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基于gyrB和rpoD序列的水稻伯克霍尔德氏菌、颖壳伯克霍尔德氏菌和唐菖蒲伯克霍尔德氏菌的系统发育研究及多重PCR检测

Phylogenetic study and multiplex PCR-based detection of Burkholderia plantarii, Burkholderia glumae and Burkholderia gladioli using gyrB and rpoD sequences.

作者信息

Maeda Yukiko, Shinohara Hirosuke, Kiba Akinori, Ohnishi Kouhei, Furuya Naruto, Kawamura Yoshiaki, Ezaki Takayuki, Vandamme Peter, Tsushima Seiya, Hikichi Yasufumi

机构信息

Laboratory of Plant Pathology and Biotechnology, Kochi University, 200 Monobe, Nankoku, Kochi 783-8502, Japan.

National Agricultural Research Center for Tohoku Region, Fukushima 960-2156, Japan.

出版信息

Int J Syst Evol Microbiol. 2006 May;56(Pt 5):1031-1038. doi: 10.1099/ijs.0.64184-0.

Abstract

In order to develop a detection method for the rice pathogens Burkholderia plantarii, Burkholderia glumae and Burkholderia gladioli, the phylogeny of six plant-pathogenic Burkholderia species was analysed using the combined nucleotide sequences of gyrB and rpoD. B. plantarii, B. glumae and B. gladioli formed tight monophyletic branches supported by high bootstrap probabilities. The high sequence similarity revealed a close phylogenetic relationship between B. glumae and B. plantarii. B. plantarii strains were divided into three subclusters comprising rice strains, whereas the single Vanda strain occupied a unique position in the phylogenetic tree. The gyrB and rpoD sequences of all B. glumae strains examined were highly conserved. In contrast, B. gladioli strains demonstrated a far greater sequence diversity, but this diversity did not correlate with pathovar, host plant or geographical origin of the strains. A multiplex-PCR protocol using specific primers from the gyrB sequences was designed that allowed the specific detection and identification of B. plantarii, B. glumae and B. gladioli in rice seeds infected with these pathogenic species.

摘要

为开发一种针对水稻病原菌水稻伯克霍尔德氏菌、颖枯伯克霍尔德氏菌和唐菖蒲伯克霍尔德氏菌的检测方法,利用gyrB和rpoD的核苷酸序列组合对六种植物致病性伯克霍尔德氏菌的系统发育进行了分析。水稻伯克霍尔德氏菌、颖枯伯克霍尔德氏菌和唐菖蒲伯克霍尔德氏菌形成了紧密的单系分支,自展概率较高。高度的序列相似性揭示了颖枯伯克霍尔德氏菌和水稻伯克霍尔德氏菌之间密切的系统发育关系。水稻伯克霍尔德氏菌菌株分为包含水稻菌株的三个亚群,而单一的万代兰菌株在系统发育树中占据独特位置。所有检测的颖枯伯克霍尔德氏菌菌株的gyrB和rpoD序列高度保守。相比之下,唐菖蒲伯克霍尔德氏菌菌株表现出更大的序列多样性,但这种多样性与菌株的致病变种、寄主植物或地理来源无关。设计了一种使用来自gyrB序列的特异性引物的多重PCR方案,可对感染这些致病物种的水稻种子中的水稻伯克霍尔德氏菌、颖枯伯克霍尔德氏菌和唐菖蒲伯克霍尔德氏菌进行特异性检测和鉴定。

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