Panchal G, Bridge P D
School of Biological and Chemical Sciences, Birkbeck College, University of London, Malet Street, London, WC1E 7HX, UK.
Mycopathologia. 2005 Jan;159(1):123-7. doi: 10.1007/s11046-004-4434-4.
The PCR primer GanET has previously been shown to be suitable for the specific amplification of DNA from Ganoderma boninense. A DNA extraction and PCR method has been developed that allows for the amplification of the G. boninense DNA from environmental samples of oil palm tissue. The GanET primer reaction was used in conjunction with a palm-sampling programme to investigate the possible infection of young palms through cut frond base surfaces. Ganoderma DNA was detected in frond base material at a greater frequency than would be expected by comparison with current infection levels. Comparisons are made between the height of the frond base infected, the number of frond bases infected, and subsequent development of basal stem rot. The preliminary results suggest that the development of basal stem rot may be more likely to occur when young lower frond bases are infected.
PCR引物GanET此前已被证明适用于从邦氏灵芝特异性扩增DNA。现已开发出一种DNA提取和PCR方法,可从油棕组织的环境样本中扩增出邦氏灵芝的DNA。GanET引物反应与棕榈采样程序结合使用,以调查幼嫩棕榈通过切割叶基表面可能受到的感染情况。与当前感染水平相比,在叶基材料中检测到灵芝DNA的频率更高。对受感染叶基的高度、受感染叶基的数量以及随后基部茎腐病的发展情况进行了比较。初步结果表明,当幼嫩的下部叶基受到感染时,基部茎腐病更有可能发生。