M. Vojvodić, D. Lazić, P. Mitrović, B. Tanović, I. Vico, A. Bulajić
{"title":"Conventional and real-time pcr assays for detection and identification of rhizoctonia solani AG-2-2, the causal agent of root rot of sugar beet","authors":"M. Vojvodić, D. Lazić, P. Mitrović, B. Tanović, I. Vico, A. Bulajić","doi":"10.2298/PIF1901019V","DOIUrl":null,"url":null,"abstract":"Soil-borne fungi belonging to the genus Rhizoctonia are considered to be among the most destructive sugar beet pathogens. Although multinucleate R. solani AG-2-2 is frequently detected as the main causal agent of root rot of sugar beet worldwide, several binucleate (AG-A, AG-E and AG-K) and multinucleate Rhizoctonia (R. solani AG-4, AG-5 and AG-8) have also been included in the disease complex. Due to their soil-borne nature and wide host range, the management of Rhizoctonia root rot of sugar beet is highly demanding. Identification of Rhizoctonia AG associated with root rot of sugar beet is the essential first step in determining a successful disease management strategy. In this paper we report a highly specific and sensitive real-time PCR protocol for detection of R. solani AG-2-2 which showed a high level of specificity after testing against 10 different anastomosis groups and subgroups, including AG-2-1 as the most closely related. Moreover, a similar conventional PCR assay showed the same specificity but proved to be at least a 100 times less sensitive. Future research will include further testing and adaptation of this protocol for direct detection and quantification of R. solani AG-2-2 in different substrates, including plant tissue and soil samples.","PeriodicalId":19801,"journal":{"name":"Pesticidi I Fitomedicina","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pesticidi I Fitomedicina","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2298/PIF1901019V","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
Soil-borne fungi belonging to the genus Rhizoctonia are considered to be among the most destructive sugar beet pathogens. Although multinucleate R. solani AG-2-2 is frequently detected as the main causal agent of root rot of sugar beet worldwide, several binucleate (AG-A, AG-E and AG-K) and multinucleate Rhizoctonia (R. solani AG-4, AG-5 and AG-8) have also been included in the disease complex. Due to their soil-borne nature and wide host range, the management of Rhizoctonia root rot of sugar beet is highly demanding. Identification of Rhizoctonia AG associated with root rot of sugar beet is the essential first step in determining a successful disease management strategy. In this paper we report a highly specific and sensitive real-time PCR protocol for detection of R. solani AG-2-2 which showed a high level of specificity after testing against 10 different anastomosis groups and subgroups, including AG-2-1 as the most closely related. Moreover, a similar conventional PCR assay showed the same specificity but proved to be at least a 100 times less sensitive. Future research will include further testing and adaptation of this protocol for direct detection and quantification of R. solani AG-2-2 in different substrates, including plant tissue and soil samples.
根丝核菌属的土壤传播真菌被认为是最具破坏性的甜菜病原体之一。虽然在世界范围内,多核番茄枯病菌AG-2-2经常被检测为甜菜根腐病的主要致病因子,但几种双核菌(AG-A、AG-E和AG-K)和多核根核菌(番茄枯病菌AG-4、AG-5和AG-8)也被包括在该疾病复合体中。甜菜根腐病因其土传性和寄主范围广,对根腐病的防治要求很高。鉴定与甜菜根腐病相关的根核菌AG是确定成功的疾病管理策略必不可少的第一步。本文报道了一种高特异性和高灵敏度的实时PCR检测方法,该方法对10个不同的吻合群和亚群进行了检测,结果显示出很高的特异性,其中AG-2-1是最接近的。此外,一种类似的传统PCR检测显示出相同的特异性,但证明其灵敏度至少低100倍。未来的研究将包括进一步测试和调整该方案,以便在不同基质(包括植物组织和土壤样品)中直接检测和定量茄茄R. ag -2。