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检测益生菌菌株大肠埃希菌 Nissle 1917(美常安)降低长期护理机构老年居民携带多重耐药大肠埃希菌的能力。

Testing probiotic strain Escherichia coli Nissle 1917 (Mutaflor) for its ability to reduce carriage of multidrug-resistant E. coli by elderly residents in long-term care facilities.

机构信息

Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.

Department of Medical and Surgical Sciences, University of Otago, Dunedin, New Zealand.

出版信息

J Med Microbiol. 2011 Mar;60(Pt 3):366-370. doi: 10.1099/jmm.0.025874-0. Epub 2010 Dec 2.

Abstract

A high carriage rate of multidrug-resistant Escherichia coli (MDREC) was observed in elderly residents in long-term care facilities. A double-blinded, placebo-controlled trial was carried out to determine whether the probiotic product E. coli strain Nissle 1917 (Mutaflor) would compete with MDREC in the bowel and thereby reduce the prevalence of the multiresistant bacteria in faeces and urine. Sixty-nine patients excreting norfloxacin-resistant E. coli were randomized to probiotic or placebo groups and administered capsules twice daily. The daily dose of probiotic was 5×10(9)-5×10(10) bacteria. Faecal and urine samples were cultured at baseline and during and after the treatment period. A reduction in baseline carriage was not influenced by probiotic administration. The probiotic strain was detected in faecal specimens collected during the treatment period of only two out of 12 probiotic group subjects that were tested. Genotyping of norfloxacin-resistant E. coli isolates showed that 32 strains were prevalent among the patients. Thus, E. coli Nissle 1917 does not have the capacity to compete effectively with MDREC in the bowel of elderly patients.

摘要

在长期护理机构的老年居民中,观察到多药耐药大肠杆菌(MDREC)的携带率很高。进行了一项双盲、安慰剂对照试验,以确定益生菌产品大肠杆菌菌株 Nissle 1917(Mutaflor)是否会与肠道中的 MDREC 竞争,从而降低粪便和尿液中多耐药菌的流行率。69 名排泄诺氟沙星耐药大肠杆菌的患者被随机分配到益生菌组或安慰剂组,并每天服用两次胶囊。益生菌的每日剂量为 5×10(9)-5×10(10)个细菌。在基线时以及治疗期间和之后采集粪便和尿液样本进行培养。基线携带量的减少不受益生菌给药的影响。在接受治疗的 12 名益生菌组受试者中,只有 2 名受试者的粪便标本中检测到益生菌菌株。对诺氟沙星耐药大肠杆菌分离株的基因分型显示,32 株菌株在患者中普遍存在。因此,大肠杆菌 Nissle 1917 没有能力在老年患者的肠道中有效地与 MDREC 竞争。

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