首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >Discrimination of Burkholderia gladioli pv.alliicola and B. cepacia complex using the gyrB gene of B. gladioli pv. alliicola
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Discrimination of Burkholderia gladioli pv.alliicola and B. cepacia complex using the gyrB gene of B. gladioli pv. alliicola

机译:用剑兰假单胞菌pv的gyrB基因鉴别剑兰假单胞菌pv.alliicola和洋葱伯克霍尔德菌复合体。阿利科拉

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摘要

The aim of the present study was to investigate the efficiency of the gyrB gene derived from Burkholderia gladioli pv.Alliicola (Bga) on the identification of Bga from the B. cepacia complex (Bcc) based on the COnsensus-DEgenerate Hybrid Oligonucleotide Primer (CODEHOP) strategy. A set of primers used for the specific amplification of the gyrB gene in Bga were designed according to the CODEHOP principle. A total of 1,644 bp of the gyrB gene sequence of Bga were acquired by CODEHOP amplification. The sequence was blasted in GenBank and it revealed an average of 86% similarity with the gyrB gene of nine genomovars of Bcc. A phylogenetic tree was constructed using the gyrB gene sequences. The microarray method was adopted to discriminate Bga from Bcc based on the specific probes designed upon the gyrB gene, and five genomovars of Bcc demonstrated a good discrimination from Bga on the microarray chip. CODEHOP strategy succeeded in amplification of the gyrB gene of Bga, which made it possible for the identification of Bga from five genomovars of Bcc.
机译:本研究的目的是基于COnsensus-DEgenerate杂交寡核苷酸引物(CODEHOP),研究源自剑兰伯克霍尔德氏菌pv.Alliicola(Bga)的gyrB基因在鉴定洋葱酒单胞菌复合物(Bcc)中的Bga方面的效率。 )策略。根据CODEHOP原理设计了一组用于特异性扩增Bga中gyrB基因的引物。通过CODEHOP扩增获得了总共1,644 bp的Bga的gyrB基因序列。该序列在GenBank中进行了blast处理,发现与9个Bcc基因型的gyrB基因的gyrB基因平均相似性为86%。使用gyrB基因序列构建了系统树。基于基于gyrB基因设计的特异性探针,采用微阵列方法将Bga与Bcc进行区分,并且在微阵列芯片上,五个Bcc基因组均表现出与Bga的良好区分。 CODEHOP策略成功扩增了Bga的gyrB基因,这使得从五个Bcc基因组中鉴定Bga成为可能。

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