首页> 美国卫生研究院文献>The Journal of Veterinary Medical Science >A PCR-RFLP assay to detect and type cytolethal distending toxin(cdt) genes in Campylobacterhyointestinalis
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A PCR-RFLP assay to detect and type cytolethal distending toxin(cdt) genes in Campylobacterhyointestinalis

机译:PCR-RFLP检测可检测和鉴定细胞致死性膨胀毒素弯曲杆菌中的(cdt)基因胃肠道

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摘要

Campylobacter hyointestinalis is considered as an emerging zoonotic pathogen. We have recently identified two types of cytolethal distending toxin (cdt) gene in C. hyointestinalis and designated them as Chcdt-I and Chcdt-II. In this study, we developed a PCR-restriction fragment length polymorphism (RFLP) assay that can differentiate Chcdt-I from Chcdt-II. When the PCR-RFLP assay was applied to 17 other Campylobacter strains and 25 non-Campylobacter strains, PCR products were not obtained irrespective of their cdt gene-possession, indicating that the specificity of the PCR-RFLP assay was 100%. In contrast, when the PCR-RFLP assay was applied to 35 C. hyointestinalis strains including 23 analyzed in the previous study and 12 newly isolated from pigs and bovines, all of them showed the presence of cdt genes. Furthermore, a restriction digest by EcoT14-I revealed that 29 strains contained both Chcdt-I and Chcdt-II and 6 strains contained only Chcdt-II, showing 100% sensitivity. Unexpectedly, however, PCR products obtained from 7 C. hyointestinalis strains were not completely digested by EcoT14-I. Nucleotide sequence analysis revealed that the undigested PCR product was homologous to cdtB but not to Chcdt-IBor Chcdt-IIB, indicating the presence of another cdtgene-variant. Then, we further digested the PCR products with DdeI in addition toEcoT14-I, showing that all three cdt genes, including a possible newChcdt variant, could be clearly differentiated. Thus, the PCR-RFLPassay developed in this study is a valuable tool for evaluating the Chcdtgene-profile of bacteria.
机译:猪肠弯曲杆菌被认为是一种新兴的人畜共患病原体。我们最近在豚肠弯曲杆菌中鉴定了两种类型的细胞致死性扩张毒素(cdt)基因,并将其命名为Chcdt-I和Chcdt-II。在这项研究中,我们开发了一种PCR限制性片段长度多态性(RFLP)分析法,可以区分Chcdt-I与Chcdt-II。当将PCR-RFLP测定法应用于其他17个弯曲杆菌属菌株和25个非弯曲杆菌属菌株时,无论其cdt基因是否存在,均未获得PCR产物,这表明PCR-RFLP测定法的特异性为100%。相反,当将PCR-RFLP测定法应用于35例猪胃肠炎菌株时,包括先前研究中分析的23种菌株和从猪和牛中新分离的12种菌株,所有菌株均显示了cdt基因的存在。此外,通过EcoT14-I的限制性消化显示29个菌株同时包含Chcdt-I和Chcdt-II,而6个菌株仅包含Chcdt-II,显示出100%的敏感性。然而,出乎意料的是,从7种猪胃肠道菌株获得的PCR产物没有被EcoT14-1完全消化。核苷酸序列分析表明,未消化的PCR产物与cdtB同源,但与Chcdt-IB同源或Chcdt-IIB,表示存在另一个cdt基因变异。然后,我们进一步用DdeI消化了PCR产物,EcoT14-I,显示所有三个cdt基因,包括可能的新Ch cdt 变体可以清楚地区分。因此,PCR-RFLP这项研究开发的检测方法是评估Ch cdt 的有价值的工具细菌的基因特征。

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