赤霉病菌对杀真菌剂抗性的田间规模基因流动以及选择压力对种群结构的影响。

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES
Leon M Hodgson, Francisco J Lopez-Ruiz, Mark R Gibberd, Geoff J Thomas, Ayalsew Zerihun
{"title":"赤霉病菌对杀真菌剂抗性的田间规模基因流动以及选择压力对种群结构的影响。","authors":"Leon M Hodgson, Francisco J Lopez-Ruiz, Mark R Gibberd, Geoff J Thomas, Ayalsew Zerihun","doi":"10.1094/PHYTO-10-23-0378-KC","DOIUrl":null,"url":null,"abstract":"<p><p>The effectiveness of fungicides to control foliar fungal crop diseases is being diminished by the increasing spread of resistances to fungicides. One approach that may help to maintain efficacy is remediation of resistant populations by sensitive ones. However, the success of such approaches can be compromised by re-incursion of resistance through aerial spore dispersal; although, knowledge of localized gene flow is lacking. Here, we report on a replicated mark-release-recapture field experiment with several treatments set up to study spore-dispersal-mediated gene flow of a mutated allele that confers demethylase inhibitor resistance in <i>Pyrenophora teres</i> f. <i>teres</i> (<i>Ptt</i>). Artificial inoculation of the host, barley (<i>Hordeum vulgare</i>), was successful across the 12-ha trial, where the introduced sensitive- and resistant-populations were, respectively, 6- and 13-fold the DNA concentration of the native <i>Ptt</i> population. Subsequent disease pressure remained low which hampered spread of the epidemic to such extent that gene flow was not detected at, or beyond 2.5 m from source points. In the absence of gene flow, plots were assessed for treatment effects; fungicide applied to populations that contained 14.3% of allele mutation increased in frequency to 24.5%, whereas sensitive populations had no change in structure. Untreated controls of native <i>Ptt</i> population remained genetically stable, yet untreated controls that were inoculated with sensitive <i>Ptt</i> had half the resistance frequency of the native population structure. The trial demonstrates the potential for management to remediate fungicide resistant pathogen populations, where localized gene flow is minimal; to safeguard chemical crop protection into the future.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Field-scale gene flow of fungicide resistance in <i>Pyrenophora teres</i> f. <i>teres</i> and the effect of selection pressure on the population structure.\",\"authors\":\"Leon M Hodgson, Francisco J Lopez-Ruiz, Mark R Gibberd, Geoff J Thomas, Ayalsew Zerihun\",\"doi\":\"10.1094/PHYTO-10-23-0378-KC\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The effectiveness of fungicides to control foliar fungal crop diseases is being diminished by the increasing spread of resistances to fungicides. One approach that may help to maintain efficacy is remediation of resistant populations by sensitive ones. However, the success of such approaches can be compromised by re-incursion of resistance through aerial spore dispersal; although, knowledge of localized gene flow is lacking. Here, we report on a replicated mark-release-recapture field experiment with several treatments set up to study spore-dispersal-mediated gene flow of a mutated allele that confers demethylase inhibitor resistance in <i>Pyrenophora teres</i> f. <i>teres</i> (<i>Ptt</i>). Artificial inoculation of the host, barley (<i>Hordeum vulgare</i>), was successful across the 12-ha trial, where the introduced sensitive- and resistant-populations were, respectively, 6- and 13-fold the DNA concentration of the native <i>Ptt</i> population. Subsequent disease pressure remained low which hampered spread of the epidemic to such extent that gene flow was not detected at, or beyond 2.5 m from source points. In the absence of gene flow, plots were assessed for treatment effects; fungicide applied to populations that contained 14.3% of allele mutation increased in frequency to 24.5%, whereas sensitive populations had no change in structure. Untreated controls of native <i>Ptt</i> population remained genetically stable, yet untreated controls that were inoculated with sensitive <i>Ptt</i> had half the resistance frequency of the native population structure. The trial demonstrates the potential for management to remediate fungicide resistant pathogen populations, where localized gene flow is minimal; to safeguard chemical crop protection into the future.</p>\",\"PeriodicalId\":20410,\"journal\":{\"name\":\"Phytopathology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytopathology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1094/PHYTO-10-23-0378-KC\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-10-23-0378-KC","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

由于对杀真菌剂的抗药性日益扩散,杀真菌剂控制作物叶部真菌病害的效果正在减弱。一种有助于保持药效的方法是用敏感种群补救抗药性种群。然而,这种方法的成功可能会因抗药性通过气生孢子传播再次扩散而受到影响;不过,目前还缺乏关于局部基因流的知识。在此,我们报告了一项重复的标记-释放-再捕获田间试验,该试验设置了几种处理方法,以研究孢子散播所介导的基因流,该基因流是一种突变的等位基因,它赋予了赤潮镰刀菌(Ptt)对去甲基化酶抑制剂的抗性。对宿主大麦(Hordeum vulgare)的人工接种在 12 公顷的试验中取得了成功,引入的敏感种群和抗性种群的 DNA 浓度分别是本地 Ptt 种群的 6 倍和 13 倍。随后的病害压力仍然很低,阻碍了疫病的传播,以至于在距离源点 2.5 米处或更远的地方都检测不到基因流。在没有基因流动的情况下,对地块的处理效果进行了评估;对含有 14.3% 等位基因变异的种群施用杀菌剂后,其变异频率增加到 24.5%,而敏感种群的结构没有变化。未处理的本地 Ptt 种群对照组在遗传上保持稳定,而接种了敏感 Ptt 的未处理对照组的抗性频率只有本地种群结构的一半。该试验表明,在局部基因流动最小的情况下,管理部门有可能对具有杀真菌剂抗性的病原体种群进行补救,以保障未来的化学作物保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Field-scale gene flow of fungicide resistance in Pyrenophora teres f. teres and the effect of selection pressure on the population structure.

The effectiveness of fungicides to control foliar fungal crop diseases is being diminished by the increasing spread of resistances to fungicides. One approach that may help to maintain efficacy is remediation of resistant populations by sensitive ones. However, the success of such approaches can be compromised by re-incursion of resistance through aerial spore dispersal; although, knowledge of localized gene flow is lacking. Here, we report on a replicated mark-release-recapture field experiment with several treatments set up to study spore-dispersal-mediated gene flow of a mutated allele that confers demethylase inhibitor resistance in Pyrenophora teres f. teres (Ptt). Artificial inoculation of the host, barley (Hordeum vulgare), was successful across the 12-ha trial, where the introduced sensitive- and resistant-populations were, respectively, 6- and 13-fold the DNA concentration of the native Ptt population. Subsequent disease pressure remained low which hampered spread of the epidemic to such extent that gene flow was not detected at, or beyond 2.5 m from source points. In the absence of gene flow, plots were assessed for treatment effects; fungicide applied to populations that contained 14.3% of allele mutation increased in frequency to 24.5%, whereas sensitive populations had no change in structure. Untreated controls of native Ptt population remained genetically stable, yet untreated controls that were inoculated with sensitive Ptt had half the resistance frequency of the native population structure. The trial demonstrates the potential for management to remediate fungicide resistant pathogen populations, where localized gene flow is minimal; to safeguard chemical crop protection into the future.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信