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首页> 外文期刊>International journal of medical microbiology: IJMM >Phenotypic and molecular characterization of Escherichia albertii: Further surrogates to avoid potential laboratory misidentification
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Phenotypic and molecular characterization of Escherichia albertii: Further surrogates to avoid potential laboratory misidentification

机译:Escherichia Albertii的表型和分子表征:避免潜在的实验室错误识别的进一步替代物

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Escherichia albertii is an emerging gastrointestinal pathogen, related to Escherichia coli, which can be misidentified as enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC), due to the presence of the eae gene in E. albertii. The aim of this study was to verify our hypothesis that E. coli cytolethal distending toxin-II (Eccdt-II) gene-positive E. coli is E. albertii and to accumulate the data regarding the bacteriological characteristics of E. albertii. For these purposes, we attempted to detect E. albertii in eae gene-positive bacteria previously identified as E. coli and to examine if re-identified E. albertii contained Eccdt-II-homologous gene and remaining eae gene-positive E. coli did not. A total of 373 eae gene-positive E. coli strains were analyzed by biochemical tests, multilocus sequence analysis and an E. albertii-specific PCR. The strains re-identified as E. albertii were also examined for the presence of cdt genes by using P-32-labled DNA probes, followed by their toxin-typing. Of the 373 strains, 17 were re-identified as E. albertii by three above-mentioned methods. Furthermore, all the 17 re-identified E. albertii possessed cdt genes highly homologous to Eccdt-II and Eacdt genes. Moreover, Eccdt-I or both Eccdt-I and stx2f genes were detected in two re-identified E. albertii strains. However, the remaining 356 strains did not carry such cdt genes. These data indicate that all re-identified E. albertii isolates specifically carried cdt genes homologous to Eccdt-II and Eacdt genes. We suggest that Eccdt-II gene-positive E. coli may be identical to E. albertii.
机译:Escherichia Albertii是一种与大肠杆菌有关的新兴胃肠病原体,其由于E.Albertii中的EAE基因存在,可以被筛选为肠道致病大肠杆菌(EBEC)和肠球鼠肠)。本研究的目的是验证我们的假设,即大肠杆菌细胞素差异的毒素-II(ECCDT-II)基因阳性大肠杆菌是E.Albertii,并积累关于E.Albertii的细菌学特征的数据。出于这些目的,我们试图检测以前鉴定为大肠杆菌的EAE基因阳性细菌中的E.Albertii,并检查重新鉴定的E.Albertii是否含有ECCDT-II-同源基因和剩余的EAE基因阳性大肠杆菌不是。通过生化试验,多层序列分析和E.Albertii-特异性PCR分析了总共373个EAE基因阳性大肠杆菌菌株。还通过使用使用P-32载DNA探针进行CDT基因的存在,将其重新鉴定为E.Albertii的菌株。在373个菌株中,通过三种上述方法重新鉴定为E. Albertii。此外,所有17重新鉴定的E.Albertii具有与ECCDT-II和EACDT基因高度同源的CDT基因。此外,在两个重新鉴定的E.Albertii菌株中检测到ECCDT-I或ECCDT-I和STX2F基因。然而,剩余的356株菌株未携带此类CDT基因。这些数据表明所有重新鉴定的E.Albertii分离物特异性地将CDT基因与ECCDT-II和EACDT基因同源。我们表明ECCDT-II基因阳性大肠杆菌可能与E. Albertii相同。

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