土壤盐度增加对基于遗传抗性(I-3 基因)的加利福尼亚加工番茄镰刀菌枯萎病(F. oxysporum f. sp. lycopercisi race 3)管理的影响。

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES
Phytopathology Pub Date : 2024-10-01 Epub Date: 2024-10-03 DOI:10.1094/PHYTO-10-23-0402-KC
Elizabeth M Hellman, Thomas Turini, Cassandra L Swett
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引用次数: 0

摘要

加利福尼亚州是美国主要的加工番茄(Solanum lycopersicum)生产地。Fusarium oxysporum f. sp. lycopercisi race 3(Fol3)是镰刀菌枯萎病的病原菌,是造成产量损失的主要原因。最近观察到 Fol3 在抗性栽培品种(I-3 R 基因)中致病,通常与土壤盐度过高有关。本研究旨在更好地了解盐度对 Fol3 抗性管理的影响。调查发现,在 44% 的受检商业田块中,土壤盐分含量高达 3.6 dS/m (P < 0.001)、高钠 (P < 0.001) 和高钠度 (SAR > 13, P < 0.001),存在盐分-Fol3-番茄相互作用的机会。在 NaCl:CaCl2 处理过的土壤中对 Fol3 进行田间对照研究时,抗 Fol3 的栽培品种要么只在盐分条件下出现枯萎病,要么只在盐分条件下出现高于行业非杂交阈值(2%)的枯萎病,试验年份为两年。没有产量差异表明病害加重对经济影响较小或没有影响(P > 0.05)。与水琼脂对照相比,NaCl、CaCl2 和 Na2SO4 对液体琼脂中 Fol3 的繁殖体产量没有影响(P > 0.05),但与离子对照(PEG)相比,CaCl2 使繁殖体数量增加了 7 倍(P = 0.036)。在有病原体侵染的番茄组织的土壤中,NaCl:CaCl2(2:1)与无盐相比,可使繁殖体数量减少 65%(P = 0.029)。这些结果共同确定了盐度-Fol3-番茄之间相互作用的机会,以及盐对基于抗性栽培品种的管理效果产生影响的潜力--这似乎并不主要是由于盐增强了病原体种群,而是盐对寄主抗性的直接影响,这一点尚未被探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impacts of Increasing Soil Salinity on Genetic Resistance (I-3 Gene)-Based Management of Fusarium Wilt (Fusarium oxysporum f. sp. lycopercisi Race 3) in California Processing Tomatoes.

California is the primary processing tomato (Solanum lycopersicum) producer in the United States. Fusarium oxysporum f. sp. lycopercisi race 3 (Fol3), the cause of Fusarium wilt, is a major driver of yield losses. Fol3 has recently been observed causing disease in resistant cultivars (I-3 R-gene), often reported in association with high soil salinity. This study was undertaken to better understand the role of salinity in compromising resistance-based management of Fol3. Surveys established opportunity for salinity-Fol3-tomato interactions in 44% of commercial fields examined, with harmful soil salt levels up to 3.6 dS/m (P < 0.001), high sodium (P < 0.001), and high sodicity (sodium adsorption ratio > 13; P < 0.001). In controlled field studies of Fol3 in NaCl/CaCl2-treated soil, Fol3-resistant cultivars either only developed wilt under salt or only developed wilt above the industry non-hybrid threshold (2%) under salt across two trial years. The absence of yield differences indicates low to no economic impact of disease enhancement (P > 0.05). NaCl, CaCl2, and Na2SO4 had no effect on Fol3 propagule production in liquid agar versus water agar controls (P > 0.05), although CaCl2 increased propagule loads sevenfold versus ionic controls (polyethylene glycol) (P = 0.036). NaCl/CaCl2 (2:1) reduced propagule loads up to 65% versus no salt (P = 0.029) in soil with pathogen-infested tomato tissue. These results together establish the opportunity for salinity-Fol3-tomato interactions and potential for salt to influence the efficacy of resistant cultivar-based management-this does not appear to be primarily due to salt enhancement of pathogen populations, pointing to a yet-unexplored direct influence of salt on host resistance.

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来源期刊
Phytopathology
Phytopathology 生物-植物科学
CiteScore
5.90
自引率
9.40%
发文量
505
审稿时长
4-8 weeks
期刊介绍: Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.
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