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中国-越南柑桔黄龙病病原16SrDNA片段的序列分析
邓崇岭1, 陈传武1, 赵小龙2, 陈国平1*, 邓光宙1, 王明召1
1.广西壮族自治区柑桔研究所, 广西 桂林 541004;2.广西壮族自治区农业厅, 南宁 530022
摘要:
采集广西、广东和越南的8个柑桔黄龙病样品,利用黄龙病的特异引物OI1/OI2c对其16S rDNA片段进行PCR扩增,将其扩增产物纯化、回收,进行序列测定。利用DNAstar软件、clustalw2软件和MEGA4.0软件进行同源性分析与系统发育分析。结果表明,越南黄龙病株系(Vietnam 0901和Vietnam 0905)与除广西样品GX 1001和广东样品GD 1002外所有亚洲种柑桔黄龙病病原的同源性都很高(97.6%~100.0%),而与非洲种、美洲种和土豆斑马条纹病的同源性相对较低(分别为96.0%/97.7%,94.7%/964%和96.2%/97.6%)。表明我国广东、广西和越南发生的HLB病原均属亚洲种,但在亚洲种之间不同地区的黄龙病病原也发生了一定变异,广西样品GX 1001和广东样品GD 1002与其它亚洲种柑桔黄龙病病原的同源性较其它亚洲种株系偏低,但聚类还是归在一个类群,表明相同地域内的黄龙病病原菌还存在一定差异。
关键词:  中国  越南  柑桔黄龙病  16S rDNA  同源性  序列分析
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Sequence analysis of 16SrDNA of Huanglongbing agents collected from China and Vietnam
DENG ChongLing1, CHEN ChuanWu1, ZHAO XiaoLong2, CHEN GuoPing1*, DENG GuangZhou1, WANG MingZhao1
1.Guangxi Citrus Research Institute, Guilin 541004, China;2.Department of Agriculture of Guangxi, Nanning 530022, China
Abstract:
In this study,eight samples of Huanglongbing(HLB) trees were collected from Guangdong,Guangxi and Vietnam. The HLB agent specific primer sets,OI1/OI2c was used to amplify DNA from the loci of 16S rDNA. PCR products were collected,purified,and sequenced. The sequences were compared to all published DNA sequences in GenBank through BLAST(http:\\www.ncbi.nlm.nih.gov)for phylogenetic analyses. The cluster analyses were performed by MEGA software. It was concluded that eight of 16S rDNA sequences from different areas were phylogentically most closely related to those of the published HLB agents. The similarities between the Vietnam samples sequences Vietnam 0901和Vietnam 0905 to that of Candidatus Liberibacter asiaticus(except GX 1001 and GD 1002)were more higher(97.6%-100.0%),to that of Ca.L.africanus were 96.0%/97.7%,to that of Ca.L.americanus were 94.7%/96.4%,and to that of Potato Zebra Chip were 96.2%/97.6%. The results indicated that the HLB agents collected from Vietnam were Ca.L.asiaticus. But there are still some differences between these Las samples.
Key words:  China  Vietnam  Huanglongbing  16S rDNA  Sequence analysis
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