{"title":"桤木树皮甲虫的潜在共生体 Neonectria bordenii sp.","authors":"D L Wertman, J B Tanney, R C Hamelin, A L Carroll","doi":"10.3114/fuse.2024.13.02","DOIUrl":null,"url":null,"abstract":"<p><p>A taxonomically comprehensive perspective on the fungal associates of bark beetles (<i>Coleoptera</i>: <i>Curculionidae</i>: <i>Scolytinae</i>), and powerful molecular tools for detection of these fungi, are imperative to understanding bark beetle impacts on forest ecosystems. The most common filamentous fungi living alongside bark beetles in infested trees are ophiostomatoids (<i>Ascomycota</i>: <i>Ophiostomatales</i> and <i>Microascales</i>), yet an undescribed species of <i>Neonectria</i> (<i>Neonectria sp. nov.</i>; <i>Ascomycota</i>: <i>Hypocreales</i>) was recently identified cohabitating with the alder bark beetle, <i>Alniphagus aspericollis</i>, in red alder, <i>Alnus rubra</i>. The hardwood-infesting alder bark beetle is found throughout the range of its red alder host in the Pacific Coast region of North America and is associated with <i>Neonectria sp. nov.</i> in southwestern British Columbia, Canada. The aim of this study was to describe and name <i>Neonectria sp. nov.</i> and to develop a quantitative PCR (qPCR) assay to enable rapid detection of <i>Neonectria sp. nov.</i> from individual adult alder bark beetles and to define the distribution of the fungus. <i>Neonectria sp. nov.</i> was phylogenetically and morphologically determined to represent a distinct species closely related to <i>N. ditissima</i> and is described herein as <i>Neonectria bordenii sp. nov. Neonectria bordenii</i> was reliably detected from individual whole-beetle DNA extractions using a probe-based qPCR assay targeting multi-copy internal transcribed spacers (ITS) of nuclear ribosomal DNA. The qPCR assay amplified the fungus from 87.8 % (36/41) of individual alder bark beetle samples and was highly sensitive to <i>N. bordenii</i>, with a lower limit of detection of 1 × 10<sup>-6</sup> ng/μL of culture DNA (or ~262 genome copies). Application of the qPCR assay developed in this study will expedite future research evaluating <i>N. bordenii</i> as a potential symbiote of the alder bark beetle. <b>Citation:</b> Wertman DL, Tanney JB, Hamelin RC, Carroll AL (2024). <i>Neonectria bordenii sp. nov.</i>, a potential symbiote of the alder bark beetle, and its detection by quantitative PCR. <i>Fungal Systematics and Evolution</i> <b>13</b>: 15-28. doi: 10.3114/fuse.2024.13.02.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11317864/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>Neonectria bordenii sp. nov.</i>, a potential symbiote of the alder bark beetle, and its detection by quantitative PCR.\",\"authors\":\"D L Wertman, J B Tanney, R C Hamelin, A L Carroll\",\"doi\":\"10.3114/fuse.2024.13.02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A taxonomically comprehensive perspective on the fungal associates of bark beetles (<i>Coleoptera</i>: <i>Curculionidae</i>: <i>Scolytinae</i>), and powerful molecular tools for detection of these fungi, are imperative to understanding bark beetle impacts on forest ecosystems. The most common filamentous fungi living alongside bark beetles in infested trees are ophiostomatoids (<i>Ascomycota</i>: <i>Ophiostomatales</i> and <i>Microascales</i>), yet an undescribed species of <i>Neonectria</i> (<i>Neonectria sp. nov.</i>; <i>Ascomycota</i>: <i>Hypocreales</i>) was recently identified cohabitating with the alder bark beetle, <i>Alniphagus aspericollis</i>, in red alder, <i>Alnus rubra</i>. The hardwood-infesting alder bark beetle is found throughout the range of its red alder host in the Pacific Coast region of North America and is associated with <i>Neonectria sp. nov.</i> in southwestern British Columbia, Canada. The aim of this study was to describe and name <i>Neonectria sp. nov.</i> and to develop a quantitative PCR (qPCR) assay to enable rapid detection of <i>Neonectria sp. nov.</i> from individual adult alder bark beetles and to define the distribution of the fungus. <i>Neonectria sp. nov.</i> was phylogenetically and morphologically determined to represent a distinct species closely related to <i>N. ditissima</i> and is described herein as <i>Neonectria bordenii sp. nov. Neonectria bordenii</i> was reliably detected from individual whole-beetle DNA extractions using a probe-based qPCR assay targeting multi-copy internal transcribed spacers (ITS) of nuclear ribosomal DNA. The qPCR assay amplified the fungus from 87.8 % (36/41) of individual alder bark beetle samples and was highly sensitive to <i>N. bordenii</i>, with a lower limit of detection of 1 × 10<sup>-6</sup> ng/μL of culture DNA (or ~262 genome copies). 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引用次数: 0
摘要
要了解树皮甲虫对森林生态系统的影响,就必须从分类学的角度全面研究树皮甲虫(鞘翅目:卷须科:鞘翅目)的真菌伴生物,并利用强大的分子工具来检测这些真菌。与树皮甲虫一起生活在受侵染树木中的最常见丝状真菌是表皮真菌(子囊菌目:表皮真菌纲和微囊真菌纲),然而最近在红赤杨(Alnus rubra)中发现了一种未被描述的新菌类(Neonectria sp.nov.;子囊菌目:Hypocreales)与赤杨树皮甲虫(Alniphagus aspericollis)共生。这种侵袭硬木的赤杨树皮甲虫遍布北美太平洋沿岸地区的红赤杨寄主,在加拿大不列颠哥伦比亚省西南部与 Neonectria sp.本研究的目的是描述和命名 Neonectria sp.经系统发育和形态学测定,Neonectria sp.使用以核核糖体 DNA 的多拷贝内部转录间隔(ITS)为目标的探针式 qPCR 分析法,可从个体全甲虫 DNA 提取物中可靠地检测到 Neonectria bordenii。该 qPCR 检测方法可从 87.8% (36/41)的桤木树皮甲虫样本中扩增出该真菌,并且对 N. bordenii 高度敏感,检测下限为 1 × 10-6 ng/μL 培养 DNA(或 ~262 个基因组拷贝)。本研究中开发的 qPCR 检测方法的应用将加速未来评估 N. bordenii 作为桤木树皮甲虫潜在共生体的研究。引用:Wertman DL, Tanney JB, Hamelin RC, Carroll AL (2024).Neonectria bordenii sp.Fungal Systematics and Evolution 13: 15-28. doi: 10.3114/fuse.2024.13.02.
Neonectria bordenii sp. nov., a potential symbiote of the alder bark beetle, and its detection by quantitative PCR.
A taxonomically comprehensive perspective on the fungal associates of bark beetles (Coleoptera: Curculionidae: Scolytinae), and powerful molecular tools for detection of these fungi, are imperative to understanding bark beetle impacts on forest ecosystems. The most common filamentous fungi living alongside bark beetles in infested trees are ophiostomatoids (Ascomycota: Ophiostomatales and Microascales), yet an undescribed species of Neonectria (Neonectria sp. nov.; Ascomycota: Hypocreales) was recently identified cohabitating with the alder bark beetle, Alniphagus aspericollis, in red alder, Alnus rubra. The hardwood-infesting alder bark beetle is found throughout the range of its red alder host in the Pacific Coast region of North America and is associated with Neonectria sp. nov. in southwestern British Columbia, Canada. The aim of this study was to describe and name Neonectria sp. nov. and to develop a quantitative PCR (qPCR) assay to enable rapid detection of Neonectria sp. nov. from individual adult alder bark beetles and to define the distribution of the fungus. Neonectria sp. nov. was phylogenetically and morphologically determined to represent a distinct species closely related to N. ditissima and is described herein as Neonectria bordenii sp. nov. Neonectria bordenii was reliably detected from individual whole-beetle DNA extractions using a probe-based qPCR assay targeting multi-copy internal transcribed spacers (ITS) of nuclear ribosomal DNA. The qPCR assay amplified the fungus from 87.8 % (36/41) of individual alder bark beetle samples and was highly sensitive to N. bordenii, with a lower limit of detection of 1 × 10-6 ng/μL of culture DNA (or ~262 genome copies). Application of the qPCR assay developed in this study will expedite future research evaluating N. bordenii as a potential symbiote of the alder bark beetle. Citation: Wertman DL, Tanney JB, Hamelin RC, Carroll AL (2024). Neonectria bordenii sp. nov., a potential symbiote of the alder bark beetle, and its detection by quantitative PCR. Fungal Systematics and Evolution13: 15-28. doi: 10.3114/fuse.2024.13.02.