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首页> 外文期刊>Journal of Clinical Microbiology >Comparison of two molecular methods for tracing nosocomial transmission of Escherichia coli K1 in a neonatal unit.
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Comparison of two molecular methods for tracing nosocomial transmission of Escherichia coli K1 in a neonatal unit.

机译:两种分子方法用于追踪新生儿单位中大肠杆菌K1的医院内传播。

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Escherichia coli K1, a normal inhabitant of the human flora, is also an important cause of serious infections in newborns. We compared two molecular methods, ribotyping and arbitrarily primed polymerase chain reaction (AP-PCR), to study the apparent nosocomial transmission of an E. coli K1 clone in a nursery for premature neonates. Sixty-two E. coli K1 strains isolated from 41 premature neonates from December 1991 to June 1992 and six strains isolated from ambient sources were studied. Eight E. coli K1 strains isolated from infants in the nursery between 1989 and September 1991 were included as controls. The properties of the strains isolated between December 1991 and June 1992 were as follows: 43 belonged to ribotype I, 12 belonged to ribotype III, and the remaining 13 isolates were distributed among 10 ribotypes. The eight control strains belonged to seven different ribotypes, but none was ribotype I. Between December 1991 and February 1992, the majority of strains from premature infants colonized with E. coli K1 were of ribotype I. Isolates from the ventilation system and from a storage shelf were also of ribotype I. When DNA from 56 selected strains was tested by AP-PCR by using the 5'-TTGTAAAACGACGGCCAG-3' oligonucleotide, 15 different profiles were obtained. Twenty-five of 56 strains were of ribotype I and had identical profiles by AP-PCR. Strains with ribotypes VI, VII, and X to XV had different profiles by AP-PCR. We conclude that ribotyping and AP-PCR correlate well and permit demonstration of the nosocomial dissemination of E. coli K1 in a unit for premature neonates.
机译:大肠杆菌K1是人类菌群的正常栖息地,也是新生儿严重感染的重要原因。我们比较了两种分子方法,即核糖分型法和任意引发的聚合酶链反应(AP-PCR),以研究早产儿在苗圃中大肠杆菌K1克隆的明显医院内传播。 1991年12月至1992年6月,从41例早产儿中分离出62株大肠杆菌K1菌株,并从环境中分离出6株。从1989年至1991年9月间从托儿所婴儿中分离出的八株大肠杆菌K1菌株作为对照。 1991年12月至1992年6月间分离出的菌株的特性如下:43个属于I型核糖体,12个属于III型核糖体,其余的13个分离株分布在10个核糖型中。八个对照菌株属于七个不同的核糖型,但没有一个是核糖型I。在1991年12月至1992年2月之间,来自大肠杆菌K1定植的早产婴儿的大多数菌株都是核糖型I。从通风系统和储藏室分离当使用5'-TTGTAAAACGACGGCCAG-3'寡核苷酸通过AP-PCR测试来自56个所选菌株的DNA时,获得了15个不同的谱。 56个菌株中有25个是I型核糖,通过AP-PCR具有相同的特征。通过AP-PCR,具有VI,VII和X至XV核糖型的菌株具有不同的谱。我们得出的结论是,核糖分型法和AP-PCR相关性很好,并可以证明早产新生儿在单位内传播大肠杆菌K1。

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