期刊文献+

两种PCR方法对木耳属菌株的遗传多样性评价(英文) 被引量:8

Assessment The Genetic Diversity of Auricularia Strains by Two PCR-Based Typing Methods
下载PDF
导出
摘要 应用ERIC和RAPD两种PCR方法对木耳属 3种 2 9个菌株进行遗传鉴别 ,其中ERIC方法是首次运用于食用菌的研究领域。在相似系数 75 %的水平上 ,ERIC和RAPD分别将供试菌株分为 9组和 6组。由ERIC所得的聚类图可将黑木耳和毛木耳两个种区分开 ,而RAPD则不能完全区分两个种 ,但两种方法得到了一个相似的结果 ,即琥珀木耳与黑木耳的亲缘关系极其相近。Southern杂交实验进一步证明了ERIC所得到的 2 9个菌株的同源性关系。分析表明 ,RAPD方法主要在种的水平上进行鉴别 ,而ERIC则可以在菌株水平上进行鉴别 ,结果与菌株栽培性状更为一致。研究结果表明ERIC PCR是一种比RAPD更快捷可靠的分子标记方法 。 Two PCR-based methods, enterobacterial repetitive intergenic consensus-PCR (ERIC-PCR) and randomly amplified polymorphic DNA (RAPD), were adopted for differentiating Auricularia strains. Taken the similarity coefficient as 75%, 29 strains of three Auricularia species were grouped into 6 and 9 clusters by RAPD and ERIC, respectively. The dendrogram from ERIC exhibited two distinct parts, one representing A. auricula and the other A. polytricha, but the dendrogram from RAPD failed to clearly distinguish between these two species. However, both methods similarly revealed high homology between A. fuscosuccinea and A. auricula. The homology relationships among the three species obtained from ERIC were validated by Southern hybridization. The analyses showed that RAPD is able to differentiate mainly at the species level, while ERIC is effective at the strain level and therefore more consistent with cultivation characteristics. The results indicate that the method of ERIC-PCR is more rapid and reliable than RAPD, and may substitute for RAPD in research related to the genetic identification and genetic diversity in Auricularia.
出处 《微生物学报》 CAS CSCD 北大核心 2004年第6期805-810,共6页 Acta Microbiologica Sinica
基金 上海市农业科学院发展基金项目~~
关键词 木耳属 ERIC-PCR RAPD 遗传多样性 Auricularia, ERIC-PCR, RAPD analysis, Genetic diversity
  • 相关文献

参考文献12

  • 1Lowy B. A morphological basis for classifying the species of Auricularia. Mycologia, 1951, 43: 351-358.
  • 2Lowy B. The genus Auricularia. Mycologia, 1952, 44:656-692.
  • 3Mark E B, Les J S, David H M. Phylogenetic relationships in auriculariaceous basidiomycetes based on 25S ribosomal DNA sequences. Mycologia, 1995, 87(6): 821-840.
  • 4Redondo V A D P, Blanco N G D. Comparison of different PCR approaches for typing of Francisella tularensis strains. Journal of Clinical Microbiology, 2000, 1016-1022.
  • 5Yves Millemann, Marie-Claude Lesage-Descauses, Jean-Pierre Lafont, et al. Comparison of random amplified polymorphic DNA analysis and enterobacterial repetitive intergenic consensus-PCR for epidemiological studies of Salmonella. FEMS Immunology and Medica
  • 6Moissenet D, Valcin M, Marchand V, et al. Comparative DNA analysis of Bordetella pertussis clinical isolates by pulsed-field gel electrophoresis, randomly amplified polymorphism DNA, and ERIC polymerase chain reaction. FEMS Microbiology Letters, 1996, 143
  • 7Kurt Houf, Lieved De Zutter, Jan Van Hoof, et al. Assessment of the genetic diversity among Arcobacters isolated from poultry products by using two PCR-based typing methods. Applied and Environmental Microbiology, 2002, 68: 2172-2178.
  • 8Wanderley Dias da Silveira, Alessandra Ferreira, Marcela Lancellotti, et al. Clonal relationships among avian Escherichia coli isolates determined by enterobacterial repetitive intergenic consensus (ERIC)-PCR. Veterinary Microbiology, 2002, 89: 323-328.
  • 9Mehta A, Mehta Y R, Tosato Y B. ERIC- and REP-PCR amplify non-repetitive fragments from the genome of Drechslera avenae and Stemphylium solani. FEMS Microbiology Letters, 2002, 211: 51-55.
  • 10Leonardo A S, Stefania Z, Ilaria D, et al. Enterobacterial repetitive intergenic consensus sequences as molecular targets for typing of Mycobacterium tuberculosis strains. Journal of Clinical Microbiology, 1998, 36:128-132.

同被引文献70

引证文献8

二级引证文献27

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部