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Disease Progress and Detection of a California Resistance-Breaking Strain of Tomato Spotted Wilt Virus in Tomato with LAMP and CRISPR-Cas12a Assays 利用 LAMP 和 CRISPR-Cas12a 检测番茄斑点萎蔫病病毒在番茄中的病害进展和加州抗性突破菌株
Pub Date : 2024-01-24 DOI: 10.1094/phytofr-05-23-0058-fi
Tatsiana Shymanovich, A. Saville, Noor Mohammad, Qingshan Wei, David Rasmussen, Kirsten A. Lahre, D. Rotenberg, A. Whitfield, J. Ristaino
Use of tomato cultivars with the Sw-5 resistance gene cluster has led to the occurrence of resistance-breaking (RB) tomato spotted wilt virus (TSWV) strains globally, including California and, recently, North Carolina and Texas. We documented disease on tomato infected with either an RB strain from California (CA-RB) or a wild type (CA-WT) strain of TSWV on tomato with (cultivar Mountain Merit) or without (cultivar Mountain Fresh Plus) the Sw-5b resistance gene and detected virus incidence over time using microneedle RNA extractions and LAMP. We developed a LAMP/Cas12a assay for detection of the CA-C118Y mutation in a CA-RB strain and tested the assay with field samples. Disease in the susceptible cultivar was less severe with CA-RB than with the CA-WT strain. In contrast, the resistant cultivar had little disease when inoculated with the CA-WT strain but exhibited stunting of greater than 50% when inoculated with the CA-RB strain. In the susceptible tomatoes, the detection rates over time by LAMP reaction were higher in CA-WT than in CA-RB-inoculated plants. In resistant tomato, CA-RB remained detectable by TSWV LAMP over 14 days, whereas the WT strain was undetectable. A two-step LAMP/Cas12a assay differentiated the two strains in 1 h. Our methods were validated with samples from TSWV-infected North Carolina fields. A phylogeny of NSm gene sequences that included North Carolina field samples revealed two independent origins of the North Carolina RB isolates. The LAMP/Cas12 assay showed excellent detection of the CA-C118Y mutation. The TSWV LAMP/Cas12a assay is adaptable for in-field applications on either a smart phone platform or heat block. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .
使用带有 Sw-5 抗性基因簇的番茄栽培品种导致全球范围内出现了抗性突破(RB)番茄斑萎病毒(TSWV)株系,包括加利福尼亚州以及最近的北卡罗来纳州和德克萨斯州。我们记录了来自加利福尼亚的 RB 株系(CA-RB)或野生型 TSWV 株系(CA-WT)在带有 Sw-5b 抗性基因的番茄(栽培品种为 Mountain Merit)或不带有 Sw-5b 抗性基因的番茄(栽培品种为 Mountain Fresh Plus)上感染番茄的病害情况,并使用微针 RNA 提取和 LAMP 方法检测了随着时间推移的病毒发生率。我们开发了一种 LAMP/Cas12a 检测法,用于检测 CA-RB 株系中的 CA-C118Y 突变,并用田间样本对该检测法进行了测试。与 CA-WT 株系相比,CA-RB 株系在易感栽培品种上的病害较轻。相反,抗性栽培品种在接种 CA-WT 株系时几乎不发病,但在接种 CA-RB 株系时,发病率超过 50%。在易感番茄中,通过 LAMP 反应,CA-WT 株系在一段时间内的检出率高于接种 CA-RB 株系的植株。在抗性番茄中,TSWV LAMP 在 14 天内仍能检测到 CA-RB,而 WT 菌株则检测不到。两步 LAMP/Cas12a 检测法可在 1 小时内将两种菌株区分开来。包含北卡罗来纳州田间样本的 NSm 基因序列系统进化显示,北卡罗来纳州 RB 分离物有两个独立的来源。LAMP/Cas12 检测方法对 CA-C118Y 突变有很好的检测效果。TSWV LAMP/Cas12a 检测法可在智能手机平台或加热块上进行现场应用。[公式:见正文] Copyright © 2024 The Author(s).本文为开放获取文章,采用 CC BY-NC-ND 4.0 国际许可证发布。
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引用次数: 0
Whole-Genome Sequence of Colletotrichum brevisporum Causing Anthracnose on Papaya (Carica papaya) 引起木瓜炭疽病的 Colletotrichum brevisporum 的全基因组序列
Pub Date : 2024-01-17 DOI: 10.1094/phytofr-07-23-0080-a
Min Yang, Chenping Zhou, R. Kuang, Xiaming Wu, Yu-Si Wei
Colletotrichum spp. are the causal agents of papaya anthracnose, which seriously affects the quality and economic value of papaya fruits. Among them, Colletotrichum brevisporum is a new and important causal pathogen of anthracnose in papaya. The infection mechanisms of C. brevisporum are still unclear, and the genome sequence of C. brevisporum has not been released. In order to systemically explore the interaction between papaya and C. brevisporum, we sequenced the whole genome of the C. brevisporum strain C1, which was isolated from an infected papaya fruit in Guangdong Province, China. The assembly consists of 18 scaffolds with a genome size of 62.66 Mb. Furthermore, we identified genes that may be associated with pathogenicity, such as carbohydrate-active enzymes, secreted proteins, and secondary metabolite gene clusters. This genome resource will provide a valuable resource for future studies on the pathogenesis of C. brevisporum and comparative genomic analyses of the Colletotrichum genus. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .
Colletotrichum spp.是木瓜炭疽病的病原菌,严重影响木瓜果实的品质和经济价值。其中,Colletotrichum brevisporum 是木瓜炭疽病新的重要病原菌。目前,C. brevisporum 的侵染机制尚不清楚,C. brevisporum 的基因组序列也尚未公布。为了系统地探索番木瓜与 C. brevisporum 之间的相互作用,我们对从中国广东省受感染的番木瓜果实中分离出的 C. brevisporum 菌株 C1 进行了全基因组测序。该基因组由 18 个支架组成,基因组大小为 62.66 Mb。此外,我们还发现了可能与致病性有关的基因,如碳水化合物活性酶、分泌蛋白和次级代谢物基因簇。该基因组资源将为今后研究 C. brevisporum 的致病机理以及对 Colletotrichum 属进行比较基因组分析提供宝贵的资源。[公式:见正文] Copyright © 2024 The Author(s).本文为开放获取文章,采用 CC BY-NC-ND 4.0 国际许可证发布。
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引用次数: 0
Complete Genome Resource of a Fungal Antagonistic Strain: Pseudomonas tohonis 真菌拮抗菌株的完整基因组资源:陶氏假单胞菌
Pub Date : 2024-01-12 DOI: 10.1094/phytofr-09-23-0124-a
Wan-Zhen Luo, Hengguang Zhu, Hong-Yue Qi, Jiangqing Song, Dan-Dan Zhang, X. Dai, Mai-He-Mu-Ti Mijiti, Jiemin Chen, Dongfei Han, Dan Wang
The KRS022 was isolated from the rhizosphere soil of a healthy plant in a pathogen-infested cotton field in Xinjiang, China. Previous studies have demonstrated that KRS022 possesses the ability to trigger plant immune responses, inhibit the growth of various pathogenic fungi, including Verticillium dahliae, and promote plant growth. The antagonistic properties of KRS022 primarily stem from its bioactive metabolites. In this study, the high-quality genome of KRS022 was obtained. The KRS022 genome consists of a chromosome of 6,369,026 bp with 67.09% GC content, possesses 5,830 ORFs, of which 5,186 genes were annotated, and 119 ncRNA genes. Additionally, eleven gene clusters of secondary metabolites biosynthesis were predicted, involving in PKS, arylpolyene, NAGGN, betalactone, ranthipeptide, RIPP-like, redox-cofactor, and NRPS clusters. It could be useful to explore the biocontrol potential of P. tohonis, implying promising application of KRS022 in biological control.
KRS022 是从中国新疆受病原菌侵染的棉田中一株健康植株的根瘤土壤中分离出来的。以往的研究表明,KRS022 具有触发植物免疫反应、抑制包括大丽轮枝菌在内的多种病原真菌生长和促进植物生长的能力。KRS022 的拮抗特性主要源于其生物活性代谢物。本研究获得了 KRS022 的高质量基因组。KRS022 基因组由一条长达 6,369,026 bp 的染色体组成,GC 含量为 67.09%,拥有 5,830 个 ORFs,其中 5,186 个基因已被注释,还有 119 个 ncRNA 基因。此外,还预测了 11 个次级代谢物生物合成基因簇,涉及 PKS、芳基聚烯、NAGGN、betalactone、ranthipeptide、RIPP-like、氧化还原因子和 NRPS 等基因簇。这对探索 P. tohonis 的生物防治潜力很有帮助,意味着 KRS022 在生物防治中的应用前景广阔。
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引用次数: 0
Phthalic Acid and Its Role in Roots of Melon Plants (Cucumis melo) 邻苯二甲酸及其在甜瓜(Cucumis melo)根中的作用
Pub Date : 2024-01-12 DOI: 10.1094/phytofr-04-23-0046-r
S. Marquez, Kevin M. Crosby, Bhimanagouda S. Patil, Amir M. H. Ibrahim, Carlos A. Avila, H. Pessoa, Jashbir Singh
Melon is an important crop worldwide. However, this crop has many problems, such as high production costs, pests, diseases, and sensitivity to abiotic stresses. Among the diseases that negatively impact its production, vine decline disease (VDD), caused by the fungus Monosporascus cannonballus, is very dangerous because it affects the plant when the fruit is almost ready to be harvested, which causes huge losses to growers. In addition, this disease is widely spread in areas where melons are grown all over the world, and its control through soil fumigation is costly and polluting. Thus, cheap and sustainable ways to combat it must be found. Therefore, this study was conducted with the objectives of identifying and quantifying phenolic compounds produced during the interaction of melon plants with the fungus M. cannonballus, which can be useful in controlling VDD, ameliorating cultural practices of this crop, and consequently reducing production costs. Two varieties were grown and inoculated with the fungus M. cannonballus: TAM-Uvalde (susceptible) and USDA PI 124104 (resistant). Their roots were sampled before inoculating with the fungus (0 h) and 24, 48, and 72 h after inoculation. The root chemicals were then analyzed using high-performance liquid chromatography. Our results indicate that phthalic acid was induced in the roots after inoculation in both varieties, which suggests that it is produced by the plant as a defensive compound. Also, the production of phthalic acid varied over time according to the variety used, which suggests its allelopathic function. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .
甜瓜是世界上重要的农作物。然而,这种作物存在许多问题,如生产成本高、病虫害和对非生物胁迫的敏感性。在对其生产造成负面影响的病害中,由真菌炮弹菌(Monosporascus cannonballus)引起的蔓枯病(VDD)非常危险,因为它会在果实即将收获时影响植株,给种植者造成巨大损失。此外,这种病害在全世界种植甜瓜的地区广泛传播,而通过土壤熏蒸来控制这种病害既昂贵又污染环境。因此,必须找到廉价且可持续的方法来防治这种病害。因此,本研究旨在鉴定和量化甜瓜植物与炮弹菌相互作用过程中产生的酚类化合物,这些化合物可用于控制 VDD,改善这种作物的栽培方法,从而降低生产成本。种植了两个品种并接种了炮弹菌:TAM-Uvalde(易感)和 USDA PI 124104(抗性)。在接种真菌前(0 小时)、接种后 24、48 和 72 小时分别对它们的根部进行采样。然后使用高效液相色谱法对根部化学物质进行分析。我们的结果表明,两个品种的根部在接种后都诱导产生了邻苯二甲酸,这表明邻苯二甲酸是植物产生的一种防御性化合物。此外,邻苯二甲酸的产生随时间的推移而变化,这表明邻苯二甲酸具有等位抗病功能。[公式:见正文] Copyright © 2024 The Author(s).本文为开放获取文章,采用 CC BY-NC-ND 4.0 国际许可证发布。
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引用次数: 0
Complete Genome Resource of Xanthomonas oryzae pv. leersiae Strain YXol-1 Isolated From Plateau Japonica Rice in Yunnan Province, China 从中国云南省高原粳稻中分离出的黄单胞菌(Xanthomonas oryzae pv. leersiae)菌株 YXol-1 的完整基因组资源
Pub Date : 2024-01-03 DOI: 10.1094/phytofr-10-23-0139-a
X. A, Le Mei, Yayun Yang, Cui-feng Tang, Feifei Zhang, Chao Dong, Bin Wang, Pengcheng Liu, Xifeng Chen, Bojun Ma, Luyuan Dai
Xanthomonas oryzae are destructive phytopathogens in rice production, and also an important model system for studying the interaction between plants and bacterial pathogens. Here, we report the isolation and complete genome sequence of a X. oryzae strain YXol-1, and through the identification of transcription activator-like effectors (TALEs) and whole genome based phylogenetic analysis, we confirmed YXol-1 belongs to a rarely reported type of X. oryzae pathovar named as X. oryzae pv. leersiae (Xol). The present work enriched the genetic resources of Xol for studying the evolution of X. oryzae strains and can contribute to a better understanding of Xol-host interaction.
黄单胞菌(Xanthomonas oryzae)是水稻生产中的毁灭性植物病原菌,也是研究植物与细菌病原菌相互作用的重要模式系统。在此,我们报告了一株 X. oryzae 菌株 YXol-1 的分离和完整基因组序列,并通过转录激活子样效应子(TALEs)的鉴定和基于全基因组的系统发育分析,证实 YXol-1 属于一种很少报道的 X. oryzae 病原变种,被命名为 X. oryzae pv. leersiae(Xol)。本研究丰富了 Xol 的遗传资源,有助于研究 X. oryzae 菌株的进化,并有助于更好地理解 Xol 与寄主的相互作用。
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引用次数: 0
Genome Resource of Bacillus subtilis KRS015, a Potential Biocontrol Agent for Verticillium dahliae 枯草芽孢杆菌 KRS015--一种潜在的大丽轮枝菌生物控制剂--的基因组资源
Pub Date : 2023-12-17 DOI: 10.1094/phytofr-08-23-0114-a
Jiangqing Song, Jiemin Chen, Dan-Dan Zhang, Ran Li, Zhiqiang Kong, Hengguang Zhu, X. Dai, Dongfei Han, Dan Wang
Bacillus subtilis, a gram-positive bacterium commonly found in soil, is an excellent organism for plant biocontrol. The B. subtilis KRS015, an endophyte isolated from the seed of Gossypium hirsutum "Zhongzhimian No. 2", has been proven as its antagonistic activity against diverse fungal pathogens of plants, including Verticillium dahliae, a fungal pathogen of Verticillium wilt in various plants such as cotton. Here, we report the complete genome sequence of B. subtilis KRS015. The size of the KRS015 genome is 4,331,506 bp. Fifteen gene clusters for antibiotics and secondary metabolites, and 412 genes involved in plant bacterial interactions were identified in this genome. These findings qualified the potential of B. subtilis KRS015 as a biocontrol agent and may help reveal the molecular basis of its antagonistic mechanisms.
枯草芽孢杆菌(Bacillus subtilis)是一种常见于土壤中的革兰氏阳性菌,是植物生物防治的优良菌种。枯草芽孢杆菌 KRS015 是一种从 "中植绵 2 号 "棉花种子中分离出来的内生菌,已被证实对植物的多种真菌病原体具有拮抗活性,包括棉花等多种植物的轮纹枯萎病真菌病原体大丽轮纹菌。在此,我们报告了枯草芽孢杆菌 KRS015 的完整基因组序列。KRS015 基因组的大小为 4,331,506 bp。在该基因组中发现了 15 个抗生素和次生代谢物基因簇,以及 412 个参与植物细菌相互作用的基因。这些发现证明了枯草杆菌 KRS015 作为生物控制剂的潜力,并可能有助于揭示其拮抗机制的分子基础。
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引用次数: 0
Phenotypic fungicide resistance and cross-resistance among Nothopassalora personata populations Nothopassalora personata 种群对杀真菌剂的表型抗性和交叉抗性
Pub Date : 2023-12-11 DOI: 10.1094/phytofr-10-23-0137-r
Hope Renfroe-Becton, Jonathan Croft, Charles Davis, Joe Varn, Albert Culbreath, David Langston, Dan Anco
Late leaf spot, caused by Nothopassalora personata, is an economically important disease of peanut which routinely requires preventative fungicide application. The objectives of this study were to quantify the risk of phenotypic fungicide resistance and potential cross-resistance among Nothopassalora personata populations. A total of 59 samples of N. personata isolates were collected from 28 grower or research fields in SC, GA, and VA. Phenotypic resistance of isolates was evaluated against 14 fungicides and a nontreated control, with active ingredients from the quinone outside inhibitor (QoI), demethylation inhibitor (DMI), and succinate-dehydrogenase inhibitor (SDHI) classes. Overall, lesion development ≥ 15% was observed with nearly all isolates for at least one of the active ingredients tested. Correlations between active ingredients, penthiopyrad and pydiflumetofen, as well as bixafen plus flutriafol and pydiflumetofen, and their lesion development risk indicates potential N. personata populations with SDHI cross-resistance. While these data do not confirm the presence of genetic resistance markers, results paired with observed reduced efficacy in the field reinforce the strong need for an integrated approach in managing late leaf spot. In areas with high probabilities for resistance to several modes of action, longer rotations out of peanut, varieties with greater levels of resistance, earlier planting, and continued incorporation of active ingredients with multi-site mode of action in fungicide programs are advised for preserving fungicide efficacy or reducing selection pressure.
由 Nothopassalora personata 引起的后期叶斑病是花生的一种重要经济病害,通常需要施用预防性杀菌剂。本研究的目的是量化 Nothopassalora personata 种群对杀真菌剂的表型抗性和潜在交叉抗性的风险。从南卡罗来纳州、佐治亚州和弗吉尼亚州的 28 个种植者或研究田中共收集了 59 份 N. personata 分离物样本。评估了分离株对 14 种杀菌剂和未处理对照的表型抗性,这些杀菌剂的有效成分来自醌外抑制剂 (QoI)、去甲基化抑制剂 (DMI) 和琥珀酸脱氢酶抑制剂 (SDHI)。总体而言,几乎所有的分离物都能观察到至少一种活性成分的病变发展≥15%。活性成分吡噻菌胺、吡氟禾草灵、苯醚甲环唑加氟螨脲和吡氟禾草灵与其病变风险之间的相关性表明,潜在的人形萘菌群具有 SDHI 交叉抗性。虽然这些数据并不能证实遗传抗性标记的存在,但这些结果与在田间观察到的药效降低相匹配,更加说明了采用综合方法防治晚发叶斑病的强烈必要性。在对几种作用模式产生抗性的概率较高的地区,建议延长花生的轮作期、种植抗性更强的品种、提早种植,并继续在杀菌剂计划中加入具有多部位作用模式的活性成分,以保持杀菌剂的药效或减少选择压力。
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引用次数: 0
Genome sequence resource of a taro bacterial soft rot pathogen Dickeya fangzhongdai ZXC1 芋头细菌软腐病病原体 Dickeya fangzhongdai ZXC1 的基因组序列资源
Pub Date : 2023-12-11 DOI: 10.1094/phytofr-07-23-0090-a
Zhongqiao Chen, Weihan Gu, Congcong Xie, Huagui Gao, Shufen Huang, Lian-hui Zhang, L. Liao
Dickeya fangzhongdai ZXC1 is a newly identified highly virulent causal agent of taro bacterial soft rot disease isolated from the taro sample showing typical soft rot symptoms at Shaoguan, Guangdong Province, China. The pathogen produces plant cell wall degrading enzymes which macerate the taro tube tissues. In this study, we report the whole genome sequencing analysis of strain ZXC1. The results showed that strain ZXC1 has one circular DNA chromosome of 5,129,951 bp with 56.59% G+C content. In addition to sharing a conserved zms gene cluster that encodes the genes for biosynthesis of phytotoxin zeamines, and 11 copies of predicted pectate lyases genes, the strain ZXC1 genome contains more prophage loci and higher number of type IV secretion system (T4SS) and type IV secretion system (T6SS) gene clusters than the D. fangzhongdai strains isolated from pears or phalaenopsis, which may account for its strong virulence phenotype. The data from this study present a valuable resource for elucidation of the pathogenic mechanisms of D. fangzhongdai, and may aid in developing new disease control approaches to safeguard taro production.
Dickeya fangzhongdai ZXC1是从中国广东省韶关市出现典型软腐症状的芋头样品中分离出来的一种新发现的芋头细菌性软腐病高致病性病原菌。该病原菌能产生植物细胞壁降解酶,使芋头管组织浸渍。本研究报告了对菌株 ZXC1 的全基因组测序分析。结果表明,菌株 ZXC1 有一个 5,129,951 bp 的环状 DNA 染色体,G+C 含量为 56.59%。与分离自梨或蝴蝶兰的方中快菌株相比,菌株 ZXC1 基因组除了共享一个保守的 zms 基因簇(编码植物毒素玉米素生物合成基因)和 11 个拷贝的预测酪酸酶基因外,还含有更多的噬菌体位点和更多的 IV 型分泌系统(T4SS)和 IV 型分泌系统(T6SS)基因簇,这可能是其具有强烈毒力表型的原因。这项研究的数据为阐明方中莱氏菌的致病机制提供了宝贵的资源,并可能有助于开发新的病害控制方法,以保障芋头生产。
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引用次数: 0
Characterization of Ralstonia pseudosolanacearum diversity and screening tomato, pepper, and eggplant resistance to manage bacterial wilt in South Asia 鉴定假丝酵母菌(Ralstonia pseudosolanacearum)的多样性,筛选番茄、辣椒和茄子的抗性,以管理南亚的细菌性枯萎病
Pub Date : 2023-12-11 DOI: 10.1094/phytofr-10-23-0136-r
N. Subedi, Tabitha Cowell, Matthew L Cope-Arguello, P. Paul, G. Cellier, Hashem Bkayrat, Nicholas Bonagura, Agela Cadatal, Rachel Chen, Ariana Enriquez, Rama Parasar, Lisa Repetto, Aracely Hernandez Rivas, Mahnoor Shahbaz, Kaitlin White, Tiffany Lowe-Power, S. A. Miller
In South Asia, bacterial wilt pathogens in the Ralstonia solanacearum species complex (RSSC) impose major constraints on eggplant, tomato, and pepper production. To improve the efficacy of bacterial wilt management, the goals of this study were to (1) conduct a survey of RSSC pathogens in Bangladesh and Nepal, (2) characterize the genetic diversity of these isolates, and (3) screen 37 tomato, eggplant, and pepper accessions for resistance to six representative isolates from South Asia. We isolated 99 isolates from Bangladesh and 20 isolates from Nepal and determined that all are phylotype I isolates of the Ralstonia pseudosolanacearum species. We sequenced and assembled draft genomes for 25 isolates. Phylogenomic analyses suggest that there is a wide diversity of endemic phylotype I isolates in South Asia, and possible introductions of two clonal phylotype I lineages into Bangladesh and Nepal. We contextualize our newly described isolates based on prior reports of RSSC diversity in South Asia and global reports of RSSC pathogens on eggplant and pepper. Greenhouse trials revealed multiple tomato, eggplant, and pepper accessions that exhibit promising levels of resistance to six phylotype I isolates from South Asia.
在南亚,Ralstonia solanacearum 菌种复合体(RSSC)中的细菌性枯萎病病原体对茄子、番茄和辣椒的生产造成了严重制约。为了提高细菌性枯萎病的防治效果,本研究的目标是:(1)对孟加拉国和尼泊尔的 RSSC 病原体进行调查;(2)描述这些分离物的遗传多样性;以及(3)筛选 37 个番茄、茄子和辣椒品种,以确定它们对来自南亚的 6 个代表性分离物的抗性。我们从孟加拉国分离了 99 个分离株,从尼泊尔分离了 20 个分离株,并确定所有分离株都是 Ralstonia pseudosolanacearum 的系统I型分离株。我们对 25 个分离株的基因组进行了测序和组装。系统发生组分析表明,南亚地区流行的系统I型分离物具有广泛的多样性,孟加拉国和尼泊尔可能引入了两个克隆系统I型系。我们根据之前关于南亚 RSSC 多样性的报道以及全球关于茄子和辣椒 RSSC 病原体的报道,对新描述的分离株进行了背景分析。温室试验发现,多个番茄、茄子和辣椒品种对来自南亚的六个系统I型分离物表现出了良好的抗性。
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引用次数: 0
Gene Expression Clusters Suggest Potential Mechanisms of Resistance to Powdery Mildew in Hop (Humulus lupulus) 基因表达集群揭示了啤酒花(Humulus lupulus)抵抗白粉病的潜在机制
Pub Date : 2023-12-01 DOI: 10.1094/phytofr-09-22-0098-r
Renée L. Eriksen, Michele S. Wiseman, A. A. Magana, Nikhilesh Dhar, Ralph L. Reed, J. Fred Stevens, D. Gent, John A. Henning
Powdery mildew, caused by Podosphaera macularis, is one of the most important diseases of hop in the Pacific Northwest of the United States. Resistant cultivars exist; however, recently, the pathogen has overcome two sources of resistance in popular cultivars. Breeding for new, emerging races of the pathogen is thus a continuing priority. We used RNA-seq to understand gene expression trends in a resistant (cv. USDA Nugget) and a susceptible (cv. Symphony) hop cultivar along a time series following inoculation. We found stronger transcriptional reprogramming in the resistant cultivar than the susceptible cultivar. Transcripts that increased in expression within 12 h post-inoculation in the resistant cultivar included genes in the jasmonic acid biosynthesis pathway, as well as phenylpropanoid biosynthesis. Transcripts that had a positive correlation with time post-inoculation in the resistant cultivar included genes involved in phosphorylation, cell-surface signaling pathways, and response to jasmonic acid. We used untargeted HPLC–HR-MS/MS analysis and confirmed an increase in jasmonic acid and several phenolic compounds. We hypothesize that resistance to powdery mildew in cv. Nugget may be at least partially due to perception of the pathogen outside of the cell, and transcriptional and metabolic reprogramming is mediated by jasmonic acid signaling. At least part of that transcriptional and metabolic reprogramming involves changes to lignin production, which might reinforce the cell wall. The multi-omics approach to describe the contrasting responses of a resistant and a susceptible hop cultivar following inoculation with this important pathogen may indicate new strategies for developing resistant germplasm and control methods. [Formula: see text] Copyright © 2023 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .
由黄斑病菌(Podosphaera macularis)引起的白粉病是美国西北太平洋地区酒花最重要的病害之一。抗病栽培品种是存在的;不过,最近病原体克服了流行栽培品种的两个抗病来源。因此,针对新出现的病原体品系进行育种仍是当务之急。我们使用 RNA-seq 来了解抗性酒花品种(cv. USDA Nugget)和易感酒花品种(cv. Symphony)在接种后的基因表达趋势。我们发现抗性栽培品种的转录重编程比易感栽培品种更强。抗性栽培品种在接种后 12 小时内表达量增加的转录本包括茉莉酸生物合成途径中的基因以及苯丙醇生物合成中的基因。在抗性栽培品种中,与接种后时间呈正相关的转录本包括参与磷酸化、细胞表面信号途径和对茉莉酸反应的基因。我们使用非靶向 HPLC-HR-MS/MS 分析,证实茉莉酸和几种酚类化合物有所增加。我们推测,变种 Nugget 对白粉病的抗性至少部分是由茉莉酸引起的。茉莉酸信号介导的转录和代谢重编程。转录和代谢重编程至少有一部分涉及木质素生产的变化,这可能会加固细胞壁。用多组学方法描述抗性酒花栽培品种和易感酒花栽培品种在接种这种重要病原体后的对比反应,可能为开发抗性种质和控制方法提供新策略。[公式:见正文] Copyright © 2023 The Author(s).本文为开放获取文章,采用 CC BY-NC-ND 4.0 国际版权许可协议发布。
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引用次数: 0
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