Kira M.T. Lynn , Michael J. Wingfield , Almuth Hammerbacher , Irene Barnes
{"title":"高分辨率熔融曲线分析:受感染桉树中桉树孢囊虫和桉树孢囊虫的检测方法","authors":"Kira M.T. Lynn , Michael J. Wingfield , Almuth Hammerbacher , Irene Barnes","doi":"10.1016/j.funbio.2024.07.011","DOIUrl":null,"url":null,"abstract":"<div><p><em>Eucalyptus</em> spp. in plantations are negatively affected by canker and wilt diseases caused by several species of <em>Ceratocystis</em>, particularly those in the Latin American Clade (LAC). <em>Ceratocystis eucalypticola</em> and <em>Ceratocystis manginecans</em> are of particular concern where disease epidemics are reported globally, with recent outbreaks emerging in South African and Indonesian <em>Eucalyptus</em> plantations. Consequently, a rapid screening protocol is required for these pathogens. In this study, a high-resolution melting curve analysis (HRMA) was developed to detect <em>C</em>. <em>eucalypticola</em> and <em>C</em>. <em>manginecans</em> that bypasses time-consuming isolation and post-PCR procedures. Primers targeting a 172 bp region of the cerato-platanin (CP) gene were designed. Using these primers, the accuracy of HRMA to detect and distinguish between these two LAC species was assessed using pure fungal DNA, and DNA extracted directly from <em>Eucalyptus</em> samples naturally infected with <em>C</em>. <em>eucalypticola</em>. The assay accurately detected the presence of <em>C. eucalypticola</em> and <em>C. manginecans</em> and quantifies their DNA, both from cultures, and directly from wood samples. HRMA further differentiated these two species from all other tested LAC individuals. This assay was also able to detect the presence of all the tested LAC species and distinguish seven of these, including <em>C. fimbriata,</em> to species level. <em>Ceratocystis polyconidia</em> was the only non-LAC off-target species detected. Based on these results, the developed assay can be used to rapidly identify <em>C. eucalypticola</em> and <em>C. manginecans</em> directly from infected plant material or fungal cultures, with the potential to also screen for several other LAC species.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1878614624001041/pdfft?md5=69d08805808447a54f673db3b2857d04&pid=1-s2.0-S1878614624001041-main.pdf","citationCount":"0","resultStr":"{\"title\":\"High-resolution melting curve analysis: A detection assay for Ceratocystis eucalypticola and C. manginecans in infected Eucalyptus\",\"authors\":\"Kira M.T. Lynn , Michael J. Wingfield , Almuth Hammerbacher , Irene Barnes\",\"doi\":\"10.1016/j.funbio.2024.07.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Eucalyptus</em> spp. in plantations are negatively affected by canker and wilt diseases caused by several species of <em>Ceratocystis</em>, particularly those in the Latin American Clade (LAC). <em>Ceratocystis eucalypticola</em> and <em>Ceratocystis manginecans</em> are of particular concern where disease epidemics are reported globally, with recent outbreaks emerging in South African and Indonesian <em>Eucalyptus</em> plantations. Consequently, a rapid screening protocol is required for these pathogens. In this study, a high-resolution melting curve analysis (HRMA) was developed to detect <em>C</em>. <em>eucalypticola</em> and <em>C</em>. <em>manginecans</em> that bypasses time-consuming isolation and post-PCR procedures. Primers targeting a 172 bp region of the cerato-platanin (CP) gene were designed. Using these primers, the accuracy of HRMA to detect and distinguish between these two LAC species was assessed using pure fungal DNA, and DNA extracted directly from <em>Eucalyptus</em> samples naturally infected with <em>C</em>. <em>eucalypticola</em>. The assay accurately detected the presence of <em>C. eucalypticola</em> and <em>C. manginecans</em> and quantifies their DNA, both from cultures, and directly from wood samples. HRMA further differentiated these two species from all other tested LAC individuals. This assay was also able to detect the presence of all the tested LAC species and distinguish seven of these, including <em>C. fimbriata,</em> to species level. <em>Ceratocystis polyconidia</em> was the only non-LAC off-target species detected. Based on these results, the developed assay can be used to rapidly identify <em>C. eucalypticola</em> and <em>C. manginecans</em> directly from infected plant material or fungal cultures, with the potential to also screen for several other LAC species.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1878614624001041/pdfft?md5=69d08805808447a54f673db3b2857d04&pid=1-s2.0-S1878614624001041-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1878614624001041\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878614624001041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
种植园中的桉树受到几种 Ceratocystis(特别是拉丁美洲支系(LAC)中的 Ceratocystis)引起的腐烂病和枯萎病的负面影响。Ceratocystis eucalypticola 和 Ceratocystis manginecans 尤其令人担忧,据报道,这两种病在全球范围内流行,最近在南非和印度尼西亚的桉树种植园中爆发。因此,需要对这些病原体进行快速筛查。本研究开发了一种高分辨率熔解曲线分析法(HRMA),用于检测桉树褐斑桉菌(C. eucalypticola)和桉树褐斑桉菌(C. manginecans),该方法绕过了耗时的分离和后 PCR 程序。所设计的引物靶向 Cerato-platanin (CP) 基因的 172 bp 区域。利用这些引物,使用纯真菌 DNA 和直接从桉树样本中提取的天然感染桉叶蝉的 DNA 评估了 HRMA 检测和区分这两种 LAC 物种的准确性。无论是从培养物中还是直接从木材样本中,该检测方法都能准确检测出桉树褐飞虱和桉树褐飞虱的存在,并对其 DNA 进行量化。HRMA 进一步将这两个物种与所有其他受测的 LAC 个体区分开来。该检测方法还能检测出所有检测过的 LAC 物种,并将其中的七个物种(包括 C. fimbriata)区分到物种级别。Ceratocystis polyconidia 是唯一检测到的非 LAC 非目标物种。基于这些结果,所开发的检测方法可用于直接从受感染的植物材料或真菌培养物中快速鉴定桉叶蝙蝠蛾和芒柄蝙蝠蛾,并有可能筛选出其他几个 LAC 物种。
High-resolution melting curve analysis: A detection assay for Ceratocystis eucalypticola and C. manginecans in infected Eucalyptus
Eucalyptus spp. in plantations are negatively affected by canker and wilt diseases caused by several species of Ceratocystis, particularly those in the Latin American Clade (LAC). Ceratocystis eucalypticola and Ceratocystis manginecans are of particular concern where disease epidemics are reported globally, with recent outbreaks emerging in South African and Indonesian Eucalyptus plantations. Consequently, a rapid screening protocol is required for these pathogens. In this study, a high-resolution melting curve analysis (HRMA) was developed to detect C. eucalypticola and C. manginecans that bypasses time-consuming isolation and post-PCR procedures. Primers targeting a 172 bp region of the cerato-platanin (CP) gene were designed. Using these primers, the accuracy of HRMA to detect and distinguish between these two LAC species was assessed using pure fungal DNA, and DNA extracted directly from Eucalyptus samples naturally infected with C. eucalypticola. The assay accurately detected the presence of C. eucalypticola and C. manginecans and quantifies their DNA, both from cultures, and directly from wood samples. HRMA further differentiated these two species from all other tested LAC individuals. This assay was also able to detect the presence of all the tested LAC species and distinguish seven of these, including C. fimbriata, to species level. Ceratocystis polyconidia was the only non-LAC off-target species detected. Based on these results, the developed assay can be used to rapidly identify C. eucalypticola and C. manginecans directly from infected plant material or fungal cultures, with the potential to also screen for several other LAC species.