苹果枝上淀粉状欧文菌的种群动态、感染途径和全身传播速度。

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES
Katherine Olive Dougherty, Cory A Outwater, George W Sundin
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引用次数: 0

摘要

由葡萄霉引起的火疫病是全世界苹果和梨最具破坏性的病害之一。幼树特别容易受到该疾病的梢枯阶段的影响,淀粉样芽孢杆菌从受感染的梢尖迅速向下传播到整个树木的根茎,经常导致形成环状溃疡病,使树木死亡。我们在野外研究中通过被感染的茎部组织对淀粉样芽孢杆菌细胞的系统迁移进行了量化和跟踪,以深入了解病原体的系统运动。在2021年和2022年,在重复的田间实验中,对“Gala”苹果芽的指定部分进行了为期20天的细菌种群监测。在有利的环境条件下,20 d取样期内,淀粉样芽孢杆菌在茎部组织中保持较高的种群数量。在接种后的第5天(9.9 cm day-1),淀粉样芽孢杆菌细胞在茎组织中最大迁移了49.5 cm,平均迁移速度为4.2 cm day-1。通过新生长的迁移速度为5.4 cm day-1,进一步的扫描电镜检查没有发现芽疤处的主要障碍物。显微检查感染茎组织使我们发现大量定植和细菌渗出形成的皮层薄壁。我们的研究完善了淀粉样芽孢杆菌在芽枯病期间系统定植的基础知识,并将过去50年来关于定植的不同研究纳入背景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population Dynamics, Route of Infection, and Velocity of Systemic Spread of Erwinia amylovora in Infected Apple Branches.

Fire blight, caused by Erwinia amylovora, is one of the most devastating diseases of apple and pear worldwide. Young trees are particularly susceptible to the shoot blight phase of the disease, and the rapid downward spread of E. amylovora from infected shoot tips throughout trees to the rootstock often results in the formation of girdling cankers that kill trees. We quantified and tracked the systemic migration of E. amylovora cells in field studies through infected shoot tissues to gain insight into the systemic movement of the pathogen. In 2021 and 2022, bacterial populations were monitored over a 20-day period in defined sections of 'Gala' apple shoots in replicated field experiments. E. amylovora reached populations >109 cfu g-1 and maintained high populations in shoot tissue throughout the 20-day sampling period under conducive environmental conditions. E. amylovora cells migrated through shoot tissue at a maximum of 49.5 cm at 5 days after inoculation (9.9 cm day-1) and exhibited an average velocity of 4.2 cm day-1. The rate of migration through the new growth was 5.4 cm day-1 and further investigations using scanning electron microscopy did not reveal major obstructions at the bud scar. Microscopic examination of infected shoot tissue enabled us to detect prolific colonization and bacterial ooze formation in the cortical parenchyma. Our study refines the fundamental knowledge of E. amylovora systemic colonization during shoot blight and contextualizes previously divergent studies of colonization from the past 50 years.

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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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