InTechOpen uses cookies to offer you the best online experience. By continuing to use our site, you agree to our Privacy Policy.

Agricultural and Biological Sciences » "Advances in International Rice Research", book edited by Jinquan Li, ISBN 978-953-51-3010-9, Print ISBN 978-953-51-3009-3, Published: March 15, 2017 under CC BY 3.0 license. © The Author(s).

Chapter 10

Genetics and Genomics of Bacterial Blight Resistance in Rice

By Yogesh Vikal and Dharminder Bhatia
DOI: 10.5772/67361

Article top

Genetics and Genomics of Bacterial Blight Resistance in Rice

Yogesh Vikal1 and Dharminder Bhatia2
Show details


Rice is an important food crop for half the world’s population and has been in cultivation for over 10,000 years. During the last few decades, rice has evolved intricate relationships with associated pathogens and pests, bacterial blight (BB) being one of the most important among them. Utilization of resistant varieties with agricultural management practices is a more effective way to control BB. Of the 42 different resistance (R) genes identified to confer BB resistance, 9 have been isolated and cloned, whereas a few of the avirulence genes and a large number of candidate pathogenicity genes have been isolated from Xanthomonas oryzae pv. oryzae. The complete genome sequences of two different rice subspecies japonica and indica and three different races of BB pathogen are available. Therefore, the interaction between rice-Xoo could be deciphered and pave a way to study the molecular aspects of bacterial pathogenesis and host counter measures like innate immunity and R gene–mediated immunity. Although several of the type III effectors of Xoo have been characterized and the host targets of a few of them identified, a relatively large number of candidate effectors remain to be studied and their functional analysis may provide key for developing broad spectrum and durable resistance to BB.

Keywords: Xanthomonas oryzae pv. oryzae, Oryza sativa, Genome structure, Xa genes, mapping

1. Introduction

Rice (Oryza sativa L.) is a staple food for a large part of the world’s human population, especially in South and Southeast Asia and tropical Latin America, making it the second most consumed cereal grain. It accounts for 35–60% of the calories consumed by more than 3 billion Asians. To meet the growing demand of nearly 5.0 billion consumers, rice-growing countries will have to produce 40% more rice by 2030 [1]. However, its production is being reduced severely by several rice diseases. Bacterial blight (BB) caused by Xanthomonas oryzae pv. oryzae (Xoo) is one of the major foliar diseases, causing yield losses by 20–30%. It was first reported by farmers in 1884 in the Southern region of Japan [2]. It is a vascular disease resulting in tannish grey to white lesions along the veins. The BB pathogen invades the host through natural openings in leaves, including hydathodes or wounds, and colonizes the xylem vessels. Under field conditions, symptoms are onset at the tillering stage and disease incidence increases with plant growth, which is maximum at the flowering stage. The kresek, a severe form of disease, occurs at the seedling stage resulting in a partial or total crop failure.

The incidence of BB has been widely reported in all rice-growing regions worldwide except North America [3]. The high degree of pathogenic variation in Xoo due to the evolution of new pathotypes often causes the breakdown of resistance. Genome structure of Xoo revealed the presence of effector (avr) genes and insertion sequences, which may be playing a major role in generating a high degree of genetic diversity and race differentiation [4]. However, with the evolution of new races, broader and more comprehensive resistance must be pursued in order to prevent super-races of Xoo, which can overcome all genetic sources of resistance, from becoming prevalent. Therefore, it is of immense interest to diversify the germplasm, scouting of resistance genes from wild species and pyramiding two or more effective resistance genes in developing rice cultivars with durable BB resistance to Xoo. For successful deployment of stable resistance (R) genes, their characterization and availability of tightly linked markers will greatly facilitate the development of new versions of cultivars. To date, more than 40 different resistance genes conferring host resistance to BB have been identified in rice so far and some of those have been characterized [5].

The rice-Xoo system is distinguished from ArabidopsisPseudomonas syringae, tomato—Cladosporium fulvum, and rice—Magnaporthe grisea, with respect to that about one-third of the R genes for Xoo resistance are recessive in nature [6]. Secondly, diverse types of proteins are encoded by the R genes such as Xa3/Xa26 and Xa21 encode leucine-rich repeat (LRR) receptor kinase-type proteins [79] that mediate race-specific resistance. Xa1 encodes a nucleotide-binding LRR protein [10]. The recessive gene xa5 encodes the γ-subunit of transcription factor IIA [11, 12]. Xa27 encodes a novel protein [13]. The recessive gene xa13 encodes a novel plasma membrane protein [14]. Thus, it is clear that Xoo has the diverse interaction mechanism within the host species. Hence, the isolation and characterization of BB resistance genes from diverse germplasm will insight depth knowledge of both pathogen and host system, which will further lead to the development of BB resistant varieties with broad spectrum and durable resistance.

2. Genetics of BB resistance

Genetic analysis of many plant-pathogen interactions has demonstrated that plants often contain a single locus that confers resistance against a complementary avirulence gene [15]. The genetic basis of host resistance to BB has been studied in depth. The genetics of resistance to bacterial blight was first carried out by Japan and IRRI, subsequently, followed by Sri Lanka, India, China, and so on. As there is diversity of Xoo strains in different countries, scientists found that it was difficult to characterize and distinguish the resistance genes. In order to compare the identified genes, the identical differential standard was set up [16]. About 42 BB resistance (R) genes, designated from Xa1 to Xa42 [5, 17, 18], conferring resistance against various strains of Xoo, have been identified from cultivated, mutant population, and wild rice species (Table 1). These genes have been mapped on six of the twelve rice chromosomes. A total of 14 recessive genes (xa5, xa8, xa13, xa15, xa19, xa20, xa24, xa25, xa26b, xa28, xa31, xa32, xa33, and xa34) in the series from Xa1 to Xa42 have been identified. Of these R genes, nine of the R genes have been cloned and characterized (Xa1, Xa3/Xa26, xa5, xa13, Xa10, Xa21, Xa23, xa25, and Xa27) encoding different types of proteins, suggesting multiple mechanisms of R-gene–mediated Xoo resistance [7, 8, 10, 11, 13, 14, 1921]. Most of these genes provide complete and race-specific resistance to Xoo and have been used singly or in combination in rice breeding for BB resistance [2232]. Since the bacterial races tend to evolve continually, influenced by the artificial and natural selection of genes resistant to BB, it is required to explore critically the new resistant resources to combat the evolved races.

Xa geneResistance to Xoo raceDonor cultivarChromosomeReference
Xa1Japanese race-IKogyoku, IRBB14[10, 33, 34]
Xa2Japanese race-IIIRBB24[33, 36]
Xa3/Xa26Chinese, Philippine, and Japanese racesWase Aikoku 3, Minghui 63, IRBB311[9, 37]
Xa4Philippine race-ITKM6, IRBB411[39, 40, 45]
xa5Philippine races I, II, IIIIRBB55[11, 40, 46]
Xa6Philippine race 1Zenith11[47]
Xa7Philippine racesDZ786[4851]
xa8Philippine racesPI2311287[52]
xa9Philippine racesKhao Lay Nhay and Sateng11[53]
Xa10Philippine and Japanese racesCas 20911[54, 55, 57]
Xa11Japanese races IB, II, IIIA, VIR83[58, 59]
Xa12Indonesian race VKogyoku, Java144[60]
xa13Philippine race 6BJ1, IRBB138[14, 6164]
Xa14Philippine race 5TN14[6567]
xa15Japanese racesM41 mutant[69]
Xa16Japanese racesTetep[70]
Xa17Japanese racesAsominori[71]
Xa18Burmese racesIR24, Miyang23, Toyonishiki[58]
xa19Japanese racesXM5 (mutant of IR24)[72]
xa20Japanese racesXM6 (mutant of IR24)[73]
Xa21Philippine and Japanese racesO. longistaminata, IRBB2111[7, 76, 77]
Xa22Chinese racesZhachanglong11[79, 80]
Xa23Indonesian racesO. rufipogon (CBB23)11[24]
xa24(t)Philippine and Chinese racesDV862[81, 82]
xa25/Xa25(t)Xa25Chinese and Philippine racesMinghui 63, HX-3 (somaclonal mutant of Minghui 63)12[85, 86]
xa26(t)Philippine racesNep Bha Bong[86]
Xa27Chinese strains and Philippine race 2 to 6O. minuta IRGC 101141, IRBB276[26, 85]
xa28(t)Philippine race2Lota sail[86]
Xa29(t)Chinese racesO. officinalis(B5)1[87]
Xa30(t)Indonesian racesO. rufipogon (Y238)11[88]
xa31(t)Chinese racesZhachanglong4[89]
Xa32(t)Philippine racesOryza australiensis (introgression line C4064)11[90]
Thai racesBa7
O. nivara
Thai racesPin Kaset
O. brachyantha
Xa35(t)Philippine racesOryza minuta (Acc. No.101133)11[94]
Xa36(t)Philippine racesC4059[95]
Xa38Indian Punjab racesO. nivara IRGC81825[17, 96]
Xa39Chinese and Philippines racesFF32911[97]
Xa40(t)Korean BB racesIR65482-7-216-1-211[5]
xa41(t)Various Xoo strainsRice germplasm[98]
xa42Japanese Xoo racesXM14, a mutant of IR243[18]

Table 1.

Summary of resistance genes to bacterial blight in rice.

Revised and updated from Ref. [147].

The Xa1 gene was identified by Sakaguchi [33] from rice cultivars Kogyoku and Java14. It conferred a high level of specific resistance to Japanese Xoo race 1. Since then, Xa1 has been extensively used in Japanese rice breeding as Xoo race 1 is the most prevalent in Japan. Later on, a high-resolution genetic map was developed for Xa1 using F2 population and RFLP markers [34]. Three markers (XNpb235, XNpb264, and C600) on chromosome 4 were found to be tightly linked to Xa1, while another RFLP marker U08750 was at 1.5 cM distance from Xa1. Screening of the YAC library with three linked markers resulted in identification of ten contiguous YAC clones. Out of these clones, Y5212 clone hybridized with all the three markers and was confirmed to possess the Xa1 locus. Sakaguchi [33] also identified another BB resistance gene, Xa2, in rice cultivar Tetep. It conferred specific resistance to T7147 (Japanese Xoo race 2). Earlier, Xa2 was mapped on chromosome 4, linked to Xa1 with a recombination frequency of 2–16% [35]. He et al. [36] reported the fine mapping of Xa2 using an F2 population of ZZA (Zhengzhui Ai) X IRBB2 and Xa2 was localized between two markers spanning approximately 190 kb region. Sequence analysis of this region revealed the presence of a homologous sequence of leucine-rich repeat (LRR) kinase, which is the product of a cloned BB resistance gene, Xa21 [7].

The Xa3 gene was identified in a japonica variety Wase Aikoku 3 [37]. It was mapped to the long arm of chromosome 11 and was found to be tightly linked to another BB resistance gene Xa4 [38, 39]. Xa3 was later known to be genetically linked to Xa26, another BB resistance gene. For characterization of Xa3, the gene was fine mapped using a population segregating for only a single resistance gene and markers developed from Xa26 gene family. Genetic analysis showed that Xa3 co-segregated with the Xa26 gene marker but segregated from the markers of other members of Xa26 gene family.

DNA fingerprinting also revealed that IRBB3 carrying Xa3 had the same copy numbers of Xa26 gene family members as were present in Minghui 63 carrying Xa26. The putative coding products of Xa3/Xa26 and the susceptible allele xa3/xa26 shared 92% homology with difference in the LRR domains, proving that Xa3 is the same as Xa26 [9].

The Xa4 and xa5 genes were identified by Petpisit et al. [40]. The dominant gene Xa4 confers resistance to Philippine race 1 of Xoo and was identified in rice cultivars TKM6, IR20, IR22, and IR72. The recessive gene xa5 confers resistance to Philippine Xoo races 1, 2, 3, and 5 [41]. Yoshimura et al. [39] reported the mapping of Xa4 and mapped an RFLP marker G181 on one flanking side of Xa4 locus on chromosome 11. However, no marker was identified on the other flanking side of Xa4 locus. The Xa4 locus was further mapped between two RFLP markers, RZ536 and L457 [41]. Wang et al. [42] localized the Xa4 locus between G181 and L1044 at a distance of 4.4 and 3.8 cM, respectively. However, using other rice molecular linkage maps as references [43, 44], Sun et al. [45] deduced that Xa4 locus reported earlier [41, 42] was not in the same position. Using an F2 population from IR24 X IRBB4 cross, Xa4 gene was genetically mapped to a region less than 1 cM. A contig map was constructed consisting of six nonredundant BAC clones, spanning approximately 500 kb length. Analysis of recombination events located Xa4 locus to one BAC “3H8” and assay of recombinants using subclones of “3H8” along with sequence analysis, further narrowed the Xa4 locus to a 47 kb fragment.

A high-resolution genetic map of the chromosomal region harboring xa5 was developed and mapped to a 0.5 cM interval between markers RS7 and RM611, which spanned an interval of 70 kb and contained 11 open reading frames. The potential candidate gene products of xa5 may be basal transcription factor IIA (TFIIA), an ABC transporter, a tRNA synthase, a MAP kinase and a cysteine protease, as well as four unknown, hypothetical or putative proteins [46].

While studying the inheritance of resistance to Xoo isolate PXO61 in five rice cultivars, Sidhu and Khush [47] observed that the same gene conferred resistance in all the cultivars. The pattern of segregation indicated a monogenic recessive factor when plants were inoculated at booting stage, but monogenic dominant when plants were inoculated during flowering. This reversal of dominance was caused by dosage effect of the resistance gene at a specific stage of growth of the plant when exposed to the bacterial inoculum. Apparently, the gene could express itself at booting stage only when present in two dosages. Heterozygous plants with one dose of resistance allele were susceptible during booting. However, at flowering, one dose was enough for expression of resistance. The new gene identified as Xa6 and was linked to Xa4 with a crossover value of 26%. Later studies on the genetics of resistance to Xoo in 74 cultivars of O. sativa using PXO61 isolate from the Philippines identified an additional dominant gene, Xa7, that conferred resistance in DZ78 [48]. A recombination value of 8.8% between Xa7 and G1091 located at 107.5 cM on chromosome 6 was determined [49]. Porter et al. [50] performed the AFLP analysis of a segregating, near-isogenic F3 population of IR24 X IRBB7, which revealed one polymorphic fragment, M1, mapped to position 107.3 cM on the rice map. Sequence comparisons of resistant and susceptible lines near M1 were used to generate additional markers linked to the rice BB resistance gene Xa7. A sequence-tagged site (STS) named M2 was mapped proximal to M1 and farther from Xa7, indicating that Xa7 lay distal to M1. Two SSRs, M3 and M4, were mapped at a distance of 0.5 and 1.8 cM from Xa7, respectively. The pattern of recombinants and the map distances indicated that Xa7 was located in the region corresponding to the ends of physically mapped Clemson University Genomics Institute (CUGI) BACs 96 and 143. A complex repeat was identified in the DNA sequence from O. sativa cultivars 93-11 and Nipponbare that matched the end of contig 96 and an EST marker (C52865S). Amplification of the repeat revealed the presence and absence of the repeat in IR24 and IRBB7, respectively. However, no recombinants were identified between Xa7 and the polymorphic repeat (M5). Comparison of the physical and genetic maps of rice in that region indicated that Xa7 lay within 40 kb of M5, a distance suitable for MAS and cloning of Xa7. A high-resolution genetic map of the chromosomal region surrounding Xa7 gene was constructed using SSR markers from the Gramene database ( based on the Xa7 gene initial mapping on chromosome 6 [51]. Primary analysis of F2 population from the cross of IRBB7 and IR24, located Xa7 in approximately 0.28 cM region. To walk closer to the target gene, recombinant F2 individuals were tested using STMS markers and the gene was finally mapped to a 0.21 cM region between markers GDSSR02 and RM20593. A contig map corresponding to Xa7 gene was constructed using reference sequence of cultivar Nipponbare through bioinformatics analysis. The target gene was assumed to span an interval of approximately 118.5 kb, containing a total of fourteen genes. Candidate gene analysis showed that the fourteen genes encoded novel domains that had no amino acid sequence similar to other cloned Xa (xa) genes.

A single recessive gene, xa8, conditioned resistance in rice germplasm accession PI 231129. Vikal et al. [52] mapped the gene between two consecutive SSR markers, RM21044 and RM21045 at 7.0 and 9.9 cM, respectively, on chromosome 7 and the physical distance between markers was 9.5 kb. This region harbors three intact genes, which codes for putative expressed proteins viz., Zinc finger A20 and AN1 domain-containing protein (LOC_Os07g07400), oxidoreductase, 2OG-Fe oxygenase family protein (LOC_Os07g07410), and Gibberellin 20 oxidase 1-B protein (LOC_Os07g07420). All the three candidate genes are responsible for plant response to various stresses.

The BB resistance in ‘Khao Lay Nhay’ and ‘Sateng’ was recessive in nature and were allelic to each other but nonallelic to and segregated independently of Xa3, Xa4, xa5, Xa7, and xa8 [53]. This new recessive gene was linked to Xa6 with a crossover value of 5.9%. This new gene for resistance was designated as xa9. The Xa10 was identified from rice cultivar Cas 209 [54, 55]. There is an extensive polymorphism on chromosome 11L between IRBB10 and IR24 and also a great distortion in Xa10 inheritance. Rice lines that carry Xa10 gene confer race-specific resistance to Xoo strains harboring avirulence (Avr) gene avrXa10. The Xa10 locus was roughly integrated to a large region between RFLP markers RG103 (~83 cM) and RG1109 (~91.4 cM) on the long arm of rice chromosome 11 [56]. High-resolution mapping by Gu et al. [57] narrowed down Xa10 to a 74 kb region between RFLP markers M491 and M419. Out of the 7 identified genes in this region, 6 are considered possible candidate genes for Xa10. Ogawa and Yamamoto [58] identified another BB resistance gene Xa11. Xa11 confers specific resistance to strains T7156, T7147, T7133, and H75304 (Japanese Xoo races IB, II, IIIA, and V, respectively). Xa11 was mapped between the loci of RM347 (2.0 cM) and KUX11 (1.0 cM) on the long arm of chromosome 3 [59]. It was reported that a single dominant gene, Xa12, controlled the resistance in Kogyoku and Java14 to BB race V of Indonesia [60].

The xa13 gene was first discovered in the rice variety BJ1 and this gene specifically confers resistance to the Philippine Xoo race 6, the most virulent race and one not overcome by most reported R genes [6163]. Sanchez et al. [63] reported the genetic and physical mapping of xa13 gene using two F2 populations of the cross between IR24 and IRBB13. The gene was fine mapped to a region less than 4 cM on the long arm of chromosome 8 between two RFLP markers, RG136 and R2027. Sequence analysis of the 14.8 kb fragment carrying xa13 gene indicated only two apparently intact candidate genes—an extensin-like gene and a homologue of nodulin (MtN3) and the 5′ end of a predicted hypothetical protein [14]. The expression of the rice gene Os8N3, a member of the MtN3 gene family from plants and animals, was elevated upon infection by Xoo strain PXO99A and depended on type III effector gene PbXo-1. Os8N3 resides near xa13 and could not be induced in rice lines with Xa13. Inhibitory RNA silencing of Os8N3 produced PX099A resistant plants [64].

Xa14 identified from Taichung Native 1 is a dominant gene against resistance to PXO112, BB race 5 of the Philippines [65]. Xa14 was located on chromosome 4 between marker RG620 and G282, with 20.1 and 19.1 cM, respectively by Tan et al. [66]. The gene was fine mapped by using two F2 populations. Combining recombination frequencies for the two populations together, the gene Xa14 was mapped to 3 BAC clones spanned approximately 300 kb in length between SSR markers HZR970-8 and HZR988-1 [67].

A series of nine genes (xa15, Xa16, Xa17, Xa18, xa19, xa20, xa26, Xa27, and xa28) have been obtained from mutagenesis which had different resistance levels and resistance spectrums [58, 6873]. A mutant rice line, XM5, was resistant to bacterial blight [72]. Allelic relationship studies with the known recessive genes, xa5, xa8, and xa13 revealed that the gene was not allelic to them and was a new gene. It was designated as xa19.

Devadath [74] identified a strain of Oryza barthii which was resistant to all the races of Xoo in India. Khush et al. [75] multiplied the strain at IRRI and studied its resistance to Philippine Xoo races. It was found that the strain was akin to Oryza longistaminata which was resistant to all the six Philippine Xoo races [76]. F1s of the cross of the strain with IR24 were resistant showing that the resistance was conferred by a dominant gene. The gene was different from the known BB resistance genes and was designated as Xa21(t). Genetic and physical analysis of Xa21 localized it in an 8.3 cM interval on chromosome 11 and the physical size of the region containing Xa21 gene was estimated to be about 800 kb [77].

Genomic DNA gel-blot analysis revealed that Xa21 belonged to a multigene family containing at least eight members. Most of these members were mapped to a single locus on chromosome 11, which is linked to at least nine other major resistance genes and one QTL for resistance [7, 77]. Wang et al. [78] studied the inheritance patterns and resistance spectra of transgenic plants carrying six Xa21 gene family members and observed that one member, designated Xa21D, conferred only partial resistance. Analysis of Xa21D sequence showed that Xa21D transcript terminated shortly after the stop codon introduced by retrotransposon. Sequence comparison of Xa21 and Xa21D provided evidence of adaptive selection. Xa21D encodes a receptor-like protein carrying LRR motifs in the presumed extracellular domain. Both functional and evolutionary evidence indicated that Xa21D LRR domain controlled race-specific pathogen interaction.

Another BB resistance gene, Xa22 was identified from landrace Zhachanglong (ZCL) of Yunnan province in Southwest China. It showed high level of resistance to 16 of the 17 BB strains tested [79]. The gene was nonallelic to Xa1, Xa2, Xa4, and Xa14 but was found to be linked to Xa4. Xa22 gene was mapped on short arm of chromosome 11, but according to new molecular map developed by Harushima et al. [43], it was present on the long arm. Xa22 provides resistance to a broad spectrum of Xoo isolates. The gene was localized to a small 100 kb fragment delimited by R1506 and a subclone from M3H8 BAC clone by a combination of genetic recombination analysis and physical mapping [80].

An interspecific cross was made between RBB16 and Jiagang30 (JG30), and the F1 plants showing highest resistance to BB were anther cultured to obtain doubled haploids for resistance. These anther-cultured progenies were inoculated with three strains of Xoo, and lines showing high resistance and improved plant type in H2 generation were advanced to H4 and collectively designated as WBB1. Zhang et al. [24] crossed WBB1 with two susceptible Chinese varieties, JG30 (indica) and 02428 (japonica), and IRBB21 (Xa21). Inoculation results with PXO99 at seedling stage suggested that a single dominant gene from Oryza rufipogon conferred resistance and the gene was nonallelic but probably linked to Xa21. PCR analysis of WBB1 with Xa21 specific primers also indicated that the gene was different from Xa21. The new gene, designated as Xa23(t), was mapped within a 0.4 cM region between markers Lj138 and A83B4, and the corresponding physical distance between these markers is 49.8 kb. Six Xa23 candidate genes have been annotated, including four candidate genes encoding hypothetical proteins, and the other two encoding a putative ADP-ribosylation factor protein and a putative PPR protein. Nine varieties (AC19-1-1, Aus 274, Chinsurah Boro II, Kalimekri 77-5, Tepa I, Long grain, Aus 295, DV85, and DV86) were crossed with BJ1 (carrying xa13) to confirm whether the resistance was due to xa13 or a new gene. The results indicated that the recessive gene identified in DV86 for resistance to race 6 was nonallelic to and independent of xa13. DV85, DV86, and Aus 295 had the same recessive resistance gene and it was designated as xa24(t) [81].

The xa24 resistance gene was fine mapped to a 71 kb DNA fragment in the long arm of chromosome 2 using PCR-based markers. It mediates resistance to the Philippine Xoo races 4, 6, and 10, and Chinese Xoo strains Zhe 173, JL691, and KS-1-21. The analysis of F2 mapping population, developed from the cross between a resistance line DV86 (Oryza sativa ssp. indica) carrying the target gene and a sensitive line IR24 (O. sativa ssp. indica), first mapped the gene to terminal region of long arm of chromosome 2 at 8.0 and 0.9 cM from RM482 and RM138, respectively. Further, fine mapping placed the xa24 gene between RM14222 and RM 14226 at a distance of 0.07 cM from both markers [82].

Xa25(t), a new dominant resistance gene, was identified in Minghui 63, a restorer line for a number of rice hybrids cultivated widely in China [83]. The gene conferred resistance to Philippine race 9 (PXO330) at both seedling and adult plant stages. Gao et al. [84] identified another dominant gene in a somaclonal mutant HX-3 providing resistance to BB strain Zhe173 and was also designated as Xa25(t). Bulked segregant analysis carried out on the DH population located the gene at the terminal region of the long arm of chromosome 4 between the two SSR markers RM6748 and RM1153 at a map distance of 9.3 and 3.0 cM, respectively.

In order to broaden the germplasm pool for breeding of disease resistance to Xoo, a wide hybridization project to transfer R genes from wild species Oryza minuta was initiated at IRRI in the late 1980s. A novel resistance (R) locus was identified from a progeny of interspecific hybrids of O. sativa cv. IR31917-45-3-2 and O. minuta acc. 101141 and was tentatively designated as Xa27(t) [85]. The genetic analysis of 21 rice cultivars for BB resistance divided the cultivars into two groups (group 1 and group 2) based on their resistance to Philippine Xoo races 1 and 2. Group 1 was resistant to race 1 and group 2 to race 2. When crossed with TN1 and evaluated for resistance with races 1 and 2, all cultivars showed monogenic inheritance of resistance. Allelic relationships of the genes were investigated by crossing these cultivars with different testers having single genes for resistance. Out of all the cultivars, three had new, undescribed genes. Nep Bha Bong had a recessive gene for moderate resistance to races 1, 2, and 3 and resistance to race 5 and was also designated as xa26(t). Arai Raj had a dominant gene for resistance to race 2 which segregated independent of Xa11 and was designated Xa27(t). Lota Sail had a recessive gene for resistance to race 2 which segregated independently of Xa10 and was designated as xa28(t) [86].

Gu et al. [26] reported the fine genetic mapping of the Xa27(t) gene by performing disease evaluation of an Xa27(t) NIL, IRBB27, with 35 Xoo strains from 11 countries. Resistance of Xa27(t) gene was developmentally regulated in IRBB27 and showed semidominant or dosage effect in the cultivar CO39 genetic background. Three markers, M336, M1081, and M1059, were closely linked to Xa27(t). The Xa27(t) locus was confirmed by chromosome landing of M1081 and M1059 markers on rice genome. Markers derived from the genomic sequence of O. sativa cv. Nipponbare finally located the Xa27(t) gene within a genetic interval of 0.052 cM on the long arm of chromosome 6 between markers M964 and M1197, and co-segregated with M631, M1230, and M449.

Another dominant Xa gene was identified from a rice line ‘B5’ derived from Oryza officinalis through introgression. It proved to be highly resistant to brown plant hopper, white-backed plant hopper and bacterial blight. The resistance gene identified in B5 was designated as Xa29(t) [87]. Bulked segregant analysis of RILs from a cross between 'B5' and 'Minghui63' located the resistance gene within a 1.3 cM region flanked by RFLP markers C904 and R596 on chromosome 1.

A new rice BB resistance germplasm (Y238) from the wild rice species O. rufipogon was identified and designated as Xa30(t) [88]. The gene was mapped on the long arm of rice chromosome 11. Linkage analysis revealed that four molecular markers RM1341, V88, C189, and 03STS were located on the same side of Xa30(t), with genetic distances of 11.4, 11.4, 4.4, and 2.0 cM to the candidate gene, respectively. Wang et al. [89] identified Xa31(t) gene for BB resistance in Zhachanglong (ZCL), a regional rice variety from Yunnan province in southwest China, which has a high level of resistance to a broad spectrum of Xoo isolates. Genetic linkage analysis and fine mapping localized Xa31(t) within a genetic distance of 0.2 cM between two RFLP markers G235 and C600 on the end of long arm of chromosome 4. The flanking markers were used to screen the MH63 BAC library and the Xa31(t) locus was limited to one BAC clone with a length of about 100 kb.

Another novel BB resistance gene from a wild rice (Oryza australiensis) introgression line, C4064, was found to be resistant to Xoo strains PXO61, PXO71, PXO99, PXO145, PXO280, PXO339, and KX085 but susceptible to PXO8 and PXO79. The gene was tentatively designated as Xa32(t). The chromosomal position of the gene was located using BSA with SSR and EST markers between two markers at the end side of long arm and four markers on centromere side. Finally, the gene was mapped within a 2.0 cM interval flanked by two SSR markers RM2064 and RM6293 on the long arm of chromosome 11 [90]. Another BB resistance gene, xa33(t) was identified from rice cultivar ‘Ba7’. The gene was localized on long arm of chromosome 6, where two other dominant genes (Xa7 and Xa27) have been reported. RM 20590 was identified as the closest linked marker. Although Xa7 and xa33 shared common markers, both showed different gene actions and were not growth stage-dependent genes [91]. Natarajkumar et al. [92] placed a new BB resistance gene, also designated as Xa33(t) from Oryza nivara, on chromosome 7 flanked by the markers RM21004 and RM21177 at a genetic distance of 2.0 and 4.5 cM, respectively.

Pin Kaset (PK), a Thai rice cultivar, had a high level of resistance to BB. The resistance gene in PK was identified using BC2F2 plants from a cross between Ba7 and PK. Phenotypic evaluation of TB0304 and genotypic analysis with SSR markers revealed that the gene was linked to RM224 on chromosome 11 [91]. The new gene was tentatively designated Xa34(t). Although Xa34(t) and other BB resistance genes are located in the same region and shared common linked markers, no evidence was obtained whether they shared the same genomic sequence or were tightly linked to each other. Also, Ram et al. [93] screened 2 introgression lines (IR65483-118-25-31-7-1-5-B and IR65483-141-2-4-4-2-5-B) derived from IR56 X O. brachyantha, against a virulent isolate DXO44 and 21 different virulent isolates of BB from 11 states of India. The ILs showed resistance to 16 isolates, moderate resistance to one and susceptibility to 4 isolates, as against the differential reaction of IRBB lines to different isolates. This indicated that the introgressed gene is different from those in IRBB lines. It was designated as Xa34(t). Crosses of ILs with IR56 and susceptibility check BPT5204 gave all resistant F1s and 3:1 ratio in F2 revealing a single dominant gene in both cases. Allelic test was done by crossing ILs with IRBB21 which showed that Xa34(t) (resistance gene from O. brachyantha) and Xa21 were nonallelic and inherited independently.

A new rice bacterial blight resistance gene Xa35(t) from the wild rice species Oryza minuta (Acc. No. IRGC101133) was identified and transferred into IR24 [94]. Through genetic analysis and identification of resistance spectrum, Xa35(t) showed a high level of resistance to PXO61, PXO112, and PXO339, but was susceptible to PXO86 and PXO99. The Xa35(t) locus was mapped to a 1.80 cM region and this locus was co-segregated with marker RM144, and was 0.7 cM from marker RM6293 on one side and 1.1 cM from marker RM7654 on the other side of the rice chromosome 11. Miao et al. [95] identified that the rice germplasm C4059 harbored a bacterial blight resistance gene and designated it as Xa36(t). The gene Xa36(t) was mapped on the long arm of rice chromosome 11 encompassing 4.5 cM region flanked by RM224 and RM2136.

An accession of O. nivara (IRGC 81825) was identified to be resistant to all the seven Xoo pathotypes prevalent in North India [96]. The F2 population derived from a cross between PR114 and O. nivara acc. 81825 segregated in a 3:1 ratio of resistant: susceptible plants, indicating that the resistance was provided by a single dominant gene. The inheritance and mapping studies using F2, BC2F2, BC3F1, and BC3F2 progenies of the cross O. sativa cv. PR114 × O. nivara acc. 81825 mapped the gene on chromosome 4L, spanning an approximate 38.4 kb region [17]. Since none of the known Xa genes mapped on chromosome 4L were effective against the Xoo pathotypes tested, the gene identified and transferred from O. nivara was considered novel and designated as Xa38.

A rice introgression line (IL), FF329, identified from a BC1F4 population derived from the cross between donor PSBRC66 (P66) and recipient Huang-Hua-Zhan (HHZ), exhibited a typical hypersensitive response (HR) with all 21 representative Xoo strains (14 Philippines races and seven Chinese pathotypes) [97]. By contrast, the parents were highly susceptible to 10 of the tested strains and resistant or moderately susceptible to 11 strains, but without HR symptoms. As FF329 showed broad-spectrum BB resistance, the gene identified was novel and was designated Xa39. Two SSR markers, RM21 and RM206, located on rice chromosome 11, were linked to the target gene by bulked segregant analysis of the F2 population derived from the HHZ/FF329 cross. The fine mapping of Xa39 locus placed the gene in the region of 97 · 4 kb interval flanked by markers RM26985 and DM13.

The japonica advanced backcross breeding lines derived from the indica line IR65482-7-216-1-2 in the background of cultivar Junam was resistant to all Korean BB races. Kim et al. [5] using two F2 populations derived from the crosses between 11325 (IR83261-3-7-23-6-2-1-1-2-1-2)/Anmi and 11325/Ilpum indicated that resistance (R) was controlled by a new resistance gene designated as Xa40(t), which was co-segregated with the markers RM27320 and ID55. Thus, based on the physical map of japonica rice Nipponbare, the Xa40(t) gene was defined by RM27320 and ID55.WA18-5 located on the BAC clone OSJNBa0036K13 spanning approximately 80 kb region on chromosome 11.

Hutin et al. [98] screened a germplasm of 169 rice accessions for polymorphism in the promoter of the major bacterial blight susceptibility “S” gene OsSWEET14, which encodes a sugar transporter targeted by numerous strains of Xoo. They identified a single allele with a deletion of 18 bp overlapping with the binding sites targeted by several TAL effectors known to activate the gene. Further, they showed that this allele, which was designated as xa41(t), confers resistance against half of the tested Xoo strains, representative of various geographic origins and genetic lineages, highlighting the selective pressure on the pathogen to accommodate OsSWEET14 polymorphism. Analysis of xa41(t) demonstrated that the resistance through TAL effector-dependent loss of S-gene expression can be greatly fostered upon knowledge-based molecular screening of a large collection of host plants.

A new mutant named ‘XM14’ was obtained by treating IR24, which was resistant to all Japanese Xoo races. The gene identified in XM14 was designated as xa42 [18]. The F population from XM14 × IR24 clearly showed 1 resistant:3 susceptible segregation, suggesting control of resistance by a recessive gene. The xa42 is located around the centromeric region of rice chromosome 3 in the chromosomal region encompassed by KGC3_16.1 and RM15189.

3. Determinants of pathogenicity

Xanthomonas oryzae pv. oryzae (Xoo) is a member of the c-subdivision of the Gram-negative proteobacteria. It continues to grow in the vascular system until the xylem vessels are clogged with bacterial cells and extracellular polysaccharide (EPS or xanthan). There are several races of Xoo, all of which secrete race-specific effectors into the xylem to trigger individualized response and cause infection. The bacteria also release factors which bind and activate transcription of genes that activate resistance response, known as resistance genes (R genes) [99]. The factors that activate Xoo resistance genes are known as avirulence factors that determine host specificity via gene-for-gene interactions, reducing the virulence of the pathogen as they are recognized by the host. Since each race of Xoo produces unique virulence and avirulence factors, R genes have evolved to provide resistance to individual races of Xoo. It has been known that the interactions of Xoo with plants are determined by hypersensitive response and pathogenicity (hrp) genes, which are required for pathogenicity in susceptible host plants and for the hypersensitive response (HR) in resistant and nonhost plants [3, 100]. A considerable effort has been made to identify genes involved in the pathogenesis of Xoo and to understand the roles of the gene products in the disease process. The knowledge of pathogenesis genes has become more clear and distinct from the genome sequence of Xoo strains KACC10331, MAFF311018, and PXO99A [4, 101, 102].

3.1. Avirulence genes

Members of the AvrBs3/PthA family of transcription activator-like effectors play a major role in the virulence of X. oryzae pv. oryzae. The avr gene family consists of a repeat sequence in the central domain of the encoded protein with each repeat of 34 amino acids. The number of repeats in different gene families varies, but the amino acids in each repeat are conserved except amino acids at positions 12 and 13, which are referred to as variable regions. The arrangements of the variable regions of all characterized family members appear to be a critical feature for the race specificity of the proteins. The carboxyl terminus of AvrXa7 and AvrXa10 contains a domain that is structurally similar to the acidic activation domain of many eukaryotic transcription factors, in addition to three nuclear localization signal (NLS) sequences as with AvrBs3 family members. It has been postulated that, two raxP and raxQ genes of Xoo are required for the activation of AvrXa21. Both raxP and raxQ resides in a genomic cluster of sulfur assimilation genes, which encodes an ATP sulfurylase and adenosine-5′-phosphosulfate (APS) kinase. These enzymes function together to produce activated forms of sulfate, APS, and 3′-phosphoadenosine-5′-phosphosulfate (PAPS). It has also been observed that the transcription activation domain and the NLS sequences in AvrXa7 are required for the virulence activity, suggesting that the avr gene products act as virulence factors that enter the host nucleus and directly affect host gene transcription [103]. Adaptation of an avirulent bacterial race to host varieties containing a single dominant R gene often results from the loss of function of the corresponding avr gene. However, the fitness penalty associated with loss of the avr gene may prevent disease epidemics [104].

3.2. Type III effectors

The interaction of many Gram-negative plant and animal pathogenic bacteria with their hosts depends on a conserved type III protein secretion system (TTSS). The TTSS is encoded by hrp genes for eliciting either HR on nonhost/resistant host plants or pathogenesis on susceptible hosts. The hrp gene-encoded TTSSs are responsible for translocation of avirulence proteins into the host plant cells. In xanthomonads, the hrp gene cluster comprises six operons (hrpA to hrpF) and is positively regulated by HrpG and HrpX [105107], repressed in nutrient-rich media, but induced in nutrient-limited media and inside the host [108111]. HrpG, which is predicted to be a member of the OmpR response regulator family of two-component signal transduction systems, regulates the expression of hrpX, encoding an AraC-type transcriptional activator, which then activates the expression of other hrp operons. The highly conserved hrp genes named hrc encode the proteins of the apparatus of the type III secretion system, and are critical for pathogenicity and the initiation of disease [100, 112, 113]. A hrp gene cluster was identified in the Xoo genome harboring 26 genes inclusive of hpa2 and hrpF. The Xoo hrp PAI (31.3 kb) was larger due to the presence of four transposase genes (about 6 kb) located between hpaB and hrpF genes than its counterparts of Xac (25.6 kb) and Xcc (23.1 kb). Strong amino acid identity was observed between several orthologous hrp genes of Xoo and Xanthomonas axonopodis pv. citri (Xac), as hpaF, hpaP, hrpD5, and hpaA had identity of 74, 76, 79, and 82% respectively, whereas hrpF (68%), hpa1 (65%), hrpB5 (66%), and hrpB7 (65%) exhibited relatively low similarity. The products of hrpF and hpa1 are predicted to be exposed or secreted components of the type III secretion system, which is responsible for contributing to their diversity due to distinct selective pressures in the different hosts. It has been demonstrated that the transcriptional regulator for hrp (trh) and phoP genes in Xoo positively regulate expression of hrpG, but not known whether the regulation is direct or indirect [114, 115]. The trh gene encodes a putative transcriptional regulator [114] and phoP encodes a putative response regulator of two-component regulatory systems [115]. It has not been reported whether trh and phoP influence the expression of other XrvA targets such as gum and rpf. It will be of interest to further study the regulation of hrpG expression by deciphering the functional relationship (if any) between xrvA, trh, and phoP to better understand hrp regulatory mechanisms. A homolog to hrpW, a proposed pectate lyase, was not readily apparent in the Xoo genome but several candidate pectate lyase genes were identified that could function similarly to hrpW.

A review classified all known and candidate TTSS effectors from strains of Xanthomonas spp. into 39 groups based on sequence and structural differences, and similarities [116]. A class of T3 effectors called transcription activator-like effectors (TALE) was first identified due to their relatedness to the T3 effector AvrBs3 from Xanthomonas campestris pv. vesicatoria [117]. Some of these TALEs have avirulence activity and three different TAL effectors avrXa7, avrXa10, and avrXa27 from Xoo have been cloned [13, 118]. All TALEs have nuclear localization signals (NLS) and an activation domain rich in acidic amino acids (AAD) at their C terminus. Each TALE also contains a central region of multiple 34- to 35-amino acid direct repeats that are nearly identical except the 12th and 13th amino acid residues (so-called repeat variable diaminoacids, or RVD) [119]. The combination of repeat number and composition of RVDs of individual TALEs determine the specificity of the targeted genes [119, 120]. Five additional T3 effectors from Xoo have known contributions to virulence under the appropriate conditions. These genes are pthXo1, pthXo2, pthXo3, pthXo6, and pthXo7. PthXo1 is the major TAL effector in many strains, including the common laboratory strain PXO99A, and induces the expression of host gene Os8N3, a member of nodulin 3 (N3) gene family and encodes a predicted membrane protein [64]. In addition to PthXo1, two other TAL effectors of PXO99A also contribute to virulence by inducing the expression of two different host genes [121]. PthXo6 and PthXo7 elevate the transcription of host genes OsTFX1 and OsTFIIAγ1, respectively. OsTFX1 is a member of bZIP family of transcription factors, which are involved in the regulation of many developmental and physiological processes. Another TAL effector gene, named pthXo8, has been identified in PXO99A with quantitative effects similar to pthXo6. Preliminary evidence indicates that the effector is involved in manipulation of the small RNA pathways of the host.

By using custom-engineered TALEs to investigate the functionality of host target genes involved in Xoo/rice interaction, it has been demonstrated that xa13 can be induced by Xoo and confer disease susceptibility, lending further evidence for Os8N3 (OsSWEET11 or Xa13) as an S gene. This approach facilitated to identify another SWEET gene (OsSWEET12) that can act as an S gene, provided that the Xoo pathogen contains a corresponding TALE. Further studies revealed that the xa27 allele can be activated and triggers resistance to the bacterium expressing a corresponding dTALE. Rice genome contains at least 21 SWEET (or N3) genes with a phylogenetic clade that harbors two known S genes (OsSWEET11 and OsSWEET14) and three additional uncharacterized SWEETs [122, 123] generated seven artificial or designer TAL effectors based on the promoter sequences of six loci in rice and transformed them into Xoo. Gene expression analyses indicated all dTALEs were active in trans-activating target genes in rice achieving a 100% success rate in engineering active dTALEs. Gene activation of three alleles (xa27, xa13, and OsSWEET12) led to phenotypic changes in disease resistance or susceptibility in response to Xoo infection, suggesting the feasibility of this approach to the gene functional analysis.

The genomic sequences are available for three strains of Xoo [4, 101, 102]. A comparison of the repetitive regions of PXO99A and MAFF311018 indicates a high degree of rearrangements and shuffling of the genes at all of the loci, to the point where only three genes of 17 in MAFF311018 are identical [96]. The genome structure of Xoo MAFF 311018 was characterized by large numbers of effector (avr) genes of the avrBs3/pth family and insertion sequences (ISs). The high degree of genetic diversity and race differentiation characteristic of this pathogen is due to the presence of mobile elements, which leads to genome inversions and rearrangements. The large numbers of TAL effector genes in these species may reflect the evolutionary “investment” the strains have in utilizing the TAL effectors for virulence. The maintenance of high gene numbers may even be exacerbated by rice breeding and R gene deployment by farmers over the millennia. It could be inferred that Xoo targets different host genes to alter the host physiology and different TAL effectors to have qualitatively different effects on host susceptibility.

3.3. Type II secretion system

The bacterial type II secretion system mediates a two-step process. The proteins that are secreted through this system carry a secretion signal at their N termini and are transported into the periplasmic space through the inner membrane by either the general secretion pathway (GSP) or the twin arginine pathway (TWP) [124, 125]. Transport across the outer membrane is facilitated by the proteins of main terminal branch (MTB) of general secretion pathway (GSP). The Xoo genome encodes a single type II secretion system in contrast to two different type II systems in Xac and Xcc [126]. Mutations in the gene cluster xps, which is required for a functional type II system, result in strains defective in virulence [127]. Type II secreted proteins are mainly toxins and enzymes that target different components of the host cell, and some of these enzymes, including xylanase, cellulase, cysteine protease, cellobiosidase, and lipases, have been characterized as contributors to Xoo virulence. Experimental evidences indicate that rice plants perceive some type II secreted proteins and respond by hypersensitive responses (HRs), and these responses are suppressed by type III secreted effectors [125]. Other factors that contribute to the virulence of Xoo include EPS, the type II general secretion system and its secreted proteins, and regulation involving genes within the rpf cluster [3128132]. The rpfB, rpfC, rpfF, and rpfG genes (regulation of pathogenicity factor) of Xoo have been shown to affect virulence in rice, EPS production, xylanase production, and motility [130132]. The virulence of Xanthomonas also depends upon cell-to-cell signaling mediated by diffusible signal factor (DSF). Two of the genes in this cluster rpfB and rpfFare involved in the synthesis of DSF. Knockout studies on rpfF indicate the role of DSF in the regulation of levels of extracellular enzymes and EPS [133]. The RpfC/RpfG two-component system couples the DSF sensing to intracellular regulatory networks through a second messenger, cyclic diGMP, and a global regulator, Clp. Protein-protein interaction between the DSF synthase RpfF and the sensor RpfC may act as a posttranslational mechanism to modulate the biosynthesis of DSF [134, 135]. Recently, an X. oryzae pv. oryzae flagellar operon region has been isolated from Xoo, which contains four ORFs. One of the ORFs, flhF, encodes a putative GTP-binding protein which is involved in chemotaxis. Mutation in flhF resulted in weak chemotaxis but did not show reduced virulence if inoculated on rice leaves with a scissors-clipping method, suggesting that chemotaxis is not required for virulence once the bacterial cells enter rice leaves [136]. EPS synthesis is directed by genes at multiple chromosomal loci; one of the loci is called the gum cluster [137]. The Xoo gum cluster in strain KACC10331 is composed of 14 ORFs arranged in a tandem array, expressed from a promoter located upstream of gumB, but internal promoters can also be found upstream of gumG, gumH, and gumM, respectively [101, 138]. Two different Xoo mutants, one with a transposon insertion in gum G and another with a spontaneous mutation due to the insertion of endogenous IS element in gum M, were incapable of EPS production and less virulent. In Xoo, EPS synthesis has been found to be controlled by the rpfC gene, which is part of a two-component system. Strains carrying a mutation in rpfC have greatly reduced EPS production and virulence but still attain maximum population levels in rice plants [130] indicating that EPS is a virulence determinant in X. oryzae pv. oryzae.

Recently, screening of a transposon mutant library of a Korean Xoo strain, KACC10331, in rice also showed that Tn5 insertion in the xrvA gene (XOO2744) led to reduced virulence; however, the mutant was not characterized in further detail [139]. The deduced protein encoded by xrvA possesses an H-NS domain. H-NS and H-NS–like proteins are modular proteins associated with the bacterial nucleoid. The discovery of xrvA as a regulator of virulence factor synthesis came from work aimed at identification of genes involved in EPS production of Xoo. Disruption of xrvA led to a significant reduction in virulence, a delay in HR elicitation, a decrease in EPS and DSF production, and an increase in glycogen accumulation.

3.4. Type I secretion systems

Type I secretion systems of Gram-negative bacteria are secretion systems that transport proteins directly to the extracellular environment from the bacterial cytoplasm through inner and outer bacterial membranes. Three highly conserved components of type I secretion systems are an ABC transporter, which forms a channel across the inner membrane, a membrane fusion protein (MFP), and an outer membrane protein called To1C [140]. PXO99A contains a type I secretion system that is involved in triggering resistance in rice cultivars which carry the Xa21 resistance gene. Transposon-induced mutations in PXO99A and subsequent screening for mutants that lost Xa21-mediated avirulence activity identified eight genes viz. raxA, raxB, raxC, raxST, raxQ, raxP, raxH, and raxR [141]. AvrXa21 activity requires the presence of raxA, raxB, and raxC genes, and these three genes encode the MFP, ABC transporter, and outer membrane protein. The AvrXa21 pathogen-associated molecule is involved in quorum sensing and the expression of raxST is regulated by a two-component regulatory system encoded by raxH and raxR [142] that responds to Xoo cell population density, and may be conserved in most Xanthomonas spp. The raxST encodes a sulphotransferase enzyme, while raxQ and raxP are involved in the production of the sulfuryl donor phosphoadenosine phosphor sulfate (PAPS). The elicitor of Xa21 immunity, Ax21, was characterized as a 194 amino acid sulfated protein, which is secreted into the extracellular environment [143]. The N-terminal 17 amino acid peptide of Ax21 is sulfated at a tyrosine residue and is sufficient to trigger Xa21-mediated resistance.

4. Molecular mechanism of BB resistance in rice

Out of 42 Xa genes identified so far, nine genes (Xa1, Xa3/Xa26, xa5, Xa10 xa13, Xa21, Xa23, xa25, and Xa27) have been characterized at molecular level and these encode various types of proteins (Table 2). Based on these studies, the molecular mechanisms of BB resistance in rice seem to be largely different from the mechanisms of resistance to rice blast, although the mechanisms of rice disease resistance remain largely to be elucidated. Most of the characterized BB resistance genes are different from the most common R protein, nucleotide-binding site-leucine-rich repeat (NBS-LRR) protein [144]. Interestingly, except for the fact that Xa21 and Xa26 encode for similar receptor-like proteins, the products of the other genes are unique and not found in other plant species [145]. These features suggest that molecular mechanism of rice-Xoo system is more complicated and a unique pathosystem to study the interactions between hosts and pathogens. The molecular mechanism of BB resistance gene has also been discussed in other book chapters [146, 147]. The nine characterized BB resistance genes fall into six different classes of proteins and thus may give a wide scenario of understanding at molecular level.

S. No.GeneEncoded proteinReference
2Xa3/Xa26Leucine-rich repeat receptor-like kinase (LRR-RLK)[8]
3xa5TFIIA Transcription factor[11, 12]
4Xa10Executor R protein, encodes 126 AA, with four potential transmembrane helices[20]
6xa21Receptor-like kinase[7]
7Xa23Executor R protein, encodes 113 AA, with four potential transmembrane helices[21]
9Xa27Apoplast (rice unique gene)[13]

Table 2.

The BB resistance genes characterized at molecular level.

4.1. BB resistance conferred by LRR receptor kinase protein

The LRR receptor kinase class of BB resistance is conferred by Xa21 and Xa3/Xa26 genes. The Xa21 was the first rice BB resistance gene characterized [7] and was one of the most intensively studied genes at molecular level. It was originally identified in the wild species O. longistaminata, and isolated by map-based cloning strategy from the IRBB21, a near-isogenic line in the background of IR24. This gene confers a race-specific resistance to Xoo, and is the most widespread BB resistance gene in the rice cultivated area, thereby providing broad-spectrum resistance. The receptor kinase-like protein encoded by Xa21 consists of putative extracellular domain containing LRR, a single pass transmembrane domain, and an intracellular domain containing serine/threonine kinase. This protein is unique in carrying the receptor domain LRR with hypothetical function in pathogen recognition, and the kinase domain that functions in subsequent signal transduction as compared to other cloned plant resistance genes [148]. The Xa21-mediated resistance is not expressed in the early developmental stages and gradually increases from the seedling stage to later stages, with 100% resistance at the adult stage [149]. The gradual increase in expression of Xa21 gene during rice development is associated with development-controlled Xa21-mediated resistance [150]. Ectopic expression of Xa21 gene can generate rice plants with a high level of resistance to Xoo at both seedling and adult stages [150, 151]. The Ax21 (avirXa21 protein; as called activator of Xa21) protein was secreted by Xoo through its type I secretion system switch on the Xa21 gene present in the host [145]. A sulfated 17-amino acid synthetic peptide derived from the N-terminal region of Ax21 is sufficient for its initiation. The Ax21 is highly conserved in many Xanthomonas species including number of pathogens of plants and human across microbial genus. Thus, Ax21 is considered a pathogen-associated molecular pattern, and thus, Xa21 can be classified both as a plant pattern recognition receptor (PRR) and an R protein [145].

The Xa21 locus is a multigene family and several key components of Xa21 protein such as E3 ubiquitin ligase/XB3, WRKY62/XB10, protein phosphatase 2C (PP2C)/XB15, ATPase/XB24, and Bip3 (also known as glucose-regulated protein), involved in defense signaling pathway have been identified. The E3 ubiquitin ligase interacts with the kinase domain of Xa21 protein and acts as a substrate for the Xa21 serine and threonine kinase activity, which is necessary for full accumulation of the Xa21 protein, thus Xa21-mediated immunity [152]. The Xa21 protein binds to WRKY62 with catalytic activity of its juxtamembrane motif and serine/threonine kinase domain. The WRKY62 and WRKY76 (another WRKY transcription factor) function as a negative regulator of Xa21-mediated resistance [153, 154]. The PP2C component interacts with juxtamembrane motif and kinase domain of Xa21 protein, and can dephosphorylate autophosphorylated Xa21, thus acting as negative regulator of Xa21-mediated resistance [155]. The XB24, an Xa21 binding protein, was isolated using yeast two-hybrid screening and belongs to a class of ATPases. The ATPase/XB24 can enhance autophosphorylation of Xa21 protein by its physical association in vivo with the juxtamembrane motif and kinase domain, and downregulates the Xa2-mediated resistance Xa21 protein by its enzymatic activity, because the activation of Xa21 following interaction with pathogen-associated molecular pattern Ax21 requires the dissociation of XB24 from Xa21 or removal of autophosphorylation. The rice plants with reduced level of XB24 expression showed enhanced level of Xa21-mediated resistance, whereas Xa21-mediated resistance overexpressing the XB24/ATPase in rice plants showed lower level of Xa21-meditated resistance, as XB24 in this case cannot readily dissociate from Xa21 and further binding of Ax21 with Xa21 leads to conformational change in Xa21 protein. The conformational change in Xa21 protein exposes it to degradation in endogenous proteases leading to lower resistance 21 protein a21 [156]. The endoplasmic reticulum chaperone Bip3 can interact with Xa21 protein in vivo. Rice plants overexpressing Bip3 have decreased Xa21 protein accumulation and inhibited Xa21 protein processing, which results in compromised Xa21-mediated resistance [157].

The Xa3/Xa26 locus was isolated as Xa26 from an indica rice cultivar Minghui 63 [8] and found to be similar to previously identified gene Xa3, therefore renamed as Xa3/Xa26 [9]. It encodes a plasma membrane-localized LRR receptor kinase-type protein with an extracellular LRR domain, a transmembrane motif, and a cytoplasmic kinase domain [8]. It also confers a broad-spectrum resistance relative to Xa21 and has been widely deployed in rice cultivars in China [158160]. Two different alleles of Xa3/Xa26 have been identified from “CC” genome of O. officinalis and O. minuta that can mediate a similar spectrum of resistance against Xoo [160]. This indicated the early origin and relatively conserved function of Xa3/Xa26 locus during evolution that can provide durable resistance against Xoo [160]. The MRKa gene, an ortholog of Xa3/Xa26 gene family in rice cultivar Mingui 63, can mediate partial resistance to Xoo when it is overexpressed [161]. The kinase domain is important for complete function of Xa3/Xa26 for resistance, as rice plants carrying truncated Xa3/Xa26 gene without kinase domain exhibits lower level of resistance. The kinase domain of MRKa protein can partially restore the function of the truncated Xa3/Xa26 gene in Xoo resistance, suggesting the partially conserved function of the orthologs of this family. This hypothesis is also supported by another study that NRKe gene from rice cultivar Nipponbare gets transcriptionally activated in response to raised temperature [162]. The kinase domain of Xa3/Xa26 protein can replace the function of the kinase domain of NRKe protein in response to temperature change.

The genetic background and development stage of rice plant affect the Xa3/Xa26-mediated resistance. The higher level of resistance was observed in japonica as compared to indica background. The Xa3/Xa26 expression gradually increases from seedling stage to adult stage and pathogen infection also differentially effects its expression in plants with different genetic backgrounds, Xoo strains at both seedling and adult stages, but has full resistance to other Xoo strains at adult stage [8, 163, 164]. Further resistance mediated by Xa3/Xa26 increases with increase in its expression and its constitutive expression provides broad-spectrum resistance at both seedling and adult stage without affecting the agronomic performance [159].

Several members functioning downstream in the Xa3/Xa26-initiated defense signaling pathway have been identified, where the downstream function of these components can mediate a broad-spectrum resistance as compared to Xa3/Xa26 protein. Two WRKY-type transcription factors namely WRKY13 and WRKY45-2 positively regulate rice resistance to Xoo, of which M. oryzae (causal organism of rice blast), with WRKY13 putatively functions upstream of WRKY45-2 in rice-Xoo interaction [165167]. Two genes namely OsDR8 encoding a protein involved in thiamine biosynthesis and C3H12, a CCCH-type zinc finger nucleic acid-binding protein, also act as positive regulator of rice resistance to Xoo in Xa3/Xa26-initiated defense pathway [152, 168]. Of these, C3H12 functions upstream of WRKY45-2. A rice tribe-specific gene OsDR10 that probably functions upstream of WRKY13, negatively regulates resistance to Xoo in Xa3/Xa26-mediated resistance pathway [169].

Both Xa21 and Xa3/Xa26 belong to multigene family; encode same type of proteins and have 53% sequence similarity [7, 8]. The only structural difference between two genes is the number of LRR, where Xa26 encodes 26 LRR, whereas Xa21 encodes 23 LRR [7]. However, the respective LRR domains of Xa3/Xa26 and Xa21 are the important determinants of race-specific recognition during rice-Xoo interactions as evidenced from experiment on domain swapping analyses, but a juxtamembrane motif of Xa3/Xa26 also seems to contribute in resistance specificity [150]. The kinase domain of Xa3/Xa26 can partially replace the function of the kinase domain of Xa21, or vice versa, in Xoo resistance, suggesting the partially conserved nature of this domain in defense signaling pathway [150]. Both Xa3/Xa26 and Xa21 genes are dose-dependent and their expression progressively increases with developmental stage. However, Xa3/Xa26 has a higher expression level in the japonica background than in an indica background [150, 164]. Further study may also be required to determine, whether Xa3/Xa26 is also a PRR in addition to being an R protein.

4.2. BB resistance conferred by MtN3/saliva class protein

The MtN3 (a homologue of nodulin protein) class of BB resistance is conferred by xa13, a fully recessive gene for BB resistance. The gene encodes a novel protein that has no sequence similarity with any known R proteins, but it shows 50% sequence identity and 68% sequence similarity to the product of a nodulin MtN3 gene in legumes [14]. The xa13 and its dominant allele Xa13, which is also named Os8N3 and OsSWEET11 [64, 122], encode identical polytopic plasma membrane proteins of the MtN3/saliva family proteins, but have crucial sequence differences in their promoter regions. Promoter swapping analysis confirms that Xa13 (Os8N3 and OsSWEET11) is a susceptibility gene, which is induced by direct binding of the transcription activator-like (TAL) effector PthXo1 of Xoo strain PXO99 to the cis element, the UPT PthXol box, on the Xa13 promoter [64, 170, 171]. The Xoo strain PXO99 that secretes PthXo1 cannot induce recessive xa13 due to the mutation of the UPT PthXo1 box in the xa13 promoter. Further, PXO99 is more sensitive to copper (an essential micronutrient of plants, is also an important element for a number of pesticides in agriculture) than other Xoo strains. The Xa13 protein interacts with two copper transporter-type proteins, COPT1 and COPT5, to promote removal of copper from xylem vessels, where Xoo multiplies and spreads to cause disease [172]. As PXO99 cannot induce recessive xa13, the copper levels in rice plants carrying the recessive xa13 gene can inhibit Xoo growth and thus plants show resistant reaction. Besides functioning against Xoo resistance, product of xa13 gene also has an essential role in pollen development. This became evident from suppressing the function of either the dominant or recessive allele of xa13 in rice transgenic plants, where xa13 not only enhanced the resistance but also caused male sterility [173]. The study showing the link between two unrelated biological processes further demands the detailed studies in the future on the functional overlap between pathogen-induced defense signaling and plant development.

The recessive xa25 gene, also named Xa25 (t), encodes a plasma membrane protein of the MtN3/saliva family similar to xa13 and confers race-specific resistance to Philippine Xoo strain PXO339 [19, 83]. The protein encoded by xa25 and its dominant allele differ in eight amino acids. The Xoo strain PXO339 can induce the expression of dominant Xa25, but not recessive xa25. The differences in proteins and expression pattern of xa25 and its dominant allele Xa25 in rice-PXO339 interaction suggest that the dominant Xa25 may be a race-specific susceptible gene, whereas the recessive xa25 has evolved as the mutant that cannot be induced by rice-Xoo interaction—similar to the recessive xa13. The developmental stage of rice plant also influences the xa25-mediated resistance. The xa25 gene regulated by its native promoter, when transferred in the rice plants homozygous for Xa25, behaves in recessive nature. The rice plants homozygous for xa25 showed resistant reaction on inoculation with PXO39. However, the rice plants heterozygous at the xa25 locus were susceptible to PXO339 at the seedling stage, but became resistant to PXO339 at the adult stage. The dominance reversal characteristic of xa25 may be because of suppression of PXO339-induced activation of dominant Xa25 at the adult stage [19]. The rice MtN3/saliva family contains more than 20 paralogs. Some MtN3/saliva proteins from different species act as glucose transporter [122, 174]. The Xa13, besides functioning as a susceptibility gene in race-specific rice-Xoo interaction, also acts as sucrose transporter. Similar role needs to be elucidated for Xa25 gene along with rice-Xoo interaction.

4.3. BB resistance conferred by TAL effector-dependent class protein

Three BB resistant genes Xa27, Xa10, and Xa23 act as transcription activator-like (TAL) effector-dependent R genes [13, 20, 21]. The Xa27 mediates race-specific resistance to diverse strains of Xoo, including Chinese and Philippine Xoo races [13]. This gene encodes an apoplast protein of 113 amino acids that has no distinguishable sequence similarity to proteins from organisms other than rice [175]. The resistant and susceptible alleles of Xa27 encode an identical protein, but they differ from each other only in the promoter region [13]. The Xa27-mediated race-specific resistance to Xoo depends upon AvrXa27, a TAL effector of Xoo that induces resistance reaction by binding to the UPTAvrXa27 box of the Xa27 promoter [176]. However, the recessive MR gene xa5 can attenuate the Xa27-mediated resistance in rice, which suggests that Xoo TAL effector could not use protein encoded by the recessive xa5 as a transcription machinery for activation of Xa27 [177]. The secondary cell wall thickening in vascular bundle elements is obviously associated with Xa27-mediated resistance [13]. According to the molecular models of plant innate immunity, pathogen-associated molecular pattern-triggered immunity (PTI) is induced by plasma membrane-localized plant pattern recognition receptors (PRRs) and effector-triggered immunity (ETI) is initiated by NBS-LRR–type R proteins present in the cytoplasm [178, 179]. The subcellular localization and sequence specificity of Xa27 protein suggest that it does not follow either PTI or ETI procedure [180], though its typical biochemical function in rice-Xoo interaction still remains to be elucidated.

Xa10, another TAL effector-dependent R gene for BB resistance contains a binding element for the TAL effector AvrXa10 (EBEAvrXa10) in its promoter, and AvrXa10 specifically induces Xa10 expression [20]. The Xa10-encoded protein consists of 126 amino acid residues, which is predicted to have four potential transmembrane helices (M1–M4), among which, M2 contains charged amino acid residues. Xa10 is an inducible protein that triggers programmed cell death by disruption of the endoplasmic reticulum (ER) and cellular Ca2+ homeostasis. The Xa10 functions not only in rice but also in other species such as Nicotiana benthamiana, and in animal kingdom such as mammalian HeLa cells [20]. The Xa10 protein localizes as hexamers in the ER and is associated with ER Ca2+ depletion in plant and HeLa cells. It shows hypersensitive response with faster cell death and shorter lesions in incompatible reactions. The variants of Xa10 that abolish programmed cell death and ER Ca2+ depletion in N. benthamiana and HeLa cells, also abolish disease resistance in rice [20]. In one of the experiment, the modified Xa10 gene designated as XA10E5 was transferred into Nipponbare and 93-11 backgrounds to generate broad-spectrum resistance to most of the BB pathogens. The XA10E5 contains five tandemly arranged effector binding elements (EBEs), each responding specifically to a corresponding virulent or avirulent TAL effector. The transgenic lines with XA10E5 showed resistance to 27 of the 28 Xoo strains collected from 11 countries [181].

Xa23, another TAL effector associated executor R gene, was isolated from O. rufipogon using map-based cloning and TAL effector-based technology [21]. It encodes 113 amino acid long proteins (same number of amino acids as in Xa27) with 64% similarity only to Xa10 protein, but nonsignificant similarity at genomic level. In addition, the predicted three transmembrane helices of Xa23 largely overlap with transmembrane helices (M2–M4) of Xa10 indicating that Xa23 could be a homolog of Xa10 [21]. A paralog of Xa23 has been found to exist in Nipponbare genome with unknown function. The AvrXa23 is responsible for activation of Xa23 transcription by a TAL effector present in all examined Xoo isolates [21]. As compared to Xa10, Xa23 is a broad-spectrum R gene and provides strong resistance to all natural Xoo strains tested so far possibly due to presence of avrXa23 in natural Xoo strains [182]. The susceptible xa23 allele Xa23 but differs in promoter region by lacking the TALE binding element (EBE) for AvrXa23. Xa23 can trigger a strong hypersensitive response in rice, tobacco, and tomato [21].

4.4. BB resistance conferred by NBS-LRR class proteins

Xa1 is the only NBS-LRR–type BB resistance gene identified so far and is an inducible gene that means its expression is induced by wounding and pathogen infection [10]. However, out of number of uncharacterized BB resistance genes, some might be providing resistance through NBS-LRR class of proteins. One such gene is Xa38, identified from O. nivara seems to be of NBS-LRR type based on the putative candidate gene sequence analysis in the targeted bacterial artificial clone (BAC) [183]. Nucleotide-binding site-leucine-rich repeat (NBS-LRR) genes play important roles in plant disease resistance. They are generally believed to be responsible for the recognition of effectors delivered by pathogens during infection and the induction of downstream disease resistance reactions [184]. Plant NBS-LRRs can be divided into several types based on the variable N-terminus. In rice, most NBS-LRRs belong to the CC-NBS-LRR (CNL) subclass, in which there is a coiled-coil domain at the N-terminus [185, 186]. In the genome of rice (O. sativa cv. Nipponbare), more than 400 NBS-LRR genes have been identified [19], but although these genes are believed to be defense-related, the functions of most of them are unknown in rice genome. Recently, a novel NBS-LRR gene was isolated from rice and designated as Oryza sativa Rp1-like 1 (OsRP1L1) based on similarity to Rp1 locus of maize, an intensively studied NBS-LRR gene providing resistance to common leaf rust in maize [187]. Overexpression of OsRP1L1 moderately elevated the resistance of plants to Xoo strains PXO86 and PXO341 in a susceptible japonica cultivar [188]. Similarly, a large number of genes out of 400 NBS-LRR in the rice genome can be isolated that could be putative candidates for BB resistance.

4.5. BB resistance conferred by other class of protein

The recessive xa5 that belongs to this class encodes a typical gamma subunit of transcription factor IIA (TFIIAγ), which is one of general transcription factors required for transcription by RNA polymerase II [11]. It mediates specific resistance to Japanese races and Philippine races 1, 2, 3, and 5 by restriction of bacterial movement, but not multiplication [11, 189]. This gene was cloned by a map-based cloning approach combined with allele sequence analysis [11], and further complementation testing confirmed this gene [12]. TFIIAγ is involved in the recruitment of the basal transcription machinery by eukaryotic transcription factors. The xa5 allele contains a missense mutation that does not seem to influence its function in the recruitment of the basal transcription machinery [12]. It is speculated that Xoo TAL effectors usurp parts of plant basal transcription machinery to regulate rice gene expression; the missense mutation of xa5 allele does not compromise its general function in transcription, but it may evade TAL virulence functions [119, 177]. The Xoo avrXa5 is an avirulence gene, which encodes a TAL-type protein, corresponding to xa5 [190]. The xa5 showed a constitutive expression pattern in different tissues, and the resistance of xa5 is not dose-dependent [11, 12].

5. Conclusion

Exploration, identification, and utilization of new resistant germplasms in rice breeding are the strategical steps to control the bacterial blight disease of rice. The Xa21 gene has been successfully introgressed into several elite rice varieties and hybrid rice parental lines all over the world either singly or in combination with other major resistance genes such as Xa4, xa5, and xa13 [2732, 191]. Traditionally, single recessive genes are overlooked in pyramiding plans since they have to be present in the homozygous condition, which is more difficult to achieve than a heterozygous- or homozygous-dominant genotype. But, in the last decades, rice genomic research has generated a wealth of information about gene function. These advances are now accessible for rice improvement, and have been applied in MAS and genetic engineering in breeding programs. Gene silencing also paves a way to utilize these genes more efficiently. Artificial microRNA (amiRNA) technology has been developed to silence the dominant allele of xa13, allowing the recessive allele to be unmasked, thereby expressing the resistant phenotype, mimicking a homozygous state. This silencing conferred a higher degree of resistance to the rice line without affecting other essential traits, such as fertility [192]. Hummel et al. [99] concluded that genetic engineering of the R gene promoter can also effectively promote resistance towards Xoo. Many R genes are turned on in the presence of TALE released from the pathogen by binding to a specific effector binding element (EBE) and initiating the resistance response. So, by fusing new EBEs to the promoter of Xa27, gene transcription could be initiated by bacterial races other than the races that normally activate Xa27. Therefore, the Xa27 gene will respond to a greater spectrum of pathogens, triggering resistance. Also, the addition of the EBEs resulted in resistance against a pathovar of Xanthamonas which is the causative agent of bacterial leaf streak, for which no R genes have yet been identified. This method creates a single gene with the expanded spectrum of traditionally pyramided lines but is less time-consuming and laborious than creating multigenic lines. Several EBEs could be added to a single promoter, greatly increasing the number of pathogens which initiate resistance. Thus, there are numerous factors impacting the resistance granted by different genes, and a complete understanding of the host-pathogen interaction dynamic would result in a better equipped scientific community.


1 - Khush GS. What will it take to feed 5.0 billion rice consumers in 2030? Plant Molecular Biology. 2005;59:1–6.
2 - Devadath S. Bacterial blight of paddy. In: Singh US, Mukhopadhyay AN, Kumar J, Chaube HS, editors. Plant Diseases of International Importance: Diseases of Cereals and Pulses. Prentice-Hall, Inc., Englewood Cliffs, NJ, USA; 1992. pp. 158–85.
3 - Nino-Liu DO, Ronald PC, Bogdanove AJ. Xanthomonas oryzae pathovars: model pathogens of a model crop. Molecular Plant Pathology. 2006;7:303–24.
4 - Ochiai H, Inoue Y, Takeya M, Sasaki A, Kaku H. Genome sequence of Xanthomonas oryzae pv. oryzae suggests contribution of large numbers of effector genes and insertion sequences to its race diversity. Japan Agricultural Research Quarterly. 2005;39:275–87.
5 - Kim SM, Suh JP, Qin Y, Noh TH, Reinke RF, Jena KK. Identification and fine-mapping of a new resistance gene, Xa40, conferring resistance to bacterial blight races in rice (Oryza sativa L.). Theoretical and Applied Genetics. 2015;128:1933–43.
6 - Zhang Q. Genetics of quality resistance and identification of major resistance genes to rice bacterial blight. In: Zhang Q, editors. Genetics and Improvement of Resistance to Bacterial Blight in Rice. Science Press, Beijing; 2007. pp. 130–77.
7 - Song WY, Wang GL, Chen L, Kim HS, Holsten T, Wang B, Zhai W, Zhu LH, Fauquet C, Ronald PC. The rice disease resistance gene, Xa-21, encodes a receptor kinase-like protein. Science. 1995;270:1804–6.
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. The Plant Journal. 2004;37:517–27.
9 - Xiang Y, Cao Y, Xu C, Li X, Wang S. Xa3, conferring resistance for rice bacterial blight and encoding a receptor kinase-like protein, is the same as Xa26. Theoretical and Applied Genetics. 2006;113:1347–55.
10 - Yoshimura S, Yamanouchi U, Katayose Y, Toki S, Wang Z, 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. Proceedings of National Academy of Sciences, USA. 1998;95:1663–8.
11 - Iyer AS, McCouch SR. The rice bacterial blight resistance gene xa5 encodes a novel form of disease resistance. Molecular Plant-Microbe Interactions. 2004;17:1348–54.
12 - Jiang GH, Xia ZH, Zhou YL, Wan J, Li DY, Chen RS, Zhai W X, Zhu LH. Testifying the rice bacterial blight resistance gene xa5 by genetic complementation and further analyzing xa5 (Xa5) in comparison with its homolog TFIIA_1. Molecular Genetics and Genomics. 2006;275:354–66.
13 - Gu K, Yang B, Tian D, Wu L, Wang D, Sreekala C, Yang F, Chu Z, Wang GL, White FF, Yin Z. R gene expression induced by a type-III effector triggers disease resistance in rice. Nature. 2005;435:1122–5.
14 - Chu Z, Fu B, Yang H, Xu C, Li Z, Sanchez A, Park YJ, Bennetzen JL, Zhang Q, Wang S. Targeting xa13, a recessive gene for bacterial blight resistance in rice. Theoretical and Applied Genetics. 2006;112:455–61.
15 - Flor HH. Current status of the gene-for-gene concept. Annual Review of Phytopathology. 1971;9:275–96.
16 - Ogawa T. Methods and strategy for monitoring race distribution and identification of resistance genes to bacterial leaf blight (Xanthomonas campestris pv. oryzae) in rice. Japanese Agricultural Research Q. 1993; 27:71–80.
17 - Cheema KK, Grewal NK, Vikal Y, Sharma R, Lore JS, Das A, Bhatia D, Mahajan R, Gupta V, Bharaj TS, Singh K. A novel bacterial blight resistance gene from Oryza nivara mapped to 38 Kb region on chromosome 4L and transferred to Oryza sativa L. Genetics Research Cambridge. 2008;90:397–407.
18 - Busungu C, Taura S, Sakagami JI, Ichitani K. Identification and linkage analysis of a new rice bacterial blight resistance gene from XM14, a mutant line from IR24. Breeding Science. 2016;66:636–645.
19 - 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. The Plant Cell Environment. 2011;34:1958–69.
20 - Tian D, Wang J, Zheng X, Gu K, Qiu C, Yang X, Zhou Z, Goh M, Luo Y, Murata-Hori M, White FF, Yin Z. The rice TAL effector-dependent resistance protein Xa10 triggers cell death and calcium depletion in the endoplasmic reticulum. The Plant Cell. 2014;26:497–515.
21 - Wang C, Zhang X, Fan Y, Gao Y, Zhu Q, Zheng C, Qin T, Li Y, Che J, Zhang M, Yang B, Liu Y, Zhao K. Xa23 is an executor R protein and confers broad-spectrum disease resistance in rice. Molecular Plant. 2014;8:290–302.
22 - Kinoshita T. Report of the committee on gene symbolization, nomenclature and linkage groups. Rice Genetics Newsletter. 1995;12:9–153.
23 - Huang N, Angeles ER, Domingo J, Magpantay G, Singh S, Zhang G, Kumaravadivel N, Benett J Khush GS. Pyramiding of bacterial blight resistance genes in rice: marker-aided selection using RFLP and PCR. Theoretical and Applied Genetics. 1997;95:313–20.
24 - Zhang Q, Lin SC, Zhao BY, Wang CL, Yang WC, Zhou YI, Li DY, Chen CB, Zhu LH. Identification and tagging a new gene for resistance to bacterial blight (Xanthomonas oryzae pv. oryzae) from O. rufipogon. Rice Genetics Newsletter. 1998;15:138.
25 - Gao DY, Xu ZG, Chen ZY, Sun LH, Sun QM, Lu F, Hu BS, Liu YF, Tang LH. Identification of a new gene for resistance to bacterial blight in a somaclonal mutant HX-3 (indica). Rice Genetics Newsletter. 2001;18:66–8.
26 - Gu K, Tian D, Yang F, Wu L, Sreekala C, Wang D, Wang GL, Yin Z. High-resolution genetic mapping of Xa27(t), A new bacterial blight resistance gene in rice, Oryza sativa L. Theoretical and Applied Genetics. 2004;108:800–7.
27 - Singh S, Sidhu JS, Huang N, Vikal Y, Li Z, Brar DS, Dhaliwal HS, Khush GS. Pyramiding three bacterial blight resistance genes (xa5, xa13 and Xa21) using marker-assisted selection into indica rice cultivar PR106. Theoretical and Applied Genetics. 2001;102:1011–5.
28 - Joseph M, Gopalakrishnan S, Sharma RK, Singh VP, Singh AK, Singh NK, Mohapatra T. Combining bacterial blight resistance and basmati quality characteristics by phenotypic and molecular marker assisted selection in rice. Molecular Breeding. 2004;13:377–87.
29 - Sundaram RM, Vishnupriya MR, Biradar SK, Laha GS, Reddy AG, Rani NS, Sarma NP, Sonti RV. Marker assisted introgression of bacterial blight resistance in Samba Mahsuri, an elite indica rice variety. Euphytica. 2008;160:411–22.
30 - Sundaram RM, Vishnupriya MR, Laha GS, Rani NS, Rao PS, Balachandran SM, Reddy GA, Sarma NP, Sonti RV. Introduction of bacterial blight resistance into Triguna, a high yielding, mid-early duration rice variety by molecular marker assisted breeding. Biotechnology Journal. 2009;4:400–7.
31 - Perumalsamy S, Bharani M, Sudha M, Nagarajan P, Arul L, Saraswathi R, Balasubramanian P, Ramalingam J. Functional marker-assisted selection for bacterial leaf blight resistance genes in rice (Oryza sativa L.). Plant Breeding. 2010;129:400–6.
32 - Pandey MK, Rani NS, Sundaram RM, Laha GS, Madhav MS, Srinivasa Rao K, Sudharshan I, Hari Y, Varaprasad GS, Subba Rao LV, Suneetha K, Sivaranjani AKP, Viraktamath BC. Improvement of two traditional Basmati rice varieties for bacterial blight resistance and plant stature through morphological and marker-assisted selection. Molecular Breeding. 2013;31(1):239–46.
33 - Sakaguchi S. Linkage studies on the resistance to bacterial leaf blight, Xanthomonas oryzae (Uyeda et Ishiyama) Dowson, in rice (in Japanese. English summary). Bulletin of National Institute of Agricultural Science Series. 1967;D16:1–18.
34 - Yoshimura S, Umehara Y, Kurata N, Nagamura Y, Sasaki T, Minobe Y, Iwata N. Identification of a YAC Clone Carrying the Xa1 allele, a bacterial blight resistance gene in rice. Theoretical and Applied Genetics. 1996;93:117–22.
35 - Yoshimura S, Kurata N, Sasaki T, Yoshimura A. Genetic analysis of bacterial blight resistance genes in rice by using molecular markers. Recent Advances in Breeding. 1994;36:33–6.
36 - He Q, Li D, Zhu Y, Tan M, Zhang D, Lin X. Fine mapping of Xa2, a bacterial blight resistance gene in rice. Molecular Breeding. 2006;17:1–6.
37 - Ezuka A, Horino O, Toriyama K, Shinoda H, Morinaka T. Inheritance of resistance of rice variety Wase Aikoku 3 to Xanthomonas oryzae. Bulletin of Tokai-Kinki National Agricultural Experimental Station. 1975;28:124–30.
38 - Yoshimura S, Nelson R, Yoshimura A, Mew TW, Iwata N. RFLP mapping of the bacterial blight resistance genes Xa3 and Xa4. Rice Genetics Newsletter. 1992;9:136–8.
39 - Yoshimura S, Yoshimura A, Iwata N, McCouch S, Abenes M, Baraoidan M, Mew TW, Nelson RJ. Tagging and combining bacterial blight resistance genes in rice using RAPD and RFLP markers. Molecular Breeding. 1995;1:375–87.
40 - Petpisit V, Khush GS, Kauffman HE. Inheritance of resistance to bacterial blight in rice. Crop Science. 1977;17:551–4.
41 - Li ZK, Luo LJ, Mei HW, Paterson AH, Zhao XH, Zhang DB, Wang YP, Yu XQ, Zhu L, Stansel JW, Ying CS. A “defeated” rice resistance gene acts as a QTL against a virulent strain of Xanthomonas Oryzae pv. oryzae. Molecular & General Genetics. 1999;261:58–63.
42 - Wang W, Zhai W, Luo M, Jiang G, Chen X, Li X, Wing R A and Zhu L. Chromosome landing at the bacterial blight resistance gene Xa4 locus using a deep coverage rice BAC library. Molecular Genetics & Genomics. 2001;265:118–25.
43 - Harushima Y, Yano M, Shomura A, Sato M, Shimano T, Kuboki Y, Yamamoto T, Lin SY, Antonio BA, Parco A, Kajiya H, Huang N, Yamamoto K, Nagamura Y, Kurata N, Khush GS and Sasaki T. A high-density rice genetic linkage map with 2275 markers using a single F2 population. Genetics. 1998;148:479–94.
44 - Wang C. Fine and Physical Mapping of Bacterial Blight Resistance Genes Xa22(t) and Xa24(t) in Rice (in Chinese). PhD thesis. Huazhong agricultural University, Wuhan, China; 1999.
45 - Sun X, Yang Z, Wang S and Zhang Q. Identification of a 47 kb DNA fragment containing Xa4, a locus for bacterial blight resistance in rice. Theoretical and Applied Genetics. 2003;106:683–7.
46 - Blair MW, Garris AJ, Iyer AS, Chapman B, Kresovich S, McCouch SR. High resolution genetic mapping and candidate gene identification at the xa5 locus for bacterial blight resistance in rice (Oryza sativa L.). Theoretical and Applied Genetics. 2003;107:62–73.
47 - Sidhu GS, Khush GS. Dominance reversal of a bacterial blight resistance gene in some rice cultivars. Phytopathology. 1978;68:461–3.
48 - Sidhu GS, Khush GS, Mew TW. Genetic analysis of bacterial blight resistance to seventy-four cultivars of rice Oryza sativa L. Theoretical and Applied Genetics. 1978;53:105–11.
49 - Kaji R, Ogawa T. Identification of the located chromosome of the resistance gene, Xa-7, to bacterial leaf blight in rice [in Japanese]. Breeding Science. 1995;45:79.
50 - Porter BW, Chittoor JM, Yano M, Sasaki T, White FF. Development and Mapping of markers linked to the rice bacterial blight resistance gene Xa7. Crop Science. 2003;43:1484–92.
51 - Chen S, Huang ZH, Zeng LX, Yang JY, Liu QG and Zhu XY. High-resolution mapping and gene prediction of Xanthomonas oryzae pv. oryzae resistance gene Xa7. Molecular Breeding. 2008;22:433–41.
52 - Vikal Y, Chawla H, Sharma R, Lore JS, Singh K. Mapping of bacterial blight resistance gene xa8 in rice (Oryza sativa L.) Indian Journal of Genetics and Plant Breeding. 2014;74(4 Suppl.):589–95.
53 - Singh RJ, Khush GS, Mew TW. A new gene for resistance to bacterial blight in rice. Crop Science. 1983;23:558–60.
54 - Mew TW, Vera Cruz CM, Reyes RC. Interaction of Xanthomonas campestris pv. oryzae and a resistant rice cultivar. Phytopathology. 1982;72:786–9.
55 - Yoshimura A, Mew TW, Khush GS, Moura T. Inheritance of resistance to bacterial blight in rice cultivar Cas 209. Phytopathology. 1983;73:1409–12.
56 - Ramalingam J, Vera Cruz CM, Kukreja K, Chittoor JM, Wu JL, Lee SW, Baraoidan M, George ML, Cohen MB, Hulbert SH, Leach JE, Leung H. Candidate defense genes from rice, barley, and maize and their association with qualitative and quantitative resistance in rice. Molecular Plant-Microbe Interactions. 2003;16:14–24.
57 - Gu K, Sangha JS, Li Y, Yin Z. High resolution genetic mapping of bacterial blight resistance gene Xa10. Theoretical and Applied Genetics. 2008;116:155–63.
58 - Ogawa T, Yamamoto T. Inheritance of resistance to bacterial blight in rice. In: Rice Genetics. Proceedings of International Rice Genetics Symposium. IRRI, Manila, Philippines; 1986. pp. 471–80.
59 - Goto T, Matsumoto T, Furuya N, Tsuchiya K, Yoshimura A. Mapping of bacterial blight resistance gene Xa11 on rice chromosome 3. Japanese Agricultural Research Quarterly. 2009;43:221–5.
60 - Ogawa T, Morinaka T, Fujii K, Kimura T. Inheritance of resistance of rice varieties of Kogyoku and Java14 to bacterial group V of Xanthomonas oryzae. Annals of Phytopathological Society of Japan. 1978;44:137–41.
61 - Ogawa T, Lin L, Tabien RE, Khush GS. A new recessive gene for resistance to bacterial blight of rice. Rice Genetics Newsletter. 1987;4:98–100.
62 - Zhang G, Angeles ER, Abenes MLP, Khush GS, Huang N. RAPD and RFLP mapping of the bacterial blight resistance gene xa13 in rice. Theoretical and Applied Genetics. 1996;93:65–70.
63 - Sanchez AC, Ilag LL, Yang D, Brar DS, Ausubel F, Khush GS, Yano M, Sasaki T, Li Z, Huang N Genetic and physical mapping of xa13, a recessive gene bacterial blight resistance gene in rice. Theoretical and Applied Genetics. 1999;98:1022–8.
64 - Yang B, Sugio A, White FF. Os8N3 is a host disease-susceptibility gene for bacterial blight of rice. Proceedings of National Academy of Sciences, USA. 2006;103:10503–8.
65 - Taura S, Ogawa T, Tabien RE, Khush GS, Yoshimura A, Omura T. The specific reaction of Taichung Native 1 to Philippine races of bacterial blight and inheritance of resistance to race 5 (Pxo112). Rice Genetics Newsletter. 1987;4:101–2.
66 - Tan Z, Zhang Q, Zhu L, Wang C. RFLP mapping of a rice bacterial blight resistance gene Xa-14. Hereditas. 1998;20:30–3.
67 - Si-Yuan B, Ming-Pu T, Xing-Hua L. Genetic mapping of a bacterial blight resistance gene Xa14 in rice. Acta Agronomica Sinica. 2010;36:422–7.
68 - Ogawa, T. Monitoring race distribution and identification of genes for resistance to bacterial leaf blight. In: Khush GS, editor. Rice Genetics III. Proceedings of the 3rd International Rice Genetics Symposium. International Rice Research Institute, Manila, Philippines; 1996. pp. 456–9.
69 - Nakai H, Nakamura K, Kuwahara S, Saito M. Genetic studies of an induced rice mutant resistant to multiple races of bacterial leaf blight. Rice Genetics Newsletter. 1998;5:101–3.
70 - Noda, T. and A. Ohuchi. A new pathogenic race of Xanthomonas campestris pv. oryzae and inheritance of resistance of differential rice variety, Tetep to it. Annals of the Phytopathological Society of Japan. 1989;55:201–7
71 - Ogawa, T., H. Kaku and T. Yamamoto, 1989. Resistance gene of rice cultivar, Asaminori to bacterial blight of rice. Japanese Journal of Breeding. 39 (Suppl. 1):196–7.
72 - Taura S, Ogawa T, Yoshimura A, Ikeda R, Omura T. Identification of a recessive resistance gene in induced mutant line XM5 of rice to bacterial blight. Japanese Journal of Breeding 1991;4:427–32.
73 - Taura S, Ogawa T, Yoshimura A, Ikeda R, Iwata N. Identification of a recessive resistance gene to rice bacterial blight of mutant line XM6, Oryza sativa L. Japanese Journal of Breeding. 1992;42(1):7–13.
74 - Devadath S. A strain of Oryza barthii, an African wild rice immune to bacterial blight of rice. Current Science. 1983;52:27–8.
75 - Khush GS, Mackill DJ, Sidhu GS. 1989. Breeding rice for resistance to bacterial blight. In: Bacterial Blight of Rice. International Rice Research Institute, Manila, Philippines;1989. pp. 207–17.
76 - Khush G S, Bacalangco E and Ogawa T. A new gene for resistance to bacterial blight from Oryza longistaminata. Rice Genetics Newsletter. 1990;7:121–2.
77 - Ronald PC, Albano B, Tabien R, Abenes L, Wu KS, McCouch S, Tanksley SD. Genetic and physical analysis of the rice bacterial blight disease resistance locus, Xa21. Molecular and General Genetics.1992;236:113–20.
78 - Wang GL, Ruan DL, Song WY, Sideris S, Chen L, Pi LY, Zhang S, Zhang Z, Fauquet C, Gaut B S, Whalen MC, Ronald PC. Xa21D encodes a receptor-like molecule with a leucine-rich repeat domain that determines race-specific recognition and is subject to adaptive evolution. The Plant Cell. 1998;10:769–75.
79 - Lin XH, Zhang DP, Xie YF, Gao HP, Zhang Q. Identification and mapping of a new gene for bacterial blight resistance in rice based on RFLP markers. Phytopathology. 1996;86:1156–9.
80 - Wang C, Tan M, Xu X, Wen G, Zhang D, Lin X. Localizing the bacterial blight resistance gene, Xa22(t), to a 100-kilobase bacterial artificial chromosome. Phytopathology. 2003;93:1258–62.
81 - Mir GN, Khush GS. Genetics of resistance to bacterial blight in rice cultivar DV86. Crop Research. 1990;3:194–8.
82 - Wu X, Li X, Xu C, Wang S. Fine genetic mapping of xa24, a recessive gene for resistance against Xanthomonas oryzae pv. oryzae in rice. Theoretical and Applied Genetics. 2008;106:1467–72.
83 - 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;92:750–4.
84 - Gao D Y, Liu MA, Zhou AH, Cheng Y, Xiang YH, Sun LH, Zhai WX. Molecular mapping of a bacterial blight resistance gene Xa-25 in rice. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 2005;32:183–8.
85 - Amante-Bordeos A, Sitch LA, Nelson R, Dalmacio RD, Oliva NP, Aswidinnoor H, Leung H Transfer of bacterial blight and blast resistance from the tetraploid wild rice Oryza minuta to cultivated rice, Oryza sativa. Theoretical and Applied Genetics. 1992;84:345–54.
86 - Lee KS, Rasabandith S, Angeles ER, Khush GS. Inheritance of resistance to bacterial blight in 21 cultivars of rice. Phytopathology. 2003;93:147–52.
87 - Tan GX, Ren X, Weng QM, Shi ZY, Zhu LL, He GC. Mapping of a new resistance gene to bacterial blight in rice line introgressed from O. officinalis. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 2004;31:724–9.
88 - Jin XW, Wang CL, Yang Q, Jiang QX, Fan YL, Liu GC, Zhao KJ. Breeding of near-isogenic line CBB30 and molecular mapping of Xa30(t), a new resistance gene to bacterial blight in rice. Scientia Agricultura Sinica. 2007;40:1094–100.
89 - Wang CT, Wen GS, Lin XH, Liu XQ, Zhang DP. Identifiation and fine mapping of the new bacterial blight resistance gene, Xa31(t), in rice. European Journal Plant Pathology. 2009; 23:235–40.
90 - Zheng CK, Wang CL, Yu YJ, Liang YT and Zhao KJ. Identification and molecular mapping of Xa32(t), a novel resistance gene for bacterial blight (Xanthomonas oryzae pv. oryzae) in rice. Acta Agronomica Sinica. 2009;35:1173–80.
91 - Korinsak S, Sriprakhon S, Sirithanya P, Jairin J, Korinsak S, Vanavichit A, Toojinda T. Identification of microsatellite markers (SSR) linked to a new bacterial blight resistance gene xa33(t) in rice cultivar ‘Ba7’. Maejo International Journal of Science and Technology. 2009;3:235–47.
92 - Natarajkumar P, Sujatha K, Laha GS, Viraktamath BC, Reddy CS, Mishra B, Balachandran SM, Ram T, Srinivasarao K, Hari Y, Sundaram RM. Identification of a dominant bacterial blight resistance gene from Oryza nivara and its molecular mapping. Rice Genetics Newsletter. 2010;25:54–6.
93 - Ram T, Laha GS, Gautam SK, Ram Deen, Madhav MS, Brar DS, Viraktamath BC. Identification of a new gene introgressed from Oryza brachyantha with broad-spectrum resistance to bacterial blight of rice in India. Rice Genetics Newsletter. 2010;25:57.
94 - Guo SB, Zhang DP, Lin XH. Identification and mapping of a novel bacterial blight resistance gene Xa35(t) originated from Oryza minuta. Scientia Agricultura Sinica. 2010;43(13).
95 - Miao LL, Wang CL, Zheng CK, Che JY, Gao Y, Wen YC, Li GQ, Zhao KJ. Molecular mapping of a new gene for resistance to rice bacterial blight. Scientia Agricultura Sinica. 2010;43(15):3051–8.
96 - Kaur R, Grewal N, Das A, Vikal Y, Singh J, Bharaj TS, Sidhu JS, Singh K. Inheritance of bacterial blight resistance in two accessions of wild rice, Oryza nivara. Rice Genetics Newsletter. 2006;22:78–82.
97 - Zhang F, Zhuoa DL, Zhang F, Huang LY, Wang WS, Xu JL, Vera Cruz C, Li ZK, Zhou YL. Xa39, a novel dominant gene conferring broad-spectrum resistance to Xanthomonas oryzae pv. oryzae in rice. Plant Pathology 2014;64:568–75.
98 - Hutin M, Sabot F, Ghesquière A, Koebnik R, Szurek B. A knowledge-based molecular screen uncovers a broad-spectrum OsSWEET14 resistance allele to bacterial blight from wild rice. The Plant Journal. 2015;84:694–703.
99 - Hummel, AW, Doyle, EL, Bognadove AJ. Addition of transcription activator-like effector binding sites to a pathogen strain-specific rice bacterial blight resistance gene makes it effective against additional strains and against bacterial leaf streak. New Phytologist. 2012;195:883–93.
100 - Alfano JR, Collmer A. The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death. Journal of Bacteriology. 1997;179:5655–62.
101 - Lee BM, Park YJ, Park DS, Kang HW, Kim JG, Song ES, Park IC, Yoon UH, Hahn JH et al. The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice. Nucleic Acids Research. 2005:33:577–86.
102 - Salzberg SL, Sommer DD, Schatz MC, Phillippy AM, Rabinowicz PD, Tsuge S, Furutani A, Ochiai H, Delcher AL et al. Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99A. BMC Genomics. 2008;9:204.
103 - Yang B, Zhu WG, Johnson WB, White FF. The virulence factor AvrXa7 of Xanthomonas oryzae pv. oryzae is a type III secretion pathway-dependent nuclear-localized double-stranded DNA-binding protein. Proceedings of National Academy of Sciences, USA. 2000;97:9807–12.
104 - Shen Y, Sharma P, Goes da Silva F, Ronald P. The Xanthomonas oryzae pv. oryzae raxP and raxQ genes encode an ATP sulphurylase and adenosine-5′-phosphosulphate kinase that are required for AvrXa21 avirulence activity. Molecular Microbiology. 2002;44:37–48.
105 - Bonas U, Schulete R, Fenselau S, Minsavage GV, Staskawicz BJ, Stall RE. Isolation of a gene cluster from Xanthomonas campestris pv. vesicatoria that determines pathogenicity and the hypersensitive response on pepper and tomato. Molecular Plant Microbe Interactions. 1991;4:81–8.
106 - Wengelnik K, Van den Ackerveken G, Bonas U. HrpG, a key hrp regulatory protein of Xanthomonas campestris pv. vesicatoria is homologous to two-component response regulators. Molecular Plant Microbe Interactions 1996;9:704–12.
107 - Wengelnik K, Bonas U. HrpXv, an AraC-type regulator, activates expression of five of the six loci in the hrp cluster of Xanthomonas campestris pv. vesicatoria. Journal of Bacteriology. 1996;178:3462–9.
108 - Arlat M, Gough CL, Barber C, Boucher C, Daniels MJ. Xanthomonas campestris contains a cluster of hrp genes related to the larger hrp cluster of Pseudomonas solanacearum. Molecular Plant Microbe Interactions. 1991;4:593–601.
109 - Schulte R, Bonas U. A Xanthomonas pathogenicity locus is induced by sucrose and sulfur-containing amino acids. The Plant Cell. 1992;4:79–86.
110 - Schulte R, Bonas U. Expression of the Xanthomonas campestris pv. vesicatoria hrp gene cluster, which determines pathogenicity and hypersensitivity on pepper and tomato, is plant inducible. Journal of Bacteriology. 1992;174:815–23.
111 - Tsuge S, Furutani A, Fukunaka R, Oku T, Tsuno K, Ochiai H, Inoue Y, Kaku H, Kubo Y. Expression of Xanthomonas oryzae pv. oryzae hrp genes in XOM2, a novel synthetic medium. Journal of General Plant Pathology. 2002;68:363–71.
112 - Bogdanove A J, Beer SV, Bonas U, Boucher CA, Collmer A, Coplin DL, Cornelis GR, Huang HC, Hutcheson SW et al. Unified nomenclature for broadly conserved hrp genes of phytopathogenic bacteria. Molecular Microbiology. 1996;20:681–3.
113 - Lahaye T, Bonas U. Molecular secrets of bacterial type III effector proteins. Trends in Plant Science. 2001;6:479–85.
114 - Tsuge S, Nakayama T, Terashima S, Ochiai H, Furutani A, Oku T, Tsuno K, Kubo Y, Kaku H. Gene involved in transcriptional activation of the hrp regulatory gene hrpG in Xanthomonas oryzae pv. oryzae. Journal of Bacteriology. 2006;188:4158–62.
115 - Lee SW, Jeong KS, Han SW, Lee SE, Phee BK, Hahn TR, Ronald P. The Xanthomonas oryzae pv. oryzae PhoPQ two-component system is required for AvrXA21 activity, hrpG expression, and virulence. Journal of Bacteriology. 2008;190:2183–97.
116 - White FF, Potnis N, Jones JB and Kloebnik R. The type III effectors of Xanthomonas. Molecular Plant Pathology. 2009;10:749–66.
117 - Bonas U, Stall RE, Staskawicz B. Genetic and structural characterization of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria. Molecular and General Genetics. 1989;218:127–36.
118 - Hopkins CM, White FF, Choi SH, Guo A, Leach JE. Identification of a family of avirulence genes from Xanthomonas oryzae pv. oryzae. Molecular Plant Microbe Interactions. 1992;5:451–9.
119 - Boch J, Bonas U. Xanthomonas AvrBs3 family-type III effectors: discovery and function. Annual Review of Phytopathology. 2010;48(1):419–36.
120 - Bogdanove AJ, Schornack S, Lahaye T. TAL effectors: finding plant genes for disease and defense. Current Opinion in Plant Biology. 2010;13:394–401.
121 - Sugio A, Yang B, Zhu T, White FF. Two type III effector genes of Xanthomonas oryzae pv. oryzae control the induction of the host genes OsTFIIAg1 and OsTFX1 during bacterial blight of rice. Proceedings of National Academy of Sciences, USA. 2007;104:10720–5.
122 - Chen LQ, Hou BH, Lalonde S, Takanaga T, Hartung ML, Qu XQ, Guo WJ, Kim JG, Underwood W, Chaudhuri B, Chermak D, Antony G, White FF, Somerville SC, Mudgett MB, Frommer WB. Sugar transporters for intercellular exchange and nutrition of pathogens. Nature. 2010;468(7323):527–32.
123 - Li T, Huang S, Zhou J, Yang B. Designer TAL Effectors Induce Disease Susceptibility and Resistance to Xanthomonas oryzae pv. oryzae in Rice. Molecular Plant. 2013;6:781–9.
124 - Voulhoux R, Ball G, Ize B, Vasil ML, Lazdunski A, Wu LF, Filloux A. Involvement of the twin-arginine translocation system in protein secretion via the type II pathway. The EMBO Journal. 2001;20:6735–41.
125 - Jha G, Rajeshwari R, Sonti RV. Bacterial type two secretion system secreted proteins: double-edged swords for plant pathogens. Molecular Plant Microbe Interactions. 2005;18:891–8.
126 - da Silva ACR, Ferro JA, Reinach FC, Farah CS, Furlan LR et al. Comparison of the genomes of two Xanthomonas pathogens with differing host specificities. Nature. 2002;417:459–63.
127 - Ray SK, Rajeshwari R, Sonti RV. Mutants of Xanthomonas oryzae pv. oryzae deficient in general secretory pathway are virulence deficient and unable to secrete xylanase. Molecular Plant-Microbe Interactions. 2000;4:394–401.
128 - Dharmapuri S, Sonti RV. A transposon insertion in gumG homologue of Xanthomonas oryzae pv. oryzae causes loss of extracellular polysaccharide production and virulence. FEMS Microbiology Letters. 1999;179:53–9.
129 - Dharmapuri S, Yashitola J, Vishnupriya MR, Sonti RV. Novel genomic locus with atypical G+ C content that is required for extracellular polysaccharide production and virulence in Xanthomonas oryzae pv. oryzae. Molecular Plant Microbe Interactions. 2001;14:1335–9.
130 - Tang JL, Feng JX, Li QQ, Wen HX, Zhou DL, Wilson TJ, Dow JM, Ma QS, Daniels MJ. Cloning and characterization of the rpfC gene of Xanthomonas oryzae pv. oryzae: involvement in exopolysaccharide production and virulence to rice. Molecular Plant Microbe Interactions. 1996;9:664–6.
131 - Chatterjee S, Sonti RV. rpfF mutants of Xanthomonas oryzae pv. oryzae are deficient for virulence and growth under low iron conditions. Molecular Plant Microbe Interactions. 2002;15:463–71.
132 - Jeong KS, Lee SE, Han JW, Yang SU, Lee BM, Noh TH, Cha JS. Virulence reduction and differing regulation of virulence genes in rpf mutants of Xanthomonas oryzae pv. oryzae. The Plant Pathology Journal 2008;24:143–51.
133 - Wang LH, He Y, Gao Y, Wu JE, Dong YH, He C, Wang SX, Weng LX, Xu JL et al. A bacterial cell-cell communication signal with cross-kingdom structural analogues. Molecular Microbiology. 2004;51:903–12.
134 - Dow M. Diversification of the function of cell-to-cell signalling in regulation of virulence within plant pathogenic Xanthomonas. Science Signaling. 2008;1:pe23.
135 - He Y-W, Zhang L-H. Quorum sensing and virulence regulation in Xanthomonas campestris. FEMS Microbiology Reviews. 2008;32:842–57.
136 - Shen Y, Chern M, Silva FG, Ronald P. Isolation of a Xanthamonas oryzae pv. oryzae flagellar operon region and molecular characterization of flhF. Molecular Plant-Microbe Interactions. 2001;14:204–13.
137 - Tseng YH, Choy KT, Hung CH, Lin NT, Liu JY, Lou CH et al. Chromosome map of Xanthomonas campestris pv. campestris 17 with locations of genes involved in xanthan gum synthesis and yellow pigmentation. Journal of Bacteriology. 1999;181:117–25.
138 - Lee CK, Lee BM, Cho JY. Identification of new internal promoters of the Xanthomonas oryzae pathovar oryzae gum gene cluster. Biotechnology Letters 2008;30:521–7.
139 - Wang JC, So BH, Kim JH, Park YJ, Lee BM, Kang HW. Genome-wide identification of pathogenicity genes in Xanthomonas oryzae pv. oryzae by transposon mutagenesis. Plant Pathology. 2008;57:136–1145.
140 - Holland IB, Schmitt L, Young J. Type 1 protein secretion in bacteria, the ABC-transporter dependent pathway. Molecular Membrane Biology. 2005;22:29–39.
141 - da Silva FG, Shen Y, Dardick C, Burdman S, Yadav RC, de Leon AL, et al. Bacterial genes involved in type I secretion and sulfation are required to elicit the rice Xa21-mediated innate immune response. Molecular Plant Microbe Interactions. 2004;17:593–601.
142 - Burdman S, Shen Y, Lee SW, Xue Q, Ronald P. RaxH/RaxR: a two component regulatory system in Xanthomonas oryzae pv. oryzae required for AvrXa21 activity. Molecular Plant Microbe Interactions. 2004;17:602–12.
143 - Lee SW, Han SW, Sririyanum M, Park CJ, Seo YS, Ronald PC. A type I–secreted, sulfated peptide triggers XA21-mediated innate immunity. Science. 2009;326:850–3.
144 - Liu J, Wang X, Mitchell T, Hu Y, Liu X, Dai L, Wang GL. Recent progress and understanding of the molecular mechanisms of the rice–Magnaporthe oryzae interaction. Molecular Plant Pathology. 2010;11(3):419–27.
145 - Dai L, Liu X, Xiao Y, Wang G. Recent advances in cloning and characterization of disease resistance genes in rice. Journal of Integrative Plant Biology. 2007;49:112–9.
146 - Li H, Wang S. Disease resistance. In: Zhang Q, Wing RA, editors. Genetics and Genomics of Rice Plant Genetics and Genomics. Springer Science + Business Media, New York; 2013. pp. 161–75.
147 - Kou Y, Wang S. Bacterial blight resistance in rice. In: Varshney RK, Tuberosa R, editors. Translational Genomics for Crop Breeding, Volume 1; Biotic Stresses. John Wiley and Sons, Inc., Iowa, USA; 2013. pp. 11–30.
148 - Wang GL, Leung L. Molecular biology of host-pathogen interactions in rice diseases. In: Shimamoto K, editor. Molecular Biology of Rice. Springer-Verlag, Tokyo, Japan; 1998. pp. 201–32.
149 - Century KS, Lagman RA, Adkisson M, Morlan J, Tobias R, Schwartz K, Smith A, Love J, Ronald PC, Whalen MC. Short communication: developmental control of Xa21-mediated disease resistance in rice. The Plant Journal. 1999;20(2):231–6.
150 - Zhao J, Fu J, Li X, Xu C, Wang S. Dissection of the factors affecting development-controlled and race-specific disease resistance conferred by leucine-rich repeat receptor kinase-type R genes in rice. Theoretical and Applied Genetics. 2009;119(2):231–9.
151 - Park CJ, Lee SW, Chern M, Sharma R, Canlas PE, Song MY, Jeon JS, Ronald PC. Ectopic expression of rice Xa21 overcomes developmentally controlled resistance to Xanthomonas oryzae pv. oryzae. Plant Science. 2010;179(5):466–71.
152 - Wang G, Ding X, Yuan M, Qiu D, Li X, Xu C, Wang S. Dual function of rice OsDR8 gene in disease resistance and thiamine accumulation. Plant Molecular Biology. 2006;60(3):437–49.
153 - Peng Y, Bartley LE, Chen X, Dardick C, Chern M, Ruan R, Canlas PE, Ronald PC. OsWRKY62 is a negative regulator of basal and Xa21-mediated defense against Xanthomonas oryzae pv. oryzae in rice. Molecular Plant. 2008;1(3):446–58.
154 - Seo YS, Chern M, Bartley LE, Han M, Jung KH, Lee I,Walia H, Richter T, Xu X, Cao P, Bai W, Ramanan R, Park CJ, Chen X, Hwang S, Jeon JS, Ronald PC. Towards establishment of a rice stress response interactome. PLoS Genetics. 2011;7(4):e1002020.
155 - Park CJ, Peng Y, Chen X, Dardick C, Ruan D, Bart R, Canlas PE, Ronald PC. Rice XB15, a protein phosphatase 2C, negatively regulates cell death and XA21-mediated innate immunity. PLoS Biology. 2008;6(9):e231.
156 - Chen X, Chern M, Canlas PE, Ruan D, Jiang C, Ronald PC. An ATPase promotes autophosphorylation of the pattern recognition receptor XA21 and inhibits XA21-mediated immunity. Proceedings of National Academy of Sciences, USA. 2010;107(17):8029–34.
157 - Park CJ, Bart R, Chern M, Canlas PE, Bai W, Ronald PC. Overexpression of the endoplasmic reticulum chaperone BiP3 regulates XA21-mediated innate immunity in rice. PLoS One. 2010;5(2):e9262.
158 - Xu Z, Sun Q, Liu F, Chen Z, Hu B, Guo Y, Liu Y, Liu H. Race monitoring of rice bacterial blight (Xanthomonas oryzae pv. oryzae) in China. Chinese Journal of Rice Science. 2004;18(5):469–72.
159 - Gao J, Zhao J, Xu C, Li X, Wang S. Development of rice germplasms conferring high-level and broad spectrum resistance to Xanthomonas oryzae pv. oryzae at both seedling and adult stages. Molecular Plant Breeding. 2010;8(3):420–5.
160 - Li H, Li X, Xiao J, Wing RA, Wang S. Ortholog alleles at Xa3/Xa26 locus confer conserved race-specific resistance against Xanthomonas oryzae in rice. Molecular Plant. 2012;5(1):281–90.
161 - Cao Y, Duan L, Li H, Sun X, Zhao Y, Xu C, Li X, Wang S. Functional analysis of Xa3/Xa26 family members in rice resistance to Xanthomonas oryzae pv. oryzae. Theoretical and Applied Genetics. 2007;115(7):887–95.
162 - Zhang H, Cao Y, Zhao J, Li X, Xiao J, Wang S. A pair of orthologs of a leucine-rich repeat receptor kinase-like disease resistance gene family regulates rice response to raise temperature. BMC Plant Biology. 2011;11(1):160.
163 - Yang Z, Sun X, Wang S, Zhang Q. Genetic and physical mapping of a new gene for bacterial blight resistance in rice. Theoretical and Applied Genetics. 2003;106(8):1467–72.
164 - Cao Y, Ding X, Cai M, Zhao J, Lin Y, Li X, Xu C, Wang S. The expression pattern of a rice disease resistance gene Xa3/Xa26 is differentially regulated by the genetic backgrounds and developmental stages that influence its function. Genetics. 2007;177(1):523–33.
165 - Qiu D, Xiao J, Ding X, et al. OsWRKY13 mediates rice disease resistance by regulating defense-related genes in salicylate- and jasmonate dependent signaling. Molecular Plant Microbe Interactions. 2007;20:492–9.
166 - Qiu D, Xiao J, Xie W, Cheng H, Li X, Wang S. Exploring transcriptional signalling mediated by OsWRKY13, a potential regulator of multiple physiological processes in rice. BMC Plant Biology. 2009;9:74.
167 - Tao Z, Liu H, Qiu D et al. A pair of allelic WRKY genes play opposite roles in rice-bacteria interactions. Plant Physiology. 2009;151:936–48.
168 - Deng H, Liu H, Li X, Xiao J, Wang S. A CCCH-type zinc finger nucleic acid-binding protein quantitatively confers resistance against rice bacterial blight disease. Plant Physiology. 2012;158:876–89.
169 - Xiao W, Liu H, Li Y et al. A rice gene of de novo origin negatively regulates pathogen-induced defense response. PLoS One. 2009;4:e4603
170 - Römer P, Recht S, Strauss T, Elsaesser J, Schornack S, Boch J, Wang S, Lahaye T. Promoter elements of rice susceptibility genes are bound and activated by specific TAL effectors from the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae. New Phytologist. 2010;87(4):1048–57.
171 - Yuan T, Li X, Xiao J, Wang S. Characterization of Xanthomonas oryzae-responsive cis-acting element in the promoter of rice race-specific susceptibility gene Xa13. Molecular Plant. 2011;4(2):300–9.
172 - Yuan M, Chu Z, Li X, Xu C, Wang S. The bacterial pathogen Xanthomonas oryzae overcomes rice defenses by regulating host copper redistribution. The Plant Cell. 2010;22:3164–76.
173 - Chu Z, Yuan M, Yao J, et al. Promoter mutations of an essential gene for pollen development result in disease resistance in rice. Genes and Development. 2006;20:1250–5.
174 - Chen LQ, Qu XQ, Hou BH, Sosso D, Osorio S, Fernie AR, Frommer WB. Sucrose efflux mediated by SWEET proteins as a key step for phloem transport. Science. 2012;335(6065):207–11.
175 - Wu L, Goh ML, Sreekala C, Yin Z. XA27 depends on an amino-terminal signal-anchor-like sequence to localize to the apoplast for resistance to Xanthomonas oryzae pv oryzae. Plant Physiology. 2008;148(3):1497–509.
176 - Boch J, Scholze H, Schornack S, Landgraf A, Hahn S, Kay S, Lahaye T, Nickstadt A, Bonas U. Breaking the code of DNA binding specificity of TAL-type III effectors. Science. 2009;326(5959):1509–12.
177 - Gu K, Tian D, Qiu C, Yin Z. Transcription activatorlike type III effector AvrXa27 depends on OsTFIIAgamma5 for the activation of Xa27 transcription in rice that triggers disease resistance to Xanthomonas oryzae pv. oryzae. Molecular Plant Pathology. 2009;10(6):829–35.
178 - Bernoux M, Ellis JG, Dodds PN. New insights in plant immunity signaling activation. Current Opinion in Plant Biology. 2011;14:512–8.
179 - Luo S, Zhang Y, Hu Q, Chen J, Li K, Lu C, Liu H, Wang W, Kuang H. Dynamic nucleotide-binding site and leucine-rich repeat encoding genes in the grass family. Plant Physiology. 2012;159:197–210.
180 - Zhang H, Wang S. Rice versus Xanthomonas oryzae pv. oryzae: a unique pathosystem. Current Opinion in Plant Biology. 2013;16:188–95.
181 - Zeng X, Tian D, Gu K, Zhou Z, Yang X, Luo Y, White FF, Yin Z. Genetic engineering of Xa10 promoter for broad-spectrum and durable resistance to Xanthomonasoryzaepv. oryzae. Plant Biotechnology Journal. 2015. doi: 10.1111/pbi.12342.
182 - Wang CL, Qin TF, Yu HM, Zhang XP, Che JY, Gao Y, Zheng CK, Yang B, Zhao KJ. The broad bacterial blight resistance of rice line CBB23 is triggered by a novel TAL effector of Xanthomonas oryzae pv. oryzae. Molecular Plant Pathology. 2014;15:333–341.
183 - Bhasin H, Bhatia D, Raghuvanshi S, Lore JS, Sahi GK, Kaur B, Vikal Y, Singh K. New PCR-based sequence tagged site marker for bacterial blight resistance gene Xa38 in rice. Molecular Breeding. 2012;30:607–11.
184 - Yue JX, Meyers BC, Chen JQ, Tian D, Yang S. Tracing the origin and evolutionary history of plant nucleotide-binding siteleucine-rich repeat (NBS-LRR) genes. New Phytologist. 2012;193:1049–63.
185 - Monosi B, Wisser RJ, Pennill L, Hulbert SH. Full-genome analysis of resistance gene homologues in rice. Theoretical and Applied Genetics. 2004;109:1434–47.
186 - Mchale L, Tan X, Koehl P, Michelmore RW. Plant NBS-LRR proteins: adaptable guards. Genome Biology. 2006;7:212.
187 - Collins N, Drake J, Ayliffe M, Sun Q, Ellis J, Hulbert S, Pryor T. Molecular characterization of the maize Rp1-D rust resistance haplotype and its mutants. The Plant Cell. 1999;11:1365–76.
188 - Wang X, Chen J, Yang Y, Zhou J, Qiu Y, Yu C, Cheng Y, Yan C, Chen J. Characterization of a novel NBS-LRR gene involved in bacterial blight resistance in rice. Plant Molecular Biology Reporter. 2013;31:649. doi:10.1007/s11105-012-0537-0.
189 - Iyer-Pascuzzi AS, Jiang H, Huang L, McCouch SR. Genetic and functional characterization of the rice bacterial blight disease resistance gene xa5. Phytopathology. 2008;98(3):289–95.
190 - Zou H, Zhao W, Zhang X, Han Y, Zou L, Chen G. Identification of an avirulence gene, avrxa5, from the rice pathogen Xanthomonas oryzae pv. oryzae. Science in China Series C Life Sciences. 2010;53(12):1440–9.
191 - Bhatia D, Sharma R, Vikal Y, Mangat GS, Mahajan R, Sharma N, Lore JS, Singh N, Bharaj TS, Singh K. Marker-assisted development of bacterial blight resistant, dwarf, and high yielding versions of two traditional basmati rice cultivars. Crop Science. 2011;51:759–70.
192 - Li C, Wei J, Lin Y, Chen H. Gene silencing using the recessive rice bacterial resistance gene xa13 as a new paradigm in plant breeding. Plant Cell Reports. 2012;21:851–62.