Skip to main content
PMC home page
International Journal of Molecular Sciences logoLink to International Journal of Molecular Sciences
. 2014 Jul 3;15(7):11847–11861. doi: 10.3390/ijms150711847

Quantitative Trait Loci Mapping for Bacterial Blight Resistance in Rice Using Bulked Segregant Analysis

Xueying Han 1,2,†, Yong Yang 2,†, Xuming Wang 2, Jie Zhou 2, Wenhao Zhang 3, Chulang Yu 2, Chen Cheng 2, Ye Cheng 2, Chengqi Yan 2,*, Jianping Chen 1,2,*
PMCID: PMC4139818  PMID: 24995697

Abstract

Oryza meyeriana is highly resistant to rice bacterial blight (BB) and this resistance trait has been transferred to cultivated rice (O. sativa) using asymmetric somatic hybridization. However, no resistance genes have yet been cloned. In the present study, a progeny of the somatic hybridization with high BB resistance was crossed with a rice cultivar with high BB susceptibility to develop an F2 population. Using bulked segregant analysis (BSA), 17 polymorphic markers that were linked to rice BB resistance were obtained through scanning a total of 186 simple sequence repeats (SSR) and sequence-tagged site (STS) markers, evenly distributed on 12 chromosomes. A genetic linkage map was then constructed based on the 17 linkage markers and the F2 segregating population, which was followed by mapping for quantitative trait loci (QTLs) for BB resistance. Three QTLs were identified on chromosomes 1, 3 and 5, respectively, and the alleles of the resistant parent at any of the QTLs increased BB resistance. All of the three QTLs had a strong effect on resistance, explaining about 21.5%, 12.3% and 39.2% of the resistance variance, respectively. These QTLs were different from the loci of the BB resistance genes that have been identified in previous studies. The QTLs mapped in this work will facilitate the isolation of novel BB resistance genes and their utilization in rice resistance breeding.

Keywords: quantitative trait loci, mapping, bacterial blight resistance, bulked segregant analysis, Oryza meyeriana

1. Introduction

Xanthomonas oryzae pv. oryzae (Xoo) causes rice bacterial blight (BB), one of the most destructive bacterial diseases of rice worldwide. It is responsible for severe yield losses to global rice production, generally in the range of 20% to 30%, and as high as 50% in years when the disease is prevalent [1]. Chemical control is temporarily effective but often causes environmental pollution. In contrast, methods that depend on the plant’s innate immune system are more acceptable and environmentally friendly. So far, at least 36 genes conferring resistance to various Xoo strains have been identified [1,2,3,4]. Most of them have been tagged with DNA markers and eight of them (Xa1, Xa3/Xa26, Xa5, Xa10, Xa13, Xa21, Xa25, Xa27) have been cloned successfully using a map-based cloning strategy [3,4,5,6,7,8,9,10]. Some of these resistance genes have been widely used in rice breeding for BB resistance and many useful cultivars have been released in Asian countries.

However, development of resistant cultivars always faces difficulties in terms of durability of resistance because of the diversity and variability of the Xoo pathogen. For example, the resistance gene Xa4 has been deployed in many resistant varieties that have played an important role in defense against rice BB disease in the tropics and in many parts of China [11,12]. However, many cultivars only carrying Xa4 have now become sensitive to the disease because of the spread of Xoo strains able to overcome the resistance [12]. Xa21 has been widely used as a broad spectrum resistance gene since it was identified in the 1990s, but new pathogen virulence that can overcome Xa21 has also been found in many areas of Korea, Philippines, Japan and China [13,14]. Therefore, it is always important for researchers to exploit new resistance genes and this strategy plays an important role in durable BB resistance of rice.

Oryza meyeriana is one of the most important wild rice resources identified in South and Southeast Asia. It is adapted to survive in harsh environments and possesses many useful traits absent in cultivated rice, including high resistance to BB [15,16,17,18]. However, no resistance genes have yet been cloned in O. meyeriana, which has delayed the utilization of this material in rice breeding. One important reason is that conventional crossing methods fail to generate fertile hybrids between cultivated rice and O. meyeriana because the two species contain different types of genome (AA and GG respectively) [19]. Somatic hybridization through the fusion of two somatic protoplasts has already been used to overcome sexual incompatibility and produce inter-species hybrids, and the improved technique of asymmetric somatic hybridization has been used to reduce the co-introduction of deleterious traits from the donor species [20]. Using this breeding technique, we have introduced BB resistance genes from O. meyeriana to a BB susceptible rice cultivar Dalixiang [17]. ASH1 (Asymmetric Somatic Hybridization 1) is one of the hybrid progenies combining the high BB resistance of O. meyeriana with the good agronomic characters of Dalixiang, and is an ideal intermediate material for cloning the novel resistance gene(s) of O. meyeriana. Our long-term aim is therefore to clone the resistance gene(s) in ASH1 through a map-based cloning strategy. In this work, we mapped quantitative trait loci (QTLs) for BB resistance in ASH1, using bulked segregant analysis (BSA), in order to provide a basis for further cloning of the resistance gene(s) and their utilization in rice breeding.

2. Results

2.1. Resistance Analysis

O. meyeriana, one parent of the asymmetric somatic hybridization, was highly resistant to all Xoo strains while the other parent, cultivated rice Dalixiang, was highly susceptible to almost all of the strains (Figure 1). The hybrid progeny ASH1 shared the high BB resistance of the wild rice (Figure 1). Because ASH1 was derived from the japonica cultivar Dalixiang, an indica cultivar IR24 was selected as another parent for QTL mapping in order to produce marker polymorphism between the parents. It has been widely reported that IR24 is highly susceptible to BB disease, which was confirmed by the data in this study (Figure 1). The significant difference in BB resistance between ASH1 and IR24 was favorable to resistance segregation in the F2 population. The frequency distribution in the F2 population exhibited a bimodal pattern with the values ranging from 1.08 to 34.43 cm (Figure 2).

Figure 1.

Figure 1

Open in a new tab

The resistance to rice bacterial blight (BB) of Oryza meyeriana, Dalixiang, ASH1 and IR24. Rice was inoculated by the leaf-clipping method with ten different Xanthomonas oryzae pv. oryzae (Xoo) strains, and for each strain, at least 16 leaves from four plants were inoculated. Lesion length was measured three weeks after inoculation. Bars indicate the standard error.

Figure 2.

Figure 2

Open in a new tab

Frequency distribution of bacterial blight lesion length in the F2 population derived from ASH1/IR24. Rice was inoculated by the leaf-clipping method with Xoo strain P10, and at least eight leaves were inoculated for each plant. Lesion length was measured three weeks after inoculation.

2.2. Markers Linked to Bacterial Blight (BB) Resistance

Bulked segregant analysis (BSA) was performed according to Michelmore et al. [21] and Zhang et al. [22]. 20 resistant and 20 susceptible individuals were selected from the F2 population, respectively (Figure 3), and two DNA bulks, R (resistant) and S (susceptible), were made by mixing equal amounts of DNA from these selected plants.

Figure 3.

Figure 3

Open in a new tab

Resistance of the rice plants in the resistant and susceptible bulk samples. Rice was inoculated by the leaf-clipping method with Xoo strain P10, and at least eight leaves were inoculated for each plant. Lesion length was measured three weeks after inoculation. The upper panel shows the lesion length of the 20 individuals from the resistant bulk, and the lower panel the susceptible bulk. Bars indicate the standard error.

The success of the bacterial inoculation is important for resistance evaluation because a rice leaf without bacterial invasion has a similar phenotype to one with high resistance, and therefore a rice plant without successful inoculation could be mis-evaluated as a resistant individual. We therefore observed the bacterial invasion in rice leaves by electron microscopy to improve the resistance evaluation. The results showed that xylem vessels at the site near the visible lesion were filled with bacteria not only in the extremely susceptible plants but also in the extremely resistant ones (Figure 4), which confirmed the resistance identification of the individuals from the two bulks.

Figure 4.

Figure 4

Open in a new tab

Electron micrograph showing the bacteria in xylem vessels in both extremely resistant and susceptible individuals from the two bulks. Left leaf and upper image were from an extremely resistant plant, and the right leaf and lower image from an extremely susceptible plant.

A total of 698 molecular markers including simple sequence repeats (SSR) and sequence-tagged site (STS) markers were screened for polymorphism between the parents of ASH1 and IR24, and 186 markers evenly distributed on 12 rice chromosomes were selected due to their polymorphism and reproducible amplification (Table S1). Subsequently, these 186 markers were used to scan the two parents and the two bulks (R bulk and S bulk) and 17 markers were identified that showed linkage to BB resistance (Table S2). Of these 17 markers, 4 were on chromosome 1, 6 on chromosome 3 and 7 on chromosome 5 (Table S2). Figure 5 illustrates the band display patterns in two parents and two bulks of the three markers RM128 (chromosome 1), R03D158 (chromosome 3) and RM6972 (chromosome 5).

Figure 5.

Figure 5

Open in a new tab

Banding patterns of three linkage markers RM128, R03D158 and RM6972 in two parents and two bulks. The numbers 1, 2, 3 and 4 represent ASH1, IR24, susceptible bulk and resistant bulk, respectively. RM128 is located on chromosome 1, R03D158 is located on chromosome 3, and RM6972 is located on chromosome 5.

The linkage markers showed heterozygous patterns from both parents in the S bulk and uniformly homozygous patterns of the resistant parent in the R bulk (Figure 5). It is most likely that the identified loci correspond to recessive resistance genes. The recessive genes for BB resistance such as Xa5 and Xa13 have quantitative, additive and broad-spectrum resistance. ASH1 possesses BB resistance with broad-spectrum (Figure 1) and the resistance loci identified here are quantitative and additive. All the results are consistent with the character of recessive genes. However, this speculation needs to be examined by further detailed studies including the separation and resistance evaluation of different resistance loci and the cloning of the corresponding resistance genes.

2.3. Quantitative Trait Loci (QTL) Mapping

To confirm the chromosome loci underlying BB resistance in ASH1, we further performed QTL analysis in the F2 population including 101 individuals using the obtained linkage markers. Three QTLs conferring BB resistance were detected on chromosomes 1, 3 and 5 (Figure 6, Table 1). ASH1 alleles at any of the three QTLs contributed to increased BB resistance. A QTL on chromosome 1, designated qBBR1 (QTL for BB resistance on chromosome 1), was located in the marker interval between RM128 and R01D144 with the nearest marker of RM128. qBBR1 explained about 21.5% of the phenotypic variance with an logarithm of odds (LOD) score of 10.1. qBBR3, with LOD score of 6.2, explained approximately 12.3% of the total resistance variance. This locus was targeted in the marker vicinity between R03D158 and RM85 on chromosome 3 with the nearest marker of R03D158. qBBR5 was mapped in the marker interval between RM7081 and RM3616 on chromosome 5, and the nearest marker was RM6972. The LOD score of qBBR5 was 17.8 and this QTL accounted for the highest resistance variance (about 39.2%). The LOD score of the three QTLs were all higher than 6.0 and they each explained more than 12% of resistance variance, which indicated that all of them were important QTLs conferring BB resistance.

Figure 6.

Figure 6

Open in a new tab

Mapping of the quantitative trait loci (QTLs) for BB resistance in the F2 population derived from ASH1/IR24. Upper, middle and bottom panels show the locations of qBBR1, qBBR3 and qBBR5, respectively. Genetic distance (cM) between adjacent markers and marker names are indicated on the left and right sides of the chromosomes. Physical distances (bp) of the markers on the chromosomes are also shown. The right part of each panel shows the graph for the distribution of the logarithm of odds (LOD) score.

Table 1.

QTLs for rice BB resistance detected in ASH1.

QTL Chromosome Marker Interval Nearest Marker LOD R2% A
qBBR1 1 RM128–R01D144 RM128 10.1 21.5 4.89
qBBR3 3 R03D158–RM85 R03D158 6.2 12.3 3.73
qBBR5 5 RM7081–RM3616 RM6972 17.8 39.2 7.36
Open in a new tab

QTL, quantitative trait locus; BB, bacterial blight; LOD, log10 likelihood; R2, the proportion of variance explained by the QTL; A, additive effect at the QTL.

Because ASH1 has broad-spectrum resistance to different Xoo strains, P10 was selected as a representative to be used in QTL mapping, resulting in the detection of three major QTLs. However, it is possible that more QTLs for BB resistance would be identified if other Xoo strains were used to characterize the F2 population because of the race specificity of the resistance loci. The race specificity to different Xoo strains of the three detected QTLs also needs to be examined despite the possibility of their broad-spectrum resistance. For future work, we have developed a larger segregating population, and are performing further fine whole-genome wide QTL mapping and related studies including race specificity examination of different QTLs. The purpose is to confirm the BSA results and to provide a solid basis for the resistance gene cloning.

3. Discussion

Many wild species of rice possess genes for resistance to BB and four genes have been identified. The first of the genes, Xa21, was discovered in O. longistaminata, and encodes for a receptor kinase-like protein with a leucine-rich repeat domain that determines race-specific recognition [5,23]. Another BB resistance gene Xa27 was cloned from O. minuta and its product is a nuclear localized type-III effector [9,24]. The other two genes, Xa23 and Xa29 were identified in O. rufipogon and O. officinalis, respectively; they have not been cloned but fine mapped in the relative chromosome regions [25,26]. These four genes have been introduced into cultivated rice through breeding programs and many resistant varieties have been developed for sustained improvement of rice productivity.

O. meyeriana is also an important wild relative of rice, and there have been many reports that it possesses high resistance to rice BB disease. Early in 1982 Peng et al. evaluated the resistance of O. meyeriana, O. officinalis and O. rufipogon, and found that O. meyeriana was highly resistant or nearly immune to BB disease [15]. Zhang et al. demonstrated that O. meyeriana’s resistance was ranked the highest among 871 accessions of 13 wild rice species [16]. Many subsequent studies have confirmed this high resistance of O. meyeriana [17,18,27]. In agreement with previous research, the results of this study also showed the trait of high BB resistance in this wild rice (Figure 1). These results suggest that O. meyeriana is a valuable genetic source that can be used for improving the BB resistance of cultivated rice. Additionally, O. meyeriana showed a wide resistance spectrum with strong resistance to all of the ten Xoo strains (Figure 1). This multiple resistance trait is particularly desirable in rice breeding for durable resistance to this disease. However, although the high resistance has been widely identified, no resistance gene(s) have yet been cloned in O. meyeriana, which has delayed the utilization of this important material in breeding programs.

At least 36 BB resistance genes have been identified in rice [1,2,3,4], and eight of them have been cloned by map-based cloning, including Xa1, Xa3/Xa26, Xa5, Xa10, Xa13, Xa21, Xa25 and Xa27 [3,4,5,6,7,8,9,10]. Xa1 is located on chromosome 4 [6], Xa3/Xa26 on chromosome 11 [28,29], Xa5 on chromosome 5 [30], Xa10 on chromosome 11 [4], Xa13 on chromosome 8 [31], Xa21 on chromosome 11 [32], Xa25 on chromosome 12 [33], and Xa27 on chromosome 6 [24]. Xa5 and the resistance locus qBBR5 identified in the present study were both mapped to chromosome 5, but their mapping regions were different. Xa5 was mapped in a 0.5 cM interval between the markers RS7 and RM611 on the front of the short arm of chromosome 5 [30], while qBBR5 was mapped in the interval between RM7081 and RM3616 on the long arm (Figure 6). Except Xa5, none of other seven genes shared the same chromosome as qBBR1, qBBR3 and qBBR5 that were identified in this study (Figure 6). Therefore, all three QTLs identified here are different from the loci of the eight Xa genes cloned in previous studies. In addition to the eight Xa genes mentioned above, more than 30 genes conferring BB resistance have been identified in different rice materials, but none of them have yet been cloned. These genes were mapped to different chromosomes from those on which qBBR1, qBBR3 and qBBR5 are located (1–4, Figure 6), except that Xa29 shares the same chromosome as qBBR1 (26, Figure 6). Tan et al. mapped Xa29 within a 1.3 cM interval flanked by the molecular markers C904 and R596 [26], a different region of chromosome 1 from the marker interval between RM128 and R01D144 to which qBBR1 was mapped (Figure 6), indicating that the loci of Xa29 and qBBR1 are also different. Taken together, qBBR1, qBBR3 and qBBR5 are three novel resistance loci that are different from any known ones associated with resistance of rice to BB disease.

ASH1 is one of the hybrid progenies of asymmetric somatic hybridization between O. meyeriana and the cultivated rice Dalixiang [17]. Dalixiang was susceptible to BB disease, while ASH1 possessed the multiple resistance of the wild rice (Figure 1), indicating that the resistance gene(s) were transferred into ASH1 from the wild rice through somatic hybridization. Three novel QTLs were mapped in ASH1 in the present study and ASH1 alleles at any of the three QTLs contributed to the increased resistance (Figure 6; Table 1). Based on these results we suggest that the three QTLs identified in ASH1 were the ones transferred from O. meyeriana corresponding to the loci of the novel resistance genes in this wild rice. Our previous studies have revealed that the high resistance of O. meyeriana to rice BB disease results from multiple causes [34,35], which suggests that this wild rice may contain more than one gene conferring its strong resistance. This is consistent with the multiple resistance loci detected in ASH1 in this study. O meyeriana can hardly be crossed with cultivated rice by traditional hybridization, so little progress has been made on mapping and cloning its resistance genes. ASH1 inherits the high resistance from O. meyeriana and can be easily crossed with cultivated rice, and so it is an ideal intermediate material that can be used for cloning the resistance genes. The QTL mapping for BB resistance in ASH1 in the present work provides an important basis for further cloning the associated genes of O. meyeriana.

4. Experimental Section

4.1. Plant Materials

O. meyeriana, a wild species of rice with high BB resistance, was provided by Professor Xinhua Wei, China National Rice Research Institute (Hangzhou, China). O. sativa ssp. japonica (cv. Dalixiang) is a high-yielding, good-quality-grain cultivar grown in southern China, but it is susceptible to rice BB disease. ASH1 is derived from asymmetric somatic hybridization using O. meyeriana as the donor and Dalixiang as the recipient, and combines the high BB resistance of O. meyeriana with the good agronomic characters of Dalixiang [17]. O. sativa ssp. indica (cv. IR24) is an elite cultivar developed by International Rice Research Institute but highly susceptible to BB disease. Dalixiang, ASH1 and IR24 were introduced from the Zhejiang Academy of Agricultural Sciences collection. An F2 population including 101 individuals was developed from self-pollinations of the F1s of the cross between ASH1 and IR24. All the materials were sown in the seedling nursery and 25-day-old seedlings were transplanted into the experimental field in Zhejiang Academy of Agricultural Sciences, Hangzhou, China. In each experiment the plots were arranged in a randomized complete block design, and the spacing was 20 cm between plants within each row and 35 cm between rows. Field management followed normal agricultural practice.

4.2. Pathogen Inoculation and Resistance Identification

The Xoo strains used in this study included P2 (PXO86), P3 (PXO79), P4 (PXO71), P5 (PXO112), P6 (PXO99), P7 (PXO280), P8 (PXO145), P9 (PXO87), P10 (PXO124) and C4 (ZHE173) (Table 2). The inoculation was carried out using the leaf-clipping method as previously described [36,37]. Briefly, at the booting stage (approximately 40 days after transplanting), the fully expanded leaves were clipped about 1 cm from the leaf tip using a pair of scissors dipped in the inoculum. The bacterial inoculum was prepared from a 48 h culture on potato semisynthetic agar (PSA) [37] slants and its density was adjusted to 109 CFU/mL. For resistance evaluation of the parents, O. meyeriana, Dalixiang, ASH1 and IR24 were inoculated with 10 Xoo strains. At least 16 leaves from four plants were inoculated with each strain. For resistance identification of the individuals in the F2 population, the plants were inoculated with Xoo strain P10, and at least 8 leaves were inoculated for each plant. Leaf length and lesion length were measured three weeks after inoculation. Additionally, electron microscopy was used to detect the sub-cellular location of Xoo pathogens in each plant.

Table 2.

Xoo strains used in this study.

Xoo Strain Origin
P2 Philippines
P3 Philippines
P4 Philippines
P5 Philippines
P6 Philippines
P7 Philippines
P8 Philippines
P9 Philippines
P10 Philippines
C4 China
Open in a new tab

4.3. Electron Microscopy

Ultrathin sections and electron microscopy were done as described by Hong et al. [38] with some minor modifications. Leaf segments (1 × 3 mm) were fixed with 2.5% (v/v) glutaraldehyde in 0.1 M phosphate buffer (pH 7.2) for 2 h at 4 °C. After post-fixation for 1 h at room temperature in phosphate buffer (pH 7.2) containing 1% (m/v) osmium tetroxide, the segments were dehydrated through an ethanol series, 15 min for each step, and finally dehydrated twice in 100% ethanol for 20 min. The samples were infiltrated in a mixture of acetone and Spurr resin, 1:1 (v/v) for 1 h and 1:3 (v/v) for 3 h at room temperature, and then in absolute Spurr resin overnight. The segments were then embedded in Spurr resin at 37 °C for 12 h followed by 78 °C for 8 h for polymerization. The polymerized blocks were cut into 70 nm ultra-thin sections with the ultramicrotome. Finally, the sections were stained with uranyl acetate and lead citrate for 15 min, and were then observed and photographed with an electron microscope (JEM-1200EX, JEOL, Tokyo, Japan).

4.4. BSA Selection of Linkage Markers

DNA was extracted from fresh young leaves of rice using a modified hexadecyltrimethylammonium bromide (CTAB) method described by Wu et al. [39]. Twenty resistant and 20 susceptible individuals were selected from the F2 population, respectively, and two DNA bulks were made by mixing equal amounts of DNA from these selected plants. A total of 698 SSR and STS markers evenly distributed on 12 chromosomes were pre-surveyed between the two parents for screening of polymorphism markers. The inter-parent polymorphic markers obtained were then surveyed in the two parents and two bulks for selecting the markers linked to BB resistance.

4.5. Genetic Map Construction and QTL Mapping

The genotypes of the linkage markers obtained were identified in the F2 population, and the genetic map was constructed by using MAPMAKER/EXP 3.0b [40]. The Kosambi mapping function was used to transform the recombination frequency to genetic distance (cM). The computer program Windows QTL cartographer 2.5 was used to perform QTL analysis in the F2 population as described previously [41]. The composite interval mapping (CIM) analysis was applied to map QTLs and estimate QTL effects. The QTL main effects were estimated using the maximum-likelihood estimation method. The logarithm of odds (LOD) threshold at the experiment-wise significance level of 0.05 was determined by using the permutation method [42]. LOD peaks for each significant QTL were used to position the QTL on the genetic map, and the additive effect (A) and the contribution of each QTL to the total variance (R2) were determined.

5. Conclusions

O. meyeriana is highly resistant to rice BB disease, but no resistance genes have yet been cloned in this wild rice, which has delayed the utilization of this important material in rice breeding programs. Previously, we introduced the BB resistance trait from O. meyeriana into a cultivated rice using asymmetric somatic hybridization. In this work, we analyzed the BB resistance of ASH1, one of the hybrid progenies, and found that ASH1 inherited the multiple resistance from O. meyeriana. An F2 population was constructed from the cross between ASH1 and a rice cultivar with high BB susceptibility. Based on BSA, 17 molecular markers that were linked to rice BB resistance were obtained using the individual plants with extremely high resistance and susceptibility selected from the F2 population. QTLs mapping was then performed based on the 17 linkage markers and the F2 segregating population, and finally three QTLs, qBBR1, qBBR3 and qBBR5 were identified on chromosomes 1, 3 and 5, respectively. All three QTLs were important gene loci having a strong effect on the BB resistance, and ASH1 alleles at any of the QTLs contributed to the increased resistance. These QTLs were three novel loci, differing from any known genes previously identified. The results will provide an important basis for further cloning of resistance genes in O. meyeriana and their utilization in rice resistance breeding.

Acknowledgments

The authors are grateful to M.J. Adams, Rothamsted Research, UK for critically reading the manuscript. This work was supported by the State Basic Program of China (2012CB722504), the National Natural Science Foundation of China for young scholar (31101208, 31201482), Zhejiang Provincial Natural Science Foundation of China (Z14C140001), and the Program for Leading Team of Agricultural Research and Innovation of Ministry of Agriculture, China.

Supplementary Files

Supplementary File 1
Click here for additional data file. (576.7KB, pdf)

Author Contributions

J.C. and Y.Y. conceived and designed the experiments. Y.Y., X.W. and C.Y. constructed the F2 population. X.H., J.Z., C.Y. and W.Z. identified the resistance. X.H., C.C. and Y.C. screened the linkage markers. Y.Y., C.Y., J.Z. and X.H. mapped the QTLs. Y.Y., X.H., X.W. and C.Y. carried out all the other experiments. Y.Y., C.Y. and J.C. wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Zhang Q. Genetics and Improvement of Resistance to Bacterial Blight in Rice. 1st ed. Science Press; Beijing, China: 2007. pp. 1–4, 157–159. [Google Scholar]
  • 2.Guo S.B., Zhang D.P., Lin X.H. Identification and mapping of a novel bacterial blight resistance gene Xa35(t) originated from Oryza minuta. Sci. Agric. Sin. 2010;43:2611–2618. [Google Scholar]
  • 3.Liu Q., Yuan M., Zhou Y., Li X., Xiao J., Wang S. A paralog of the MtN3/saliva family recessively confers race-specific resistance to Xanthomonas oryzae in rice. Plant Cell Environ. 2011;34:1958–1969. doi: 10.1111/j.1365-3040.2011.02391.x. [DOI] [PubMed] [Google Scholar]
  • 4.Tian D., Wang J., Zeng X., Gu K., Qiu C., Yang X., Zhou Z., Goh M., Luo Y., Murata-Hori M., et al. The rice TAL effector-dependent resistance protein XA10 triggers cell death and calcium depletion in the endoplasmic reticulum. Plant Cell. 2014;26:497–515. doi: 10.1105/tpc.113.119255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Song W.Y., Wang G.L., Chen L.L., Kim H.S., Pi L.Y., Holsten T., Gardner J., Wang B., Zhai W.X., Zhu L.H., et al. A receptor kinase-like protein encoded by the rice disease resistance gene, Xa21. Science. 1995;270:1804–1806. doi: 10.1126/science.270.5243.1804. [DOI] [PubMed] [Google Scholar]
  • 6.Yoshimura S., Yamanouchi U., Katayose Y., Toki S., Wang Z.X., Kono I., Kurata N., Yano M., Iwata N., Sasaki T. Expression of Xa1, a bacterial blight-resistance gene in rice, is induced by bacterial inoculation. Proc. Natl. Acad. Sci. USA. 1998;95:1663–1668. doi: 10.1073/pnas.95.4.1663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Iyer A.S., McCouch S.R. The rice bacterial blight resistance gene Xa5 encodes a novel form of disease resistance. Mol. Plant Microbe Interact. 2004;17:1348–1354. doi: 10.1094/MPMI.2004.17.12.1348. [DOI] [PubMed] [Google Scholar]
  • 8.Sun X., Cao Y., Yang Z., Xu C., Li X., Wang S., Zhang Q. Xa26, a gene conferring resistance to Xanthomonas oryzae pv. oryzae in rice, encodes an LRR receptor kinase-like protein. Plant J. 2004;37:517–527. doi: 10.1046/j.1365-313X.2003.01976.x. [DOI] [PubMed] [Google Scholar]
  • 9.Gu K., Yang B., Tian D., Wu L., Wang D., Sreekala C., Yang F., Chu Z., Wang G.L., White F.F., Yin Z. R gene expression induced by a type-III effector triggers disease in rice. Nature. 2005;435:1122–1125. doi: 10.1038/nature03630. [DOI] [PubMed] [Google Scholar]
  • 10.Chu Z., Yuan M., Yao J., Ge X., Yuan B., Xu C., Li X., Fu B., Li Z., Bennetzen J.L., et al. Promoter mutations of an essential gene for pollen development result in disease resistance in rice. Genes Dev. 2006;20:1250–1255. doi: 10.1101/gad.1416306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Khush G.S., Mackill D.J., Sidhu G.S. Bacterial Blight of Rice. 1st ed. International Rice Research Institute; Manila, Philippines: 1989. Breeding rice for resistance to bacterial blight; pp. 207–217. Volume 1. [Google Scholar]
  • 12.Huang N., Angeles E.R., Domingo J., Magpantay G., Singh S., Zhang G., Kumaravadivel N., Bennett J., Khush G.S. Pyramiding of bacterial blight resistance genes in rice: Marker-assisted selection using RFLP and PCR. Theor. Appl. Genet. 1997;95:313–320. doi: 10.1007/s001220050565. [DOI] [Google Scholar]
  • 13.Lee S.W., Choi S.H., Han S.S., Lee D.G., Lee B.Y. Distribution of Xanthomonas oryzae pv. oryzae strains virulent to Xa21 in Korea. Phytopathology. 1999;89:928–933. doi: 10.1094/PHYTO.1999.89.10.928. [DOI] [PubMed] [Google Scholar]
  • 14.Zhang Q., Wang C.L., Zhao K.J., Zhao Y.L., Caslana V.C., Zhu X.D., Li D.Y., Jiang Q.X. The effectiveness of advanced rice lines with new resistance gene Xa23 to rice bacterial blight. Rice Genet. Newsl. 2001;18:71–73. [Google Scholar]
  • 15.Peng S.Q., Wei Z.S., Mao C.X., Huang H.Q., Xiao F.H., Luo K. Identification of multiresistance of O. meyeriana, O. officinalis and O. sativa f. spantanea growing in Yunan province. Acta Phytopathol. Sin. 1982;12:58–60. [Google Scholar]
  • 16.Zhang Q., Wang C., Shi A., Bai J., Ling S., Li D., Chen C., Pang H. Evaluation of resistance to bacterial blight (Xanthomonas oryzae pv. oryzae) in wild rice species. Sci. Agric. Sin. 1994;27:1–9. [Google Scholar]
  • 17.Yan C.Q., Qian K.X., Yan Q.S., Zhang X.Q., Xue G.P., Huangfu W.G., Wu Y.F., Zhao Y.Z., Xue Z.Y., Huang J., et al. Use of asymmetric somatic hybridization for transfer of the bacterial resistance trait from Oryza meyeriana L. to O. sativa L. ssp. japonica. Plant Cell Rep. 2004;22:569–575. doi: 10.1007/s00299-003-0732-4. [DOI] [PubMed] [Google Scholar]
  • 18.Cheng Z.Q., Yan H.J., Geng X.S., Yin F.Y., Sun Y.D., Zhang C., Huang X.Q. Identification of Oryza granulata for resistance to Xanthomonas oryzae pv. oryzae and observation of leaf tissue. Acta Phytopathol. Sin. 2008;38:582–591. [Google Scholar]
  • 19.Aggarwarl R.K., Brar D.S., Khush G.S. Two new genomes in the Oryza complex identified on the basis of molecular divergence analysis using total genomic DNA hybridization. Mol. Gen. Genet. 1997;254:1–12. doi: 10.1007/s004380050384. [DOI] [PubMed] [Google Scholar]
  • 20.Kinoshita T., Mori K. In vitro techniques for genomic alteration in rice plants. Euphytica. 2001;120:367–372. doi: 10.1023/A:1017506100359. [DOI] [Google Scholar]
  • 21.Michelmore R.W., Paran I., Kesseli R.V. Identification of markers linked to disease-resistance genes by bulked segregant analysis: A rapid method to detect markers in specific genomic regions by using segregating populations. Proc. Natl. Acad. Sci. USA. 1991;88:9828–9832. doi: 10.1073/pnas.88.21.9828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Zhang Q.F., Shen B.Z., Dai X.K., Mei M.H., Saghai Maroof M.A., Li Z.B. Using bulked extremes and recessive class to map genes for photoperiod-sensitive genic male sterility in rice. Proc. Natl. Acad. Sci. USA. 1994;91:8675–8679. doi: 10.1073/pnas.91.18.8675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Wang G.L., Ruan D.L., Song W.Y., Sideris S., Chen L.L., Pi L.Y., Zhang S., Zhang Z., Fauquet C., Gaut B.S., et al. Xa21D encodes a receptor-like molecule with a leucine-rich repeat domain that determines race-specific recognition and is subject to adaptive evolution. Plant Cell. 1998;10:765–779. doi: 10.1105/tpc.10.5.765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Gu K., Tian D., Yang F., Wu L., Sreekala C., Wang D., Wang G.L., Yin Z. High-resolution genetic mapping of Xa27(t), a new bacterial blight resistance gene in rice, Oryza sativa L. Theor. Appl. Genet. 2004;108:800–807. doi: 10.1007/s00122-003-1491-x. [DOI] [PubMed] [Google Scholar]
  • 25.Wang C.L., Chen L.T., Zeng C.Z., Zhang Q.Y., Liu P.Q., Liu Y.G., Fan Y.L., Zhang Q., Zhao K.J. Chromosome walking for fine mapping of Xa23 gene locus by using genomic libraries. Chin. J. Rice Sci. 2006;20:355–360. [Google Scholar]
  • 26.Tan G.X., Ren X., Weng Q.M., Shi Z.Y., Zhu L.L., He G.C. Mapping of a new resistance gene to bacterial blight in rice line introgressed from Oryza officinalis. Acta Genet. Sin. 2004;31:724–729. [PubMed] [Google Scholar]
  • 27.Liu J.M., Cheng Z.Q., Yang M.Z., Wu C.J., Wang L.X., Sun Y.D., Huang X.Q. Cloning and sequence analysis of disease resistance gene analogues from three wild rice species in Yunnan. Sci. Agric. Sin. 2003;36:273–280. [Google Scholar]
  • 28.Yang Z., Sun X., Wang S., Zhang Q. Genetic and physical mapping of a new gene for bacterial blight resistance in rice. Theor. Appl. Genet. 2003;106:1467–1472. doi: 10.1007/s00122-003-1205-4. [DOI] [PubMed] [Google Scholar]
  • 29.Xiang Y., Cao Y.L., Xu C.G., Li X.H., Wang S.P. Xa3, conferring resistance for rice bacterial blight and encoding a receptor kinase-like protein, is the same as Xa26. Theor. Appl. Genet. 2006;113:1347–1355. doi: 10.1007/s00122-006-0388-x. [DOI] [PubMed] [Google Scholar]
  • 30.Blair M.W., Garris A.J., Iyer A.S., Chapman B., Kresovich S., McCouch S.R. High resolution genetic mapping and candidate gene identification at the Xa5 locus for bacterial blight resistance in rice (Oryza sativa L.) Theor. Appl. Genet. 2003;107:62–73. doi: 10.1007/s00122-003-1231-2. [DOI] [PubMed] [Google Scholar]
  • 31.Zhang G., Angeles E.R., Abenes M.L.P., Khush G.S., Huang N. RAPD and RFLP mapping of the bacterial blight resistance gene Xa-13 in rice. Theor. Appl. Genet. 1996;93:65–70. doi: 10.1007/BF00225728. [DOI] [PubMed] [Google Scholar]
  • 32.Ronald P.C., Albano B., Tabien R., Abenes L., Wu K.S., McCouch S., Tanksley S.D. Genetic and physical analysis of the rice bacterial blight disease resistance locus, Xa21. Mol. Gen. Genet. 1992;236:113–120. doi: 10.1007/BF00279649. [DOI] [PubMed] [Google Scholar]
  • 33.Chen H., Wang S., Zhang Q. New gene for bacterial blight resistance in rice located on chromosome 12 identified from Minghui 63, an elite restorer line. Phytopathology. 2002;92:750–754. doi: 10.1094/PHYTO.2002.92.7.750. [DOI] [PubMed] [Google Scholar]
  • 34.Yang Y., Yu C.L., Wang X.M., Yan C.Q., Cheng Y., Chen J.P. Inoculation with Xanthomonas oryzae pv. oryzae induces thylakoid membrane association of Rubisco activase in Oryza meyeriana. J. Plant Physiol. 2011;168:1701–1704. doi: 10.1016/j.jplph.2011.02.012. [DOI] [PubMed] [Google Scholar]
  • 35.Yang Y., Xie L., Yan C.Q., Wang X.M., Yu C.L., Cheng X.Y., Cheng Y., Chen J.P. Xylem secondary cell-wall thickening involved in defense responses of Oryza meyeriana to Xanthomonas oryzae pv. oryzae. Acta Phytopathol. Sin. 2012;42:505–514. [Google Scholar]
  • 36.Kauffman H.E., Reddy A.P.K., Hsieh S.P.Y., Merca S.D. An improved technique for evaluating resistance of rice varieties to Xanthomonas oryzae. Plant Dis. Rep. 1973;57:537–541. [Google Scholar]
  • 37.Sanchez A.C., Ilag L.L., Yang D., Brar D.S., Ausubel F., Khush G.S., Yano M., Sasaki T., Li Z., Huang N. Genetic and physical mapping of Xa13, a recessive bacterial blight resistance gene in rice. Theor. Appl. Genet. 1999;98:1022–1028. doi: 10.1007/s001220051163. [DOI] [Google Scholar]
  • 38.Hong J., Jiang D.A., Weng X.Y., Wang W.B., Hu D.W. Leaf anatomy, chloroplast ultrastructure, and cellular localisation of ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) and RuBPCO activase in Amaranthus tricolor L. Photosynthetica. 2005;43:519–528. doi: 10.1007/s11099-005-0084-0. [DOI] [Google Scholar]
  • 39.Wu S.B., Wirthensohn M.G., Hunt P., Gibson J.P., Sedgley M. High resolution melting analysis of almond SNPs derived from ESTs. Theor. Appl. Genet. 2008;118:1–14. doi: 10.1007/s00122-008-0870-8. [DOI] [PubMed] [Google Scholar]
  • 40.Lander E.S., Green P., Abrahamson J., Barlow A., Daly M.J., Lincoln S.E., Newberg L.A. MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics. 1987;1:174–181. doi: 10.1016/0888-7543(87)90010-3. [DOI] [PubMed] [Google Scholar]
  • 41.Wang S., Basten C.J., Zeng Z.B. Windows QTL Cartographer 2.5. Department of Statistics, North Carolina State University; Raleigh, NC, USA: 2007. [Google Scholar]
  • 42.Churchill G.A., Doerge R.W. Empirical threshold values for quantitative trait mapping. Genetics. 1994;138:963–971. doi: 10.1093/genetics/138.3.963. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary File 1
Click here for additional data file. (576.7KB, pdf)

Articles from International Journal of Molecular Sciences are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES