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种间马铃薯育种系在感染后表现出不同的定殖模式和诱导防御反应。

Interspecific Potato Breeding Lines Display Differential Colonization Patterns and Induced Defense Responses after Infection.

作者信息

Ferreira Virginia, Pianzzola María J, Vilaró Francisco L, Galván Guillermo A, Tondo María L, Rodriguez María V, Orellano Elena G, Valls Marc, Siri María I

机构信息

Departamento de Biociencias, Facultad de Química, Universidad de la RepúblicaMontevideo, Uruguay.

Unidad de Horticultura, INIA Las BrujasCanelones, Uruguay.

出版信息

Front Plant Sci. 2017 Aug 28;8:1424. doi: 10.3389/fpls.2017.01424. eCollection 2017.

DOI:10.3389/fpls.2017.01424
PMID:28894453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5581342/
Abstract

Potato ( L.) is one of the main hosts of , the causative agent of bacterial wilt. This plant pathogen bacteria produce asymptomatic latent infections that promote its global spread, hindering disease control. A potato breeding program is conducted in Uruguay based on the introgression of resistance from the wild native species Dun. Currently, several backcrosses were generated exploiting the high genetic variability of this wild species resulting in advanced interspecific breeding lines with different levels of bacterial wilt resistance. The overall aim of this work was to characterize the interaction of the improved potato germplasm with . Potato clones with different responses to were selected, and colonization, dissemination and multiplication patterns after infection were evaluated. A strain belonging to the phylotype IIB-sequevar 1, with high aggressiveness on potato was genetically modified to constitutively generate fluorescence and luminescence from either the green fluorescence protein gene or operon. These reporter strains were used to allow a direct and precise visualization of fluorescent and luminescent cells in plant tissues by confocal microscopy and luminometry. Based on wilting scoring and detection of latent infections, the selected clones were classified as susceptible or tolerant, while no immune-like resistance response was identified. Typical wilting symptoms in susceptible plants were correlated with high concentrations of bacteria in roots and along the stems. Tolerant clones showed a colonization pattern restricted to roots and a limited number of xylem vessels only in the stem base. Results indicate that resistance in potato is achieved through restriction of bacterial invasion and multiplication inside plant tissues, particularly in stems. Tolerant plants were also characterized by induction of anatomical and biochemical changes after infection, including hyperplasic activity of conductor tissue, tylose production, callose and lignin deposition, and accumulation of reactive oxygen species. This study highlights the potential of the identified tolerant interspecific potato clones as valuable genetic resources for potato-breeding programs and leads to a better understanding of resistance against in potato.

摘要

马铃薯(L.)是青枯病菌(细菌性萎蔫病的病原体)的主要寄主之一。这种植物病原细菌会产生无症状的潜伏感染,促进其在全球传播,阻碍病害防治。乌拉圭开展了一项马铃薯育种计划,其基础是将野生本地物种邓恩薯(Dun)的抗性基因渗入进来。目前,利用该野生物种的高遗传变异性进行了多次回交,培育出了具有不同青枯病抗性水平的高级种间育种系。这项工作的总体目标是表征改良马铃薯种质与青枯病菌的相互作用。选择了对青枯病菌有不同反应的马铃薯克隆,并评估了感染后病菌的定殖、传播和繁殖模式。一株属于IIB -序列变种1的青枯病菌株,对马铃薯具有高侵袭性,经过基因改造后可组成性地从绿色荧光蛋白基因或操纵子产生荧光和发光。这些报告菌株用于通过共聚焦显微镜和发光测定法直接精确地观察植物组织中的荧光和发光细胞。根据萎蔫评分和潜伏感染检测,将所选克隆分为易感型或耐受型,未发现类似免疫的抗性反应。易感植物的典型萎蔫症状与根和茎中高浓度的细菌相关。耐受克隆的定殖模式仅限于根部,且仅在茎基部的少数木质部导管中存在。结果表明,马铃薯的抗性是通过限制病菌在植物组织内,特别是在茎中的侵入和繁殖来实现的。耐受植物还表现出在感染青枯病菌后诱导的解剖学和生化变化,包括传导组织的增生活性、侵填体产生、胼胝质和木质素沉积以及活性氧的积累。本研究突出了所鉴定的耐受种间马铃薯克隆作为马铃薯育种计划宝贵遗传资源的潜力,并有助于更好地理解马铃薯对青枯病菌的抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/28a850650a42/fpls-08-01424-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/7d3b4528c320/fpls-08-01424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/e46c0d81fec7/fpls-08-01424-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/35a7d6fcb1ab/fpls-08-01424-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/646fc62d7797/fpls-08-01424-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/b95d6029cb2a/fpls-08-01424-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/a28b1805347c/fpls-08-01424-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/0dfc38361e98/fpls-08-01424-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/28a850650a42/fpls-08-01424-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/7d3b4528c320/fpls-08-01424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/e46c0d81fec7/fpls-08-01424-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/35a7d6fcb1ab/fpls-08-01424-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/646fc62d7797/fpls-08-01424-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/b95d6029cb2a/fpls-08-01424-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/a28b1805347c/fpls-08-01424-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/0dfc38361e98/fpls-08-01424-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5581342/28a850650a42/fpls-08-01424-g008.jpg

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