Fine mapping and identification of candidate genes for a QTL affecting Meloidogyne incognita reproduction in Upland cotton
- Pawan Kumar†1,
- Yajun He†1, 7,
- Rippy Singh1,
- Richard F. Davis2,
- Hui Guo3,
- Andrew H. Paterson3,
- Daniel G. Peterson4,
- Xinlian Shen1, 6,
- Robert L. Nichols5 and
- Peng W. Chee1Email author
Received: 17 December 2015
Accepted: 19 July 2016
Published: 8 August 2016
Abstract
Background
The southern root-knot nematode (Meloidogyne incognita; RKN) is one of the most important economic pests of Upland cotton (Gossypium hirsutum L.). Host plant resistance, the ability of a plant to suppress nematode reproduction, is the most economical, practical, and environmentally sound method to provide protection against this subterranean pest. The resistant line Auburn 623RNR and a number of elite breeding lines derived from it remain the most important source of root-knot nematode (RKN) resistance. Prior genetic analysis has identified two epistatically interacting RKN resistance QTLs, qMi-C11 and qMi-C14, affecting gall formation and RKN reproduction, respectively.
Results
We developed a genetic population segregating only for the qMi-C14 locus and evaluated the genetic effects of this QTL on RKN resistance in the absence of the qMi-C11 locus. The qMi-C14 locus had a LOD score of 12 and accounted for 24.5 % of total phenotypic variation for egg production. In addition to not being significantly associated with gall formation, this locus had a lower main effect on RKN reproduction than found in our previous study, which lends further support to evidence of epistasis with qMi-C11 in imparting RKN resistance in the Auburn 623RNR source. The locus qMi-C14 was fine-mapped with the addition of 16 newly developed markers. By using the reference genome sequence of G. raimondii, we identified 20 candidate genes encoding disease resistance protein homologs in the newly defined 2.3 Mb region flanked by two SSR markers. Resequencing of an RKN resistant and susceptible G. hirsutum germplasm revealed non-synonymous mutations in only four of the coding regions of candidate genes, and these four genes are consequently of high interest.
Conclusions
Our mapping results validated the effects of the qMi-C14 resistance locus, delimiting the QTL to a smaller region, and identified tightly linked SSR markers to improve the efficiency of marker-assisted selection. The candidate genes identified warrant functional studies that will help in identifying and characterizing the actual qMi-C14 defense gene(s) against root-knot nematodes.
Keywords
Background
Plant-parasitic nematodes are important pests in agriculture and are found across a broad range of climatic conditions. The genus Meloidogyne includes more than 70 species; four species – M. incognita, M. arenaria, M. javanica and M. hapla – account for approximately 95 % of the total crop area infested by this genus [1]. The Southern root-knot nematode (Meloidogyne incognita, RKN) is the most important parasitic nematode of Upland cotton inflicting economic losses through direct damage to the plant root system and indirectly through increasing severity of other root diseases such as Fusarium Wilt caused by Fusarium oxysporum f. sp. vasinfectum. Yield loss due to RKN has dramatically increased in the U.S. from 1 % in 1987 to 5.5 % in 2006, resulting in losses of more than 300 million pounds (4.4 %) of cotton valued over $235 million (Cotton Disease Loss Estimate Committee Report 2012). Recommended management practices to control RKN include crop rotation and nematicide application. The broad host-range of RKN leaves cotton growers with few profitable options to adopt crop rotation as a means of nematode management [2]. Nematicides applied at planting fail to provide season long protection; moreover, the future availability of most widely used cotton nematicide, aldicarb, is uncertain.
Host plant resistance can be an efficient RKN management tool in cotton production. Resistant varieties can offer good to excellent pest control efficacy and are also environmentally sound alternatives. Both cultivated and wild relatives of Upland cotton have been screened to identify germplasm displaying high levels of RKN resistance [3], and a few resistance sources were identified. Currently, the Auburn 623 RNR germplasm line is the most important source of RKN resistance because it displays near immunity to RKN infection. The resistance in Auburn 623 RNR is believed to have originated from transgressive segregation in a cross between two moderately resistant parents, Clevewilt 6 and Wild Mexican Jack Jones [4, 5]. Resistance in Auburn 623 RNR was transferred to several adapted cultivars through backcrossing, resulting in the release of M-lines with improved agronomic qualities while retaining near-immunity to RKN [4].
Quantitative trait locus (QTL) mapping studies have identified regions on the long arm of Chromosome 11 and the short arm of Chromosome 14 that confer RKN resistance in Auburn 623 RNR derived M-lines [6–8]. Origin of the resistance loci was traced to the two moderately resistant parents of Auburn 623 RNR, with the qMi-C11 locus on Chromosome 11 inherited from Clevewilt 6 [8] and the qMi-C14 locus on Chromosome 14 inherited from Wild Mexican Jack Jones [7, 8]. The qMi-C11 locus was recently fine mapped to a 3.6 cM interval [6], however the QTL region near qMi-C14 remains sparsely mapped [8, 9].
Recent studies suggested that the qMi-C11 locus predominanly affects root gall suppression whereas the qMi-C14 locus largely reduces egg production but has little effect on galling [9]. Further, while the main effects of each QTL appeared to serve as the major genetic basis in conferring resistance for both galling and egg production phenotypes, additive x additive epistatic interaction was important in suppressing nematode egg production, resulting in a near-immunity to infection when both QTLs are present [9]. These studies support earlier histo-pathological observations indicating that a two-stage defense mechanism was responsible for resistance in Auburn 623 RNR. The first stage involved suppressing the development of giant cells at 6 days post penetration and the second stage involved reducing the egg production of M. incognita females at 24 days post penetration [10, 11].
The presence of two or more unlinked resistance loci with different mechanisms in the Auburn 623 RNR source has complicated elucidating the mode of inheritance and determining the genetic effects of each resistance gene. For example, Zhou et al. [12] reported that RKN resistance in the Auburn 623 RNR source involved a partially dominant and a recessive gene. However, McPherson et al. [13] suggested that resistance in the Auburn 623 RNR source was due to a dominant and an additive gene, and Zhang et al. [14] concluded that resistance was controlled by at least two additive genes. To better determine the genetic effects of each resistance locus and to investigate the hypothesis of independent resistance genes controlling plant responses to suppression of root galling and nematode reproduction in this resistance source would require testing a genetic population segregating for only a single resistance locus.
Host-plant resistance to root-knot nematodes was first identified in Lycopersicum peruvianum Mill., a wild relative of cultivated tomato [15] where a single dominant Mi gene conferred resistance to three major root-knot nematodes M. arenaria, M. incognita and M. hapla. Further molecular characterization of the Mi gene revealed that it encodes a protein with nucleotide-binding site leucine-rich repeat (NBS-LRR) motifs [16] and triggers a hypersensitive response in the host plant. Based on the amino acid motifs and their membrane spanning domains [17], disease resistance genes in plants are grouped into eight classes and a majority of these genes are characterized by the presence of Leucine Rich Repeat (LRRs) motifs. The several classes of LRR-containing proteins that exist in plants have diverse overall structures and functions. They provide an early warning system for the presence of potential pathogens and activate protective immune signaling in plants [18, 19]. In addition, they act as a signal amplifier in the case of tissue damage, establishing symbiotic relationships and affecting developmental processes [20].
In this study, we developed a genetic population segregating only for the qMi-C14 resistance locus. Our objectives were to: (1) develop and map new SSR markers to construct a dense linkage map near the qMi-C14 locus, (2) estimate the genetic effect of qMi-C14 on RKN resistance and (3) predict putative candidate genes responsible for the qMi-C14 resistance by identifying genes that encode for LRR-containing proteins within the QTL interval.
Methods
Population development
The mapping population was derived from an interspecific cross between the highly resistant Upland cotton line M-120 RNR, and an RKN susceptible G. barbadense cultivar Pima S-6 as described by Shen et al. [7]. A total of 1252 F2 individuals were planted in a greenhouse and screened with previously published SSRs mapped to chromosomes 11 and 14 [6, 7, 9]. Seven F2 individuals that were completely heterozygous at the qMi-C14 locus on Chromosome 14 as determined by five previously mapped co-dominant SSR markers (CIR246, JESPR156, UGT045, CGR5668, and STV30) [9] but were homozygous for the Pima S-6 allele at the qMi-C11 locus as determined by CIR069 and CIR316 on chromosome 11 (for absence of resistance allele) were identified. All seven plants were self-pollinated to yield a genetic population consisting of 513 plants segregating only for the qMi-C14 locus.
Phenotypic screening and data analysis
The mapping population was planted in a greenhouse along with ten plants each of the parental lines, M-120 RNR and Pima S-6, as resistant and susceptible checks, respectively. The screening method to determine the level of resistance to RKN has been described previously by Shen et al [7]. One hour prior to inoculation, nematode eggs were collected by agitating infected eggplant roots (Solanum melongena L.) in 0.5 % sodium hypochlorite solution for two minutes [21]. Three week old plants were inoculated with approximately 8000 eggs of M. incognita race 3 (approximately 450 eggs 150 cm-3 soil). Inoculum was distributed into two holes about 2.5 cm deep in soil on opposite sides of the seedling and the holes were covered with soil after inoculation. The soil temperatures varied between 17 °C and 28 °C. Plants were evaluated for the amount of M. incognita reproduction at 56 to 58 days after inoculation. Phenotypic data collected included root galling index (RGI), total number of eggs extracted, and the number of eggs per gram of fresh root. Roots were washed free of soil, evaluated for galling, weighed, cut into 5-cm pieces, and agitated in a 1 % v/v sodium hypochlorite solution in a 1-liter flask for four minutes [21]. Eggs were collected and rinsed with tap water on nested 150- over 25-μm-pore sieves. Root galling index (RGI) was evaluated using the 0 to 10 scale where 0 = no galling, 1 = 1–10 % of the root system galled, 2 = 11–20 % of the root system galled, up to 10 = 91–100 % of the root system galled [22]. Roots of each plant were harvested and weighed immediately prior to extraction of eggs. Eggs were extracted from the whole root system and counted. The mean number of eggs per gram of fresh root (eggs/g of root) was evaluated in order to standardize egg counts.
Statistical parameters describing the population for each phenotypic trait were calculated using SAS (SAS, ver. 9.3). Fisher’s Least Significant Difference (LSD) test was used to compare phenotypic means for all traits between mapping parents. Data for total egg count and eggs per gram of root weight were Log10 (x + 1) transformed to achieve a normalized distribution for QTL analysis.
SSR mining and primer design
He et al. [9] and Gutierrez et al. [8] indicated that the RKN resistance locus on chromosome 14 is flanked by BNL3545 and CGR5668; therefore, we used the sequences from which these two SSRs (available at www.cottongen.org) to BLAST search the genome sequence of G. raimondii at www.phytozome.net (version 9.1). The physical location of the qMi-C14 locus was found to be on the distal end of G. raimondii chromosome 05. More than 4 Mbp of sequence from the distal end of this chromosome was downloaded in fasta file format, divided into two equal segments of 2Mbp each, and scanned for short repeating units using a web based microsatellite repeat finder (insilico.ehu.es/mini_tools/microsatellites). Search parameters were: minimum number of repeats = 5, minimum repeat unit length = 2, maximum repeat unit length = 10. Fifty microsatellites that were between 10–25 repeats long were selected; these microsatellites are fairly uniformly distributed along the 4 Mbp region. Three hundred base pairs on each side of each microsatellite were selected for primer development using the web based BatchPrimer3 software [23]. Primers were 20–22 nt long and designed to amplify 150–200 bp PCR products at melting temperatures between 50–55 °C. Primers were commercially synthesized by Eurofins MWG Operon (Huntsville, AL).
PCR reaction conditions were slightly modified from a previously described protocol [24]. PCR amplification was performed in a PTC-100 or PTC-200 thermocycler (MJ Research Inc.). A 10 μl reaction contained 10 ng of template DNA, 0.5 μM primer mix, 100 μM dNTPs, 1.5 mM MgCl2, 3U of DNA polymerase, and 1X reaction buffer (100 mM Tris-HCl, pH 8.3, 500 mM KCl). The cycling conditions for PCR were 94 °C for 3 min, followed by 35 cycles of 94 °C for 1 min, 55 °C for 1 min, and 72 °C for 1.2 min. After the last cycle, reactions were incubated at 72 °C for 6 min before cooling to 4 °C. The amplified PCR products were separated by electrophoresis on a 10 % w/v non-denaturing polyacrylamide gel (PAGE) and visualized by staining with silver nitrate following published procedures [25].
Linkage map construction and QTL mapping
Procedures for linkage map development and QTL analysis were as described by He et al. [9]. Briefly, all markers were first tested for their ability to detect polymorphism between the M-120 RNR and Pima S-6 parents. Primers that detected clear polymorphism between parents were utilized to genotype the entire mapping population. Linkage groups were constructed using the Mapmaker/EXP 3.0 [26] software. Linkage group assembly was done using the ‘group’ command with a LOD score of 3.0 and a maximum recombination fraction of 30 cM. Recombination units were converted into genetic distances by using the Kosambi mapping function [27] with the “error detection” command on. New markers were added to the framework using the ‘try’ and ‘compare’ commands. The final order of markers on a linkage group was confirmed using the ‘ripple’ command.
Detection of QTLs and estimation of various genetic parameters were performed by Composite Interval Mapping (CIM) function implemented in the software WinQTL Cartographer version 2.5 [28]. Likelihood ratio (LR) threshold values (α = 0.05) for declaring the presence of QTLs were estimated after 1000 permutations [29]. Mapping was performed at 1 cM walk speed in a 10 cM window using five background cofactors selected via forward-backward stepwise regression. QTLs were defined by one-LOD likelihood intervals on either side of the peak position.
Identification of potential candidate genes
The reference genome sequence of the D genome diploid G. raimondii and the assembled Dt subgenome of the tetraploid G. hirsutum were downloaded from CottonGen (http://www.cottongen.org) along with their GFF3 gene annotation files. The physical region between markers BNL3545 and STV030 was identified in both genome sequences and scanned for annotated genes using the Multiple Sequence Comparison by Log-Expectation software [30]. Genes with Leucine Rich Repeat (LRR) N-terminal domains were shortlisted as potential candidate genes that may be involved in a nematode resistance. Protein sequences encoded by these genes were further used for blastp (protein-protein blast) search to identify protein homologs in the protein database of GenBank. A neighbor joining method was utilized to construct the phylogenetic tree using the MEGA 6.0 software [31].
Identification of single nucleotide variations
Genomes of an RKN susceptible cotton line, Acala ‘Maxxa’ (SRA061309), and an RKN resistant line, GA120R1B3 (SRA068148), were sequenced at 82x and 30x read depth respectively by Illumina sequencing of paired-end libraries [32]. Using the cotton D-genome sequence as reference [33], short reads were aligned using the Burrows-Wheeler Aligner (BWA) [34]. Single nucleotide polymorphism (SNPs) between candidate gene alleles in RKN resistant and susceptible lines were called with Samtools/bcftools [35, 36] using reads with mapping quality >30 and base quality >30 [32].
Results
Population biometrical parameters
Phenotypic distribution of Root Galling Index (RGI) and egg production in an F2 population segregating for the M. incognita resistance QTL qMi-C14
New SSR marker development and mapping
A total of 801 microsatellites were found on the 4 Mb region of G raimondii chromosome 05 between the two SSR markers BNL3545 and CGR5668, thought to contain qMi-C14, 405 microsatellites were identified in the first 2 Mb and 396 in the next 2 Mb region. The distribution of di, tri, tetra, penta and hexa repeats on the two regions is presented in Additional file 1: Figure S1. Of the 801 microsatellites identified, 624 (77.9 %) di-nucleotide repeats and 135 were tri-nucleotide repeats with unit copy numbers from 5–28. Forty-five SSRs occurring at approximately uniform intervals were selected to fine-map the region between BNL3545 and CGR5668. A polymorphism survey found 27 (60 %) SSRs to be polymorphic between M-120 RNR and Pima S-6, with 12 (27 %) being monomorphic and 6 (13 %) failing to amplify.
Genetic and physical position of qMi-C14 on chromosome 14. a LOD profile of the QTL region affecting RKN egg production; b Linkage map of the telomeric region; and c Physical location of the three clusters of candidate genes, identified with different colors
Association analyses
Because these phenotypes displayed a non-normal distribution, log transformed data for total eggs and eggs g-1 of root phenotypes were used for further analysis. Composite interval mapping detected a major QTL for total eggs and eggs g-1 root near the marker UGT1432, with the allele from the resistant parent M-120 RNR increasing nematode resistance for all phenotypes. The QTL peak for both phenotypes was located at the 12.9 cM position with a LOD value of 10.7 and 11.8, respectively. These QTLs explained up to 21.5 % and 24.6 % of phenotypic variation for total eggs and eggs g-1 root, respectively. The likelihood interval, circumscribed by a one LOD score drop on either side of the peak, covered 3.9 cM and was flanked by markers UGT1426 and UGT1414 (Fig. 2). The d/a ratio was 0.1 for both phenotypes, indicating that the gene action for this QTL is additive. Interestingly, there was no significant association with RGI suggesting that this region has no effect on suppressing root galling.
Mean difference between the three genotypic classes in the BNL3545 -- STV030 interval. Means were compared (P < 0.001) between individuals completely homozygous for the M-120 allele (Homo M120), completely homozygous for Pima S-6 alleles (Homo Pima S6) and completely heterozygous (Hetero)
Potential candidate genes
Physical locations of genes with Leucine Rich Repeat (LRR) domain between SSR markers BNL3545 and STV030 on chromosome 5 of G. raimondii and chromosome D02 of G. hirsutum
Gene name | Physical location | Group |
|---|---|---|
Gorai.005G026300 | 2297846 - 2301061 | I |
Gorai.005G026400 | 2313103 - 2316975 | I |
Gorai.005G026500 | 2345315 - 2348063 | I |
Gorai.005G026600 | 2349170 - 2352262 | I |
Gorai.005G026700 | 2361518 - 2365096 | I |
Gorai.005G028600 | 2501120 - 2504324 | II |
Gorai.005G028900 | 2553716 - 2557308 | II |
Gorai.005G029000 | 2565325 - 2569455 | II |
Gorai.005G029100 | 2585224 - 2589560 | II |
Gorai.005G029200 | 2596425 - 2600231 | II |
Gorai.005G029300 | 2613108 - 2617044 | II |
Gorai.005G029400 | 2632315 - 2635858 | II |
Gorai.005G031500 | 2804242 - 2806833 | III |
Gorai.005G031600 | 2810110 - 2813150 | III |
Gorai.005G031700 | 2819656 - 2825365 | III |
Gorai.005G031800 | 2833071 - 2838460 | III |
Gorai.005G031900 | 2852829 - 2859789 | III |
Gorai.005G032000 | 2870255 - 2876978 | III |
Gorai.005G032100 | 2880034 - 2881241 | III |
Gorai.005G032200 | 2898234 - 2905491 | III |
Gh D02G0233 | 2749065 - 2751671 | I |
Gh D02G0234 | 2757983 - 2759275 | I |
Gh D02G0235 | 2766873 - 2769728 | I |
Gh D02G0236 | 2780046 - 2781380 | I |
Gh D02G0237 | 2787974 - 2791318 | I |
Gh D02G0238 | 2800055 - 2803296 | I |
Gh D02G0257 | 2942631 - 2946086 | II |
Gh D02G0258 | 2962327 - 2965794 | II |
Gh D02G0259 | 2979373 - 2983290 | II |
Gh D02G0277 | 3219359 - 3311044 | III |
Gh D02G0280 | 3391502 - 3393436 | III |
Gh D02G0281 | 3410121 - 3412647 | III |
Gh D02G0282 | 3466152 - 3467675 | III |
Phylogenetic relationships among the candidate genes with LRR motifs near the qMi-C11 locus, from G. raimondii (panel a) and G. hirsutum (panel b). Red dots, blue squares and green diamond represent genes from Group I, II, and III, respectively
SNP between RKN resistant and susceptible alleles
Details of non-synonymous SNPs that differentiate genes from GA120R1B3 (RKN resistant) and Acala Maxxa (susceptible) lines in the QTL region flank by Gorai.005G026300 and Gorai.005G032200
Gene ID | Position | Strand | Ref allele | Susceptible allele | Resistant allele | Ref aa | Susceptible aa | Resistant aa | SNP location | Pfam | Annotated function |
|---|---|---|---|---|---|---|---|---|---|---|---|
Gorai.005G026500 | 2345728 | + | T | T | G | F | F | L | CDS | PF08263,PF00560,PF13855 | receptor like protein 7 |
Gorai.005G027700 | 2415658 | - | T | T | G | . | . | . | 3-UTR | PF02826,PF05221 | S-adenosyl-L-homocysteine hydrolase |
Gorai.005G028100 | 2458792 | - | T | T | C | . | . | . | 3-UTR | PF00076 | glycine-rich RNA-binding protein 2 |
Gorai.005G028100 | 2459025 | - | A | A | G | . | . | . | 3-UTR | PF00076 | glycine-rich RNA-binding protein 2 |
Gorai.005G028100 | 2460937 | - | A | A | T | . | . | . | 5-UTR | PF00076 | glycine-rich RNA-binding protein 2 |
Gorai.005G028500 | 2499549 | + | C | C | T | . | . | . | 3-UTR | PF05653 | Protein of unknown function (DUF803) |
Gorai.005G028600 | 2502813 | + | T | T | A | S | S | R | CDS | PF08263,PF00560,PF13855 | receptor like protein 7 |
Gorai.005G028600 | 2502817 | + | G | G | A | D | D | N | CDS | PF08263,PF00560,PF13855 | receptor like protein 7 |
Gorai.005G029200 | 2599856 | + | G | G | T | K | K | N | CDS | PF08263,PF13855 | receptor like protein 6 |
Gorai.005G029200 | 2599857 | + | A | A | T | I | I | F | CDS | PF08263,PF13855 | receptor like protein 6 |
Gorai.005G029400 | 2632994 | + | T | T | C | V | V | A | CDS | PF08263,PF13855 | receptor like protein 6 |
Gorai.005G029400 | 2634053 | + | G | G | C | S | S | T | CDS | PF08263,PF13855 | receptor like protein 6 |
Gorai.005G029600 | 2657576 | + | G | G | A | A | A | A | CDS | PF00119 | ATPase, F0 complex, subunit A protein |
Gorai.005G029600 | 2657842 | + | G | G | A | R | R | Q | CDS | PF00119 | ATPase, F0 complex, subunit A protein |
Gorai.005G030200 | 2695818 | - | T | T | A | . | . | . | 3-UTR | PF01564,PF08241 | S-adenosyl-L-methionine-dependent methyltransferases superfamily protein |
Gorai.005G030800 | 2750823 | - | G | G | A | . | . | . | 5-UTR | PF05856 | protein binding |
Gorai.005G031000 | 2760819 | + | C | C | T | . | . | . | 5-UTR | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2761040 | + | A | A | C | . | . | . | 5-UTR | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2761073 | + | A | A | G | . | . | . | 5-UTR | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2761385 | + | C | C | A | R | R | S | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2761993 | + | G | G | C | K | K | N | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2761995 | + | C | C | G | T | T | S | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2762049 | + | A | A | G | E | E | G | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2768718 | + | A | A | G | N | N | D | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Gorai.005G031000 | 2768729 | + | A | A | T | P | P | P | CDS | PF02892,PF02902,PF05699 | BED zinc finger ;hAT family dimerisation domain |
Discussion
Transgressive segregation for RKN resistance from the Auburn 623RNR cotton germplasm is due to the effects of pyramiding of at least two QTLs inherited from different parents; each individually confers moderate resistance, although the two QTLs interact epistatically to confer near-immunity. The qMi-C11 and qMi-C14 loci map to chromosome 11 and 14, respectively [8, 9]. Study of these loci shows that two phenotypes commonly used to measure resistance reaction to RKN, specifically galling index and egg production, could be partly genetically independent, and the qMi-C11 and qMi-C14 loci may provide resistance via different mechanisms [8, 9]. Full characterization of qMi-C11 and qMi-C14 will advance our understanding of defense mechanisms against parasitism from RKN, elucidate host-pathogen interactions at the molecular level, and facilitate their use in cotton improvement.
The genetic population used in the current study, consisting of 513 F2:3 plants, was developed using F2 plants that were heterozygous (and therefore segregating) at the qMi-C14 locus but homozygous for the susceptible parent allele at the qMi-C11 locus. Without the confounding effects from the qMi-C11 QTL, our data confirmed prior QTL analyses suggesting that the qMi-C14 locus had a highly significant effect on egg production but little or no effect on root galling (Fig. 3). The estimated main genetic effects for this locus was 21.5 to 24.5 % PV explained, lower than the 45 to 47 % PV explained in our earlier study when both QTLs were segregating in the population [9]. The suppression of egg production with qMi-C14 alone appears to be lower in the absence of the qMi-C11 locus, further supporting the hypothesis that the combination of both QTLs with different modes of action provides the genetic basis for transgressive segregation in the Auburn 623RNR germplasm [8, 9]. Similar transgressive resistance to root-knot nematode resulting from epistatic interaction have been reported in cotton. For example, Wang et al. [37] reported that the gene RKN2 from the susceptible G. barbadense cultivar Pima S-7 can significantly enhance the level of resistance to RKN in the Acala NemX resistance source. In addition to cotton, interlocus interactions among main effect resistance QTLs have been observed in pepper [38] and soybean [39], suggesting that epistasis is common and constitutes a major component of host-plant resistance to pest and disease pathogens.
The reference genome sequence of the diploid G. raimondii [33] and draft sequence of the tetraploid Upland cotton G. hirsutum [40, 41] have provided the cotton community an unprecedented resource for genome analysis. In this study, we were able to narrow the confidence interval for qMi-C14 to a 3.9 cM region and identify 20 candidate resistance genes with conserved LRR domains clustering in three groups (Fig. 4). This is not surprising as NBS-LRR genes are frequently clustered in plant genomes, and can contain genes conferring resistance to diverse pathogens, thereby acting as reservoirs of genetic variation for resistance specificities [17]. More importantly, of the six RKN resistance genes that have now been cloned in plants, all fall into a family of genes with the classic LRR motif typical of disease resistance genes (R-genes) [42]. Not all genes may be expressed at a given time but specific R genes may be triggered by the avirulence (Avr) factor of the invading pathogen, and result in activation of a gene-for-gene resistance mechanism. Since a majority of disease resistance genes are comprised of arrays of hypervariable potential ligand-binding sites, inter-allelic recombination within these arrays along with unequal recombination may be the primary mechanism behind rapid evolution of R genes and their clustering in the genome [43].
To further investigate the role of these LRR genes in disease resistance, we performed a Blast search of GenBank to identify annotated genes from species for which the genome sequence is available. Except for the gene Gorai.005G026700 and its tetraploid genome counterpart Gh D02G0238 that showed high similarity with a Theobroma cacao leucine-rich repeat protein kinase family protein isoform (accession No. XP_007034190.1), all other candidate genes from cluster I and II (Group I and II on the cladogram) showed high similarity with a Theobroma cacao Verticillium wilt disease resistance-like protein (up to 82 % sequence similarity to accession XM_007034192.1). Genes in cluster III showed high homology with a Theobroma cacao receptor like protein (accession XM_007010859.1). This observation is not uncommon - as noted in earlier studies, R genes in a disease resistance cluster encode protein motifs that are components of signal transduction systems including genes coding for protein receptors and protein kinases. For example, the Xa21 R gene cluster in rice is composed of more than eight LRR and protein kinase genes while the M locus in flax and RPP5 locus in Arabidopsis are comprised of genes with NBS-LRR and Toll-interleukin like protein receptor domains [44]. Molecular studies have shown that some R genes in a disease resistance cluster share some degree of sequence similarity with other genes but are functionally divergent. For example, Prf, an NBS-LRR R gene, is located within a cluster of five protein kinase homologs (Pto). Both Prf and Pto genes are required for resistance to Pseudomonas syringae pv. tomato [44], suggesting that resistance is conferred by a haplotype rather than an individual gene.
Among 20 positional candidate LRR genes, sequencing of the QTL interval of the resistant germplasm GA120R1B3 (derived from Auburn 623RNR) revealed only four to have non-synonymous mutations in the coding region (Table 2), suggesting these to be more probable candidates than the others. The observation that the SNP containing LRR gene Gorai.005G026500 belongs to cluster-I and Gorai.005G028600, Gorai.005G029200, and Gorai.005G029400 belong to cluster-II implicates one of these two clusters in RKN resistance. Such non-synonymous mutations in the coding region are likely to have caused changes in the structure and function of the encoded protein, but the effects of these mutations are currently unknown.
Although no nematode resistance genes have been cloned via map-based cloning in cotton, a polypeptide called Meloidogyne Induced Cotton or MIC protein has been observed to be differentially expressed in root galls of resistant and susceptible cotton plants [45]. Further analyses on the MIC protein led to the identification of the MIC-3 gene family with at least 15 MIC-like cDNAs that encode cotton-specific pathogenesis-related proteins [46, 47]. Overexpression of MIC-3 in a RKN susceptible cotton line showed 60–70 % reduction in RKN egg production when compared to non-transgenic controls [40]. Further, overexpression of MIC-3 does not affect RKN-induced root galling. Therefore, the MIC gene family produced a similar phenotypic effect as qMi-C14, reducing nematode egg production but not root galling. However, our BLAST search against the G. hirsutum genome database using the MIC sequence (Accession No. AY072783) showed no MIC-like genes in or near the qMi-C14 region, precluding MIC family members as candidate genes for this QTL. Nonetheless, given that MIC expression and effects are strongly correlated with RKN resistance, it is possible that this gene family represents a type of pathogenesis-related gene in which the effect is at the ‘end-point” in the signaling cascade that is regulated by gene(s) annotated in the qMi-C14 locus.
From a practical breeding perspective, until the causal gene for qMi-C14 is identified, it might be prudent to simultaneously target all three clusters of R genes from the resistant parent to ensure horizontal and possibly stable RKN immunity of new cultivars. Tightly linked markers are therefore important for detecting recombination events that may result in segregation of these R gene clusters, as well as to identify the zygosity of selected plants during marker-assisted selection. Our results further point to the dominant nature of this QTL as indicated by non-significant differences between the heterozygous and homozygous classes of resistance alleles. This scenario can potentially render selection based solely on phenotypic observation less effective in cotton breeding populations, and may have contributed to difficulties in fixing resistance alleles during the development of the highly resistant germplasm line GA 120R1B3 [48].
Conclusion
In this study, we validated an earlier observation that the qMi-C14 resistance locus mostly suppress egg production but has little effect on galling, further supporting the hypothesis that the effectiveness of RKN resistance from Auburn 623RBR is due to synergistic effects of two different mechanisms of RKN resistance. In addition, we have delimited qMi-C14 to a physical contig of about 2.3 Mb and identified 20 positional candidate LLR genes, including four of which containing non-synonomous mutation in the coding region. The candidate genes identified warrant functional studies that will help in identifying and characterizing the actual qMi-C14 defense gene(s) against root-knot nematodes.
Abbreviations
LRR, leucine rich repeat, LOD, likelihood of odds ratio, NBS, nucleotide binding site, QTL, quantitative trait locus, RKN, root-knot nematodes, RNR, root-knot nematode resistant, SSR, simple sequence repeats
Declarations
Acknowledgments
We thank Jennifer McCurdy for technical assistance; Ed Lubbers and Mychele Batista Da Silva for valuable comments.
Funding
We appreciate financial support from the Georgia Cotton Commission and Cotton Incorporated.
Availability of data and materials
The sequences of all candidate genes were obtained from the reference genome sequence of G. raimondii and G. hirsutum, which are publicly available in the CottonGen database (http://www.cottongen.org). The data utilized in the alignment and phylogenetic analysis can be found in Treebase (http://purl.org/phylo/treebase/phylows/study/TB2:S19559).
Authors’ contributions
YH, PK, RS and XS developed the interspecific F2 population and performed the SSR genotyping work. RD performed the phenotypic evaluations. HG, AP, and DP analyzed the genome sequences of Acala Maxxa and GA120R1B3. BN, AP, DP, and PC assisted in drafting of the manuscript. All authors read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Consent for publication
Not applicable.
Ethics approval and consent to participate
Not applicable.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Authors’ Affiliations
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