{"title":"椰子“致黄”型疾病多样性、变异性及诊断研究进展","authors":"M. Dollet, R. Quaicoe, F. Pilet","doi":"10.1051/OCL.2009.0246","DOIUrl":null,"url":null,"abstract":"Coconut palms (Cocos nucifera L.) can be affected by several types of Lethal Yellowing (LY) diseases worldwide. Some of the syndromes are caused by phytoplasmas, small bacteria that are impossible to detect by light microscopy. Amplification of a given gene of the phytoplasmas by polymerase chain reaction (PCR) is the most convenient diagnosis method. The problem is that there are at least 28 “groups” of phytoplasmas and only one pair of primers -P1/P7- commonly used for PCR. As these primers belong to a very conserved gene, false positives are frequent. Consequently, alternative primers specific to one “strain” (or subgroup) have to be used, such as LY-F/LY-R for the Caribbean LY, Rohde primers for LD Tanzania. Such specific primers are sometimes restrictive. Indeed, there is variability within each strain and the sequence of the primers has to be adapted to that variability. There are at least five LY subgroups. The subgroups can only be identified by restriction fragment length polymorphism or sequencing. In Africa, two subgroups of LY phytoplasmas have been identified so far.","PeriodicalId":30815,"journal":{"name":"Oleagineux Corps gras Lipides","volume":"47 1","pages":"97-101"},"PeriodicalIF":0.0000,"publicationDate":"2009-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"26","resultStr":"{\"title\":\"Review of Coconut “Lethal Yellowing” type diseases Diversity, variability and diagnosis\",\"authors\":\"M. Dollet, R. Quaicoe, F. Pilet\",\"doi\":\"10.1051/OCL.2009.0246\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Coconut palms (Cocos nucifera L.) can be affected by several types of Lethal Yellowing (LY) diseases worldwide. Some of the syndromes are caused by phytoplasmas, small bacteria that are impossible to detect by light microscopy. Amplification of a given gene of the phytoplasmas by polymerase chain reaction (PCR) is the most convenient diagnosis method. The problem is that there are at least 28 “groups” of phytoplasmas and only one pair of primers -P1/P7- commonly used for PCR. As these primers belong to a very conserved gene, false positives are frequent. Consequently, alternative primers specific to one “strain” (or subgroup) have to be used, such as LY-F/LY-R for the Caribbean LY, Rohde primers for LD Tanzania. Such specific primers are sometimes restrictive. Indeed, there is variability within each strain and the sequence of the primers has to be adapted to that variability. There are at least five LY subgroups. The subgroups can only be identified by restriction fragment length polymorphism or sequencing. In Africa, two subgroups of LY phytoplasmas have been identified so far.\",\"PeriodicalId\":30815,\"journal\":{\"name\":\"Oleagineux Corps gras Lipides\",\"volume\":\"47 1\",\"pages\":\"97-101\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"26\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oleagineux Corps gras Lipides\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1051/OCL.2009.0246\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oleagineux Corps gras Lipides","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/OCL.2009.0246","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 26
摘要
在世界范围内,椰子树(Cocos nucifera L.)可受到几种致命黄化(LY)疾病的影响。有些综合征是由植物原体引起的,植物原体是一种不可能通过光学显微镜检测到的小细菌。用聚合酶链反应(PCR)扩增植物原体的特定基因是最方便的诊断方法。问题是至少有28个植物原体“群”,而通常用于PCR的引物只有一对——p1 /P7。由于这些引物属于非常保守的基因,因此经常出现假阳性。因此,必须使用针对一个“菌株”(或亚群)的替代引物,例如针对加勒比LY的LY- f /LY- r引物,针对坦桑尼亚LD的Rohde引物。这种特定的引物有时是限制性的。事实上,每个菌株都有变异,引物序列必须适应这种变异。至少有五个LY子组。亚群只能通过限制性片段长度多态性或测序来识别。在非洲,迄今已确定了LY植物原体的两个亚群。
Review of Coconut “Lethal Yellowing” type diseases Diversity, variability and diagnosis
Coconut palms (Cocos nucifera L.) can be affected by several types of Lethal Yellowing (LY) diseases worldwide. Some of the syndromes are caused by phytoplasmas, small bacteria that are impossible to detect by light microscopy. Amplification of a given gene of the phytoplasmas by polymerase chain reaction (PCR) is the most convenient diagnosis method. The problem is that there are at least 28 “groups” of phytoplasmas and only one pair of primers -P1/P7- commonly used for PCR. As these primers belong to a very conserved gene, false positives are frequent. Consequently, alternative primers specific to one “strain” (or subgroup) have to be used, such as LY-F/LY-R for the Caribbean LY, Rohde primers for LD Tanzania. Such specific primers are sometimes restrictive. Indeed, there is variability within each strain and the sequence of the primers has to be adapted to that variability. There are at least five LY subgroups. The subgroups can only be identified by restriction fragment length polymorphism or sequencing. In Africa, two subgroups of LY phytoplasmas have been identified so far.