首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Use of digoxigenin-labelled oligonucleotide DNA probes for VT2 and VT2 human variant genes to differentiate Vero cytotoxin-producing Escherichia coli strains of serogroup O157.
【2h】

Use of digoxigenin-labelled oligonucleotide DNA probes for VT2 and VT2 human variant genes to differentiate Vero cytotoxin-producing Escherichia coli strains of serogroup O157.

机译:用洋地黄毒苷标记的VT2和VT2人类变异基因寡核苷酸DNA探针区分O157血清群的产生Vero细胞毒素的大肠杆菌菌株。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Digoxigenin-labelled oligonucleotide DNA probes specific for B-subunit genes of Vero cytotoxin 2 (VT2) and a variant of VT2 (VT2vha) were used to differentiate 116 strains of Escherichia coli serogroup O157 belonging to phage types 1, 2, 4, 8, 14, and 49. Of these strains, 38% had sequences for both VT2 and VT2vha, 38% had sequences for VT2 only, and 24% had sequences for VT2vha only. Oligonucleotide probe hybridization subdivided strains of all of the phage types except phage type 1. The greatest variation in toxin gene pattern was observed with strains of phage type 14, for which there were six distinct patterns when the presence or absence of VT1 genes was also considered. Two strains from each phage type group were examined for bacteriophages encoding VT production. Two of the six VT2vha-producing strains carried phage from which DNA hybridized with the VT2vha-specific probe. Phages were not detected in the remaining four VT2vha strains, suggesting that genes may be chromosomally located or associated with a defective prophage. In contrast, seven of the eight VT2 strains carried phages from which DNA hybridized with the VT2-specific probe. Two strains of E32511 (O157:H-) were also investigated. One strain (E32511A) possessed gene sequences for both VT2 and VTvha and was shown to carry phage possessing gene sequences for VT2. With strain E32511B, however, phages were not detected and DNA hybridized only with the VT2vha probe. Analysis of total genomic DNA digested with restriction endonuclease EcoRI showed that polymorphisms were seen with VT2 strains and not with VT2vha strains.
机译:使用洋地黄毒苷标记的Vero细胞毒素2(VT2)B亚基基因和VT2变体(VT2vha)特异的寡核苷酸DNA探针来区分属于噬菌体类型1,2,4,8的116株大肠杆菌O157血清群。分别参见图14和图49。在这些菌株中,有38%的菌株同时具有VT2和VT2vha的序列,38%的菌株仅具有VT2的序列,24%的菌株仅具有VT2vha的序列。寡核苷酸探针杂交将除了噬菌体1型以外的所有噬菌体类型的菌株细分。在噬菌体14型菌株中观察到毒素基因模式的最大变化,当同时考虑是否存在VT1基因时,有六个不同的模式。检查来自每个噬菌体类型组的两个菌株的编码VT产生的噬菌体。六株产生VT2vha的菌株中有两株带有噬菌体,DNA与VT2vha特异性探针杂交。在其余四个VT2vha菌株中未检测到噬菌体,这表明基因可能位于染色体上,或与缺陷的原噬菌体相关。相反,八株VT2菌株中有七株带有噬菌体,DNA与VT2特异性探针杂交。还研究了两株E32511(O157:H-)。一种菌株(E32511A)同时具有VT2和VTvha的基因序列,并显示携带具有VT2的基因序列的噬菌体。但是,对于E32511B菌株,未检测到噬菌体,DNA仅与VT2vha探针杂交。用限制性核酸内切酶EcoRI消化的总基因组DNA分析表明,在VT2菌株中观察到多态性,而在VT2vha菌株中观察不到。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号