Beretta M J G, Barthe G A, Ceccardi T L, Lee R F, Derrick K S
Instituto Biologico, Sao Paulo, Brazil, CP07119,01064-970.
Citrus Research and Education Center, IFAS, University of Florida, Lake Alfred 33850.
Plant Dis. 1997 Oct;81(10):1196-1198. doi: 10.1094/PDIS.1997.81.10.1196.
Polymerase chain reaction amplification of DNA from various strains of Xylella fastidiosa with tRNA consensus primers produced three different fingerprint groups. The citrus variegated chlorosis (CVC) and mulberry leaf scorch strains were unique and readily separated from each other and all other strains tested. Internal primers were designed based on the sequence of a DNA fragment unique to the CVC strain. An assay was developed with a mixture of these primers and those reported to detect 18 strains of X. fastidiosa. The assay was used to survey citrus in Brazil. The strain identified to be the cause of CVC was found in constant association with trees with CVC symptoms. On occasion, trees with no symptoms were found to have the CVC strain; this was presumably due to presymptomatic infections. No other strains were found in this survey, and X. fastidiosa was not associated with citrus blight.
用tRNA共有引物对不同菌株的木质部难养菌DNA进行聚合酶链反应扩增,产生了三个不同的指纹图谱组。柑橘杂色黄化病(CVC)菌株和桑树叶焦枯病菌株是独特的,彼此之间以及与所有其他测试菌株都很容易区分。基于CVC菌株特有的DNA片段序列设计了内部引物。开发了一种检测方法,将这些引物与报道的用于检测18种木质部难养菌菌株的引物混合使用。该检测方法用于对巴西的柑橘进行调查。发现被确定为CVC病因的菌株总是与有CVC症状的树木相关联。偶尔也会发现无症状的树木带有CVC菌株;这可能是由于症状出现前的感染。在本次调查中未发现其他菌株,且木质部难养菌与柑橘枯萎病无关。