A New Recessive Gene Conferring Resistance Against Rice Blast
© The Author(s). 2016
Received: 10 July 2016
Accepted: 10 September 2016
Published: 15 September 2016
Rice blast (causative pathogen Magnaporthe oryzae) represents a major biotic constraint over rice production. While numerous genes for resistance have been found in both japonica and indica germplasm, as yet the diversity harbored by aus germplasm has not been widely exploited.
The blast resistance present in the aus type cultivar AS20-1 was shown, via an analysis of segregation in the F2 generation bred from a cross with the highly blast susceptible cultivar Aichi Asahi, to be due to the action of a single recessive gene, denoted pi66(t). The presence of pi66(t) gave an intermediate level control to plants infected with the blast pathogen isolate EHL0635. A bulked segregant analysis indicated that four microsatellite loci (SSRs) mapping to chromosome 3 were probably linked to pi66(t). Localized mapping using chromosome 3-based SSRs and Indels defined a genetic window for pi66(t), flanked by the markers F04-j2 and M19-i12, which physically equals to 27.7 and 49.0 kb, respectively, in the reference genomes of cultivars Nipponbare and 93–11. This physical interval does not harbor any major gene currently associated with disease resistance.
pi66(t) is one of just three recessive genes controlling rice blast, and is the first major gene for resistance to be mapped to chromosome 3.
Rice, a crop which feeds half of the world’s population, has been cultivated for at least 8,000 years (Khush 1997; The 3,000 rice genome project 2014; Travis et al. 2015). Five distinct groups of rice germplasm have long been recognized: they are referred to as indica, aus, basmati/sadri, tropical japonica and temperate japonica (The 3,000 Rice Genomes Project 2014; Travis et al. 2015). The aus group has developed in the north-eastern region of the Indian sub-continent, where both the climate and the growing environment are highly variable (Mahender et al. 2012; Travis et al. 2015). In recent years, aus germplasm has grown in importance as a source of genes for rice improvement, especially in the context of breeding for resistance/tolerance to abiotic and biotic stress (Travis et al. 2015 and references therein).
Rice blast (causative pathogen Magnaporthe oryzae) is a major constraint over rice production, inducing grain yield losses of up to 90 % (He et al. 2012; Singh et al. 2015). Although breeders have so far been able to rely on a number of sources of genetic resistance, the pathogen is adept at evolving new races, with the result that mongenic resistances typically break down quite rapidly (Wu et al. 2014; Singh et al. 2015; Zhang et al. 2015). To date, some one hundred rice blast resistance (Pi) genes have been identified, many of which have been shown to map within a cluster or even in form of a tandem array; they are dispersed on eleven of the twelve rice chromosomes (Sharma et al. 2012; Singh et al. 2015; Tanwaeer et al. 2015 and references therein). All but two of the Pi genes are functionally dominant (Fukuoka et al. 2009; He et al. 2012), and about 30 have been isolated: their products mostly belong to the large group of nucleotide-binding site (NBS)-leucine-rich repeat (LRR) proteins. The two exceptions are Pid-2 and pi21 (Chen et al. 2006b; Fukuoka et al. 2009; Liu et al. 2011). Here, a third recessive gene, denoted pi66(t), has been identified in the aus cultivar (cv.) AS20-1, and its genomic position has been defined.
Resistance Reaction and Spectrum
Reactions shown by four rice cultivars infected by a M. oryzae isolate representative of each of the five Chinese populations, and the frequency of resistance exhibited among the collected isolates from each population
Specific reactions selected from the five Mo populationsa
Resistance frequencies in the five Mo populations (%)b
Segregation for resistance in the F2 population bred from the cross cv. AS20-1 x cv. Aichi Asahi, following inoculation with the M. oryzae isolate EHL0635
No. of plantsa
Additional nine polymorphic SSR markers developed in the region defined by the flanking markers RM16 and RM55 were subjected to the second round of linkage analysis (Additional file 2: Table S2). The results showed that there were 31 to 22 recombinants detected among the seven marker loci [B07 (31), G02 (30), H15 (30), N03 (30), P23 (30), N11 (29), L18 (25), M23 (22)] on the centromere side, and only 8 distinct recombinants at RM135 locus on the telomere side (Fig. 2a). A total of 14 additional Indel markers developed in the narrower region flanked by markers M23 and RM135 were subjected to the third round of linkage analysis (Additional file 2: Table S2). The results showed that there were 15 to 2 recombinants detected among the six marker loci [D21 (15), E06 (9), I20 (7), I24 (2), F04 (2), F04-j2 (2)] on the centromere side, and 7 to 1 recombinant(s) detected among the eight marker loci [G23 (7), E01 (4), M19 (3), M19-4 (3), M19-3 (2), M19-2 (2), M19-1 (1), M19-i12 (1)] on the telomere side (Fig. 2a). The target locus, pi66(t), was closely flanked by F04-j2 and M19-i12, which equals to 27.7 and 49.0 kb, respectively, in the reference genomes of cvs Nipponbare and 93–11 (Fig. 2a).
The pi66(t) region was represented by the two cv. Nipponbare overlapping BACs OSJNBb0009F04 and OSJNBa0092M19 (Fig. 2b). The number of genes present within this region was six in cv. Nipponbare and 14 in cv. 93–11 (Additional file 3: Table S3). Genome comparison and presence/absence (P/A) analyses revealed that there were three substantial Indel events that resulted in six genome-specific genes in the region. That is, both pi66-2j and pi66-3j in Indel I present in two genomes of cvs Nipponbare and AS20-1; pi66-1i-2 (a duplication of pi66-1i-1) in Indel II, pi66-5i and pi66-6i in Indel III in that of both cvs 93–11 and AS20-1; and pi66-2i in Indel II in that of cv 93–11, only (Fig. 2c, Additional file 4: Figure S1). Notably, there were six transposon-like genes (pi66-1j, -2j, -3j, 1i-1, 1i-2, -6i), of which both pi66-2j and -3j were scattered across the entire genomes except for the target region of cv. 93–11, thereby ruling out for P/A analyis (Additional file 4: Figure S1; Additional file 3: Table S3). Furthermore, there were three chimeric genes in both 93–11 and AS20-1 genomes (Fig. 2c and Additional file 4: Figure S1). By excluding six transposon-like genes, there were three most possible candidates (pi66-5a, -6a, -7a) for pi66(t) (Fig. 2c; Additional file 3: Table S3).
Chinese rice breeders have to date largely ignored aus germplasm, even though it has acquired a growing reputation for harboring genes for resistance/tolerance to abiotic and biotic stress (Travis et al. 2015). Rather, efforts to improve indica have concentrated on materials developed in SE Asia, while those directed at japonica have relied on germplasm from Japan (Wu et al. 1991). In addition to pi66(t), aus germplasm has also yielded both Pi16 and an allele of Pik (Pan et al. 1999). More recently, nine already recognized Pi genes have been identified as present in materials originating in NE and E India (Imam et al. 2014), which is the center of origin of aus germplasm. Notably, the donor of pi66(t) also harbors a gene conferring resistance against the brown plant hopper; this gene also lies on chromosome 3, but at some distance from pi66(t) (Chen et al. 2006a). Such works clearly indicated that aus cvs are valuable and promising genetic resources for withstanding biotic pressures including rice blast disease, and will greatly enlarge the gene pool for rice breeders.
Plant disease resistance genes have been classified into two types, the most frequent of which encode an NBS-LRR protein. Non-NBS-LRR genes encode a wide diversity of products (Chauhan et al. 2015; Olukolu et al. 2016), tend to confer partial (rather than complete) resistance and are typically more durable than the NBS-LRR type genes. The most well documented non-NBS-LRR type is barley mlo, a gene which encodes a G protein-coupled receptor residing in the plasma membrane (Kim et al. 2002); the gene confers durable resistance to a broad spectrum of powdery mildew races (Acevedo-Garcia et al. 2014). A second example is the wheat gene Lr34, which encodes an ATP-binding cassette transporter; its product protects against five distinct foliar fungal pathogens (Kratttinger et al. 2009; Chauhan et al. 2015). The maize gene ZmWAK encodes a plasma membrane-related receptor-like kinase; its presence has been correlated with a reduction in the incidence of head smut disease (Zuo et al. 2015). Finally, the rice gene xa5 encodes a small subunit of the transcription factor IIA (TFIIA); this gene confers resistance against bacterial blight (Iyer-Pascuzzi 2004). Before the identification of pi66(t), all but two of the Pi genes characterized to date act as dominant alleles. The exceptions are pi21 and pi55. The former gene encodes a proline-rich protein harboring a probable heavy metal-binding domain and some predicted protein-protein interaction motifs; the resistant allele differs from the wild type dominant one by two deletions affecting the latter motifs, and which are thought to be responsible for the allele's determination of non-race-specific resistance (Fukuoka et al. 2009). One of candidate genes for pi55 encodes a protein rather similar to that encoded by pi21. Although a substantial number of major Pi genes have been intra-chromosomally mapped, pi66(t) is the first to be located on chromosome 3. Two quantitative trait loci mapping to this chromosome (Os03g0122000 and Os03g0120400) have been associated with blast resistance (Wang et al. 2014), but both lie outside the critical RM16-RM55 interval. The pi66 identified in the current study that is the third recessive Pi gene located on the virgin land, where no any known Pi protein (domain) is identifiable (Additional file 3: Table S3). It is noteworthy that the bph19 derived from the donor cv. AS20-1 was also recognized as non-NBS-LRR resistance gene (Chen et al. 2006a). It has been argued that durable and broad-spectrum resistance may be more readily achieved by deploying non-NBS-LRR genes, perhaps in combination with NBS-LRR ones, than by attempting to stack genes which each (at least for some time) confer immunity (Fukuoka et al. 2009; Acevedo-Garcia et al. 2014; Chauhan et al. 2015; Zuo et al. 2015). This hypothesis can only be tested by exploiting genes such as pi66(t) in a rice breeding program.
This research has confirmed that novel resistance genes against blast can be recovered from aus germplasm. The gene pi66(t) identified here is the third recessive Pi gene to be identified, and is also the first major Pi gene to be located on chromosome 3.
The pi66(t) donor cv. AS20-1, along with the Pia carrier cv. Aichi Asahi, the Pi36 carrier cv. Kasalath and the Pita-2 carrier cv. IRBLta2-Pi were challenged with 60 M. oryzae isolates collected from each of Guangdong (GD), Guangxi (GX), Yunnan (YN), Sichuan (SC) and Heilongjiang (HLJ) provinces. Inoculation and scoring methods were adapted from those described by Pan et al. (1996, 2003). Plants were assigned a score of either 0–1 (resistant: R), 2–3 (moderately resistant: MR), 4 (moderately susceptible: MS) or 5 (susceptible: S). The frequency of resistance for each of the four cultivars within each of the five M. oryzae populations was calculated from [(R + MR)/(R + MR) + (MS + S)]. The typical reactions of cv. AS20-1, cv. Aichi Asahi and the cv. AS20-1 x cv. Aichi Asahi F1 plants were quantified using a quantitative PCR (qPCR) assay, according to the protocols previously described (Berruyer et al. 2006; Kawano et al. 2010; Zhang et al. 2015). Oryza sativa OsUbi (Gene ID: 4332169) and M. oryzae Pot2 (Gene ID: 2680652) were used as the reference genes for, respectively, the host and the pathogen DNA.
The donor cv. AS20-1 was crossed with the highly susceptible cv. Aichi Asahi, and their F2 progenies were screened for reaction to inoculation with M. oryzae isolate EHL0635. The F2 population showing monogenic segregation was regarded as the mapping population, thereby subjecting to the bulked-segregant assay (BSA) for quickly mapping chromosomal region involving the target gene. Genomic DNAs of the F2 plants as well as the parental plants were extracted from frozen leaves using the CTAB method. Two contrast bulks that were constructed by pooling equimolar amounts of DNAs from 10 resistant or 10 susceptible F2 plants. The two bulks, along with both parental DNAs, were then assayed with a set of 180 simple sequence repeat (SSR) markers (Temnykh et al. 2000, 2001), selected to span the full rice genome, following the methods given by He et al. (2012).
Genomic map of target gene were established through three rounds of linkage analysis using genomic position-ready molecular markers (He et al. 2012). The first round was carried out with candidate markers defined by BSA for screening recombinants on both sides of the target locus. The second round was carried out with additional SSR markers in the target region flanked by the closest markers derived from the first round of linkage analysis, which were developed on the basis of reference sequence of cv. Nipponbare, except for RM135 that was adopted from the rice SSR marker maps (Temnykh et al. 2000, 2001). The third round was carried out in the recombinant progeny with insertion/deletion (Indel) markers those were developed de novo based on differential sequences between the two reference sequences of japonica cv. Nipponbare and indica cv. 93–11. Linkage marker search and prime designation were performed in the way essentially same way as previously described (Liu et al. 2005; Zeng et al. 2011; He et al. 2012). Genomic map of the target locus was constructed on the basis of both reference sequences.
Candidate Gene Indentification
Candidates for pi66(t) were predicted based on gene annotations provided by BLASTN (www.ncbi.nlm.nih.gov/BLAST), RiceGAAS (ricegaas.dna.affrc.go.jp) and FGENSH (www.softberry.com) software. The two reference sequences proved to be rather diverse in the target region, so candidates that encode proteins with over 200 aa was validated by PCR-based presence/absence (P/A) test against the four DNAs of cvs AS20-1, Aichi Asahi, 93–11, and Nipponbare, following Zhai et al. (2011).
We acknowledge funding from the National Key R&D Project (2016YDF0100601), the National Transgenic Research Project (2015ZX08001-002), and the National Natural Science Foundation of China (U1131003). Materials used in the current study were obtained from our own collection with great helps from Dr. X. Zhu at the Guangdong Academy of Agricultural Sciences, Dr. R. Li at Guangxi University, Dr. Y. Zhu at Yunnan Agricultural University, Dr. D. Lu at Sichuan Academy of Agricultural Sciences, and Ms. Y. Zhang at Heilongjiang Bayi Agricultural University.
The authors declare that they have no competing interests.
Project conception (QP). Resistance phenotyping (QP, LW). Mapping population construction (QP, LW). Linkage analysis (ZL, QP), Candidate gene analysis (ZL, QP). Manuscript preparation (QP). All authors read and approved the final manuscript.
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