- Original article
- Open Access
High-resolution mapping and breeding application of a novel brown planthopper resistance gene derived from wild rice (Oryza. rufipogon Griff)
- Zhihua Li†1,
- Yanxia Xue†1, 2,
- Hailian Zhou†1,
- Yang Li1,
- Babar Usman1,
- Xiaozhen Jiao1,
- Xinyi Wang1,
- Fang Liu1,
- Baoxiang Qin1,
- Rongbai Li1Email author and
- Yongfu Qiu1Email author
© The Author(s). 2019
- Received: 3 December 2018
- Accepted: 11 April 2019
- Published: 4 June 2019
The brown planthopper (Nilaparvata lugens Stål; BPH), one of the most destructive pests of rice, has proven to be a substantial threat, conferring enormous production losses in Asia and becoming a difficult challenge to manipulate and control under field conditions. The continuous use of insecticides promotes the resurgence of BPH, which results in resistant varieties adapting through the upgrading of new BPH biotypes. To overcome resistance acquired by BPH against resistance varieties, different forms of novel resistant gene fusions act as functional domains for breeding to enhance insect resistance.
The current study reports on the novel BPH resistance gene Bph36 derived from two introgression lines (RBPH16 and RBPH17) developed from wild rice GX2183 which was previously reported to be resistant to BPH. Using two F2 crossing populations (Kangwenqizhan × RBPH16 and Huanghuazhan × RBPH17) in a bulked segregant analysis (BSA) for identification of resistant genes and QTL analysis, two QTLs for BPH resistance were generated on the long and short arms of chromosome 4, which was further confirmed by developing BC1F2:3 populations by backcrossing via marker assisted selection (MAS) approach. One BPH resistance locus on the short arm of chromosome 4 was mapped to a 38-kb interval flanked by InDel markers S13 and X48, and then was named Bph36, whereas another locus on the long arm of chromosome 4 was also detected in an interval flanked by RM16766 and RM17033, which was the same as that of Bph27. An evaluation analysis based on four parameters (BPH host selection, honeydew weight, BPH survival rate and BPH population growth rate) shows that Bph36 conferred high levels antibiosis and antixenosis to BPH. Moreover, Bph36 pyramided with Bph3, Bph27, and Bph29 through MAS into elite cultivars 9311 and MH511 (harbored Xa23), creating different background breeding lines that also exhibited strong resistance to BPH in the seedling or tillering stage.
Bph36 can be utilized in BPH resistance breeding programs to develop high resistant rice lines and the high-resolution fine mapping will facilitate further map-based cloning and marker-assisted gene pyramiding of resistant gene. MAS exploited to pyramid with Bph3, Bph27, Bph29, and Xa23 was confirmed the effectiveness for BPH resistance breeding in rice and provided insights into the molecular mechanism of defense to control this devastating insect.
- Oryza rufipogon Griff
- Brown planthopper (Nilaparvata lugens Stål)
- Resistance gene
- Gene mapping
- Marker-assisted selection
- Near isogenic line
- Pyramided line
The brown planthopper (Nilaparvata lugens Stål; BPH) is the most destructive insect pest of rice found throughout tropical Asia where rice is widely planted (Cha et al. 2008). The BPH causes direct damage to rice by sucking the plant’s sap and indirect damage by transmitting viral diseases such as grassy and ragged stunt viruses, resulting in severe yield reduction or complete crop losses referred as a result of the “hopper burn” phenomenon (Rivera et al. 1966; Ling et al. 1978; Sōgawa 1982; Normile 2008). According to the Statistics of China Agriculture Yearbook, over 25 million hectares of rice were infested with rice planthoppers in each year of 2005–2007. To manage the pest, the extensive use of chemical pesticides has generally worked well over the past decades, but the long term application of pesticides resulted in increased BPH resistance to chemical insecticides and presents the risk of destroying the environment (Heinrichs et al. 1982; Tanaka et al. 2000). However, ensuring the genetic resistance of host plants is the most effective and environmentally-friendly approach for the BPH management. Therefore, it is very necessary and imperative to detect more novel resistant genes and to then elucidate the resistance mechanism.
Thirty- five major BPH-resistance genes have been identified from cultivated rice and wild Oryza species (Wang et al. 2018). Wild rice species and their introgression lines have been progressively used as resistance harbors, and almost half of BPH resistance genes are derived from them (Ali and Chowdhury, 2014; Hu et al., 2016a, b). For example, resistance genes Bph10 and Bph18(t) were detected from introgression lines of O. australiensis with the EE genome (Ishii et al. 1994; Jena et al. 2006). Resistance genes bph11(t), bph12(t), Bph13(t), Bph14, Bph15, and QBph4.1 were identified from introgression lines of O. officinalis with the CC genome (Hirabayashi et al., 1998, 1999; Renganayaki et al. 2002; Du et al. 2009; Lv et al. 2014; Hu et al. 2015). Resistance gene Bph12 was derived from the introgression line B14 of O. latifolia with the CCDD genome (Qiu et al. 2012). Resistance genes Bph20(t) and Bph21(t) were identified from O. minuta with the CCDD genome and were mapped to chromosomes 4 and 12, respectively (Rahman et al. 2009). Finally, Bph27 and Bph29 were identified from O. rufipogon with the AA genome (Huang et al. 2013; Wang et al. 2015). Considerable efforts have been made to clone major BPH-resistance genes, and a few successes have been achieved over the past ten years. For instance, Bph14, Bph9, and Bph6 were successfully map-based cloned and to encode one type of NB-LRR protein (Du et al. 2009; Zhao et al. 2016; Guo et al. 2018). Resistance gene Bph3, a cluster of three repeated genes, encodes plasma membrane–localized lectin receptor kinases, confers broad-spectrum insect resistance and serves as a reference for the molecular breeding of insect-resistant cultivars (Liu et al., 2015). Bph29 is a recessive gene derived from O. rufipogon and has been found to contain a B3 DNA-binding domain (Wang et al. 2015).
The interaction of plants and insects is complex and can be described in relation to physical, chemical, cellular, or molecular aspects. To limit damage from insects to plants, one may employ antixenosis, antibiosis, or insect tolerance through physiological functions (Kennedy et al. 1987; Alam and Cohen, 1998). Several BPH resistance genes have been demonstrated to confer one or more types of resistance mechanisms. For instance, Panda and Heinrichs (1983) determined that rice varieties carrying the Bph1 gene exhibit antibiosis and tolerance and observed moderate resistance to the BPH. Moreover, resistance genes Bph6 and Bph14 have been characterized to have antibiotic and antixenotic effects on insects (Qiu et al. 2010; Du et al. 2009). Together, different BPH resistance genes may possess different resistance mechanisms. Thus, it is still necessary to demonstrate resistance mechanisms and to identify resistance effects observed when one novel BPH resistance gene is detected, which should facilitate resistant rice breeding.
The identified BPH resistance genes provide a wealth of resistance resources for rice breeding and improvement. However, it must be noted that the BPH insects can adapt to rice varieties with single resistance gene and then develop new biotypes for practical rice cultivation. For example, two BPH resistance varieties, IR26 and IR36, harboring BPH resistance genes Bph1 and bph2, respectively, were widely cultivated in the 1970s and 1980s, but they have become susceptible in the last few years due to changes in BPH biotypes and infestation patterns (Claridge and Hollander, 1980; Pathak et al. 1969). Previous studies have indicated that rice lines pyramiding two or more BPH resistance genes via marker-assisted selection (MAS) can efficiently improve resistance levels (Qiu et al. 2012; Hu et al., 2016a, b; Jena et al. 2017). Thus, there is still an urgent need to pyramid multiple BPH resistance genes and to develop stronger and more durable varieties that are resistant to BPH.
GX2183, a wild species of O. rufipogon with the AA genome, shows broad spectrum resistance to BPH biotypes, including biotypes 1 and 2, Bangladesh (collected from Bangladesh), Cuu Long (collected from Vietnam), and Pantnagar (collected from India) (Li et al. 2006). Major resistance gene Bph27 has been finely mapped to an 86.3-kb region harbored by markers RM16846 and RM16853 (Huang et al. 2013). Meanwhile, this study reveals the presence of more than one major BPH resistance gene in the rice species of GX2183. In the present study, introgression lines of GX2183 were used to develop the mapping population, near isogenic lines (NILs), and pyramiding lines (PYLs) to map and apply the BPH resistance gene. We identified and finely mapped a new BPH resistance gene Bph36 flanked by InDel markers S13 and X48 on the short arm of rice chromosome 4 and incorporated this gene into the elite rice cultivars via MAS.
Mapping population, NIL, and PYL development
RBPH16 and RBPH17, two introgression lines derived from O. rufipogon accession GX2183, are highly resistant to BPH and were used as the donor. Rice varieties Kangwenqingzhan (abbreviated as KW) and Huanghuazhan (abbreviated as HHZ) are widely cultivated in southern China and are highly susceptible to BPH. RBPH16 and RBPH17 were respectively crossed with KW and HHZ to develop F2:3 mapping populations. Based on the QTL analysis, the positive F1 (KW/RBPH16) individuals were continuously backcrossed with KW to developed BC1F1, BC2F1, BC3F1, and BC4F1 populations, and each backcrossed individual was verified with tightly linked markers. From the developed populations, single-gene individuals carrying the novel resistance gene were self-crossed twice to develop a BC1F2 population, and then they were used to verify the resistance gene and for fine mapping. Positive BC4F1 individuals were then self-crossed twice to obtain BC4F2 lines homozygous to the resistance genes and taken as NILs.
RBPH54, an introgression line derived from O. rufipogon, carries BPH-resistance gene Bph29 (Wang et al. 2015). Rice variety PTB33 has been indicated to be highly resistant to BPH and includes resistance gene Bph3 in the short arm of chromosome 4 (Liu et al., 2015). Both were used to develop PYLs with BPH resistance genes. MH511, carrying the Xa23 resistance gene, is a bacterial blight resistant line. Rice line 9311 is a merit restoring line that is highly susceptible to BPH. To develop PYLs with different BPH resistance genes, RBPH16 was first crossed with RBPH54 and PTB33, and then the positive individuals were backcrossed with RBPH16 twice. Next, BC2F1 individuals derived from RBPH16/RBPH54 or RBPH16/PTB33 were crossed and self-crossed twice. Then, the BC2F2 lines were evaluated based on BPH resistance levels, and highly BPH- resistant lines were crossed with MH511 or 9311. Susceptible lines MH511 and9311 were taken as recurrent parents to develop BC3F1, and each backcrossed individual was verified with the tightly linked markers (Additional file 1: Figure S1).
Wild rice accession GX2183 was collected from Guangxi province of China and was stored at Guangxi University. Rice lines RBPH16, RBPH17, RBPH54, and MH511 were developed in our laboratory. Rice varieties 9311, KW, and HHZ were collected and stored in our laboratory as germplasm.
BPH insects and evaluation of BPH resistance
The BPH insects were collected from rice fields in Nanning, Guangxi province of China, and were maintained on Taichung Native 1 (TN1, a susceptible indica variety) under natural conditions in a greenhouse at Guangxi University. A bulk seedling test was conducted to evaluate BPH resistance as described by Qiu et al. (2010). The pre-germinated seeds were sown in rows spaced 3.5 cm apart with 20 seeds in each line in a plastic box (58 × 38 × 7 cm) with a seed bed of 3-cm thick fine puddled soil. Susceptible control TN1, resistant control PTB33 and parents of the mapping population were sown in thecenter. Seedlings of the third-leaf stage (13 or 14 days old) were infested with second- to third-instar hopper nymphs at a density of eight insects per seedling. Temperature and humidity were respectively maintained at 28 ± 2 °C and 75 ± 5% for evaluation. Phenotypic values for the individual plants were recorded on a scale on 0–9 when all plants of susceptible control TN1 were killed. This was done following the Standard Evaluation System (SES) for rice (IRRI, 1996) based on the following scale: 0 = no visible damage; 1 = partial yellowing in first leaf; 3 = first and second leaves have become partially yellow; 5 = pronounced yellowing or minor stunting; 7 = wilting while, the plant is still alive; and 9 = the plant has completely wilted or died. Three replicates of each line were carried out, and all resistance tests were repeated twice.
Marker analysis, QTL detection and gene mapping
Total genomic DNA of the plant leaves was extracted by the CTAB method (Murray and Thompson, 1980). PCR was performed as described by Qiu et al. (2010), and the PCR products were separated on 7% denaturing polyacrylamide gels and visualized by silver staining. Simple sequence repeat (SSR) primer sequences were obtained from the Gramene database (www.gramene.org/archive),and InDel makers were developed through a comparison of genome sequences of japonica cv. Nipponbare and indica cv. 9311.
A bulked segregant analysis (BSA) was performed to identify markers linked to BPH resistance (Michelmore et al. 1991). According to the results of our BPH resistance evaluation, ten extremely resistant and ten extremely susceptible individuals were used to construct two contrasting DNA pools. SSR and InDel markers were screened for polymorphism between the two pools. All polymorphic markers within the study region were used to genotype the F2 individuals. Genetic linkage maps of SSR and InDel markers with BPH resistance loci were constructed using JoinMap 3.0. Genetic linkage maps and phenotypes of the primary mapping population were used for QTL analysis via inclusive composite interval mapping (ICIM) with MapQTL 5.0. QTLs were identified when LOD scores exceeded 3.0.
BPH host selection test
To perform the BPH host selection test, each rice line with a single gene (NIL-Bph36), two genes (NIL-Bph36 + Bph27), and KW were sown into one row with 15 healthy seedlings (4 weeks old) in a plastic bucket containing rice field soil. The second- to third-instar BPH nymphs were released into an average of eight heads per plant. The number of BPH insects attached to each line was counted every day after infestation. After each observation, the base of each rice plant was gently tapped to allow BPH insects to be evenly distributed throughout the water and to select the host plant once again. Three replications were conducted each time and the test was repeated twice.
BPH honeydew excretion measurement
The parafilm sachets method was used to measure BPH honeydew excretion (Pathak et al. 1982). One fifth-instar BPH insect was enclosed in a rectangular (3.5 cm × 3 cm) parafilm bag with a pipette, and then was fastened to the test plants (4 weeks old). Each plant had one or two bags and eight bags for each line of NIL-Bph36, NIL-Bph36 + Bph27, or KW wereused. After 2 days of insect infestation, the bags were removed and the total weight of the bag enclosing the honeydew was weighed as W1. Then, the honeydew was wiped with absorbent cotton and the bag was weighed again (W2). Therefore, the weight of honeydew excretion was calculated as W1 – W2. The test was repeated three times.
BPH survival and growth measurement
The BPH survival rate was determined according to the method described by Qiu et al. (2010). The 5-week-old seedlings were only composed of main stems and were covered with a plastic cup with a hole in the base. Then, each plant was infested with ten third-instar nymphs. The surviving insects were counted 1 d, 2 d, 3 d, 4 d, and 5 d after BPH release. Six plants were arranged for each line of NIL-Bph36, NIL-Bph36 + Bph27, and KW, and the experiment was repeated three times.
To measure the population growth rate (PGR) of the BPH, the rice seedlings were treated as they were for the BPH survival test. The 5-week-old seedlings were infested with 15 pre-weighed second- to third-instar nymphs and then covered with a plastic cup with a hole sealed with absorbent cotton. The weight of the surviving BPH was measured after 4 days of insect infestation. The PGRs of BPH were calculated following the method described by Qiu et al. (2010). Six plants were used for each line of NIL-Bph36, NIL-Bph36 + Bph27, and KW, and the test was repeated three times.
Bacterial blight resistance test
To perform the bacterial blight resistance test, Xanthomonas oryzae pv. oryzae GX1070 was collected from rice plants from Guangxi province of China and was cultured on nutrient agar (NA) media at 28 °C for 4 days. The bacteria were then collected and dissolved with ddH2O to an optical density concentration of OD600 = 1.0. The 8-week-old plants were then inoculated with bacteria using the leaf-clipping method, and then each leaf was measured and scored after 3 weeks of inoculation (Kauffman et al. 1973). Six plants were used for each line, and the test was repeated twice.
MAS for the resistance genes
According to the above study, molecular markers RHD9, RH007, and RHC10 were co-segregated with Bph3 (Liu et al., 2015), and BYL8, BID2, BID3, and BYL7 were tightly linked to Bph29 (Wang et al. 2015). Bph27 was found in the region flanked by SSR markers RM16846 and RM16888, which were used for MAS (Huang et al. 2013). These markers were verified for RBPH16, RBPH54, PTB33, 9311, and MH511 to select suitable markers for MAS.
Agronomic trait measurement
To detect agronomic traits of the developed BPH-resistance lines, each line was composed of five rows and each row included ten plants at a planting density of 20 × 30 cm (20-cm spacing between plants and 30-cm spacing between rows distance). Together with the recurrent parents, three repeats of each line were randomly distributed across the rice field. Then, 20 plants from each repeat were subjected to agronomic trait measurements, (i.e., plant height, effective panicle number, the number of grains per panicle, 1000-grain weight, and seed setting percentage). Field management followed normal agronomic practices. The test was repeated over two seasons.
The Chi-square test for goodness-of-fit was performed with GraphPad Prism 7; and the resistance data were analyzed using one-way ANOVA and comparing the LSD test at a 5% or 1% significance level. The survival rates of insects (%) were arcsine transformed prior to analysis.
Genetic analysis of BPH resistance
Primary mapping of resistance genes
QTL scanning results using 140 lines (KW/RBPH16) and 120 lines (HHZ/RBPH17) resistance scores and marker genotypes of F2 population by MapQTL 5
Verification and fine mapping of Bph36
Polymorphic InDel molecular markers used for fine mapping
Forward primer (5′-3′)
Reverse primer (5′-3′)
In consideration of the target region, four candidate genes were contained in the corresponding genomic region of Nipponbare. They are hypothetical protein (LOC_Os04g11800), acyltransferase family protein (LOC_Os04g11810), white-brown complex homolog protein (LOC_Os04g11820), and TCP family transcription factor (LOC_Os04g11830). Acyltransferase is a large family of proteins that play an important role in the biosynthesis of some plant secondary metabolites for defensing against insect (Chedgy et al. 2015). White-brown complex (WBC) family protein, is a part of ABC superfamily protein, has been reported to participate in a multitude of physiological processes that allow the plant to adapt to changing environments and cope with biotic and abiotic stresses (Kretzschmar et al. 2011). TCP family transcription factor participate in plant developmental processes, such as development of leaf and flower (Koyama et al. 2017; Yin et al. 2018).
Characterization of the BPH resistance of NILs
According to our BPH honeydew excretion measurements for the different genotypic plants, we observed 14.46, 4.10, and 3.82 mg/BPH in KW, NIL-Bph36, and NIL-Bph36 + Bph27, respectively (Fig. 4b). To measure resistance effects on the insects, the PGR of BPH was calculated from changes in weight observed before and after feeding the resistant and susceptible plants. Consequently, the PGRs of resistant plants NIL-Bph36 and NIL-Bph36 + Bph27 and of susceptible plants KW were measured as 0.0196, 0.0184, and 0.0623 mg/BPH/d, respectively (Fig. 4c). Significantly less honeydew excretion levels and PGRs were detected from the resistant plants than from the susceptible plants (P < 0.001 for NIL-Bph36 and KW or NIL-Bph36 + Bph27 and KW).
We surveyed the survival number of BPHs left 1 d, 2 d, 3 d, 4 d, and 5 d after treatment. BPH survival rates declined quickly for resistant plants NIL-Bph36 and NIL-Bph36 + Bph27 compared to those of the susceptible plants. After 2 d of infestation, BPH survival rates for the resistant plants were less than 60%while remaining at above 80% for the susceptible plants (P < 0.05 for NIL-Bph36 and KW or NIL-Bph36 + Bph27 and KW). After 5 d of infestation, BPH survival rates of the resistant plants were only measured at 5%, but a value of 62% was measured for the susceptible plants (P < 0.01 for NIL-Bph36 and KW or NIL-Bph36 + Bph27 and KW, Fig. 4d). We must also note that survival rates of NIL-Bph36 + Bph27 were still lower than those of NIL-Bph36 during the observation period, and a statistical difference was detected 2 d and 3 d after infestation (P < 0.05). Taken together the resistant plants had a strong antibiotic effect on the insects and the pyramided line had a stronger effect than the single gene line.
BPH resistance evaluation for PYLs
Selected PYLs carring multiple BPH resistance genes
1.59 ± 0.41
1.76 ± 0.32
2.18 ± 0.26
2.53 ± 0.68
2.53 ± 0.81
2.73 ± 0.22
2.95 ± 0.18
Breeding applications of resistance genes
Agronomic traits of recurrent parents and breeding lines
Plant height (cm)
Number of effective panicle per plant
Number of grains per panicle
Setting rate (%)
1000-grain weight (g)
108.6 ± 0.70
8.7 ± 0.37
168.9 ± 5.06
84.7 ± 1.53
27.8 ± 0.35
106.9 ± 0.92
8.5 ± 0.44
176.8 ± 4.15
84.0 ± 1.28
25.4* ± 0.16
96.4 ± 2.21
6.9 ± 0.57
141.6 ± 5.06
86.4 ± 2.15
21.3 ± 0.23
95.4 ± 1.15
7.0 ± 0.42
139.7 ± 7.46
85.1 ± 1.56
21.6 ± 0.37
94.9 ± 1.76
6.8 ± 0.52
141.8 ± 5.24
84.8 ± 1.72
20.9 ± 0.68
BPHexerts chronic biotic stress and severely constrains rice production in Asia and in other parts of the world. Accordingly, BPH resistance gene identification, mapping and characterization are valuable in ensuring long-term resistance against diverse predominant biotypes for sustainable rice outputs. Previous reports demonstrate the highly resistant wild rice accession GX2183 contains more than one major gene for BPH resistance. In this study, RBPH16 and RBPH17 originating from GX2183 were employed as donor parents and were respectively crossed to KW and HHZ to develop F2:3 mapping populations. Subsequently, with the exception of the previously detected gene Bph27 (Huang et al. 2013), novel resistance gene Bph36 was identified via high-resolution mapping to accupy a 38-kb region harbored by markers S13 and X48. Rice chromosomes 4 and 12 have been considered as the mainframe of BPH resistance genes (Jena and Kim 2010; Fujita et al. 2013; Hu et al., 2016a, b). For instance, thirteen genes are found in two distinct clusters of chromosome 4. Six of them (Bph6, bph12, Bph27, bph18(t), Bph27(t), and Bph34) are clustered on the long arm of chromosome 4 (Qiu et al. 2010, 2012; Huang et al. 2013; Fujita et al. 2013; Kumar et al. 2018); and seven genes (Bph3, Bph12, Bph15, Bph17, Bph20(t), Bph30, and Bph33) are found on the short arm of chromosome 4 (Liu et al., 2015; Yang et al. 2002; Sun et al. 2005; Yang et al. 2004; Rahman et al. 2009; Wang et al. 2018; Hu et al. 2018). According to the present study Bph36 also occupies this cluster, and via high-resolution mapping, it was successfully identified on the short arm of chromosome 4 roughly 2 Mb downstream from the Bph12, Bph17, Bph15, and Bph20 regions (Yang et al. 2002; Sun et al. 2005; Yang et al. 2004; Rahman et al. 2009) and 0.6 Mb upstream from Bph3 in the Nipponbare genome (Liu et al., 2015). Gene Bph36 presented a large LOD score and accounts for the considerable variance in BPH resistance observed as shown in Table 1. This was also proved through the characterization of NILs and PYLs as shown in Figs. 4 and Fig. 5.
Plants generally apply antixenosis, antibiosis, and tolerance against insect attacks. Previous studies indicate that BPH resistance genes such as Bph6, Bph14, and Bph27 have strong antixenotic and antibiotic effects on the insects (Qiu et al. 2010; Du et al. 2009; Huang et al. 2013), while the resistance gene Bph7 mainly confers tolerance to BPH (Qiu et al. 2014). Moreover, plants pyramiding with two or more genes significantly increase resistance to BPH insects (Qiu et al. 2012; Hu et al. 2012). According to tests on BPH host choices, honeydew excretion, survival rates, and PGR, lines of NIL-Bph36 and NIL-Bph36 + Bph27 show significant antixenotic and antibiotic effects on insects relative to those of susceptible plants, and it must be noted that lines of NIL-Bph36 + Bph27 have significantly stronger resistance effects than NIL-Bph36 as shown in host choice and BPH survival rates (Fig. 4).
Wild rice species offer natural and unique pools of resistance genes with strong resistance to all BPH biotypes (Heinrichs et al. 1982; Hu et al. 2015). At the same time, modern technologies offer means of using molecular markers in molecular breeding approaches to accelerate the identification and application of resistance loci (Ashkani et al. 2015). Recently, Jiang et al. (2018) introduced six dominant BPH-resistance genes into Jin23B using MAS and in turn improved BPH-resistance breeding lines. Moreover, Hu et al. (2016a, b) pyramided Bph3, Bph14, and Bph15 into elite indica cultivar Heimeizhan and obtained high BPH resistance breeding lines. Via high-resolution mapping, Bph36 has been found to include tightly linked markers that are effective and efficient for MAS performance (Additional file 2: Figure S2). We also pyramided Bph36 with Bph27, Bph29, and Bph3 by continuous backcrossing and MAS, and obtained several highly resistant PYLs. Of these, VP1720 and VP1728 were found to be homozygous across all four BPH-resistance genes and exhibited strong resistance to insects (Table 3). Then, VP1728 was backcrossed with MH511 and 9311 to develop approximate resistant breeding lines with diverse backgrounds. Consequently, an agronomic trait survey suggests that the developed breeding lines are almost the same as the recurrent parents (Table 4). Therefore, the developed PYLs may be applied for insect resistance rice breeding.
Regarding agricultural traits of the developed PYLs, setting rates of BR1658 (85.1%) and BR1660 (84.8%) declined relative to those of MH511 (86.4%) (F = 5.6, P = 0.06 for BR1658 and MH511; F = 4.8 P = 0.046 for BR1660 and MH511). The 1000-grain weight of BR1693 (25.4 g) was also lower than that of 9311 (27.8 g) (F = 16.4, P = 0.042, Table 4). This suggests that linkage drag remains a serious problem when pyramiding different genes via MAS. Many previous studies have revealed the same problem. For instance, a previous study shows that Bph3 from Rathu Heenati is positioned very close to the Wxa allele (roughly 380 kb), which confers amylose content in rice (Jairin et al. 2007, 2009). However, the authors acquired breeding lines with Bph3 and without Wxa alleles by screening large backcrossed individuals (Jairin et al. 2009). However, Hu et al. (2016a, b) failed to break up linkages of Wxa while pyramiding Bph3 with Bph14 and Bph15 in Hemeizhan, as the numbers of screened backcrossed individuals was still too low. Therefore, more backcrosses and MAS tests are needed to break up unexpected linkage genes for breeding purposes.
Our results validate the usefulness of the Bph36 gene for the control of BPH and show that applying it to susceptible rice varieties produces resistance effect by suppressing the feeding behavior, growth and longevity of BPH insects. This can in turn facilitate the development of BPH-resistant rice varieties in the future and help limit herbicide use. Tightly linked markers will facilitate the marker-assisted breeding and high-resolution mapping of Bph36, laying the foundation for insect resistance mechanism research, map-based cloning and functional analysis and providing a theoretical basis and intermediate materials to facilitate resistance to BPH.
This research was supported by the National Key R&D Program of China (2016YFD0100600), the National Natural Science Foundation of China (31560423), the Guangxi Natural Science Foundation (2013GXNSFGA019009), and Guangxi innovation-driven development special funding project (Guike-AA17204070).
This research was supported by the National Key R&D Program of China (2016YFD0100600), the National Natural Science Foundation of China (31560423), the Guangxi Natural Science Foundation (2013GXNSFGA019009), and Guangxi innovation-driven development special funding project (Guike-AA17204070).
Availability of data and materials
All relevant data are provided as Additional file 3: Table S1.
ZH L, YF Q, and RB L conceived the idea and wrote the manuscript. ZH L, YX X, and HL Z conducted the experiments and performed data analysis. Y L, B U, XZ J, XY W, F L and BX Q participated in material development and sample preparation. All authors read and approved the final manuscript.
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