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首页> 外文期刊>Infection control and hospital epidemiology >Molecular characterization of methicillin-resistant coagulase-negative staphylococci from a neonatal intensive care unit.
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Molecular characterization of methicillin-resistant coagulase-negative staphylococci from a neonatal intensive care unit.

机译:新生儿重症监护病房的耐甲氧西林凝固酶阴性葡萄球菌的分子特征。

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摘要

OBJECTIVE: To evaluate clonal dissemination of methicillin-resistant coagulase-negative staphylococci (CNS). SETTING: Neonatal intensive care unit of a 180-bed, university-affiliated general hospital. PATIENTS: Neonates admitted to the neonatal intensive care unit between March 1999 and October 2000, from whom CNS were isolated as a unique pathogen. Patients from other wards from whom epidemiologically unrelated staphylococci strains were obtained served as control-patients. METHODS: Conventional methods were used for phenotypic characterization of CNS. Methicillin resistance was determined by mecA polymerase chain reaction (PCR) amplification. Genotypic characterization was done by random amplification of DNA with degenerated primers (RAPD) and repetitive element sequence-based PCR (rep-PCR). RESULTS: Forty methicillin-resistant CNS isolates obtained from neonates were characterized as Staphylococcus epidermidis (33), S. hominis (5), S. warneri (1), and S. auricularis (1). Both RAPD and rep-PCR indicated the presence of 4 different clones among the 33 S. epidermidis isolates. In turn, the 4 randomly selected, epidemiologically unrelated methicillin-resistant CNS strains obtained from control-patients showed 3 new profiles by RAPD and 2 by rep-PCR, which differed from the corresponding patterns mentioned earlier. Persistence of S. hominis in a neonate could be assessed by both genotypic techniques. CONCLUSIONS: The molecular characterization of the methicillin-resistant CNS studied indicated dissemination of one particular methicillin-resistant CNS clone among the neonates in the ward studied. Although RAPD showed a superior power to discriminate among methicillin-resistant CNS isolates, both RAPD and rep-PCR detected intraspecific and interspecific genomic diversity.
机译:目的:评估耐甲氧西林凝固酶阴性葡萄球菌(CNS)的克隆传播。地点:大学附属综合医院,拥有180张床的新生儿重症监护室。患者:1999年3月至2000年10月间进入新生儿重症监护室的新生儿,从中分离出CNS作为独特的病原体。从其他病区获得流行病学无关的葡萄球菌菌株作为对照患者。方法:采用常规方法对中枢神经系统进行表型鉴定。通过mecA聚合酶链反应(PCR)扩增确定对甲氧西林的耐药性。通过用简并引物(RAPD)随机扩增DNA和基于重复元件序列的PCR(rep-PCR)进行基因型鉴定。结果:从新生儿获得的40株耐甲氧西林的CNS分离株的特征为表皮葡萄球菌(33),人沙门氏菌(5),华氏链球菌(1)和耳形链球菌(1)。 RAPD和rep-PCR均表明在33种表皮葡萄球菌分离物中存在4个不同的克隆。反过来,从对照患者那里随机选择的4种与流行病学无关的耐甲氧西林CNS菌株通过RAPD显示3个新图谱,通过rep-PCR显示2个新图谱,这与前面提到的相应模式不同。两种基因型技术均可评估人乳链球菌在新生儿中的持久性。结论:耐甲氧西林的中枢神经系统的分子特征表明在病房中有一个特定的耐甲氧西林的中枢神经系统克隆在新生儿中传播。尽管RAPD表现出更好的区分耐甲氧西林CNS分离物的能力,但RAPD和rep-PCR均可检测到种内和种间基因组多样性。

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