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首页> 外文期刊>Journal of Clinical Microbiology >Molecular typing of Salmonella typhi strains from Dhaka (Bangladesh) and development of DNA probes identifying plasmid-encoded multidrug-resistant isolates.
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Molecular typing of Salmonella typhi strains from Dhaka (Bangladesh) and development of DNA probes identifying plasmid-encoded multidrug-resistant isolates.

机译:来自达卡(孟加拉国)的鼠伤寒沙门氏菌菌株的分子分型和鉴定质粒编码的耐多药分离株的DNA探针的开发。

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Seventy-eight Salmonella typhi strains isolated in 1994 and 1995 from patients living in Dhaka, Bangladesh, were subjected to phage typing, ribotyping, IS200 fingerprinting, and PCR fingerprinting. The collection displayed a high degree of genetic homogeneity, because restricted numbers of phage types and DNA fingerprints were observed. A significant number of the S. typhi strains (67%) were demonstrated to be multiple drug resistant (MDR). The vast majority of the MDR strains were resistant to chloramphenicol, ampicillin, trimethoprim, streptomycin, sulfamethoxazole, and tetracycline (R type CATmSSuT), a resistance phenotype that has also frequently been observed in India. Only two strains displayed a distinct MDR phenotype, R type AT-mSSuT. Pulsed-field gel electrophoresis demonstrated the presence of large plasmids exclusively in the MDR strains of both R types. The plasmids present in the S. typhi strains of R type CATmSSuT could be conjugated to Escherichia coli and resulted in the complete transfer of the MDR phenotype. PCR fingerprinting allowed discrimination of MDR and susceptible strains. The DNA fragments enabling discrimination of MDR and susceptible S. typhi strains by PCR were useful genetic markers for identifying MDR encoded by large plasmids of the H1 incompatibility group.
机译:1994年和1995年从孟加拉国达卡市的患者中分离出的78株伤寒沙门氏菌菌株进行了噬菌体分型,核糖分型,IS200指纹图谱和PCR指纹图谱。该集合显示出高度的遗传同质性,因为观察到数量有限的噬菌体类型和DNA指纹。大量伤寒沙门氏菌菌株(67%)被证明具有多重耐药性(MDR)。绝大多数MDR菌株对氯霉素,氨苄青霉素,甲氧苄啶,链霉素,磺胺甲恶唑和四环素(R型CATmSSuT)具有抗性,这种抗性表型在印度也很常见。仅两种菌株显示出独特的MDR表型,R型AT-mSSuT。脉冲场凝胶电泳表明,两种R型MDR菌株都只存在大型质粒。 R型CATmSSuT的伤寒链球菌菌株中存在的质粒可以与大肠杆菌缀合,并导致MDR表型的完全转移。 PCR指纹图谱可区分MDR和易感菌株。能够通过PCR区分MDR和易感伤寒链球菌菌株的DNA片段是有用的遗传标记,可用于鉴定由H1不相容性组的大质粒编码的MDR。

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