一种快速有效的将树干溃疡病病原菌引入叶片的体内接种方法:适用于杨树育种后代的大规模抗性评估。

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Zheng Li, Bingyu Zhang, Yuchen Fu, Yutian Suo, Yinan Zhang, Jinxia Feng, Long Pan, Wanna Shen, Huixiang Liu, Xiaohua Su, Jiaping Zhao
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引用次数: 0

摘要

背景:杂交育种作为一种直接有效的树种疾病控制和管理策略,目前受到抗性克隆选择方法——“离体茎段接种法”的限制。这种方法受接种材料的限制,不能快速、有效和经济地筛选所有杂交克隆的抗性。为了克服这些局限性,我们引入了一种新的病原菌接种方法来评估杨树-雪梨病系杂交无性系的抗性。这种方法包括在宿主叶片上接种茎溃疡病病原体,这是一种独特而有前途的方法,我们已经成功验证了。结果:茎溃疡病病原菌V. sordida在接种菌丝体5 d后可诱导扩大的坏死灶,甚至诱导叶片表面形成pypydium结构和分生孢子;(1)上部5 ~ 7叶的抗病性高于中部18 ~ 20叶;(2)遮荫条件比光照条件诱发的症状更严重;(3)杨树叶片对培养4 d的幼菌丝比培养7 d的老菌丝更敏感。本研究结果证明了“叶片体内接种法”在揭示杨树杂交无性系抗性分化方面的稳健性。根据叶片坏死面积病指数,将这些杨树无性系分为7个不同的抗性类群。采用“离体茎段接种法”,对15个杨树无性系进行叶片鉴定。结果表明,两种方法的有效性是一致的。此外,研究结果还揭示了叶片接种法病原菌种群的致病性多样性。结论:与常规的“茎段离体接种法”相比,叶片法具有接种材料丰富、操作简便、发病快、对寄主几乎无不良影响等优点。特别适用于杨树茎秆抗病性育种中所有后代的抗性筛选和抗病性杨树无性系的早期(幼苗)表型选择。“叶片体内接种法”在杨树育种、树木病理学和树干疾病分子生物学研究中具有重要的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rapid and efficient in vivo inoculation method for introducing tree stem canker pathogens onto leaves: suitable for large-scale assessment of resistance in poplar breeding progeny.

Background: Hybrid breeding, a direct and efficient strategy for disease control and management in tree species, is currently limited by the selection method of resist clones: the "in vitro stem segment inoculation method". This method, constrained by the availability of inoculating materials, cannot rapidly, efficiently, and cost-effectively screen the resistance of all hybrid clones. To overcome these limitations, we introduce a novel pathogen inoculation method for the resistance assessment of hybrid clones in the poplar-Valsa sordida pathosystem. This method involves inoculating the stem canker pathogen on the host leaf, a unique and promising approach we have successfully validated.

Results: Results showed that stem canker pathogen V. sordida induced the extended necrotic lesion and even induced the formation of pycnidium structure and conidia on the leaf surface 5 days after mycelium inoculation; (1) the upper 5-7thleaves exhibited higher resistance than the middle 18-20th leaves; (2) the shading conditions induced more severe symptoms on the leaves than lighting conditions; (3) the poplar leaves were more susceptible to the juvenile mycelium inoculums (4-day-cultured) than the old ones (7-day-cultured). Our results demonstrate the robustness ofthe "in vivo leaf inoculation method" in revealing the resistance differentiation in poplar hybrid clones. According to the leaf necrotic area disease index, we divided these poplar clones into seven different resistance groups. The resistance assessed by leaf assessment was validated in 15 selected poplar clones using the "in vitro stem segment inoculation method". Results showed that the effectiveness of these two methods was consistent. Moreover, results also revealed the pathogenicity diversity of the pathogen population of tree species using leaf the inoculation method.

Conclusions: Compared to the conventional "in vitro stem segment inoculation method", the leaf method has the advantages of abundant inoculation materials, easy operation, rapid disease onset, and almost no adverse effect on the host. It is particularly suitable for the resistance screening of all progeny and the early (seedling) phenotypic selection of resistant poplar clones in poplar stem disease resistance breeding. The "in vivo leaf inoculation method" holds significant promise in poplar breeding, tree pathology, and molecular biology research on tree stem diseases.

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来源期刊
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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