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一种用于检测和区分柑橘黑点病菌(Guignardia citricarpa)和内生菌芒果拟盘多毛孢(Guignardia mangiferae)的一日敏感方法。

A One-Day Sensitive Method to Detect and Distinguish Between the Citrus Black Spot Pathogen Guignardia citricarpa and the Endophyte Guignardia mangiferae.

作者信息

Meyer L, Sanders G M, Jacobs R, Korsten L

机构信息

Department of Microbiology and Plant Pathology, Forestry and Agricultural Biotechnology Institute, University of Pretoria, Pretoria, 0002, South Africa.

出版信息

Plant Dis. 2006 Jan;90(1):97-101. doi: 10.1094/PD-90-0097.

Abstract

If South African citrus exporters wish to retain their competitive edge in the European market and access new markets such as the United States of America, it is of quarantine importance to distinguish between the citrus black spot pathogen, Guignardia citricarpa, and the harmless endophyte, G. mangiferae. The endophyte is not a sanitary or phytosanitary concern. This paper describes the design of species-specific primers that are able to detect and distinguish between these two Guignardia species. Application of the primer set CITRIC1 and CAMEL2 in conjunction with the ITS4 primer yielded polymerase chain reaction (PCR) amplicons of approximately 580 bp and 430 bp for G. citricarpa and G. mangiferae, respectively. Results obtained with these primers are in accordance with sequence data, and repeated tests verified accuracy and sensitivity. A BLAST search revealed no matches other than G. citricarpa and G. mangiferae, and no positive PCR results were obtained with Colletotrichum gloeosporioides, which is the most common contaminant in black spot lesions. We are, therefore, able to distinguish G. citricarpa and G. mangiferae unequivocally using a PCR-based method. This method was further improved to directly isolate DNA from fruit lesions by means of the DNeasy Plant Mini Kit (Qiagen). This eliminates the prior need for culturing the slow-growing organism, thereby shortening the time required to one day to test for and verify the presence or absence of the pathogenic G. citricarpa in export consignments.

摘要

如果南非柑橘出口商希望在欧洲市场保持其竞争优势并打入诸如美国等新市场,区分柑橘黑点病菌(Guignardia citricarpa)和无害内生菌芒果拟盘多毛孢(G. mangiferae)具有检疫重要性。该内生菌不是卫生或植物检疫方面的问题。本文描述了能够检测和区分这两种拟盘多毛孢属物种的种特异性引物的设计。引物组CITRIC1和CAMEL2与ITS4引物联合使用时,分别对柑橘黑点病菌和芒果拟盘多毛孢产生了约580 bp和430 bp的聚合酶链反应(PCR)扩增子。用这些引物获得的结果与序列数据一致,重复试验验证了准确性和灵敏度。BLAST搜索显示除了柑橘黑点病菌和芒果拟盘多毛孢外没有其他匹配项,并且用炭疽菌(Colletotrichum gloeosporioides)未获得阳性PCR结果,炭疽菌是黑点病斑中最常见的污染物。因此,我们能够使用基于PCR的方法明确区分柑橘黑点病菌和芒果拟盘多毛孢。该方法进一步改进为通过DNeasy植物微量提取试剂盒(Qiagen)直接从果实病斑中分离DNA。这消除了先前对培养生长缓慢的生物体的需求,从而将检测和验证出口货物中致病性柑橘黑点病菌是否存在所需的时间缩短至一天。

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