Hyun J W, Peres N A, Yi S-Y, Timmer L W, Kim K S, Kwon H-M, Lim H-C
Subtropical Environment Division, National Institute of Subtropical Agriculture, R.D.A. Jeju, 699-803, Korea.
University of Florida, Gulf Coast Research and Education Center, Wimauma 33598.
Plant Dis. 2007 Jul;91(7):865-870. doi: 10.1094/PDIS-91-7-0865.
Two scab pathogens of citrus, Elsinoë fawcettii and E. australis, cause citrus scab and sweet orange scab, respectively, and pathotypes of each species have been described. The two species cannot be readily distinguished by morphological or cultural characteristics and can be distinguished only by host range and the sequence of the internal transcribed spacer (ITS) region. In this study, random amplified polymorphic DNA (RAPD) assays clearly distinguished E. fawcettii and E. australis, and the sweet orange and natsudaidai pathotypes within E. australis also could be differentiated. We developed specific primer sets, Efaw-1 for E. fawcettii; Eaut-1, Eaut-2, Eaut-3, and Eaut-4 for E. australis; and EaNat-1 and EaNat-2 for the natsudaidai pathotype within E. australis using RAPD products unique to each species or pathotype. Other primer sets, Efaw-2 and Eaut-5, which were specific for E. fawcettii and E. australis, respectively, were designed from previously determined ITS sequences. The Efaw-1 and Efaw-2 primer sets successfully identified E. fawcettii isolates from Korea, Australia, and the United States (Florida) and the Eaut-1 to Eaut-5 primer sets identified both the sweet orange pathotype isolates of E. australis from Argentina and the natsudaidai pathotype isolates from Korea. The EaNat-1 and EaNat-2 primer sets were specific for isolates of the natsudaidai pathotype. The Efaw-1 and Efaw-2 primer sets successfully detected E. fawcettii from lesions on diseased leaves and fruit from Korea and primer pairs Eaut-1, Eaut-2, Eaut-3, Eaut-4, and Eaut-5 detected E. australis from lesions on sweet orange fruit from Brazil.
柑橘的两种痂病菌,法氏痂圆孢(Elsinoë fawcettii)和澳洲痂圆孢(E. australis),分别引起柑橘痂病和甜橙痂病,并且已描述了每个物种的致病型。这两个物种不能通过形态学或培养特征轻易区分,只能通过寄主范围和内部转录间隔区(ITS)序列来区分。在本研究中,随机扩增多态性DNA(RAPD)分析清楚地区分了法氏痂圆孢和澳洲痂圆孢,并且澳洲痂圆孢内的甜橙致病型和夏橙致病型也能够被区分。我们利用每个物种或致病型特有的RAPD产物,开发了特异性引物组,用于法氏痂圆孢的Efaw - 1;用于澳洲痂圆孢的Eaut - 1、Eaut - 2、Eaut - 3和Eaut - 4;以及用于澳洲痂圆孢内夏橙致病型的EaNat - 1和EaNat - 2。其他引物组,分别针对法氏痂圆孢和澳洲痂圆孢的Efaw - 2和Eaut - 5,是根据先前确定的ITS序列设计的。Efaw - 1和Efaw - 2引物组成功鉴定了来自韩国、澳大利亚和美国(佛罗里达州)的法氏痂圆孢分离株,而Eaut - 1至Eaut - 5引物组鉴定了来自阿根廷的澳洲痂圆孢甜橙致病型分离株和来自韩国的夏橙致病型分离株。EaNat - 1和EaNat - 2引物组对夏橙致病型分离株具有特异性。Efaw - 1和Efaw - 2引物组成功地从韩国患病叶片和果实的病斑中检测到了法氏痂圆孢,引物对Eaut - 1、Eaut - 2、Eaut - 3、Eaut - 4和Eaut - 5从巴西甜橙果实的病斑中检测到了澳洲痂圆孢。