- Open Access
Identification of QTLs and possible candidate genes conferring sheath blight resistance in rice (Oryza sativa L.)
© Yadav et al.; licensee Springer. 2015
- Received: 24 December 2014
- Accepted: 30 March 2015
- Published: 11 April 2015
Sheath blight, caused by the pathogenic fungus Rhizoctonia solani Kühn, is one of the most devastating diseases in rice. Breeders have always faced challenges in acquiring reliable and absolute resistance to this disease in existing rice germplasm. In this context, 40 rice germplasm including eight wild, four landraces, twenty- six cultivated and two advanced breeding lines were screened utilizing the colonized bits of typha. Except Tetep and ARC10531 which expressed moderate level of resistance to the disease, none could be found to be authentically resistant. In order to map the quantitative trait loci (QTLs) governing the sheath blight resistance, two mapping populations (F2 and BC1F2) were developed from the cross BPT-5204/ARC10531. Utilizing composite interval mapping analysis, 9 QTLs mapped to five different chromosomes were identified with phenotypic variance ranging from 8.40 to 21.76%. Two SSR markers namely RM336 and RM205 were found to be closely associated with the major QTLs qshb7.3 and qshb9.2 respectively and were attested as well in BC1F2 population by bulk segregant analysis approach. A hypothetical β 1–3 glucanase with other 31 candidate genes were identified in silico utilizing rice database RAP-DB within the identified QTL region qshb9.2. A detailed insight into these candidate genes will facilitate at molecular level the intricate nature of sheath blight, a step forward towards functional genomics.
- Sheath blight
- QTL mapping
- Bulk segregant analysis (BSA)
- Defense response genes
Sheath blight, caused by Rhizoctonia solani Kühn of the anastomosis group AG1- IA, is potentially a devastating disease of rice (Oryza sativa) in the temperate and tropical rice growing regions of the world (Teng et al. 1990). In recent years, the disease has assumed serious epiphytotic proportions causing earnest crop losses under intensive rice production systems characterized by abundant application of nitrogenous fertilizers, high planting density, and extensive adoption of high-yielding cultivars (Slaton et al. 2002).
Breeding for sheath blight (ShB) resistance has been a futile exercise so far, mainly because of lack of reliable stable sources of resistance in rice germplasm (Jia et al. 2009; Zuo et al. 2010; Srinivasachary and Savary 2011; Liu et al. 2013). Though rice literature is replete with reports on the occurrence of sources with varied levels of resistance have been found as in Teqing (Li et al. 1995; Pinson et al. 2005), Jasmine 85 (Pan et al. 1999; Zou et al. 2000; Liu et al. 2009), Minghui63 (Han et al. 2002), Xiangzaoxian 19 (Che et al. 2003), WSS2 (Sato et al. 2004), Pecos (Sharma et al. 2009) and Tetep (Sha and Zhu, 1989; Channamallikarjuna et al. 2010) and wild rices O. rufipogon, O. nivara etc. (Ram et al. 2008; Eizenga et al. 2013). Intensive study of the resistance in such sources reveals it to be quantitative in nature controlled possibly by polygenes (Sha and Zhu 1989; Li et al. 1995; Pinson et al. 2005; Zuo et al. 2013 It is widely believed that quantitative nature of resistance could be the expedient for evolving varieties with durable/horizontal resistance (Young, 1996; Poland et al. 2009). Precise mechanism underlying the quantitative resistance as yet not well understood, could be attributed to the host plant defense system through PR proteins in response to attack by pathogen (Datta et al. 1999; Vanloon and Strien 1999). Over-expression of PR proteins, including chitinases (PR-3), β-1, 3-glucanases (PR-2), thaumatin like proteins (PR-5), and other plant or microbe derived antifungal proteins in transgenic plants is known to provide resistance to sheath blight (Lin et al. 1995 and Datta et al. 2001).
With the rapid development of molecular marker technology, there have been significant advances in mapping ShB resistance QTLs: To date, around 50 ShB resistance quantitative trait loci (ShBR QTLs) have been mapped to all the 12 rice chromosomes (Jia et al. 2009; Zuo et al. 2010; Xu et al. 2011 and Wang et al. 2012). Several recent studies have explore the possible candidate genes viz. Chitinase, Glucanase, Glutathione S-Transferase and Kinase protein within the mapped QTL region may responsible for sheath blight resistance (Channamallikarjuna et al. 2010; Silva et al. 2012; Zuo et al. 2014). Though most of the ShBR QTLs identified so far are of only limited effects on ShB resistance, instances of some showing expected effect were not uncommon. For instance Zuo et al. (2007) reported introgression of the QTL, qSB-11 LE and observed reduced grain loss by 10.71% in Lemont background under severe disease infestation in field trials. Pinson et al. (2005) predicted that qSB-9 TQ and qSB-3 TQ could possibly reduce the crop loss due to ShB by 15% when introduced into Lemont. Yin et al. (2010) and Wang et al. (2012) have found that pyramiding of diverse ShBR QTLs could help achieve higher levels of resistance to ShB. Thus, it is likely that the level of resistance to the disease could be raised by pyramiding diverse ShBR QTLs differing in their level of moderate resistance.
Keeping in view this possibility the present investigation was conducted to i) identify ShB resistance source(s), ii) establish their genetic diversity by molecular mapping of the QTLs associated with sheath blight resistance by using F2:3, iii) validation of markers associated with sheath blight resistance in BC1F2, iv) to identify the possible candidate genes in the QTL region by in silico analysis.
List of rice germplasm screened for Sheath Blight Resistance
Oryza rufipogon AC100488
O. rufipogon AC 100368
O. rufipogon AC 100490
O. rufipogon AC100483
O. nivara AC100456
O. nivara AC100396
O. nivara AC 100395
O. nivara AC 100110
NRCPB- New Delhi
Advanced Breeding Lines
NRCPB- New Delhi
NRCPB- New Delhi
Evaluation of rice germplasm for sheath blight resistance
The screening for the disease reaction was carried out in Kharif 2011 at the Institute of Biotechnology, ANGRAU under the artificial epiphytotic conditions in a hot humid chamber. The material was sown in 3 replications in separate pots and maintained in the humid chamber at optimum humidity (90%) and temperature (28-30°C), which are very favorable for the disease development.
Multiplication of the pathogen
In the present study, the most virulent local Rajendranagar isolate of rice sheath blight pathogen R. solani AG 1-IA (Wamishe et al. 2007) obtained from the Division of Plant Pathology, Directorate of Rice Research, Hyderabad and utilized used for disease screening.
Before the inoculation, the fungus was cultured in potato dextrose agar (PDA) medium at 28°C for 3–4 days, followed by transferring of disc of medium with mycelia for multiplication. The inoculum of the virulent isolate was multiplied by following the procedure described by Bhaktavatsalam et al. (1978). Typha stem bits of 4–5 cm long were washed exhaustively and soaked in typha medium for 5 minutes. Subsequently, they were filled loosely to 1/3 volume of 500 ml conical flask and autoclaved for 20 minutes each for two consecutive days. The sterilized flasks with typha were inoculated with 5 mm diameter disk of actively growing mycelium of R. solani AG1-IA and incubated for one week at 28 ± 2°C. Then colonized typha stem bits so developed were utilized as inoculum.
Pathogen inoculation and disease scoring
In the present study, ARC10531 and Tetep were identified as moderately resistant to sheath blight among the 40 rice germplasm screened. Tetep is a known source for moderate resistance to the disease and QTLs relating to resistance has already been reported by Channamallikarjuna et al. (2010). Hence, the present study was confined to ARC 10531 for development of mapping population and mapping of QTLs conferring resistance.
One mapping population consisted of 210 F2:3 progeny lines derived from the cross between the susceptible BPT-5204 and moderately resistant ARC10531. The susceptible parent BPT-5204 is the late -maturing, fine grain, semi-dwarf and high yielding variety but highly susceptible to R. solani. The resistant parent ARC 10531 is a late-maturing, bold grain and tall land race from Assam with moderate resistance to ShB. The other mapping population (BC1F2) comprising 150 plants derived from the same cross (BPT-5204/ARC10531) planted in the green house at IBT (ANGRAU) were used to validate the markers linked to sheath blight resistance QTLs.
Phenotyping of F2:3 and BC1F2 population
The 210 plants of F2:3 and 150 of BC1F2 population derived from the cross (BPT-5204/ARC10531) were grown in pots as well as under soil bed conditions. The plants were inoculated with R. solani multiplied in typha bits and disease reaction for the disease was recorded as per the Standard Evaluation System described earlier.
Bulk segregant analysis
Bulk Segregant Analysis (BSA) is as an efficient strategy for identifying the DNA markers linked to the gene(s) or genomic regions of interest (Michelmore et al. 1991). By making DNA bulks, all loci are randomized, except for the region containing the gene of interest. In this approach, the markers are screened across the parents and two bulks. Polymorphic markers may represent markers that are linked to the gene or QTL of interest (Collard et al. 2005). DNA bulks of plants showing resistant reaction and of those found susceptible were prepared from BC1F2 population. This was done by pooling aliquots, containing equivalent amounts of DNA approximately, 50 ng/μl from each of ten highly resistant and ten highly susceptible plants of the BC1F2 generation predicated on phenotypic observations. Seventy polymorphic SSR primers were utilized for screening the parents and the two bulk DNA samples.
Construction of molecular linkage map
The total genomic DNA was extracted of young leaves from each of the F2 plants along with those of the two parental lines - BPT5204 and ARC10531as per the method described by Murray and Thompson (1980). The concentration of the DNA was detected with the aid of ultraviolet spectrophotometer. The DNA quality was judged by running on 0.8% agarose gel electrophoresis stained with ethidium bromide (EtBr) (10 mg/ml) using 1× TAE buffer at constant voltage 70 V for 30 minutes and visualized under UV light. The DNA was amplified through PCR using reaction mixture (total volume 10 μl), containing 20 ng template DNA, 10 mM Tris–HCl, 50 mM KCl, 2.5 mM MgCl2, 10 mM dNTPs, 5 pmol each primers and 1.0 U Taq DNA polymerase. The PCR reaction was performed as DNA denaturation at 94°C for 4 minutes followed by 35 cycles (94°C for 1 minutes, 55°C for 1 minutes, 72°C for 1 minutes) and final extension step (at 72°C for 10 minutes). The PCR product was subjected to electrophoresis on 4% metaphor agarose. The DNA fragments were then visualized under UV-transilluminator and documented using a gel documentation system (BIO-RAD Gel Doc™ XR, USA).
Identification of sufficient number of markers revealing polymorphism among the parental lines is a prerequisite for the construction of a genetic linkage map. In this study, parental polymorphism survey was carried out between the two parents (ARC10531 and BPT-5204) using a total of 500 SSR markers spanning all the 12 chromosomes of rice (http://www.gramene.org/). The list of polymorphic markers with their details is depicted in Additional file 1: Table S2.
Seventy polymorphic markers were used for genotyping of the 210 F2 individuals along with parental lines. A linkage map was constructed by using MAPMAKER 3.0 (Cambridge, MA, USA; Lander et al. 1987). The map distances were calculated based on Kosambi’s function (Kosambi, 1944).
Identification of QTLs for ShB resistance was completed using the software QTL cartographer v. 2.5 (Wang et al. 2004 http://statgen.ncsu.edu/qtlcart/WQTLCart.htm). To identify additional QTLs that may have been masked by the major QTLs, composite interval mapping (CIM) method was employed. Genome-wide threshold values (α = 0.05) were used to detect putative QTLs on the basis of the results of 1000 permutations (Churchill and Doerge 1994). The likelihood-ratio (LR) test statistic used was -2ln (L0/L1), where L0/L1 is the ratio of the likelihood under the null hypothesis (there is no QTL in the interval) and the alternative hypothesis (there is a QTL in the interval). The presence of a putative QTL was declared if the LOD threshold was larger than 3.0 (Basten et al. 2002). The QTLs were deemed to exist only at positions where an LOD score exceeded the corresponding significant threshold. Estimation of the position, genetic effects, and percentage of phenotypic variation of the QTLs were done at the significant LOD peak in the region under consideration. The proportion of phenotypic variation explained by each QTL was calculated as R2 value, and the degree of dominance of a QTL was estimated as the ratio of dominance effect to additive effect.
Screening of rice germplasm for sheath blight resistance
Grouping of rice genotypes based on their reactions against the fungus R. solani, AG1-IA
Relative lesion height (%)
RIL-140 of cross HP2216× Tetep, Swarnadhan, MTU 1061, Kavya, Naveen, Oryza rufipogon AC 100490,
Rajeswari, Moroberakan, Vandana, Lalnakandha, MTU 1001, Oryza nivara AC100395, AC100396, Oryza rufipogon AC100488, Sonasali and Pusa Basmati,
TKM-6, Nilagiri, Jyothi, WGL32100, Chandan,N-22,Ghanteswari, MTU-1010, Jaya, Jaganath, WGL14, Surekha, JGL-3844,IR-64, Khandagiri, Oryza nivara AC100456, AC100110Oryza rufipogon AC100483 and AC100368, RIL-45 of cross HP2216x Tetep, BPT-5204,
Several researchers have attempted in the past to identify sources of resistance to ShB by screening a large number of wild species, landraces, local and improved cultivars, advanced breeding lines using different screening techniques (Srinivasachary and Savary 2011). They broadly included use of colonized typha bits (Bhaktavatsalam et al. 1978), a toothpicks infected with R. solani (Zou et al. 2000), broadcasting of inoculum on rice plants (Li et al. 1995; Savary et al. 1995; Singha and Borah 2000 and Han et al. 2002), infected rice grain–hull mixtures (Pan et al. 1999; Willocquet et al. 2000), detached leaf technique (Prasad and Eizenga, 2008) and micro-chamber method (Jia et al. 2009) under controlled greenhouse conditions. In comparison with field ShB evaluation, the micro-chamber and mist-chamber assays were simple, precise and more reliable assays methods in tagging ShB resistance (Liu et al. 2009; Jia et al. 2009). In the present study controlled chamber method was adopted by keeping the potted plants inoculated with typha bits under greenhouse condition, maintained at optimum humidity (90%) and temperature (28-30°C) for disease development.
As for disease development and expression, earlier reports suggest plant height to be related to disease severity (Sharma et al. 2009; Liu et al. 2014) reveal relatively tall statured plants favor disease escape delaying the spread of the pathogen to canopy. In the present study, ARC 10531 and Tetep exhibited low RLH% possibly due to a well-developed mechanism against sheath blight disease as well as their tall stature nature which delays the spread of the pathogen to the canopy in these moderately resistant line. The statement cannot be generalized as in the present study other varieties and wild accessions tall in stature expressed susceptibility towards ShB disease. Pace of disease development need not be due to plant height alone. Possibly there may be other factors associated with the resistance gene warranting more detailed study of such an association. Channamallikarjuna et al. 2010 similarly viewed that sheath blight resistance quantified in Tetep might be due to the molecular mechanisms involved in host- pathogen interaction and not due to any morphological adaptation to evade disease. The heading date is also associated significantly with ShB resistance and the varieties with later maturing are generally more resistant to ShB (Zuo et al. 2010; Srinivasachary and Savary 2011).
The present study though could not succeed in finding a strong source of resistance to sheath blight, assumes importance in identifying additional source of moderate resistance to the diseases in ARC10531 besides the already known source Tetep. If they are found to be of diverse genetics, they would prove a base for pyramiding them and expect enhanced level of resistance.
Phenotype distribution analysis
Linkage map construction and QTL analysis
QTLs identified for Sheath Blight Resistance by Composite Interval Mapping (CIM)
On chromosome 1, the QTLs qshb1.1 was found linked to the markers RM151 and RM12253 respectively with phenotypic variance of 10.99% and 12.18%, explaining involvement of additive gene action. Earlier workers too mapped ShB resistance to chromosome 1, but at locations different from the presently identified location (Liu et al. 2009; Jia et al. 2012). For ShB QTL on chromosome 6 (qshb6.1), the genomic region identified in the present study were same as the ones reported earlier by Zou et al. (2000) and Liu et al. (2009), but the peak markers were different. Thus, the markers linked to the ShB resistances QTLs on chromosome 1, 6 and 8 were different and reported for the first time. Likewise the QTL qshb8.1 was found at almost the same genomic region as that of the QTL reported by Li et al. (1995) and Channamallikarjuna et al. (2010).
On chromosome 7, three QTLS qshb7.1, qshb7.2, and qshb7.3 were mapped and phenotypic variance of 21.76% was observed for QTL qshb7.3 denoting strong additive gene action. Four studies detected QTLs for sheath blight around the chromosomal region of qshb7.3 (Pan et al. 1999; Zou et al. 2000; Kunihiro et al. 2002 and Liu et al. 2009).
Some of the chromosomal regions containing ShBR QTLs and its associated markers identified in present investigation were also reported earlier by different researchers. However, the genomic locations of these QTLs were observed to be different in different populations. These might be due to the use of different sources of resistance to sheath blight in different studies, varying methodologies of assessing sheath blight resistance, or the use of different marker densities as earlier expressed by Channamallikarjuna et al. (2010).
A QTL region qshb7.3 identified on chromosome 7 associated with marker RM336 was in agreement with the previously reported result of Channamallikarjuna et al. (2010) with different genomic location. The alleles explained 21.76% of total phenotypic variance in contrast with the report of Channamallikarjuna et al. (2010) depicting only 10.02% for this QTL. This might be due to interaction of favorable alleles in this source (ARC10531) of resistance. The QTL region qshb7.3 associated with same peak marker RM336 in both the studies represents the stability of the QTL for sheath blight resistance.
The major QTL qshb9.2 identified on chromosome 9 associated with marker RM205 was earlier reported by Tan et al. (2005) in F2 population derived from a Lemont/Teqing. The QTL location, associated marker and phenotypic variance identified in their study was quite similar to that observed in our study. The QTL qshb9.2 identified in this study not only helped in validation of QTL once again, but also provided an alternate source of resistance for introgression of the QTL into any elite variety. This consistent QTL region qshb-9 for sheath blight resistance on chromosome 9 has been verified by various independent researches (Li et al. 1995; Tan et al. 2005; Pinson et al. 2005; Liu et al. 2009; Yin et al. 2010; Zuo et al. 2014) and in the present study, indicating its authenticity and potentially breeding value in practice. These may be candidate regions to explore in ShB resistance breeding programme. The major ShB-QTLs qshb7.3and qshb9.2 identified in the present study, as a favorable QTL can be readily transferred using MAS into elite cultivars to strengthen their resistance levels. In addition, we have identified other minor ShB QTLs, which can be used to develop new cultivars with improved resistance to this important disease.
Although the present findings are preliminary and QTL were identified under controlled condition, the validation of identified QTLs in other populations with adequate size and number of markers tested across multiple environments would add additional landmark in regards to identify resistance genes against sheath blight.
Confirmation of linked microsatellite markers associated with sheath blight resistance in rice
Channamallikarjuna et al. (2010) utilized an F2 population derived from resistant parent Tetep, to confirm the linked marker associated with sheath blight QTL identified in RIL population. They validated the marker RM224 linked to major QTL, qSBR11-1 identified during their earlier study with RILs of same cross. In the present study, the two microsatellite markers RM336 and RM205 associated with major QTLs, qshb7.3 and qshb9.2 were reconfirmed in the BC1F2 population by using BSA approach. The evaluation of stable line phenotypically at the ShB hot spot location to study the stability of the identified major QTL could speed up the process of authenticating markers for phenotypically complex traits viz sheath blight and can be particularly useful for mapping genes whose phenotypes cannot be easily separated into discrete classes.
In silico analysis for presence of defense responsive candidate genes within the identified QTLs
In order to navigate for the presence of candidate defense responsive genes present in the chromosomal regions associated with sheath blight resistance, a search was done in silico using rice data base RAP-DB. This in silico search was done for the presence of defense responsive genes as well as genes associated with signal transduction of biotic stresses.
List of candidate genes identified in the QTL mapped region qShb 9.2
Position start – end (bp)
Description (RAP-DB annotation)
Similar to CBF-like protein
Cyclin-like F-box domain containing protein
Similar to Hd1-like protein
Cytochrome P450 family protein
Proteinase inhibitor, propeptide domain containing protein
Similar to β-1, 3-glucanase precursor (EC 184.108.40.206).
Similar to Heat shock protein 82
Transcription initiation factor IIB (TFIIB).
Conserved Hypothetical protein.
Curculin-like (mannose-binding) lectin domain containing protein.
Exodeoxyribonuclease III xth family protein.
Ribonuclease T2 family protein
Eukaryotic transcription factor, DNA-binding domain containing protein
Similar to Plasma membrane intrinsic protein (Aquaporin).
Similar to 26S proteasome subunit RPN3a.
Transferase family protein.
Similar to Glutathione S-transferase GST 16 (EC 220.127.116.11).
Glucose/ribitol dehydrogenase family protein.
Cyclin-like F-box domain containing protein.
Ribosomal protein L18P/L5E family protein.
Protein kinase domain containing protein.
Similar to NADC homolog.
Similar to 26S protease regulatory subunit 6B
Similar to mutator-like transposase [Oryza sativa (japonica cultivar- group)].
Similar to RuBisCO subunit binding-protein alpha subunit, chloroplast precursor (60 kDa chaperonin alpha subunit)
Lipoprotein, type 6 family protein
Similar to Beta-amylase (EC 18.104.22.168) (1,4-alpha-D-glucan maltohydrolase).
Similar to Calmodulin-binding heat-shock protein
Beta-lactamase-like domain containing protein
Zuo et al. (2014) reported 12 candidates within the QTL region qSB-9 TQ responsible for transferase family proteins glutathione S-transferase and kinase protein. Silva et al. (2012) identified four candidate genes within the major QTL qShB9-2, mapped by Liu et al. (2009). In their study, they found the pathogenesis-related (PR) protein glucan endo-1, 3-β-glucosidase (glucanase) at two loci on chromosomes 8 and 9. Interestingly in our study also, same kind of gene (β -1, 3 glucanase like protein) with single copy spanning 21770245…21771297 bp was identified on chromosome 9 within the QTL qshb9.2 linked with marker RM205. A wealth of scientific reports (Sridevi et al. 2003; Kalpana et al. 2006) accumulated on plant β -1,3-glucanases has enabled us to understand their structure, regulation of expression and the multitude of roles they play directly and indirectly in plants. β -1, 3- glucanases are most studied with respect to their expression during pathogen infection and their broad spectrum anti-fungal, antimicrobial activity (Ignacimuthu and Antony 2012). Channamallikarjuna et al. (2010) predicted 11 tandem repeats of chitinase genes near the QTL qSBR11-1 on chromosome 11 may be responsible for sheath blight resistance in rice line Tetep. Our study revealed, β-1, 3-glucanase precursor (EC 22.214.171.124) a PR protein within QTL (qshb9.2) on chromosome 9. Hence, pyramiding of these two major QTLs into one background gives the possibility of combined effect of chitinase and β-1, 3-glucanase may be the feasible strategy to produce resistant cultivar against ShB.
In present study two SSR markers namely, RM336 and RM205 were found to be closely associated with the major QTLs qshb7.3 and qshb9.2, respectively in the newly identified source ARC10531 and same were confirmed as well in BC1F2 population by bulk segregant analysis approach. The presence of defense responsive gene β 1–3 glucanase as well as genes associated with signal transduction of biotic stresses within ShB resistance QTL (qshb9.2) may be responsible for sheath blight resistance in rice line ARC10531. Further, the approach of pyramiding QTLs identified in this source with earlier identified diverse QTLs for ShB resistance may help in developing cultivars with enhanced and durable resistance to this disease.
The authors wish to thank the Director, Institute of Biotechnology, Acharya N.G. Ranga Agricultural University, Hyderabad-500 030, India for providing all the facilities to carry out this present work. The ICAR-SRF fellowship received by SHAILESH YADAV is gratefully acknowledged.
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