Hagen Ralf Matthias, Hinz Rebecca, Frickmann Hagen
Department of Tropical Medicine at the Bernhard Nocht Institute, German Armed Forces Hospital of Hamburg , Germany.
Department of Tropical Medicine at the Bernhard Nocht Institute, German Armed Forces Hospital of Hamburg , Germany ; Institute for Microbiology and Immunology, University Medicine Rostock , Germany.
Eur J Microbiol Immunol (Bp). 2015 Oct 21;5(4):281-4. doi: 10.1556/1886.2015.00037. eCollection 2015 Dec.
ESBL (extended-spectrum-β-lactamase)-positive Enterobacteriaceae, which colonized European soldiers in tropical Western African Mali, were subjected to a molecular assessment of their resistance determinants. By doing so, a better insight into the locally endemic pattern of ESBL-associated β-lactamase genes was aspired. From a previous study on diarrhea in European soldiers on deployment in tropical Mali, 15 ESBL-positive Escherichia coli with demonstrated high clonal diversity and one positive Klebsiella pneumoniae were assessed. Polymerase chain reactions (PCRs) for blaTEM and blaSHV β-lactamase genes with subsequent sequencing for the discrimination of ESBL- and non-ESBL variants were performed, followed by four group-specific PCRs for blaCTX-M genes. Non-ESBL-associated blaTEM-1 was identified in six out of 15 (40%) E. coli strains, while 100% of the assessed strains were positive for group I blaCTX-M . Considering the known clonal diversity of the assessed strains, the striking restriction to one group of blaCTX-M genes accounting for the ESBL phenotypes of the isolates suggests little genetic exchange in the local setting. Under such circumstances of restricted numbers of locally endemic target genes, PCR-based screening approaches for ESBL colonization might be promising.
产超广谱β-内酰胺酶(ESBL)的肠杆菌科细菌定殖于在热带西非马里的欧洲士兵体内,对其耐药决定因素进行了分子评估。通过这样做,旨在更好地了解ESBL相关β-内酰胺酶基因的本地流行模式。根据之前一项关于在热带马里部署的欧洲士兵腹泻情况的研究,对15株具有高度克隆多样性的ESBL阳性大肠杆菌和1株肺炎克雷伯菌阳性菌株进行了评估。进行了blaTEM和blaSHVβ-内酰胺酶基因的聚合酶链反应(PCR),随后进行测序以区分ESBL和非ESBL变体,接着对blaCTX-M基因进行了四组特异性PCR。在15株大肠杆菌菌株中的6株(40%)中鉴定出了非ESBL相关的blaTEM-1,而100%的评估菌株I组blaCTX-M呈阳性。考虑到所评估菌株已知的克隆多样性,导致分离株出现ESBL表型的blaCTX-M基因仅局限于一组,这表明在当地环境中基因交换很少。在本地流行的靶基因数量有限的这种情况下,基于PCR的ESBL定植筛查方法可能很有前景。