期刊文献+

PCR法制备地高辛标记探针斑点杂交检测鳗弧菌 被引量:4

Detection of Vibrio anguillarum by Dot Blot Hybridization with Digoxigenin Labeled Probe by PCR
下载PDF
导出
摘要 以鳗弧菌(Vibrio anguillarum)toxR基因内366~571bp之间的基因序列为靶序列,采用PCR法制备对鳗弧菌特异性的地高辛标记DNA探针,探针长度为206bp。选取2株鳗弧菌和8株与鳗弧菌亲缘关系非常接近的常见水产动物致病弧菌,通过斑点杂交法对制备的探针进行特异性检测,结果显示该探针对鳗弧菌杂交阳性,而与弧菌属的其它8株细菌均无交叉反应。这表明该地高辛标记探针具有很强的特异性,它能够很好地对鳗弧菌感染进行检测。 A digoxigenin labeled DNA probe was produced by PCR method using toxR gene between 366 bp and 571 bp of Vibrio anguillarum as a target. The length of probe was 206 bp. Together with two V. anguillarum strains, ten pathogenic vibrio strains were chosen to detect the specificity of probe for V. anguillarum by dot blot hybridization. Result showed that the probe was able to hybridize with V. anguillarum. And no hybridization signals were observed using other eight vibrio strains most close to V. anguillarum, which demonstrated that the probe had strong specificity and had high value in detecting V. anguillarum.
出处 《淮海工学院学报(自然科学版)》 CAS 2008年第2期66-69,共4页 Journal of Huaihai Institute of Technology:Natural Sciences Edition
基金 淮海工学院自然科学基金资助项目(Z2006036)
关键词 鳗弧菌 PCR法 地高辛标记探针 斑点杂交 V. anguillarum PCR digoxigenin labeled DNA probe dot blot hybridization
  • 相关文献

参考文献12

  • 1郑国兴,沈亚林,李何.中国对虾病原菌(鳗弧菌)的研究[J].水产学报,1990,14(1):1-7. 被引量:57
  • 2EGIDIUS E. Vibriosis: pathogenicity and pathology: a review[J]. Aquaculture, 1987,67 : 15-28.
  • 3QIN Lei, WANG Yingeng, ZHANG Zheng, et al. The first report on fin rot disease of cultured turbot, cophthalmus maximus (L) in China[J]. Journal of Aquatic Animal Health, 2006,18 : 83-89.
  • 4VIVARES C P,GUESDON J. Nucleic acid probes in aquatic bacteriology [J]. Aquaculture, 1992, 107: 147- 154.
  • 5REICH K A,SCHOOLNIK G K. The light organ symbiont Vibrio fischeri possesses a homolog of the Vibrio cholerae transmembrane transcriptional activator toxR [J ]. Journal of Bacteriology, 1994, 176 ( 10 ) : 3085- 3088.
  • 6VUDDHAKUL V T,NAKAI T,MATSUMOTO C,et al. Analysis of the gyrB and toxR gene sequences of Vibrio hollisae and the development of the gyrB-and toxR- targeted PCR methods for isolation of V. hollisae from the environment its identification[J]. Applied Environment Microbiology, 2000, 66 (8): 3506-3514.
  • 7KIM Y B,OKUDA J, MATSUMOTO C,et al. Identification of Vibrio parahaemolyticus strains at the species level by PCR targeted to the toxR gene[J]. Journal of Clinical Microbiology, 1999,37(4) : 1173-1177.
  • 8余俊红,陈吉祥,厉云,苟万里,纪伟尚,徐怀恕.聚合酶链反应(PCR)检测花鲈鳗弧菌感染[J].黄渤海海洋,2002,20(2):60-64. 被引量:17
  • 9GONZALEZ S F,OSORIO C R, SANTOR Y, et al. Development of a PCR-based method for the detection of Listonella anguillarum in fish tissues and blood samples[J]. Diseases of Aquatic Organisms, 2003,55 (2) :109-115.
  • 10REHNSTAM A S, NORQVIST A, WORF-WATZ H,et al. Identification of Vibrio anguillarum in fish by using partial 16S rRNA sequences and a specific 16S rRNA oligonucleotide probe[J]. Applied Environment Microbiology, 1989,55(8) : 1907-1910.

二级参考文献4

共引文献71

同被引文献78

引证文献4

二级引证文献20

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