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问号钩端螺旋体黄疸出血型和哥本哈根型血清型的限制性内切酶DNA分析

Restriction endonuclease DNA analysis of Leptospira interrogans serovars Icterohaemorrhagiae and Copenhageni.

作者信息

Tamai T, Sada E, Kobayashi Y

机构信息

First Department of Internal Medicine, Faculty of Medicine, Ehime University.

出版信息

Microbiol Immunol. 1988;32(9):887-94. doi: 10.1111/j.1348-0421.1988.tb01450.x.

Abstract

Leptospira interrogans serovar icterohaemorrhagiae strains Ictero No. I and RGA and serovar copenhageni strains M20, Shiromizu and Shibaura were examined by restriction endonuclease DNA analysis. Fifteen endonucleases (AluI, BamHI, BglII, EcoRI, HaeIII, HhaI, HindIII, KpnI, PstI, SacI, SalI, SmaI, StyI, XbaI and XhoI) were used as the digesting enzymes. Strain Ictero No. I showed endonuclease cleavage patterns which differed from those of the other four strains only when it was digested with enzymes KpnI and HindIII. When digested with KpnI, an extra band of about 5.4 kb was clearly produced, and when digested with HindIII, an extra band of about 25 kb was produced. When the other 13 enzymes were used, no differences were found between the endonuclease cleavage patterns among the five strains. Moreover, strains RGA, M20, Shiromizu and Shibaura could not be distinguished by the restriction endonuclease DNA analysis using all 15 endonucleases. In addition, six newly isolated leptospires from patients with leptospirosis and from Rattus norvegicus were compared with the Ictero No. I and M20 strains, by restriction endonuclease DNA analysis using enzymes KpnI and HindIII. Three leptospires belonging to serovar icterohaemorrhagiae showed the same endonuclease cleavage patterns as the M20 strain. The other three strains, which belong to serovar copenhageni, showed almost the same endonuclease cleavage patterns as the M20 strain; only the Kai ima 702 strain produced an extra band which was not identical to the Ictero No. I-specific extra band when digested with HindIII. The leptospiral restriction endonuclease DNA analysis has revealed taxonomic structures that are unrecognized by serology alone.

摘要

采用限制性内切酶DNA分析法对问号钩端螺旋体黄疸出血群菌株Ictero No. I和RGA以及哥本哈根群菌株M20、白水和芝浦进行了检测。使用了15种内切酶(AluI、BamHI、BglII、EcoRI、HaeIII、HhaI、HindIII、KpnI、PstI、SacI、SalI、SmaI、StyI、XbaI和XhoI)作为消化酶。菌株Ictero No. I仅在用KpnI和HindIII酶消化时,其内切酶切割模式与其他四种菌株不同。用KpnI消化时,明显产生了一条约5.4 kb的额外条带;用HindIII消化时,产生了一条约25 kb的额外条带。当使用其他13种酶时,这五种菌株的内切酶切割模式之间没有差异。此外,使用所有15种内切酶进行限制性内切酶DNA分析,无法区分菌株RGA、M20、白水和芝浦。此外,通过使用KpnI和HindIII酶进行限制性内切酶DNA分析,将6株新分离的来自钩端螺旋体病患者和褐家鼠的钩端螺旋体与Ictero No. I和M20菌株进行了比较。三株属于黄疸出血群的钩端螺旋体显示出与M20菌株相同的内切酶切割模式。另外三株属于哥本哈根群的菌株显示出与M20菌株几乎相同的内切酶切割模式;只有Kai ima 702菌株在用HindIII消化时产生了一条额外条带,该条带与Ictero No. I特异性额外条带不同。钩端螺旋体限制性内切酶DNA分析揭示了仅靠血清学无法识别的分类结构。

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