首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Typing and Subtyping of 83 Clinical Isolates Purified from Surgically Implanted Silicone Feeding Tubes by Random Amplified Polymorphic DNA Amplification
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Typing and Subtyping of 83 Clinical Isolates Purified from Surgically Implanted Silicone Feeding Tubes by Random Amplified Polymorphic DNA Amplification

机译:通过随机扩增的多态性DNA扩增从外科植入硅胶喂食管中纯化的83种临床分离株的分型和分型。

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摘要

In this study, 83 clinical isolates purified from biofilms colonizing 18 silicone gastrostomy devices (12 “buttons” and six tubes converted to skin level devices) were selected for subtype characterization utilizing genetic analysis. The tubes, previously used for feeding, remained in place for 3 to 47 months (mean, 20.0 months) in children ranging in age from 6 months to 17 years. Classification of specific microbes using random amplified polymorphic DNA (RAPD) analysis revealed genetic similarities and differences among isolates belonging to the same genus. Both gram-positive and -negative bacteria were investigated, including 2 isolates of Bacillus brevis, 4 isolates of Bacillus licheniformis, 2 isolates of Bacillus pumilus, 3 isolates of Enterococcus durans, 19 isolates of Enterococcus faecalis, 8 isolates of Enterococcus faecium, 2 isolates of Enterococcus hirae, 7 isolates of Escherichia coli, 8 isolates of Lactobacillus plantarum, 19 isolates of Staphylococcus aureus, 2 isolates of Staphylococcus epidermidis, and 7 isolates of Staphylococcus saprophyticus. Amplified DNA fragments (amplicons) provided species-specific fingerprints for comparison by agarose gel electrophoresis. A total of 62 distinct RAPD types were categorized from the five genera studied. Typing analysis suggested cross acquisition of E. coli, E. faecalis, and S. aureus in three patient pairs. Genomic polymorphism detection proved efficient and reliable for classifying bacterial subtypes isolated from biofilms adhering to various portions of commonly employed enteral access tubes.
机译:在这项研究中,选择了83个从生物膜中纯化的临床分离株,这些生物膜定居于18个硅酮胃造口术设备(12个“纽扣”和6个转换为皮肤水平设备的试管)中,以利用遗传分析进行亚型表征。以前用于喂养的试管在6个月至17岁的儿童中保留了3到47个月(平均20.0个月)。使用随机扩增多态性DNA(RAPD)分析对特定微生物进行分类,揭示了属于同一属的分离株之间的遗传相似性和差异。对革兰氏阳性和阴性细菌均进行了调查,包括短杆菌芽孢杆菌2株,地衣芽孢杆菌4株,短小芽孢杆菌2株,杜兰肠球菌3株,粪肠球菌19株,粪肠球菌8株,粪肠球菌2株。平肠球菌,大肠杆菌7株,植物乳杆菌8株,金黄色葡萄球菌19株,表皮葡萄球菌2株,腐生葡萄球菌7株。扩增的DNA片段(扩增子)提供了物种特异性的指纹,可通过琼脂糖凝胶电泳进行比较。从研究的五个属中总共归类出62种不同的RAPD类型。分型分析建议在三对患者中交叉采集大肠杆菌,粪肠球菌和金黄色葡萄球菌。基因组多态性检测被证明是有效和可靠的,用于对从粘附在常用肠管的各个部分的生物膜分离出的细菌亚型进行分类。

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