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Search Results (181)

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22 pages, 1042 KiB  
Article
Effects of Climatic Conditions and Agronomic Practices on Health, Tuber Yield, and Mineral Composition of Two Contrasting Potato Varieties Developed for High and Low Input Production Systems
by Gultekin Hasanaliyeva, Ourania Giannakopoulou, Juan Wang, Marcin Barański, Enas Khalid Sufar, Daryl Knutt, Jenny Gilroy, Peter Shotton, Halima Leifert, Dominika Średnicka-Tober, Ismail Cakmak, Levent Ozturk, Bingqiang Zhao, Per Ole Iversen, Nikolaos Volakakis, Paul Bilsborrow, Carlo Leifert and Leonidas Rempelos
Agronomy 2025, 15(1), 89; https://doi.org/10.3390/agronomy15010089 - 31 Dec 2024
Viewed by 279
Abstract
Modern potato varieties from high-input, conventional farming-focused breeding programs produce substantially (up to 45%) lower yields when grown in organic production systems, and this was shown to be primarily due to less efficient fertilization and late blight (Phytophthora infestans) control methods [...] Read more.
Modern potato varieties from high-input, conventional farming-focused breeding programs produce substantially (up to 45%) lower yields when grown in organic production systems, and this was shown to be primarily due to less efficient fertilization and late blight (Phytophthora infestans) control methods being used in organic farming. It has been hypothesized that the breeding of potato varieties suitable for the organic/low-input sector should (i) focus on increasing nutrient (especially N) use efficiency, (ii) introduce durable late blight resistance, and (iii) be based on selection under low-input conditions. To test this hypothesis, we used an existing long-term factorial field experiment (the NEFG trials) to assess the effect of crop management practices (rotation design, fertilization regime, and crop protection methods) used in conventional and organic farming systems on crop health, tuber yield, and mineral composition parameters in two potato varieties, Santé and Sarpo mira, that were developed in breeding programs for high and low-input farming systems, respectively. Results showed that, compared to Santé, the variety Sarpo mira was more resistant to foliar and tuber blight but more susceptible to potato scab (Streptomyces scabies) and produced higher yields and tubers with higher concentrations of nutritionally desirable mineral nutrients but lower concentrations of Cd. The study also found that, compared to the Cu-fungicides permitted for late blight control in organic production, application of synthetic chemical fungicides permitted and widely used in conventional production resulted in significantly lower late blight severity in Sante but not in Sarpo mira. Results from both ANOVA and redundancy analysis (RDA) indicate that the effects of climatic (precipitation, radiation, and temperature) and agronomic (fertilization and crop protection) explanatory variables on crop health and yield differed considerably between the two varieties. Specifically, the RDA identified crop protection as a significant driver for Santé but not Sarpo mira, while precipitation was the strongest driver for crop health and yield for Sarpo mira but not Santé. In contrast, the effect of climatic and agronomic drivers on tuber mineral and toxic metal concentrations in the two varieties was found to be similar. Our results support the hypothesis that selection of potato varieties under low agrochemical input conditions can deliver varieties that combine (i) late blight resistance/tolerance, (ii) nutrient use efficiency, and (iii) yield potential in organic farming systems. Full article
(This article belongs to the Section Agroecology Innovation: Achieving System Resilience)
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Figure 1

Figure 1
<p>Bi-plot resulting from the RDA showing the associations between climate and agronomic explanatory variables/drivers and potato health and tuber yield response variables for the varieties Santé and Sarpo mira. Data included were from three growing seasons/years (2010, 2011, 2012). For the variety Santé, the horizontal axis 1 explains 31.7% of the variation and the vertical axis 2 a further 10.2%. For the variety Sapro mira, the horizontal axis 1 explains 24.4% of the variation and the vertical axis 2 a further 12.9%. NC, not computed. <b>Continuous explanatory variables (△): PRE</b>, precipitation; <b>RAD</b>, radiation; <b>TEMP</b>, temperature. <b>Fixed explanatory variables (▲): CP</b>, conventional crop protection; <b>OP</b>, organic crop protection; <b>CF</b>, conventional fertilization (mineral NPK); <b>OF</b>, organic fertilization (farmyard manure). <b>Response variables (<span style="color:#FF0000">▲</span>):</b> <span class="html-italic">fwy</span>, fresh weight yield, <span class="html-italic">dwy</span>, dry weight yield; <span class="html-italic">my+ST</span>, marketable fresh weight yield including tubers with scab; <span class="html-italic">my-ST</span>, marketable fresh weight yield excluding tubers with scab; <span class="html-italic">fb</span>, foliar blight (AUDPC); <span class="html-italic">tb</span>, % of tubers with tuber blight; <span class="html-italic">sc</span>, % of tubers with scab; <span class="html-italic">sl</span>, % of tubers with slug damage; gt, % of green tubers; ct, % cracked tubers.</p>
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<p>Bi-plot resulting from the RDA showing the associations between climate and agronomic explanatory variables/drivers and potato health and tuber yield response variables for the varieties Santé and Sarpo mira. Data included were from three growing seasons/years (2010, 2011, 2012). For the variety Santé, the horizontal axis 1 explains 34.7% of the variation and vertical axis 2 a further 10.0%. For the variety Sapro mira, horizontal axis 1 explains 25.6% of the variation and vertical axis 2 a further 8.0%. NC, not computed. <b>Continuous explanatory variables (△): PRE</b>, precipitation; <b>RAD</b>, radiation; <b>TEMP</b>, temperature. <b>Fixed explanatory variables (▲): CP</b>, conventional crop protection; <b>OP</b>, organic crop protection; <b>CF</b>, conventional fertilization (mineral NPK); <b>OF,</b> organic fertilization (farmyard manure). <b>Response variables (<span style="color:#FF0000">▲</span>): <span class="html-italic">Macronutrients</span>:</b> <span class="html-italic">N</span>, nitrogen; <span class="html-italic">P</span>, phosphorus; <span class="html-italic">K</span>, potassium; <span class="html-italic">S</span>, sulfur; <span class="html-italic">Ca</span>, calcium; <span class="html-italic">Mg</span>, magnesium. <b><span class="html-italic">Micronutrients</span>:</b> <span class="html-italic">B</span>, boron; <span class="html-italic">Cu</span>, copper; <span class="html-italic">Fe</span>, iron; <span class="html-italic">Zn</span>, zinc; <b><span class="html-italic">Toxic metals</span>:</b> <span class="html-italic">Al</span>, aluminum; <span class="html-italic">Cd</span>, cadmium; <span class="html-italic">Ni</span>, nickel; <span class="html-italic">Pb</span>, lead.</p>
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17 pages, 3441 KiB  
Article
Identification and Functional Analysis of the Ph-2 Gene Conferring Resistance to Late Blight (Phytophthora infestans) in Tomato
by Chunyang Pan, Xin Li, Xiaoxiao Lu, Junling Hu, Chen Zhang, Lianfeng Shi, Can Zhu, Yanmei Guo, Xiaoxuan Wang, Zejun Huang, Yongchen Du, Lei Liu and Junming Li
Plants 2024, 13(24), 3572; https://doi.org/10.3390/plants13243572 - 21 Dec 2024
Viewed by 387
Abstract
Late blight is a destructive disease affecting tomato production. The identification and characterization of resistance (R) genes are critical for the breeding of late blight-resistant cultivars. The incompletely dominant gene Ph-2 confers resistance against the race T1 of Phytophthora infestans in tomatoes. [...] Read more.
Late blight is a destructive disease affecting tomato production. The identification and characterization of resistance (R) genes are critical for the breeding of late blight-resistant cultivars. The incompletely dominant gene Ph-2 confers resistance against the race T1 of Phytophthora infestans in tomatoes. Herein, we identified Solyc10g085460 (RGA1) as a candidate gene for Ph-2 through the analysis of sequences and post-inoculation expression levels of genes located within the fine mapping interval. The RGA1 was subsequently validated to be a Ph-2 gene through targeted knockout and complementation analyses. It encodes a CC-NBS-LRR disease resistance protein, and transient expression assays conducted in the leaves of Nicotiana benthamiana indicate that Ph-2 is predominantly localized within the nucleus. In comparison to its susceptible allele (ph-2), the transient expression of Ph-2 can elicit hypersensitive responses (HR) in N. benthamiana, and subsequent investigations indicate that the structural integrity of the Ph-2 protein is likely a requirement for inducing HR in this species. Furthermore, ethylene and salicylic acid hormonal signaling pathways may mediate the transmission of the Ph-2 resistance signal, with PR1- and HR-related genes potentially involved in the Ph-2-mediated resistance. Our results could provide a theoretical foundation for the molecular breeding of tomato varieties resistant to late blight and offer valuable insights into elucidating the interaction mechanism between tomatoes and P. infestans. Full article
(This article belongs to the Section Horticultural Science and Ornamental Plants)
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Figure 1
<p>Analysis of gene expression within the candidate interval (<b>A</b>) Heatmap of expression of genes within the candidate interval after inoculation; (<b>B</b>) Heatmap–bubble of the 15 genes stably expressed in the candidate interval.</p>
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<p>Targeted knockout and Complementation analysis of the <span class="html-italic">RGA1</span> (<b>A</b>) <span class="html-italic">RGA1</span> mutations generated through <span class="html-italic">CRISPR/Cas9</span> gene editing; (<b>B</b>) Comparison of phenotypes after inoculations between <span class="html-italic">RGA1cr-1</span>, <span class="html-italic">RGA1cr-6</span> and LA3152; (<b>C</b>) Comparison of phenotypes after inoculations between MM (<span class="html-italic">Ph-2</span>) and MM (<span class="html-italic">ph-2</span>); (<b>D</b>) Comparison of disease index after inoculations between resistant and susceptible genotypes. Asterisks indicate a significant difference (****, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Identification of resistance to <span class="html-italic">Ph</span>-2 driven by the 35S promoter.</p>
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<p>The subcellular localization of Ph-2 and ph-2.</p>
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<p>Evaluation of the capacity of Ph-2 and its domains to induce HR (<b>A</b>) HR response elicited by the transient expression of Ph-2; (<b>B</b>) Trypan blue staining; (<b>C</b>) Evaluation of the capacity of the Ph-2 domains to elicit HR; (<b>D</b>) Trypan blue staining.</p>
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<p>Comparative transcriptome analysis of NILs in <span class="html-italic">Ph-2</span> (<b>A</b>) The Venn diagram of DEGs of resistant and susceptible genotypes at 24 hpi; (<b>B</b>) The Venn diagram of DEGs of resistant and susceptible genotypes at 48 hpi; (<b>C</b>) The specific DEGs enriched in the ko04626 pathway at 48 hpi in the resistant genotype; (<b>D</b>) The specific DEGs enriched in the ko04626 pathway at 48 hpi in the susceptible genotype.</p>
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17 pages, 3081 KiB  
Article
The Induction of Disease Resistance by Scopolamine and the Application of Datura Extract Against Potato (Solanum tuberosum L.) Late Blight
by Zhiming Zhu, Shicheng Liu, Yi Liu, Xinze Zhang, Zhiwen Shi, Shuting Liu, Zhenglin Zhu and Pan Dong
Int. J. Mol. Sci. 2024, 25(24), 13442; https://doi.org/10.3390/ijms252413442 - 15 Dec 2024
Viewed by 545
Abstract
Late blight, caused by Phytophthora infestans, is a devastating disease of potato. Our previous work illustrated that scopolamine, the main bioactive substance of Datura extract, exerts direct inhibitory effects on P. infestans, but it is unclear whether scopolamine and Datura extract [...] Read more.
Late blight, caused by Phytophthora infestans, is a devastating disease of potato. Our previous work illustrated that scopolamine, the main bioactive substance of Datura extract, exerts direct inhibitory effects on P. infestans, but it is unclear whether scopolamine and Datura extract can boost resistance to late blight in potato. In this study, P. infestans is used to infect scopolamine-treated potato pieces and leaves, as well as whole potatoes. We found that scopolamine-treated potato is resistant to P. infestans both in vitro and in vivo. The treatment of 4.5 g/L scopolamine reduces the lesion size of whole potato to 54% compared with the control after 20 d of the infection of P. infestans. The disease-resistant substance detection based on the kit method shows that scopolamine triggers the upregulation of polyphenoloxidase, peroxidase, superoxide dismutase activities, and H2O2 contents in potato tubers, and the decline of phenylalanine ammonia lyase and catalase activity. A total of 1682 significantly differentially expressed genes were detected with or without scopolamine treatment through high-throughput transcriptome sequencing and the DESeq2 software (version 1.24.0), including 705 upregulated and 977 downregulated genes. Scopolamine may affect the genes functioning in the cell wall, membrane and the plant-pathogen interaction. The addition of Datura extract could directly inhibit the mycelial growth of P. infestans on rye plate medium. In addition, P. infestans was found to be resistant to late blight in potato pieces treated with Datura extract. Datura extract can also be utilized in combination with the chemical fungicide Infinito in field experiments to lessen late blight symptoms and enhance potato yield. To our knowledge, this is the first study to detect the induction of disease resistance by scopolamine, and it also explores the feasibility of Datura extract in potato disease resistance. Full article
(This article belongs to the Special Issue Biocontrol of Plant Diseases and Insect Pests)
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Figure 1
<p>Scopolamine induces potatoes to resist late blight. Late blight symptoms of ‘Favorita’ potato leaves (<b>A</b>) and pieces (<b>B</b>) pretreated with different concentrations of scopolamine. (<b>C</b>) Late blight symptoms of ‘Qingshu 9’, ‘Xisen 6’, and ‘Hongmei’ potato pieces pretreated with scopolamine. (<b>D</b>) Symptoms of late blight in whole ‘Marco’ potatoes with or without scopolamine treatment. Proportion of lesion size of ‘Favorita’ potato leaves (<b>E</b>), pieces (<b>F</b>), and whole ‘Marco’ potatoes (<b>G</b>). d: days post inoculation with <span class="html-italic">P. infestans</span>. Tukey’s multiple comparisons test * <span class="html-italic">p</span> &lt; 0.0332, ** <span class="html-italic">p</span> &lt; 0.0021, *** <span class="html-italic">p</span> &lt; 0.0002, **** <span class="html-italic">p</span> &lt; 0.0001. 3 replicates per group.</p>
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<p>Change of disease-resistant substances in potato tubers with or without scopolamine treatment. (<b>A</b>) Phenylalanine ammonia (PAL) activity, (<b>B</b>) polyphenols oxidase (PPO) activity, (<b>C</b>) peroxidase (POD) activity, (<b>D</b>) superoxide dismutase (SOD) activity, (<b>E</b>) catalase (CAT) activity, (<b>F</b>) H<sub>2</sub>O<sub>2</sub> content in control group and scopolamine-treated group. h: hours after scopolamine treatment. d: days post-inoculation with <span class="html-italic">P. infestans</span>. Three replicates per group. Values represent the means ± standard error of 3 independent samples (Tukey’s multiple comparisons test, * <span class="html-italic">p</span> &lt; 0.0332, ** <span class="html-italic">p</span> &lt; 0.0021, *** <span class="html-italic">p</span> &lt; 0.0002).</p>
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<p>Main information of transcriptome sequencing in potato tubers under scopolamine treatment. (<b>A</b>) Distribution of differentially expressed genes. (<b>B</b>) qRT-PCR result. (<b>C</b>) GO annotation analysis diagram. The <span class="html-italic">X</span>–axis represents the number of genes compared to the secondary classification. (<b>D</b>) GO enrichment analysis. The horizontal axis represents the ratio of sample number of genes enriched in the rich factor (GO term) to the background number of annotated gene, and the color of the dot corresponds to different <span class="html-italic">p</span>-adjust ranges. (<b>E</b>) Histogram of KEGG. The <span class="html-italic">X</span>–axis is the number of genes annotated to the pathway. (<b>F</b>) KEGG enrichment analysis. The horizontal axis represents the ratio of rich factor (sample number of genes enriched in this pathway to background number of annotated genes). Three replicates per group.</p>
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<p><span class="html-italic">Datura</span> extract has dual effects to resist potato late blight. (<b>A</b>) Growth state of <span class="html-italic">Phytophthora infestans</span> on the medium supplemented with different concentrations of <span class="html-italic">Datura</span> extract. (<b>B</b>) The growth of <span class="html-italic">Phytophthora infestans</span> on the potato pieces pretreated with different concentrations of scopolamine. (<b>C</b>) The inhibition ratio of <span class="html-italic">Datura</span> extract against <span class="html-italic">Phytophthora infestans</span>. (<b>D</b>) The proportion of lesion size of potato pieces. Three replicates per group. Dunnett’s multiple comparisons test, * <span class="html-italic">p</span> &lt; 0.0332, ** <span class="html-italic">p</span> &lt; 0.0021, *** <span class="html-italic">p</span> &lt; 0.0002.</p>
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<p><span class="html-italic">Datura</span> extract could control late blight of potato and increase potato yield. (<b>A</b>) Late blight status of potato leaves at harvest. (<b>B</b>) Harvested potatoes. (The total length of the sign in the picture is 0.36 m) (<b>C</b>) Disease index of each treatment group. (The five surveys were given on 2, 6, 13, 19 April, and 5 May 2023). (<b>D</b>) Average yield of each treatment group. Treatment method: group 1. Control, treated with water; group 2. Infinito (1.5 mL); group 3. <span class="html-italic">Datura</span> extract (40 g); group 4. Infinito (0.15 mL); group 5. <span class="html-italic">Datura</span> extract (40 g) + Infinito (0.15 mL). (Tukey’s multiple comparisons test, * <span class="html-italic">p</span> &lt; 0.0332, ** <span class="html-italic">p</span> &lt; 0.0021.).</p>
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27 pages, 3135 KiB  
Article
Potato Late Blight Outbreak: A Study on Advanced Classification Models Based on Meteorological Data
by Parama Bagchi, Barbara Sawicka, Zoran Stamenkovic, Dušan Marković and Debotosh Bhattacharjee
Sensors 2024, 24(23), 7864; https://doi.org/10.3390/s24237864 - 9 Dec 2024
Viewed by 706
Abstract
While past research has emphasized the importance of late blight infection detection and classification, anticipating the potato late blight infection is crucial from the economic point of view as it helps to significantly reduce the production cost. Furthermore, it is necessary to minimize [...] Read more.
While past research has emphasized the importance of late blight infection detection and classification, anticipating the potato late blight infection is crucial from the economic point of view as it helps to significantly reduce the production cost. Furthermore, it is necessary to minimize the exposure of potatoes to harmful chemicals and pesticides due to their potential adverse effects on the human immune system. Our work is based on the precise classification of late blight infections in potatoes in European countries using real-time data from 1980 to 2000. To predict the potato late blight outbreak, we incorporated several hybrid machine learning models, as well as a unique combination of stacking classifier and logistic regression, achieving the highest prediction accuracy of 87.22%. Further enhancements of these models and the use of new data sources may lead to a higher late blight prediction accuracy and, consequently, a higher efficiency in managing potatoes’ health. Full article
(This article belongs to the Special Issue Sensors and Artificial Intelligence in Smart Agriculture)
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Figure 1
<p>Potato late blight: (<b>a</b>) Leaf form <span class="html-italic">P. infestans</span>; (<b>b</b>) Stem form of potato blight on late cv. ‘Amarant’; (<b>c</b>) Potato infection with late blight in ‘Boryna’ cv.; (<b>d</b>) <span class="html-italic">P. infestans</span> plantation infection, 2°, scale 9°, ‘Irga’ cv.; (<b>e</b>) Potato late blight on the tuber; (<b>f</b>) Potato blight on the cross-section of tubers; Source: own.</p>
Full article ">Figure 1 Cont.
<p>Potato late blight: (<b>a</b>) Leaf form <span class="html-italic">P. infestans</span>; (<b>b</b>) Stem form of potato blight on late cv. ‘Amarant’; (<b>c</b>) Potato infection with late blight in ‘Boryna’ cv.; (<b>d</b>) <span class="html-italic">P. infestans</span> plantation infection, 2°, scale 9°, ‘Irga’ cv.; (<b>e</b>) Potato late blight on the tuber; (<b>f</b>) Potato blight on the cross-section of tubers; Source: own.</p>
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<p>Analysis of meteorological data.</p>
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<p>First symptoms of <span class="html-italic">P. infestans</span> in the years 1987–1989.</p>
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<p>Linear regression model for predicting potato blight infection in period 1987–1989.</p>
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<p>Potato blight infections affecting different varieties of potato over the years 1987–1989. SA—Sencor before emergence; SB—Sencor after emergence in the 10–15 cm phase of potato plants; AF—Afalon 50 WP used before potato emergence as a control plant.</p>
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<p>Regression analysis based on potato blight infection data for the year 1987: (<b>a</b>) Anova; (<b>b</b>) Regression statistics.</p>
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<p>Regression analysis based on potato blight infection data for the year 1988: (<b>a</b>) Anova; (<b>b</b>) Regression statistics.</p>
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<p>Regression analysis based on potato blight infection data for the year 1989; (<b>a</b>) Anova; (<b>b</b>) Regression statistics.</p>
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15 pages, 3821 KiB  
Article
Antifungal Activity of Bacillus velezensis X3-2 Against Plant Pathogens and Biocontrol Effect on Potato Late Blight
by Peixia Wei, Mengying Gao, Shuang Zhou, Guohui Liu, Pan Wang, Chunguang Liu, Fengshan Yang and Haiyan Fu
Agriculture 2024, 14(12), 2224; https://doi.org/10.3390/agriculture14122224 - 5 Dec 2024
Viewed by 524
Abstract
Late blight of potato is caused by the pathogen Phytophthora infestans, which has been considered to be the most destructive disease affecting potato crops worldwide. In recent years, the use of antagonistic microorganisms to control potato late blight has become a green [...] Read more.
Late blight of potato is caused by the pathogen Phytophthora infestans, which has been considered to be the most destructive disease affecting potato crops worldwide. In recent years, the use of antagonistic microorganisms to control potato late blight has become a green and environmentally friendly means of disease control, greatly reducing the use of chemical pesticides. To obtain antagonistic bacteria with a high biocontrol effect against potato late blight, a total of 16 antagonistic bacterial strains with an inhibition rate of more than 50% against P. infestans were screened from potato rhizosphere soil by double-culture method, among which the bacterial isolate (X3-2) had the strongest inhibitory activity against P. infestans, with an inhibition rate of 81.97 ± 4.81%, respectively, and a broad-spectrum inhibitory activity. The bacterial isolate (X3-2) was identified as Bacillus velezensis based on its 16S rDNA gene sequence and morphological as well as biochemical properties. The results of our in vitro experiments demonstrated that X3-2 was a potent inducer of resistance in potato tubers and leaflets against late blight. In greenhouse experiments, it was confirmed that the biological preparation X3-2 exhibits an anti-oomycete effect, demonstrating a significant control efficacy on potato late blight. Further analyses showed that the antagonistic substances of X3-2 were distributed both intracellularly and extracellularly. In addition, screening for plant-growth-promoting (PGP) traits showed that X3-2 has the ability to produce siderophores and secrete indole acetic acid (IAA). The findings from this research suggest that B. velezensis X3-2 exhibits promise as a biocontrol agent for managing late blight. In the future, the composition and mechanism of the action of its antimicrobial substances can be studied in depth, and field trials can be carried out to assess its actual prevention and control effects. Full article
(This article belongs to the Section Crop Protection, Diseases, Pests and Weeds)
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Figure 1
<p>Effect of strain X3-2 on the growth of <span class="html-italic">Phytophthora infestans</span>. (<b>a</b>) A single culture of <span class="html-italic">P. infestans</span>. (<b>b</b>) The mycelial morphology of <span class="html-italic">P. infestans</span> under X3-2 confrontation. (<b>c</b>) The colony diameter of <span class="html-italic">P. infestans</span> under X3-2 confrontation. All treatments were performed with three replicates and values were expressed as average ± SD. **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Taxonomic identification of strain X3-2. (<b>a</b>) Morphological characteristics of X3-2 colonies on LB medium. (<b>b</b>) Morphological characteristics of X3-2 colonies on LB medium under the stereoscope. (<b>c</b>) The phylogenetic tree of strain X3-2.</p>
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<p>The effect of X3-2 on the growth of other plant pathogens in vitro. (<b>a</b>) Colony morphology under antagonistic conditions on PDA plates of X3-2 and plant pathogens. (<b>b</b>) Colony diameter of other plant pathogens by X3-2. All treatments were performed with three replicates, and values were expressed as average ± SD. **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Biological control of potato late blight by the formulated X3-2 bioagents. (<b>a</b>) Photograph of late blight symptoms in treated and control potato plants 10 d after inoculation with <span class="html-italic">P. infestans</span>. (<b>b</b>) Disease incidence in treated and control potato plants after inoculation with <span class="html-italic">P. infestans</span>. (<b>c</b>) Disease index of treated and control potato plants after inoculation with <span class="html-italic">P. infestans</span>. All treatments were performed with three replicates, and values were expressed as average ± SD. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effect on mycelial growth of <span class="html-italic">P. infestans</span> by different concentrations of X3-2 cell-free filtrates (CFS) and distribution of antagonistic components against <span class="html-italic">P. infestans</span>. (<b>a</b>) Effect of different concentrations of X3-2 CFS on the mycelial growth of <span class="html-italic">P. infestans</span>; <span class="html-italic">P. infestans</span> mycelial discs inoculated in the center of rye agar medium served as blank control and named as CK; Rye agar medium supplemented with 10% LB served as positive control and named LB; CFS (10%, 20%, and 30%) was added to the medium to test the effect of CFS on <span class="html-italic">P. infestans</span> mycelial growth. (<b>b</b>) Colony diameter of <span class="html-italic">P. infestans</span> treated with different concentrations of CFS. (<b>c</b>) The inhibition rate of <span class="html-italic">P. infestans</span> by different concentrations of CFS. (<b>d</b>) Colony morphology of <span class="html-italic">P. infestans</span> under different X3-2 component confrontations. (<b>e</b>) Colony diameter of <span class="html-italic">P. infestans</span> under different compositional treatments of X3-2. Each treatment group was performed three times, and values were expressed as average ± SD. **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Detection of extracellular enzymes and traits of plant growth promoting (PGP) of X3-2. (<b>a</b>–<b>d</b>) The appearance of transparent circle around the bacterial colony on the plate indicates extracellular enzyme production by X3-2. (<b>e</b>) The presence of an orange halo around colony on the plate indicates the production of siderophore by X3-2. (<b>f</b>) The pink-colored centrifuge tube contained IAA-producing bacteria and a negative control (LB with 0.5 mg/mL tryptophan). Arrows of different lengths represent the size of the halo.</p>
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19 pages, 1088 KiB  
Review
Deciphering Fire Blight: From Erwinia amylovora Ecology to Genomics and Sustainable Control
by Rafael J. Mendes, Laura Regalado, Fabio Rezzonico, Fernando Tavares and Conceição Santos
Horticulturae 2024, 10(11), 1178; https://doi.org/10.3390/horticulturae10111178 - 7 Nov 2024
Viewed by 1057
Abstract
Fire blight is a highly destructive plant disease that affects the pome fruit value chain, with high economic impacts. Its etiological agent is the Gram-negative bacterium Erwinia amylovora. The origin of fire blight goes back to the late 1700s in North America, [...] Read more.
Fire blight is a highly destructive plant disease that affects the pome fruit value chain, with high economic impacts. Its etiological agent is the Gram-negative bacterium Erwinia amylovora. The origin of fire blight goes back to the late 1700s in North America, and the disease since then has spread to New Zealand, Europe, North Africa, the Middle East, and Asia. Due to its worldwide dissemination, advances have been made to identify and characterize E. amylovora strains from different regions and understand their evolutionary adaptation. Additionally, many efforts have been made in recent decades to stop the occurrence and impacts of fire blight, but in many countries, only preventive measures have been applied, as the application of antibiotics and copper-based compounds has become more restricted. Thus, new sustainable methods to control the pathogen are constantly required. This article presents a comprehensive review of the pathogen, from the phenotypic and molecular characterization methods applied to advances in comparative genomics and the development of new compounds for sustainable control of E. amylovora. Full article
(This article belongs to the Special Issue The Diagnosis, Management, and Epidemiology of Plant Diseases)
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<p>World distribution of <span class="html-italic">Erwinia amylovora</span>. <a href="https://gd.eppo.int/taxon/ERWIAM/distribution" target="_blank">https://gd.eppo.int/taxon/ERWIAM/distribution</a> (accessed on 20 March 2024).</p>
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<p>Diagram of different control measures against fire blight.</p>
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<p>Models of antibacterial mechanisms of antimicrobial peptides (AMPs).</p>
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15 pages, 951 KiB  
Article
The Effects of Tomato Intercropping with Medicinal Aromatic Plants Combined with Trichoderma Applications in Organic Cultivation
by Magdalena Szczech, Beata Kowalska, Frederik R. Wurm, Magdalena Ptaszek, Anna Jarecka-Boncela, Paweł Trzciński, Kaja Borup Løvschall, Sara T. Roldan Velasquez and Robert Maciorowski
Agronomy 2024, 14(11), 2572; https://doi.org/10.3390/agronomy14112572 - 1 Nov 2024
Viewed by 975
Abstract
To increase biodiversity in tomato cultivation, two herbal aromatic plants, thyme (Thymus vulgaris) and basil (Ocimum basilicum L.), were introduced as companion plants. Their role was to improve crop plant growth and stress resistance. Moreover, the effect of the soil [...] Read more.
To increase biodiversity in tomato cultivation, two herbal aromatic plants, thyme (Thymus vulgaris) and basil (Ocimum basilicum L.), were introduced as companion plants. Their role was to improve crop plant growth and stress resistance. Moreover, the effect of the soil application of Trichoderma microbial preparations on tomato growth parameters and yield, in combination with companion plants, was studied. Ligno-cellulose multi-layer microcapsules with Trichoderma atroviride TRS14 spores (MIC14) and the commercial preparation Trianum G (TG) were used as microbial preparations. This experiment was carried out in a certified organic field. Tomato plants were intercropped with thyme or basil in the arrangement of two tomato rows alternating with one herbal row. In all intercropping arrangements and in the control (tomato plants grown without herbs), subplots were sectioned. The soil in the subplots was amended with the MIC14 and TG preparations used at a concentration of 104 spores g−1 of the soil and planted with tomato transplants. No control measures were applied during tomato growing, and the plants were naturally infected with late blight. Tomato plant growth parameters and yield were assessed, and late blight severity was monitored. The degree of soil colonization by Trichoderma fungi and the effect of these applications on soil microbial activity and biodiversity (dehydrogenases activity, EcoPlates AWCD, and Shannon index) were evaluated. The results clearly showed a significant influence of thyme and basil on tomato growth and yield in organic production. The cultivation of thyme adjacent to tomatoes had a beneficial effect on the development of the root system and the number of flowers and fruits on the crop plants. Basil, on the other hand, clearly decreased tomato yield and adversely affected the effect of Trichoderma applications by reducing root system development. Moreover, basil as a companion plant increased late blight symptoms. Both Trichoderma strains colonized soil, but they had no significant effect on the microbial activity or metabolic potential measured on the EcoPlates with the use of the BIOLOG system. However, a decrease in dehydrogenases activity was noted. In organic cultivation, the Trichoderma preparations used had no significant effect on tomato yield, opposite to its increase in integrated tomato production. Full article
(This article belongs to the Section Farming Sustainability)
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<p>The marketable yield of tomato plants intercropped with thyme and basil in the years 2022 and 2023. The same letters above the bars in each year indicate not significant differences at <span class="html-italic">p</span> = 0.05 according to DMRT.</p>
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<p>The effect of thyme and basil on the growth parameters of tomato plants. The same letters above bars indicate not significant differences at <span class="html-italic">p</span> = 0.05, according to DMRT.</p>
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12 pages, 2363 KiB  
Article
Transcriptional Modulation of Plant Defense Genes by a Bipartite Begomovirus Promotes the Performance of Its Whitefly Vector
by Wen-Ze He, Shu-Sheng Liu and Li-Long Pan
Viruses 2024, 16(11), 1654; https://doi.org/10.3390/v16111654 - 23 Oct 2024
Viewed by 793
Abstract
The majority of plant viruses rely on insect vectors for inter-plant transmission. Amid virus transmission, vector-borne viruses such as begomoviruses may significantly modulate host plants in various ways and, in turn, plant palatability to insect vectors. While many case studies on monopartite begomoviruses [...] Read more.
The majority of plant viruses rely on insect vectors for inter-plant transmission. Amid virus transmission, vector-borne viruses such as begomoviruses may significantly modulate host plants in various ways and, in turn, plant palatability to insect vectors. While many case studies on monopartite begomoviruses are available, bipartite begomoviruses are understudied. More importantly, detailed elucidation of the molecular mechanisms involved is limited. Here, we report the mechanisms by which an emerging bipartite begomovirus, the Sri Lankan cassava mosaic virus (SLCMV), modulates plant defenses against whitefly. SLCMV infection of tobacco (Nicotiana tabacum) plants significantly downregulated defenses against whitefly, as whitefly survival and fecundity increased significantly on virus-infected plants when compared to the controls. We then profiled SLCMV-induced transcriptomic changes in plants and identified a repertoire of differentially expressed genes (DEGs). GO enrichment analysis of DEGs demonstrated that the term defense response was significantly enriched. Functional analysis of DEGs associated with defense response revealed that four downregulated DEGs, including putative late blight resistance protein homolog R1B-17 (R1B-17), polygalacturonase inhibitor-like (PGI), serine/threonine protein kinase CDL1-like (CDL1), and Systemin B, directly contributed to plant defenses against whitefly. Taken together, our findings elucidate the role of novel plant factors involved in the modulation of plant defenses against whitefly by a bipartite begomovirus and shed new light on insect vector–virus–host plant tripartite interactions. Full article
(This article belongs to the Special Issue Molecular Virus-Insect Interactions, 2nd Edition)
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<p>Effect of SLCMV infection of tobacco plants on plant phenotype and whitefly performance. (<b>A</b>) picture of tobacco plants. Tobacco plants were inoculated with pBINPLUS (empty vector, control) or SLCMV DNA-A+DNA-B. At 25 days post inoculation, plants showing typical symptoms were used for photographing. (<b>B</b>,<b>C</b>) survival and fecundity of Asia II 1 whiteflies on tobacco plants. Ten Asia II 1 whiteflies were released into leaf-clip cages that were placed on tobacco leaves. Whitefly survival and fecundity were recorded seven days post whitefly release. N = 27 for B and C. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 (independent <span class="html-italic">t</span>-test).</p>
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<p>Pearson’s correlation coefficients of overall gene expression patterns between samples. The coefficient values are presented and indicated by the red color.</p>
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<p>Volcano plot of differentially expressed genes in SLCMV vs. pBINPLUS. The <span class="html-italic">x</span>-axis represents the log fold change, and the <span class="html-italic">y</span>-axis represents the log significance (<span class="html-italic">p</span> value). Blue dots represent downregulated genes, and red dots represent upregulated genes.</p>
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<p>Distribution of the top twenty GO terms in the GO database. The <span class="html-italic">Y</span>-axis represents the name of the GO term, and the <span class="html-italic">X</span>-axis indicates the rich factor. The <span class="html-italic">p</span> value was indicated by the color of the dots, and the number of genes in each term was indicated by the size of the dots.</p>
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<p>Effect of SLCMV infection of tobacco plants on the expression of DEGs. (<b>A</b>,<b>B</b>) expression of DEGs. Tobacco plants were inoculated with pBINPLUS (empty vector) and SLCMV DNA-A+DNA-B. Plants were sampled for gene expression analysis at 25 days post inoculation. The number of replicates was 5–6. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 (independent <span class="html-italic">t</span>-test).</p>
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<p>Effects of DEG silencing on whitefly performance. (<b>A</b>,<b>D</b>,<b>G</b>,<b>J</b>,<b>M</b>) Silencing efficiency; (<b>B</b>,<b>E</b>,<b>H</b>,<b>K</b>,<b>N</b>) survival rate of whiteflies on control and virus-induced gene silencing (VIGS) plants; (<b>C</b>,<b>F</b>,<b>I</b>,<b>L</b>,<b>O</b>) fecundity of whiteflies on control and VIGS plants. The number of replicates was 7–19 for (<b>A</b>,<b>D</b>,<b>G</b>,<b>J</b>,<b>M</b>) and 22–31 for (<b>B</b>,<b>C</b>,<b>E</b>,<b>F</b>,<b>H</b>,<b>I</b>,<b>K</b>,<b>L</b>,<b>N</b>,<b>O</b>). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 (independent <span class="html-italic">t</span>-test).</p>
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19 pages, 11091 KiB  
Article
Endophyte Bacillus vallismortis BL01 to Control Fungal and Bacterial Phytopathogens of Tomato (Solanum lycopersicum L.) Plants
by Vladimir K. Chebotar, Maria S. Gancheva, Elena P. Chizhevskaya, Anastasia V. Erofeeva, Alexander V. Khiutti, Alexander M. Lazarev, Xiuhai Zhang, Jing Xue, Chunhong Yang and Igor A. Tikhonovich
Horticulturae 2024, 10(10), 1095; https://doi.org/10.3390/horticulturae10101095 - 14 Oct 2024
Viewed by 3044
Abstract
Some strains of Bacillus vallismortis have been reported to be efficient biocontrol agents against tomato pathogens. The aim of our study was to assess the biocontrol ability of the endophytic strain BL01 Bacillus vallismortis through in vitro and field trials, as well as [...] Read more.
Some strains of Bacillus vallismortis have been reported to be efficient biocontrol agents against tomato pathogens. The aim of our study was to assess the biocontrol ability of the endophytic strain BL01 Bacillus vallismortis through in vitro and field trials, as well as to verify its plant colonization ability and analyze the bacterial genome in order to find genes responsible for the biocontrol activity. We demonstrated in a gnotobiotic system and by confocal laser microscopy that the endophytic strain BL01 was able to colonize the endosphere and rhizosphere of tomato, winter wheat and oilseed rape. In vitro experiments demonstrated the inhibition activity of BL01 against a wide range of phytopathogenic fungi and bacteria. BL01 showed biological efficacy in two-year field experiments with tomato plants against black bacterial spotting by 40–70.8% and against late blight by 47.1% and increased tomato harvest by 24.9% or 10.9 tons per hectare compared to the control. Genome analysis revealed the presence of genes that are responsible for the synthesis of biologically active secondary metabolites, which could be responsible for the biocontrol action. Strain BL01 B. vallismortis can be considered an effective biocontrol agent to control both fungal and bacterial diseases in tomato plants. Full article
(This article belongs to the Section Plant Pathology and Disease Management (PPDM))
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<p>The number of bacilli in the rhizosphere and endosphere of tomatoes (10<sup>6</sup> CFU per 1 root of the tomato plant) (<b>a</b>) and spring wheat (10<sup>6</sup> CFU per 1 root of the wheat plant) (<b>b</b>). Bars represent the mean ± SD of three replications.</p>
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<p>(<b>a</b>) IMARIS-edited CLSM picture of BL01 <span class="html-italic">B. vallismortis</span>-primed oilseed rape, old root parts. Rendered root parts (green), Firmicutes (red). (<b>b</b>,<b>c</b>) IMARIS-edited CLSM pictures of matured roots in the root hair zone treated with BL01 <span class="html-italic">B. vallismortis</span>. The view is from various directions, and the arrow points to endophytic cells of BL01 <span class="html-italic">B. vallismortis</span>.</p>
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<p>Inhibitory effects of <span class="html-italic">B. vallismortis</span> BL01 on <span class="html-italic">Diaporthe eres</span> 18-001 (<b>a</b>), <span class="html-italic">Alternaria solani</span> 747151 (<b>b</b>), <span class="html-italic">Plenodomus lindquistii</span> 19-007 (<b>c</b>), <span class="html-italic">Fusarium oxysporum</span> 70523 (<b>d</b>), <span class="html-italic">F. sporotrichioides</span> 86093 (<b>e</b>) and <span class="html-italic">F. culmorum</span> 46504 (<b>f</b>).</p>
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<p>Antifungal activity (%) of <span class="html-italic">B. vallismortis</span> BL01 against phytopathogenic fungi <span class="html-italic">Diaporthe eres</span> 18-001, <span class="html-italic">Alternaria solani</span> 747151, <span class="html-italic">Plenodomus lindquistii</span> 19-007, <span class="html-italic">Fusarium oxysporum</span> 70523, <span class="html-italic">F. sporotrichioides</span> 286093 and <span class="html-italic">F. culmorum</span> 46504. Bars represent the mean ± SD of three replications.</p>
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<p>Inhibitory effects of <span class="html-italic">B. vallismortis</span> BL01 on <span class="html-italic">Fusarium culmorum</span> 58800, <span class="html-italic">Rhizoctonia solani</span> and <span class="html-italic">Sclerotinia sclerotiorum</span> N149 in co-cultivation in one Petri dish.</p>
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<p>Antibacterial activity (lysis zones, mm) of strain BL01 <span class="html-italic">B. vallismortis</span> against phytopathogenic bacteria: <span class="html-italic">Erwinia carotovora</span> 3304, <span class="html-italic">Erwinia carotovora</span> pv. <span class="html-italic">atroseptica</span> 822, <span class="html-italic">Xanthomonas campestris</span> pv. <span class="html-italic">vesicatoria</span> 7767, <span class="html-italic">Pseudomonas syringae</span> pv. <span class="html-italic">tomato</span> 8949, <span class="html-italic">Pseudomonas syringae</span> pv. <span class="html-italic">atrofaciens</span> P-88, <span class="html-italic">Pseudomonas syringae</span> 213. Bars represent the mean ± SD of three replications.</p>
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<p>Bactericidal activity of <span class="html-italic">B. vallismortis</span> BL01 against black bacterial spotting. Box plots were drawn using the R boxplot() function. The box of a boxplot starts in the first quartile (25%) and ends in the third (75%). Hence, the box represents 50% of the central data, with a line inside that representing the median. Standard—Phytolavin (streptotricin antibiotic complex). ***, <span class="html-italic">p</span>-value &lt; 0.001; das—days after sowing.</p>
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<p>The effect of <span class="html-italic">B. vallismortis</span> BL01 on late blight disease (<b>a</b>) and yield (<b>b</b>) of tomato compared with control and standard Phytolavin (streptotricin antibiotic complex). Box plots were drawn using the R boxplot () function. The box of a boxplot starts in the first quartile (25%) and ends in the third (75%). Hence, the box represents 50% of the central data, with a line inside that representing the median. ***, <span class="html-italic">p</span>-value &lt; 0.001.</p>
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<p>Map of the <span class="html-italic">B. vallismortis</span> BL01 genome constructed by Proksee (<a href="https://proksee.ca/" target="_blank">https://proksee.ca/</a>, accessed on 28 August 2024).</p>
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<p>Protein comparison among <span class="html-italic">B. vallismortis</span> BL01 and related species <span class="html-italic">(B. spizizenii</span> str. W23, <span class="html-italic">B. amyloliquefaciens</span> UMAF6639, <span class="html-italic">B. subtilis</span> HJ5 and <span class="html-italic">B. velezensis</span> FZB42). The Venn diagram illustrates the overlap and unique clusters among <span class="html-italic">Bacillus</span> species. The bar plot displays the total cluster content for each <span class="html-italic">Bacillus</span> species analyzed.</p>
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11 pages, 1045 KiB  
Article
Genetic Diversity and Pathogenicity of Phytophthora infestans Isolates on Four Solanum tuberosum (Potato) Cultivars in Nariño, Colombia
by Pedro Alexander Velasquez-Vasconez, Reyven Yair Chaves-Ordoñez, Juan David Pantoja Unigarro, Tharling Yadhannia Hernandez Diaz, Luz Estela Lagos Mora, Carlos Betancourth García and Claudia Salazar-Gonzalez
Int. J. Plant Biol. 2024, 15(4), 1021-1031; https://doi.org/10.3390/ijpb15040072 - 9 Oct 2024
Viewed by 762
Abstract
Phytophthora infestans remains a major threat to global potato production. This study focused on characterizing and assessing the pathogenicity of P. infestans isolates on detached potato leaves and in greenhouse trials across four cultivars. Seven isolates were obtained from high potato-producing regions in [...] Read more.
Phytophthora infestans remains a major threat to global potato production. This study focused on characterizing and assessing the pathogenicity of P. infestans isolates on detached potato leaves and in greenhouse trials across four cultivars. Seven isolates were obtained from high potato-producing regions in the department of Nariño, Colombia. The isolates were analyzed using 12 microsatellite markers to determine genetic distances. Two genetically distinct isolates showed markedly different pathogenicity on detached leaves: isolate P00921 caused complete infection by day five, whereas P00321 showed no symptoms. These two isolates (P00921 and P00321) selected for having the greatest genetic distance and highest pathogenicity among the seven analyzed were further tested in a greenhouse setup on four potato cultivars using a randomized block design. Disease progression was monitored over nine days. The results indicated significant variations in pathogenicity linked to genetic diversity among isolates. Notably, Capiro and Margarita cultivars were more prone to severe disease than Suprema and Única. These findings highlight the complex nature of host–pathogen interactions and suggest the need for tailored approaches in disease management and cultivar selection. Full article
(This article belongs to the Section Plant–Microorganisms Interactions)
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<p>Progression of infection and genetic relationships among seven <span class="html-italic">P. infestans</span> isolates. (<b>A</b>) Progression of infection over time in seven <span class="html-italic">P. infestans</span> isolates on detached leaves. The lines represent the average of four values. (<b>B</b>) Dendrogram representing the genetic distance among seven <span class="html-italic">P. infestans</span> isolates based on Bruvo distances for microsatellite markers. Isolate codes are displayed on the right, each representing a unique genetic profile collected for the study.</p>
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<p>Differential response of four potato genotypes to two distinct isolates of <span class="html-italic">P. infestans</span> isolates over time. The P00921 strain rapidly increases the number of affected leaflets, particularly in the Capiro and Margarita cultivars.</p>
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<p>Differential response of four potato cultivars to <span class="html-italic">P. infestans</span> infection. (<b>A</b>) Number of affected leaves, (<b>B</b>) number of necrotic spots (2 mm<sup>2</sup>), and (<b>C</b>) number of necrotic spots (1 cm<sup>2</sup>), measured at 2, 4, 6, and 9 days post-inoculation.</p>
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33 pages, 2829 KiB  
Review
Genome-Wide Association Studies for Key Agronomic and Quality Traits in Potato (Solanum tuberosum L.)
by Jianlong Yuan, Lixiang Cheng, Yuping Wang and Feng Zhang
Agronomy 2024, 14(10), 2214; https://doi.org/10.3390/agronomy14102214 - 26 Sep 2024
Viewed by 1614
Abstract
Deciphering the genetic mechanisms underlying key agronomic and quality traits in potato (Solanum tuberosum L.) is essential for advancing varietal improvement. Phenotypic instability in early clonal generations and inbreeding depression, coupled with the complexity of tetrasomic inheritance, pose significant challenges in constructing [...] Read more.
Deciphering the genetic mechanisms underlying key agronomic and quality traits in potato (Solanum tuberosum L.) is essential for advancing varietal improvement. Phenotypic instability in early clonal generations and inbreeding depression, coupled with the complexity of tetrasomic inheritance, pose significant challenges in constructing mapping populations for the genetic dissection of complex traits. Genome-wide association studies (GWASs) offer an efficient method to establish trait–genome associations by analyzing genetic recombination and mutation events in natural populations. This review systematically examines the application of GWASs in identifying agronomic traits in potato, such as plant architecture, yield components, tuber shape, and resistance to early and late blight and nematodes, as well as quality traits including dry matter, starch, and glycoalkaloid content. Some key chromosomal hotspots identified through GWASs include chromosome 5 associated with tuber yield, starch content, and late blight resistance; chromosome 4 and 10 associations with tuber shape and starch content; chromosomes 1, 9, and 11 associated with plant height, tuber number, glycoalkaloid content, and pest resistance. It elucidates the advantages and limitations of GWASs for genetic loci identification in this autotetraploid crop, providing theoretical insights and a reference framework for the precise localization of key genetic loci and the discovery of underlying genes using GWASs. Full article
(This article belongs to the Section Crop Breeding and Genetics)
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<p>Overview of the steps for potato GWAS. Components of GWAS include population selection, phenotyping, genotyping, population stratification, and association analysis. The Manhattan plot displays SNPs significantly associated with the number of leaves, where each dot represents a SNP, the <span class="html-italic">x</span>-axis indicates chromosome position, and the y-axis represents the -log10 (<span class="html-italic">p</span>-value) associated with the phenotype. After identifying the associated <span class="html-italic">loci</span>, linkage disequilibrium analysis refines the <span class="html-italic">loci</span> and identifies candidate genes. Functional genomics techniques validate these genes and facilitate the development of molecular breeding markers.</p>
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17 pages, 3448 KiB  
Article
Konjac Glucomannan Oligosaccharides (KGMOS) Confers Innate Immunity against Phytophthora nicotianae in Tobacco
by Md Mijanur Rahman Rajib, Kuikui Li, Md Saikat Hossain Bhuiyan, Wenxia Wang, Jin Gao and Heng Yin
Agriculture 2024, 14(8), 1289; https://doi.org/10.3390/agriculture14081289 - 5 Aug 2024
Viewed by 975
Abstract
In this study, KGMOS (DP, 2-13), derived from KGM (Konjac glucomannan), was applied to elucidate plant immunity in a Nicotiana benthamiana Phytophthora nicotianae model. Application of KGMOS (25–100 mg/L) notably inhibited P. nicotianae, resulting in reduced disease indices and a significant accumulation [...] Read more.
In this study, KGMOS (DP, 2-13), derived from KGM (Konjac glucomannan), was applied to elucidate plant immunity in a Nicotiana benthamiana Phytophthora nicotianae model. Application of KGMOS (25–100 mg/L) notably inhibited P. nicotianae, resulting in reduced disease indices and a significant accumulation of defense molecules such as H2O2 and callose. Transcriptomic analysis revealed that genes shared between KGMOS-treated and control plants are involved in signaling pathways, transcription regulation, hydrogen peroxide catabolism, and oxidative stress response. This suggests that KGMOS triggers H2O2 accumulation, callose deposition, and activation of the salicylic acid (SA) and jasmonic acid/ethylene (JA/ET) pathways after pathogen inoculation. Upregulated defense-response genes in the KGMOS group included SA-related late blight-resistant, pathogenesis-related (PR), and JA/ET-related ethylene response factor (ERF) genes. Heatmap analysis showed more upregulated defense genes (PR and NPR) related to SA in the KGMOS-treated group than in controls. RT-qPCR validation revealed significant upregulation of SA and JA/ET pathway genes in KGMOS-treated plants. Higher SA content in these plants suggests enhanced disease resistance. This study concludes that KGMOS pre-treatment induced resistance against P. nicotianae, especially at a lower concentration (25 mg/L). These findings could offer valuable insights for the future application of KGMOS in controlling plant diseases for sustainable agriculture and postharvest management. Full article
(This article belongs to the Section Crop Protection, Diseases, Pests and Weeds)
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<p>KGMOS-mediated disease resistance and fungal inhibition in <span class="html-italic">N. benthamiana</span>. (<b>A</b>) Disease symptoms in tobacco leaves under control and KGMOS treatments. (<b>B</b>) Disease index of KGMOS pre-treated and non-treated infected leaves. (<b>C</b>) Mycelial growth of <span class="html-italic">P. nicotianae</span> under control and KGMOS treatments. (<b>D</b>) Antifungal activity by KGMOS and control treatments. CK = control (sterilized water), PC = positive control (carbendazim 50% @ 1 g/L). Values are presented as the means ± SD of three independent measurements. IBM software SPSS (version 22) was used to analyze data, and means were compared with LSD at 0.05. Asterisks indicate significant differences (* <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>KGMOS induced H<sub>2</sub>O<sub>2</sub> and callose deposition in <span class="html-italic">N. benthamiana</span>. (<b>A</b>) The ROS in leaves through DAB staining. (<b>B</b>) Average optical density of H<sub>2</sub>O<sub>2</sub> accumulation. (<b>C</b>) Callose deposition in leaves through aniline blue staining. Scale bar—50 μm. (<b>D</b>) Average optical density of callose molecules. Values are presented as the means ± SD from three technical replicates. IBM software SPSS (version 22) was used to analyze data, and means were compared with LSD at 0.05. Asterisks indicate significant differences (** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>DEGs from <span class="html-italic">N. benthamiana</span> at 3 days after <span class="html-italic">P. nicotianae</span> infection. (<b>A</b>) Volcano plot displaying DEGs of the control group (PC) compared to the mock group. (<b>B</b>) Volcano plot displaying DEGs of the KGMOS group (PK) compared to the mock group, identified with [log2(fold change) &gt; 1] and <span class="html-italic">p</span>-value &lt; 0.05. (<b>C</b>) KEGG enrichment analysis of upregulated DEGs between the control and mock groups. (<b>D</b>) KEGG enrichment analysis of upregulated DEGs between the KGMOS and mock groups. (<b>E</b>) Distinct and overlapped DEGs in between the PK/mock and PC/mock groups. (<b>F</b>) GO annotation of overlapped DEGs between PK/mock and PC/mock. The horizontal axis represents the rich ratio, while the vertical axis represents the pathway names. Gene number: DEGs number; Q value: False discovery rate (FDR) adjusted <span class="html-italic">p</span>-value. Generally, a Q value ≤ 0.05 is regarded as a significant enrichment.</p>
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<p>Transcriptomic analysis of distinct and overlapped genes in mock, control, and KGMOS groups. (<b>A</b>) KEGG pathway of unique genes in the control group (PC). (<b>B</b>) KEGG pathway of unique genes in the KGMOS group (PK). (<b>C</b>) KEGG pathway analysis of overlapped genes between control and KGMOS. (<b>D</b>) GO enrichment analysis of overlapped genes between control and KGMOS. The horizontal axis represents the rich ratio, while the vertical axis represents the pathway names. Gene number: DEGs number; Q value: FDR adjusted <span class="html-italic">p</span>-value.</p>
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<p>Heatmap analysis of defense genes among mock, control (PC), and KGMOS groups (PK). (<b>A</b>) The expression of upregulated defense genes in the KGMOS group compared to control and mock. (<b>B</b>) The expression of <span class="html-italic">PR</span> genes among mock, control, and KGMOS groups. (<b>C</b>) The expression of SA signaling pathway-related genes among mock, control, and KGMOS groups. TPM = transcripts per kilobase million.</p>
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<p>KGMOS induced SA and JA/ET pathway in <span class="html-italic">N. benthamiana</span>. (<b>A</b>) The relative expression of SA pathway genes detected by RT-qPCR. The control (CK) was normalized as 1. (<b>B</b>) The content of SA in infected leaves pre-treated with KGMOS. SPSS (version 22) was used to analyze data, and means were compared with the LSD at 0.05. Values are presented as the means ± SD of three independent measurements. Asterisks indicate significant differences (* <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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14 pages, 6532 KiB  
Article
Population Structure of Phytophthora infestans in Israel Changes Frequently Due to the Import of Asymptomatic Late Blight-Infected Potato Seed Tubers from Europe
by Yigal Cohen
J. Fungi 2024, 10(8), 549; https://doi.org/10.3390/jof10080549 - 4 Aug 2024
Viewed by 1034
Abstract
Late blight, caused by the oomycete Phytophthora infestans, is a devastating disease of potato worldwide. In Israel, potatoes are grown twice a year, in autumn and spring, with late blight causing extensive damage in both seasons. While tuber seeds for the autumn [...] Read more.
Late blight, caused by the oomycete Phytophthora infestans, is a devastating disease of potato worldwide. In Israel, potatoes are grown twice a year, in autumn and spring, with late blight causing extensive damage in both seasons. While tuber seeds for the autumn planting are produced locally, seed tubers for the spring planting are imported from Europe due to dormancy of local tubers. Here, we demonstrate that seed tubers imported from Europe for the spring season carry asymptomatic infection with EU genotypes of P. infestans, which alters the population structure of the pathogen each spring. The proportion of imported tubers carrying asymptomatic infections ranged between 1.2 and 3.75%, varying by year and cultivar. Asymptomatic tubers produced late blight-infected sprouts about one month after planting. The sporangia produced on these sprouts served as primary inoculum, causing intensive foliage attacks on neighboring plants. When sprout-infected plants were uprooted and the mother tuber was washed, sliced, and placed in moistened dishes at 18 °C, profuse sporulation of P. infestans developed on the slices’ surfaces within 1–2 days. The dominant genotype of P. infestans in the autumn season in Israel is 23A1, but genotypes in the following spring season changed to include 13A2 or 36A2. Surprisingly, genotype 43A1, which might be resistant to CAA and OSBPI fungicides and appeared in Europe in 2022, emerged in Israel in spring 2024. The immigrating genotypes do not persist in the country, allowing 23A1 to regain predominance in the following autumn. Long-term monitoring data suggest that the population structure of P. infestans changes yearly but temporarily due to the import of new genotypes from Europe. Full article
(This article belongs to the Special Issue Plant Fungal Diseases and Crop Protection)
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<p>Potato seed tubers (<span class="html-italic">cv</span> Nicola, imported from Holland) carrying asymptomatic infection with <span class="html-italic">Phytophthora infestans</span> developed late blight symptoms upon germination. Tubers were sown on 6 December 2016. Symptoms were seen on 11 January 2017, 36 days after planting. (<b>A</b>) The appearance of 500 plants 5 weeks after sowing. (<b>B</b>) Emerging sprouts showing late blight symptoms. (<b>C</b>) Below-ground stems showing necrotic symptoms of late blight, while mother tuber appears healthy. (<b>D</b>) Sporulation of <span class="html-italic">Phytophthora infestans</span> on tuber slices (arrows) that were taken from the mother tuber shown in (<b>C</b>).</p>
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<p>Potato seed tubers imported from Europe carrying asymptomatic infection with <span class="html-italic">Phytophthora infestans</span> developed late blight symptoms upon germination. Tubers were sown on 5 January 2017. Symptoms were detected on 15 February 2017, 41 days after sowing. (<b>A</b>) Nicola plants in net house 1. (<b>B</b>) Mondial plants in net house 9. (<b>C</b>) symptoms (arrow) of late blight at ground level. (<b>D</b>) symptoms of late blight on sprout apex (arrows). (<b>E</b>) sporulation of <span class="html-italic">Phytophthora infestans</span> on a tuber slice of cv Nicola. (<b>F</b>) Sporulation of <span class="html-italic">Phytophthora infestans</span> on a tuber slice of cv Mondial.</p>
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<p>Meteorological conditions prevailing in Spring 2024 at BIU Farm during the epidemics of late blight caused by <span class="html-italic">Phytophthora infestans</span> in eight cultivars of potato whose seeds were imported from Europe. (<b>A</b>) rain (total = 370 mm). (<b>B</b>) air temperature (mean = 14.6 °C; min = 5.8 °C; max = 26.6 °C). (<b>C</b>) % RH (mean = 76.2%; min = 14%; max = 98%).</p>
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<p>Potato seed tubers (<span class="html-italic">cv</span> Rosana and VR 808) carrying asymptomatic infection with <span class="html-italic">Phytophthora infestans</span> developed late blight symptoms upon germination. Imported tubers were sown on 1 January 2024 and sprout symptoms were observed on 7 February 2024, 36 days after sowing. (<b>A</b>) Net house with germinating potato plants at 36 days after planting. (<b>B</b>–<b>D</b>) Late blight symptoms on a germinating plant cultivar Rosana with no external symptoms on tubers. (<b>E</b>) An infected plant of cv VR 808 at 40 days after planting. Note the two healthy plants alongside. (<b>F</b>,<b>G</b>) Sporulation of <span class="html-italic">P. infestans</span> on surface of tuber slices cut from symptomless tubers of VR-808 and Rosana, respectively.</p>
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<p>Compatibility to potato and tomato of genotypes 23A1 and 13A2 retrieved from potato. (<b>A</b>) In detached tomato and potato leaves. (<b>B</b>,<b>C</b>) In tomato fruits. (<b>D</b>,<b>E</b>) In tomato leaves. Note heavy sporulation of 23A1 on tomato fruits and leaves as against hypersensitive response to 13A2 with no sporulation.</p>
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<p>Progress of late blight on foliage of eight cultivars of imported potato cultivars. (<b>A</b>) Disease progresses in each cultivar during a 76-day period after planting. (<b>B</b>) Area under disease progress curves (derived from data in (<b>A</b>)). Different letters on curves or columns indicate a significant difference between cultivars at α = 0.05 (Tukey’s HDS).</p>
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<p>Annual frequency of genotypes of <span class="html-italic">Phytophthora infestans</span> in potato crops in Israel during the period 2004–2024.</p>
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18 pages, 7892 KiB  
Article
GamaNNet: A Novel Plant Pathologist-Level CNN Architecture for Intelligent Diagnosis
by Marcio Oliveira, Adunias Teixeira, Guilherme Barreto and Cristiano Lima
AgriEngineering 2024, 6(3), 2623-2639; https://doi.org/10.3390/agriengineering6030153 - 2 Aug 2024
Cited by 1 | Viewed by 843
Abstract
Plant pathologies significantly jeopardise global food security, necessitating the development of prompt and precise diagnostic methods. This study employs advanced deep learning techniques to evaluate the performance of nine convolutional neural networks (CNNs) in identifying a spectrum of phytosanitary issues affecting the foliage [...] Read more.
Plant pathologies significantly jeopardise global food security, necessitating the development of prompt and precise diagnostic methods. This study employs advanced deep learning techniques to evaluate the performance of nine convolutional neural networks (CNNs) in identifying a spectrum of phytosanitary issues affecting the foliage of Solanum lycopersicum (tomato). Ten thousand RGB images of leaf tissue were subsampled in training (64%), validation (16%), and test (20%) sets to rank the most suitable CNNs in expediting the diagnosis of plant disease. The study assessed the performance of eight well-known networks under identical hyperparameter conditions. Additionally, it introduced the GamaNNet architecture, a custom-designed model optimised for superior performance on this specific type of dataset. The investigational results were most promising for the innovative GamaNNet and ResNet-152, which both exhibited a 91% accuracy rate, as evidenced by their confusion matrices, ROC curves, and AUC metrics. In comparison, LeNet-5 and ResNet-50 demonstrated lower assertiveness, attaining accuracies of 74% and 69%, respectively. GoogLeNet and Inception-v3 emerged as the frontrunners, displaying diagnostic preeminence, achieving an average F1-score of 97%. Identifying such pathologies as Early Blight, Late Blight, Corynespora Leaf Spot, and Septoria Leaf Spot posed the most significant challenge for this class of problem. Full article
(This article belongs to the Special Issue Recent Trends and Advances in Agricultural Engineering)
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Graphical abstract
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<p>Tomato leaf tissue in classes: (<b>A</b>) Bacterial Leaf Spot, (<b>B</b>) Alternariosis, (<b>C</b>) Asymptomatic, (<b>D</b>) Late Blight, (<b>E</b>) Leaf Mould, (<b>F</b>) Septoria Leaf Spot, (<b>G</b>) Spider Mite, (<b>H</b>) Corynespora Leaf Blight, (<b>I</b>) TYLCV, and (<b>J</b>) ToMV.</p>
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<p>Workflow for classifying plant diseases in tomato leaves.</p>
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<p>Representation of the general structure of convolutional neural networks (CNN).</p>
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<p>(<b>a</b>) Accuracy during the training and validation of ResNet-50; (<b>b</b>) loss during the training and validation of ResNet-50.</p>
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<p>(<b>a</b>) ResNet-50 confusion matrix with 2000 unseen images; (<b>b</b>) ResNet-50 multiclass ROC curve.</p>
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<p>(<b>a</b>) GoogLeNet confusion matrix with 2000 unseen images; (<b>b</b>) GoogLeNet multiclass ROC curve.</p>
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<p>(<b>a</b>) Inception-v3 confusion matrix with 2000 unseen images; (<b>b</b>) Inception-v3 multiclass ROC curve.</p>
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<p>(<b>a</b>) Accuracy during GamaNNet training and validation; (<b>b</b>) loss during GamaNNet training and validation.</p>
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<p>(<b>a</b>) GamaNNet confusion matrix with 2000 unseen images; (<b>b</b>) GamaNNet multiclass ROC curve.</p>
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<p>Feature extraction after each convolutional layer of the GamaNNet architecture.</p>
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<p>(<b>a</b>) Sensitivity, specificity, and F1-score for GoogLeNet; (<b>b</b>) Sensitivity, specificity, and F1-score for Inception-v3.</p>
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<p>Detailed samples from the BDFH group of plant pathologies.</p>
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12 pages, 2150 KiB  
Article
Optimized Crop Disease Identification in Bangladesh: A Deep Learning and SVM Hybrid Model for Rice, Potato, and Corn
by Shohag Barman, Fahmid Al Farid, Jaohar Raihan, Niaz Ashraf Khan, Md. Ferdous Bin Hafiz, Aditi Bhattacharya, Zaeed Mahmud, Sadia Afrin Ridita, Md Tanjil Sarker, Hezerul Abdul Karim and Sarina Mansor
J. Imaging 2024, 10(8), 183; https://doi.org/10.3390/jimaging10080183 - 30 Jul 2024
Viewed by 1748
Abstract
Agriculture plays a vital role in Bangladesh’s economy. It is essential to ensure the proper growth and health of crops for the development of the agricultural sector. In the context of Bangladesh, crop diseases pose a significant threat to agricultural output and, consequently, [...] Read more.
Agriculture plays a vital role in Bangladesh’s economy. It is essential to ensure the proper growth and health of crops for the development of the agricultural sector. In the context of Bangladesh, crop diseases pose a significant threat to agricultural output and, consequently, food security. This necessitates the timely and precise identification of such diseases to ensure the sustainability of food production. This study focuses on building a hybrid deep learning model for the identification of three specific diseases affecting three major crops: late blight in potatoes, brown spot in rice, and common rust in corn. The proposed model leverages EfficientNetB0′s feature extraction capabilities, known for achieving rapid high learning rates, coupled with the classification proficiency of SVMs, a well-established machine learning algorithm. This unified approach streamlines data processing and feature extraction, potentially improving model generalizability across diverse crops and diseases. It also aims to address the challenges of computational efficiency and accuracy that are often encountered in precision agriculture applications. The proposed hybrid model achieved 97.29% accuracy. A comparative analysis with other models, CNN, VGG16, ResNet50, Xception, Mobilenet V2, Autoencoders, Inception v3, and EfficientNetB0 each achieving an accuracy of 86.57%, 83.29%, 68.79%, 94.07%, 90.71%, 87.90%, 94.14%, and 96.14% respectively, demonstrated the superior performance of our proposed model. Full article
(This article belongs to the Special Issue Imaging Applications in Agriculture)
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<p>Hybrid model architecture.</p>
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<p>Dataset distribution.</p>
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<p>Sample from the dataset.</p>
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<p>EfficientNetB0 model architecture.</p>
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<p>Hybrid model structure diagram.</p>
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<p>Hybrid plot training &amp; validation accuracy values and validation loss values.</p>
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