机构地区: 华中农业大学植物科学技术学院
出 处: 《园艺学报》 2006年第5期947-952,共6页
摘 要: 建立了一种同时检测柑橘黄龙病病原类细菌(CandidatusLiberibacterasiaticus,HLB)、柑橘裂皮类病毒(Citrusexocortisviroid,CEVd)、柑橘衰退病病毒(Citrustristezavirus,CTV)的多重RT-PCR技术体系。运用根据3种病原核苷酸保守区序列设计的特异性引物,成功的对同一样品中的HLB、CEVd、CTV进行多重RT-PCR扩增,得到1160bp、371bp、273bp3条特异性大小与试验设计相符的条带。就影响多重PCR的主要因素引物浓度和退火温度进行了一系列优化,建立了能同时检测HLB、CEVd、CTV的多重RT-PCR技术体系。该体系最低能从10pg总RNA中检测出黄龙病类细菌和柑橘裂皮类病毒,从1pg总RNA中检测到柑橘衰退病毒。对采自田间37份材料的实际检测表明:存在两种或3种病原的复合侵染。 A multiplex RT-PCR was successfully established to simultaneously detect Citrus Huanglongbing pathogen ( Candidatus Liberibacter asiaticus, HLB) , Citrus exocortis viroid (CEVd) and Citrus tristeza virus (CTV). Using three sets of specific primers designed according to the converted sequences of these three pathogens respectively, expected fragments of 1 160 bp (HLB), 371 bp (CEVd) and 273 bp (CTV) were successfully amplified by this multiplex RT-PCR systerm. To optimize the multiplex RT-PCR, the concentration of primers and annealing temperature were repeatedly tried. Final results showed that a multiplex RT-PCR system to simultaneously detect HLB, CEVd and CTV was firstly established successfully. Sensibility test showed: it could detect out HLB, CEVd in 10 pg, and CTV in 1 pg total RNA respectively. To confirm the utilization of the multiplex RT-PCR system, 37 samples collected from field were tested. The results showed: two or three pathogens mix-infection was in existence in fields.