Naihui Guo, Ruihu An, Zongliang Ren, Jun Jiang, Bonian Cai, Shikai Hu, Gaoneng Shao, Guiai Jiao, Lihong Xie, Ling Wang, Fengli Zhao, Shaoqing Tang, Zhonghua Sheng, Peisong Hu
{"title":"Developing super rice varieties resistant to rice blast with enhanced yield and improved quality","authors":"Naihui Guo, Ruihu An, Zongliang Ren, Jun Jiang, Bonian Cai, Shikai Hu, Gaoneng Shao, Guiai Jiao, Lihong Xie, Ling Wang, Fengli Zhao, Shaoqing Tang, Zhonghua Sheng, Peisong Hu","doi":"10.1111/pbi.14492","DOIUrl":null,"url":null,"abstract":"<p>Rice blast, caused by the <i>Magnaporthe oryzae</i>, is the most detrimental disease to rice. Yield losses caused by this disease were from 10% to 30% in rice planting areas (Skamnioti and Gurr, <span>2009</span>); severe cases may even lead to complete cessation of production (Parker <i>et al</i>., <span>2008</span>). Cloning rice blast resistant genes and applying them to cultivate resistant varieties is a practical and effective method for controlling rice blast disease. So far, more than 70 disease resistance genes and QTLs have been identified, of which at least 25 have been cloned and used in disease resistance breeding (Luo <i>et al</i>., <span>2017</span>). The <i>Pi2</i> gene encodes a protein with a nucleotide-binding site and leucine-rich repeat (LRR) domain (Zhou <i>et al</i>., <span>2006</span>), and is one of the most broad-spectrum and efficient resistance genes to rice blast, exhibiting resistance to 36 out of 43 rice blast strains from 13 countries (Liu <i>et al</i>., <span>2002</span>). However, many elite varieties do not carry <i>Pi2</i> gene, which seriously hinders the widespread and sustainable promotion of these varieties.</p><p>Marker-assisted selection (MAS) is one of the important technologies in modern breeding. It uses molecular markers to quickly detect individual plants carrying target genes, greatly improving breeding efficiency and saving breeding costs. Previously, Jiang <i>et al</i>. (<span>2015</span>) developed blast-resistant thermosensitive genic male sterile (TGMS) lines by employing MAS. High-density whole genome single nucleotide polymorphism (SNP) chips are also a technology that accelerates the breeding process. Therefore, combining MAS and SNP chips can make breeding improvement faster and more accurately. For example, Guo <i>et al</i>. (<span>2024</span>) used MAS and Green Super Rice 40K (GSR40K) detection to screen improved strains with high genetic similarity to the receptor in BC<sub>1</sub>F<sub>2</sub>. In this study, we successfully generated an improved rice germplasm with blast-resistant by integrating MAS and GSR40K detection technology.</p><p>F<sub>1</sub> plants obtained from the cross of Zhonghui261 (ZH261; a good quality restoring line of Huazheyou 261 [HZY261], which was selected as a demonstration and promotion variety of super rice in 2024) and Yuenongsimiao (YNSM; carrying <i>Pi2</i>), were backcross with ZH261 to generate BC<sub>1</sub>F<sub>1</sub>. Among 1025 BC<sub>1</sub>F<sub>1</sub> plants, we selected 70 strains that similar to ZH261 and 26 individual plants were identified to carry <i>Pi2</i> (Heterozygous) using the marker <i>Pi2</i>-CM1. Then, the single plant out of 26 with 89.72% of genetic background reversion was selected by detecting with GSR40K. The single plant was backcrossed again with ZH261 to generate 964 BC<sub>2</sub>F<sub>1</sub> plants. We selected 10 strains that are similar to ZH261 and three individual plants were identified to carry <i>Pi2</i> (Heterozygous) using the marker <i>Pi2</i>-CM1. The single plant out of three with 97.86% of genetic background reversion was selected to selfing and generate BC<sub>2</sub>F<sub>2</sub>. The single plant named ZH261-Pi2 was selected from BC<sub>2</sub>F<sub>2</sub> by employing MAS and detecting with GSR40K (Figure 1a). ZH261-Pi2 exhibited 97.81% genetic similarity to ZH261 and 99.97% purity (Figure 1b). Based on 48 simple sequence repeats (SSR) markers followed by the protocol NY/T 1433-2014, only one pair of SSR marker (RM176) was different between ZH261 and ZH261-<i>Pi2</i> (Figure 1c), indicating that ZH261 and ZH261-<i>Pi2</i> were the same variety. Finally, we hybridised with Huazhe2A using ZH261 and ZH261-<i>Pi2</i>, respectively, to produce HZY261 and HZY261-<i>Pi2</i>, and evaluated their rice blast resistance, yield and quality traits (Figure 1a).</p><p>We found that ZH261-<i>Pi2</i> and HZY261-<i>Pi2</i> significantly increased resistance to blast compared to ZH261 and HZY261 (Figure 1d–g). ZH261-<i>Pi2</i> showed a similar grain numbers per panicle, but higher tiller numbers per plant, 1000 grain weight and grain yield per plant than that of ZH261 (Figure 1h–k). On the other hand, HZY261-<i>Pi2</i> displayed lower 1000 grain weight, but higher grain numbers per panicle, tiller numbers per plant and grain yield per plant compared with HZY261 (Figure 1h–k). Together, our results indicate that introduction of <i>Pi2</i> in ZH261 by integrating MAS and GSR40K detection can simultaneously enhance rice blast resistance and yield.</p><p>Amylose content is the most critical parameter determining rice eating and cooking quality (Wang <i>et al</i>., <span>2024</span>). ZH261-<i>Pi2</i> showed a similar length–width ratio, alkali spreading value and amylose content, but higher gel consistency than that of ZH261 (Figure 1l–o). HZY261-<i>Pi2</i> had higher length–width ratio, but lower amylose content and gel consistency than that of HZY261 (Figure 1l–n). As for alkali spreading value, no significant difference was observed between HZY261-<i>Pi2</i> and HZY261 (Figure 1o).</p><p>Balancing the yield, quality and resistance to disease is a daunting challenge in crop breeding due to the negative relationship among these traits (Xiao <i>et al</i>., <span>2021</span>). However, it is feasible to improve the rice blast resistance, yield and quality of existing rice varieties through molecular design breeding (Mao <i>et al</i>., <span>2021</span>). Our work provides a molecular design strategy to rapidly improve rice blast resistance, yield and quality by integrating MAS and GSR40K detection. In particular, the improved varieties can be directly applied to production, providing an important guarantee for food security.</p><p>H.P., T.S. and S.Z. designed the research; G.N., A.R., R.Z., J.J., C.B., H.S., S.G., J.G., X.L., W.L. and Z.F. performed the experiments; S.Z. and G.N. analysed the results and wrote the manuscript.</p><p>The authors declare no conflict of interests.</p>","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"23 1","pages":"232-234"},"PeriodicalIF":10.5000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/pbi.14492","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/pbi.14492","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Rice blast, caused by the Magnaporthe oryzae, is the most detrimental disease to rice. Yield losses caused by this disease were from 10% to 30% in rice planting areas (Skamnioti and Gurr, 2009); severe cases may even lead to complete cessation of production (Parker et al., 2008). Cloning rice blast resistant genes and applying them to cultivate resistant varieties is a practical and effective method for controlling rice blast disease. So far, more than 70 disease resistance genes and QTLs have been identified, of which at least 25 have been cloned and used in disease resistance breeding (Luo et al., 2017). The Pi2 gene encodes a protein with a nucleotide-binding site and leucine-rich repeat (LRR) domain (Zhou et al., 2006), and is one of the most broad-spectrum and efficient resistance genes to rice blast, exhibiting resistance to 36 out of 43 rice blast strains from 13 countries (Liu et al., 2002). However, many elite varieties do not carry Pi2 gene, which seriously hinders the widespread and sustainable promotion of these varieties.
Marker-assisted selection (MAS) is one of the important technologies in modern breeding. It uses molecular markers to quickly detect individual plants carrying target genes, greatly improving breeding efficiency and saving breeding costs. Previously, Jiang et al. (2015) developed blast-resistant thermosensitive genic male sterile (TGMS) lines by employing MAS. High-density whole genome single nucleotide polymorphism (SNP) chips are also a technology that accelerates the breeding process. Therefore, combining MAS and SNP chips can make breeding improvement faster and more accurately. For example, Guo et al. (2024) used MAS and Green Super Rice 40K (GSR40K) detection to screen improved strains with high genetic similarity to the receptor in BC1F2. In this study, we successfully generated an improved rice germplasm with blast-resistant by integrating MAS and GSR40K detection technology.
F1 plants obtained from the cross of Zhonghui261 (ZH261; a good quality restoring line of Huazheyou 261 [HZY261], which was selected as a demonstration and promotion variety of super rice in 2024) and Yuenongsimiao (YNSM; carrying Pi2), were backcross with ZH261 to generate BC1F1. Among 1025 BC1F1 plants, we selected 70 strains that similar to ZH261 and 26 individual plants were identified to carry Pi2 (Heterozygous) using the marker Pi2-CM1. Then, the single plant out of 26 with 89.72% of genetic background reversion was selected by detecting with GSR40K. The single plant was backcrossed again with ZH261 to generate 964 BC2F1 plants. We selected 10 strains that are similar to ZH261 and three individual plants were identified to carry Pi2 (Heterozygous) using the marker Pi2-CM1. The single plant out of three with 97.86% of genetic background reversion was selected to selfing and generate BC2F2. The single plant named ZH261-Pi2 was selected from BC2F2 by employing MAS and detecting with GSR40K (Figure 1a). ZH261-Pi2 exhibited 97.81% genetic similarity to ZH261 and 99.97% purity (Figure 1b). Based on 48 simple sequence repeats (SSR) markers followed by the protocol NY/T 1433-2014, only one pair of SSR marker (RM176) was different between ZH261 and ZH261-Pi2 (Figure 1c), indicating that ZH261 and ZH261-Pi2 were the same variety. Finally, we hybridised with Huazhe2A using ZH261 and ZH261-Pi2, respectively, to produce HZY261 and HZY261-Pi2, and evaluated their rice blast resistance, yield and quality traits (Figure 1a).
We found that ZH261-Pi2 and HZY261-Pi2 significantly increased resistance to blast compared to ZH261 and HZY261 (Figure 1d–g). ZH261-Pi2 showed a similar grain numbers per panicle, but higher tiller numbers per plant, 1000 grain weight and grain yield per plant than that of ZH261 (Figure 1h–k). On the other hand, HZY261-Pi2 displayed lower 1000 grain weight, but higher grain numbers per panicle, tiller numbers per plant and grain yield per plant compared with HZY261 (Figure 1h–k). Together, our results indicate that introduction of Pi2 in ZH261 by integrating MAS and GSR40K detection can simultaneously enhance rice blast resistance and yield.
Amylose content is the most critical parameter determining rice eating and cooking quality (Wang et al., 2024). ZH261-Pi2 showed a similar length–width ratio, alkali spreading value and amylose content, but higher gel consistency than that of ZH261 (Figure 1l–o). HZY261-Pi2 had higher length–width ratio, but lower amylose content and gel consistency than that of HZY261 (Figure 1l–n). As for alkali spreading value, no significant difference was observed between HZY261-Pi2 and HZY261 (Figure 1o).
Balancing the yield, quality and resistance to disease is a daunting challenge in crop breeding due to the negative relationship among these traits (Xiao et al., 2021). However, it is feasible to improve the rice blast resistance, yield and quality of existing rice varieties through molecular design breeding (Mao et al., 2021). Our work provides a molecular design strategy to rapidly improve rice blast resistance, yield and quality by integrating MAS and GSR40K detection. In particular, the improved varieties can be directly applied to production, providing an important guarantee for food security.
H.P., T.S. and S.Z. designed the research; G.N., A.R., R.Z., J.J., C.B., H.S., S.G., J.G., X.L., W.L. and Z.F. performed the experiments; S.Z. and G.N. analysed the results and wrote the manuscript.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.