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16 pages, 1644 KiB  
Article
Exploring Distribution and Evolution of Pi-ta Haplotypes in Rice Landraces across Different Rice Cultivation Regions in Yunnan
by Hengming Luo, Lin Lu, Qun Wang, Zhixiang Guo, Lina Liu, Chi He, Junyi Shi, Chao Dong, Qiaoping Ma and Jinbin Li
Genes 2024, 15(10), 1325; https://doi.org/10.3390/genes15101325 (registering DOI) - 15 Oct 2024
Viewed by 319
Abstract
Background: Rice blast, caused by Magnaporthe oryzae, seriously damages the yield and quality of rice worldwide. Pi-ta is a durable resistance gene that combats M. oryzae carrying AVR-Pita1. However, the distribution of the Pi-ta gene in rice germplasms in Yunnan [...] Read more.
Background: Rice blast, caused by Magnaporthe oryzae, seriously damages the yield and quality of rice worldwide. Pi-ta is a durable resistance gene that combats M. oryzae carrying AVR-Pita1. However, the distribution of the Pi-ta gene in rice germplasms in Yunnan Province has been inadequately studied. Methods: We analyzed the potential molecular evolution pattern of Pi-ta alleles by examining the diversity in the coding sequence (CDS) among rice varieties. Results: The results revealed that 95% of 405 rice landraces collected from different ecological regions in Yunnan Province carry Pi-ta alleles. We identified 17 nucleotide variation sites in the CDS regions of the Pi-ta gene across 385 rice landraces. These variations led to the identification of 28 Pi-ta haplotypes, encoding 12 novel variants. Among these, 5 Pi-ta haplotypes (62 rice landraces) carried R alleles. The evolutionary cluster and network of the Pi-ta haplotypes suggested that the Pi-ta S alleles were the ancestral alleles, which could potentially evolve into R variants through base substitution. Conclusions: This study suggests that Pi-ta alleles are diverse in the rice landraces in Yunnan, and the Pi-ta sites resistant to blast evolved from the susceptible plants of the rice landraces. These results provide the basis for breeding resistant varieties. Full article
(This article belongs to the Section Genes & Environments)
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Figure 1
<p>Diversification of <span class="html-italic">Pi-ta</span> in rice landraces in Yunnan. Distribution of variation of the <span class="html-italic">Pi-ta</span> alleles was analyzed using sliding window. X-axis shows the distribution of variation within the full CDS regions. Lower pane indicates the corresponding schematic presentation of the two exons of <span class="html-italic">Pi-ta</span>. Window length: 10; step size: 1. π value corresponds with the level of variation at each site, because it is the sum of pair-wise differences divided by the number of pairs within the population.</p>
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<p>Neighbor joining phylogenetic tree of <span class="html-italic">Pi-ta</span> resistance (<span class="html-italic">R</span>)/susceptibility (<span class="html-italic">S</span>) alleles. (<b>A</b>), systematical evolution of 44 <span class="html-italic">Pi-ta</span> alleles. <span class="html-italic">R/S</span> alleles of the <span class="html-italic">Pi-ta</span> can be divided into 2 different clusters. Cluster I contained 4 <span class="html-italic">Pi-ta</span> haplotypes (wild <span class="html-italic">O. barthii</span>, <span class="html-italic">O. glaberrima</span>, <span class="html-italic">O. sativa f. spontanea</span>, and <span class="html-italic">O. sativa Indica</span> Group), while Cluster II contained wild <span class="html-italic">Oryza rufipogon</span> and <span class="html-italic">Oryza glaberrima,</span> and all of <span class="html-italic">Pi-ta</span> haplotypes in rice landraces in Yunnan. (<b>B</b>), the phylogenetic relationship of <span class="html-italic">Pi-ta R/S</span> alleles. The <span class="html-italic">Pi-ta R</span> alleles were derived from <span class="html-italic">S</span> alleles in rice landraces in Yunnan. These <span class="html-italic">Pi-ta</span> haplotype alleles were obtained from rice landraces in Yunnan (28 <span class="html-italic">Pi-ta</span> haplotype alleles, H01–H28) and the published GenBank (16 <span class="html-italic">Pi-ta</span> haplotype alleles, accession number: AF207842.1, EU770206.1, EU770207.1, EU770208.1, EU770209.1, EU770210.1, EU770211.1, EU770212.1, EU770213.1, EU770214.1, EU770215.1, EU770216.1, EU770217.1, EU770218.1, EU770219.1, EU770220.1).</p>
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<p>The haplotype network for the 28 <span class="html-italic">Pi-ta</span> alleles and the 13 reference <span class="html-italic">Pi-ta</span> alleles in rice. Haplotype network analysis was performed using TCS1.21 (<a href="http://darwin.uvigo.es/" target="_blank">http://darwin.uvigo.es/</a>). The Pi-ta haplotypes were major divided into 5 evolutionary clades. Clade A contained 4 <span class="html-italic">Pi-ta</span> orthologues and they derived from the published sequences in GenBank. Clade D possessed the most <span class="html-italic">Pi-ta</span> orthologues, but not contained its <span class="html-italic">R</span> allele. In contrast, clade B, C, and E included the <span class="html-italic">Pi-ta R</span> allele at least one and derived from the <span class="html-italic">S</span> orthologues. The original <span class="html-italic">Pi-ta</span> alleles were designated as the H01 haplotype in the network. Each <span class="html-italic">Pi-ta</span> haplotype was separated by mutational events. The node in the network represents an extinct or a missing haplotype not found among the samples. All haplotypes were displayed as circles. The size of the circles corresponded to the haplotype frequency. H01–H28 were obtained from 385 rice landraces in Yunnan. The AF207842.1, EU770206.1, EU770207.1 (same with H02), EU770209.1 (same with H07), EU770211.1 (same with H05), EU770212.1 (same with H01), EU770214.1, EU770215.1 (same with H06), EU770216.1, EU770217.1 (same with H11), EU770218.1, EU770219.1, and EU770220.1 (GenBank accession number) of the <span class="html-italic">Pi-ta</span> haplotypes were obtained from GenBank. White color indicates the susceptibility alleles of <span class="html-italic">Pi-ta</span> gene, and yellow color indicates the resistance alleles of <span class="html-italic">Pita</span> gene. A to E, 5 major haplotypes of <span class="html-italic">Pi-ta</span> in Yunnan Province of China, are shaded.</p>
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13 pages, 3107 KiB  
Article
A Novel SPOTTED LEAF1-1 (SPL11-1) Gene Confers Resistance to Rice Blast and Bacterial Leaf Blight Diseases in Rice (Oryza sativa L.)
by Shaojun Lin, Niqing He, Zhaoping Cheng, Fenghuang Huang, Mingmin Wang, Nora M. Al Aboud, Salah F. Abou-Elwafa and Dewei Yang
Agronomy 2024, 14(10), 2240; https://doi.org/10.3390/agronomy14102240 - 28 Sep 2024
Viewed by 412
Abstract
Programmed cell death (PCD) plays critical roles in plant immunity but must be regulated to prevent excessive damage. In this study, a novel spotted leaf (spl11-1) mutant was identified from an ethyl methane sulfonate (EMS) population. The SPL11-1 gene was genetically [...] Read more.
Programmed cell death (PCD) plays critical roles in plant immunity but must be regulated to prevent excessive damage. In this study, a novel spotted leaf (spl11-1) mutant was identified from an ethyl methane sulfonate (EMS) population. The SPL11-1 gene was genetically mapped to chromosome 12 between the Indel12-37 and Indel12-39 molecular markers, which harbor a genomic region of 27 kb. Annotation of the SPL11-1 genomic region revealed the presence of two candidate genes. Through gene prediction and cDNA sequencing, it was confirmed that the target gene in the spl11-1 mutant is allelic to the rice SPOTTED LEAF (SPL11), hereafter referred to as spl11-1. Sequence analysis of SPL11 revealed a single bp deletion (T) between the spl11-1 mutant and the ‘Shuangkang77009’ wild type. Moreover, protein structure analysis showed that the structural differences between the SPL11-1 and SPL11 proteins might lead to a change in the function of the SPL11 protein. Compared to the ‘Shuangkang77009’ wild type, the spl11-1 mutant showed more disease resistance. The agronomical evaluation showed that the spl11-1 mutant showed more adverse traits. Through further mutagenesis treatment, we obtained the spl11-2 mutant allelic to spl11-1, which has excellent agronomic traits and more improvement and may have certain breeding prospects in future breeding for disease resistance. Full article
(This article belongs to the Special Issue New Insights into Pest and Disease Control in Rice)
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Figure 1
<p>The <span class="html-italic">spl11-1</span> mutant showed brown necrotic spots on leaves. Under field planting conditions, during the tillering stage, the <span class="html-italic">spl11-1</span> mutant exhibited obvious brown necrotic spots on the leaves, whereas ‘Shuangkang77009’ did not.</p>
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<p>Main agronomic characteristics between the <span class="html-italic">spl11-1</span> mutant, <span class="html-italic">spl11-2</span> mutant, and ‘Shuangkang77009’. (<b>a</b>–<b>j</b>) indicate the differences in heading date, plant height, panicle length, number of effective panicles, spikelets per panicle, seed setting rate, grain length, grain width, 1000-grain weight, and yield per plant, respectively, between ‘Shuangkang77009’, the <span class="html-italic">spl11-1</span> mutant, and the <span class="html-italic">spl11-2</span> mutant. These data are detailed in <a href="#app1-agronomy-14-02240" class="html-app">Supplementary Table S1</a>. Taking ‘Shuangkang77009’ as the control, ** indicates <span class="html-italic">p</span> ≤ 0.01, * indicates <span class="html-italic">p</span> ≤ 0.05, and NS indicates no significant difference.</p>
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<p>The <span class="html-italic">spl11-1</span> mutant showed high resistance to bacterial blight. Using the bacterial blight caused by <span class="html-italic">Xanthomonas oryzae</span> strain <span class="html-italic">PXO99</span>, the resistance levels of the <span class="html-italic">spl11-1</span> mutant and ‘Shuangkang77009’ were identified. The <span class="html-italic">spl11-1</span> mutant exhibited high resistance to bacterial blight, while the wild-type ‘Shuangkang77009’ showed high susceptibility to bacterial blight.</p>
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<p>Fine mapping of the <span class="html-italic">spl11-1</span> gene. (<b>a</b>) Preliminary gene mapping of <span class="html-italic">spl11-1</span>. <span class="html-italic">spl11-1</span> localized between the markers RM4125 and RM235. (<b>b</b>) Intermediate mapping of <span class="html-italic">spl11-1</span>. <span class="html-italic">spl11-1</span> narrowed down between the markers Indel12-10 and Indel12-13. (<b>c</b>) Detailed mapping of <span class="html-italic">spl11-1</span>. <span class="html-italic">spl11-1</span> precisely mapped between the markers Indel12-28 and Indel12-30. (<b>d</b>) High-resolution mapping of <span class="html-italic">spl11-1</span>. The <span class="html-italic">spl11-1</span> gene was eventually mapped to a 27 kb region. (<b>e</b>) The 27kb genomic region contains two candidate genes, <span class="html-italic">LOC_Os12g38210</span> and <span class="html-italic">LOC_Os12g38220</span>.</p>
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<p>Sequence comparison between <span class="html-italic">spl11-1</span>, <span class="html-italic">spl11-2,</span> and <span class="html-italic">spl11</span>. There was only a 1 bp deletion (T) between the <span class="html-italic">spl11-1</span> mutant (<span class="html-italic">spl11-1</span>) and ‘Shuangkang77009’ (<span class="html-italic">SPL11</span>) of <span class="html-italic">LOC_Os12g38210</span>. The genotype of <span class="html-italic">spl11-2</span> was the same as that of <span class="html-italic">spl11-1</span>.</p>
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<p>The structure comparison between SPL11 and spl11-1. The 3D structural diagrams of the SPL11 and spl11-1 proteins were drawn using PyMol-2.5.7, showing significant changes in structures except for the same structure in the red square area.</p>
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17 pages, 5705 KiB  
Article
Improvement of Quality and Disease Resistance for a Heavy-Panicle Hybrid Restorer Line, R600, in Rice (Oryza sativa L.) by Gene Pyramiding Breeding
by Haipeng Wang, Gen Wang, Rui Qin, Chengqin Gong, Dan Zhou, Deke Li, Binjiu Luo, Jinghua Jin, Qiming Deng, Shiquan Wang, Jun Zhu, Ting Zou, Shuangcheng Li, Yueyang Liang and Ping Li
Curr. Issues Mol. Biol. 2024, 46(10), 10762-10778; https://doi.org/10.3390/cimb46100639 - 25 Sep 2024
Viewed by 281
Abstract
The utilization of heavy-panicle hybrid rice exemplifies the successful integration of architectural enhancement and heterosis, which has been widely adopted in the southwest rice-producing area of China. Iterative improvement in disease resistance and grain quality of heavy-panicle hybrid rice varieties is crucial to [...] Read more.
The utilization of heavy-panicle hybrid rice exemplifies the successful integration of architectural enhancement and heterosis, which has been widely adopted in the southwest rice-producing area of China. Iterative improvement in disease resistance and grain quality of heavy-panicle hybrid rice varieties is crucial to promote their sustainable utilization. Here, we performed a molecular design breeding strategy to introgress beneficial alleles of broad-spectrum disease resistance and grain quality into a heavy-panicle hybrid backbone restorer line Shuhui 600 (R600). We successfully developed introgression lines through marker-assisted selection to pyramid major genes (Wxb + ALKA-GC + Pigm + Xa23) derived from three parents (Huanghuazhan, I135, I488), which significantly enhance grain quality and confer resistance to rice blast and bacterial blight (BB). The improved parental R600 line (iR600) exhibited superior grain quality and elevated disease resistance while maintaining the heavy-panicle architecture and high-yield capacity of R600. Moreover, the iR600 was crossed with male sterility line 608A to obtain a new heavy-panicle hybrid rice variety with excellent eating and cooking quality (ECQ) and high yield potential. This study presents an effective breeding strategy for rice breeders to expedite the improvement of grain quality and disease resistance in heavy-panicle hybrid rice. Full article
(This article belongs to the Section Molecular Plant Sciences)
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<p>Co-improvement of high quality and disease resistance in R600. R600 was selected as a recurrent parent; I135, I488, and HHZ were chosen as donor parents. The schedule shows the breeding procedure for crossing and backcrossing. To pyramid four target genes in one iR600 line, several successive backcrossing processes were performed, and the backcrossing population was screened to select the desirable individuals. The three digits within the bracket indicate the screening parameters for each backcrossing population, representing the number of individuals evaluated (the first digit), the targeted gene numbers (the second digit), and the selected individuals for backcrossing (the third digit).</p>
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<p>Molecular marker-assisted selection in this study. (<b>a</b>) Polymorphism analysis of <span class="html-italic">Pigm</span> among recurrent parent R600, donor parent I135, and improved line iR600. The double bands indicated the presence of the <span class="html-italic">Pigm</span> locus from the donor parent I135. (<b>b</b>) Polymorphism analysis of <span class="html-italic">Xa23</span> among R600, I488, and iR600. The band genotype of <span class="html-italic">Xa23</span> in I488 and iR600 was significantly smaller than that of R600. (<b>c</b>,<b>d</b>) KASP genotyping results of <span class="html-italic">Wx</span> and <span class="html-italic">ALK</span>. The blue circle represents the homozygous allele derived from the donor parent HHZ, while the purple circle signifies heterozygosity, and the red circle denotes alleles originating from R600.</p>
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<p>Graphical genotype maps of iR600. The green bars represent the chromosome fragments derived from R600. The red lines represent chromosome fragments derived from donor parents. The black dots indicate the positions of <span class="html-italic">Wx<sup>b</sup></span> and <span class="html-italic">ALK<sup>A-GC</sup></span> genes from the donor parent of HHZ. The blue dot indicates the position of the <span class="html-italic">Pigm</span> gene from the donor parent of I135. The yellow dot indicates the position of the <span class="html-italic">Xa23</span> gene from the donor parent of I488.</p>
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<p>Analysis of grain appearance quality in improved lines. (<b>a</b>) The appearance of head rice. Scale bar, 1 cm. (<b>b</b>) HD, analysis of head rice (<span class="html-italic">n</span> = 3). (<b>c</b>) CGP, analysis of chalky grain percentage (<span class="html-italic">n</span> = 3). (<b>d</b>) CGG, analysis of chalky grain grade (<span class="html-italic">n</span> = 3). (<b>e</b>) LWR, analysis of length–width ratio (<span class="html-italic">n</span> = 10). (<b>f</b>) AC, analysis of amylose content (<span class="html-italic">n</span> = 3). (<b>g</b>) GC, analysis of gel consistency (<span class="html-italic">n</span> = 3). (<b>h</b>) ASV, analysis of alkali spreading value (<span class="html-italic">n</span> = 3). (<b>i</b>) CTS, analysis of comprehensive taste score (<span class="html-italic">n</span> = 3). (<b>j</b>) AS, analysis of appearance score (<span class="html-italic">n</span> = 3). (<b>k</b>) TS, analysis of taste score (<span class="html-italic">n</span> = 3). (<b>l</b>) Analysis of hardness (<span class="html-italic">n</span> = 3). (<b>m</b>) Analysis of viscosity (<span class="html-italic">n</span> = 3). The significant comparison object is R600. A two−tailed Student’s t-test was used to generate <span class="html-italic">p</span>-values. ** indicate a significant difference at <span class="html-italic">p</span> &lt; 0.01; Values are means ± SD. Error bars represent SDs.</p>
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<p>The RVA characteristic curves of improved lines. (<b>a</b>) The RVA characteristic curves. (<b>b</b>) GT, analysis of gelatinization temperature (<span class="html-italic">n</span> = 3). (<b>c</b>) HPT, analysis of hot paste viscosity (<span class="html-italic">n</span> = 3). (<b>d</b>) CPT, analysis of cool paste viscosity (<span class="html-italic">n</span> = 3). (<b>e</b>) BV, analysis of breakdown values (<span class="html-italic">n</span> = 3). (<b>f</b>) SV, analysis of setback values (<span class="html-italic">n</span> = 3). (<b>g</b>) CV, analysis of consistency values (<span class="html-italic">n</span> = 3). The significant comparison object is R600. A two−tailed Student’s t-test was used to generate <span class="html-italic">p</span>-values. ** indicate a significant difference at <span class="html-italic">p</span> &lt; 0.01. Values are means ± SD. Error bars represent SDs.</p>
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<p>Evaluation and analysis of disease resistance of improved lines. (<b>a</b>) Rice blast is naturally induced. (<b>b</b>) Incidence of leaf blast. Scale bar, 1 cm. (<b>c</b>) Disease analysis of rice blast (<span class="html-italic">n</span> = 3). (<b>d</b>) Bacterial blight inoculation. (<b>e</b>) Incidence of bacterial blight. Scale bar, 1 cm. (<b>f</b>) Analysis of leaf blight spot length (<span class="html-italic">n</span> = 10). The significant comparison object is R600. The red arrow represents the inoculated leaves. A two−tailed Student’s <span class="html-italic">t</span>-test was used to generate <span class="html-italic">p</span>-values. ** indicate a significant difference at <span class="html-italic">p</span> &lt; 0.01. Values are means ± SD. Error bars represent SDs.</p>
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<p>Evaluation of main agronomic characters in improved lines. (<b>a</b>) Main panicles. Scale bar, 10 cm. (<b>b</b>) Plant morphology. Scale bar, 20 cm. (<b>c</b>) YP, yield per plant (<span class="html-italic">n</span> = 10). (<b>d</b>) TN, tiller number (<span class="html-italic">n</span> = 10). (<b>e</b>) PH, plant height (<span class="html-italic">n</span> = 10). (<b>f</b>) SGP, spike grain per panicle (<span class="html-italic">n</span> = 10). (<b>g</b>) SR, setting rate (<span class="html-italic">n</span> = 10). (<b>h</b>) SL, spike length (<span class="html-italic">n</span> = 10). (<b>i</b>) PB, primary branches (<span class="html-italic">n</span> = 10). (<b>j</b>) SD, spikelet density (<span class="html-italic">n</span> = 10). (<b>k</b>) 1000-grain weight (<span class="html-italic">n</span> = 10). The significant comparison object is R600. A two−tailed Student’s <span class="html-italic">t</span>-test was used to generate <span class="html-italic">p</span>-values. * and ** indicate a significant difference at <span class="html-italic">p</span> &lt; 0.05 and 0.01. Values are means ± SD. Error bars represent SDs.</p>
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<p>Analysis of rice quality in hybrid combinations. (<b>a</b>) Whole-milled rice appearance of 608A/R600. Scale bar, 1 cm. (<b>b</b>) Whole-milled rice appearance of 608A/iR600. Scale bar, 1 cm. (<b>c</b>) CGP, chalky grain percentage of hybrid combinations (<span class="html-italic">n</span> = 3). (<b>d</b>) CGG, chalky grain grade of hybrid combinations (<span class="html-italic">n</span> = 3). (<b>e</b>) CTS, comprehensive taste score of hybrid combinations (<span class="html-italic">n</span> = 3). (<b>f</b>) AC, amylose content of hybrid combinations (<span class="html-italic">n</span> = 3). (<b>g</b>) GC, gel consistency of hybrid combinations (<span class="html-italic">n</span> = 3). (<b>h</b>) ASV, alkali spreading value of hybrid combinations (<span class="html-italic">n</span> = 3). The significant comparison objects are the cross combinations of R600 corresponding to male sterile line. A two-tailed Student’s <span class="html-italic">t</span>-test was used to generate <span class="html-italic">p</span>-values. ** indicate a significant difference at <span class="html-italic">p</span> &lt; 0.01. Values are means ± SD. Error bars represent SDs.</p>
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<p>Major agronomic phenotypes of hybrid combinations. (<b>a</b>–<b>c</b>) Field growth of hybrid combinations. (<b>d</b>) Yield of hybrid combination (<span class="html-italic">n</span> = 3). (<b>e</b>) Plant height of hybrid combination (<span class="html-italic">n</span> = 10). (<b>f</b>) Tiller number of hybrid combinations (<span class="html-italic">n</span> = 10). Values are means ± SD. Error bars represent SDs. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> ≤ 0.05; one−way ANOVA).</p>
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11 pages, 2538 KiB  
Article
The Effects of Rice Husk Ash as Bio-Cementitious Material in Concrete
by Mays Mahmoud Alsaed and Rafal Latif Al Mufti
Constr. Mater. 2024, 4(3), 629-639; https://doi.org/10.3390/constrmater4030034 - 23 Sep 2024
Viewed by 622
Abstract
Concrete is one of the most commonly used materials in civil engineering construction, and it continues to have increased production. This puts pressure on the consumption of its constituent materials, including Portland cement and aggregates. There are environmental consequences related to the increased [...] Read more.
Concrete is one of the most commonly used materials in civil engineering construction, and it continues to have increased production. This puts pressure on the consumption of its constituent materials, including Portland cement and aggregates. There are environmental consequences related to the increased emission of CO2 that are associated with the production process of Portland cement. This has led to the development and use of alternative cementitious materials, mainly in the form of condensed silica fume, pulverised fuel ash, and ground granulated blast furnace slag. All of these are by-products of the silicon, electrical power generation, and iron production industries, respectively. In recent years, attention has turned to the possible use of sustainable bio-waste materials that might contribute to the replacement of Portland cement in concrete. This research investigates the effects of using rice husk ash as cement replacement material on the 1 to 28-day concrete properties, including the compressive strength, workability, and durability of concrete. The findings indicate that including rice husk ash in concrete can improve its strength at 3–28 days for percentage replacements of 5% to 20% (ranging from 2.4% to 18.7% increase) and improvements from 1 day for 20% replacement (with 11.1% increase). Any percentage replacement with rice husk ash also reduced the air permeability by 21.4% and therefore improved the durability, while there was a small reduction in the workability with increased replacement. Full article
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<p>RHA-production process [<a href="#B12-constrmater-04-00034" class="html-bibr">12</a>].</p>
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<p>Particle size distribution for rice husk ash.</p>
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<p>Pan-type mixer.</p>
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<p>Slump workability test.</p>
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<p>Effects of RHA replacement on workability/consistency of concrete.</p>
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<p>The compressive strength of the five concrete mixes with age.</p>
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<p>The variation in concrete density with percentage of RHA.</p>
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14 pages, 8796 KiB  
Article
MoHG1 Regulates Fungal Development and Virulence in Magnaporthe oryzae
by Xin Pu, Aijia Lin, Chun Wang, Sauban Musa Jibril, Xinyun Yang, Kexin Yang, Chengyun Li and Yi Wang
J. Fungi 2024, 10(9), 663; https://doi.org/10.3390/jof10090663 - 21 Sep 2024
Viewed by 675
Abstract
Magnaporthe oryzae causes rice blast disease, which threatens global rice production. The interaction between M. oryzae and rice is regarded as a classic model for studying the relationship between the pathogen and the host. In this study, we found a gene, MoHG1, [...] Read more.
Magnaporthe oryzae causes rice blast disease, which threatens global rice production. The interaction between M. oryzae and rice is regarded as a classic model for studying the relationship between the pathogen and the host. In this study, we found a gene, MoHG1, regulating fungal development and virulence in M. oryzae. The ∆Mohg1 mutants showed more sensitivity to cell wall integrity stressors and their cell wall is more easily degraded by enzymes. Moreover, a decreased content of chitin but higher contents of arabinose, sorbitol, lactose, rhamnose, and xylitol were found in the ∆Mohg1 mutant. Combined with transcriptomic results, many genes in MAPK and sugar metabolism pathways are significantly regulated in the ∆Mohg1 mutant. A hexokinase gene, MGG_00623 was downregulated in ∆Mohg1, according to transcriptome results. We overexpressed MGG_00623 in a ∆Mohg1 mutant. The results showed that fungal growth and chitin contents in MGG_00623-overexpressing strains were restored significantly compared to the ∆Mohg1 mutant. Furthermore, MoHG1 could interact with MGG_00623 directly through the yeast two-hybrid and BiFC. Overall, these results suggest that MoHG1 coordinating with hexokinase regulates fungal development and virulence by affecting chitin contents and cell wall integrity in M. oryzae, which provides a reference for studying the functions of MoHG1-like genes. Full article
(This article belongs to the Section Fungal Pathogenesis and Disease Control)
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<p><span class="html-italic">MoHG1</span> influences the fungal development. (<b>A</b>) The amino acid sequence alignment between MoHG1 and MGG_14388. (<b>B</b>) Phylogenetic analyses of MoHG1 homologous sequences in different host-infecting strains. (<b>C</b>) Colonic phenotypes of ∆<span class="html-italic">Mohg1</span> at CM and MM plates. (<b>D</b>–<b>H</b>) The diameter of the colony, dry weight, spore production, spore germination, and appressorium formation. Each experiment was conducted with 3 biological repeats and statistically significant differences were calculated by Student’s <span class="html-italic">t</span>-test, ** <span class="html-italic">p</span> &lt; 0.01. Error bars represent the means ± SD.</p>
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<p><span class="html-italic">MoHG1</span> regulates fungal cell wall integrity in <span class="html-italic">M. oryzae</span>. (<b>A</b>,<b>B</b>) ∆<span class="html-italic">Mohg1</span> mutants show more sensitivity to CR (600 μg/mL), SDS (100 μg/mL), and CFW (4 μg/mL). (<b>C</b>,<b>D</b>) ∆<span class="html-italic">Mohg1</span> mutants show more sensitivity to sorbitol (1 mol/L), KCl (0.7 mol/L), and NaCl (0.7 mol/L). (<b>E</b>,<b>F</b>) The released protoplast in WT and ∆<span class="html-italic">Mohg1</span> mutants. Each experiment was conducted with 3 biological repeats and statistically significant differences were calculated by Student’s <span class="html-italic">t</span>-test, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01. Error bars represent the means ± SD. (<b>G</b>) The fungal cell wall staining in ∆<span class="html-italic">Mohg1</span> and WT.</p>
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<p><span class="html-italic">MoHG1</span> plays an essential role in pathogenicity. (<b>A</b>,<b>B</b>) The pathogenicity of ∆<span class="html-italic">Mohg1</span> mutants on rice. (<b>C</b>–<b>G</b>) The expressions of basal defense genes in rice inoculated by ∆<span class="html-italic">Mohg1</span> and WT. (<b>H</b>) The fluorescent signal of MoHG1-GFP in <span class="html-italic">M. oryzae</span> during infection. Each experiment was conducted with 3 biological repeats and statistically significant differences were calculated by Student’s <span class="html-italic">t</span>-test, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01. Error bars represent the means ± SD.</p>
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<p>Transcriptome analysis between WT and ∆<span class="html-italic">Mohg1</span>. (<b>A</b>) The volcano plot of DEGs in ∆<span class="html-italic">Mohg1</span>. GO enrichment and KEGG pathway analysis of downregulated (<b>B</b>) and upregulated (<b>C</b>) genes in ∆<span class="html-italic">Mohg1</span>. The DEGs involving glycerol synthesis (<b>D</b>), synthesis pentose (<b>E</b>), and MAPK pathway (<b>F</b>) in <span class="html-italic">M. oryzae</span>. The box background in green or red means the decrease or increase of gene expression according to the transcriptome, respectively.</p>
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<p>The carbohydrate contents in ∆<span class="html-italic">Mohg1</span>. (<b>A</b>–<b>H</b>) The content of 8 carbohydrates. Each experiment was conducted with 3 biological repeats and statistically significant differences were calculated by Student’s <span class="html-italic">t</span>-test, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01. Error bars represent the means ± SD.</p>
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<p>Overexpressing of <span class="html-italic">MGG_00623</span> in the ∆<span class="html-italic">Mohg1</span> mutant restored the fungal growth and chitin contents. (<b>A</b>) The relative expressions of <span class="html-italic">MGG_00623</span> in ∆<span class="html-italic">Mohg1</span>. Each experiment was conducted with 3 biological repeats and statistically significant differences were calculated by Student’s <span class="html-italic">t</span>-test, ** <span class="html-italic">p</span> &lt; 0.01. (<b>B</b>,<b>C</b>) Overexpression of <span class="html-italic">MGG_00623</span> in ∆<span class="html-italic">Mohg1</span> partially restored the fungal growth. Each experiment was conducted in 3 biological repeats. The different letters above each bar graph indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) calculated by ANOVA and Duncan’s test. Error bars represent the means ± SD. (<b>D</b>,<b>E</b>) Overexpression of <span class="html-italic">MGG_00623</span> in ∆<span class="html-italic">Mohg1</span> restored CWI staining and chitin contents. The scale bar represents 25 μm. The different letters above each bar graph indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) calculated by ANOVA and Duncan’s test. Error bars represent the means ± SD. (<b>F</b>) Yeast two-hybrid and (<b>G</b>) BiFC assays show MoHG1 interacts with MGG_00623. The scale bar represents 20 μm.</p>
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17 pages, 7634 KiB  
Article
Rice Varieties Intercropping Induced Soil Metabolic and Microbial Recruiting to Enhance the Rice Blast (Magnaporthe Oryzae) Resistance
by Xiao-Qiao Zhu, Mei Li, Rong-Ping Li, Wen-Qiang Tang, Yun-Yue Wang, Xiao Fei, Ping He and Guang-Yu Han
Metabolites 2024, 14(9), 507; https://doi.org/10.3390/metabo14090507 - 20 Sep 2024
Viewed by 577
Abstract
[Background] Intercropping is considered an effective approach to defending rice disease. [Objectives/Methods] This study aimed to explore the resistance mechanism of rice intraspecific intercropping by investigating soil metabolites and their regulation on the rhizosphere soil microbial community using metabolomic and microbiome analyses. [Results] [...] Read more.
[Background] Intercropping is considered an effective approach to defending rice disease. [Objectives/Methods] This study aimed to explore the resistance mechanism of rice intraspecific intercropping by investigating soil metabolites and their regulation on the rhizosphere soil microbial community using metabolomic and microbiome analyses. [Results] The results showed that the panicle blast disease occurrence of the resistant variety Shanyou63 (SY63) and the susceptible variety Huangkenuo (HKN) were both decreased in the intercropping compared to monoculture. Notably, HKN in the intercropping system exhibited significantly decreased disease incidence and increased disease resistance-related enzyme protease activity. KEGG annotation from soil metabolomics analysis revealed that phenylalanine metabolic pathway, phenylalanine, tyrosine, and tryptophan biosynthesis pathway, and fructose and mannose metabolic pathway were the key pathways related to rice disease resistance. Soil microbiome analysis indicated that the bacterial genera Nocardioides, Marmoricola, Luedemannella, and Desulfomonile were significantly enriched in HKN after intercropping, while SY63 experienced a substantial accumulation of Ruminiclostridium and Cellulomonas. Omics-based correlation analysis highlighted that the community assembly of Cellulomonas and Desulfomonile significantly affected the content of the metabolites D-sorbitol, D-mannitol, quinic acid, which further proved that quinic acid had a significantly inhibitory effect on the mycelium growth of Magnaporthe oryzae, and these three metabolites had a significant blast control effect. The optimal rice blast-control efficiency on HKN was 51.72%, and Lijiangxintuanheigu (LTH) was 64.57%. [Conclusions] These findings provide a theoretical basis for rice varieties intercropping and sustainable rice production, emphasizing the novelty of the study in elucidating the underlying mechanisms of intercropping-mediated disease resistance. Full article
(This article belongs to the Section Microbiology and Ecological Metabolomics)
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<p>Disease investigation and associated enzyme assay. (<b>A</b>) Field image of rice intercropping of Shanyou63 (SY63) and Huangkenuo (HKN). (<b>B</b>) Field image of rice monoculture of SY63 and HKN. (<b>C</b>) The disease index on rice blast of HKN and SY63 under monoculture and intercropping patterns. (<b>D</b>) The incidence rate on rice blast of HKN and SY63 under monoculture and intercropping patterns. (<b>E</b>) The protease activity of HKN and SY63 under monoculture and intercropping patterns. (<b>F</b>) The nitrate reductase activity of HKN and SY63 under monoculture and intercropping patterns. (<b>G</b>) The urease activity of HKN and SY63 under monoculture and intercropping patterns. Mono-HKN indicates rice susceptible variety HKN in the monoculture planting pattern. Inter-HKN indicates rice susceptible variety HKN in the intercropping planting pattern. Mono-SY63 indicates rice-resistant variety SY63 in the monoculture planting pattern. Inter-SY63 indicates rice-resistant variety SY63 in the intercropping planting pattern. Each column represented the average value of twelve independent experiment replicates, and the standard error was represented by the error bars. Letters above the column indicate the significant differences at <span class="html-italic">p</span> &lt; 0.05 according to the ANOVA and Tukey’s HSD.</p>
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<p>Soil metabolites and principal component analysis. (<b>A</b>) PCA of mass spectrometry data of each group of samples and quality control samples. X axis represents the first principal component, and Y axis represents the second principal component. (<b>B</b>) Identified metabolite’s types and proportion of two different rice varieties. (<b>C</b>) PCA loading plot of soil metabolites of Mono-HKN and Inter-HKN. (<b>D</b>) PCA loading plot of soil metabolites of Mono-SY63 and Inter-SY63. Inter-HKN indicates rice susceptible variety HKN in the intercropping planting pattern. Mono-SY63 indicates rice-resistant variety SY63 in the monoculture planting pattern. Inter-SY63 indicates rice-resistant variety SY63 in the intercropping planting pattern.</p>
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<p>The differential metabolites and metabolic pathways enriched by HKN and SY63 under different planting patterns. (<b>A</b>) The volcanic plot of differential metabolites of Mono-HKN and Inter-HKN. (<b>B</b>) The volcanic plot of differential metabolites of Mono-SY63 and Inter-SY63. (<b>C</b>) The bubble plot of differential metabolic pathways of Mono-HKN and Inter-HKN. (<b>D</b>) The bubble plot of differential metabolic pathways of Mono-SY63 and Inter-SY63. Mono-HKN indicates rice susceptible variety HKN in the monoculture planting pattern. Inter-HKN indicates rice susceptible variety HKN in the intercropping planting pattern. Mono-SY63 indicates rice-resistant variety SY63 in the monoculture planting pattern. Inter-SY63 indicates rice-resistant variety SY63 in the intercropping planting pattern.</p>
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<p>Differential bacterial community of Shanyou63 (SY63) and Huangkenuo (HKN) in intercropping and monoculture. (<b>A</b>) Principal component analysis of bacterial communities in HKN under different planting patterns. (<b>B</b>) Principal component analysis of bacterial communities in SY63 under different planting patterns. (<b>C</b>) Significant differential bacteria genus in Inter-HKN vs. Mono-HKN. (<b>D</b>) Significant differential bacteria genus in Inter-SY63 vs. Mono-SY63. Mono-HKN indicates rice susceptible variety HKN in the monoculture planting pattern. Inter-HKN indicates rice susceptible variety HKN in the intercropping planting pattern. Mono-SY63 indicates rice-resistant variety SY63 in the monoculture planting pattern. Inter-SY63 indicates rice-resistant variety SY63 in the intercropping planting pattern.</p>
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<p>The correlation heat map of soil metabolites and rhizosphere bacterial genus. Asterisk (*) indicates the significance level of the correlation at <span class="html-italic">p</span> &lt; 0.05. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The control effect of metabolites on rice blast of plate-antagonistic assay in vitro. (<b>A</b>) The plate-antagonistic graphic of D-sorbitol, D-mannitol, and quinic acid. The text below the plates indicates the corresponding metabolite concentration. (<b>B</b>) The pathogen mycelium diameter in the sorbitol-contained PDA plate. (<b>C</b>) The pathogen mycelium diameter in the mannitol-contained PDA plate. (<b>D</b>) The pathogen mycelium diameter in the quinic-acid-contained PDA plate. Each column represented the average value of three independent experiment replicates, and the standard error was represented by the error bars. Letters above the column indicate the significant differences at <span class="html-italic">p</span> &lt; 0.05 according to the ANOVA and Tukey’s HSD.</p>
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<p>The control effect of metabolites on rice blast of pot experiment in vivo. (<b>A</b>) The disease symptoms of HKN after application of D-sorbitol, D-mannitol, and quinic Acid. (<b>B</b>) The disease index of HKN after application of D-sorbitol. (<b>C</b>) The disease index of HKN after application of D-mannitol. (<b>D</b>) The disease index of HKN after application of quinic Acid. (<b>E</b>) The disease symptoms of LTH after application of D-sorbitol, D-mannitol, and quinic Acid. (<b>F</b>) The disease index of LTH after application of D-sorbitol. (<b>G</b>) The disease index of LTH after application of D-mannitol. (<b>H</b>) The disease index of LTH after application of quinic acid. Letters above the column indicate the significance among the treatments at <span class="html-italic">p</span> &lt; 0.05.</p>
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20 pages, 27362 KiB  
Article
SMARTerra, a High-Resolution Decision Support System for Monitoring Plant Pests and Diseases
by Michele Fiori, Giuliano Fois, Marco Secondo Gerardi, Fabio Maggio, Carlo Milesi and Andrea Pinna
Appl. Sci. 2024, 14(18), 8275; https://doi.org/10.3390/app14188275 - 13 Sep 2024
Viewed by 488
Abstract
The prediction and monitoring of plant diseases and pests are key activities in agriculture. These activities enable growers to take preventive measures to reduce the spread of diseases and harmful insects. Consequently, they reduce crop loss, make pesticide and resource use more efficient, [...] Read more.
The prediction and monitoring of plant diseases and pests are key activities in agriculture. These activities enable growers to take preventive measures to reduce the spread of diseases and harmful insects. Consequently, they reduce crop loss, make pesticide and resource use more efficient, and preserve plant health, contributing to environmental sustainability. We illustrate the SMARTerra decision support system, which processes daily measured and predicted weather data, spatially interpolating them at high resolution across the entire Sardinia region. From these data, SMARTerra generates risk predictions for plant pests and diseases. Currently, models for predicting the risk of rice blast disease and the hatching of locust eggs are implemented in the infrastructure. The web interface of the SMARTerra platform allows users to visualize detailed risk maps and promptly take preventive measures. A simple notification system is also implemented to directly alert emergency responders. Model outputs by the SMARTerra infrastructure are comparable with results from in-field observations produced by the LAORE Regional Agency. The infrastructure provides a database for storing the time series and risk maps generated, which can be used by agencies and researchers to conduct further analysis. Full article
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<p>A schematic description of the back-end and front-end of the SMARTerra decision support system.</p>
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<p>The digital elevation model (DEM) of Sardinia, with the island’s main rice-growing areas (<b>left</b>). The DEM was obtained by processing <math display="inline"><semantics> <mrow> <mn>10</mn> <mo> </mo> <mi mathvariant="normal">m</mi> </mrow> </semantics></math> resolution rasters downloaded from the geoportal of the region of Sardinia [<a href="#B14-applsci-14-08275" class="html-bibr">14</a>]. On the (<b>right</b>), the locations of the meteorological stations of the Regional Meteorological Network (RUR) are shown in yellow, and the nodes of the grid points for which the BOLAM model provides weather forecasts are shown in white.</p>
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<p>A schematic description of the InfluxDB time-series-oriented database storing the weather measurements from the RUR network and BOLAM forecasts. After preprocessing, the data are put into the database and organized into measurements and fields. Then, the data become available for the interpolation techniques by query via API.</p>
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<p>Temperature distribution for a selected geographic window at a specific day and time. Enabling the “Station” flag displays all stations (shown as blue dots) within the window. Detailed variations of the selected variable are shown for each station (dark popup), along with the relative trend of the value from the nearest BOLAM grid point (blue popup). The white dots represent the location of the 4 nodes of the BOLAM model closest to the selected station.</p>
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<p>Detail of the rice blast (“brusone”) risk map on a given day, highlighting the paddy field areas. The dark popup allows users to view specific information about the selected parcel, including the name of the farm, technical features like area, the rice cultivar, and other relevant details.</p>
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<p>Daily maximum temperature (<b>left</b>) and daily rainfall accumulation (<b>right</b>) spatially interpolated from measured data with the KED technique.</p>
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<p>Thumbnails from the PDF report. From (<b>top left</b>) to (<b>bottom right</b>), the hourly mean temperature, mean relative humidity and rainfall from the measured and forecast data, the daily maximum and mean temperature and rainfall from the measured data, the risk indices and alert levels for the rice blast disease, and the threshold dates and accumulation totals for the locust egg hatching prediction.</p>
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<p>Risk indices (<b>top</b>, <b>bottom left</b>) and alert levels (<b>bottom right</b>) maps for the rice blast disease obtained from interpolated measured and forecast weather data. See <a href="#sec2dot2dot5-applsci-14-08275" class="html-sec">Section 2.2.5</a> for details.</p>
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<p>The cumulative sum of degree days (<b>left</b>), starting for each pixel of the map once the rain accumulation threshold <math display="inline"><semantics> <mrow> <msub> <mi>R</mi> <mi>th</mi> </msub> <mo>=</mo> <mn>100</mn> <mo> </mo> <mrow> <mi mathvariant="normal">m</mi> <mi mathvariant="normal">m</mi> </mrow> </mrow> </semantics></math> has been reached, and the predicted dates for locust egg hatching (<b>right</b>). The white areas indicate regions where the summation of <math display="inline"><semantics> <mrow> <msub> <mi>D</mi> <mi>th</mi> </msub> <mo>=</mo> <mn>200</mn> <mo> </mo> <mrow> <mo>°</mo> <mi mathvariant="normal">C</mi> </mrow> </mrow> </semantics></math> degree days has not yet occurred. Compare with the former map, where the darkest red areas correspond to regions where the summation of degree days is below the threshold <math display="inline"><semantics> <msub> <mi>D</mi> <mi>th</mi> </msub> </semantics></math>. See <a href="#sec2dot2dot6-applsci-14-08275" class="html-sec">Section 2.2.6</a> for details.</p>
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<p>Comparison of observed and predicted alert levels for rice blast disease in the Oristano rice districts. Observed (<b>top left</b>) and predicted (<b>top right</b>) alert levels for 17 July 2023. Observed (<b>bottom left</b>) and predicted (<b>bottom right</b>) alert levels for 18 July 2023.</p>
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<p>Spatial distribution of <math display="inline"><semantics> <msub> <mo>Δ</mo> <mi>d</mi> </msub> </semantics></math> for egg hatching predicted by the default (literature) model (<b>left</b>) and a slightly modified model (<b>right</b>), both with a superimposed OpenStreetMap layer (<b>top</b>), a map of the dates for <math display="inline"><semantics> <msub> <mi>day</mi> <mn>2</mn> </msub> </semantics></math> when the rain threshold <math display="inline"><semantics> <msub> <mi>R</mi> <mi>th</mi> </msub> </semantics></math> is reached and the accumulation of degree days starts (<b>middle</b>), and a map representing <math display="inline"><semantics> <msub> <mi>day</mi> <mn>3</mn> </msub> </semantics></math>, the predicted dates of the hatching of locust eggs (<b>bottom</b>). The region of interest is partitioned into hexagons, each of which is assigned a color according to the average of the <math display="inline"><semantics> <msub> <mo>Δ</mo> <mi>d</mi> </msub> </semantics></math> values of the records within the area of the hexagon itself.</p>
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15 pages, 3488 KiB  
Article
Multi-Population Analysis for Leaf and Neck Blast Reveals Novel Source of Neck Blast Resistance in Rice
by Ashim Debnath, Hage Sumpi, Bharati Lap, Karma L. Bhutia, Abhilash Behera, Wricha Tyagi and Mayank Rai
Plants 2024, 13(17), 2475; https://doi.org/10.3390/plants13172475 - 4 Sep 2024
Viewed by 641
Abstract
Rice blast is one of the most devastating biotic stresses that limits rice productivity. The North Eastern Hill (NEH) region of India is considered to be one of the primary centres of diversity for both rice and pathotypes of Magnaporthe grisea. Therefore, [...] Read more.
Rice blast is one of the most devastating biotic stresses that limits rice productivity. The North Eastern Hill (NEH) region of India is considered to be one of the primary centres of diversity for both rice and pathotypes of Magnaporthe grisea. Therefore, the present study was carried out to elucidate the genetic basis of leaf and neck blast resistance under Meghalaya conditions. A set of 80 diverse genotypes (natural population) and 2 F2 populations involving resistant parent, a wildtype landrace, LR 5 (Lal Jangali) and susceptible genotypes Sambha Mahsuri SUB 1 (SMS) and LR 26 (Chakhao Poireiton) were used for association analysis of reported major gene-linked markers with leaf and neck blast resistance to identify major effective genes under local conditions. Genotyping using twenty-five gene-specific markers across diverse genotypes and F2 progenies revealed genes Pi5 and Pi54 to be associated with leaf blast resistance in all three populations. Genes Pib and qPbm showed an association with neck blast resistance in both natural and LR 5 × SMS populations. Additionally, a set of 184 genome-wide polymorphic markers (SSRs and SNPs), when applied to F2-resistant and F2-susceptible DNA bulks derived from LR 5 × LR 26, suggested that Pi20(t) on chromosome 12 is one of the major genes imparting disease resistance. Markers snpOS318, RM1337 and RM7102 and RM247 and snpOS316 were associated with leaf blast and neck blast resistance, respectively. The genotypes, markers and genes will help in marker-assisted selection and development of varieties with durable resistance. Full article
(This article belongs to the Special Issue Pre-Breeding in Crops)
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<p>Representative photos showing (<b>A</b>) leaf, nodal and neck blast symptoms in experimental plot. (<b>B</b>) Differential disease reaction for leaf blast showing disease severity on a scale from 0 to 5. (<b>C</b>) Susceptible variety (SMS) showing severe blast in the field conditions. (<b>D</b>) Variation in panicle architecture and blast symptoms in selected progenies of biparental cross (LR 5 × LR 26) as compared to parents (Chakhao Poireiton (LR 26)—susceptible; Lal Jangali (LR 5)—resistant).</p>
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<p>Frequency distribution of genotypes for leaf and neck blast. Leaf blast and neck blast score in F<sub>2</sub> progenies of two biparental populations, viz., LR 5 × LR 26 and LR 5 × SMS. X-axes represent disease severity score for leaf (0–5 scale; based on lesion length on leaves) and neck blast (percentage (%) of panicles affected by neck blast), respectively. Y-axes represent number of progenies. LR 5—Lal Jangali (resistant landrace); LR 26—Chakhao Poireiton (susceptible genotype); SMS—Sambha Mahasuri SUB1 (susceptible variety).</p>
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<p>Population structure estimation of the 43 rice lines based on SSR markers with STRUCTURE software output at K = 4. (<b>A</b>) Natural population. The serial numbers of genotypes are labelled on the x-axis (<a href="#app1-plants-13-02475" class="html-app">Table S5 (from Supplementary File)</a>), while y-axis denotes percentage ancestry. (<b>B</b>) Net nucleotide distance between clusters. (<b>C</b>) Genotypic clustering of blast resistance and susceptible pools for LR 5 × LR 26. Net nucleotide distance between four clusters computed using point estimates of P. Triangle plot showing genotypic clustering of blast resistance and susceptible pools (LR 5 × LR 26). Leaf blast—LB and neck blast—NB.</p>
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<p>Association of candidate gene-based/-linked markers with leaf blast (LB) and neck blast (NB) resistance. (<b>A</b>) Timely sown upland, (<b>B</b>) late-sown upland, (<b>C</b>) timely sown lowland conditions. The x-axis shows the candidate gene-based/-linked markers (<a href="#app1-plants-13-02475" class="html-app">Table S3 (from Supplementary File)</a>). The y-axis represents 1-<span class="html-italic">P</span>(α) value for t distribution where <span class="html-italic">P</span>(α) is the probability of type-I error. The marker bars above 0.95 on Y-axis show significant association.</p>
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<p>Markers associated with neck blast resistance and leaf blast resistance in three populations. (<b>A</b>) Map shows position of reported blast markers associated with three populations. (<b>B</b>) Summary of significant markers for LR 5 × LR 26, along with phenotypic percentage variation, explained (<span class="html-italic">R</span><sup>2</sup> values).</p>
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20 pages, 5278 KiB  
Article
Priming of Exogenous Salicylic Acid under Field Conditions Enhances Crop Yield through Resistance to Magnaporthe oryzae by Modulating Phytohormones and Antioxidant Enzymes
by Wannaporn Thepbandit, Anake Srisuwan and Dusit Athinuwat
Antioxidants 2024, 13(9), 1055; https://doi.org/10.3390/antiox13091055 - 30 Aug 2024
Viewed by 566
Abstract
This study explores the impact of exogenous salicylic acid (SA) alongside conventional treatment by farmers providing positive (Mancozeb 80 % WP) and negative (water) controls on rice plants (Oryza sativa L.), focusing on antioxidant enzyme activities, phytohormone levels, disease resistance, and yield [...] Read more.
This study explores the impact of exogenous salicylic acid (SA) alongside conventional treatment by farmers providing positive (Mancozeb 80 % WP) and negative (water) controls on rice plants (Oryza sativa L.), focusing on antioxidant enzyme activities, phytohormone levels, disease resistance, and yield components under greenhouse and field conditions. In greenhouse assays, SA application significantly enhanced the activities of peroxidase (POX), polyphenol oxidase (PPO), catalase (CAT), and superoxide dismutase (SOD) within 12–24 h post-inoculation (hpi) with Magnaporthe oryzae. Additionally, SA-treated plants showed higher levels of endogenous SA and indole-3-acetic acid (IAA) within 24 hpi compared to the controls. In terms of disease resistance, SA-treated plants exhibited a reduced severity of rice blast under greenhouse conditions, with a significant decrease in disease symptoms compared to negative control treatment. The field study was extended over three consecutive crop seasons during 2021–2023, further examining the efficacy of SA in regular agricultural practice settings. The SA treatment consistently led to a reduction in rice blast disease severity across all three seasons. Yield-related parameters such as plant height, the number of tillers and panicles per hill, grains per panicle, and 1000-grain weight all showed improvements under SA treatment compared to both positive and negative control treatments. Specifically, SA-treated plants yielded higher grain outputs in all three crop seasons, underscoring the potential of SA as a growth enhancer and as a protective agent against rice blast disease under both controlled and field conditions. These findings state the broad-spectrum benefits of SA application in rice cultivation, highlighting its role not only in bolstering plant defense mechanisms and growth under greenhouse conditions but also in enhancing yield and disease resistance in field settings across multiple crop cycles. This research presents valuable insights into the practical applications of SA in improving rice plant resilience and productivity, offering a promising approach for sustainable agriculture practices. Full article
(This article belongs to the Section ROS, RNS and RSS)
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<p>Effects of different treatments on antioxidant enzyme activity in plants at pre (0 h) and post inoculated with <span class="html-italic">Magnaporthe oryzae</span> over a 72-h period. (<b>A</b>) Peroxidase (POX) activity, (<b>B</b>) polyphenol oxidase (PPO), (<b>C</b>) catalase (CAT) activity, and (<b>D</b>) superoxide dismutase (SOD). Different letters (a, b, c, d) indicate significant differences via Duncan’s multiple range test at <span class="html-italic">p</span> ≤ 0.05. “ns” denotes non-significant differences.</p>
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<p>Effects of different treatments on endogenous salicylic acid and indole-3-acetic acid levels in plants at pre (0 h) and post inoculated with <span class="html-italic">Magnaporthe oryzae</span> over a 72-h period. (<b>A</b>) Quantification of endogenous SA content. (<b>B</b>) Quantification of IAA content. Different letters (a, b, c) indicate significant differences via Duncan’s multiple range test at <span class="html-italic">p</span> ≤ 0.05. “ns” denotes non-significant differences.</p>
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<p>The effectiveness of exogenous salicylic acid elicitors on growth parameters and yield components of rice cv. KDML 105: (<b>A</b>) plant height; (<b>B</b>) number of tillers and panicles per hill; (<b>C</b>) number of grains per panicle; (<b>D</b>) 1000-grain weight; and (<b>E</b>) yield. Data presented as the mean ± SD (n = 12). Different letters (a, b, c) signify significant differences as determined by Duncan’s multiple range test at <span class="html-italic">p</span> ≤ 0.05. “ns” denotes non-significant differences.</p>
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<p>The efficacy of exogenous salicylic acid on the severity of rice blast disease on rice KDML 105 was evaluated during the following periods: (<b>A</b>) August–November 2021, (<b>B</b>) August–November 2022, and (<b>C</b>) August–November 2023. Data are presented as the mean ± SD (n = 12). Significant differences are denoted by different letters (a, b, c) according to Duncan’s multiple range test at <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>A proposed schematic model of antioxidative enzymes and hormonal responses in plant defense against <span class="html-italic">Magnaporthe oryzae</span> after being treated with exogenous salicylic acid.</p>
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20 pages, 3140 KiB  
Article
Detection of Rice Leaf SPAD and Blast Disease Using Integrated Aerial and Ground Multiscale Canopy Reflectance Spectroscopy
by Aichen Wang, Zishan Song, Yuwen Xie, Jin Hu, Liyuan Zhang and Qingzhen Zhu
Agriculture 2024, 14(9), 1471; https://doi.org/10.3390/agriculture14091471 - 28 Aug 2024
Viewed by 781
Abstract
Rice blast disease is one of the major diseases affecting rice plant, significantly impacting both yield and quality. Current detecting methods for rice blast disease mainly rely on manual surveys in the field and laboratory tests, which are inefficient, inaccurate, and limited in [...] Read more.
Rice blast disease is one of the major diseases affecting rice plant, significantly impacting both yield and quality. Current detecting methods for rice blast disease mainly rely on manual surveys in the field and laboratory tests, which are inefficient, inaccurate, and limited in scale. Spectral and imaging technologies in the visible and near-infrared (Vis/NIR) region have been widely investigated for crop disease detection. This work explored the potential of integrating canopy reflectance spectra acquired near the ground and aerial multispectral images captured with an unmanned aerial vehicle (UAV) for estimating Soil-Plant Analysis Development (SPAD) values and detecting rice leaf blast disease in the field. Canopy reflectance spectra were preprocessed, followed by effective band selection. Different vegetation indices (VIs) were calculated from multispectral images and selected for model establishment according to their correlation with SPAD values and disease severity. The full-wavelength canopy spectra (450–850 nm) were first used for establishing SPAD inversion and blast disease classification models, demonstrating the effectiveness of Vis/NIR spectroscopy for SPAD inversion and blast disease detection. Then, selected effective bands from the canopy spectra, UAV VIs, and the fusion of the two data sources were used for establishing corresponding models. The results showed that all SPAD inversion models and disease classification models established with the integrated data performed better than corresponding models established with the single of either of the aerial and ground data sources. For SPAD inversion models, the best model based on a single data source achieved a validation determination coefficient (Rcv2) of 0.5719 and a validation root mean square error (RMSECV) of 2.8794, while after ground and aerial data fusion, these two values improved to 0.6476 and 2.6207, respectively. For blast disease classification models, the best model based on a single data source achieved an overall test accuracy of 89.01% and a Kappa coefficient of 0.86, and after data fusion, the two values improved to 96.37% and 0.95, respectively. These results indicated the significant potential of integrating canopy reflectance spectra and UAV multispectral images for detecting rice diseases in large fields. Full article
(This article belongs to the Special Issue Multi- and Hyper-Spectral Imaging Technologies for Crop Monitoring)
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<p>Experimental site map.: (<b>a</b>) Zhenjiang is in Jiangsu province.; (<b>b</b>) The experimental field is in Jurong City, Zhenjiang; (<b>c</b>–<b>f</b>) Four experimental areas and sampling plots. The disease severity is distinguished by four colors: green for level 0, yellow for level 1, orange for level 2, and red for level 3.</p>
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<p>Canopy Spectral Data Analysis. In a boxplot, the upper edge of the box and the lower edge of the box represent the 75th and 25th percentiles of the data, respectively, while the line in the middle of the box represents the median of the data. The height of the box, known as the interquartile range (IQR), reflects the concentration of the data. The whiskers extending from the box show the range of the data, typically defined as extending up to 1.5 times the IQR from the quartiles, with the dimonds outside the box as outliers. (<b>a</b>) Average canopy reflectance spectra of samples with different disease severity levels. (<b>b</b>) Boxplot of disease levels for 520–590 nm band. (<b>c</b>) Boxplot of disease levels for 730–850 nm band.</p>
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<p>Distribution of different physiological parameters of rice at various disease severity levels. The <span class="html-italic">p</span>-values indicate the probability of observing the test results under the null hypothesis, which states that all groups have the same median. In the boxplot, the diamonds outside the box are outliers. (<b>a</b>) Distribution of SPAD values. (<b>b</b>) Distribution of Ft values. (<b>c</b>) Distribution of top canopy LAI values. (<b>d</b>) Distribution of mid-canopy LAI values.</p>
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<p>Adjusted <span class="html-italic">p</span>-values for different physiological parameters of rice at various disease severity levels after Dunn’s Test. The heatmap displays the results of Dunn’s Test, showing the adjusted <span class="html-italic">p</span>-values for pairwise comparisons between different severity levels. The gray color indicates that the difference between the two groups of samples is significant, while the yellow color indicates that the difference is nonsignificant. (<b>a</b>) Adjusted <span class="html-italic">p</span>-values for SPAD values after Dunn’s Test. (<b>b</b>) Adjusted <span class="html-italic">p</span>-values for Ft values After Dunn’s Test. (<b>c</b>) Adjusted <span class="html-italic">p</span>-values for mid-canopy LAI values after Dunn’s Test.</p>
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<p>Correlation coefficients between SPAD values and different VIs for the 137 samples were calculated by Pearson correlation analysis. The higher the absolute value of the correlation coefficient, the higher the correlation between the VI and SPAD values.</p>
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<p>Correlation coefficients between disease severity level and different VIs for the 137 samples calculated by gray relational analysis. The larger the correlation coefficient, the higher the correlation between the VI and disease severity level.</p>
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<p>Regression between observed and predicted SPAD values by four representative SPAD inversion models (<b>a</b>) Raw-PLSR model. (<b>b</b>) SG-PLSR model. (<b>c</b>) SNV-BPNN model. (<b>d</b>) BC-BPNN model.) based on ground full-wavelength canopy reflectance spectrum (450–850 nm) corresponding to <a href="#agriculture-14-01471-t004" class="html-table">Table 4</a>. The red lines are the regression lines between observed and predicted SPAD values of the validation set.</p>
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<p>Regression between observed and predicted SPAD values by four representative SPAD inversion models (<b>a</b>) (Raw-CARS-SPA) + VIs-PLSR model. (<b>b</b>) (SG-CARS-SPA) + VIs-PLSR model. (<b>c</b>) (SNV-CARS-SPA) + VIs-BP model. (<b>d</b>) (BC-CARS-SPA) + VIs-BP model.) based on effective bands of ground spectra and UAV VIs corresponding to <a href="#agriculture-14-01471-t005" class="html-table">Table 5</a>. The red lines are the regression lines between observed and predicted SPAD values of the validation set.</p>
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17 pages, 15463 KiB  
Article
Research on Lightweight Rice False Smut Disease Identification Method Based on Improved YOLOv8n Model
by Lulu Yang, Fuxu Guo, Hongze Zhang, Yingli Cao and Shuai Feng
Agronomy 2024, 14(9), 1934; https://doi.org/10.3390/agronomy14091934 - 28 Aug 2024
Viewed by 391
Abstract
In order to detect rice false smut quickly and accurately, a lightweight false smut detection model, YOLOv8n-MBS, was proposed in this study. The model introduces the C2f_MSEC module to replace C2f in the backbone network for better extraction of key features of false [...] Read more.
In order to detect rice false smut quickly and accurately, a lightweight false smut detection model, YOLOv8n-MBS, was proposed in this study. The model introduces the C2f_MSEC module to replace C2f in the backbone network for better extraction of key features of false smut, enhances the feature fusion capability of the neck network for different sizes of false smut by using a weighted bidirectional feature pyramid network, and designs a group-normalized shared convolution lightweight detection head to reduce the number of parameters in the model head to achieve model lightweight. The experimental results show that YOLOv8n-MBS has an average accuracy of 93.9%, a parameter count of 1.4 M, and a model size of 3.3 MB. Compared with the SSD model, the average accuracy of the model in this study increased by 4%, the number of parameters decreased by 89.8%, and the model size decreased by 86.9%; compared with the YOLO series of YOLOv7-tiny, YOLOv5n, YOLOv5s, and YOLOv8n models, the YOLOv8n-MBS model showed outstanding performance in terms of model accuracy and model performance detection; compared to the latest YOLOv9t and YOLOv10n models, the average model accuracy increased by 2.8% and 2.2%, the number of model parameters decreased by 30% and 39.1%, and the model size decreased by 29.8% and 43.1%, respectively. This method enables more accurate and lighter-weight detection of false smut, which provides the basis for intelligent management of rice blast disease in the field and thus promotes food security. Full article
(This article belongs to the Section Pest and Disease Management)
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<p>Scientific Experiment Base of Shenyang Agricultural University.</p>
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<p>Early, mid, and late images of rice false smut.</p>
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<p>Partial Data Enhancement Picture.</p>
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<p>YOLOv8n-MBS structure diagram and C2f module structure.</p>
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<p>C2f_MSEC network structure diagram.</p>
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<p>Schematic diagram of PANet feature fusion structure; BiFPN feature fusion diagram; Improved feature fusion diagram.</p>
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<p>Structure diagram of the shared convolutional lightweight detection head.</p>
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<p>Plot of training results for different models.</p>
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<p>Plot of training results for different models.</p>
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<p>Comparison of detection results taken at the same horizontal line.</p>
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<p>Comparison of detection results taken at the same horizontal line.</p>
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<p>Comparison of detection results taken at a tilt of 30 degrees.</p>
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<p>Feature visualization heat.</p>
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<p>Effectiveness of early testing of rice false smut in 2024.</p>
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<p>Effectiveness of mid-term test for rice false smut in 2024.</p>
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15 pages, 641 KiB  
Article
Yield Performance of RD6 Glutinous Rice near Isogenic Lines Evaluated under Field Disease Infection at Northeastern Thailand
by Jirapong Yangklang, Jirawat Sanitchon, Jonaliza L. Siangliw, Tidarat Monkham, Sompong Chankaew, Meechai Siangliw, Kanyanath Sirithunya and Theerayut Toojinda
Agronomy 2024, 14(8), 1871; https://doi.org/10.3390/agronomy14081871 - 22 Aug 2024
Viewed by 460
Abstract
RD6, the most popular glutinous rice in Thailand, is high in quality but susceptible to blast and bacterial blight disease. It was thus improved for disease resistance through marker-assisted backcross selection (MAS). The objective of this study was to evaluate the performance of [...] Read more.
RD6, the most popular glutinous rice in Thailand, is high in quality but susceptible to blast and bacterial blight disease. It was thus improved for disease resistance through marker-assisted backcross selection (MAS). The objective of this study was to evaluate the performance of improved near isogenic lines. Eight RD6 rice near isogenic lines (NILs) derived from MAS were selected for evaluation with RD6, a standard susceptible check variety, as well as recurrent parent for a total of nine genotypes. The experiment was conducted during the wet season under six environments at three locations, Khon Kaen, Nong Khai, and Roi Et, which was repeated at two years from 2019 to 2020. Nine genotypes, including eight RD6 rice near isogenic lines (NILs) selected from two in-tandem breeding programs and the standard check variety RD6, were evaluated to select the high-performance new improved lines. The first group, including four NILs G1–G4, was gene pyramiding of blast and BB resistance genes, and the second group, including another four NILs G5–G8, was gene pyramiding of blast resistance and salt tolerance genes. Field disease screening was observed for all environments. Two disease occurrences, blast (leaf blast) and bacterial blight, were found during the rainy season of all environments. The NILs containing blast resistance genes were excellent in gene expression. On the other hand, the improved lines containing the xa5 gene were not highly resistant under the severe stress of bacterial blight (Nong Khai 2020). Notwithstanding, G2 was greater among the NILs for yield maintenance than the other genotypes. The agronomic traits of most NILs were the same as RD6. Interestingly, the traits of G2 were different in plant type from RD6, specifically photosensitivity and plant height. Promising rice RD6 NILs with high yield stability, good agronomic traits, and disease resistance were identified in the genotypes G1, G2, and G7. The high yield stability G1 and G7 are recommended for widespread use in rain-fed areas. The G2 is specifically recommended for use in the bacterial blight (BB) disease prone areas. Full article
(This article belongs to the Special Issue Advances in Crop Molecular Breeding and Genetics)
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<p>Rainfall (mm) per week during experimental planting of individual six environments: Khon Kaen 2019 (<b>a</b>), Nong Khai 2019 (<b>b</b>), Roi Et 2019 (<b>c</b>), Khon Kaen 2020 (<b>d</b>), Nong Khai 2020 (<b>e</b>), and Roi Et 2020 (<b>f</b>). TP = Transplant, MT/PI = Maximum tiller number/Panicle primodia initiation, FL = Flowering, M = Maturity, Blast = Blast disease screening, BB = Bacterial blight disease screening.</p>
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<p>Yield stability analysis by GGE-biplot.</p>
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17 pages, 4179 KiB  
Article
Strategy for Monitoring the Blast Incidence in Crops of Bomba Rice Variety Using Remote Sensing Data
by Alba Agenjos-Moreno, Constanza Rubio, Antonio Uris, Rubén Simeón, Belén Franch, Concha Domingo and Alberto San Bautista
Agriculture 2024, 14(8), 1385; https://doi.org/10.3390/agriculture14081385 - 16 Aug 2024
Viewed by 560
Abstract
In this paper, we investigated the monitoring and characterization of the pest Magnaporthe oryzae, known as rice blast, in the Bomba rice variety at the Albufera Natural Park, located in Valencia, Spain during the 2022 and 2023 seasons. Using reflectance data from [...] Read more.
In this paper, we investigated the monitoring and characterization of the pest Magnaporthe oryzae, known as rice blast, in the Bomba rice variety at the Albufera Natural Park, located in Valencia, Spain during the 2022 and 2023 seasons. Using reflectance data from different Sentinel-2 satellite bands, various vegetative indices were calculated for each year. Significant differences in reflectance in the visible (B4), infrared (B8), red-edge (B6 and B7), and SWIR (B11) bands were detected between healthy and unhealthy fields. Additionally, variations were observed in the vegetation indices, with RVI and IRECI standing out for their higher accuracy in identifying blast-affected plots compared to NDVI and NDRE. Early differences in band values, vegetative indices, and spectral signatures were observed between the unhealthy and healthy plots, allowing for the anticipation of control treatments, whose effectiveness relies on timely intervention. Full article
(This article belongs to the Special Issue Smart Agriculture Sensors and Monitoring Systems for Field Detection)
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<p>Location of the experiment and the study area. (<b>a</b>) Location of Valencia in Comunitat Valenciana, Spain. (<b>b</b>) Location of Albufera in the area of Valencia.</p>
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<p>Mean daily temperature (T mean) and humidity (HR meand) from March to September in the experimental area for 2022 and 2023 and optimal conditions for the development of rice blast.</p>
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<p>Phenological cycle of the <span class="html-italic">Bomba</span> variety rice crop in days after sowing.</p>
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<p>Study plots of the 2022 and 2023 seasons (red) situated at the studied area (yellow).</p>
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<p>Evolution of healthy and unhealthy plots in the 10 m spectral resolution bands: B4 (<b>A</b>) and B8-NIR (<b>B</b>) in days after sowing (DAS). Vertical bars indicate standard error interval.</p>
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<p>Evolution of B4 band of healthy and unhealthy fields over the course of a season.</p>
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<p>Evolution of the healthy and unhealthy plots in the 20 m spectral resolution bands: B6 (<b>A</b>) and B7 (<b>B</b>) in days after sowing (DAS). The vertical bars indicate standard error interval.</p>
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<p>Evolution of the VI NDVI (<b>A</b>), RVI (<b>B</b>), NDRE (<b>C</b>), and IRECI (<b>D</b>) of the healthy and unhealthy plots in DAS of the 2022 and 2023 seasons. Vertical bars indicate the standard error interval.</p>
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<p>Evolution of RVI index over the course of a season for healthy and unhealthy fields.</p>
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<p>Spectral signature at 45 DAS during the 2022 and 2023 seasons.</p>
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16 pages, 4997 KiB  
Article
Improvement of Flowering Stage in Japonica Rice Variety Jiahe212 by Using CRISPR/Cas9 System
by Dengmei He, Ran Zhou, Chenbo Huang, Yanhui Li, Zequn Peng, Dian Li, Wenjing Duan, Nuan Huang, Liyong Cao, Shihua Cheng, Xiaodeng Zhan, Lianping Sun and Shiqiang Wang
Plants 2024, 13(15), 2166; https://doi.org/10.3390/plants13152166 - 5 Aug 2024
Viewed by 743
Abstract
The flowering period of rice significantly impacts variety adaptability and yield formation. Properly shortening the reproductive period of rice varieties can expand their ecological range without significant yield reduction. Targeted genome editing, like CRISPR/Cas9, is an ideal tool to fine-tune rice growth stages [...] Read more.
The flowering period of rice significantly impacts variety adaptability and yield formation. Properly shortening the reproductive period of rice varieties can expand their ecological range without significant yield reduction. Targeted genome editing, like CRISPR/Cas9, is an ideal tool to fine-tune rice growth stages and boost yield synergistically. In this study, we developed a CRISPR/Cas9-mediated multiplex genome-editing vector containing five genes related to three traits, Hd2, Ghd7, and DTH8 (flowering-stage genes), along with the recessive rice blast resistance gene Pi21 and the aromatic gene BADH2. This vector was introduced into the high-quality japonica rice variety in Zhejiang province, Jiahe212 (JH212), resulting in 34 T0 plants with various effective mutations. Among the 17 mutant T1 lines, several displayed diverse flowering dates, but most exhibited undesirable agronomic traits. Notably, three homozygous mutant lines (JH-C15, JH-C18, and JH-C31) showed slightly earlier flowering dates without significant differences in yield-related traits compared to JH212. Through special Hyg and Cas marker selection of T2 plants, we identified seven, six, and two fragrant glutinous plants devoid of transgenic components. These single plants will serve as sib lines of JH212 and potential resources for breeding applications, including maintenance lines for indicajaponica interspecific three-line hybrid rice. In summary, our research lays the foundation for the creation of short-growth-period CMS (cytoplasmic male sterility, CMS) lines, and also provides materials and a theoretical basis for indicajaponica interspecific hybrid rice breeding with wider adaptability. Full article
(This article belongs to the Special Issue Molecular Breeding and Germplasm Improvement of Rice—2nd Edition)
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<p>Target site location data. (<b>a</b>–<b>e</b>) correspond to <span class="html-italic">Hd2</span>, <span class="html-italic">Ghd7</span>, <span class="html-italic">DTH8</span>, <span class="html-italic">Pi21</span>, and Bad<span class="html-italic">h2</span>, respectively. The letters in the red box indicate the PAM sequence.</p>
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<p>Expression vector construction procedure.</p>
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<p>PCR screening T<sub>0</sub> generation positive strains. M, 2K DNA marker; 1–34 is the test line number.</p>
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<p>The mutant genotype of the positive T<sub>1</sub> plants tested. The green letters indicate the PAM sequence; the red letters and hyphens indicate base insertions and missing bases, respectively. (<b>a</b>) The six mutation types of <span class="html-italic">Hd2</span>; (<b>b</b>) the four mutation types of <span class="html-italic">DTH8</span>; (<b>c</b>) the eight mutation types of <span class="html-italic">Ghd7</span>; (<b>d</b>) the nine mutation types of <span class="html-italic">Pi21</span>.</p>
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<p>PCR screening of T<sub>2</sub> generation mutant lines without transgenic components and the phenotype of the three selected homozygotes lines. (<b>a</b>,<b>b</b>) PCR screening of the Cas9 vector region and <span class="html-italic">Hygromycin</span> region in the single plants sampled from the three selected homozygotes lines. M, 2K DNA marker; 1–3, are negative control, distilled water, positive control, 4–16 are strains of JH-C15, 17–30 are strains of JH-C18, a31–a45 and 31–45 are strains of JH-C31. (<b>c</b>,<b>e</b>,<b>g</b>) the phenotype of JH-C15, JH-C18, and JH-C31 at flowering stage; (<b>d</b>,<b>f</b>,<b>h</b>) the phenotype of JH-C15, JH-C18, and JH-C31 at harvest stage.</p>
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<p>qPCR analysis of flowering-related genes in the selected homozygotes lines. (<b>a</b>–<b>c</b>) Relative expression levels of flowering stage related genes in the homozygous mutant lines JH-C15, JH-C18 and JH-C31, respectively.</p>
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<p>Analysis of grain shape and agronomic traits of the selected homozygotes lines. (<b>a</b>–<b>h</b>), grain appearance and shape, thousand-grain weight, length mean, width mean, length and width mean ratio, effective tiller number, and yield per plant. The data were analyzed using <span class="html-italic">t</span>-test, * and ** indicate significance at <span class="html-italic">p</span> ≤ 0.05 and <span class="html-italic">p</span> ≤ 0.01 levels, respectively. The data represent mean ± standard deviation.</p>
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13 pages, 1334 KiB  
Article
Detection and Evaluation of Blast Resistance Genes in Backbone Indica Rice Varieties from South China
by Liqun Tang, Jian Song, Yongtao Cui, Honghuan Fan and Jianjun Wang
Plants 2024, 13(15), 2134; https://doi.org/10.3390/plants13152134 - 1 Aug 2024
Viewed by 531
Abstract
Rice blast caused by the pathogenic fungus Magnaporthe oryzae poses a significant threat to rice cultivation. The identification of robust resistance germplasm is crucial for breeding resistant varieties. In this study, we employed functional molecular markers for 10 rice blast resistance genes, namely [...] Read more.
Rice blast caused by the pathogenic fungus Magnaporthe oryzae poses a significant threat to rice cultivation. The identification of robust resistance germplasm is crucial for breeding resistant varieties. In this study, we employed functional molecular markers for 10 rice blast resistance genes, namely Pi1, Pi2, Pi5, Pi9, Pia, Pid2, Pid3, Pigm, Pikh, and Pita, to assess blast resistance across 91 indica rice backbone varieties in South China. The results showed a spectrum of resistance levels ranging from highly resistant (HR) to highly susceptible (HS), with corresponding frequencies of 0, 19, 40, 27, 5, and 0, respectively. Yearly correlations in blast resistance genes among the 91 key indica rice progenitors revealed Pid2 (60.44%), Pia (50.55%), Pita (45.05%), Pi2 (32.97%), Pikh (4.4%), Pigm (2.2%), Pi9 (2.2%), and Pi1 (1.1%). Significant variations were observed in the distribution frequencies of these 10 resistance genes among these progenitors across different provinces. Furthermore, as the number of aggregated resistance genes increased, parental resistance levels correspondingly improved, though the efficacy of different gene combinations varied significantly. This study provides the initial steps toward strategically distributing varieties of resistant indica rice genotypes across South China. Full article
(This article belongs to the Special Issue Molecular Breeding and Germplasm Improvement of Rice—2nd Edition)
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<p>Distribution of blast resistance genes among backbone varieties of <span class="html-italic">indica</span> rice.</p>
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<p>Percentage and distribution of blast resistance gene combinations among backbone varieties of <span class="html-italic">indica</span> rice. (<b>a</b>) Percentage of various blast resistance gene combinations. (<b>b</b>) Spatial distribution frequency of blast resistance combination. Numbers 1–6: The number of blast resistance genes among different regions.</p>
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<p>Geographical distribution of rice blast resistance genes across different provinces.</p>
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<p>Correlation analysis of gene type with blast resistance in backbone varieties of <span class="html-italic">indica</span> rice.</p>
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