related to allocation patterns and nutrient uptake, antioxidant production, biomass production, photorespiration, photosynthesis, plant growth, and storage capacity are involved (Rosenthal and Kotanen, 1994; Heng-Moss et al., 2003; Boyko et al., 2006; Reddy et al., 2013; Donze-Reiner et al., 2017). Despite the conceptual separation of these categories, it is difficult to isolate them in terms of the actual mechanisms that cause the resistance (Smith and Clement, 2012).
The deployment of insect resistance in elite varieties requires significant investments from the germplasm identification to the development of parental lines and breeding itself. Because phenotypic selection methods are complicated to apply in the field, breeding for insect resistance is a challenging task in large breeding programs that pursue the development of elite germplasm with ample yield gain, stability and resistance to other relevant biotic and abiotic factors. Nonetheless, marker assisted breeding (MAB) can be an efficient tool to utilize in breeding programs to transfer and select resistance to aphids. The successful implementation of MAB lies in the identification of molecular markers closely linked to resistance genes, which is achieved through genetic analyses, linkage mapping (QTL analysis), or linkage disequilibrium related methods.
Previous studies have identified genes (Gb2 and Gb6) on chromosome 1R from rye (Puterka and Peters, 1989; Lu et al., 2010) and in Aegilops speltoides Tausch (Gb5) (Tyler et al., 1987; Dubcovsky et al., 1998; Crespo-Herrera et al., 2013). Synthetic hexaploid wheats (SHWs) are other highly valuable source of resistance to S. graminum (Lage et al., 2003). The SHWs are the product of the human-induced hybridization between tetraploid species carrying the “A” and “B” genomes of wheat, with accessions of the “D” genome ancestor goat grass (Aegilops tauschii Coss). SHWs can be directly crossable with the adapted germplasm, hence transfer of desirable traits from wild relatives is possible. Studies have identified resistance genes on chromosome 7DL of A. tauschii, i.e., Gb3, Gb4, Gb7, Gba, Gbb, Gbc, Gbd, Gbx, and Gbz, and it has been demonstrated that these are single dominant genes (Puterka and Peters, 1989; Zhu et al., 2005; Crespo-Herrera et al., 2014; Tan et al., 2017). However, the relationships between the SHW identified genes need to be established.
The bread-wheat breeding program at the International Maize and Wheat Improvement Centre (CIMMYT) has recently undertaken the task of transferring resistance to aphids (S. graminum and Rhopalosiphum padi L.) to elite breeding germplasm. As part of this endeavor, CIMMYT germplasm was screened for resistance against these pests, which allowed the identification of the drought tolerant line “Sokoll” (Reynolds et al., 2007) also resistant to S. graminum. Sokoll is a synthetic hexaploid derived line, pedigree: “PASTOR/3/ALTAR 84/A. squarrosa (TAUS)//OPATA,” and has been used in CIMMYT’s wheat breeding program to develop drought tolerant germplasm.
The objectives of our study were: (1) to identify the genomic regions associated with resistance to S. graminum in the CIMMYT’s synthetic hexaploid derived wheat Sokoll; (2) characterize the marker-S. graminum resistance association in a set of Sokoll derived lines; and (3) determine the association of the resistance between Sokoll and Gba, Gbb, and Gbd S. graminum resistance genes of SHW origin through allelism tests, since the A. squarrosa (A. tauschii) accession in Sokoll is unknown.
Materials and Methods
Three sets of germplasm, developed at the International Maize and Wheat Improvement Centre (CIMMYT), were evaluated: (1) 228 F6 recombinant inbred lines (RILs) derived from the cross of the SHW derived line Sokoll (S. graminum resistant) with Weebill1 (S. graminum moderately susceptible), (2) A set of 46 Sokoll derived breeding lines, and (3) Four F2 derived F3 populations of 94, 92, 98, and 98 families from the crosses between Sokoll and the SHWs previously reported to carry S. graminum resistance genes: “Ceta/A. squarrosa (1027),” “Seri//T. dicoccon PI94623/A. Squarrosa (1027),” “Croc_1/A. Squarrosa (224)”, and “Altar 84/A. Squarrosa (328)” (Lage et al., 2003; Zhu et al., 2005; Crespo-Herrera et al., 2014).
Clones of S. graminum were collected from wheat fields at CIMMYT’s experimental station located in Ciudad Obregon, Sonora, Mexico (27° 37’ N, 109° 93’ W). Aphids were reared on the CIMMYT’s bread wheat line “Reedling #1” under controlled conditions at 24 ± 2°C and 16:8 (light:dark) photoperiod with high-pressure sodium lamps as light source.
After the establishment of the aphid cultures, the S. graminum the virulence/avirulence pattern was determined by evaluating a set of differential lines, the parents of the RILs and the F2:F3 families (Table 4). The virulence/avirulence pattern of the aphid population was similar to the biotype I in the United States (Porter et al., 1997).
Phenotyping and Data Analysis
The plant materials were evaluated at seedling stage. Five seeds of each of the Sokoll/Weebill1 RILs were planted as tufts in flats of 40 cm × 53 cm × 7 cm. The evaluations consisted of two treatments, infested vs. non-infested, arranged in augmented incomplete blocks where the resistant (Sokoll) and susceptible (Weebill1) progenitors of the RILs were replicated 8 and 6 times in each flat as controls, respectively. After emergence, each tuft was carefully thinned to allow the growth of one seedling of similar size for both treatments. The flats were grown side by side in growth chambers with controlled light (16:8) and temperature (22 ± 2°C).
Each seedling of the infested treatment was exposed to 15–20 individuals of S. graminum at the 2nd–3rd leaf stage. The infestations were conducted every second day during 10–12 days to ensure high and homogeneous aphid pressure within flats. Since the flats were grown side by side, the non-infested flats were treated with a 0.2% solution of Admire® (Bayer, Imidacloprid @ 30.2%) 1 day before the infestation treatment was applied, with the objective to avoid aphid establishment and movement from the infested flats. This insecticide is a commercially available product in Mexico, and its active ingredient has been tested to assess the resistance to aphids in wheat (Dunn et al., 2007).
Chlorophyll content was measured on each seedling with a SPAD meter (Minolta®). Three readings along the first fully developed leaves were taken and averaged. In addition, a visual assessment of the aphid damage on a 0–100 scale was also recorded, the scale was based on the percentage of chlorosis displayed by the plants under aphid feeding. Data were collected when the susceptible check displayed 60–70% damage (chlorosis). The evaluation of RILs was repeated three times, i.e., once a full round of evaluations was finished with the augmented design, the RILs were evaluated two more times.
A similar procedure was followed for the Sokoll derived lines and the F2:F3 populations to conduct the allelism tests, except that the tufts were not thinned, and the non-infested treatment was not established, hence we evaluated between 460 and 490 total seedlings per populations. The susceptible check for this evaluations was “Pavon F76”, a hard-white spring wheat variety highly susceptible to aphids (Crespo-Herrera et al., 2013) and the resistant check was Sokoll. Only the qualitative scores (S, susceptible; R, resistant) were given based on the seedling response to the aphid feeding.
The classification of each of the F2:F3 families were used to assess the hypothesis of 15:1 (Resistant:Susceptible) ratio for two independent dominant genes in a Chi-squared test, given that each family is expected to segregate in that ratio for two independent genes. The families displaying any sign of damage, or abnormal observations were re-evaluated to confirm the results by exposing each family to aphid feeding. For this, Twenty-five seeds of each family and the susceptible check were planted in rows on the flats previously described, and each row of seedlings were infested following the same procedures as described above.
Phenotypic data were analyzed with the package lme4 (Bates et al., 2015) in the R software v.3.4 (R Development Core Team, 2013). Best linear unbiased estimators (BLUEs) were obtained from the analysis of the RILs by fitting the lines and treatments as fixed effects, whereas the incomplete blocks and the experiment repetitions where considered as random effects. We obtained heritability estimates for the mapping population from the variance components by fitting the RILs as random effects, but keeping the parental lines and treatments as fixed effects in the linear mixed model.
The Sokoll/Weebill1 RILs and the Sokoll derived lines were genotyped with the Diversity Array Technology (DArT), and DArT-Seq at the laboratory of Genetic Analysis Service for Agriculture in CIMMYT, Mexico. The DArT-Seq procedure consists on digestion, primer and barcode ligation, amplification and sequencing processes of the DNA samples (Sansaloni et al., 2011). Unlike DArT-Seq, the array procedure (DArT) lacks the sequencing process and yields a presence/absence pattern of the markers by hybridizing the probes to the wheat array (Wenzl et al., 2004; Akbari et al., 2006). In total there were 95,958 markers processed prior to the linkage analysis. Markers not considered for further analysis were those with more than 20% missing data, minor allele frequency lower than 5% and those that were monomorphic between the parents of the RILs.
Linkage and QTL Analysis
Linkage and QTL analyses were performed for the Sokoll/Weebill1 RIL population. Markers were first grouped with the ICIMapping software (Meng et al., 2015) using the DArT chromosome locations as anchoring information and a high LOD threshold (30.0) for grouping unanchored markers. Subsequently, each group was ordered using the ASMap package (Taylor and Butler, 2017), which contains the linkage map functions of the MSTMap (Wu et al., 2008) for R language. The program takes the minimum spanning tree of a graph for grouping and ordering. The utilization of these two tools allowed us the use of the prior knowledge of the markers (ICIMapping) and the ordering efficiency of ASMap.
The QTL analysis was conducted with the R package R/qtl (Broman and Sen, 2009) to identify genomic regions associated with chlorophyll content, chlorophyll loss and aphid damage. First, interval mapping was implemented with the Haley-Knott regression method (Haley and Knott, 1992). Significant genomic regions were identified after a 1,000 permutations run at a threshold of the 5% tail of the null distribution. Significant main effect QTL were then further examined in a multiple interval mapping framework to refine positions, estimate QTL effects and the proportion of variance explained by the QTL and the QTL model.
Phenotypic Analysis of Recombinant Inbred Lines (RILs)
In the infested treatment, seedlings of the parental lines, Sokoll (resistant) and Weebill1 (susceptible), displayed 28.3 and 11.5 units of chlorophyll content (SPAD units), respectively in contrast to 31.3 (Sokoll) and 29.1 (Weebill1) units for their non-infested treatments, which resulted in chlorophyll losses of 9.4 and 60.3% on average, respectively for the two parents. The visual damage score for Sokoll and Weebill1 was 1 and 68.4% on average, respectively. The analysis of the phenotypic data indicated a significant variation between RILs for all recorded traits. The damage score ranged from 3.5 to 84.3% (F229,392.9 = 1.24, P < 0.0001), and the heritability (h2) was 0.52. The chlorophyll content of the RILs in the infested treatment, ranged from 4.6 to 35.2 (F229,615 = 11.72, P < 0.0001) and h2 = 0.89, whereas in the non-infested treatment it ranged from 23.3 to 39.4 (F229,627 = 2.07, P < 0.0001) and h2 = 0.49. The chlorophyll loss, expressed as percentage of SPAD units and as a function of chlorophyll content between infested vs. non-infested treatments, ranged from −24.46 to 84.15%.
The correlation analysis between recorded traits indicated a significantly positive (r = 0.27, p < 0.001) association between the chlorophyll content of the RILs in both treatments, but an insignificant close to zero (r = −0.07, p = 0.9) correlation between chlorophyll loss and chlorophyll content in the non-infested treatment (Figure 1). High and significant (r > |0.9|, p < 0.001) correlations were detected between the traits related to the infested treatment (Figure 2).
Figure 1. Trait distribution and correlation. The diagonal displays the histogram for each recorded trait. The panels below and above the diagonal represent the scatter plots and correlation values between traits, respectively. ∗∗p = 0.01, ∗∗∗p < 0.001.
Figure 2. Adjusted mean trait (±SE) of main QTL effects across Sokoll/‘Weebill1 RILs. (A–C) Correspond to damage score of QTL on 2B, 3A, and GbSkl in 7DL, respectively. (D–F) Correspond to chlorophyll content (SPAD units) of QTL on 3A, 7B, and GbSkl, respectively.
The histograms of chlorophyll content, loss and damage scores, displayed a significant departure (D = 0.04, p < 0.005) from a unimodal distribution according to the Hartigan’s dip test for unimodality. The Sarle’s bimodality coefficient of the recorded traits in the infested treatments was b > 0.6, which suggests a bimodal distribution, which for genetic interpretations indicates the presence of a gene with a major effect segregating in the RIL population.
Linkage and QTL Analysis
We used 5,259 DNA markers for QTL analysis after conducting the quality control of the genotypic data. From these, 24 linkage groups (LGs) were built, one for each wheat chromosome plus additional LGs for each of the chromosomes 3B, 5B, and 6B. The number of markers per LG ranged from 20 (4D) to 650 (7B). The size of the LGs spanned from 33.34 cM (4D) to 597.13 cM (6A), and the total distance of the LG summed to 6,507.03 cM. On average, the LG were comprised by one marker every 1.24 cM, but this value ranged for individual LG from 0.29 cM (1B) to 5.78 cM (5D). The markers were distributed across the three wheat genomes as follows: 32.7, 55.1, and 12.2%, for the A, B, and D genomes, respectively.
The QTL models explained 37.8, 40.2, and 37.1% of the total phenotypic variation for damage score, chlorophyll content and chlorophyll loss, respectively (Table 1). For all recorded traits, the QTL analysis of the Sokoll/Weebill1 RILs indicated the presence of a genomic region with large effect (Table 1 and Figures 2C,F, 3B) on chromosome 7DL (Figure 4) of Sokoll that explained between 16.5 and 24.1% of the phenotypic variation (Table 1). This locus is herein referred as GbSkl. The closest marker to GbSkl was m3222388 (Figure 4). An additional QTL (QGb.cimmyt-3A) was also found for all traits on chromosome 3A of Weebill1 that explained a lesser amount of phenotypic variation, up to 5.4% (Table 1 and Figures 2B,D, 3A). Other minor QTL were found on chromosomes 2B (QGb.cimmyt-2B) for damage score, which accounted for a reduced amount of phenotypic variation (Table 1 and Figure 2A), and another on chromosome 7B (QGb.cimmyt-7B) for chlorophyll content which explained 3.9% of the phenotypic variation (Table 1 and Figure 2E). The closest marker to these QTL were m3951322 and m4439909, respectively.
Table 1. Quantitative trait loci (QTL) for S. graminum resistance identified in the Sokoll/Weebill1 mapping population.
Figure 3. Adjusted mean trait (±SE) of chlorophyll loss for main QTL effect across Sokoll/Weebill1 RILs. (A) Chlorophyll loss for QTL on 3A. (B) Chlorophyll loss for GbSkl on 7DL.
Figure 4. LOD profile of damage score, chlorophyll content and loss on linkage group (LG) assigned to chromosome 7D.
Sokoll Derived Lines
Among the Sokoll derived lines evaluated, 13% exhibited a resistant phenotypic reaction (Table 2). The full list of lines with their pedigree, marker and phenotypic response is given in the Supplementary Table S1.
For marker m3222388, linked to GbSkl, 2.1% lines displayed a false negative response, while 19.5% showed false positive responses (Supplementary Table S1). For marker m1407691, also flanking the 7DL QTL, there were 4.3% false negatives and 10.8% false positives. The combined response of these markers had 8.7% false positive and 2.1% false negative rates.
For the QTL on 3A the flanking markers displayed a 4.3% false negative responses, and 15.2 and 45.7% false positive responses for markers m3385293 and m1070254, respectively. The combined response of these two markers had 13% false positives, however; none had a false negative response.
We did not observe any susceptible seedlings or segregating families in the F2:F3 populations derived between the crosses of Sokoll and Gba, Gbb, and Gbd sources (Table 3). Hence, with the Chi-squared test the null hypothesis of 15:1 (Resistant:Susceptible) phenotypic segregation ratio was rejected for the GbSkl and Gba, Gbb, and Gbd, indicating that the presence of an allelic gene or tightly linked genes could be involved in the resistance to S. graminum.
Incorporating HPR to insects in elite germplasm that can potentially become commercial varieties is of great value due to environmental considerations associated with reduced insecticide use, as well as benefits to non-targeted organisms including human, and reduction of production costs and health risks to farmers. The accurate identification and clear understanding of the genetics of resistance are important for breeding programs to efficiently incorporate HPR to insects as a selection trait, either directly (phenotypic selection) and/or indirectly (MAB).
The analysis of the phenotypic data supports the conclusion that a major gene controls the resistance to S. graminum in Sokoll, as the population could be classified in two groups but with phenotypic variation within the groups according to the bimodality parameters.
The observed correlation patterns of the phenotypic data demonstrate that the chlorophyll content in non-infested treatments is not indicative of resistance to S. graminum (Figure 1). The low but significant correlation of chlorophyll content between the evaluated treatments indicated that plants with higher chlorophyll content tended to also have higher chlorophyll content when exposed to aphids, but not to the level of exhibiting resistance, which is supported by the null association between chlorophyll loss and content in the non-infested treatment (Figure 1). Furthermore, given the high correlation exhibited between chlorophyll content, chlorophyll loss and damage score, despite the null association between chlorophyll loss and chlorophyll content in non-infested plants, it is possible to conclude that, taking SPAD measurements in infested treatments may be sufficient as a rapid evaluation of resistance, as long as appropriate controls are included in the experimental design. Another important aspect to note for phenotyping purposes is that the visual score was highly correlated with chlorophyll content and loss, indicating that this alone can be a good parameter to assess tolerance in mapping studies, as the same important genomic regions were detected using the SPAD meter related traits (Table 1).
Our study aimed to evaluate quantitatively the ability of Sokoll/Weebill1 RILs and additional Sokoll derived material to withstand S. graminum damage (tolerance) under high aphid pressure in seedling experiments, and map the genomic regions conferring resistance in Sokoll. Typically, tolerance to S. graminum is evaluated qualitatively for gene mapping studies (Weng and Lazar, 2002; Zhu et al., 2004, 2005; Weng et al., 2005). Although SPAD measurements had been used for evaluating tolerance (Lage et al., 2003; Boina et al., 2005), it had not been used as a trait for genetic studies.
Our screening methodology allowed us to identify genomic regions with small effects that are associated with S. graminum tolerance, in addition to a region harboring the major effect resistance gene GbSkl on chromosome 7DL (Weng and Lazar, 2002; Boyko et al., 2004; Zhu et al., 2005). Interestingly, the QGb.cimmyt-2B and QGb.cimmyt-3A alleles from Weebill1 contributed small effects to the phenotypic variation of the evaluated traits (Figures 2A,B,D, 3A). Such a small effects alone are not enough for the lines to display acceptable levels of protection, however, in combination with GbSkl they can play an important role in conferring higher levels of resistance. It is relevant to note that these QTL with small effects were located on the “A” and “B” genomes of wheat, unlike most of the reported genes on the “D” genome from A. tauschii. Another, reported gene in wheat, but not in the “D” genome is Gby on chromosome 7A, which confers tolerance and antibiosis (Boyko et al., 2004; Boina et al., 2005).
Sokoll has been used as one of the parents for the development of CIMMYT’s drought tolerant germplasm. Even though, DArT-Seq markers cannot be readily used for MAB and require further efforts to be transformed in user friendly assays, the results from the marker response highlight the importance of having flanking markers to reduce the false positive rate for MAB purposes. Furthermore, the recombinant lines can be used for fine mapping and developing molecular markers that are in tighter linkage to the resistance gene (Table 2). Efforts are underway to characterize a larger set of Sokoll derivatives in CIMMYT breeding germplasm to determine the phenotypic and marker responses using KASP assays we developed based on additional studies we conducted (Crespo-Herrera et al., 2014).
The sequence of the DArT-seq markers flanking GbSkl were investigated in the reference wheat genome sequence (IWGSC RefSeq v1.0) in the Ensembl database (Zerbino et al., 2018), these markers (m3222388 and m1407691) were located 5.7 Mbp apart on 7DL between the physical position of 593.4 and 599.1 Mbp, a region that encloses 56 genes predicted to code for 35 protein superfamilies. The superfamilies include: ricin B-like lectins, terpenoid cyclases/protein prenyltransferases, terpenoid synthases, serine metabolism enzymes, cysteine proteinases, and leucine rich repeats, which can be related to plant defenses to aphids (Goggin, 2007; Smith and Boyko, 2007).
The results from the allelism tests suggest that the major gene in Sokoll, GbSkl, could be allelic or in tight linkage with Gba, Gbb, and Gbd reported genes, as the F2:F3 populations did not segregate for S. graminum resistance (Table 3). Additional testing is required to determine the allelic relations between these genes and other sources, such as Gb7, Gbc, and Gbz. Due to a lack of seed availability we could not develop these additional populations. Derived from the pedigree information, it is possible that GbSkl is related to Gb7, however, this cannot be confirmed by pedigree alone as the A. tauschii accession that is the source of Gb7 appears to be different from GbSkl (Tan et al., 2017). There is reported evidence that Gbd is different from Gbz (Zhu et al., 2005), and also that Gbz is allelic or tightly linked to Gb3 (Zhu et al., 2004). Therefore, it could be inferred that Gba, Gbb, Gbd and GbSkl are different from Gb3. However, more work is required to determine the relationship between all these S. graminum resistance genes. A definite way to fully deciphering it is by cloning the genes involved in the resistance.
Our results contribute to unraveling the genetic relationships between certain S. graminum resistance genes, and in the identification of key genomic regions that contribute to the phenotypic variation for S. graminum resistance in Sokoll wheat. Our results also suggest that measuring chlorophyll content with a SPAD meter in S. graminum infested plants can be a quick and standardized evaluation method for determining resistance. Breeding efforts are undergoing to transfer the resistance to newer elite germplasm and the resistant materials being distributed to CIMMYT collaborators for evaluation in local environments where this aphid is a concern.
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.
LC-H established the screening methodology, conducted the phenotyping, data analysis, and wrote the main manuscript. LC-H, JH-E, and RS conducted the data analysis, developed the parental lines of RILs, and the allelism test populations. MR developed the RILs. All authors reviewed and approved the final version of the manuscript.
Conflict of Interest Statement
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.
We are grateful to the Bill and Melinda Gates Foundation (OPPGD1389) and the Department for International Development from the United Kingdom for supporting the CIMMYT’s wheat breeding and research activities through the Delivering Genetic Gains in Wheat (DGGW) project. We thank the United States Agency for International Development (USAID) and the Indian Council of Agricultural Research (ICAR) for their financial support.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2019.00782/full#supplementary-material
TABLE S1 | Marker S. graminum response of selected Sokoll derived germplasm.
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Keywords: wheat, genetics, resistance, greenbug, tolerance, genes
Citation: Crespo-Herrera L, Singh RP, Reynolds M and Huerta-Espino J (2019) Genetics of Greenbug Resistance in Synthetic Hexaploid Wheat Derived Germplasm. Front. Plant Sci. 10:782. doi: 10.3389/fpls.2019.00782
Received: 28 February 2019; Accepted: 29 May 2019;
Published: 13 June 2019.
Edited by:Soren K. Rasmussen, University of Copenhagen, Denmark
Reviewed by:Jackie C. Rudd, Texas A&M AgriLife Research and Extension Center at Amarillo, United States
Ken Chalmers, The University of Adelaide, Australia
Copyright © 2019 Crespo-Herrera, Singh, Reynolds and Huerta-Espino. 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: Leonardo Crespo-Herrera, L.Crespo@cgiar.org