Pub Date : 2026-02-02DOI: 10.1094/PHYTO-06-25-0203-R
Qi Luo, Xiaotong Feng, Delu Wang, W M W W Kandegama, Qiang Bian, Zhuo Chen
Osthole exhibits strong inhibitory activity against phytopathogenic fungi; however, its antifungal mechanism remains unclear. This study assessed osthole's inhibitory effects on several phytopathogenic fungi, revealing a half-maximal effective concentration of 73.03 μg/ml against the hyphal growth of Botrytis cinerea. Micromorphological analysis showed that osthole caused abnormalities in the hyphae, including unclear organelle boundaries and organelle dissolution. Integrated transcriptomic and metabolomic assays and correlation analysis indicated that osthole induced differentially expressed genes and differentially abundant metabolites, which were enriched particularly in the pathways of glyoxylate and dicarboxylate metabolism, tyrosine metabolism, glycerophospholipid metabolism, fructose and mannose metabolism, citrate cycle, biosynthesis of unsaturated fatty acids, and ABC transporters. Molecular docking and molecular dynamics simulation assays demonstrated that osthole binds stably to amidase, a key enzyme in energy metabolism, with a relatively lower binding energy of -8.5 kcal/mol compared with osthole's analogs, suggesting that amidase may be a potential target protein in the fungus. A microscale thermophoresis assay indicated that the dissociation constant (Kd) value for osthole binding to amidase was significantly lower compared with that of osthole's analog 7-methoxycoumarin. Overall, this study demonstrates that osthole disrupts energy metabolism, nitrogen metabolism, substance transport, and the metabolism of the hyphal cell wall and cell membrane, potentially targeting the amidase of B. cinerea. These findings highlight the potential of osthole for controlling gray mold.
{"title":"The Natural Product Osthole, Known for Its Insecticidal and Antimicrobial Properties, Potentially Binds to Amidase, Offering a Novel Approach for Controlling Tomato Gray Mold for the First Time.","authors":"Qi Luo, Xiaotong Feng, Delu Wang, W M W W Kandegama, Qiang Bian, Zhuo Chen","doi":"10.1094/PHYTO-06-25-0203-R","DOIUrl":"10.1094/PHYTO-06-25-0203-R","url":null,"abstract":"<p><p>Osthole exhibits strong inhibitory activity against phytopathogenic fungi; however, its antifungal mechanism remains unclear. This study assessed osthole's inhibitory effects on several phytopathogenic fungi, revealing a half-maximal effective concentration of 73.03 μg/ml against the hyphal growth of <i>Botrytis cinerea</i>. Micromorphological analysis showed that osthole caused abnormalities in the hyphae, including unclear organelle boundaries and organelle dissolution. Integrated transcriptomic and metabolomic assays and correlation analysis indicated that osthole induced differentially expressed genes and differentially abundant metabolites, which were enriched particularly in the pathways of glyoxylate and dicarboxylate metabolism, tyrosine metabolism, glycerophospholipid metabolism, fructose and mannose metabolism, citrate cycle, biosynthesis of unsaturated fatty acids, and ABC transporters. Molecular docking and molecular dynamics simulation assays demonstrated that osthole binds stably to amidase, a key enzyme in energy metabolism, with a relatively lower binding energy of -8.5 kcal/mol compared with osthole's analogs, suggesting that amidase may be a potential target protein in the fungus. A microscale thermophoresis assay indicated that the dissociation constant (Kd) value for osthole binding to amidase was significantly lower compared with that of osthole's analog 7-methoxycoumarin. Overall, this study demonstrates that osthole disrupts energy metabolism, nitrogen metabolism, substance transport, and the metabolism of the hyphal cell wall and cell membrane, potentially targeting the amidase of <i>B. cinerea</i>. These findings highlight the potential of osthole for controlling gray mold.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"PHYTO06250203R"},"PeriodicalIF":3.1,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145030326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-21DOI: 10.1094/PHYTO-05-25-0164-R
Alexander Mullens, Tao Zhong, Alexander Lipka, Peter Balint-Kurti, Tiffany Jamann
How host genotype shapes pathogen tissue tropism remains poorly understood. Vascular and nonvascular tissues represent distinct habitats within a plant for bacteria to colonize. Host plants often utilize different mechanisms to defend themselves against vascular and nonvascular pathogens, and mechanisms of resistance employed by the host can vary by organ. Xanthomonas vasicola pv. vasculorum (Xvv) is an emerging bacterial maize pathogen, and this pathosystem offers an opportunity to study how host resistance differs in response to the vascular and nonvascular lifestyles exhibited by a single bacterial phytopathogen. We used different inoculation techniques to induce vascular and nonvascular disease and evaluated maize populations using both techniques to map resistance to vascular and nonvascular disease caused by Xvv. Xvv can colonize both vascular and nonvascular tissues, depending on the genotype. Different inoculation techniques can be used to induce vascular or nonvascular colonization. Independent loci control variation in resistance to Xvv during vascular and nonvascular pathogenesis. We confirmed the role of those regions in resistance to vascular and nonvascular infection. This study offers insights into how host resistance shapes how bacterial pathogens adapt to both vascular and nonvascular lifestyles. We show that host genotype can dictate which tissues a pathogen can infect. This system can serve as a model to understand tissue-specific host resistance to plant pathogens and tissue specificity in pathogens.
{"title":"Vascular Pathogenicity of <i>Xanthomonas vasicola</i> pv. <i>vasculorum</i> in Maize Is Modulated by Tissue-Specific Host Resistance.","authors":"Alexander Mullens, Tao Zhong, Alexander Lipka, Peter Balint-Kurti, Tiffany Jamann","doi":"10.1094/PHYTO-05-25-0164-R","DOIUrl":"10.1094/PHYTO-05-25-0164-R","url":null,"abstract":"<p><p>How host genotype shapes pathogen tissue tropism remains poorly understood. Vascular and nonvascular tissues represent distinct habitats within a plant for bacteria to colonize. Host plants often utilize different mechanisms to defend themselves against vascular and nonvascular pathogens, and mechanisms of resistance employed by the host can vary by organ. <i>Xanthomonas vasicola</i> pv. <i>vasculorum</i> (<i>Xvv</i>) is an emerging bacterial maize pathogen, and this pathosystem offers an opportunity to study how host resistance differs in response to the vascular and nonvascular lifestyles exhibited by a single bacterial phytopathogen. We used different inoculation techniques to induce vascular and nonvascular disease and evaluated maize populations using both techniques to map resistance to vascular and nonvascular disease caused by <i>Xvv</i>. <i>Xvv</i> can colonize both vascular and nonvascular tissues, depending on the genotype. Different inoculation techniques can be used to induce vascular or nonvascular colonization. Independent loci control variation in resistance to <i>Xvv</i> during vascular and nonvascular pathogenesis. We confirmed the role of those regions in resistance to vascular and nonvascular infection. This study offers insights into how host resistance shapes how bacterial pathogens adapt to both vascular and nonvascular lifestyles. We show that host genotype can dictate which tissues a pathogen can infect. This system can serve as a model to understand tissue-specific host resistance to plant pathogens and tissue specificity in pathogens.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"285-297"},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144966075","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.1094/PHYTO-10-25-0336-SC
R Rabekijana, H Raveloson, A Dereeper, C Sciallano, G Boulard, F Auguy, N M Rakotonanahary, H Rakotonary, E Thomas, L Brottier, S Cunnac, B Szurek, M Hutin
Xanthomonas oryzae pv. oryzae (Xoo) causes bacterial leaf blight (BLB), a major rice disease causing up to 70% yield loss in Asia and West Africa. First described in Japan in 1884 and later reported in West Africa in the 1970s, BLB recently emerged in East Africa, with an epidemic reported in Tanzania in 2019. Remarkably, the disease was detected for the first time in Madagascar the same year, representing a serious threat to food security. To investigate the origin of BLB in Madagascar, we isolated 73 Xoo strains from symptomatic rice leaves collected between 2019 and 2023. MLVA genotyping revealed 19 haplotypes forming a single clonal complex, indicating low diversity and a likely recent introduction. In order to come up with disease control strategies, IRBB-based race-typing was achieved and identified four resistance genes (Xa8, xa13, Xa21, Xa23) that confer resistance to all Malagasy strains tested, while the 19 Malagasy varieties assessed were susceptible. The analysis of SWEET knock-out lines confirmed that Malagasy strains rely on the susceptibility gene OsSWEET11 for full virulence. Whole-genome sequencing and TALEs repertoire analyses of two strains allowed the identification of a PthXo1 ortholog predicted to induce OsSWEET11. SNP-based phylogenetic analyses clustered Malagasy strains within Asian lineages, most closely related to strains originated from India. Malagasy strains did not cluster with recently reported Tanzanian Xoo, suggesting independent introductions. Overall, our study demonstrates that BLB in Madagascar results from a recent and single introduction from Asia and identifies effective resistance genes for deployment.
{"title":"Emergence of Bacterial Leaf Blight of Rice in Madagascar: A Recent Introduction from Asia.","authors":"R Rabekijana, H Raveloson, A Dereeper, C Sciallano, G Boulard, F Auguy, N M Rakotonanahary, H Rakotonary, E Thomas, L Brottier, S Cunnac, B Szurek, M Hutin","doi":"10.1094/PHYTO-10-25-0336-SC","DOIUrl":"https://doi.org/10.1094/PHYTO-10-25-0336-SC","url":null,"abstract":"<p><p><i>Xanthomonas oryzae</i> pv. <i>oryzae</i> (<i>Xoo</i>) causes bacterial leaf blight (BLB), a major rice disease causing up to 70% yield loss in Asia and West Africa. First described in Japan in 1884 and later reported in West Africa in the 1970s, BLB recently emerged in East Africa, with an epidemic reported in Tanzania in 2019. Remarkably, the disease was detected for the first time in Madagascar the same year, representing a serious threat to food security. To investigate the origin of BLB in Madagascar, we isolated 73 <i>Xoo</i> strains from symptomatic rice leaves collected between 2019 and 2023. MLVA genotyping revealed 19 haplotypes forming a single clonal complex, indicating low diversity and a likely recent introduction. In order to come up with disease control strategies, IRBB-based race-typing was achieved and identified four resistance genes (<i>Xa8, xa13, Xa21, Xa23</i>) that confer resistance to all Malagasy strains tested, while the 19 Malagasy varieties assessed were susceptible. The analysis of <i>SWEET</i> knock-out lines confirmed that Malagasy strains rely on the susceptibility gene <i>OsSWEET11</i> for full virulence. Whole-genome sequencing and TALEs repertoire analyses of two strains allowed the identification of a PthXo1 ortholog predicted to induce <i>OsSWEET11</i>. SNP-based phylogenetic analyses clustered Malagasy strains within Asian lineages, most closely related to strains originated from India. Malagasy strains did not cluster with recently reported Tanzanian <i>Xoo</i>, suggesting independent introductions. Overall, our study demonstrates that BLB in Madagascar results from a recent and single introduction from Asia and identifies effective resistance genes for deployment.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146100444","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.1094/PHYTO-12-25-0399-R
Li Zhang, Housong Cui, Song Yu, Renlan Yan, Bao Wang, Runmao Lin, Tong Liu
Trichoderma Gene Prediction Web server (TGP-WEB) is designed for accurate gene prediction in genomes of Trichoderma species, the biological control agents and the plant-beneficial microorganisms. It employs a hybrid gene prediction strategy, combining ab initio (Augustus and GeneMark) and homology-based (Braker utilizing fungal protein sequences from NCBI Refseq database) methods. Predictions are integrated and prioritized using a ranking framework, followed by functional assessment via domain annotation. After uploading a single-genome FASTA file, users can download TGP-WEB prediction results (including GFF3 files with gene locations, and FASTA files for both the predicted nucleotide and amino acid sequences) within ~4 hours. TGP-WEB demonstrates high accuracy in gene prediction across 177 genomes. When benchmarked against 42 published genomes with annotated gene sets available on NCBI, it recovers more than 90.00% of reported genes in 37 (88.00%) genomes. For 135 previously unannotated genomes, TGP-WEB generates complete gene sets, now available on the web server. BUSCO evaluation shows greater than 97.00% completeness for 94.92% (168/177) of genomes. TGP-WEB predictions enable the identification of 2100 single-copy genes from Trichoderma genomes. These genes are used to construct a robust phylogenetic tree, which clarifies the taxonomy of 49 strains. The robust performance of TGP-WEB prediction will contribute to the increasing studies of Trichoderma genomes, and it is freely available from www.fungalgenomics.cn/geneprediction.
{"title":"TGP-WEB: A Server for Automatic Gene Prediction of <i>Trichoderma</i> Genomes.","authors":"Li Zhang, Housong Cui, Song Yu, Renlan Yan, Bao Wang, Runmao Lin, Tong Liu","doi":"10.1094/PHYTO-12-25-0399-R","DOIUrl":"https://doi.org/10.1094/PHYTO-12-25-0399-R","url":null,"abstract":"<p><p><i>Trichoderma</i> Gene Prediction Web server (TGP-WEB) is designed for accurate gene prediction in genomes of <i>Trichoderma</i> species, the biological control agents and the plant-beneficial microorganisms. It employs a hybrid gene prediction strategy, combining <i>ab initio</i> (Augustus and GeneMark) and homology-based (Braker utilizing fungal protein sequences from NCBI Refseq database) methods. Predictions are integrated and prioritized using a ranking framework, followed by functional assessment via domain annotation. After uploading a single-genome FASTA file, users can download TGP-WEB prediction results (including GFF3 files with gene locations, and FASTA files for both the predicted nucleotide and amino acid sequences) within ~4 hours. TGP-WEB demonstrates high accuracy in gene prediction across 177 genomes. When benchmarked against 42 published genomes with annotated gene sets available on NCBI, it recovers more than 90.00% of reported genes in 37 (88.00%) genomes. For 135 previously unannotated genomes, TGP-WEB generates complete gene sets, now available on the web server. BUSCO evaluation shows greater than 97.00% completeness for 94.92% (168/177) of genomes. TGP-WEB predictions enable the identification of 2100 single-copy genes from <i>Trichoderma</i> genomes. These genes are used to construct a robust phylogenetic tree, which clarifies the taxonomy of 49 strains. The robust performance of TGP-WEB prediction will contribute to the increasing studies of <i>Trichoderma</i> genomes, and it is freely available from www.fungalgenomics.cn/geneprediction.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146100520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-21DOI: 10.1094/PHYTO-12-24-0389-R
Sita Paudel, Neil Olszewski, Shauna Mason, Benham Lockhart, Dimitre Mollov, Brett Arenz, Robert Alvarez-Quinto
The family Caulimoviridae comprises plant-infecting pararetroviruses that replicate by reverse transcription and encapsidate a circular double-stranded DNA genome. They can occur as episomal (encapsidated and replicative forms) and endogenous forms integrated into the host genome. Some endogenous sequences can give rise to episomal forms. In this study, we report and characterize a new badnavirus infecting Pelargonium × hortorum. We propose the name Pelargonium vein banding virus (PVBV). The episomal genome is 7,586 bp in length. Endogenous PVBV (ePVBV) DNA was identified in healthy plants and characterized. Southern blotting and PCR suggest that in many cultivars, the ePVBV consists of a tandem array of the complete PVBV genome. The ePVBV tandem array was not detected in 'Maverick White'. The major parents of P. × hortorum hybrids are P. zonale and P. inquinans. P. zonale contained ePVBV, but P. inquinans did not. The sequence of ePVBV recovered from the cultivar 'BullsEye Salmon' was >99% identical to the episomal sequence. Agroinoculation experiments demonstrated that ePVBV is infectious. Bacilliform-shaped virions with a modal particle length of 144 nm and 33 nm in diameter were recovered from leaves of agroinfected Maverick White exhibiting mosaic symptoms and chlorosis surrounding the veins. P. zonale and P. × hortorum varieties with full ePVBV genomes were not infected. Interestingly, P. inquinans, which does not contain ePVBV, was also not infected.
{"title":"Elucidation of the Nature of Pelargonium Vein Banding Virus Sequences Present in <i>Pelargonium × hortorum</i>.","authors":"Sita Paudel, Neil Olszewski, Shauna Mason, Benham Lockhart, Dimitre Mollov, Brett Arenz, Robert Alvarez-Quinto","doi":"10.1094/PHYTO-12-24-0389-R","DOIUrl":"10.1094/PHYTO-12-24-0389-R","url":null,"abstract":"<p><p>The family <i>Caulimoviridae</i> comprises plant-infecting pararetroviruses that replicate by reverse transcription and encapsidate a circular double-stranded DNA genome. They can occur as episomal (encapsidated and replicative forms) and endogenous forms integrated into the host genome. Some endogenous sequences can give rise to episomal forms. In this study, we report and characterize a new badnavirus infecting <i>Pelargonium × hortorum</i>. We propose the name Pelargonium vein banding virus (PVBV). The episomal genome is 7,586 bp in length. Endogenous PVBV (ePVBV) DNA was identified in healthy plants and characterized. Southern blotting and PCR suggest that in many cultivars, the ePVBV consists of a tandem array of the complete PVBV genome. The ePVBV tandem array was not detected in 'Maverick White'. The major parents of <i>P. × hortorum</i> hybrids are <i>P. zonale</i> and <i>P. inquinans. P. zonale</i> contained ePVBV, but <i>P. inquinans</i> did not. The sequence of ePVBV recovered from the cultivar 'BullsEye Salmon' was >99% identical to the episomal sequence. Agroinoculation experiments demonstrated that ePVBV is infectious. Bacilliform-shaped virions with a modal particle length of 144 nm and 33 nm in diameter were recovered from leaves of agroinfected Maverick White exhibiting mosaic symptoms and chlorosis surrounding the veins. <i>P. zonale</i> and <i>P. × hortorum</i> varieties with full ePVBV genomes were not infected. Interestingly, <i>P. inquinans</i>, which does not contain ePVBV, was also not infected.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"327-335"},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145280933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Puccinia striiformis f. sp. tritici, causing stripe rust, is one of the most prominent pathogens of wheat worldwide. The biotrophic and obligate fungus is capable of rapidly developing new virulent races that can overcome race-specific resistance in host plants. The traditional virulence characterization of the pathogen requires strict conditions for testing isolates on wheat differentials with specific resistance genes, which is time-consuming. Developing molecular markers for avirulence genes could provide an efficient method for monitoring virulence changes in the pathogen population. In this study, secreted protein gene-based single-nucleotide polymorphism markers previously identified to be associated with avirulence genes of the pathogen were converted to kompetitive allele-specific PCR (KASP) markers. The KASP markers were screened with a diverse panel of 192 isolates selected from various countries based on their virulent races and molecular genotypes. The markers significantly correlated with the avirulence/virulence phenotypic data of the 192 isolates were further validated with 845 isolates collected from the United States in 2019 to 2021. Based on the results of both the screening and validation data, 21 KASP markers significantly associated with different avirulence genes were developed. Seventeen of the 21 markers were significantly associated with two or more avirulence genes, and except AvrYr10, and the remaining 15 avirulence genes had two or more markers. Different combinations of up to three markers could be used for specific detection of 16 avirulence genes in monitoring the pathogen population.
{"title":"Development of KASP Markers in Association with Avirulence Genes of <i>Puccinia striiformis</i> f. sp. <i>tritici</i>, the Wheat Stripe Rust Pathogen.","authors":"Hannah Merrill, Arjun Upadhaya, Meinan Wang, Qing Bai, Bingbing Jiang, Chongjing Xia, Yuxiang Li, Xianming Chen","doi":"10.1094/PHYTO-02-25-0074-R","DOIUrl":"10.1094/PHYTO-02-25-0074-R","url":null,"abstract":"<p><p><i>Puccinia striiformis</i> f. sp. <i>tritici</i>, causing stripe rust, is one of the most prominent pathogens of wheat worldwide. The biotrophic and obligate fungus is capable of rapidly developing new virulent races that can overcome race-specific resistance in host plants. The traditional virulence characterization of the pathogen requires strict conditions for testing isolates on wheat differentials with specific resistance genes, which is time-consuming. Developing molecular markers for avirulence genes could provide an efficient method for monitoring virulence changes in the pathogen population. In this study, secreted protein gene-based single-nucleotide polymorphism markers previously identified to be associated with avirulence genes of the pathogen were converted to kompetitive allele-specific PCR (KASP) markers. The KASP markers were screened with a diverse panel of 192 isolates selected from various countries based on their virulent races and molecular genotypes. The markers significantly correlated with the avirulence/virulence phenotypic data of the 192 isolates were further validated with 845 isolates collected from the United States in 2019 to 2021. Based on the results of both the screening and validation data, 21 KASP markers significantly associated with different avirulence genes were developed. Seventeen of the 21 markers were significantly associated with two or more avirulence genes, and except <i>AvrYr10</i>, and the remaining 15 avirulence genes had two or more markers. Different combinations of up to three markers could be used for specific detection of 16 avirulence genes in monitoring the pathogen population.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"263-276"},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145131843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-21DOI: 10.1094/PHYTO-06-25-0223-R
J A Abbey, S Singh, K A Neugebauer, T D Miles
Highbush blueberries (Vaccinium corymbosum) are an important fruit crop worldwide, and Michigan is one of the largest producers within the United States. Botrytis blossom blight and fruit rot are major diseases in this region. Although Botrytis cinerea has long been considered the primary causal agent, a recent study identified a novel species in Michigan. In this article, we describe a new species, B. michiganensis, as an additional pathogen causing blossom blight. This study aimed to characterize B. michiganensis through multilocus phylogenetic analysis (G3PDH, HSP60, RPB2, NEP1, and NEP2), morpho-cultural traits, and fungicide sensitivity. Phylogenetic analyses, using both individual and concatenated gene sequences, placed B. michiganensis in a distinct clade closely related to B. fabiopsis, B. caroliniana, and B. galanthina. The isolates exhibited diverse cultural and morphological characteristics on potato dextrose agar, ranging from white to gray fluffy/cottony mycelia. None of the isolates produced conidia on artificial media but developed typical Botrytis-like conidiophores and conidia on inoculated plant tissues, characterized by hyaline to pale brown, elliptical to ovoid conidia and branching conidiophores. Pathogenicity tests on blueberry tissues, green grapes, and white rose petals confirmed its ability to cause Botrytis blossom blight and fruit rot, with disease severity comparable to B. cinerea. Fungicide sensitivity assays revealed that B. michiganensis isolates were sensitive to all tested fungicides except cyprodinil. These findings provide new insights into the Botrytis species complex affecting blueberries and highlight the need for further diversity studies.
高丛蓝莓(Vaccinium corymbosum)是世界范围内重要的水果作物,密歇根州是美国最大的蓝莓生产国之一。葡萄枯萎病和果腐病是本地区的主要病害。虽然灰霉病一直被认为是主要的致病因子,但最近的一项研究在密歇根州发现了一种新物种。本文描述了一种新的引起花枯萎病的病原菌——密歇根芽孢杆菌。本研究旨在通过多位点系统发育分析(G3PDH、HSP60、RPB2、NEP1和NEP2)、形态培养性状和杀菌剂敏感性等方法对黑僵菌进行鉴定。系统发育分析,使用个体和连接的基因序列,将B. michiganensis置于与B. fabiopsis, B. caroliniana和B. galanthina密切相关的独特分支中。菌株在马铃薯葡萄糖琼脂上表现出不同的培养和形态特征,菌丝从白色到灰色不等。这些菌株在人工培养基上均未产生分生孢子,但在接种植株组织上发育了典型的葡萄孢样分生孢子和分生孢子,其特征为透明至浅棕色,椭圆形至卵圆形,分生孢子分枝。对蓝莓组织、绿葡萄和白玫瑰花瓣的致病性测试证实了它能引起葡萄枯萎病和果实腐烂,其疾病严重程度与灰葡萄球菌相当。杀菌剂敏感性试验表明,除环虫腈外,密歇根芽孢杆菌对其他杀菌剂均敏感。这些发现为了解影响蓝莓的葡萄孢菌种类复合体提供了新的见解,并强调了进一步多样性研究的必要性。
{"title":"<i>Botrytis michiganensis</i>: A New <i>Botrytis</i> Species Causing Blossom Blight on Highbush Blueberries.","authors":"J A Abbey, S Singh, K A Neugebauer, T D Miles","doi":"10.1094/PHYTO-06-25-0223-R","DOIUrl":"10.1094/PHYTO-06-25-0223-R","url":null,"abstract":"<p><p>Highbush blueberries (<i>Vaccinium corymbosum</i>) are an important fruit crop worldwide, and Michigan is one of the largest producers within the United States. Botrytis blossom blight and fruit rot are major diseases in this region. Although <i>Botrytis cinerea</i> has long been considered the primary causal agent, a recent study identified a novel species in Michigan. In this article, we describe a new species, <i>B. michiganensis</i>, as an additional pathogen causing blossom blight. This study aimed to characterize <i>B. michiganensis</i> through multilocus phylogenetic analysis (<i>G3PDH</i>, <i>HSP60</i>, <i>RPB2</i>, <i>NEP1</i>, and <i>NEP2</i>), morpho-cultural traits, and fungicide sensitivity. Phylogenetic analyses, using both individual and concatenated gene sequences, placed <i>B. michiganensis</i> in a distinct clade closely related to <i>B. fabiopsis</i>, <i>B. caroliniana</i>, and <i>B. galanthina</i>. The isolates exhibited diverse cultural and morphological characteristics on potato dextrose agar, ranging from white to gray fluffy/cottony mycelia. None of the isolates produced conidia on artificial media but developed typical <i>Botrytis</i>-like conidiophores and conidia on inoculated plant tissues, characterized by hyaline to pale brown, elliptical to ovoid conidia and branching conidiophores. Pathogenicity tests on blueberry tissues, green grapes, and white rose petals confirmed its ability to cause Botrytis blossom blight and fruit rot, with disease severity comparable to <i>B. cinerea</i>. Fungicide sensitivity assays revealed that <i>B. michiganensis</i> isolates were sensitive to all tested fungicides except cyprodinil. These findings provide new insights into the <i>Botrytis</i> species complex affecting blueberries and highlight the need for further diversity studies.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"252-262"},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145065362","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-30DOI: 10.1094/PHYTO-06-25-0199-R
Jae Young Hwang, Sharmodeep Bhattacharyya, Shirshendu Chatterjee, Thomas L Marsh, Joshua F Pedro, David H Gent
The economic value of cultivars resistant to disease is of great interest, but how growers change their fungicide use in response to host resistance may be nuanced. We draw upon a well-described data set of the incidence of hop plants with powdery mildew and associated production metadata and demonstrate the utility of Bayesian networks as a framework for quantifying causal relationships for fungicide use and cost in response to host resistance. Conditional Gaussian Bayesian network models applied to cultivars differing in race-specific resistance to powdery mildew revealed cultivar resistance to powdery mildew influenced disease levels in early spring, which had a causal effect on how often and what fungicides growers later applied. Annual costs depended on not only the number of applications made but also the specific types of fungicides growers selected. Fungicide costs were little changed on cultivars that possessed race-specific resistance to only one of two extant strains of the pathogen. For cultivars with resistance to both pathogen strains, annual costs of fungicides were reduced commensurate with the level of resistance. Predicted values from the Bayesian networks and simulation indicate that growers apply a baseline level of fungicide, independent of cultivar resistance. Fungicide cost savings result from how fungicide inputs differentially scale with the incidence of powdery mildew and the type of fungicides used. Our analyses indicate that for a high-value crop, deployment of disease resistance may cause complex and unexpected changes in growers' fungicide use patterns that may not be obvious in simplified randomized controlled trials.
{"title":"How Do Growers Respond to Host Resistance? A Conditional Gaussian Bayesian Network for Causal Inference of Fungicide Cost Savings.","authors":"Jae Young Hwang, Sharmodeep Bhattacharyya, Shirshendu Chatterjee, Thomas L Marsh, Joshua F Pedro, David H Gent","doi":"10.1094/PHYTO-06-25-0199-R","DOIUrl":"10.1094/PHYTO-06-25-0199-R","url":null,"abstract":"<p><p>The economic value of cultivars resistant to disease is of great interest, but how growers change their fungicide use in response to host resistance may be nuanced. We draw upon a well-described data set of the incidence of hop plants with powdery mildew and associated production metadata and demonstrate the utility of Bayesian networks as a framework for quantifying causal relationships for fungicide use and cost in response to host resistance. Conditional Gaussian Bayesian network models applied to cultivars differing in race-specific resistance to powdery mildew revealed cultivar resistance to powdery mildew influenced disease levels in early spring, which had a causal effect on how often and what fungicides growers later applied. Annual costs depended on not only the number of applications made but also the specific types of fungicides growers selected. Fungicide costs were little changed on cultivars that possessed race-specific resistance to only one of two extant strains of the pathogen. For cultivars with resistance to both pathogen strains, annual costs of fungicides were reduced commensurate with the level of resistance. Predicted values from the Bayesian networks and simulation indicate that growers apply a baseline level of fungicide, independent of cultivar resistance. Fungicide cost savings result from how fungicide inputs differentially scale with the incidence of powdery mildew and the type of fungicides used. Our analyses indicate that for a high-value crop, deployment of disease resistance may cause complex and unexpected changes in growers' fungicide use patterns that may not be obvious in simplified randomized controlled trials.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"239-251"},"PeriodicalIF":3.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145207407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}