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通过16S rDNA序列分析估算水稻(Oryza sativa L.)根内生细菌多样性。

Endophytic bacterial diversity in rice (Oryza sativa L.) roots estimated by 16S rDNA sequence analysis.

作者信息

Sun Lei, Qiu Fubin, Zhang Xiaoxia, Dai Xin, Dong Xiuzhu, Song Wei

机构信息

College of Life Sciences, Capital Normal University, Beijing 100037, People's Republic of China.

出版信息

Microb Ecol. 2008 Apr;55(3):415-24. doi: 10.1007/s00248-007-9287-1. Epub 2007 Aug 10.

DOI:10.1007/s00248-007-9287-1
PMID:17690836
Abstract

The endophytic bacterial diversity in the roots of rice (Oryza sativa L.) growing in the agricultural experimental station in Hebei Province, China was analyzed by 16S rDNA cloning, amplified ribosomal DNA restriction analysis (ARDRA), and sequence homology comparison. To effectively exclude the interference of chloroplast DNA and mitochondrial DNA of rice, a pair of bacterial PCR primers (799f-1492r) was selected to specifically amplify bacterial 16S rDNA sequences directly from rice root tissues. Among 192 positive clones in the 16S rDNA library of endophytes, 52 OTUs (Operational Taxonomic Units) were identified based on the similarity of the ARDRA banding profiles. Sequence analysis revealed diverse phyla of bacteria in the 16S rDNA library, which consisted of alpha, beta, gamma, delta, and epsilon subclasses of the Proteobacteria, Cytophaga/Flexibacter/Bacteroides (CFB) phylum, low G+C gram-positive bacteria, Deinococcus-Thermus, Acidobacteria, and archaea. The dominant group was Betaproteobacteria (27.08% of the total clones), and the most dominant genus was Stenotrophomonas. More than 14.58% of the total clones showed high similarity to uncultured bacteria, suggesting that nonculturable bacteria were detected in rice endophytic bacterial community. To our knowledge, this is the first report that archaea has been identified as endophytes associated with rice by the culture-independent approach. The results suggest that the diversity of endophytic bacteria is abundant in rice roots.

摘要

采用16S rDNA克隆、扩增核糖体DNA限制性分析(ARDRA)和序列同源性比较的方法,对生长在中国河北省农业试验站的水稻(Oryza sativa L.)根内的内生细菌多样性进行了分析。为有效排除水稻叶绿体DNA和线粒体DNA的干扰,选择了一对细菌PCR引物(799f - 1492r),直接从水稻根组织中特异性扩增细菌16S rDNA序列。在内生菌16S rDNA文库的192个阳性克隆中,根据ARDRA条带图谱的相似性鉴定出52个操作分类单元(OTU)。序列分析揭示了16S rDNA文库中细菌的不同门类,包括变形菌门的α、β、γ、δ和ε亚类、噬纤维菌/屈挠杆菌/拟杆菌(CFB)门、低G + C革兰氏阳性菌、嗜热放线菌、酸杆菌和古菌。优势菌群为β-变形菌(占总克隆数的27.08%),最优势的属为嗜麦芽窄食单胞菌。超过14.58%的总克隆与未培养细菌具有高度相似性,表明在水稻内生细菌群落中检测到了不可培养细菌。据我们所知,这是首次通过非培养方法将古菌鉴定为与水稻相关的内生菌的报道。结果表明,水稻根内的内生细菌多样性丰富。

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